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, Loud Noises (Equipment/Machinery), 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.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse, Will work with hazardous/toxic materials

Job Description

Join Thermo Fisher Scientific and contribute to a team that's making a remarkable impact in the world. Here, you’ll engage in important work, supported by collaborative colleagues and ample opportunities within a global leader. Our ambitious and growing organization is passionate about a robust strategy for the future. Become part of our outstanding team and help us make the world healthier, cleaner, and safer!

The Sr Formulation Technician will perform various tasks and activities listed below, ensuring compliance with cGMP, company and department SOPs, and safety regulations.

Responsibilities

Setup and operate pharmaceutical production equipment including high-speed filling lines, autoclave, parts and vial washers, depyrogenation tunnel, formulation process, HMI, and automatic CIP/SIP processes.Complete formulation activities for production batches, including dispensing of drug substances and excipients.Prepare and sterilize parts and materials.Package and transfer the final product to the freezer.Complete all relevant training before performing tasks.Perform materials and process transactions at each manufacturing step.Adhere strictly to aseptic techniques for aseptic operations.Clean and maintain production equipment and classified areas.Conduct routine QC sampling and in-process testing throughout manufacturing.Complete batch records and logbooks with adherence to GDP.Transfer materials for batch manufacturing.Perform FIT (filter integrity testing) and prepare filters for testing.Load/unload batches from equipment during production.Check consumable stock and inform Manager/Lead Technician of needs.Follow safety and quality compliance at all times and report anomalies promptly.Participate in EHS, Business Compliance, cGMP, and other compliance-related matters.Report quality issues immediately to Manager or Lead Technician.Perform microbial sampling and swabbing of room and equipment as required.Liaison with external vendors for instrument calibration and maintenance.Conduct chemical and mathematical calculations to determine product potency and endotoxin levels, if needed.Perform visual inspection, labeling, and packaging on finished drug products.Conduct in-process inspection and checks.Perform any other duties as assigned by the Manager.

Education

Minimum “O” Level, NITEC/ITE education/Diploma in relevant field.

Experience

3 to 5 years of relevant experience in the pharmaceutical industry.

Knowledge, Skills, Abilities

Good understanding GDP, CGMP and Safety.Highly motivated to work in the pharmaceutical industry.Ability to work collaboratively as part of a team.Willingness to work rotating shifts.

Take this opportunity to advance your career in a world-class organization!