eBay Classifieds  » Jobs » Biotech, R&D, & science » 1-50 of 83 ads in San Francisco Bay Area

Green Key Resources is currently seeking an experienced Clinical Data Manager for an immediate 12-month renewable contract. Summary:  • Manages and supports team of Data Management professionals to efficiently deliver Data Management deliverables per corporate timeline.  • Manages services providers to ensure the quality and timelines are met.  • Manages and supports staff dedicated to the implementation of the Data Management activities from study start-up to study close-out.  • Liaise with the ...

PRIMARY JOB FUNCTION: Provides support to the Manufacturing organization to facilitate efficient operations within the production area to optimize existing processes, and ensure that production goals are met. Develops and/or monitors performance of components of medical devices and corrects equipment problems or process parameters that produce non-conforming products, low yields, or product quality issues from a Mechanical Engineering perspective. Creates and/or updates Solidworks models for existing ...

  Major Specialty Sales organization expanding their neuroscience sales division  looking for a top performing sales representative, with neuroscience/specialty sales experience in the San Francisco,CA geography Position will be calling exclusively on specialists and institutions. Need at least 7-10 years specialty pharmaceutical sales in current position. Documented awards and rankings required. Please send resume in MS word Format. No LinkedIn profiles please.

We are seeking an energetic, self-motivated and independent scientist to join efforts in our infectious disease department discovering novel antiviral therapies in a dynamic, fast-paced research setting. Responsibilities: • The responsibilities of the successful candidate will be in the efforts of producing and titrating viral stocks, running cell-based viral assays, quantifying viral DNA by real-time PCR, and screening small molecule inhibitors. • The candidate should be able to demonstrate ...

Responsibilities: The successful candidate will help perform innovative research in the preparation of novel organic molecules to aid in the discovery and development of new therapeutically relevant compounds. Specifically, the candidate will: • Perform design and synthesis of biologically active compounds, document methods and create data presentations • Carry out retrosynthetic analyses • Characterize compounds using analytical instrumentation such as HPLC, LCMS, IR and NMR • Present ...

Responsibilities: • Propagate, test, maintain and distribute mammalian and/or microbial cell lines for master cell bank. • Preparation of high quality reagents. • Use and maintain laboratory equipment, and ensure quality and sterility of materials by using aseptic techniques. • Maintain complete and accurate laboratory documentation and electronic files. • Provide information about existing cell lines, investigate new cell lines, and provide help/guidance for culturing difficult cell lines. • ...

Responsibilities • Candidate with experience in techniques that include rodent handling, health monitoring, blood and tissue collection, and dosing via multiple routes. Skills • 5-10 years of hands-on experience conducting studies using experimental rodent models. • Basic molecular biology skills required. • Must have strong written and verbal communication skills. • Must be proficient using Excel, Word and PowerPoint. • Must be a strong team player who quickly learns new in vivo ...

Contract Length - 12 months Title of Position:  Medical Science Liaison I 12m Location: City/State: South San Francisco, CA Zip Code: 94080 # of positions:  1     REQUIRED:   An advanced clinical degree (e.g. PharmD, PhD, MD, MSN) with previous Pharmaceutical/MSL experience is preferred. A candidate with clinical experience in the area of Neuroscience is desirable, while a candidate with multiple Sclerosis experience is highly desirable. *ORL     Job Description: The Medical Science Liaison I will: ...

  Overview: ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries.  We offer the excitement of a consistently evolving career.  Our team is continually learning and working on new and exciting projects in a variety of regions.  We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and ...

  Overview: ProPharma Group is an industry leader providing validation, compliance and technical services to the pharmaceutical, biotechnology, medical device and related industries.  We offer the excitement of a consistently evolving career.  Our team is continually learning and working on new and exciting projects in a variety of regions.  We look for people who excel in their technical area of expertise, believe in our values of Experience, Integrity and Commitment and ...

Contract:  6 Months - possible extension REQUIRED:    • Bachelor’s degree in science or engineering required. PMP Certification a plus. • 3+ years experience of relevant work in project management within biotech or the pharmaceutical industry with a sound knowledge of drug development processes Job Description: The Senior Regulatory Associate/Project Manager will be responsible for project management activities to support one or more products in the pipeline for global market applications as well ...

Hello,   My name is Francheska and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Associate Research Scientist for a prominent client of ours.  This position is located in Emeryville, CA. Details for the positions are as follows:   Core Qualifications:   Propagate, test, maintain and distribute mammalian and/or microbial cell lines for master cell bank. Preparation of high quality reagents. Use and maintain laboratory equipment, and ensure quality and ...

Hello,   My name is Francheska and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Scientific Associate for a prominent client of ours.  This position is located in Emeryville, CA. Details for the positions are as follows:   Core Qualifications: Experience in techniques that include rodent handling, health monitoring, blood and tissue collection, and dosing via multiple routes. If you are interested in hearing more about the position please respond to ...

Hello,   My name is Francheska and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Complaint Manager for a prominent client of ours.  This position is located in Emeryville, CA. Details for the positions are as follows:   Core Responsibilities:   Manage complaints and deviation investigations primarily associated with products previously manufactured at the Bayer Emeryville facility, Extavia, MenC, PDGF and Proleukin.  Communicate with other Novartis ...

 Hello,   My name is Bryson Jackson and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Associate Research Scientist Level I for a prominent client of ours.  This position is located in Emeryville, CA. Details for the positions are as follows:   Job Description:   Propagate, test, maintain and distribute mammalian and/or microbial cell lines for master cell bank. Preparation of high quality reagents. Use and maintain laboratory equipment, and ensure ...

*Please Note: Candidates cannot begin an assignment without a completed and successful drug/ background screening. *1 year contract assignment* The Production Laboratory Technician will operate wet chemical and vacuum semiconductor process equipment in the fabrication of silicon solar cells. Run processes per Standard Operation Procedures and instructions of Device Engineers, and help characterize the materials that are produced. Execute a variety of process sequences using wet chemical tools and ...

 Hello,   My name is Smita Desai and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Training Coordinator (LMS Specialist) for a prominent client of ours.  This position is located in South San Francisco, CA_. Details for the positions are as follows:   Job Description: ·         Intake, process and subsequently communicate Learning Management System (i.e. LSO) training requests to the Shared Service Center in accordance with PD Quality Services training ...

 Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Installer Job ID: 1635853 Industry: Telecommunication Location: Burlingame, CA Duration: 8 Month Contract Hours per Week: 40 Installer is responsible for FNE installation not covered by an installation contract. These installations would include but are not limited to: Cabinet ...

Qtech-Sol Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed by Clinical Research Associates and Clinical Research Monitor.   Internship includes prior training, which follows real time experience and exercise learning pattern. Training is required and may take 1.5 months to complete. Internship takes approximately 2 months depending on project needs. The students will be selected and toward ONE of the career pathways for learning. ...

Qtech Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as Business Analysts towards Clinical Research and Safety Reporting / Financial Risk and Credit Banking / Medical Healthcare Claim / Insurance and System Analyst with clients: Internship includes prior training, which follows real time experience and exercise learning pattern. Educational Qualifications: Bachelor Degree or Higher in Business Management / Computers / IT Only students ...

Qtech Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as SAS programmer towards Clinical Research / Financial Banking / Risk / Credit / Healthcare Claims / Adjudication Analysts with clients. Training is required prior to the internship. Internship is provided for 3-6 months depending on the project and performance during initial training. The students will be selected and qualified for one of the career pathways for learning. ...

Qtech-Sol Internship program develops technical skills and knowledge pertaining to roles and responsibility to be performed as Drug Safety Associates.   Before the internship the professional training is required, which provides real time experience and exercise learning pattern.   Educational Qualifications: Bachelor Degree or Higher in Life Science             Preferred degree in: Anatomy, Biochemistry, Biotechnology, Biology, Biomedical             Science, Biomedical Engineering, Chemistry, ...

 Our San Francisco Peninsula Client  has a need for both full time and a contract SAS Programmer,  the ideal candidate will provide statistical programming support and validation of analysis datasets, create statistical tables, graphs and listings for clinical trial data and assist in developing software to support project teams analysis requirements.  CDISC experience (i.​e.​ SDTM & ADaM) required.  Qualified applicants must have minimum of 5 years of SAS programming in a pharmaceutical/biotech/CRO ...

The Senior Statistician is a skilled statistician with training and significant experience in statistics, drug development, and clinical research. This person will provide biostatistics and biometrics leadership and oversight for all phases of clinical trials and drug development programs, including regulatory submissions. This individual is also responsible for production of biostatistics deliverables, either personally or by supervising one or more statisticians. RESPONSIBILITIES • Works with ...

Shall develop manufacturing processes of bacterial strains for the production of novel biochemicals and biofuels. Candidate must possess: *** Experience with industrial microbiology, metabolic pathway engineering, and fermentation *** Track record of successful scale-up processes *** Understanding of Small scale strain screening technologies and prediction of large scale results *** Exposure to troubleshooting aseptic operations and processes *** PhD in Chemical Engineering, Microbiology ...

Hello,   My name is Smita Desai and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a _Staff Scientist  for a prominent client of ours.  This position is located in _South San Francisco, CA. Details for the positions are as follows:   Job Description: Education: PHD/MD Drug Safety Scientist The Drug Safety Scientist (DSS) is responsible for implementing and coordinating safety surveillance procedures for delegated products. Responsibilities of the DSS ...

This position is responsible for developing and validating release, in-process and cleaning methods in support of immunodiagnostic products. This role will interact with Technology Development, Manufacturing, Research & Development, Quality Control and Quality Assurance staff to ensure that method validation and transfer studies are appropriate for the methods’ intended use(s) and comply with applicable regulatory and company validation requirements. Responsibilities: • Assist with development ...

• Experience working with laboratory rodents is a positive. • Excellent organizational and communication skills. • Self-motivated and autonomous. • Strong time-management skills. • Capable of self-direction and able to manage multiple projects at once. • Ability to occasionally work in a group situation. • Innovative and creative thinker to aid in trouble shooting issues. Skills • 1-3 years industry experience • Competent in Excel and Word with strong ...

We are looking for a highly motivated individual to join our Small Molecule Open Access and Expert Purification team (part of the Analytical Group) that supports Medicinal Chemistry. Job Description: The successful candidate will demonstrate a high level of creativity and independence in designing new high throughput small molecule purification and analytical functions Responsibilities: • Demonstrates highly productivity in high throughput purification and is able to lead the purification ...

Assist with in-house monitoring of data from clinical sites including:Documentation of review of data Preparing enrollment tracking spreadsheets and graphs Communication with study team Assistance with preparation for site visits Assist with study preparation phase including: Review study protocol and Case Report Forms (CRFs) Assist with or lead production and qualification of test panels including documentation Ordering study supplies Assemble panels   Assist with study testing phase ...

The associate is responsible for the growth and recovery of microorganisms used in the manufacture and development of biopharmaceuticals. Major Activities: • Manufacture recombinant antigens to ensure commercial product demands are met: • Provides necessary support for all production activities associated with the Antigen Fermentation. • Operates complex fermentation, filtration and centrifugation equipment • Participates in equipment and process qualification and troubleshooting • Maintains ...

SUMMARY Igenica, Inc. is a biopharmaceutical company dedicated to serving the unmet medical needs of cancer patients through the discovery and development of breakthrough antibody-based therapeutics.  We are looking for an experienced cellular and molecular biologist capable of both in vitro and in vivo target drug development.  The successful applicant will focus on the functional evaluation of novel anti-tumor antibodies for diverse programs using cellular, molecular, and biochemical in vitro ...

 I represent The Fountain Group.  We are a national staffing firm and are currently seeking to fill a Clinical Safety Associate position for a prominent client of ours.  This position will work South San Francisco, CA Details for the positions are as follows:     Demonstrated knowledge of safety concepts, per ICH and FDA guidelines per drug safety reporting requirements. Performs a review of ancillary documentation accompanying ICSR reports and identifies pertinent clinical information for ...

I am Jimmy Cole from Nelson Engineering and Research, With reference to your resume, This is an Excellent Job Opportunity with a Pharmaceutical company in Novato, CA. This is with one of our leading clients and your skills & professional experience seems to be a good match to this opportunity. Please review the job description given below.   Job Title:              Sr Associate/Manager, Regulatory Affairs Location:             Novato, CA Position:              Full time/Regular Industry:              ...

Seeking extensive clinical development experience to help guide discovery strategies and focus pre-clinical resources and efforts most effectively for big pharma research & development activities. Must be a strategic expert and savvy diplomat to work closely with global pharma CEO in the analysis, selection and internal promotion of drug development strategies from evidence-based medicine to sustainable therapeutic solutions. Requires MD-Ph.D, MD, or Ph.D and well rounded research executive with ...

Seeking PhD and 2+ years experience in formulating delivery methods such as metered dose inhalers, dry powder inhalers, nasal sprays, and nebulizers. Must be familiar with: *** Formulation and analytical expertise with particle sizing, blending, in vitro permeation testing, and rheometry. *** Aerosol and powder characterization: cascade impaction, moisture sorption isotherm, bulk density, surface area. *** Scale-up, tech transfer, and process optimization. *** Contributing to regulatory ...

Perform experiments on animal models to test the efficacy and tolerability of novel cardio renal therapeutics. Required: *** 2+ years experience developing and validating animal models for pharmacological targets. *** Extensive experience performing hands on animal modeling and surgery. *** Ph.D Life Sciences, Pharmacology, or related field. High growth visible position with top company. Salary $100,000 to $150,000 plus bonus plan; company paid full family coverage medical, dental, ...

Responsibilities: • Perform microbial fermentations to produce recombinant proteins using soluble and insoluble expression systems. • These efforts will be towards scale down characterization studies to support Validation efforts and Manufacturing process. • We are seeking a highly motivated individual with proven abilities who will be involved in the execution and analysis of upstream fermentation experiments. • Contribute to the group by collaborating with colleagues to support company goals. • ...

our client in Santa Rosa, CA is looking for a Chemist. This is a long term consulting position. If interested, please apply to this ad Job #: 37566 Job Description: Perform analytical method validations, and has the experience and drive to aid in analysis and characterization of combination small molecule drug/medical device products.,The Chemist will analyze samples from drug stability, method development, method validation and product development activities. Develops an validates new methods and ...

Job Requirements Experience with evaluation of software lifecycle (SLC) deliverables for compliance with Operating Procedures, FDA requirements and the CFR including 21 CFR Part 11. Lead or participate in various reviews, risk analyses and other software quality assurance activities. Knowledge or experience in requirements gathering, analysis techniques, software verification/validation techniques. This candidate will be to overhauling the site’s software validation process and will also Identify ...

We are currently looking for a Microbiologist (PHM or CLS with micro specific experience) for a full time contract to hire opportunity with a hospital client of ours in the Eat Bay, CA. This is a full time position working Monday-Friday. Responsibilities Include: •Operating and maintaining test equipment, monitoring and evaluating testing quality, verifying and reporting test results. Performing routine bench microbiology. Requirements: • B.S. in a biological science, medical technology, or ...

Work Description Candidates must posses 7 or more years experience supporting validation programs and possess a BS degree, preferable in the Science or Engineering fields. Give attention to detail, perform critical analysis of situations and provide recommendations, work independently with structured guidance, good follow up skills, clearly define and communicate issues both verbally and in writing. Experience with evaluation of software lifecycle (SLC) deliverables for compliance with Operating ...

GENERAL SUMMARY Under limited supervision but in compliance with policies and regulations, assists in the design,  implementation and monitoring of clinical trials, preparation of integrated medical reports(INDs), periodic reports,  New Drug Applications (NDA’s) and Biological License Applications(BLA’s) etc. Participates in the design and writing of protocols, Case Report Forms (CRFs), and informed consent forms for clinical trials. Productive in recruitment/selection of new investigators, contract ...

 Job Title: Associate Research Scientist II Responsibilities: Conducts incoming and finished products lot release, stability and product support testing in a timely and compliant manner. Conducts testing in a GMP environment following local and global SOPs. Assists in method verifications or validations according to approved protocols. Produces competent and reproducible results to a high technical and compliant standard. Makes detailed observations and analyzes data to ...

  One of the worlds leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care.    Stryker offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives Corporate Paralegal Under the supervision of the Legal Counsel, works directly with other attorneys in ...

SUMMARY Igenica has an exciting opportunity for a highly motivated individual to join a drug discovery team in our research organization and play a key role in applying and advancing our antibody-drug conjugate (ADC) technologies to identify new targeted therapeutics for cancer.  The candidate will have the opportunity to work closely with other high caliber scientists with diverse scientific expertise.   PRIMARY RESPONSIBILITIES The candidate will work within our ADC discovery team and will ...

Job Description IntegraGen, Inc. is seeking a Regional Account Manager to grow the company’s revenue in the Western part of the United States. This field sales position will be based in California and be responsible for the growth of IntegraGen’s ARISk® Autism Risk Assessment Test (www.arisktest.com) within the assigned geography through selling and promotional activities to targeted clinicians.    Applicants MUST currently reside in either the Los Angeles or San Francisco Bay area. No relocation ...

We are hiring a Statistical Programmer to work onsite in the Bay area:    Job Description:    Key Accountabilities/Core Job Responsibilities:   Performs data analysis using primarily the SAS programming language for the summary and interpretation of clinical trial data. Create CDISC SDTM and ADaM files, SAS export files and Define.xml use for Electronic Submission from the data received in non-standard form from various sources. Performs Data analysis, statistical analysis, generate safety and ...

We are seeking a highly motivated, enthusiastic, an independent Research Associate/Senior Research Associate to join the Clinical Pharmacology Group in the Department of Development Sciences.  Responsibilities:  The candidate will provide technical support for the pharmacokinetic and pharmacodynamics assessment of drug candidates and marketed products.  The overall scope and focus of this position is to support pharmacokinetic analyses, which seek to optimize dose regimens and strategies to ...

Based on the protocol, CRF, existing final study report, and high-level description of additional desired analyses, prepare detailed TLG and derived variable specifications in order for the analyses to be implemented by our statistical programming group.  Performs detailed QC of TLGs and derived datasets programmed by our statistical programming group, including possible double-programming of key variables or tables  Programs ad hoc or exploratory analyses (Tables, Graphs, Exploratory modeling) in ...