Hybrid Lead Formulation Technician bei Thermo Fisher Scientific Inc.
Thermo Fisher Scientific Inc. · Singapore, Singapur · Hybrid
- Senior
- Optionales Büro in Singapore
Work Schedule
12 hr shift/nightsEnvironmental 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 materialsJob Description
Job Title: Lead Formulation Technician
Reports to: Operations Manager
How Will You Make an Impact?
Thermo Fisher Scientific Inc. is a key player in the science industry, generating around $40 billion in annual revenue. Our mission is to support customers in making the world healthier, cleaner, and safer. We aid in life sciences research, analytical problem-solving, and outstanding lab efficiency with our distributed team.
What will you do?
As a Lead Formulation Technician at Thermo Fisher Scientific, you will have the outstanding opportunity to coordinate and optimize production processes, ensuring world-class quality and efficiency! Your role is crucial in maintaining our exceptionally high standards of cGMP, safety, and housekeeping. You will collaborate with a dedicated team to successfully implement production schedules and achieve detailed results.
Responsibilities
- Monitor production activities to ensure processes adhere strictly to SOPs and quality standards.
- Assist in day-to-day production activities and approve production cycles.
- Ensure efficient allocation of personnel and equipment, liaising with associated departments.
- Investigate and troubleshoot quality deviations, ensuring timely resolution.
- Maintain accurate batch documentation and ensure adherence to cGMP and GDP.
- Provide oversight during preventive and breakdown maintenance.
- Lead Continuous Improvement activities to improve Quality and Efficiency.
- Operate pharmaceutical production equipment and perform formulation activities as required.
- Ensure all tasks are completed with strict compliance to SOPs and GMP.
- Participate in EHS, Business Compliance, and other compliance-related matters.
How will you get here?
Education
- Minimum “O” Level, NITEC/ITE education/Diploma in a relevant field.
Experience
- Minimum 5 years of relevant experience in the pharmaceutical industry.
Knowledge, Skills, Abilities
- Good understanding of safe working practices and cGMP.
- Highly motivated to work in the pharmaceutical industry.
- Strong great teammate with the ability to work rotating shifts.