Job Description

Are you passionate about quality in pharmaceutical manufacturing? My client, a cutting-edge biopharmaceutical company, is seeking a Pharmaceutical Quality Assurance Specialist to play a critical role in ensuring compliance, conducting audits, and improving quality processes. This is an opportunity to make a real impact in a fast-paced environment where your expertise will help drive innovation and regulatory excellence.

Why You Should Apply

• Work with a growing biopharmaceutical company focused on groundbreaking product development.
• Play a key role in maintaining quality, compliance, and process improvements.
• Gain exposure to GLP and cGMP audits, vendor certification, and quality system oversight.
• Collaborative and fast-paced environment with opportunities for professional growth.

What You’ll Be Doing

• Conducting GLP, cGMP, and internal audits, ensuring compliance with regulations.
• Leading product nonconformance investigations and preparing impact assessments.
• Reviewing batch production records and ensuring proper QA documentation.
• Managing vendor certifications and auditing external suppliers.
• Assisting in the qualification of new analytical procedures and instruments.

About You

• Be able to do the job as described.
• Strong understanding of pharmaceutical manufacturing, GMPs, and validation processes.
• Experience with laboratory environments, data analysis, and quality documentation.
• Ability to problem-solve and manage multiple priorities in a dynamic setting.

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send an email to ccupo@jacobsmgt.com and tell me why you’re interested. Or, if you do have a resume ready, apply here.

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