Quality Assurance Specialist
Listed on 2026-10-11
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Quality Assurance - QA/QC
Production QC/QA, Quality Engineering
Location: Salt Lake City, UT - Onsite Role
Job Summary:The Quality Assurance Specialist will play a role in supporting GMP operations and ensuring the highest quality standards are being met in all areas across the facility, with a heavy focus on the floor support for manufacturing operations.
Duties and Responsibilities:- Execute QA on the Floor program - 50% of the time
- Conduct manufacturing and warehouse walkthroughs
- Provide quality support to manufacturing operations
- Review batch records, test data, and logs
- Disposition materials
- Escalate quality issues
- Work with manufacturing on the floor proactively and in collaboration
- Other duties as assigned
Qualifications:
- 4+ years of experience in Biotech Manufacturing / Quality Assurance / MSAT
- Familiarity with large molecule drug substance manufacturing
- Knowledge of current USP/Ph. Eur./FDA/ISO/GMP standards and guidance
- Previously experienced working in a GMP-regulated facility
- Well-developed verbal and written communication skills
- Ability to closely follow quality standards and pay attention to detail
- Excellence in execution through accuracy, right first time, and a proactive nature
- Familiar with Master Control, Electronic Batch Records
GMP quality assurance, QA floor support, Biotech manufacturing/MSAT experience (4+ years), Large molecule drug substance manufacturing, Manufacturing and warehouse walkthroughs, Batch record/test data/log review, Material disposition, Deviation review, Change control, CAPA review, Quality issue escalation, USP/Ph. Eur./FDA/ISO standards, Master Control, Electronic batch records, Verbal and written communication, Cross-functional collaboration, Attention to detail, Accurate and proactive execution, BS in a scientific discipline
Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate.
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