Quality Data Reviewer

Join a Cutting-Edge Pharma Tech Company as a Quality Data Reviewer!
Location: Clearwater, FL
Industry: Pharmaceutical (GMP Environment)
Salary: $18/hr
Employment Type: 6-Month Contract

About Our Client:

Step into a dynamic and innovative pharmaceutical technology company where your contributions make a real impact! This forward-thinking organization thrives in a fast-paced, growth-driven environment and is a leader in contract development manufacturing. With a focus on oral solid dosage, they empower their employees with ownership and foster a supportive, team-oriented culture. If you re looking to make a difference in a company that prioritizes both professional development and a collaborative work atmosphere, this is your chance!

Your Role:

As a Quality Data Reviewer, you'll play a key role in ensuring the highest standards of quality are maintained across the production and testing processes. If you're detail-oriented, thrive in fast-paced environments, and have experience in quality control in the pharmaceutical industry, we want to hear from you! Your responsibilities will include:

• Ensuring compliance with company procedures and regulatory standards in a GMP setting
• Auditing critical documentation such as batch records, reports, and certificates
• Supporting document control systems to ensure accuracy and integrity
• Combining lab data with executed batch records for comprehensive review
• Reviewing laboratory data to ensure compliance with industry standards
• Managing key metrics such as analyst errors, batch record reviews, and more
• Reviewing and approving calibrations, cleaning validations, process validations, and drug product specifications
• Supporting preparation for health authority inspections and customer audits
• Approving equipment change controls and metrology reviews to ensure smooth operations

What We re Looking For:

To thrive in this role, you'll need to bring your strong background in GMP-regulated environments, and have hands-on experience with lab equipment and quality systems. Here s what you ll need:

• 1-2 years of experience in a GMP-regulated quality department
• 1-2 years in pharmaceutical quality control (lab experience highly preferred)
• Experience with HPLC and spectrophotometers (a plus!)
• Strong proficiency in MS Office (Word, Excel, Outlook)
• An AS in Chemistry or a closely related discipline

Why Join Us?

• Make an Impact: This is an opportunity to be part of a company that's revolutionizing the pharmaceutical industry.
• Collaborative Culture: You ll work with talented professionals in a company that values teamwork and innovation.
• Career Growth: Our client offers a fast-paced environment where your skills and expertise will be valued, and your career can evolve with the company.
• Flexible Work Environment: Enjoy the benefits of a supportive and flexible work culture that promotes work-life balanc

Ready to Take Your Career to the Next Level?
If you re a detail-driven, results-oriented professional with a passion for quality control in the pharmaceutical industry, we want to meet you! Apply now and take your next career step with us.

SRG provides flexible staffing solutions nationwide, offering contract, contract-to-hire, direct hire, and executive search services. We leverage a cutting-edge platform and a proprietary database of over a million candidates to match the best talent with top-tier opportunities in industries like pharmaceuticals, biotechnology, and more.

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