Documentation Specialist

Overview :

TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing scientific expertise and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients Bioscience Biopharmaceuticals Custom manufacturing Biotechnology Life science ingredients Nutrition Microbial Control Agriculture Materials Science Personal Care and cell and gene therapy.

Job Title : Documentation Specialist / QA Documentation Specialist I

Location : Bend OR

Duration : 6 Months

Job Type : Temporary Assignment

Work Type : Onsite

Shift Days : Monday to Friday

Summary

The role involves supporting the implementation and continuous improvement of Quality Systems in compliance with GMP regulations. It includes managing controlled records and documents maintaining proper documentation processes and assisting in audit activities to ensure regulatory compliance.

Key Responsibilities

• Continuously develop and maintain knowledge of GMP regulations.
• Support implementation and continuous improvement of Quality Systems.
• Manage record control including receipt reconciliation scanning verification check-in / check-out and maintaining scanned backups.
• Issue and track controlled documents and numbering.
• Support internal and external audit activities.
• Perform additional duties as assigned.

Level of Authority

Required Skills

TekWissen Group is an equal opportunity employer supporting workforce diversity.

Key Skills

Environment,Ado,Carpentry,Drafting,Front Office Management,Airlines

Employment Type : Full Time

Experience : years

Vacancy : 1