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The Steely Group
http://www.thesteelygroup.com
http://www.thesteelygroup.com
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Senior Associate, Quality Assurance
Posted: 05/12/2025
2025-05-12
2025-06-14
Employment Type:
Contract
Job Category: Quality
Job Number: 4416
Job Description
Primarily responsible for quality oversight of GMP documents related to site startup activities.
Some of these activities include reviewing and approving GMP documents, communicating with site SMEs for document adequacy, communicating action progress to Sr Manager level.
Requirements / Qualifications:
Some of these activities include reviewing and approving GMP documents, communicating with site SMEs for document adequacy, communicating action progress to Sr Manager level.
Requirements / Qualifications:
- High school/GED + 4 years work experience or Associate + 2 years work experience or Bachelor + 6 months work experience or Masters Degree
- Knowledge of process and facility equipment, ability to interpret and apply Good Manufacturing Practices (GMP)
- Experience reviewing and approving GMP documents from a Quality role
- Experience working in a fast paced environment
- Ability to interpret and apply Good Manufacturing Practices (GMP)
- Document management experience
- Quality assurance or manufacturing experience in the pharmaceutical or medical device industry;
- Written and spoken fluency required in English.
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