QA Specialist (Biotech / Pharmaceutical manufacturing)

Dawar Consulting, Inc.; Oceanside (CA); On-site; USD 37,000 - 53,000; Full time

Benefits offered by this job

Medical

Dental

Vision

Paid Sick Leave

401K

Job summary

JobRx, Inc. is hiring a QA Specialist in Oceanside, CA for biotech/pharmaceutical manufacturing. This long-term contract involves QA oversight, batch record reviews, and maintaining compliance with regulatory standards.

The ideal candidate will have experience in QC and strong GMP knowledge, alongside familiarity with tools like MS Office and Veeva. Benefits include medical and 401K.

Qualifications

• QC experience (analytical, virology, microbiology).
• Strong GMP knowledge (US/EU).

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.

Skills

QA

Batch Records

QC

GMP Manufacturing

Tools

MS Office

Veeva

Smartsheet

LIMS

Job description

Job Description

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 [e-mail]/[e-mail]

Skill Set

QA, Batch Records, QC, GMP Manufacturing