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manufacturing in Newark

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    1. Process Operator Specialist

      Kelly Services has provided outstanding employment opportunities to the most talented individuals in the marketplace. Today, we are proud to offer an excellent long term contract opportunity for a Process Operator with our client located in Skillman, NJ . JOB DUTIES • ...

    2. Regulatory Affairs Specialist

        Regulatory Affairs Specialist Leading Pharmaceutical Manufacturer Located in Central NJ   DESCRIPTION: Assist in labeling changes for new and existing products prescriptions. Interact with other departments and cross functional teams in the US and India.   ...

    3. Quality Engineer - Utility and Facility Validation

      Experience: Minimum of three (3) years’ relevant experience performing utility and facility qualification/validation activities within a pharmaceutical, diagnostic, biotechnical, or chemical processing environment. Experience within an aseptic manufacturing and processing ...

    4. Quality Engineer – Process and Validation

      Experience: Minimum of three (3) years’ relevant experience performing validation activities within an aseptic pharmaceutical environment.   Education: Bachelor’s degree or higher in Engineering, Life Sciences or related discipline (Engineering, Chemical Engineering, ...

    5. SAP Validation

      The candidate will be responsible for developing procedures and documentation to support the validation maintenance and compliance of Client’s GxP and business systems. The incumbent will oversee the Client’s IT validation program in accordance with departmental standards, ...

    6. Director of R&D

      Director of Research and Development Top Competitive Salary Near Princeton, NJ (Semiconductors)     Duties and Responsibilities Work directly with the internal and external customer on new product ideas. Lead and direct the department heads for mechanical design ...

    7. Regulatory Affairs Manager

      Great perm opportunity for a Regulatory Affairs Specialistto move to the next level. Great Benefits Location-Princeton NJ 1. Responsiblefor the coordination and preparation of document packages for regulatorysubmissions to ensure the timely preparation of organized and ...

    8. ASSOCIATE DIRECTOR, SUPPLY CHAIN (BIOLOGICS)

      This position reports into the Vice President, Biologics External Manufacturing and is responsible for all materials management, production planning and logistics activities that are outsourced from global Contract Manufacturing Organizations; accountable to deliver ...

    9. ASSOCIATE DIRECTOR, SUPPLY CHAIN (BIOLOGICS)

      This position reports into the Vice President, Biologics External Manufacturing and is responsible for all materials management, production planning and logistics activities that are outsourced from global Contract Manufacturing Organizations; accountable to deliver ...

    10. Nutrition & Regulatory Manager

      Contact Kristine at (815) 756-1221 / [email removed] for more information. Key responsibilities include the following: *Ensure regulatory compliance of products, labels, advertising and promotions as well as adherence to policies and guidelines *Manage and develop staff ...

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