Sr. Associate Metrologist (Secondment 12 Months)

WHY PATIENTS NEED YOU

Every day our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible innovative and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development maintenance compliance or research analysis your contributions have a direct impact on patient care. Our dedication to quality and safety drives everything we do fostering a dynamic environment where your role is crucial in advancing healthcare solutions.

WHAT YOU WILL ACHIEVE

A position within Pfizer Global Supply GTEL Laboratory Operations Center function providing GMP compliant services to PGS within GTEL ES & MDCP. The applicant must have awareness of cGMPs good lab practices and good housekeeping practices. The candidate must also have experience with laboratory equipment and demonstrated compliance to procedures.

HOW YOU WILL ACHIEVE IT

The Sr. Associate Metrologist:

• Primary oversight for service providers and/or performs occasional validation qualification calibration/preventative maintenance for laboratory instrumentation used for GMP testing.

• Responsible for generating and/or reviewing documentation in support of the metrological activities stated above. Including maintaining these records and filing according to eRIM policies

• Responsible for updating and maintaining calibration database

• Responsible for scheduling and managing calibration/maintenance service contracts with outside vendors

• Performing/documenting investigations for non-conformances associated with laboratory equipment.

• Assisting with troubleshooting equipment and equipment software applications as well as makes recommendations to Laboratory Team Leaders and Analysts.

• Ensuring compliance to Quality Agreement between SLS and Pfizer Pharmaceutical Sciences Lake Forest

• Ensuring compliance per Pfizer Quality Standards for Service Providers (e.g. obtains procedures and training records).

• Responsible for providing support during regulatory inspections and on-site audits.

QUALIFICATIONS

Must-Have

• Applicant must have a bachelors degree with 0 years of experience; ORan associates degree with 4 years of experience; OR a high schooldiploma (or equivalent) and 6 years of relevant experience.

• Experience with laboratory equipment such as Balances Calipers etc.

• Strong written and oral communication skills

• Demonstrated proficiency with CMMS software

• Demonstrated computer literacy in Microsoft Office or equivalent programs familiarity with document management systems and databases

• Familiarity with GMPs and applicable regulations guidelines (e.g. CFR EMA and ICH publications) and standard operating procedures

• Ability to work independently and effectively in a team environment with colleagues of diverse backgrounds

• Ability to complete work within reasonable timelines and to a high-quality standard

• Ability to commit to the Pfizer Values & work in a regulated environment

• Experience with MS Word MS Excel QTS Calibration database and PDOCS as well as a demonstrated ability to learn and master new applications software is desired

PHYSICAL/MENTAL REQUIREMENTS

• This position will be expected to work in an office setting as well as in a mechanical and wet-laboratory setting. Proper handling of hazardous chemicals and adherence to safety procedures.

• This position may involve lifting moderately heavy equipment with assistance from others. This position will also involve office work. This individual will be expected to handle multiple projects and responsibilities as well as adapt to changing priorities within the business.

NON-STANDARD WORK SCHEDULE TRAVEL OR ENVIRONMENT REQUIREMENTS

• This position is based at the Pfizer Parsippany NJ site and may require travel (<10%) to other Pfizer or vendor locations.

• Work Location Assignment:On Premise

OTHER JOB DETAILS

• Last Date to Apply for Job:October 30 2025

• Additional Location Information:NO

• Eligible for Relocation Package NO

• Secondment 12 months

• If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

• There will be no change to your current work location.

Relocation assistance may be available based on business needs and/or eligibility.