C = ContractCH = Contract to HireDP = Direct PlacementDOE = Depending on experienceGTW = Go To Work (no interview)

HOTTEST OPENINGS ARE HIGHLIGHTED

Research Associate, Downstream x3 – CH – UTC $17-30/hr DOE

From the hiring manager: “I have been asked to begin recruiting 3 Research Associate Positions for my Downstream PD Team. I am looking for candidates that satisfy all (or some) of the following criteria:

Junior and/or entry level in general, although not necessary, if other qualifications line up and the candidate is willing to discuss the situation.

The position will involve projects dedicated to developing purification protocols that yield an antibody product that meets our specifications of purity and stability.

General science education (BS is fine) and/or some degree of experience in the lab Specific areas of knowledge and/or experience that would be regarded as a plus:

o Protein purification: column chromatography principles and techniques, familiarity with AKTA systems and Unicorn software

o Buffer preparationo Centrifugation and filtrationo General understanding of protein biochemistry

“I would rather see more than less of the available resumes to get a feel for the breadth of available talent. The most important attributes I will be looking for is enthusiasm and trainability, and how those lines up with their education and experience.”

Project Coordinator – CH – UTC $17-25/hr Bachelor's Degree in the biology or chemistry is preferred. Minimum of 3-4 years of college

coursework in the sciences, or equivalent work experience is required. Aseptic manufacturing experience is strongly preferred. Good documentation, strong organizational and record keeping skills are essential. Excellent verbal and written communication skills are required. Must be a team player, customer service oriented, willing to learn, and able to work flexible

hours. The Project Coordinator is responsible for coordinating and running processes associated with the

manufacture of the customer's product in manufacturing. This includes working with Project Managers in communication with the customer, ensuring inventory is available to begin the process, and coordinating the scheduling of the job including the needs of personnel, equipment and space. The Project Coordinator is directly involved in the set-up, formulation and aseptic filling and lyophilization of buffers and solutions, and the timely completion of all associated documentation throughout the entire process. They are to ensure that personnel follow all regulations and written procedures applicable to the job. Project Coordinators will also write procedures, perform validations, and investigate failures as necessary. The ideal candidate should

be able to work with minimal instructions, and should be able to provide some direction to area technicians

Director, Upstream – DP – UTC $DOE BS/MS or PhD with 5 years+ upstream processing, prefer prior director- would probably look at

associate director DEPARTMENT: MANUFACTURING/OPERATIONS As a member of the senior management team, this individual will be involved in the production

and processing of recombinant proteins for clinical use. ESSENTIAL DUTIES AND RESPONSIBILITIES: Manage a complex workload for cell line development, upstream process development, and

upstream manufacturing activities. Responsible for leading a team of supervisors and technicians. Provide support to cross-functional teams to meet production or timeline demands. Demonstrate understanding and provide oversight on technical operations, safety, and Good

Manufacturing Practice. Provide oversight on upstream processes as well as cleanroom facility and equipment operations. Develop staff capabilities, creating a culture of safety, maintain training objectives, compliance

and collaboration while implementing process improvements where applicable Initiate, review, and revise cGMP Batch Production Records, SOP’s, Process Development

reports, and Manufacturing Summary reports. Ensure the completeness and accuracy of manufacturing documentation per approved procedures. JOB REQUIREMENTS: Expert in cell line development, upstream process development and upstream manufacturing

processes PhD’s degree in Life Sciences or Chemical Engineering with more than 7 years of relevant

experience in GMP production including aseptic processing or a BS / MS degree in Life Sciences or Chemical Engineering with more than 15 years of relevant experience.

Practical Experience with cGMP operations. More than 5 years of supervisory experience Must be proficient in Word and Excel.

Doc Control Specialist - CH - UTC $20/hr.+ We need a Document Control Assistant who has a strong quality background and mindset who

will be an advocate for the Quality system changes we are making (in other words, able to accept changes and able to think creatively to help with change. This individual will also need:

A minimum of two years of Quality Assurance experience, preferably within a cGMP environment within the Pharmaceutical / Biotech Industry.

Experience with Batch record and document review Experience with area / line clearance Experience with performing and writing investigations

Quality Operations Associate – C/CH – Torrey Pines $20-24/hr 70% on Document Control/Review (for next 2 months), 30% on QA role (product batch review,

QA release, daily kit verifications) ALL manual documentation The role’s process: Obtain the document à Doc Control, Doc Change Process à formatting,

editing, bounce back à get approval signatures à put into document mold MUST be a good communicator = Will be interfacing with reagent manufacturing, product

managers, quality consultants, regulatory head Will have weekly 1 on 1 with the hiring manager to touch base/check in since this is a BRAND

NEW ROLE MUST HAVES: good with Excel AND word, computer savvy, 3+ years of experience in this

field, self-motivated, attention to detail, ability to multi-taskPreferred experience:

College courses and experience in the appropriate scientific and quality disciplines. Three or more years of relevant industry experience in a Manufacturing Quality role. Proficient with office equipment, computer systems and other tools of the administration function

assigned. Proficient in using MS Office, WORD, Excel and other data systems is required Excellent written and verbal communication skills Must be detail-oriented with strong prioritization and organization skills Able to handle multiple tasks and work in a fast paced environment

Responsibilities: Assist with document authoring and editing under the document change control system including

creation and revision of SOPs to support quality processes. This responsibility requires formatting and routing the document including obtaining the appropriate approvals throughout the process.

Review of production documents including manufacturing/production batch records. Generate Certificate of Analysis (CoA) for products. Perform transactions such as Incoming Material Inspection. Responsible for exhibiting professional behavior with both internal/external business associates

that reflects positively on the company and is consistent with the company’s policies & practices. Understands and is aware of the quality consequences which may occur from the improper

performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.

Knowledgeable of federal and other regulations, e.g. QSR’s, ISO, ISO 13485, CMDR a plus.

Manufacturing Associate II AND III – DP – Sorrento Valley $45-55k for level II, $55-65k for level III The Manufacturing Associate III will assist with all aspects of production, including the

production of master mixes, controls, and assay kits. This position will manufacture products adhering to existing Quality System Regulations that are

accompanied by appropriate documentation.

The Manufacturing Associate III will review, edit, create, and maintain documents, including Standard Operating Procedures, Batch Records, and Purchasing Specifications.

Some administrative work may be required (maintaining inventory, and other duties as necessary).

Requires knowledge and skills normally acquired through the successful completion of a BS Degree in a scientific discipline.

Requires 2+ years of experience in a GMP regulated industry or equivalent combination of education and experience.

SKILLS / KNOWLEDGE / ABILITIES Direct working knowledge of a production environment, including use of SOPs, batch records,

ERP systems and purchasing specifications. Ability to recognize deviation from accepted practice is required. Strong working knowledge of PCR and molecular biology. Experience with sterile techniques and accurate pipetting skills. Meticulous and detailed oriented. Ability to follow Standardized Operating Procedures (SOPs) as well as written and verbal

instructions. Ability to work independently as well as in a team environment. Excellent written and verbal communication skills with the ability to train employees. Ability to manage multiple projects and changing priorities. Willingness to learn and take on new challenges. Able to use Adobe Acrobat, Illustrator, and

Photoshop for art work and graphics in documents.

Development Associate I, II, III – DP – Torrey Pines Pays $40-65k DOE Molecular Biologist with industry experience Will be doing development, supporting manufacturing Supports manufacturing technical support projects that can include generating analytical data for

an FDA submission. Performs the design, execution and documentation of moderately complex experiments that

support existing reagents and assays. Experimental design will include all of the appropriate controls.

Independently writes study protocols and reports that may be auditable. Maintains a laboratory notebook that records all aspects of experimental design and results,

following good documentation practices. When applicable, maintains electronic copies of experiments, procedures, instructions, data and analysis in appropriate locations.

Uses laboratory techniques such as preparation of buffers and media, aseptic technique, cell culture, specimen processing, PCR, gel and capillary electrophoresis and sequencing.

Independently operates laboratory equipment such as thermocyclers, spectrophotometers, fluorometers, centrifuges, cell counters, autoclaves, scales, capillary electrophoresis instrumentation, sequencers, real-time PCR platforms and DNA isolation workstations.

Performs data analysis using available software such as Microsoft Excel, JMP and GeneMapper. Cooperates and respectfully communicates with external customers and internal customers. Other duties, as assigned.

3+ years of experience in R&D (not just research), development and/or manufacturing Supports manufacturing technical support projects that can include generating analytical data for

an FDA submission. Performs the design, execution and documentation of moderately complex experiments that

support existing reagents and assays. Experimental design will include all of the appropriate controls.

Independently writes study protocols and reports that may be auditable. Maintains a laboratory notebook that records all aspects of experimental design and results,

following good documentation practices. When applicable, maintains electronic copies of experiments, procedures, instructions, data and analysis in appropriate locations.

Labeler – C – Sorrento Valley $13/hr AS or BS, labelling experience is ideal Must be good with attention to detail Requires knowledge and skills normally acquired through the successful completion of a BS

Degree in a scientific discipline. Prefers accessioning exp. data entry, accessioning

QC Analyst II x2 – C/CH – Torrey Pines $16-25/hr DOE The purpose of the QC Analyst II is to carry out assigned laboratory duties which may include

sampling, testing, and evaluating analytical data on samples such as raw materials, in-process and final products. In addition, will also participate in the development and validation of analytical methods.

2 years of relevant hands-on laboratory experience. BS degree in scientific discipline from an accredited college or university or equivalent

experience. Demonstrated computer proficiency, e.g., word processing, spreadsheets, graphing, etc Good knowledge of cGMPs and laboratory practices. Proficient in the operation and maintenance of basic laboratory instruments such as HPLC and

GC. Excellent observation skills and problem solving abilities. Ability to follow analytical procedures and protocols. Good laboratory techniques. Conduct laboratory tests in compliance with established internal Standard Test Methods,

compendial and vendor/partner supplied methods. Maintain organized records of tests performed and results obtained following company policies Assist in performing laboratory investigations. Write investigation report as required. Maintain a level of technical knowledge and understanding in the assigned areas of responsibility

that are consistent with the current scientific requirements of the company. Understand and comply with all company policies, safety procedures, and SOPs, including

cGMPs and cGLPs Assist in the preparation of analytical data for internal and external meetings and presentations.

Provide technical assistance and training to other laboratory personnel. Participate in the transfer of methods to/from the Quality Control department. Represent functional area in Project Teams, as required. Write documents for GMP compliance such as standard test methods, validation reports, and

SOPs.

Manufacturing Technician – CH – Sorrento Valley $15-25/hr DOE Bachelor’s Degree in Biochemistry, Biology, Chemistry, or a related field 1-5 years of experience in antibody purification or protein purification Solid understanding of antibody structure and hands-on experience with chromatography Good computer skills Follow SOP’s Perform all essential functions related to antibody purification manufacturing, including

centrifugation, making buffers, using the spectrophotometer, running SDS-PAGE gels, and performing endotoxin tests

Perform basic math calculations to determine the concentration and amount of antibodies Perform column chromatography manually as well as using FPLC Use of ERP database to execute production orders Maintenance of laboratory equipment and supplies

Manufacturing, Data Entry Clerk – C – Sorrento Valley $14/hr Job Description: The Manufacturing Data Entry Clerk will work closely with all of the

Manufacturing teams to understand and streamline Manufacturing production processes. The person in this position will be responsible for finishing production orders, creating labels for QC samples and bulks made by Manufacturing teams, working closely with inventory controllers to create Bin locations for purified and conjugated bulks and maintaining their accuracy, and reviewing, verifying, and scanning/attaching batch records into ERP system. This position will also be responsible for helping the Inventory and Planning teams to resubmit re-test samples and will perform other duties as necessary.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Helping to finish production orders and creating labels for QC samples and bulk materials Assisting with batch records (reviewing/verification and scanning/attaching) Helping the inventory controller to identify Bin locations and helping Planning teams to resubmit

re-test samples Performing job duties under ISO requirements such as following " line of clearance" rule and

following SOP's or work instructions Other duties as assigned Work Environment: work at computer in protein production lab Qualifications: BS Degree. open to non-degree with experience Perform antibody conjugation and purification

Follow SOPs to perform experiments. Use ERP database and other database to document activities.

Set up production specification for manufacturing Trouble-shooting problematic conjugations with emphasis on optimizing reaction condition

Recombinant Antibody Manager – DP – Sorrento Valley $120-145k The Recombinant Antibody Manager will be responsible for leading the Recombinant Antibody

group by developing methods of achieving a high level of antibody expression and ensuring that those methods are implemented to product high quality antibodies. This position will functional as an integral part of the Recombinant Antibody Development and Production Teams.

PhD in Biochemistry, molecular biology, cell biology, bioengineering or related Biological Science area

5 years of related industry experience, focusing on transient and/or cell line development for recombinant antibody expression and production

Previous project management and personnel management experience Expertise with stable cell line development for recombinant antibody production Extensive experience with recombinant antibody engineering and development Expertise with high level expression of recombinant antibodies in different expression systems

such as CHO, NS0, and HEK 293 Technical expertise in cell culture and stable cell line generation, process development, and

optimization Experience with the scale up recombinant antibody production to an industrial level Extensive experience with media optimization and scaling-up of bioreactor processes Strong Microsoft Word, EXCEL, PowerPoint, and FM database skills Familiarity with ISO 9001/ ISO13485, GLP or GMP compliance Lead the Recombinant Antibody Program, which will include designing and optimizing

recombinant antibody expression in both transient and stable expression systems Develop and maintain detailed and accurate electronic records related to cell line development to

support recombinant antibody manufacturing and process improvement Interface with manufacturing groups to provide on time and accurate material transfer support Analyze results of data and prepare recommendations for improvement or trouble shooting

Receptionist – CH – Sorrento Valley $12-15/hr Hours are 8-4:30pm. Mon-Fri Prefer a Sci background (degree or exp in a lab setting). NOTE: They do animal research so it

has to be someone that is ok with this. Job is answering phones, filing, client interaction, ordering supplies, etc. Will learn the business

side of things over time.

Lab Technician II – C – Sorrento Valley Up to $21/hr PART TIME – looking for a candidate who is IN SCHOOL that can work 20-30 hours per week

Job Description Buffer & media preparation, washing glassware, autoclaving, ordering lab supplies, preparing

fermenter vessels for use, general lab cleaning. Performs a wide variety of laboratory tasks. May make detailed observations, analyze data and interpret results. Maintains laboratory

equipment and inventory levels for laboratory supplies buffers/media. Will be responsible for buffer & media preparation in the research and development area,

including experiments as required and outlined. May also develop and maintain record keeping for experiments performed. Performs limited troubleshooting and calibration of instruments. Will perform glassware washing. MUST HAVES Buffer/media preparation experience, glassware cleaning experience, science lab background

and/or coursework, basic understanding Microsoft Office Skills/Experience High school diploma or associate degree with relevant work experience, prefer someone without

a bachelor's degree. Typically requires a minimum of 1-2 years of related experience. Professional or academic lab experience Previous buffer and/or media preparation is required, lab support experience including cleaning

glassware, autoclaving, able to learn tasks quickly and multitask, efficient in pipetting & sterile technique, able to work well in a team, preferred but not required experience – SDS-PAGE analysis, ELISA assay, protein purification, fermentation, protein conjugation

Doc Control Analyst II – C – Sorrento Valley Up to $22/hr FROM THE CLIENT: I don’t suggest much for the Doc Control. Candidates NEED to have

strong excel macro skills and word skills and be able to interpret technical data. The worker would really only be converting documents and handling change control.

Top Three Skills: excel, document control, word, QA, documentation, medical device Job Description:

The main function of the Document Control Analyst is to maintain and modify all required documentation for the company to ensure adherence to the Company’s Quality Management System (QMS). More specifically the Document Control Analyst will ensure all products manufactured at the company currently using Branan Medical Corp (BMC) documents are converted into the QMS.

Need someone to build/convert forms and handle change control of documents highly skilled in excel with macro and formulas, able to convert forms in word to excel form,

highly skilled in macros Highly skilled in word, able to convert/format documents. Use form building functions in word Key components of role, don’t necessarily need to have QA/Doc control background, but need to

be able to interpret/translate technical information. Work Environment: Classic document control position: need someone to build/convert forms

and handle change control of documents.

Key components of role, doesn't necessarily need to have QA/Doc control background, but need to be able to interpret/translate technical information.

Strong Administrative organization skill set. Knowledge of MS Outlook, Word, Excel, and PowerPoint in an office setting Experience and Education: High school Diploma- could also be fresh out of college as long as have Word/Excel skills listed

above 2-4 years of administrative experience Responsibilities Aid in writing, formatting and subsequent processing of documents (SOPs, MPs, RMS, Labeling)

relating to the implementation of BMC products into the AMDT QMS. Write/update procedures by using a template/feedback provided by a subject matter experts

(R&D, Quality, Operations). Initiate required forms to process the documents through an electronic or paper based document

management system. Work both independently and in a team environment Manage release and control of updates to documents. Control distribution of new releases and recall/destruction of obsolete documents Interview Information: Interview: Will have 1 hour phone screen, hour of standard Q&A, 2nd

half quiz on excel/word skills.

QA Assistant – C – Sorrento Valley Up to $19/hr As needed perform the following tasks: Assist with data entry and metric data collection for batch records, Send data update emails, logs, and forms as necessary Maintain logs as necessary Provide support to QA activities for regulatory compliance meetings and audits, (i.e.

Management Review support, FDA inspections, or regulatory audits). Assist with internal audits and agency audits. Log documents send into and returned from document vault Pull, copy and deliver documents to document vault Assist with Document Control activities as needed Filing various documents when required Assist with document retention activities Assist with maintaining the Document Control Room Pull documents as requested Review and disposition batch records if necessary Other responsibilities as assigned Responsible for exhibiting professional behavior with both internal/external business associates

that reflects positively on the company and is consistent with the company’s policies and practices

Preferred educational background: Bachelor’s Degree in relevant field (scientific)

Will take a new college grad, but candidate must have some type of work experience (does not necessarily need to be related, that is a bonus). Manager wants candidate to be accountable and have exposure to being in a work environment.

***great role for someone trying to get their foot in the door! Preferred experience: 1year of Quality Assurance experience in manufacturing environment preferred. QC experience

may work as well Prefer experience with 21 CFR 820, ISO 13485 regulations Experience in a GMP type environment (production, lab) preferred GMP good manufacturing

practices Some knowledgeable of federal and other regulations, e.g. QSR’s, ISO, ISO 13485, CMDR

bonus associate

Research Associate (5662) – C – Torrey Pines TOP PHARMA COMPANY Up to $20/hr We are seeking a highly motivated Research Associate to conduct in vivo studies. In particular, this person will be responsible for formulation preparation, animal dosing, blood

sampling and plasma preparations in a fast-pace drug discovery setting. Responsibilities also include harvest tissues in support of tox/pharmacology studies. Experience with automatic blood sampler and surgery will be a plus. A BS or an equivalent degree in biology or pharmaceutical-related discipline with 1 - 2 years of

industrial animal research experience and proficiency in formulation work, animal handling, dosing and sampling in rodents.

This individual is also expected to be highly organized, detail oriented and responsive to instructions, a team player, enthusiastic about drug discovery, and a strong communicator with strong work ethics.

Research Associate (5561) – C – Torrey Pines TOP PHARMA COMPANY Up to $28/hr Highly motivated Scientist to conduct bio-analytical work to measure small molecules in

different biological matrices. This work will involve extraction of samples in biological matrices collected from in vitro and in

vivo studies and quantitative analysis of small molecules using LC-MS/MS methods in a fast-pace drug discovery setting.

BS degree with 3-6 years of industrial research experience or MS degree with 2-4 years industrial research experience.

The ability to independently operate a triple-quad LC-MS/MS for quantification purposes is REQUIRED, no exceptions.

The individual will be proficient in sample preparation, LC-MS/MS operations for quantification of small molecules in biological matrices, and data processing using various software.

The experience in the use of Pheonix (WinNonLin) software, conduct of in vitro ADME assays (such as metabolic stability, permeability, and protein binding), and carrying out metabolite identification studies is a plus.

This individual is also expected to be highly organized, a team player, enthusiastic about drug discovery, and a strong communicator with strong work ethics.

Regulatory Specialist (5503) – C – Torrey Pines Up to $90/hr BS/BA degree in Scientific Discipline (Masters or higher preferred) with a minimum of 7 years in

the pharmaceutical industry, and a minimum of 5 years CMC regulatory (biologics preferred) experience.

Must have experience with CMC regulatory documents (NDA, MAA, CTD, BLA, supplements, responses and IND/CTAs)

Experience in the development of CMC regulatory strategy with a focus on BLA and global biologic marketing applications.

Thorough knowledge of FDA, EMEA and ICH guidelines. Knowledge of rest of world pre- and post-approval guidelines Have a solution-oriented approach to problem solving Expertise in the biologic drug development process and post approval activities Ability to work on complex projects and within cross-functional teams Prior supervisor or project management experience Experience with global CMC regulations for biological compounds. Responsible for the development of the CMC regulatory strategy for submissions. These

submissions include IND/CTA/BLA, NDA, CTD and MAA regulatory filings. Lead the preparation and review CMC submission documents, registration dossiers, health

authority briefing packages, and responses to health authorities with other relevant line functions. Interact with regulatory agencies and represent Regulatory CMC at regulatory agency meetings.

Prepare SMEs for health authority meetings as required. Responsible for the management of CMC activities related to specific developmental or

commercial compounds. Responsible for the regulatory evaluation of CMC change controls. Represent Regulatory CMC on cross-functional teams such as GPDO development/commercial

and Regulatory Affairs teams. Take a leadership role in the CMC development/commercial teams. Maintain knowledge of global regulatory environment, regulations and procedures.

GMP/QC Chemist – CH – Sorrento Valley $14-30/hr DOE BS degree in Chemist, Chem Eng, Pharm Chem (maybe Biochem) Must have experience working in an industry lab (clean room) Will train on HPLC and Oligo purification and reagent prep. To assist with the manufacturing of synthetic compounds. “The ideal candidate must be flexible and able to multi-task in a fast pace laboratory

environment. Good organizational skills and attention to detail are required. A great attitude and

the desire to learn are attributes of a successful candidate. GMP and clean room background and experience is a plus!

This individual will be involved in the synthesis, processing and purification of synthetic DNA and RNA compounds for research, diagnostic or therapeutic application. Techniques include oligonucleotide synthesis, HPLC analysis and purification, gel electrophoresis, gel filtration, conjugation chemistry and spectral analysis.”

mRNA Assistant/Associate Biologist – CH – Sorrento Valley $15-24/hr BS/MS in Biology, Biochemistry, Molecular Biology, Cell Biology with experience with PCR,

DNA handling, reagents, solutions, buffers, pipetting Immediate opening for a Molecular Biologist to assist in the development of novel PCR and other

molecular biology products. Bachelors Science degree minimum. Cleanroom experience of 1 year and GMP; Strong writing skills, attention to detail, and the ability to work independently is a must.

Will work with mRNA. Utilize PCR, gels, MS, pipetting

Product Management Assistant – CH – Sorrento Valley $15-20/hr BS Degree in sci. Marketing /customer service role, phone work, office Assist PM/Associate in managing assigned product lines, which may include quotes, customer

correspondence, inventory control, sales reports, marketing reports and projections. Assist with various projects as needed to support the Marketing & Sales department PM Assistant, The position would be to take orders, so great customer service, some filing and

attention to detail. Science background

QA Specialist – CH – Sorrento Valley $15-30/hr Seeking an individual to release final products. BS in science required, preferably in chemistry. 2-5 years’ experience in a controlled industrial environment a required (cGMP/GLP). Good writing skills, high degree of organization and excellent attention to detail are necessary. The successful candidate will also demonstrate an ability to work independently. Upon conversion, this position will also assist the Director of Quality Assurance in internal

audits, drafting quality assurance documentation, raw material analysis and release, CAPA & NCMR systems, light lab support duties/facilities assistance in GMP lab environment as a cross train into QC tactic.

QA/QC Technician (Raw Materials) – CH – Sorrento Valley $15-25/hr The responsibilities will depend somewhat on the aptitude of the candidate. The primary responsibility for the position will be processing incoming raw materials including

ordering qualification tests and maintaining the related documentation. The candidate must have a BS in science and one year experience in the lab or QA.

They should have enough experience to have a basic understanding of the materials they are handling.

**DEGREE IS NOT REQUIRED IF THEY HAVE THE RIGHT INDUSTRY EXPERIENCE Raw Materials Release Detail oriented is essential as well as accuracy and simple math & organized.

Lab Support – CH – Sorrento Valley $12-14/hr Highly motivated individual to support or manufacturing facility. Duties to include

laboratory/instrument maintenance, stocking of supplies, buffer preparation, disposing of chemicals and washing glassware.

Critical skills to include: Attention to detail, desire to learn, a cheerful personality. High school diploma or equivalent

required.

Technical Manager – DP – Sorrento Valley $90-100k ESSENTIAL FUNCTIONS: Trains, develops and coaches Team to continuously improve their knowledge, productivity and

effectiveness in projecting a professional image and providing excellent customer satisfaction whenever interacting with a Customer (internal or external). Typical contact points would be: telephone and or email communication, meetings and training classes as requested by Sales or Marketing.

Actively participates in Customer Complaint Committee Meetings. Effectively communicates with cross functional

Teams with respect to inquiries and complaints received by end use customers and/or distributors, as well as results of customer satisfaction surveys.

Creates, analyzes and reports on department metrics and efficiencies. Works closely with IS to ensure best practice and continuous improvement in LN and/or other

operating systems. Manages and monitors global customer complaint system to ensure procedures are being

followed according to ISO requirements and that Quidel’s corporate goal for processing time is being met.

Takes lead on international complaints and ensures proper training on handling and communication.

Collaborates with cross functional teams to resolve escalated customer complaints. Participate in internal and external audits pertaining to functions of Technical Support Team Provides and/or coordinates training for internal employees, distributors, and end-use customers

as needed. May provide training in person, via WebEx or via phone. Manages, monitors, and reports to Marketing and Management Team on all applicable

proficiency programs. Works closely with R & D regarding any troubleshooting and/or improvements required based on proficiency results.

Responsible for monitoring and maintaining the instrument tracking system in our ERP system and for assisting with any instrument upgrade programs.

Education/Experience B.S. /B.A. in Life Sciences, or equivalent experience 6 years related experience Minimum 3 years in Technical Support in leadership role Experience with diagnostics industry, hospital, and/or physician office laboratory strongly

preferred Knowledge/Skills Lead, motivate and mentor individuals with different personalities that require different levels of

support Able to maintain a professional attitude at all times and work calmly under pressure Quality focused High degree of ethics and professionalism while interacting with customers, vendors and co-

workers. A positive attitude demonstrated during company functions and public events to encourage team

camaraderie and enthusiasm for growth in market share and revenue. Ability to work in a fast-paced, and results-oriented environment, handling time sensitive projects

often with short notice

Manufacturing Technician – C/CH – Sorrento Valley $16-24/hr Minimum of High School with 2 plus years experiences in biotech/pharmaceutical industry.

Associate or Bachelor degree is preferred. cGMP manufacturing for biological product required Proficient with Microsoft Word and Excel Ability to work with pressurized systems, steam, and corrosive chemicals with necessary safety

cautions. 1 - Under supervision, employee will perform routine manufacturing activities in GMP

manufacturing areas including solution preparation, bioprocessing support and autoclave operation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Fundamental knowledge of current biologics regulations and cGMP for drug substance operation are preferred. Employee will perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Candidate must be detailed oriented, a strong team player and has ability to collaborate cross functionally. Flexible shift schedule and overtime may be required.

2 - Under supervision, employee will perform routine manufacturing activities in GMP manufacturing areas including cell culture/fermentation and the associated sub-processes/preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Fundamental knowledge of current biologics regulations and cGMP for drug substance operation are preferred. Employee will perform manufacturing steps, execute routine batch records, and regularly draft and revise documents such as batch records, SOPs and technical reports. Candidate must be detailed oriented, a strong team player and has ability to collaborate cross functionally. Flexible shift schedule and overtime may be required.

Production Support – CH – Sorrento Valley $20-22/hr 1-2 years of experience in GMP Will be preparing buffers used for purification/support manufacturing Will be cleaning lines and bioreactors (CIP/SIP)

Research Associate – CH – Sorrento Valley RA I: $12 - $14 (0 – 3 months experience) RA II: $14 - $16 ( 3 – 12 months experience RA III: $16 - $18 ( > 1 year) This position requires a broad knowledge of anatomy, physiology and biochemistry to help

develop and support in vivo models to screen therapeutics and devices being developed for various disorders. Experience with surgical, dosing and sampling techniques is required. Prior experience working with other in vivo models may be considered even if there is no direct experience working with medical devices, stem cells or ophthalmology.

Bachelor’s degree in pharmaceutical sciences, life sciences, or pharmacology Minimum 1-3 years relevant industry experience depending on education level Background in lab animal (in vivo) research is a must. Working knowledge of in vivo techniques

and imaging modalities will be a plus. Position requires good communication skills and attention to detail Strong work ethic, self-motivation, and ability to adapt in a dynamic team environment are keys

for success Participate in study design and preparation of preclinical studies. Fully support execution of preclinical studies Help in the preparation of study protocols and reports May be required to serve on the Institutional Animal Care and Use Committee (IACUC) Interface with different teams including in vivo scientists, QC/QA, Account Managers/Sales Maintain accurate records in various internal databases Support internal research projects to optimize service offerings Perform other duties as directed by Management.

QA Associate/Doc Control – C – Sorrento Valley $70-90k Manage and support document control processes and systems for GxP activities in compliance

with internal procedures and policies as well as regulatory requirements. Manage the approval, distribution and archival of new and revised controlled documents. Scans documents for archival, maintains paper and electronic filing system and other related tasks

as required. Manages and maintains documents from Contract Manufacturing and Testing Organizations. Ensures controlled documents are periodically reviewed for relevance and accuracy to ensure

actual practices are reflected as defined in applicable procedures. Maintains records management system including secure storage (on and off-site), retrieval,

retention and destruction.

Develop and deliver training and/or site guidance on document and records management roles, and processes to internal and external customers.

Perform Quality metrics Supports internal and external audits as needed. Supports regulatory audits and submissions as needed. Provides recommendations to improve efficiency and compliance Bachelor’s degree in Sciences or related discipline Minimum of 2-4 years of experience in a GMP related field within a biotechnology / biologics

manufacturing facility, with a hands-on role in document management. Proficiency with Microsoft Office applications Word, Excel, Visio, and Adobe Acrobat Attention to detail, clear and effective verbal and written communication skills Excellent project management skills. Ability to multi-task and work well under pressure Highly organized and ability to manage multiple priorities Ability to communicate, relate and work independently with various work groups Excellent documentation skills and attention to detail Demonstrated initiative and accountability in a fast paced environment. Knowledge of Good Manufacturing Practices, Good Documentation practices and regulatory

agencies is a plus

Production Associate – C – Sorrento Valley $15-25/hr DOE Perform commercial vaccine production related activities Operate and maintain 50L Blender, Filler, Washer, and CIP Skid Clean and maintain GMP equipment (Filler, Blender, Washer, CIP Skid, etc.) Troubleshoot equipment issues in a timely manner Assist other team members and management in implementing equipment upgrades and process

improvements Assist with drafting and revising manufacturing SOPs and batch records Author investigations and deviations/incidents Collaborate with Facilities department to schedule Preventive Maintenance and Calibration

activities around production schedule Escort vendors into GMP area to perform activities Qualification Requirements: Minimum of 3 years of relevant industry experience Bachelors of Science/Engineering in Biology, Chemistry, Chemical Engineering, or related

discipline is preferred Capable of lifting up to 50 lbs. Team player and quick learner Demonstrated ability to follow SOPs and attention to detail Ability to effectively communicate and collaborate with other team members and departments

Sr. Project Analyst x5, Method Development – CH – Sorrento Valley $29-31/hr Bachelor’s degree (BA or BS) in Science or related discipline

3+ years of relevant laboratory experience Assist Principal Investigator in developing and validating analytical assays to meet final

requirements of QAU review and release. Responsible for following GLP guidelines for validation of assays and sample analysis. Review of validation data. Write final validation reports and QC raw data that go to the reports.

Organize raw data notebooks. Review of analytical data (sample analysis). Writing of Bioanalytical Procedures/SOPs and contribution to final written SOPs in the

laboratory. Responsible for scheduling analysts, supervising QC preparation, reagent tracking, and ordering

necessary reagents. Responsible for accurate record keeping with regards to sponsor’s samples, data and reports. Responsible for general lab safety with regard to employees and clients. Responsible for keeping accurate inventory of supplies for laboratory operations. Interact with Principal Investigator on new and on-going projects. Discussion of development works with Principal Investigator and analysts.

Project Analyst x4, Sample Analysis – CH – Sorrento Valley $20—22/hr Bachelor’s degree (B.A. or B.S.) in Science or related discipline. MUST have at least 1-2 years

post graduate experience in academic or industry setting Will be expected to dilute specimens, run ELISA assays, validate assays, etc. following SOP's. Candidates MUST have experience multi-tasking, MUST be able to communicate effectively. Culture fit is VERY important Run assays (mainly ELISA) to meet final requirements of QAU review and release. Develop and validate analytical assays to meet final requirements of QAU review and release. Perform assays according to GLP guidelines. Writing of SOPs and contribution to final written SOPs in the laboratory. Write final validation reports and QC raw data that go into the report. Organize raw data

notebooks. Responsible for following GLP guidelines for validation of assays. Responsible for general lab safety with regard to employees and clients. Responsible for keeping accurate inventory of supplies for laboratory operations. Responsible for accurate record keeping with regards to sponsor’s samples, data and reports. Responsible for communicating with client with regards to project.

Lab Assistant x2 – CH – Sorrento Valley $14-16/hr Entry-level position High School Diploma required Responsible for preparation and documentation of reagents. Responsible for general lab safety with regard to employees and clients. Fill pipette tip boxes. Wash glassware.

Stock lab supplies. Take out biohazard trash. Assist with laboratory duties as assigned.

Lab Technician – CH – Vista $15-18/hr Essential Duties & Responsibilities: Core duties and responsibilities include the following. Other duties may be assigned. Responsible for filling Sales department sample order requests • Provide product formulation

support by accurately preparing laboratory beverages and concentrates Perform material inspections/analysis of ingredients, work in progress and finished products •

Maintain laboratory and sample inventory of ingredients and supplies • Maintain laboratory equipment

Assists in preparation of shelf life reports and documentation of other trial tests. • Support Product Developers in conducting production runs, managing ingredient orders, handling, ensuring product meets specifications

Assists in gathering product or ingredient related information from vendors Tracking of sample shipments Maintain safe and clean work environment by complying with procedures, rules and regulations

and Good Manufacturing Practices Skill Requirements: Must have a minimum of 2-years’ experience in the in a food and beverage laboratory Or a

Bachelor’s of Science degree. Qualitative analytical capacity Quantitative capability Knowledge of Manufacturing Quality Systems Sensory Evaluation Organization Skills Thoroughness Proficient in Microsoft Word and Excel Ability to work in a production environment. Able to lift up to 20 lbs. - Ability to work well in a fast-paced ‘hands-on’ environment and under

pressure situations

Sr. Research Associate (In-vivo) x2 – DP – Sorrento Valley $60-75k

EDUCATION AND/OR EXPERIENCE Bachelors in an appropriate biological discipline leading to a college level understanding of

mammalian physiology, such as: biology, biological sciences, biochemistry, physiology, or pharmaceutical sciences, physiology/pharmacology related in vivo laboratory environment.

REQUIRED EXPERIENCE Minimum 3-5 years of In Vivo experience. Knowledge of Vivarium and/or InVivo procedures and processes, preclinical study

implementation and conduct.

Working knowledge of the process of conduction of non-clinical discovery and development studies in all relevant laboratory animal species.

Familiar with Drug Development Process and regulatory and clinical considerations. Knowledge of Good Laboratory Practice regulations and ICH guidelines. Understanding of USDA animal welfare regulations and AALAC guidelines is essential. Additional experience working with cancer/diabetes/inflammation model highly desirable.

EQUIPMENT, TOOLS & SKILLS An employee in this position must be knowledgeable and skilled in the safe use and maintenance

of the following equipment and tools: Knows to use protective devices: gloves, goggles, mask, non-skid water safe shoes, etc. Maintains awareness of proper safety precautions at all times. Always uses products and/or machines as recommended by the manufacturer’s safety

instructions.DUTIES & RESPONSIBILITIES INCLUDE:

The position is responsible for helping the company meet their goals in serving and maintaining clients and engaging in a number of projects in parallel, with multiple responsibilities in preclinical research. You will be responsible for supporting studies assigned to the team by consistently executing procedures according to protocol and associated SOPs in GLP and non/GLP settings.

Sr. Research Associate (Instrumentation Specialist) – CH/DP – Sorrento Valley $60k Participate in development of rapid immunoassay for IVD applications. Conduct testing of IVD

instruments and evaluate performance of various clinical chemistry methods and immunoassays. Execute testing in accordance with pre-written protocols; document, analyze and summarize results; integrate the documentation and results into reports to support completion of project assignments. Maintain in-house reference instruments in best condition and be a main contact for service and troubleshooting. Approach assigned duties with professional independence and self-motivation and demonstrate adequate ability to work on multiple projects as required.

Bachelor's degree in a scientific discipline (chemistry, biochemistry, molecular biology, virology, immunology or related field) with at least three (3) years of research or industrial laboratory experience, or Master's degree in same with at least one (1) year of experience and demonstrated working knowledge of scientific principles. Competence in working with common laboratory equipment and analytical instruments. Adequate understanding of immunochemistry and quantitative immunoassays. Working knowledge of monoclonal and polyclonal antibodies and basic protein chemistry. Experience with designing and executing experiments independently. Skill set must include flexibility, creativity and critical thinking. Must poses analytical and problem solving abilities.

Work effectively with own team members and other personnel. Design and perform laboratory experiments and other assignments as directed. Write experimental summaries and technical reports for own data. Write reports covering data and non-data project topics. Conduct literature reviews; summarize and evaluate data obtained. Supports product transfer from development to manufacturing and associated product

manufacturing activities. Maintain reference instruments in best condition and keep logs.

Be a main contact with service provider or instrument manufacturer for routine service and troubleshooting.

Contribute to preparation of SOPs for IQ, OQ and PQ. Ensure new staff members are properly trained to use instruments.

ADDITIONAL INFO: This person will be working as part of the product development team under some of the senior

scientists If they have a bachelor’s degree they need 3 years of industry experience, if they have a masters

they need 2 years of industry IVD (in vitro diagnostics) experience is required – people that come from Alere, Accriva,

Genmark backgrounds would be a good match 1st shift Monday – Friday This position is open because the workload has increased so they need to bring on this additional

RA to help This is a hands on role – if they have a chemistry background that is a plus They will be working on multiple projects and have to wear many hats (this is a smaller company

so it is great for people to get experience on more techniques) They want someone that is curious about what they do at this company – they want them to come

in and learn all about what they do and why they do rather than just come in and suggest changes

Production Technician – CH – Carlsbad $14-15/hr This is a very entry level position – pay is $14/15 per hour. Schedule is M-F 7am-330,

sometimes they come in early on Friday 6am-230 so that they can leave early on Fridays. Conducts bulk manufacturing of medical point-of-care diagnostic products. Responsible for

production and manufacturing of lateral flow rapid test for enteric and infectious diseases. Works with Production Associate(s) in POC to manufacture products. Collaborates with other departments as required. Assists in activities in the POC Production Department. Engages in the company’s need for continuous improvement in POC Production.

BS in chemistry, biochemistry, biology or related field and prefer a minimum of one (1) year of related laboratory work experience in lateral flow rapid test manufacturing. Prefer working knowledge of GMP, QWRs, QSRs and ISO 9001 with the ability to maintain documentation of process in a cGMP, FDA and ISO approved facility. Experience in bio-related laboratory skills, such as buffer preparation, pipetting, immunoassay, and aseptic technique.

The POC manufacturing group is responsible for the production of lateral flow rapid test for enteric and infectious diseases. Will perform and execute duties as instructed by the Production Associate(s) in POC. Under the direction of the Production Associate(s) in POC, the Production Technician must have the ability to perform routine tasks.

Lab Operations Specialist – CH – Sorrento Valley $14-15/hr Responsibilities:

Maintains re-usable laboratory materials such as glassware and ceramic vessels by sandblasting, sonicating, tumbling or otherwise cleaning and re-distributing to stock locations, ensuring minimum quantities on hand are maintained.

Keeps laboratory supplies ready by inventorying stock, placing orders, verifying receipt and re-stocking to ensure minimum quantities on hand are maintained.

Operates and maintains cleaning and dispensing equipment such as tumbler, sonicator, sandblaster and dispenser.

Prepares materials for chemical experiments, including pre-weighing and pre-stocking materials. Skills: Ability to effectively and safely operate, adapt and maintain cleaning and dispensing equipment. Ability to utilize computer hardware and software. Ability to keep detailed and precise records. Ability to communicate and work effectively and cooperatively with lab technicians, engineers,

research associates and scientists. Basic knowledge of health and safety practices and precautions applicable to a chemistry

laboratory. Education and Training / Experience: Associate’s degree in a scientific field such as chemistry, biology or materials science, or a high

school diploma plus equivalent work experience. Two or more years of laboratory experience. Qualifications: To perform this job successfully, an individual must be able to perform each essential duty

satisfactorily. The requirements listed below are representatives of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Manufacturing Supervisor – DP – Carlsbad $70-85k 2 openings 1st shift, 1 opening 2nd shift (5% shift differential), 1 opening 3rd shift (10% shift

differential) The Supervisor provides leadership and technical support to the manufacturing organization. In

this role, you will assist in development of, drive and achieve departmental short and long-term goals enabling the manufacturing organization to achieve New Product Development, Continuous Improvement, Quality, Compliance and Operational objectives.

Essential Duties and Responsibilities Supervise production personnel and activities to effectively meet forecast, customer demand,

R&D and New Product Introduction requirements. Develop and execute manufacturing training plans to ensure proper resources and talent are in

place to support manufacturing requirements. Develop production schedules in alignment with forecast and customer demand. Develop, implement, analyze, summarize and report key performance indicator data and metrics

for areas of responsibility. Responsible for identification of root cause and implementation of sustainable corrective actions for missed targets.

Responsible for ensuring compliance to quality systems (FDA, GMP, QSR, ISO), product specifications, process instructions, safety requirements and company policies.

Responsible for identification, resolution and follow-up on manufacturing issues that may arise. Responsible for identification and resolution of non-conformances via NCR and CAPA process

including initiation, root cause analysis and implementation of sustainable corrective action. Collaborate with and provide manufacturing input and support to New Product teams, including

the design for manufacturing (DFM) guidance, input on process / tooling development and developing/refining manufacturing instructions.

Collaborate closely with Engineering, R&D, Technical Operations, Quality Assurance and Regulatory teams to ensure proper implementation, sustainability and compliance of manufacturing processes and systems.

Utilize lean manufacturing principles to improve quality, increase productivity, reduce costs and reduce cycle times.

Responsible for management of Kanban system for manufacturing components and supplies in close collaborate with Planning, Supply Chain, Quality, Finance and Logistic teams.

Build and provide leadership for an effective team in a high growth environment including hiring, on-boarding, developing, goal setting and performance improvement in alignment with individual, department and company goals and objectives.

Evaluate and perform written evaluation of direct report performance on an annual basis. Develop and execute performance improvement plans and disciplinary actions in conjunction with HR, as required.

Provide technical guidance and input regarding new processing strategies and associated equipment procurement.

Develop and sustain the manufacturing team as a quality minded culture driven by focusing on customer service (external and internal), outstanding compliance, continuous improvement activities that support business objectives.

Supervisory Responsibilities Up to 30 non-exempt personnel, additional exempt and/or non-exempt personnel as required Position Requirements B.S. degree in Engineering or Science, or AA degree plus 5 years supervisory experience in

medical device, pharmaceutical or similarly regulated environment, or High School Diploma plus 7 years supervisory experience in medical device, pharmaceutical or similarly regulated environment

A minimum of 10 years of manufacturing experience in a medical device, pharmaceutical or similarly regulated environment.

Skills – Technical Working knowledge of quality system requirements (QSR), good manufacturing practices

(GMP), ISO and FDA regulations. Experience with a clean room environment including development and implementation of

environmental procedures. Working knowledge of manufacturing/MRP systems (QAD preferred) Experience, training and/or certification in LEAN Manufacturing principles and/or Six Sigma

methodologies. Experience with Statistical Process Control a plus. Hands-on with a strong sense of urgency, discipline, commitment and organization

Skills – General Strong time management and organizational skills in a dynamic, constantly changing

environment Effective interpersonal communication skills with a demonstrated ability to interact with all

levels within the organization as well as external customers in a professional manner. Hands-on, self-directed, results-driven organized and conscientious Completes work in a timely, accurate and thorough manner Ability to write, comprehend, edit and analyze complex documents Adept at influencing, gaining consensus and overcoming resistance through effective presentation Ability to work autonomously, exhibit a professional manner and establish constructive working

relationships Strong, analytical problem-solving, judgment and decision making skills are required Work Environment The essential functions of the job are usually performed in an environmentally controlled facility

where the noise level in the work environment is usually moderate. This position may involve a combination of office and biotechnology laboratory environments. The employee may be exposed to hazardous chemicals, blood borne pathogens and automated equipment.

While performing the job duties, the employee is regularly required to sit; reach with hands and arms and talk or hear. The employee is frequently required to stand and walk. The employee may sometimes be required to lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision and ability to adjust focus.

The work environment and physical demands described are representative of those required by an employee to perform the essential functions of this job with or without reasonable accommodations.

Operations & Quality Coordinator – CH – Vista $16-24/hr Provide quality and technical expertise, regulation interpretation and recommendations to

leadership team including but not limited to gap analysis and improvements on existing programs and processes and/or new programs and processes as needed to ensure regulatory compliance and optimal business efficiencies. Responsible for updates within Salesforce CRM and development of various initiatives including, but not limited to, developing reports, dashboards, and supporting the organization’s aggressive growth goals. Responsible for supporting operations team with daily deadlines surrounding orders and/or customer requests.

Qualifications Bachelor’s degree required, with at least 3-5 years’ experience in a quality and operations.

Industry experience in food/dietary supplements and/or sports nutrition preferred Preventative Controls Qualified Individual Preferred (PCQI certified) Salesforce experience preferred Must have broad business knowledge and database management experience. Knowledge of sales

processes, policies, and procedures Previous experience implementing HACCP, Food Safety, cGMPs, FDA 21CFR Part 110, 111,

117 and FSMA

Ability to present technical and business solution concepts to all levels (including non-technical audiences)

Must excel and be effective and professional in written and verbal forms of communication Must be computer literate and able to demonstrate proficiency in MS Word, Excel, PowerPoint,

Outlook Must possess the following characteristics:

Procurement Sourcing Technical Specialist – Vista This position is responsible for managing and coordinating all raw material related projects

including, but not limited to, raw material sourcing and qualification, evaluation of technical information, facilitation of the documentation process, regulatory assessment and specification requirements compliance.

Select new and/or replacement ingredients and new and/or replacement suppliers to maintain competitive pricing, meet production and customer requirements. Analyze the market place and material supply to improve quality, and reduce cost. Lead special projects as necessary.

Bachelor's degree in Life Sciences or related fields with 5 plus years previous work experience in the nutritional supplement or food industry in technical and project management areas is required.

Ability to work with minimal supervision. Strong written and oral communication skills; must be able to communicate with all levels of the

organization. Effective interpersonal, negotiation, and decision-making skills. Must be highly organized & disciplined about completing tasks within deadlines. Ability to manage multiple tasks where changing priorities is necessary. Knowledge of material management and MRP systems. Prior Baan system experience is a plus. Must be proficient with computer applications such as Microsoft Word and Excel. Must have analytical laboratory or manufacturing experience in the food, nutritional supplement

or related industries. Statistical analysis skills; must be able to analyze trends and statistical data and make appropriate

decisions and recommendations. Strong commitment to ongoing process improvements and being an integral part of the success of

the organization.

Research Associate/Sr. Research Associate – CH – Sorrento Valley $17-25/hr

Job Summary: Seeking highly motivated and self-starting Biologist or Biochemist to work in the Sample

Collection Product Development Department. The candidate’s responsibilities will include characterization of biological samples (blood and saliva) for key biomarkers using immunofluorescent and colorimetric readouts. The candidate should be experienced in immunochemistry, molecular biology, experimental design, and assay development. The candidate should have excellent scientific writing and communication skills, be highly organized, and be enthusiastic about working in a dynamic, fast-paced, cross-functional environment. Additionally, the candidate should be a team player, have an entrepreneurial spirit, and want to participate in developing products with revolutionary core technologies.

Qualifications BS in biology, biochemistry, or equivalent 2+ years of laboratory experience (5+ years for Senior Research Associate) Previous experience with flow cytometry, ELISA, Western blotting, and/or other

immunochemical techniques Previous experience with nucleic acid techniques (DNA/RNA purification, PCR, NGS) Proficiency in writing detailed technical documentation Familiarity with Quality Management System and GLP/GMP/ISO 13485 regulations a plus Basic statistical knowledge Willingness to work with biological specimens (blood, saliva, urine, etc.) Competent in Microsoft Office software (Word, Excel, PowerPoint) Essential Skills and Abilities Strong ownership of technical success Ability to work independently to plan and execute experiments Ability to work in a fast-paced, goal-oriented team environment Team player with excellent interpersonal skills Excellent oral and written communication skills

Duties and Responsibilities Optimization and execution of biochemical techniques for the characterization of key

biomolecules (nucleic acids and proteins) Experimental design and execution Scientific trouble-shooting and problem solving Data analysis and presentation Technical report writing Professional, ethical, and moral conduct at all times Adherence to regulatory guidelines Additional duties based on dynamic business priorities

Research Associate/Associate Scientist – C – Poway Will be to support in vivo pharmacological studies. Hands-on experience working with rodents

(rats and mice) is a must. The successful candidate must have strong rodent handling skills (both rats and mice) and the candidate will be working in the vivarium for >70% of the working hours. The candidate must be proficient with all routes of drug administration (i.e., i.p., s.c., p.o.) in both rats and mice and must also be proficient in rodent brain tissue necropsy. Experience with rodent EEG studies is strongly recommended. Experience with rodent stereotaxic surgery is preferred. The candidate will be working in reverse-light-dark cycles behavioral rooms with dim light. Experience with other rodent behavioral models is desirable. Some weekend work is expected.

The candidate will preferably have a scientific background in neuroscience and/or pharmacology and will be working in a creative, fast-paced environment supporting multiple drug discovery projects. The position requires team-oriented execution of time-dependent experiments. Thus, the candidate must have excellent interpersonal skills and collaborate with other members of the team. The candidate will be expected to follow directions and SOPs and be able to carry out in vivo experiments independently as well as in close collaboration with other members of the team.

The candidate must be well-organized and with good time-management skills. The candidate must be able to document and report study procedures and results in a timely and precise manner.

Qualifications/Requirements: BS or MS preferably in a Neuroscience or Pharmacology-related discipline and 2+ years’

experience. Strong hands-on in vivo skills with demonstrated proficiency in animal handling (rats and mice) Strong hands-on skills with all routes of drug administration (ip, po, sc) with rats and mice Solid behavioral training and tissue necropsy (rats and mice); Experience with survival surgery recommended (rats and mice); Experience with rodent EEG studies desired; Capability of trouble-shooting and assay development; Proficiency using basic scientific software especially Microsoft office (Excel, PowerPoint), Prism Excellent collaboration, communication (oral and written) and multitasking skills and able to

present work formally to Scientific Research Committees. Team-oriented with good communication skills (oral, written) Strong work ethic with a can-do attitude