Commissioning & Qualification process Engineer/Lead

HMI TECH PTE. LTD.; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A biopharmaceutical company based in Singapore is seeking an experienced C&Q Execution Leader. The role requires a minimum of 8 years of experience in C&Q execution within the pharmaceutical sector, including leadership responsibilities, and expertise in DeltaV. The successful candidate will oversee project documentation, coordinate with various stakeholders, and ensure compliance with regulatory standards.

Qualifications

• 8 years minimum C&Q execution experience in the pharmaceutical sector.
• Minimum of 1 year in a C&Q execution leadership role.
• Knowledge of GMP's and regulatory requirements.

Responsibilities

• Lead a team in preparing and executing Biopharmaceutical Process Equipment C&Q documents.
• Provide technical oversight to assure technical work quality.
• Coordinate with Engineering Compliance, QA, and other stakeholders.

Skills

C&Q execution experience

Leadership skills

Teamwork

DeltaV proficiency

Education

Degree in engineering (M. Sc. / B. Sc.) or equivalent

Job description

Key Responsibilities:

• Abide by all safety requirements and procedures pertaining to their role; serve as a positive model to others in this regard; re‑enforce in meetings, perform periodic field observation and feedback as needed.
• Lead a team as the system owner in preparing and executing Biopharmaceutical Process Equipment C&Q documents, ensuring achievement of the project schedule, track and report progress to the C&Q Manager.
• Provide a strong working technical knowledge of Biopharmaceutical Process Equipment systems regarding the development of protocols, their execution, and close out.
• Provide technical oversight to a Biopharmaceutical Process Equipment C&Q team to assure technical work quality, consistency, and alignment with the C&Q programme.
• Work in the Kneat platform for preparation, review and approval of C&Q documentation with a key focus on traceability to User Requirements throughout.
• Coordinate with the Engineering Compliance team, the QA team and other stakeholders in assuring all decisions on the document preparation for Biopharmaceutical Process Equipment systems are aligned and agreed.
• Work collaboratively with the other project disciplines (e.g. automation, construction, engineering, end user) to support integration of activities.
• Train Biopharmaceutical Process Equipment personnel on the C&Q programme and it’s implementation in execution.
• Report on any proposals for deviating from the C&Q program during doc development and execution to ensure they are addressed and, if agreed on, documented in a timely manner.
• Report issues for escalation where agreed document review and approval (pre and post, where applicable) turnaround times are not being adhered to.
• Report issues for escalation where agreed execution timelines are not being adhered to.
• Report any other issues which need to be escalated when no resolution is clear with the stakeholders internally.

Qualifications and Requirements:

• 8 years minimum C&Q execution experience in the pharmaceutical sector with a minimum of 1 in a C&Q execution leadership role.
• Degree in engineering (M. Sc. / B. Sc.) or equivalent.
• Demonstrated leadership and people management skills.
• Knowledge of GMP’S, regulatory requirements, equipment commissioning and qualification.
• Ability to work well in a team environment.
• Able to manage multiple parties and coordination.
• Proficient in the use of DeltaV.