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2013…..NOW HIRING in San Diego…. Medical Director…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea Biosciences is seeking a Medical Director who will participate in the development and implementation of the organization’s clinical development strategy for our gout franchise, for US and ...

2013…..NOW HIRING in San Diego….QA Manager Validation…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is searching for a QA Manager, Validation to join the team. The successful candidate will assure software validation compliance with applicable regulatory requirements including ...

Ambrx is a biopharmaceutical company enabling a new field of protein medicinal chemistry, using a fundamentally new technology that directs incorporation of amino acids beyond nature’s conserved set into biosynthetic proteins to produce high value biologics products. Ambrx is seeking a highly motivated scientist to be a key member of a fast-paced and dynamic organization. As part of a team, the ideal candidate will produce therapeutic proteins in mammalian cells and to help mature Ambrx’s ...

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases We are seeking a medical writer who will be responsible for writing and/or revising regulatory documents in support of drug development, including clinical protocols, clinical study reports, patient narratives and investigator brochures. Responsibilities include: •Write and/or ...

Please Note - Candidate will be required to be onsite. Responsibilities - Writing and review of protocols and/or reports for manufacturing process characterization studies - Writing of protocols/batch records for manufacturing process validation - Writing and/or review of other CMC documents as needed - All activities will need to be performed in close collaboration with key team members Skills/Experience: - Excellent technical writing and reviewing skills for process development and ...

Experienced Product Manager will provide marketing insight and direction to optimize new product launch. Will be responsible for developing marketing strategy, product positioning and pre-launch and launch plans for a first-in-class oncology immunotherapeutic. Responsibilities: •Perform strategic market analysis including market size and drivers, segmentation analysis, competitive landscape, opportunities and factors for success. Translate results into product positioning and marketing strategy. ...

Description/ Responsibilities: Application engineering POC for Mobile Broadband data products including but not limited to embedded WWAN modem modules, USB dongles, WiFi hotspots, Wireless CPE, etc. The POC will work at NA R&D Center MBB Product which is a remote technical team to interface with HQ, Ecosystem, Customer Reference Design Teams, and occasional technically support onsite to customers. •Responsible for North America customer platform reference design WWAN integration, including co ...

2013…..NOW HIRING in San Diego….Director/Sr. Director, Regulatory & Scientific Communications…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. The successful candidate will be responsible for managing and directing the medical writing function as well as producing documents for regulatory ...

Major Specialty Sales organization looking for a top performing sales representative, with specialty experience in the San Diego geography to cover the San Diego (Orange County) territory. Position will be calling exclusively on specialists and institutions. Need at least 3-7 years pharmaceutical in current position. Documented awards and rankings required. Please send resume in MS word Format. No LinkedIn profiles please. San Diego, CA (Orange County)

Summary/Scope The Vivarium Technician I will operate equipment associated with washing and sanitizing caging equipment, fill cages and water bottles as well as maintain the general cleanliness of the Vivarium. Must be able to work weekends and holidays as needed. Responsibilities will include, but are not limited to, the following: 1. Sanitation and operation of the cage/rack washer and autoclave 2. Filling clean cages with bedding 3. Filling and autoclaving water bottles 4. Restocking laboratory ...

We are currently looking to hire Permanent Regional CRAs Job Description   The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification ...

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking a GCP QA Manager/Senior Associate to join it's dynamic team. The successful candidate will provide consultation in interpretation of GCP regulations, guidelines, policies, and procedures; plan and conduct independent Good Clinical Practice (GCP) quality ...

This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor: Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects Conduct Pre-Study Site Visits (or calls), Study Initiation ...

 This position is responsible for performing any/all of the following tasks and responsibilities, as well as any other tasks deemed appropriate by the Supervisor:   Monitor activities at assigned clinical study sites to assure adherence to ICH GCPs, local regulatory requirements, TRIO Standard Operating Procedures (SOPs), Standard Guidelines (SGs), Instruction Manuals (IMs), study protocols and study-specific SGs/IMs, for multiple projects Conduct Pre-Study Site Visits (or calls), Study Initiation ...

We are a small biopharmaceutical company located in Sorrento Valley. Our exciting product is entering into a new late phase of clinical trials. We are looking for a hands-on Quality Assurance CMC Sr. Manager/ Director to lead the strategy for CMC (chemistry, manufacturing and controls) activities leading to submission and approval of product marketing applications. The incumbent will assist in planning, reviewing, and preparing CMC documentation in CTD format to support clinical development and ...

Novartis Pharmaceuticals Description: To investigate the role and therapeutic applications of cellular aging and senescence. Contributes to the leading drug discovery projects and intiates new lead discovery projects targeting established and novel molecular pathways. Responsibiities include fostering scientific and operational excellence, supervising associates, developing and optimizing biochemical or cell-based assays for hit identification and lead optimization. Requirements: Ph.D. or M.D ...

Prestigious Pharmaceutical Company is seeking an experience Medical Collections Specialist! Requirements: (2+) Years in Medical Billing Customer Service Role Knowledge of Medical Coding, HIPPA, Medical Terminology, Insurance Classifications High School Diploma Duties: Provide high level of customer service telephonically and electronically to insurance companies, doctors' offices, patients, direct bill accounts, and internal staff Process faxes, emails, and mail from patients, insurance companies, ...

The HR/Talent Manager is primarily responsible for the talent management function. This responsibility includes developing effective and creative sourcing strategies; building and maintaining a diverse pool of top talent; focusing on targeted recruiting, social media branding, employee onboarding, training and development needs, and retention; industry networking and building/maintaining relationships; managing the ATS; participating in employee relations issues; and other HR related tasks as needed. ...

Millennium Laboratories is a national, research-based medication monitoring company whose test panels, technology, customer support, educational resources and experts are specifically focused on clinicians who treat chronic pain. We utilize the latest cutting-edge technology, Liquid Chromatography/Mass Spectrometry/Mass Spectrometry (LC-MS/MS). This allows Millennium to provide the fastest turn-around time in the industry for determining the presence and precise levels of drugs in a patient’s urine, ...

Prestigious Life Science Company is seeking a highly motivated customer service representative. Requirements:Bachelor’s Degree - Science Degree is preferred 3+ years of customer service experience Related experience in Medical Device, Life Science, Bioscience, Pharmaceutical Industry Duties: Provide customer service support to clients, patients, vendors, and clinics. Collaborate with sales reps and provide sales support Learn extensive and complex product knowledge  

Develop and implement strategies focused on molecularly driven oncology programs integrating data from clinical trials, journals and medical records into biomarker development, discovery research, patient selection and clinical research. Collaborate with clinical personnel, research teams, academic institutions and other scientific professionals to drive the development of novel therapeutics. Qualifications: *** MD, MD-PhD or PhD in a relevant scientific field such as pathology, molecular biology ...

Strategic leader needed to oversee a program in cancer immunotherapy with a focus on translating findings from preclinical studies into the design and implementation of collaborative clinical trials. Shall: *** Lead the review, analysis and interpretation of study data to develop preclinical strategies for biomarker discovery *** Provide scientific expertise for evaluation of licensing opportunities *** Establish collaborations and interact with external clinical groups to drive the ...

  The Surgical Regulatory Affairs Manager handles all regulatory development aspects for surgical devices as assigned. These include IOLs, Inserters and Solutions. The incumbent participates on the product development team to provide regulatory guidance for surgical devices assigned. They also manage relevant regulatory strategy components and interactions with Regulatory Authorities for their assigned surgical products and may perform due diligence efforts on new product opportunities.   ...

Our client, a leading biopharmaceutical company, is looking for a Lab Technician to join their team. Responsibilities: Routine small animal husbandry, animal health monitoring, cage changing, sanitation and operation of the cage washer and autoclave. The work may include occasional holiday and weekend duties. Qualifications: Requires a high school diploma or equivalent. Experience with small animal husbandry and ability to follow established SOPs. Must be able to lift 50 Ibs. Experience with ...

Our client, a water service company, is currently seeking a Laboratory Technician to join their team. This person will be responsible for conducting laboratory tests for chemical and bacteriological analysis of potable and raw water, and treated wastewater. DUTIES • Collects potable and recycled water samples from specified locations in the distribution systems and Water Reclamation Facility. • Performs physical, chemical and bacteriological tests on potable water, raw water and ...

HUNDREDS OF SCIENCE/BIOTECH POSITIONS - CLS'S, MOLECULAR, FISH, CYTO HUNDREDS OF BIOTECH POSITIONS AVAILABLE NATIONWIDE MOLECULAR; CYTOGENETICS; FISH; HISTO'S, PATHOLOGIST'S, CLS'S-NATIONWIDE, ETC..... Description: WE SPECIALIZE IN RECRUITING FOR ALL POSITIONS AND JOB LEVELS WITHIN THE BIOTECH/PHARMA INDUSTRY NATIONWIDE! WE REPRESENT SEVERAL HUNDRED CLIENTS THAT HAVE THE FOLLOWING POSITIONS AVAILABLE AT THIS PRESENT TIME... PLEASE SEE BELOW LIST: JOB OPPORTUNITIES: CLINICAL LABORATORY ...

Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea Biosciences is searching for a Regulatory CMC Manager/Associate Director to join the team. The Regulatory CMC Manager/Associate Director leads the regulatory strategy for, and execution of, global CMC (chemistry, manufacturing and controls) activities leading to ...

Allied Search Partners is looking for a qualified Molecular Genetic Technologist (Licensed CLS) candidate for a state of the art facility in the Oceanside, CA area. This position is full time permanent. Know someone for this position? We offer a $$ bonus if we place your referral in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Position: Molecular Technologist (Must be a licensed CLS) Schedule: ...

2013…..NOW HIRING….GMP QA Associate…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking an Associate Director, Analytical Sciences to join its’ dynamic team. The successful candidate will assure cGMP compliance with applicable regulatory requirements including audits and ...

2013…..NOW HIRING….Biostatistics Consultant…..Ardea Biosciences/Astra Zeneca Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is seeking an Associate Director, Analytical Sciences to join its’ dynamic team. The Biostatistics Consultant is responsible for providing input to statistical analysis plans, and executing on ...

   Sr. RCRA – West Coast – Oncology, Rheumatology, Diabetes Key Accountabilities   Ø  Assume the ability to meet the requirements of a CRA I and II with a high degree of proficiency and autonomy Ø  Shows solid understanding of therapeutic indications and study hypothesis. Ø  Act as an independent CRA Coordinator on complex or multiple projects, CRA Coordinator on smaller projects Ø  Represent function in external client meetings and presentations such as investigator meetings and bid defenses as ...

- The Manufacturing associate will be responsible for supporting manufacturing operations by working as an operator in all aspects of plasmid DNA manufacturing, including fermentation, lysis, and chromatographic processes and applying knowledge to troubleshoot problems as well as improve manufacturing procedures. - The Manufacturing Associate will work to execute and troubleshoot equipment during Manufacturing runs. - In addition, the Manufacturing Associate will assist the Facilities department ...

Are you a self-starter that thrives in team environments? Do you enjoy analyzing data for process experiments? Are you able to prioritize multiple projects and tasks to accomplish goals on time? Is this the type of challenge you are looking for in your career? Our client is hiring! Our client is growing its Bioprocess Development team and we are seeking a hardworking, team member to be part of our bioprocess development group working on the fermentation and downstream recovery of recombinant ...

Our client is a pioneer and recognized leader in the development and commercialization of high-performance enzymes for use in industrial processes. Are you a self-starter that thrives in team environments? Do you enjoy analyzing data for process experiments? Are you able to prioritize multiple projects and tasks to accomplish goals on time? Is this the type of challenge you are looking for in your career? Our client is hiring! Our client is growing its Bioprocess Development team and we are ...

Essential Duties & Responsibilities: - Maintains safe, organized and clean work environment. - Performs analytical testing on designated laboratory samples. - Performs chemical and physical testing on raw materials, in-process and finished products as assigned. - Operates and maintains laboratory instruments and equipment. - Performs sample log-in of receipts. Initiates the shipment of samples and tracking documents for outside contract laboratory tests. - Performs administrative tasks ...

Our client assists customers in rapidly developing, manufacturing and commercializing point of care lateral flow, flow through and ELISA assays for any market segment. Our client develops products for markets as broad as clinical diagnostics, veterinary diagnostics, food science, and microbiology and operates under design controls and GMP as required. They are seeking a Research Associate who will be responsible for research and development of products from feasibility through clinical trials and ...

Bio-Medical Equipment Technician Job Description: Biomeds are involved in the total management of healthcare technology beyond repairs and scheduled maintenance; such as, project management, designing interfaces and integrating medical systems, training end-users to utilize medical technology, and evaluating new devices for acquisition. BMETs educate and advise staff and other agencies on theory of operation, physiological principles, and safe clinical application of biomedical equipment. BMET is ...

 Senior/Associate Principal/Principal/Team Lead Medical Writers This leading regulatory writing company with US locations in CA (San Diego), TX (Austin), TN (Nashville), PA (Malvern), DE (Wilmington), and MA (Cambridge) is seeking regulatory writing talent at a variety of levels for on-site, full-time, permanent positions. The company enjoys a 25 year-plus track record of stability and offers its employees excellent growth potential, competitive salaries, profit sharing, and benefits, as well as, ...

 Clinical Operations Leader Responsible for coordinating the functional team members and their activities across all geographies, liaising with project leadership and the sponsor to ensure that the Global Research Operations deliverables (timeline, quality, productivity) are met. The ClinicalOperations Leader has overall accountability for the execution of the clinical operations strategy on the project. May act as Project Leader for projects involving a small number of services, where no Project ...

Looking for a qualified SAS Programmer (home based) Requirements include but are not limited to the following: BA/BS degree in computer science, statistics, biostatistics, mathematics or related field. MA/MS degree is desirable  3-5 years of programming and clinical research or related experience Must have database management, SAS or PL/SQL programming experience Or equivalent combination of education, training, and experience that provides the individual with the required knowledge, skills ...

We are a small biopharmaceutical company located in Sorrento Valley. Our exciting product is entering into a new late phase of clinical trials. We are looking for a hands-on CMC Project Manager to oversee internal CMC team in collaboration with the project team leader, integration of project deliverables/ activities and proactive communication with stakeholders. Facilitates the creation and maintenance of clear, concise Integrated CMC Plan consistent with guidance documents and drives the ...

DUTIES: - Support the Manufacturing department by working effectively to meet department goals, objectives and tasks to achieve desired results. - Responsible for completing assigned tasks which include cleaning, sterilizing, and prepping glassware and parts used in the manufacturing environment. - Work with senior technicians and leads to prioritize tasks and assignments and make recommendations to maximize efficiency and productivity based on shift needs. - May also include ...

AltheaDx performs assay development and clinical testing services for biopharma customers and physicians. Our biopharma service menu covers early stage biomarker discovery through companion diagnostics development, clinical trials and regulatory submission to FDA. AltheaDx is bringing theranostics into clinical use. Please visit our website http://www.altheadx.com for additional details. Clinical Lab Scientist (CLS) The successful candidate will be responsible for performing assay validation, CLIA ...

Ardea Biosciences/Astra Zeneca…NOW HIRING...Sharepoint Administrator, San Diego, CA Ardea Biosciences, a wholly owned subsidiary of AstraZeneca, is headquartered in San Diego, CA. We are a biotechnology company focused on the development of small-molecule therapeutics for the treatment of serious diseases. Ardea is searching for a Sharepoint Administrator to join the team. The overall responsibility is to provide support and administration of corporate Intranet and Extranet, and daily support ...

Ardea Biosciences/Astra Zeneca…NOW HIRING in San Diego... Senior Project Manager Ardea Biosciences, Inc. a wholly owned subsidiary of Astra Zeneca based in San Diego is a Biotechnology Company focused on the development of small molecule therapeutics for the treatment of serious diseases. Ardea Biosciences is searching for a Senior Project Manager to join the team. The overall responsibility will be to apply project management and leadership skills to programs through all stages of the candidate ...

In this position, you will need to work effectively as part of a team responsible for ensuring successful and efficient cell culture/fermentation processes for the production of marketed recombinant proteins. This group provides ongoing technical and scientific support and oversight for the unit operations utilized in the manufacture of these marketed products. Additionally, the group conducts laboratory experiments and full-scale studies to continually improve and optimize process performance. Note: ...

Essential Duties & Responsibilities: - Candidates must be able to work during normal business hours 8am-5:00pm. - The Administrative Assistant will lend support to the Research and Development and Manufacturing Departments and will report directly to the COO. Summary of Job functions: - Maintains records, prepares reports, and composes correspondence relative to the work. - Reviews, analyzes, records and resolves customer complaints about quality control issues. Responds to and makes ...

Accelovance is currently seeking females between the ages of 18-50 who have been diagnosed with Type 1, Type 2, or Gestational Diabetes to participate in a clinical research study. This study will be evaluating an investigational non-invasive diabetes screening device. The study will require one visit that will last approximately 2.5 Hours. Volunteers will be compensated for their participation. For more information please contact Accelovance at 619-291-2845

Essential Duties & Responsibilities: This position is responsible for the following: • Collecting environmental and personnel monitoring samples • Processing environmental and personnel monitoring samples • Recording test data and trending test data. • Assisting with environmental excursion investigations • Writing technical documents in a clear and concise manner. • Maintaining adequate inventory of test supplies • Ordering general supplies as necessary • Performing daily equipment ...

The major responsibility for the QA Associate is to monitor the work performed by manufacturing personnel in the custom mix area to ensure that information found in the formula are correct. The position may also involve review of other documentation, verification of work processes in accordance with SOPs and directions of the QA Manager. Other tasks include assistance with batch record review and documentation, such as training records. Aseptic processing knowledge and/or experience is a plus. The ...