Process Engineer - Pharma Manufacturing - West
Occupation
PROCESS ENGINEER
Job Description & Requirements
1-year renewable contract
Normal office hours
Tuas site
Responsibilities:
• Develop Manufacturing/Operating Instructions and Standard Operating Procedures
• Develop, maintain and troubleshoot the process control system recipes/models
• Investigate, report, and troubleshoot findings on both quality and EHS related issues observed during manufacturing / 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
• Perform production review on batch records
• Proactively monito, identify, develop and implement improvements in processes and equipment
• Train process technicians on processes and procedures
• Focus on safety and GMP compliance as operational priorities and as performance measures. This includes alarm reductions, CPV, etc.
• Be the subject matter experts of assigned topics for internal and external audits.
• Perform other tasks necessary to support site compliance to Center and regulatory requirements
Qualifications:
Must-Have
• Bachelor's Degree, preferably in Chemical Engineering
• Demonstrated ability to provide technical solutions for complex problems through equipment and process understanding
• Working knowledge of Food and Drug Administration Regulations, and Good Manufacturing Practices
• Proactive, has experience with high-performance teams, strong interpersonal and project management skills
• Strong written and verbal communication skills
Nice-to-Have
- Demonstrated experience in a relevant manufacturing environment
- API experience is good to have
- Chemical Plant experience
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