Ready to take the next step in your career?
Join our dynamic team, and become a part of the NPC community.
PHARMA/BIOTECH
Process/Project Engineer
This position is responsible for the validation of enterprise resource planning systems, automated equipment and/or control systems. Familiarity in DCS (Distributed Control System), PLC/SCADA and OSI PI is a plus. In this role, the engineer has to work in accordance with the company’s policies and procedures to ensure validation is performed in accordance with quality requirements and regulations.
Manufacturing Biotechnologist Downstream/Central Services (Pharma/Biopharma)
The candidate will be expected to support day to day production activities and troubleshoot process related issues.
Manufacturing Engineer
Candidate is responsible for leading the development of operational protocols, execute Change Records and Continuous Process Improvements, manage projects, troubleshoot issues, and collaborate for enhanced manufacturing processes in compliance with GMP regulations.
CQV Engineer
The candidate is responsible to support equipment qualification, system qualification and cleaning validation. In this role, the engineer must ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements.
CSV Engineer
This position is responsible for the validation of automated equipment and/or control systems. Familiarity in DCS (Distributed Control System), PLC/SCADA and OSI PI is a plus and also have thermal mapping experience. In this role, the engineer has to work in accordance with the company’s policies and procedures to ensure validation is performed in accordance with quality requirements and regulations.
QA Production Associate
Responsible for providing oversight for Quality on-the-floor and operations support, the QA Associate will support manufacturing operations and IPC testing through purposeful presence on the floor, and support of complex manufacturing investigations, change control, and unexpected result investigations. Required to perform a 12-hour shift (full night shift preferably).
Senior Validation Engineer
Support equipment qualification, system qualification, and cleaning validation.
Quality Operations Specialist
Quality Operations Specialists must assist site management to oversee the quality system execution on the manufacturing and production areas at all times.
The personnel are required to observe, document, discuss, and report quality adverse events related to the manufacturing of the product and are responsible to ensure highest quality and compliance of released batches.
Manufacturing Biotechnologist Upstream
As our Biotechnologist, you will be expected to perform routine manufacturing processes and troubleshoot process related issues.
Validation Engineer
The candidate is responsible for supporting validation activities including develop, support and implementation. In this role, the engineer has to ensure qualification activities are performed in accordance with the company’s policies and procedures, and regulatory requirements.
EHS Engineer (F&B Alternative Food Technology)
This role involves supporting the development and implementation of EHS policies. It also includes conducting risk assessments, enforcing safe management measures, coordinating audits, maintaining safety documentation, and overseeing workplace safety, including drills and emergency management exercises.
Process Engineer (Active Pharmaceutical Ingredient)
This role involves leading improvement initiatives for manufacturing processes, supporting operational efficiency goals, troubleshooting process, equipment issues, conducting risk assessments, and ensuring quality documentation for SOPs, reports, and protocols.
Laboratory Analyst (Pharma/Biotech)
The position involves conducting biochemistry and analytical testing for lot release of products, ensuring compliance with quality standards, maintaining laboratory equipment and cleanliness, supporting operations like method transfer and documentation management, and participating in regulatory audits and continuous improvement initiatives.
