- Experience
- 1–5 yrs
- Salary
- —
- Openings
- 1
- Posted
- 3 weeks ago
- Work mode
- In office
- Education
- NITEC/ITE/Diploma
- Resume
- Required to apply
Where you'll work
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Job description
Work Schedule and Environment
The standard working days are Monday through Friday. The role requires the ability to lift up to 40 pounds without assistance and compliance with rigorous Good Manufacturing Practices (GMP) safety standards. Working in a cleanroom setting imposes restrictions such as no use of hair products, jewelry, makeup, nail polish, perfume, exposed piercings, or facial hair. Personal Protective Equipment such as safety glasses, gowns, gloves, lab coats, and ear plugs must be worn. Standing for the entire shift is also necessary.
About the Role
Joining Thermo Fisher Scientific means becoming part of a collaborative and supportive global leader with a promising strategy for growth. This position contributes significantly to biopharmaceutical advancements by carrying out various technical manufacturing tasks while complying fully with company and industry regulations.
Responsibilities
- Assemble Single-Use Bio-Processing Containers used in critical sterile liquid-handling within the biopharmaceutical sector.
- Adhere to standard operating procedures and accurately interpret technical drawings to maintain product consistency.
- Strictly comply with ISO 13485:2016, ISO 22301:2019, and cGMP documentation standards ensuring regulatory and quality compliance.
- Complete mandatory training sessions before undertaking any manufacturing tasks.
- Timely and accurate batch record completion, following Good Documentation Practices.
- Engage in Practical Process Improvement initiatives aimed at enhancing production and product quality.
- Maintain workplace safety by following all protocols and guidelines.
- Collaborate with engineers, quality assurance, and maintenance teams.
- Communicate clearly with supervisors and colleagues to support efficient production flows.
- Manage the correct storage and handling of materials to avoid contamination or damage.
- Perform additional duties as assigned by management.
Requirements
- Minimum qualifications include an "O" Level certification, NITEC/ITE education, or Diploma in a relevant discipline.
- Possess 1 to 2 years of experience in the pharmaceutical field or 3 to 5 years in any industry.
- Sound knowledge of safe working practices and cGMP principles.
- Strong motivation to develop a career in pharmaceutical manufacturing.
- Capability to work effectively as part of a team.
- Flexibility to work rotating shifts.
Minimum education
Diploma / ITI / Vocational