Work Schedule

12 hr shift/days

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

Job Description

At Thermo Fisher Scientific, you’ll do important work that makes a difference. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can provide. Our respected, growing organization has an outstanding strategy for the near term and beyond. Take your place on our strong team and help us make meaningful contributions to the world.

ResponsibilitiesOperate pharmaceutical production equipment like filling lines, autoclave, washers, formulation process, and packaging equipment following SOPs.Perform formulation activities of production batches which includes formulation and/or dispensing of all the available drug substance(s) and excipients.Prepare parts, wash, and sterilize materials.Package and transfer the final product to the Freezer.Complete all relevant training before performing any task.Follow aseptic techniques and practices for aseptic operations.Clean and maintain the production equipment and classified areas in the manufacturing area.Timely complete relevant batch records and logbooks for tasks performed with adherence to GDP (Good Documentation Practice).Transfer materials for manufacturing batches.Prepare filters for test execution and perform FIT (filter Integrity testing).Load/unload loads/batches from equipment during production activities.Perform stock checks of consumables and inform Manager/Lead technician for required materials.Follow safety and quality compliance at all times and communicate any anomalies to the manager promptly.Participate in EHS, Business Compliance, cGMP, and other compliance-related matters, where applicable.Perform all tasks in accordance with standard operating procedures and maintain strict compliance to GMP. Report all quality issues immediately to Manager or Lead technician.Perform visual inspection, labeling, and packaging on finished drug products. Conduct in-process sampling on semi-finished drug products, and in-process inspection and checks.Perform any other duties as assigned by the Manager.

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

Experience

1 to 2 years of relevant experiences in pharmaceutical industry or 3 to 5 years of working experience in any industry.

Knowledge, Skills, Abilities

Good understanding of safe working practices and cGMP.Highly motivated to work in pharmaceutical Industry.Able to work as a team.Able to work rotating shift.