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Sr Associate, Manufacturing (Technical Authoring/Deviation Investigations)) at Amgen - ApplyBlast

Sr Associate, Manufacturing (Technical Authoring/Deviation Investigations))

Amgen

4 months ago

3.6 on Glassdoor

New Albany, OH

Hybrid

Full Time

Senior

0 applicants

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About this role

A Sr Associate in Manufacturing at Amgen provides technical expertise to draft and revise Standard Operating Procedures, protocols, and training materials within a GMP-regulated environment. The role involves supporting the manufacturing team with documentation, data collation, and deviation investigations to ensure quality system compliance. Collaboration with cross-functional departments and continuous process improvement projects are also key aspects of this position.

Responsibilities

Draft and revise Standard Operating Procedures and technical reports
Support deviation investigations and change control processes
Collaborate with manufacturing teams to update training documentation
Ensure compliance with Quality System records and GMP standards
Participate in continuous process improvement and troubleshooting projects

Skills

Qualifications

Bachelor's Degree or equivalent experienceGMP Pharmaceutical ExperienceBachelor's in Science or EngineeringMaster's Degree

About Amgen

amgen.com

Headquarters

Thousand Oaks, California, United States

Company Size

10001+ employees

Founded

1980

View Profile

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics.