Biotechnologist (Pharma Manufacturing/ Contract)

Biotechnologist (Pharma Manufacturing/ Contract) 12-Months Contract Location: Buona Vista Salary: Up to $4,800 depending on experience Industry : 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 RecoveryDownstream: Chromatography, Filtration, Ultrafiltration, Final FillingCentral 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: • Degree 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) - Apple.lim@manpower.com.sg Recruitment Consultant (R2090579) Manpower Staffing Services (S) Pte Ltd EA Licence: 02C3423