Senior Process Engineer (Pharmaceutical)

AMARIS GROUP SA; Singapore; On-site; SGD 90,000 - 130,000; Full time

Benefits offered by this job

Internal Academy

Global team culture

ESG & sustainability initiatives

Job summary

AMARIS GROUP SA in Singapore is seeking a Senior Process Engineer to support pharmaceutical/biopharmaceutical manufacturing. You will design processes, develop P&IDs, URS, risk assessments, and manage lifecycle documentation while driving safety, reliability, and efficiency on site.

You will lead design reviews, qualification activities, FAT/SAT/IQ/OQ/PQ, and GMP-compliant change controls, deviations, and CAPAs.

Qualifications

• Degree in Chemical Engineering or related field.
• Experience in process design, P&ID development, URS, risk assessments.
• Experience with design reviews and HAZOP.
• Knowledge of FAT/SAT/IQ/OQ/PQ and requalification.

Responsibilities

• Develop process designs, P&IDs, URS, SRA/FRA and other engineering docs.
• Participate in design reviews, design qualification, and HAZOP.
• Lead lifecycle documentation and change controls, deviations, and CAPAs.
• Support qualification, validation activities and commissioning.
• Lead process systems ownership including CIP/SIP, washers, and autoclaves.
• Collaborate with MS&T, Automation, Manufacturing, Quality, and Engineering teams.

Skills

Process design

P&ID development

URS/SRA/FRA documentation

HAZOP participation

Qualification & validation (FAT/SAT/IQ

CAPA management

Troubleshooting

Cross-functional collaboration

Education

Bachelor's degree in Chemical Engineering

Job description

Senior Process Engineer (Pharmaceutical)

Permanent Job

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.)
• At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support.

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.