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  1. Pharmacy Manager Clinical Research at Biotrial, Inc.

    Registered Pharmacist/Pharm D with active license in NJ. Manage the Pharmacy Operations in accordance with Good Manufacturing Practices and Good Clinical...

  2. Director, Client Services (Project Management) at Medidata Solutions

    To be the most innovative cloud company in Life Sciences. We sit at the intersection of technology and Life Sciences industries....

  3. Executive Director, Strategic Product Leader, Immuno-Oncology Brands at BMS

    Establish priorities across Site Operations, Manufacturing Science & Technology, Quality, Supply Chain, GRS, and align annual objectives....

  4. Software Development Lead - Oracle at Topps

    BS - Information Technology / Computer Science. Technical knowledge of several EBS modules supporting Finance, SCM, Trade Management, Manufacturing, Order...

  5. Director, Development Quality Assurance (Operations) at Celgene

    D. Motivating team member to be leaders. § Thorough understanding of the GMPs as related to Clinical Manufacturing....

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    1. Clinical Research Pharmacy Manager (438866)

      OVERVIEW:The Pharmacy Manager is responsible for the operational management of the Newark Clinical Pharmacology Unit Pharmacy and ensures the effective operations of the pharmacy at all times including during hours outside of normal working times.Responsibilities:•    Manage the Pharmacy Operations in accordance with Good Manufacturing Practices and Good Clinical Practices.•    Oversee and ...

    1. Plant Controller at OWENS CORNING

      Global in scope and human in scale, the company’s market-leading businesses use their deep expertise in materials, manufacturing and building science to develop...

    1. Formulation Scientist

       Formulation Scientist   A Pharmaceutical Formulation Scientist is needed to design and execute pre-formulation activities for solubility, stability and excipient compatibility testing of new products; manage scale-up and manufacturing of soft gel and liquid dosage forms; test and characterize active pharmaceutical ingredients using techniques such as particle size analysis, impurity and ...

    1. Director, Pharmaceutical Development at Celgene

      Responsible for ensuring adequate transition plans to transfer knowledge to clinical and commercial manufacturing....

    1. Quality Assurance Manager

      Due to unprecedented growth our client a generic pharmaceutical company located in New Jersey currently has approval to add to its staff a Manager of Quality Assurance.JOB SUMMARY:The Manager of Quality Assurance provides for the development and implementation of computerized and other processes that will assure that primary documentation systems encompassing records mandated to comply with ...

    1. Accounts Payable Clerk at PixarBio Corporation

      Frank is a neurological R&D expert and he has filed a wide range of patents covering NeuroScaffolds, NeuroRelease, and neuro-biomaterials cGMP manufacturing....

    1. Quality Assurance Auditor - Full Time - Princeton, NJ

      Our client is currently seeking a Quality Assurance Auditor to join their Quality Assurance & Auditing (QA) Department reporting to QA Management. This position requires experience in planning and conducting both cGMP and GCP audits (supplier, internal process and investigator site) with a focus on new drug application preparation activities and will include responsibilities for providing ...

    1. Senior Director,Regulatory Affairs at Celgene

      With a presence in more than 70 countries - and growing - we look for talented people to grow our business, advance our science and contribute to our unique...

    1. Quality Assurance Specialist

      Quality Assurance SpecialistJOB SUMMARY:The Quality Assurance Specialist, under the direct supervision of the Supervisor Quality Assurance is directly responsible for performing inspection and auditing within the facility. Areas where inspection and/or audits are conducted include; warehouse, granulation, compression, packaging and laboratories.ESSENTIAL FUNCTIONS:The QA Specialist is ...

    1. NEW DRIVERS: Earn up to $70,000 yr, Home Weekends, Paid Flatbed Training! (6760906) at TMC Transportation

      CDL license, cdl jobs, truck driving opportunities, owner operator, O/O, regional driver, trucking company, Class A truck driver, class A cdl, semi driver,...

    1. Business Development Associate

      We are looking for a dynamic, self-starter with the ability to communicate clearly and a passion for finding new business opportunities.  Using his/her strong computer/financial modeling skills as well as outgoing personality, the Bus. Dev. Assoc. will develop ideas backed by data and present them to manufacturing partners while negotiating contractual terms.  The ideal candidate will have ...

    1. Director/Senior Director, Regulatory Affairs (Promotional Review) at Lexicon Pharmaceuticals, Inc.

      Minimum of 8-10 years’ experience in a regulatory position within a biotech, pharmaceutical or clinical research organization....

    1. Scientific Quality Auditor

      *Please note that this is a 6 month contract assignment. Candidates cannot start an assignment until background check and drug test is completed*Responsibilities: Under the direction of CMC Auditing supervision, the Auditor conducts routine document audits of CMC data and information included in regulatory submissions to ensure data accuracy and integrity and compliance with Standard ...

    1. Head of Clinical Microbiology at ContraFect Corporation

      ContraFect Corporation, a clinical-stage biotechnology company focused on the discovery and development of protein therapeutics and antibody products for life

    1. Formulation Scientist

      Formulation ScientistFormulation Scientist Near Union, NJ Job Description:The formulation scientist involved in the recording of the developmental programs designed for the gel formulation products for a pharmaceutical firm. Performs proper analysis, arrangement, and reassessment of the examination reports. Responsibilities:• Collect, documentation, and survey of validation processes that are ...

    1. Formulation Leader at Celgene

      Execute experiments to characterize drug product formulations and manufacturing processes utilizing various technologies....

    1. Quality Manager

      Hello, My name is Shannon and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Manager for a prominent client of ours.  This position is located near East Hanover, NJ. Details for the position are as follows: Job SummaryResponsible for preparation and review of the Annual Product Review Reports for marketed products and select third party ...

    1. Scientist I, Drug Substance Development at Celgene

      Develop scalable chemical manufacturing processes. Familiarity with GMP manufacturing and IND/NDA filings are a plus....

    1. Methods Development Chemist

      Methods Development ChemistAjulia Executive SearchLocated near Linden, New Jersey COMPENSATIONCompetitive Salary, Full Benefits, 4 -6 Month Temp Assignment RESPONSIBILITIES· Manage the analytical development and conduct QC analysis of new soft gelatin RX/ capsules, OTC products, and shelf life studies· Write stability, procedures, practice, validation protocols/ reports, partaking in customer ...

    1. Principal Scientist, Product Formulation at Celgene

      Knowledge of cGMPs during pharmaceutical development and clinical manufacturing. With minimum of 12 years in Pharmaceutics, Pharmaceutical Science or related...

    1. Formulation Scientist

      Formulation ScientistLocation- Near New Brunswick,NJFull-Time Position with BenefitsJob Requirements:Bachelors in Pharmaceutics.Must have prior formulation development experience in the generic drug pharmaceutical industry.Must be proficient in Microsoft Office Suite (PowerPoint, Word, and Excel specifically).Require Hands on experience or knowledge to operate Tablet, Capsule, Granulation ...

    2. Quality Assurance Auditor - Full Time - Princeton, NJ

      Our client is currently seeking a Quality Assurance Auditor to join their Quality Assurance & Auditing (QA) Department reporting to QA Management. This position requires experience in planning and conducting both cGMP and GCP audits (supplier, internal process and investigator site) with a focus on new drug application preparation activities and will include responsibilities for providing ...

    3. Quality Assurance Specialist

      Quality Assurance SpecialistJOB SUMMARY:The Quality Assurance Specialist, under the direct supervision of the Supervisor Quality Assurance is directly responsible for performing inspection and auditing within the facility. Areas where inspection and/or audits are conducted include; warehouse, granulation, compression, packaging and laboratories.ESSENTIAL FUNCTIONS:The QA Specialist is ...

    4. Senior Pharmaceutical Project Manager (Drug Development PM Experience

      *Please note that this is a 1 year contract assignment. Candidates cannot start an assignment until background check and drug test are completed*Responsibilities:Under the broad guidance of the Executive Director or the VP/SVP, GPM, the core responsibility of this senior PM role will be to independently manage development programs and / or due diligence/business development activities, ...

    5. Quality Control Analytical Lab Chemist

      Job Description:This position will perform chemical analysis and testing on raw materials, stability samples, bulk formulations, and finished product with quality compliance; under supervision from the Quality Control Supervisor. This position performs analytical testing and data review in accordance with cGMP requirements.Role and Responsibilities:o Provide cGMP compliant laboratory ...

    6. Product Development Manager

      We are seeking a Product Development Manager to become an integral part of our team! You will develop and design manufactured products in accordance with company standards. Product Development ManagerWill be responsible for color matching, new product development, working with sales to commercialize new products and provide technical support to customersBS or MS in Chemistry, Chemical ...

    7. Associate Manager, Global Supply Chain Planning

      DEPARTMENT Global Supply Chain Planning, Technical OperationsPREREQUISITES Planner with three to five years experience in the Pharmaceutical or Healthcare Industry. Bachelor’s Degree in Business or Engineering is required, APICS certification, or equivalent, is desiredClient is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. ...

    8. SQF Practitioner, Quality Manager 24.16AM

      :: If you meet the qualifications listed below and would like more information contact Amanda at 815-756-1221 Attach resume when responding to this posting :: The SQF Practitioner, Quality Manager will be responsible for creating a culture of quality throughout the organization and articulating the unique requirements for the manufacturing of nutritional products and products with special ...

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      No Telecommute

    9. Senior Pharmaceutical Project Manager (Drug Development PM Experience

      *Please note that this is a 1 year contract assignment. Candidates cannot start an assignment until background check and drug test are completed*Responsibilities:Under the broad guidance of the Executive Director or the VP/SVP, GPM, the core responsibility of this senior PM role will be to independently manage development programs and / or due diligence/business development activities, ...

    10. Shipping and Receiving Coordinator - Forklift Certified

      MUST have Fork-Lift and warehouse experience, pharmaceutical a plus.This position will be responsible and accountable for handling all shipping and receiving functions while on facility premises. This role provides accurate documentation of all incoming and outgoing material in compliance with GMP, cGMP, FDA and DEA regulations, and company protocol.Role and Responsibilities:Under Supervision ...

      1. Drivers: Earn up to $80,000 yr, Home Weekends and up to $2,500 Sign On Bonus! (6754002) at TMC Transportation

        CDL license, cdl jobs, truck driving opportunities, owner operator, O/O, regional driver, trucking company, Class A truck driver, class A cdl, semi driver,...

      2. Postdoc Fellow - Translational Development / Clinical Pharmacology at Celgene

        Experience in NONMEM and R or SAS, is a plus. Basic scientific computing and programming skills in a variety of computational tools such as MATLAB, Monolix,...

      3. Senior Scientist, Analytical Technical Services at Celgene

        Interacts with various departments (Commercial Manufacturing Organization (internal and external), Commercial Technical Services (API and drug product),...

      4. Senior Engineer, Drug Substance Development at Celgene

        Supported by a multidisciplinary team, you will then transfer your scaleable technology to the manufacturing sites where it will be used to produce high quality...

      5. Senior Software Engineer at The Macaluso Group

        Bachelor degree, Computer Science. Build leading edge solutions in pharmacy, biotech, retail, and payment processing. The Macaluso Group....