Key Responsibilities
- Engage with Business SMEs and Key Users to gather, analyze, and document manufacturing requirements
- Translate business needs into functional and technical MES solutions
- Collaborate with MES engineers to design, configure, and test system functionalities
- Design and develop Process Instructions (PIs) aligned with site-specific manufacturing processes
- Identify commonalities across sites and develop global PIs/templates for reuse and standardization
- Perform validation activities for MES solutions in compliance with regulatory standards (e.g., GxP)
- Create and maintain project documentation, including: User Requirement Specifications (URS) Functional Requirement Specifications (FRS) Design Specifications (DS) Test Scripts (IQ/OQ/PQ support)
- Lead a team of consultants/engineers, assign tasks, and ensure timely delivery
- Provide regular status updates to internal management and customer stakeholders
- Support system deployment, user training, and post-go-live activities
- Any other adhoc duties as assigned.
Required Qualifications
- Bachelor's degree in Engineering, Computer Science, or related field
- 4-10+ years of experience in MES, preferably in pharma or life sciences
- Hands-on experience with Siemens Opcenter Execution Pharma (Simatic IT eBR)
- Strong understanding of electronic batch records (eBR) and manufacturing workflows
- Experience with validation processes in regulated environments (GxP, CSV)
- Proven experience in documentation (URS, FRS, DS, test protocols)
- Leadership experience or ability to manage small teams
Interested applicants, please Email , and look for
Jensen Fang Lifa
Recruit Express Pte Ltd
EA License No. 99C4599
EA Personnel Registration Number: R2197080
We regret that only shortlisted candidates will be contacted.
