Process Engineer (Adv PCP) - 2 Years Contract

Job Description

THE OPPORTUNITY

• Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2021, 2022, 2023).
• Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.

Our Engineers support internal and external manufacturing operations to remain operational, continuously improve, and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities, and Validation.

WHAT YOU WILL DO

As a Process Engineer, you will provide process engineering support for manufacturing operations to support continuous improvement to drive safety, quality, process efficiency, and compliance in a cGMP manufacturing environment. You are expected to support various initiatives leveraging quality, safety, and project management platforms, engineering standards, codes, technology, and support department business goals and objectives.

Other main responsibilities include:

• Provide Process Engineering Support for API manufacturing plants in support of business continuity to meet Safety, Quality, environmental, continuous improvement, regulatory, and compliance objectives.
• Support Deviation management related to the equipment, systems in response to deviations/adverse events to investigate and identify point of occurrence, root cause, and corrective/preventative actions.
• Support global change management under various company execution platforms to ensure the equipment, facility, and system changes are executed complying with design standards, safety standards, and quality procedures.
• Support minor capex projects through evaluation of scope, feasibility, design, project proposals, sourcing plan, installation, commissioning & qualification with adherence to site change control procedures within the allotted timeline, budget, design requirements, and established quality standards.
• Demonstrate good project management skills (e.g. define core team and activities, project scheduling, stakeholder management, and issues escalation, etc.), and demonstrate the ability to manage/influence the project team.
• Execute portfolio projects to introduce new technology, engineering standards recommendations, and new codes and practices to support process & energy efficiencies, process safety, and quality compliance.
• Provide technical support during quality and safety external audits/internal inspections in providing technical representation and/or assessments in response to the auditing firms and other regulatory agencies.
• Perform gap assessment & periodic review of current engineering & business procedures, update SOPs, and train the impacted personnel.
• Demonstrate leadership behaviors and lead personal career development with manager assistance through Performance Management and Employee Development Plan (EDP).
• Participate in process hazards analyses (PHA) and applicable Process Safety Management (PSM) activities related to new/inline products. Support EHS audits and Safety incident investigations.
• Support energy initiatives & cost reduction projects.
• Any other duties as assigned by the Supervisor.

WHAT YOU MUST HAVE

• Bachelor’s degree in chemical engineering or biochemical engineering.
• 1 to 3 years technical experience in the manufacturing industry preferred. Fresh graduates are welcome to apply.
• Knowledge of GMP systems, equipment qualification, and commissioning.
• Possess unit operations, equipment knowledge, and troubleshooting skills.
• Perform Process hazard analysis, FMEA, and Risk assessments.
• Application of engineering fundamentals to carry out feasibility studies and develop implementation plans.
• Project management skills to scope, plan, cost, and implement actions in collaboration with multi-functional teams.

This is an Advanced Professional Conversion Program under Workforce Singapore (WSG) and candidates must meet the following criteria and are open to the following conditions:

• Singaporeans/Singapore PRs only.
• Fresh graduates with relevant internships are welcome to apply.
• PMETs/Mid-Careerists with no prior work experience in the Biopharma industry are welcome to apply.

WHAT YOU CAN EXPECT

• Opportunities across various functional groups within biopharmaceutical manufacturing.
• Diverse and dynamic team that focuses on development and success.

Our Manufacturing & Supply Division is committed to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities, along with our external contractors, suppliers, and partners, create an interdependent global manufacturing network that’s committed to delivering a high quality, reliable supply to customers and patients on time, every time.

We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace.

Current Employees apply HERE

Current Contingent Workers apply HERE