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Manufacturing Documentation Specialist Jobs

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Training Specialist

Penumbra, Inc.

Job opening ID38 Posting titleTraining Specialist Roles and responsibilitiesAs a Training Specialist at Penumbra, you will develop and execute training programs to support the growth of our Production environments. You will be tasked with increasing the knowledge and

8/26/2014  Alameda, CA  Save This Job

Up to Lead Validation Specialist

Scientific Protein Laboratories

Position Summary Responsible for cGMP compliance of validation functions for pancreatin, heparin, and those contract manufacturing products that require cGMP status, based upon regulatory commitments for each product. Essential Responsibilities (Critical) Participates in all

8/27/2014  Waunakee, WI  Save This Job

Engineering Administration Specialist

Evenflo Company, Inc.

Description General Responsibilities: The Engineering Administration Specialist is responsible to assign new component part numbers, support management of tooling documentation and manage and track Engineering Change (EC) documentation for domestic and international products

8/25/2014  Miamisburg, OH  Save This Job

Senior Specialist, QA Compliance

Merrimack Pharmaceuticals

Merrimack Pharmaceuticals is a biopharmaceutical company discovering, developing and preparing to commercialize innovative medicines paired with companion diagnostics for the treatment of serious diseases, with an initial focus on cancer. Merrimack currently has six targeted

7/19/2014  Cambridge, MA  Save This Job

Lead QS Specialist

Scientific Protein Laboratories

Lead QS Specialist 1 st Shift Monday - Friday Grade Level: Up to E09 This position is responsible for assuring SPL maintains a strong quality system by ensuring deadlines are met, tasks are completed accurately the first time and mistakes have appropriate corrective and

8/27/2014  Waunakee, WI  Save This Job

Document Control Analyst - Temporary

Jawbone

Jawbone is seeking a Product Life Cycle/Document Control Specialist to join our Manufacturing team to ensure integrity of our production documentation, including Manufacturing BOMs, ECOs, and Deviations. Responsibilities: Assist with BOM creation and PLM in support of Jawbone

9/10/2014  Sunnyvale, CA  Save This Job

Quality Engineer/CAPA and EtQ Administrator

Second Sight Medical Products

Administers the CAPA system. Facilitates CAPA movement through processing phases. Ensures adequate documentation for CAPAs as they are closed. Provides metrics that enable management to gage the effectiveness of this system. Develops, implements and maintains quality

8/3/2014  Sylmar, CA  Save This Job