Senior Process Engineer (Pharmaceutical)

Amaris Consulting; Singapore; On-site; SGD 90,000 - 130,000; Full time

Benefits offered by this job

International team

Internal Academy training

Team events

Job summary

Amaris Consulting in Singapore seeks an experienced Process Engineer to provide process engineering support in pharmaceutical/biopharmaceutical manufacturing. You will design, qualify, troubleshoot, automate, and continuously improve process systems while ensuring safe and reliable site operations.

Responsibilities include leading change controls, CAPAs, and qualification activities across SIP/CIP and autoclaves; collaborating with MS&T and Automation teams, and supporting validation and

Qualifications

• 5–8 years of experience in process engineering within regulated pharma/biotech manufacturing.
• Experience with process design, P&ID development, URS, risk assessments, design reviews, and HAZOP.
• Knowledge of qualification/validation activities including FAT, SAT, IQ, OQ, PQ, and requalification.

Responsibilities

• Develop process designs, P&IDs, URS, SRA, FRA and other engineering documentation.
• Participate in design reviews, design qualification activities, and HAZOP studies.
• Generate, review and maintain process engineering documentation through its lifecycle.
• Support FAT, SAT, IQ, OQ, PQ, qualification, requalification and validation activities.
• Lead and manage process engineering change controls, deviations and CAPAs.
• Own process systems and equipment, including SIP, CIP, washers and autoclaves.
• Provide independent technical support to ensure safe, reliable site operations.
• Lead process improvements focused on equipment performance, yield optimization and cycle-time reduction.
• Act as link between MS&T and Automation teams; translate process requirements into automation modules, recipes and parameters.
• Support recipe testing and collaborate with Automation teams to implement system changes.
• Lead troubleshooting, design reviews and optimization to minimize risks; provide on-call support as needed.
• Assist during absences and represent function in delegated meetings.
• Provide guidance to assigned resources when required.
• Support continuous improvement initiatives.

Skills

Process engineering

P&ID development

URS & risk assessments

HAZOP studies

Qualification & validation

CAPA management

Troubleshooting

Cross-functional collaboration

On-call support

Education

Degree in Chemical/Process Engineering

Job description

You’ll have the opportunity to work within our Life Sciences team, providing process engineering support in a pharmaceutical or biopharmaceutical manufacturing environment. You will contribute to equipment and process design, qualification, troubleshooting, automation changes, and continuous improvement while helping ensure safe and reliable site operations.

About The Job

• Develop process designs, P&IDs, User Requirement Specifications (URS), System Risk Assessments (SRA), Functional Risk Assessments (FRA), and other engineering documentation
• Participate in design reviews, design qualification activities, and HAZOP studies
• Generate, review, and maintain process engineering documentation throughout its lifecycle
• Support FAT, SAT, IQ, OQ, PQ, qualification, requalification, and validation activities
• Lead and manage process engineering change controls, deviations, and CAPAs
• Take ownership of process systems and equipment, including SIP, CIP, washers, and autoclaves
• Provide independent technical support to ensure safe, reliable, and efficient site operations
• Lead process and engineering improvements focused on equipment performance, yield optimization, and cycle-time reduction
• Act as the link between Manufacturing Science and Technology (MS&T) and Automation teams
• Translate process requirements into the required automation equipment modules, recipes, and parameters
• Support recipe testing and collaborate with Automation teams to implement system changes
• Lead process and engineering troubleshooting, design reviews, and optimization activities to minimize operational and supply risks
• Provide on-call support for complex process issues according to operational requirements, which may include support outside regular working hours
• Support lead responsibilities during absences and represent the function in delegated meetings
• Provide guidance or limited oversight to assigned resources when required
• Support continuous improvement initiatives and perform other responsibilities assigned by the manager

About You

• Degree in Chemical Engineering, Process Engineering, Pharmaceutical Engineering, Biotechnology, Mechanical Engineering, or a related field
• 5–8 years of experience in process engineering within a pharmaceutical, biopharmaceutical, biotechnology, or similarly regulated manufacturing environment.
• You have experience with process design, P&ID development, URS, risk assessments, design reviews, and HAZOP
• You understand qualification and validation activities, including FAT, SAT, IQ, OQ, PQ, and requalification
• You have practical knowledge of CIP, SIP, washers, autoclaves, or comparable pharmaceutical process systems
• You are experienced in managing change controls, deviations, investigations, and CAPAs
• You understand automated manufacturing processes, including equipment modules, recipes, and process parameters
• You can collaborate effectively with MS&T, Automation, Manufacturing, Quality, Validation, and Engineering teams
• You demonstrate strong troubleshooting, analytical, documentation, and problem-solving skills
• You can work independently, propose practical solutions, and assume lead responsibilities when required
• You are available to provide on-call technical support according to operational needs

WHY AMARIS?

• An international community bringing together 110+ different nationalities
• An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
• A robust training system with our internal Academy and 250+ available modules
• A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)

Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Who are we?

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. With more than 1,000 clients across the globe, we have been rolling out solutions in major projects for over a decade – this is made possible by an international team of 7,600 people spread across 5 continents and more than 60 countries. Our solutions focus on four different Business Lines: Information System & Digital, Telecom, Life Sciences and Engineering. We’re focused on building and nurturing a top talent community where all our team members can achieve their full potential. Amaris is your steppingstone to cross rivers of change, meet challenges and achieve all your projects with success.