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NUSAntara Prime Consulting Pte Ltd Jobs: 48+ Job Opportunities in Singapore

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Laboratory Analyst (Microbiology)

Main Responsibilities Conduct environmental monitoring sampling across various cleanroom classifications. Perform utilities monitoring (e.g., Water System, Compressed Gas System). Execute bench microbiological testing including incubation/plate reading, bioburden, endotoxin, ...

QC S&T Analyst (Pharma/Biotech)

Responsibilities Supports team task to support laboratory operation and infrastructure in the areas of examples: Equipment, Data Systems, Method) needs Participates in the management of laboratory equipment and computerized systems in QC laboratory to ensure business continuity and s ...

IT System Analyst (Pharma/Biotech)

This role undertakes projects related to onboarding new Manufacturing, Lab, or Shopfloor systems, applications, and devices. It requires working in a team, proficiency in Manufacturing systems, Lab systems, network and security standards and the System Life Cycle process, as well as effective problem-solvi ...

Quality Assurance Specialist (Pharma/Biotech)

Responsibilities: Ensure adherence to the Change Control management systems and processes. Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed. Evaluate C ...

Laboratory Analyst (Pharma/Biotech)

Responsibilities Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freez ...

Senior Laboratory Analyst (Pharma/Biotech)

Responsibilities Responsible for the timely completion and data verification of all testing of raw material, intermediates, in-process control samples and final product Maintain up-to-date, complete and precise records of all tests performed Ensure that all test equipmen ...

Warehouse/Logistics Assistant (Pharma/Biotech)

Responsibilities: Ensure accurate and timely receiving and issuance of materials to production from internal warehouse and 3PL to ensure no production stoppages. Raising of materials damage report, materials disposition authorization and any other document to track th ...

QA Operation

Responsible for overseeing manufacturing, testing and validation activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities: Oversee routine quality control for on-site GMP production and testing, ensuring all GMP activities a ...

Warehouse Operation

Overview This position is responsible for supporting all aspects of production within the distribution area. This includes assembly, test, loading of customer-specific software, packaging, inventory control, shipping, and any other tasks required to meet production targets. Main Responsibi ...

Laboratory Analyst (Microbiology)

Main Responsibilities Conduct environmental monitoring sampling across various cleanroom classifications. Perform utilities monitoring (e.g., Water System, Compressed Gas System). Execute bench microbiological testing including incubation/plate reading, bioburden, endotoxin, and growth promotion ...

QC S&T Analyst (Pharma/Biotech)

Responsibilities Supports team task to support laboratory operation and infrastructure in the areas of examples: Equipment, Data Systems, Method) needs Participates in the management of laboratory equipment and computerized systems in QC laboratory to ensure business continuity and system data mainte ...

IT System Analyst (Pharma/Biotech)

This role undertakes projects related to onboarding new Manufacturing, Lab, or Shopfloor systems, applications, and devices. It requires working in a team, proficiency in Manufacturing systems, Lab systems, network and security standards and the System Life Cycle process, as well as effective problem-solving ...

CSV Validation Engineer (Pharma/Biotech)

Responsibilities Work with a cross functional team in providing Quality oversight in computerized system life cycle procedure and ensure compliance to GXP standards and company policies and procedures. As the Subject Matter Expert (SME) in CSV topics, provide guidance and support to establish systems ...

Laboratory Analyst (Pharma/Biotech)

Responsibilities Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, water bath, etc. ...

Process/Project Engineer (Pharma/Biotech)

Overview The role is responsible for Equipment Package Ownership (full lifecycle – Engineering Design, Build, Testing (FAT), Installation and Commissioning), including experience in commissioning and qualification of process equipment. Responsibilities Experience in upstream / downstream / Centra ...

Senior Laboratory Analyst (Pharma/Biotech)

Responsibilities Responsible for the timely completion and data verification of all testing of raw material, intermediates, in-process control samples and final product Maintain up-to-date, complete and precise records of all tests performed Ensure that all test equipment is used and maintained p ...

Manufacturing Engineer

Responsibilities: Lead and execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for Production, Support Change Records Assessment and GMP documentation Review. Responsible for providing support ...

Process/Project Engineer

The role is responsible for Equipment Package Ownership (full lifecycle – Engineering Design, Build, Testing (FAT), Installation and Commissioning), including experience in commissioning and qualification of process equipment. Responsibilities: Experience in upstream / downstream / Central ...

Validation Engineer

This role is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer must ensure qualification activities are performed in accordance with the company's policies and procedures, and regulatory requirements. Responsibilities: <li ...

Senior Laboratory Analyst

Responsibilities: Responsible for the timely completion and data verification of all testing of raw material, intermediates, in-process control samples and final product Maintain up-to-date, complete and precise records of all tests performed Ensure that all test equipment is use ...

Project Engineer

Responsibilities: Assist in the design, operation, control and optimization of biological processes To be part of the commissioning and qualification effort of the process equipment and associated systems. Design, install and commission new production units, monitoring modificati ...

Process Engineer

Responsibilities: Support new product introduction (NPI) and technology transfer activities Support process validation and characterization studies. Develop process validation and process characterization study protocols/reports in accordance with relevant policies, standards, pr ...

Project Engineer

Responsibilities: Assist in the design, operation, control and optimization of biological processes To be part of the commissioning and qualification effort of the process equipment and associated systems. Design, install and commission new production units, monitoring modificati ...

Manufacturing Biotechnologist Upstream

Responsibilities: 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. Perfor ...

Cleaning Supervisor

Responsibilities: Supervision of facility GMP cleaner. Training of GMP cleaners. Resource and schedule management of GMP cleaners. Material and consumable management. Conduct regular safety inspections and implement corrective actions. Develop and enfor ...

Manufacturing Biotechnologist Downstream/Central Services

Responsibilities: 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. Perfor ...

Laboratory Analyst

Responsibilities: Perform biochemistry, analytical and raw material of in-process and marketed products for lot release in accordance with quality standards and procedures Responsible for housekeeping duties in the lab. Perform Quality Tag Out for laboratory equipment such as freezer, wat ...

Change Control Specialist

Responsibilities: Raise change control from end to end Serve as the primary manufacturing representative for initiating, assessing, and implementing change controls impacting production processes, equipment, materials, and procedures. Collaborate with cross-functional teams (QA, ...

Quality Assurance Specialist

Responsibilities: Ensure adherence to the Change Control management systems and processes. Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed. Evaluate Change Control request ...

CQV Engineer

Responsibilities: Ensure validation activities comply with cGDP and ALCOA guidelines. Draft & implement approved protocols, identify non-conformances to User Requirements Maintain detailed documentation and provide regular updates to stakeholders. Any other task as assig ...

Warehouse/Logistics Assistant

Responsibilities: Ensure accurate and timely receiving and issuance of materials to production from internal warehouse and 3PL to ensure no production stoppages. Raising of materials damage report, materials disposition authorization and any other document to track the movement of invento ...

QC S&T Analyst

Roles & Responsibilities Responsibilities: Supports team task to support laboratory operation and infrastructure in the areas of examples: Equipment, Data Systems, Method) needs Participates in the management of laboratory equipment and computerized systems in QC laboratory t ...

Change Control Specialist

Roles & Responsibilities Responsibilities: Raise change control from end to end Serve as the primary manufacturing representative for initiating, assessing, and implementing change controls impacting production processes, equipment, materials, and procedures. Colla ...

Warehouse/Logistics Assistant

Roles & Responsibilities Responsibilities: Ensure accurate and timely receiving and issuance of materials to production from internal warehouse and 3PL to ensure no production stoppages. Raising of materials damage report, materials disposition authorization and any other doc ...

Manufacturing Biotechnologist Downstream/Central Services

Roles & Responsibilities Responsibilities: 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 ...

Change Control Specialist

Roles & Responsibilities Responsibilities: Raise computerized system change control Coordinate CSCC review/approval Work with validation on test case generation Assist in design document revision About You: At least 2 years of r ...

Warehouse Operation

Roles & Responsibilities This position is responsible for supporting all aspects of production within the distribution area. This includes assembly, test, loading of customer-specific software, packaging, inventory control, shipping, and any other tasks required to meet production targets. M ...

Senior CQV Engineer

Responsibilities: The incumbent will lead commissioning, qualification, and validation (CQV) activities for Lab Equipment. About You: Diploma/Degree in Engineering or Science Disciplines with at least 5 years' experience in lab equipment CSV (computer system validation). ...

QA Operation

Responsible for overseeing manufacturing, testing and validation activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities: Oversee routine quality control for on-site GMP production and testing, ensuring all GMP activities are executed in strict ...

Laboratory Analyst

Main Responsibilities: Conduct environmental monitoring sampling across various cleanroom classifications. Perform utilities monitoring (e.g., Water System, Compressed Gas System). Execute bench microbiological testing including incubation/plate reading, bioburden, endotoxin, and ...

Process Engineer

Responsibilities: Support new product introduction (NPI) and technology transfer activities Support process validation and characterization studies. Develop process validation and process characterization study protocols/reports in accordance with relevant policies, standards, pr ...

Process/Project Engineer

The role is responsible for Equipment Package Ownership (full lifecycle – Engineering Design, Build, Testing (FAT), Installation and Commissioning), including experience in commissioning and qualification of process equipment. Responsibilities: Experience in upstream / downstream / Central ...

Warehouse Operator

This position is responsible for supporting all aspects of production within the distribution area. This includes assembly, test, loading of customer-specific software, packaging, inventory control, shipping, and any other tasks required to meet production targets. Main Responsibilities: En ...

Manufacturing Engineer

Responsibilities: Lead and execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for Production, Support Change Records Assessment and GMP documentation Review. Responsible for providing support ...

CQV Engineer

Responsibilities: Ensure validation activities comply with cGDP and ALCOA guidelines. Draft & implement approved protocols, identify non-conformances to User Requirements Maintain detailed documentation and provide regular updates to stakeholders. Any other task as assig ...

Senior CQV Engineer

Responsibilities: The incumbent will lead commissioning, qualification, and validation (CQV) activities for Lab Equipment. About You: Diploma/Degree in Engineering or Science Disciplines with at least 5 years' experience in lab equipment CSV (computer system validation). ...

Quality Assurance Specialist

Responsibilities: Ensure adherence to the Change Control management systems and processes. Develop competency and proficiency in the QA Change Control process and the associated tools, supporting the delivery of training for change users as needed. Evaluate Change Control request ...

QA Operation

Main Responsibilities: Responsible for overseeing manufacturing, testing and validation activities, ensuring compliance with internal procedures and regulatory requirements. Responsibilities: Oversee routine quality control for on-site GMP production and testing, ensuring all GMP act ...

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    Nusantara-Prime-Consulting-Pte-Ltd Jobs in Singapore Job Search Guide, Trends and Insights

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