Siemens MES – Opcenter Engineer

Location: Singapore Employment Type: Fulltime

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.

• 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.

• Bachelors 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 crossfunctional teams.

• Level: MidSenior
• Availability: Immediate/ASAP

• Work on cuttingedge MES projects in the pharmaceutical sector.
• Gain exposure to global compliance and validation standards.
• Be part of a collaborative growthoriented environment with career progression opportunities.