Metrologist

About the role

Ensure laboratory instrument calibration and preventive maintenance (PM) programs are performed as scheduled, including reviewing and maintaining all calibration and PM documentation. Coordinate outside contractors for calibration, preventive maintenance, and equipment service, ensuring services are scheduled, approved, completed, and compliant with industry guidelines. Create, review, and maintain internal and external calibration and preventive maintenance master documentation to ensure required checks and assessments are completed in compliance with applicable guidelines. Serve as the laboratory system administrator and a member of the data integrity team, evaluating laboratory systems for compliance with 21 CFR Part 11 and corporate data integrity requirements, including periodic system reviews. Provide technical support to laboratory personnel by performing initial troubleshooting, serving as the primary point of contact for laboratory systems, and coordinating communication with corporate teams and local users. Attend external training to become a subject matter expert on laboratory instrumentation and provide ongoing technical support and guidance to laboratory personnel. Lead capital equipment requests, oversee the decommissioning of outdated laboratory instruments, and ensure the computerized maintenance management system (CMMS) remains current and accurate. Perform and assist with calibration and preventive maintenance activities while ensuring appropriate controls are in place to support regulatory compliance and data integrity requirements. Other duties as assigned. The Candidate 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, or instrumentation intense position in a GMP-regulated environment required. Work experience in cGMP laboratory is required. Experience as laboratory administrator is preferred but not required. Previous experience handling regulatory/customer audit for laboratory systems is preferred but not required. Prior experience troubleshooting of electronic and electrical circuits. 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

Benefits

Additional Information

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 Metrologist is responsible for the general oversight and support of laboratory instrumentation. Solves problems, provide Validation support, support Preventive Maintenance and Calibration, lead capital appropriate requests and provide troubleshooting and repair support, assist in training of personnel on instrumentation.

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