Lead Metrologist, Quality Control

Lead Metrologist, Quality Control

Position Summary

• Work Schedule: Standard Hours; Monday through Friday

• 100% on-site

Join Catalent’s flagship softgel development and manufacturing facility in North America, located in St. Petersburg, FL, with a capacity of 18 billion capsules per year. This role offers competitive pay, day-one benefits, and career growth in a state-of-the-art, turn-key facility.

The Lead Metrologist plays a critical role within Catalent’s Quality Control laboratory, ensuring all measurement and test equipment remains calibrated, qualified, and fully GMP‑compliant to support accurate testing and product release across manufacturing operations. This position partners closely with Manufacturing, Technical Services, Validation, and Quality teams, contributing to protocols, continuous improvement, and the training of junior colleagues while maintaining the highest regulatory and safety standards. Supported by a close‑knit, collaborative Quality team with a strong culture of internal growth, hands‑on learning, and long‑term career development, this role offers both technical leadership and meaningful impact.

The Role

• Manage the QC calibration program for laboratory instruments and equipment, including scheduling, execution, documentation, and compliance with internal procedures, GMP, and regulatory requirements.

• Perform, review, and approve calibrations, verifications, and preventive maintenance; investigate instrument failures or out‑of‑tolerance conditions and support impact assessments, deviations, and CAPAs.

• Maintain complete and accurate equipment records, calibration certificates, as‑found/as‑left data, and master equipment lists in accordance with data integrity and SOP requirements.

• Establish, revise, and govern metrology‑related SOPs, work instructions, calibration standards, plans, and templates to ensure consistency, traceability, and audit readiness.

• Serve as the metrology Subject Matter Expert during audits, inspections, and cross‑functional activities, supporting IQ/OQ/PQ, lifecycle management, validation, and engineering utility impacts.

• Qualify, manage, and periodically re‑qualify calibration service vendors, including review of certificates for uncertainty, traceability, acceptance criteria, contracts, KPIs, and on‑site service coordination.

• Train laboratory staff on proper instrument use and verification practices, trend equipment performance data, and forecast resources and budget to support continuous improvement and operational demands.

• Other duties as assigned.

Qualifications

• Bachelor’s degree in Metrology, Engineering, Chemistry, Physics, or related scientific discipline required. Advanced degree preferred but not required.

• 5+ years of experience in metrology, equipment calibration, or laboratory instrumentation in a GMP-regulated environment required.

• Demonstrated understanding of CVS, calibration principles, measurement uncertainty, and equipment lifecycle management required. Experience leading investigations, CAPAs, or change controls strongly preferred.

• Experience with laboratory instrumentation typical to QC environments (e.g., balances, pipettes, pH meters, HPLC/GC, incubators, spectrophotometers).

• Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds.

• Vision requirements include ability to differentiate color, have 20/30 vision in each eye with or without corrective lenses, read written documents and frequent use of a computer monitor.

Why You Should Join Catalent

• Tuition reimbursement to support educational goals

• WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants

• 152 hours of PTO plus 8 paid holidays

• Medical, dental, and vision benefits effective day one

• Defined career path with annual performance reviews & strong potential for career growth within a mission-driven organization

• Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives

Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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