Biotechnologist - (Pharma MNC, full training provided, GMP) #HCL

Roles & ResponsibilitiesResponsibilities: Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP, etc.) Support day to day production activities and record data according to Electronic Batch Record (EBR) in compliance with GMP, Environmental, Health and Safety guidelines. Perform equipment and process monitoring Able to...

Roles & ResponsibilitiesResponsibilities:Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP, etc.) Support day to day production activities and record data according to Electronic Batch Record (EBR) in compliance with GMP, Environmental, Health and Safety guidelines. Perform equipment and process monitoring Able to communicate...

Roles & ResponsibilitiesResponsibilities:· Assist in Project Execution: Support the execution of capital projects, including equipment hookup and installation.· Stakeholder Engagement: Coordinate with internal teams and contractors to ensure project requirements are understood.· Project Planning & Reporting: Assist in planning, monitoring, and reporting...

Roles & ResponsibilitiesQA Specialist (Validation/ GMP/ CAPA/ Pharma)12 Months ContractLocation: TuasUp to $5,000 depending on experienceIndustry: PharmaceuticalOur client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to...

Roles & ResponsibilitiesQA Specialist (Validation/ GMP/ CAPA/ Pharma)12 Months ContractLocation: TuasUp to $5,000 depending on experienceIndustry: PharmaceuticalOur client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to...

Roles & ResponsibilitiesResponsibilities: Revise and review Standard Operating Procedures (SOPs) to ensure compliance and quality standards. Review executed Manufacturing Batch Records (MBR) / Equipment Batch Records (EBR) for completeness and accuracy. Provide quality oversight and support to the manufacturing team, addressing any quality-related...

Accounts Payable Analyst (Pharma MNC, ERP System)Job Scope: Maintain AP sub-ledger including checking completeness & accuracy of expenses and staff claims and preparing payments Month-end Closing including, but not limited to: Journal Posting Reconciliations/Audit Schedules (Accounts Payables related)Respond to ad-hoc requests for financial information/...

Roles & ResponsibilitiesResponsibilities: Revise and review Standard Operating Procedures (SOPs) to ensure compliance and quality standards. Review executed Manufacturing Batch Records (MBR) / Equipment Batch Records (EBR) for completeness and accuracy. Provide quality oversight and support to the manufacturing team, addressing any quality-related...

Roles & ResponsibilitiesPES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our...

Roles & ResponsibilitiesJobscope: Raise project proposal (STP - Situation, Target & Proposal), Project Investment Proposal (PIP) and justification paper Communication and escalation of project progress, key risk areas and support requirements enabling successful delivery of the project and benefit realization Manage and execute the project in compliance...

Roles & ResponsibilitiesJobscope: Raise project proposal (STP - Situation, Target & Proposal), Project Investment Proposal (PIP) and justification paper Communication and escalation of project progress, key risk areas and support requirements enabling successful delivery of the project and benefit realization Manage and execute the project in compliance...

Roles & ResponsibilitiesJob Description80%• Perform loading and Operating of Autoclave• Responsible for MFR (Manufacturing Formulation Record)/SOP creation and revision• Perform monitoring for process and equipment performance during operation as per SOP/MFR, identify and report if there’s any atypical events• Support investigation to event and...

Roles & ResponsibilitiesKey Responsibilities: Provide Siemens PCS support to manufacturing operations. Perform manual interventions to ensure continuous process operation. Collaborate with production teams and document all activities. Assist with shift handovers and resolve technical tasks with Automation Engineers.Safety and Compliance: Adhere to...

Roles & ResponsibilitiesKey Responsibilities: Provide Siemens PCS support to manufacturing operations. Perform manual interventions to ensure continuous process operation. Collaborate with production teams and document all activities. Assist with shift handovers and resolve technical tasks with Automation Engineers.Safety and Compliance: Adhere to...

Senior/Executive, GMP Procurement & Logistics, ACTRIS Overview The Consortium for Clinical Research and Innovation, Singapore (CRIS) brings together six national R&D, clinical translation and service programmes to advance clinical research and innovation for Singapore, and establish important capabilities for a future-ready healthcare system. The Business...

Roles & ResponsibilitiesQA Specialist (Validation/ GMP/ CAPA/ Pharma)12 Months ContractLocation: TuasUp to $5,000 depending on experienceIndustry: PharmaceuticalOur client aims at creating a new manufacturing concept consisting of a new generation of evolutive multi-product facilities, modular, adaptable, and agile, leveraging new disruptive technologies, to...

Roles & ResponsibilitiesJob ObjectivesEstablish DSSG Quality Management System (QMS) in GMP QA through review and improvement of operational process, and ready for obtaining the importation license and new product launch. Promote GMP/GDP QA activities and enhance QMS. As a result, contributed to the stable supply of the highest quality products and DS's...

Roles & ResponsibilitiesJoin a well-established pharma MNC as a Receptionist & Admin Assistant, providing front desk and administrative support in a dynamic office environment.5-day work week in a stable MNC environment Convenient Central-East location near a mall Yearly renewable contract with bonuses, leave, and medical benefitsResponsibilitiesReception...

At CRIS, we value expertise in logistics management and material qualification processes. Our ideal candidate will ensure compliance with SOP/GMP guidelines and coordinate materials release for production runs.Key responsibilities include:Performing incoming material inspectionManaging inventory and coordinating materials releaseLiaising with various...

Role SummaryThe Quality Operation Specialist is responsible for ensuring site compliance with GMP requirements and corporate policies and procedures. This role involves reviewing and approving GMP documents, collaborating with operations teams, and coordinating shop floor routine compliance.Key ResponsibilitiesEnsure timely delivery of quality oversight...