Job Description

Work Schedule

Rotational shift nights/weekends

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse, Will work with hazardous/toxic materials

Join Thermo Fisher Scientific Inc. as a Formulation specialist and contribute to our mission of making the world healthier, cleaner, and safer. This is an outstanding opportunity to work with a team of professionals who are dedicated to delivering world-class results while encouraging an inclusive and collaborative environment.

Set up and operate pharmaceutical production equipment, including high-speed filling lines for sterile products, autoclave, parts and vial washers, depyrogenation tunnel, formulation process, HMI, and automatic CIP/SIP processes, as well as inspection and packaging line equipment, following relevant SOPs and the Batch Record. Conduct formulation activities for production batches, including the formulation and/or dispensing of all available drug substances and excipients. Prepare, wash, and sterilize parts and materials. Package and transfer the final product to the freezer. Complete all relevant training before performing any tasks. Adhere strictly to aseptic techniques and practices for aseptic operations. Maintain and clean production equipment and classified areas in the manufacturing area. Complete batch records and logbooks timely and with adherence to GDP standards. Transfer materials for batch manufacturing. Prepare filters for test execution and perform FIT (filter integrity testing). Load/unload batches from equipment during production activities. Perform stock checks of consumables and inform the Manager/Lead technician of required materials. Adhere to safety and quality standards consistently and promptly notify the manager of any irregularities. Participate in EHS, business compliance, cGMP, and all other compliance-related matters. Carry out duties following SOPs and uphold GMP regulations consistently. Conduct visual inspections, labeling, and packaging on finished drug products, and perform in-process sampling and checks on semi-finished drug products. Complete any other duties as assigned by the Manager.

Education

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Minimum "O" Level, NITEC/ITE education, or Diploma in a relevant field.

Experience

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1 to 2 years of applicable experience in the pharmaceutical sector or 3 to 5 years of professional experience in any field.

Knowledge, Skills, Abilities

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Good understanding of safe working practices and cGMP. Eager to embark on a career within the pharmaceutical sector. Strong ability to work collaboratively as part of a team. * Flexibility to work rotating shifts.