QA Specialist (Biotech / Pharmaceutical manufacturing)

Reposted 21 Days Ago
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Oceanside, CA, USA
In-Office
45-45 Hourly
Mid level
HR Tech • Information Technology • Professional Services • Consulting
The Role
Provide on‑the‑floor QA oversight for biopharma manufacturing: review batch records, perform line clearance, support QC activities, approve shipments, manage deviations/CAPAs/change controls/investigations/holds, support regulatory inspections, ensure GMP compliance, and maintain document control and procedures.
Summary Generated by Built In
Our client, a world leader in biotechnology and life sciences, is seeking a "QA Specialist (Biotech / Pharmaceutical manufacturing).

Location: Oceanside, CA
Duration: Long-Term Contract (Possibility Of Further Extension)
Pay Rate: $45/hr on W2
Company Benefits: Medical, Dental, Vision, Paid Sick Leave, 401K

Job Summary:

This role provides on‑the‑floor QA oversight, batch record review, QC support, and ensures compliance with regulatory and site quality standards.

Key Responsibilities:
• Review batch records, perform line clearance, and provide floor QA support
• QA oversight of QC activities (method transfer, COAs, stability)
• Approve shipments and support packaging operations
• Manage deviations, CAPAs, change controls, investigations, and hold events
• Support regulatory inspections and GMP compliance
• Perform walkthroughs, document control tasks, and update procedures/forms

Preferred Skills:
• QC experience (analytical, virology, microbiology)
• Strong GMP knowledge (US/EU)
• MS Office; Veeva/Smartsheet/LIMS a plus

If interested, please share your updated resume at [email protected]/[email protected]

Skills Required

  • Batch record review and line clearance experience
  • QA oversight of QC activities (method transfer, COAs, stability)
  • Approve shipments and support packaging operations
  • Manage deviations, CAPAs, change controls, investigations, and hold events
  • Support regulatory inspections and GMP compliance
  • Perform walkthroughs, document control tasks, and update procedures/forms
  • QC experience (analytical, virology, microbiology)
  • Strong GMP knowledge (US/EU)
  • MS Office proficiency
  • Experience with Veeva, Smartsheet, or LIMS
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The Company
Year Founded: 2009

What We Do

Dawar Consulting Inc. is a professional services and staff augmentation firm specializing in IT consulting, workforce solutions, and HCM/HRIS services. They provide technology and business consulting, project delivery, and IT support to help clients achieve their strategic goals. With expertise across IT, Engineering, and Finance, they deliver best-in-class workforce solutions and innovative strategies to drive operational efficiency and business success.

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