Biotechnologist | Step Into Biopharma Manufacturing #HDCA
Roles & Responsibilities
Ready to take your biotechnology expertise into the world of biopharmaceutical manufacturing?
Join a fast-paced and highly regulated biopharma environment where your technical skills, attention to detail and GMP knowledge can make a real impact. We’re looking for a Biotechnologist with solid GMP experience to support critical manufacturing operations and contribute to quality-driven processes.
Why This Opportunity?
Gain valuable exposure to biopharmaceutical manufacturing operations
Work within a GMP-regulated environment with established processes and quality standards
Collaborate with multidisciplinary teams across manufacturing, quality and technical functions
Be involved in process execution, documentation, troubleshooting and continuous improvement
Build deeper expertise in the biopharma and life sciences industry
Your Key Responsibilities
Execute day-to-day biopharmaceutical manufacturing activities in accordance with approved SOPs and GMP requirements.
Perform manufacturing processes accurately while ensuring adherence to safety, quality and compliance standards.
Complete batch records, manufacturing documentation and other relevant records accurately and in a timely manner.
Monitor processes and equipment, identifying and escalating abnormalities or deviations when required.
Support investigations, corrective and preventive actions, and continuous improvement initiatives.
Work closely with Quality, Engineering and other relevant teams to ensure smooth and compliant operations.
Maintain a clean, organised and compliant manufacturing environment.
What You Bring
Diploma or Degree in Biotechnology, Life Sciences, Biological Sciences, Biochemistry or a related discipline.
GMP experience is strongly preferred.
Experience within pharmaceutical, biopharmaceutical, biologics or other regulated manufacturing environments is advantageous.
Familiarity with GMP documentation, SOPs and quality systems.
Strong attention to detail with a commitment to accuracy, quality and compliance.
A proactive and collaborative approach to working in a manufacturing environment.
Ready for Your Next Biopharma Opportunity?
If you have GMP experience and are keen to grow your technical exposure within the biopharmaceutical industry, this could be an exciting opportunity to take your career further.
📩 Send your updated CV to:
healthcaretemps@recruitexpress.com.sg
EA License Information
Leon Leong De Cong
R1551708
Recruit Express Pte Ltd
EA License No. 99C4599
Tell employers what skills you have
manufacturing environment
CGMP manufacturing
Deviations
Pharmaceutical Manufacturing
Quality Management
monitoring of equipment
GMP
Operational Delivery Teams
Biotechnology Industry
Biotechnology
Preventive Actions
Organic Chemistry
Process Safety Management
Continuous Improvement Programme
Standards Compliance
Molecular Biology
Project Coordination
producing documentation
Life Sciences
Laboratory