Current jobs related to Pharmaceutical Equipment Validation Specialist - Singapore - PROCESS ENGINEERING SPECIALISTS PTE. LTD.

  • Pharmaceutical Validation Specialist

    2 weeks ago

    Singapore Wood Full time

    At Wood, we are seeking a highly skilled Pharmaceutical Validation Specialist to join our team. This role is responsible for ensuring that our pharmaceutical manufacturing processes, equipment, and systems comply with regulatory requirements, industry standards, and company policies.Key Responsibilities:Develop and implement validation plans for laboratory...

  • Process Equipment Validation Specialist

    1 week ago

    Singapore PROCESS ENGINEERING SPECIALISTS PTE. LTD. Full time

    About the RolePES International is seeking a skilled Process Equipment Validation Specialist to join our team. As a key member of our team, you will be responsible for ensuring the quality and compliance of our equipment and processes in the Life Sciences industry.Key ResponsibilitiesAssist in qualifying and validating new equipment or replacing existing...

  • Validation Specialist

    1 week ago

    Singapore RECRUIT EXPRESS PTE LTD Full time

    Job SummaryA highly skilled Validation Specialist is needed to join our team at Recruit Express Pte Ltd. The successful candidate will be responsible for ensuring the validation and qualification of equipment, processes, and facilities in a cGMP manufacturing environment. This role requires a strong understanding of quality regulations and standards,...

  • CSV Validation Specialist

    2 weeks ago

    Singapore Amaris Consulting Full time

    Job Title: CSV Validation SpecialistJob Summary:Amaris Consulting is seeking a skilled CSV Validation Specialist to join our team. The ideal candidate will have a strong background in computer systems validation within the pharmaceutical industry.Key Responsibilities:Develop and implement CSV strategy and validation plans for computerized systems.Create and...

  • QC Validation Specialist

    1 month ago

    Singapore NO DEVIATION PTE. LTD. Full time

    Roles & ResponsibilitiesNo Deviation PTE. LTD. is a leading provider of patient-centric solutions for the pharmaceutical industry. We are seeking a highly skilled QC Validation Specialist to join our team.We are committed to upholding our core values of Empathy, Integrity, and Transparency, and we strive to create a collaborative, innovative, and inclusive...

  • Pharmaceutical Engineer

    2 months ago

    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesJob Summary:We are seeking a highly motivated and skilled Pharmaceutical Engineer to join our team. The successful candidate will play a pivotal role in the design, development, and manufacturing of pharmaceutical products. This position requires a deep understanding of pharmaceutical processes, regulatory compliance, and quality...

  • QC Specialist

    1 week ago

    Singapore PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. Full time

    Job Title: QC SpecialistJob Summary:PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. is seeking a highly skilled QC Specialist to join our Quality Control Team. The successful candidate will be responsible for performing analytical equipment lifecycle management, equipment qualification, and ensuring real-time documentation and data integrity.Key...

  • QA Validation Expert

    2 months ago

    Singapore MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD Full time

    Roles & ResponsibilitiesQA Validation Expert (Pharmaceutical/Commissioning/ Quality)Location: Gul CircleUp to $8,500 depending on experience12 Months ContractIndustry: PharmaceuticalJob Purpose Responsible to partner with cross-functional teams to provide quality oversight to commissioning, qualification, and validation (CQV) lifecycle activities ensuring...

  • Validation Specialist

    1 week ago

    Singapore ANTAES ASIA PTE. LTD. Full time

    Roles & ResponsibilitiesJob Description: Contribute to Life Science projects for Antaes Asia clients Manage change control processes for computer systems, ensuring accurate documentation, risk assessment, and approval workflow. Coordinate with relevant departments to assess the impact of changes and ensure successful integration into existing systems. ...

  • QC Validation Expert

    2 months ago

    Singapore NO DEVIATION PTE. LTD. Full time

    Roles & ResponsibilitiesNo Deviation PTE. LTD. is a leading provider of patient-centric solutions for the pharmaceutical industry. We are seeking a highly skilled QC Validation Specialist to join our team.We uphold our core values of Empathy, Integrity, and Transparency, and strive to create a collaborative, innovative, and inclusive work environment that...

  • Computer System Validation Engineer

    2 months ago

    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...

  • Validation Engineer

    2 months ago

    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Roles & ResponsibilitiesPharmEng Technology has been providing quality services to leading manufacturers of healthcare and pharmaceutical products since 1997. Our specialists hold expertise in Commissioning & Qualification, Validation, Quality Systems, Regulatory Affairs, Engineering, and Training to ensure that our clients can keep on providing the world...

  • CSV Validation Specialist

    1 week ago

    Singapore NUSANTARA PRIME CONSULTING PTE. LTD. Full time

    Job Summary:As a CSV Validation Specialist at NUSANTARA PRIME CONSULTING PTE. LTD., you will be responsible for managing the Computer System Validation Lifecycle from design to execution phases. This includes creating and executing validation documents, protocols, and test cases using valgenesis software. You will work closely with Subject Matter Experts...

  • LIMS QC Specialist in Pharmaceutical Environment

    1 week ago

    Singapore MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD Full time

    Job SummaryThis is a 9-month contract position as a LIMS QC Specialist in a pharmaceutical environment. The role involves implementation of LIMS in QC, alongside master data collection, writing and executing LIMS IQ and UAT test cases, writing LIMS-related SOPs, and conducting end-user training. Additionally, the successful candidate will support the...

  • QC Validation Specialist

    2 months ago

    Singapore NO DEVIATION PTE. LTD. Full time

    Roles & ResponsibilitiesNo Deviation is a provider of patient-centric solutions for the pharmaceutical industry, and we are currently seeking individuals who are passionate about joining our team. Our areas of expertise include engineering consultancy, Commissioning Qualification Validation (CQV), as well as Quality, Compliance, and Regulatory services.We...

  • Pharmaceutical Laboratory Specialist

    4 days ago

    Singapore Thermo Fisher Scientific Full time

    At Thermo Fisher Scientific, we are committed to enabling our customers to make the world healthier, cleaner and safer.As a Pharmaceutical Laboratory Specialist, you will play a critical role in supporting our customers in the life sciences industry.Key responsibilities include:Providing technical support and training to customers on our pharmaceutical...

  • Compounding Technician

    1 week ago

    Singapore RECRUIT EXPRESS PTE LTD Full time

    Job SummaryCompounding Technician - Pharmaceutical SpecialistCompounding Technicians are responsible for preparing and dispensing medications to patients. In this role, you will work closely with healthcare professionals to ensure the safe and effective preparation of medications.ResponsibilitiesPrepare and dispense medications to patients in accordance with...

  • Validation Engineer

    1 week ago

    Singapore T0SS-EX S PTE. LTD. Full time

    Roles & ResponsibilitiesJob PurposeThe Commissioning & Validation Engineer provides specialized scientific and technical support for the validation, revalidation, and requalification of laboratory equipment and computerized systems. These activities are performed in strict adherence to current Good Manufacturing Practices (cGMPs), Standard Operating...

  • HVAC Systems Qualification and Validation Specialist

    1 week ago

    Singapore SURPASS STAFFING PTE. LTD. Full time

    Roles & ResponsibilitiesResponsibilities: Execute commissioning, qualification, and validation (CQV) activities for mechanical equipment and systems utilized in Biopharma manufacturing facilities, adhering to regulatory standards and industry best practices. Create, assess, and implement validation protocols and reports for mechanical systems and...

  • Computer System Validation Expert

    1 week ago

    Singapore PHARMENG TECHNOLOGY PTE. LTD. Full time

    Computer System Validation Consultant RoleAt PHARMENG TECHNOLOGY PTE. LTD., we are seeking an experienced Computer System Validation Consultant to help drive our solution-based business model and take our designs to the next level. Our consultants have the chance to work hands-on with several business divisions to design, develop, test industry-leading...

Pharmaceutical Equipment Validation Specialist

2 months ago

Singapore PROCESS ENGINEERING SPECIALISTS PTE. LTD. Full time
Job Title: QC/Lab Equipment Validation Engineer- Pharma

PES International, a leading provider of project management, construction management, commissioning, and qualification services, is seeking a highly skilled QC/Lab Equipment Validation Engineer to join our team.

We are a global company with offices across Europe, Asia, and the US, serving multinational clients in the pharmaceutical, nutritional, and related sectors. Our focus on delivering high-quality outcomes has been key to our success over the past 20 years.

The successful candidate will be responsible for:

  • Assisting in qualifying and validating new equipment or replacing existing equipment.
  • Collaborating across multiple functions to coordinate and plan execution activities smoothly.
  • Preparing and drafting qualification and validation protocols and reports.
  • Conducting equipment qualification and validation according to applicable policies, standards, procedures, and guidelines, ensuring timely completion.
  • Implementing safety policies through site activities, including pre-planning, reviewing safe work plans, preparing site documentation, and monitoring safe work methods during execution.
  • Managing qualification and validation exceptions, deviations, and investigations encountered during acceptance testing.
  • Providing support for other technical changes and additional duties as needed.

We are an equal-opportunity employer and welcome applications from candidates with a strong background in equipment validation, project management, and regulatory requirements. If you are a motivated and detail-oriented professional looking to join a dynamic team, please submit your CV for consideration.