Process Engineer (Equipment Validation/ Pharma) Duration: 6 months Location: Tuas Salary : Up to $7,500 depending on experience Our Client is a US MNC and a pioneering leader in the Pharmaceutical industry. They are currently seeking experienced and forward-thinking professionals to join their team in Singapore Job Purpose Provides technical supply support on the commercialization and manufacture of all drug products either independently or with minimal support (seeking support/ escalating efficiently where needed).Supports/ leads all technical/ process activities (for example) investigations, validation and qualification processes, risks assessments, process safety management activities under his/ her responsibilities and could be responsible for technical product stewardship activities.Supports continuous process improvement activities to enhance site performance metrics and contributes to the global organization technical network to share site experiences/ knowledge and continuously expands on personal expertise.Supports/leads the introduction of new products to the site and the transfer of drug products to other facilities.ResponsibilitiesLead and support new product introductions, including process scale-up, equipment qualification (IQ/OQ/PQ), PPQ execution, and validation documentation for sterile pharmaceutical manufacturingDesign and execute process experiments to evaluate equipment and process changes, troubleshoot manufacturing issues, and implement improvements to ensure robust and compliant operationsProvide technical support for sterile manufacturing, including monitoring CPPs, CQAs, Cpk, and sterile boundaries to maintain validated state and product qualityInvestigate deviations, product complaints, and adverse events to determine root causes and implement effective CAPA in compliance with GMP requirements.Support regulatory audits, change control management, cleaning validation, continued process verification, and lifecycle management activities within a pharmaceutical manufacturing environmentRequirements:Bachelor's degree in chemical or mechanical engineering, Chemistry, Biological sciences, or Pharmaceutical Sciences At least 3 years' experience in the process engineering with hands-on experience in equipment validation and sterile manufacturingExperience in the Pharmaceutical Manufacturing IndustryLim Pey Chyi - .sg Recruitment Consultant (R2090579) Manpower Staffing Services (S) Pte Ltd EA Licence: 02C3423 Desired Skills and ExperienceBachelor's degree in chemical or mechanical engineering, Chemistry, Biological sciences, or Pharmaceutical SciencesAt least 3 years' experience in the process engineering with hands-on experience in equipment validation and sterile manufacturingExperience in the Pharmaceutical Manufacturing IndustryApple, Pey Chyi Lim EA License No.: 02C3423 Personnel Registration No.: R2090579Please note that your response to this advertisement and communications with us pursuant to this advertisement will constitute informed consent to the collection, use and/or disclosure of personal data by ManpowerGroup Singapore for the purpose of carrying out its business, in compliance with the relevant provisions of the Personal Data Protection Act 2012. To learn more about ManpowerGroup's Global Privacy Policy, please visit