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Biotechnologist (Pharma Manufacturing/ Contract)
Job reference: 159897
Industry: Pharmaceuticals- brand-id: R2090579
Brand Name: 02C3423
Biotechnologist (Pharma Manufacturing/ Contract)
12-Months Contract
Location: Buona Vista
Salary: Up to $6,000 depending on experience
Indsutry : Biopharmaceutical
Our client is a global biopharmaceutical company that develops innovative medicines in areas such as immunology, oncology, neuroscience, eye care and aesthetics. Its Singapore office serves as a regional commercial hub supporting healthcare innovation and patient care.
Primary Function:
- Performs functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components, and final materials.
- Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner.
- Supports operations & troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan.
Responsibilities:
Operations and Technical
- Adhere to cGMP and safety requirements
- Executes manufacturing operations to perform operations including but not limited to equipment cleaning and set up as well as stream specific operations like:
- Upstream: Vial Thaw, Inoculation, Cell Culture and Recovery
- Downstream: Chromatography, Filtration, Ultrafiltration, Final Filling
- Central Service: Buffer/ Media Preparation, Autoclave, Glasswash and cleaning processes, Sampling of raw materials.
- Carry out daily tasks as assigned by Lead Biotechnologist or Manufacturing Supervisor
- Accurately completing documentation on time, accurately and legibly.
- Maintains inventory levels to minimize distress
- Ensures training is complete and current.
- Responsible for overall plant upkeep during the shift.
- Reports any anomalous processing events to Lead Biotechnologist or Manufacturing Supervisor timely.
Safety
- Adhere to and support all EHS & E standards, procedures, and policies.
Quality
- Accurately completes documentation on time, accurately and legibly
- Reviews documentation for the completeness and accuracy.
- Ensure that all batch related document errors are resolved in a timely manner
- Support in preparation for regulatory audits and inspections
Schedule
- Adheres to production schedule
- Escalates to Lead Biotechnologist or Manufacturing Supervisor in events of unplanned downtimes
Requirements:
- NITEC / Diploma in Sciences, Engineering, or equivalent.
- Min. 2 years of relevant work experience in Biotechnology / Pharmaceutical industry
- Good working knowledge of cGMP and regulatory requirements related to Manufacturing
- Experience with SAP, LIMS, MES systems
- Possess problem-solving and troubleshooting skills.
- Rotational shift work is required
Lim Pey Chyi (Apple) - [email protected]
Recruitment Consultant (R2090579)
Manpower Staffing Services (S) Pte Ltd
EA Licence: 02C3423
