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Process/ Project Engineer Responsibilities: Experience in upstream / downstream / Central services process operation, (experience in equipment design for process equipment will be an advantage). Responsible for basic and detailed design, commissioning and qualification activities, including URS development, FAT, SAT, DQ, IQ, OQ and PQ. Review industry practices for best-in-class approach. Ensure that the appropriate Quality standards are applied consistent with best practice and internal Quality Standards and expectations. Engage with project teams to deliver the project from conceptual through implementation phase, encompassing support for a wide range of engineering and construction requirements. Coordinates with different functions like manufacturing, project engineering team, validation and quality for implementation of changes associated with the project. Work independently and/or with the project manager to complete the engineering projects within schedule, budget and quality constraints. Any other task as assigned by Supervisor/Manager. About You: Diploma/Degree in Chemical Engineering, Chemistry or equivalent with at least 5 years' experience in a process engineering role or similar role with a biologics manufacturing plan At least 2-5 years of relevant working experience in the Pharmaceutical / Biologics manufacturing industry with experience in Process Engineer In Biologics industry with understanding of cGMP requirement Should have Design experience at various stages of project (Base, Detailed design) Preferably handling the Autoclave, Glove box, CIP Skid during project phase Able to support Installation, Commissioning & Qualification activity at site. Any other task given related to Process. Submit your resume to recruitment@nusaprime.com. Only shortlisted candidates will be contacted.

Upstream MSAT Specialist Responsibilities: Perform routine lab cell culture tasks, including subculturing, passaging, and maintaining cell lines in compliance with established protocols. Monitor cell health, viability, and growth characteristics, reporting any deviations or anomalies promptly. Prepare and sterilize cell culture media, supplements, and reagents. Ensure accurate documentation of media preparation procedures and maintain inventory levels Adhere to rigorous quality control standards to ensure the integrity and purity of cell cultures. Maintain detailed records of all cell culture activities, documenting parameters such as cell counts, passage numbers, and viability. Ensure cleanliness and organization of the laboratory space, including benchtops, equipment, and storage areas Dispose of biological waste and hazardous materials in accordance with safety guidelines and regulations. Operate, clean, and maintain laboratory equipment, including incubators, biosafety cabinets, centrifuges, and microscopes. Report any equipment malfunctions or irregularities to the supervisor for timely resolution. Implement and uphold strict aseptic techniques to prevent contamination of cell cultures. Perform routine cleaning and sterilization of work areas and equipment to maintain a controlled environment. Contribute to the development and optimization of protocols for cell culture procedures. Collaborate with peers and supervisors to design and validate new experimental techniques. Generate comprehensive reports summarizing experimental procedures, results, and observations. Compile and analyze data, ensuring accuracy and completeness prior to submission. Collaborate with multidisciplinary teams to achieve project objectives. Assist in experimental design and troubleshooting as needed. Perform any other tasks as assigned by the manager. About You: Diploma/Bachelor's degree in a relevant life science field (e.g., biology, biotechnology, biochemistry). Previous experience in cell culture techniques and aseptic procedures is required. 3-6 years lab cell culture experience is preferred. Familiarity with laboratory equipment and techniques associated with cell culture operations. Strong attention to detail, organizational skills, and the ability to work independently or in a team. Excellent communication skills, both written and verbal, in English. Adherence to safety protocols and regulatory compliance Submit your resume to recruitment@nusaprime.com. Only shortlisted candidates will be contacted.

PIONEERING LEAN, HOLISTIC SOLUTIONS FOR PHARMACEUTICAL , LIFE SCIENCES AND F&B INDUSTRIES ACROSS ASIA HOW DO WE DO IT? NUSANTARA PRIME CONSULTING is a Singapore-based company that focuses on technical consulting solutions led by a team of industry practitioners. We have been delivering solutions to clients since 2019 with an impressive portfolio of professional consulting services that are completely customizable for your business. Interested to be part of us? Submit your resume to recruitment@nusaprime.com OUR OFFERING S Whatever your needs may be, we can make it happen. Get in touch with us today. BOOK CONSULTATION Design Solution Projects Staff Augmentation Technology Transfer Management Validation Support Health Authority Audit Training Expansion Consulting Waste Management Consulting MES TECHNOlogy support Contact Us Address Location Singapore Office NUSANTARA PRIME CONSULTING (NPC) 12 Arumugam Road, #06-04, LTC Building B Singapore 409958 Contact Phone Mail : +65 6910-8368 : hello@nusaprime.com : NUSANTARA PRIME CONSULTING PTE LTD (Nusaprime) Location Indonesia Office PT ANTERO TEKNIK UNGGUL INDONESIA (PT ATUI) CYBER 2 TOWER, 18TH Floor JL H.R. Rasuna Said Blok X-5, Kav 13 Kuningan Timur, Setiabudi Jakarta Selatan – DKI Jakarta Mail :hello@ptatui.com : PT Antero Teknik Unggul Indonesia