Siemens Opcenter MES Engineer (Pharma, CSV, Validation)

Advanced Manufacturing Tech Solutions; Singapore; On-site; SGD 70,000 - 90,000; Full time

Job summary

Advanced Manufacturing Tech Solutions is seeking a Siemens MES – Opcenter Engineer to join their team in Singapore. The role involves implementing and supporting Siemens MES solutions in the pharmaceutical sector, ensuring compliance, validation, and operational excellence. Candidates should have at least 5 years of relevant industry experience.

This position provides an opportunity to work on cutting-edge projects, contributing to global compliance and validation standards while being part of a collaborative environment with career progression opportunities.

Qualifications

• Minimum 5 years of experience in pharmaceutical manufacturing or life sciences projects.
• Proven expertise in MES, preferably Siemens Opcenter.
• Strong knowledge of CSV, deviation writing, and change control processes.

Responsibilities

• Configure and implement Siemens MES – Opcenter modules in pharma manufacturing.
• Lead CSV activities, including deviation handling and change control.
• Collaborate with QA and Document Control teams for compliance.

Skills

Siemens MES – Opcenter

CSV processes

Communication skills

Stakeholder management

Documentation skills

Education

Bachelor’s degree in Engineering, Computer Science, or related discipline

Tools

Kneat

Job description

Job Title: Siemens MES – Opcenter Engineer

Location: Singapore Employment Type: Full‑time

About The Role

We are looking for experienced professionals with 5+ years of pharmaceutical industry experience to join our team in Singapore. The role focuses on implementing and supporting Siemens MES – Opcenter solutions for life sciences manufacturing, ensuring compliance, validation, and operational excellence.

Key Responsibilities

• Configure and implement Siemens MES – Opcenter modules in pharma manufacturing environments.
• Lead and support CSV (Computer System Validation) activities, including deviation handling, change control, and documentation.
• Develop and maintain operating plans and validation protocols.
• Collaborate with QA, Tech Control, and Document Control teams to ensure compliance with GMP and regulatory standards.
• Utilize tools such as Kneat for validation and compliance documentation.
• Provide technical support, troubleshoot issues, and contribute to continuous improvement initiatives.
  
  
  

Requirements

• Bachelor’s degree in Engineering, Computer Science, or related discipline.
• Minimum 5 years of experience in pharmaceutical manufacturing or life sciences projects.
• Proven expertise in MES (preferably Siemens Opcenter).
• Strong knowledge of CSV, deviation writing, and change control processes.
• Familiarity with Kneat or similar compliance tools is a plus.
• Excellent communication, documentation, and stakeholder management skills.
• Ability to work independently and in cross‑functional teams.
  
  
  

Employment Details

• Level: Mid‑Senior
• Availability: Immediate/ASAP
  
  
  

Why Join Us

• Work on cutting‑edge MES projects in the pharmaceutical sector.
• Gain exposure to global compliance and validation standards.
• Be part of a collaborative, growth‑oriented environment with career progression opportunities.