Clinical Supply Operations Packaging Technician - Groton, CT

Pfizer's Purpose

Pfizer's purpose is to deliver breakthroughs that change patients' lives. Research and Development is at the heart of fulfilling Pfizer's purpose as we work to translate advanced science and technologies into the therapies and vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world.

Job Description

You must maintain daily compliance to Standard Operating Procedures (SOPs), in accordance with current Good Manufacturing Practice (cGMP) guidelines and be responsible for performing operations to support the packaging and labelling of clinical trial supplies. Your role performs both Primary Packaging and Secondary Packaging Operations. This may include (but is not limited to): solid dose drug product by way of manual hand count filling into bottles or by use of minor equipment for automated filling, packaging finished dosage forms such as filled bottles, ointments, pre-filled vials and labelling of other pre-packaged finished material. This position is also responsible to maintain the packaging equipment for daily use including cleaning.

Your knowledge and skills will contribute towards the goals and objectives of the team. Your focus and ability to meet team targets will help in completing critical deliverables. Your innovative use of technology, including AI, communication tools and techniques will facilitate in explaining difficult issues and establishing consensus between teams. It is your hard work and focus that will make Pfizer ready to achieve new milestones and help patients across the globe.

Responsibilities

Responsible for performing primary and secondary operations in a GMP environment, executing operations following instructions on the approved packaging batch records in accordance with cGMPs and safety regulations. Responsible for completing required GMP documentation to ensure records of equipment used and packaging activities performed are maintained contemporaneously in applicable documentation. Responsible for adhering to SOPs, cGMPs, and all safety requirements involving handling and movement of clinical trial materials. Responsible for using EMD365 to scan material and perform tasks required for packaging operations. Responsible for supporting routine daily, weekly, monthly, and quarterly maintenance, inspection and cleaning of the rooms and equipment in the GMP packaging areas as directed. Follow and adhere to production schedules and timelines. Support and assist resolution of common equipment/process failures. Responsible for attending required meetings as necessary for business updates. Utilize AI platforms in job responsibilities where applicable.