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Pharma Manufacturing & Quality Careers (Multiple Openings – cGMP)

Company: PrideStaff on behalf of a Premier Pharmaceutical Contract Manufacturer

Location: Northwestern Palm Beach County, FL (Palm Beach Gardens / Jupiter area)

Employment Type: Full-Time, Direct Hire & Temp-to-Hire Opportunities

Compensation: $25.00 - $30.00 / hour (Depending on Role & Experience)

Ready to plant roots and build a long-term career with a rapidly expanding industry leader? At PrideStaff West Palm Beach, we have partnered with a premier Pharmaceutical Contract Manufacturing Organization (CMO) that is experiencing massive growth.

Why this opportunity is different: Our client is not just looking for temporary staff—they are actively seeking dedicated, career-minded employees who want to grow alongside the organization. As they expand their footprint and capabilities, they are offering incredible career longevity, room for advancement, and a stable, thriving workplace.

If you thrive in a fast-paced, highly regulated environment and have a passion for precision, quality, and cGMP excellence, we want to talk to you! We are currently hosting a major talent search for multiple critical positions within their state-of-the-art facility.

Available cGMP Career Tracks ($25 - $30/hr):

1. Raw Material Quality Specialist

Ensure the foundation of our product is flawless before production even begins.

• What you’ll do: Oversee the inspection, sampling, testing, and disposition of incoming active ingredients and excipients. Ensure full compliance with cGMP, FDA, and internal specifications.
• What you need: Strong background in raw material inspection, sampling protocols, and strict documentation compliance.

2. Quality Lab Supervisor

Lead from the front in a state-of-the-art testing environment.

• What you’ll do: Oversee daily laboratory operations, manage testing schedules, and mentor a team of analysts. Ensure all laboratory equipment is calibrated, validated, and that data integrity (ALCOA+) is strictly maintained.
• What you need: Prior leadership or senior-level experience in a cGMP QC laboratory setting, with strong troubleshooting and regulatory audit familiarity.

3. Document Control Trainer

Shape the culture of compliance and continuous improvement.

• What you’ll do: Manage the lifecycle of SOPs, batch records, and deviations. Simultaneously, you will head the facility’s cGMP training program, ensuring all personnel are thoroughly trained, assessed, and fully compliant with current regulations.
• What you need: Exceptional organization, experience with Electronic Document Management Systems (EDMS), and a knack for training/coaching others.

The Ideal Candidate Profile:

• Career Mindset: Individuals looking for longevity who want to grow their skill sets and advance within an expanding organization.
• cGMP Expertise: A rock-solid understanding of current Good Manufacturing Practices (FDA 21 CFR Parts 210/211).
• Attention to Detail: A "first-time right" mindset with an emphasis on data integrity and flawless documentation.
• Team Player: Strong communication skills and the ability to collaborate across production, quality, and warehouse teams.

Why Join Our Client's Team?

Our client isn't just a manufacturer; they are a fast-growing innovator. Located in beautiful Northwestern Palm Beach County, they offer a cutting-edge work environment, highly competitive shift structures, and a clear path for professional advancement. By joining through PrideStaff, you gain a dedicated career advocate who will champion your resume straight to the hiring managers.

Apply Today to Invest in Your Future!

Positions in this growing sector fill quickly. Submit your updated resume today, and a specialized PrideStaff scientific/manufacturing recruiter will reach out to discuss which of these premier, long-term roles best aligns with your expertise.

Great Opportunity !