Manufacturing Technician II
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What you'll do
- Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
- Follow standard work instructions and interpret technical drawings to ensure consistent product quality.
- Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.
- Complete all relevant training before performing any task.
- Timely completion of relevant batch records with adherence to Good Documentation Practice (GDP).
- Participate in Practical Process Improvements (PPI) to improve production efficiency and product quality.
- Adhere to all safety protocols and guidelines to maintain a safe working environment.
- Work collaboratively with team members, including engineers, quality assurance, and maintenance personnel.
- Communicate effectively with supervisors and colleagues to ensure smooth production operations.
- Ensure accurate storage and handling of materials to prevent contamination or damage.
- Perform any other duties as assigned by the Manager.
What they're looking for
- Minimum “O” Level, NITEC/ITE education/Diploma in relevant field.
- 1 to 2 years of relevant experiences in pharmaceutical industry or 3 to 5 years of working experience in any industry.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shiftJob Description
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. Surrounded by collaborative colleagues, you’ll have the support and opportunities that only a global leader can give you. 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.
The incumbent will perform various tasks and activities listed below for which they are appropriately trained and are in compliance with the cGMP, company and department SOPs and the safety regulations.
Responsibilities
- Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
- Follow standard work instructions and interpret technical drawings to ensure consistent product quality.
- Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.
- Complete all relevant training before performing any task.
- Timely completion of relevant batch records with adherence to Good Documentation Practice (GDP).
- Participate in Practical Process Improvements (PPI) to improve production efficiency and product quality.
- Adhere to all safety protocols and guidelines to maintain a safe working environment.
- Work collaboratively with team members, including engineers, quality assurance, and maintenance personnel.
- Communicate effectively with supervisors and colleagues to ensure smooth production operations.
- Ensure accurate storage and handling of materials to prevent contamination or damage.
- Perform any other duties as assigned by the Manager.
Education
- Minimum “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.
Company
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