Responsibilities
- Develop Manufacturing/Operating Instructions and necessary Standard Operating Procedures.
- Develop, maintain and troubleshoot the process control system recipe/Models.
- Investigate, report and troubleshoot findings on both quality and EHS related issues observed during manufacturing or during batch record review.
- Develop, implement and monitor robust preventive measures for processing issues.
- Play a pro-active role in ensuring the site safety and quality standards are adhered to.
- Proactively monitor, identify, develop and implement improvements in processes and equipment.
- Communicate on a regular basis to the plant personnel on process updates.
- Train the process technicians on the process and procedures as required.
- Ensure we adhere to our approved procedures and update these as required.
- Own one or more multiple equipment/GMP systems in production and present the system overview with evidence compliance to internal and external auditors.
Requirements
- Degree in Engineering, preferably in Chemical Engineering or Degree in Science with major in Chemistry.
- Preferably 2-3 years’ experience in a relevant Pharmaceutical manufacturing environment.
- Candidates without working experience but have Pharmaceutical GMP intern experience are welcome as training will be provided
- Open to rorating 12 hours shifts
All qualified applicants, please send in your resume to:
Tricia Celestine Goh (R1981653)
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