QA Specialist (Biotech / Pharmaceutical manufacturing)

Dawar Consulting

Oceanside, California

Apply

JOB DETAILS

SKILLS

Biology, Biotech and Pharmaceutical, Change Control, Drug Manufacturing, GMP (Good Manufacturing Practices), Laboratory Information Management System (LIMS), Maintain Compliance, Operational Support, Order Picking/Packing, Quality Assurance, Quality Control, Quality Metrics, Regulations, Regulatory Compliance

LOCATION

Oceanside, California

POSTED

16 days ago

Our client, a world leader in biotechnology and life sciences, is seeking a "QA Specialist (Biotech / Pharmaceutical manufacturing)<\/b>.
<\/div>

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

<\/div>
Job Summary:<\/b>
<\/div>

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

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

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

<\/div>
If interested, please share your updated resume at
hr@dawarconsulting.com
lakshmi@dawarconsulting.com

About the Company

Dawar Consulting

Resume Resources

Free Resume Templates Free Resume Builder