Equipment validation lead
6 days ago
Process Engineering Specialists is an international services company providing Project Management, Construction Management, Commissioning & Qualification, and Automation services to our clients in the pharmaceutical, nutritional, and related sectors. With offices across Europe, Asia, and the US, our core focus is on consistently delivering high-quality outcomes for our multinational clients. We are currently looking for a QC Equipment Validation Lead to join us in a permanent role to help us deliver various projects in the Life Sciences Industry. What we’re looking for: Must have experience leading a small team. Develop and execute validation documents, including URS, IQs, OQs, PQs, QPs, QRs, and audit trail reviews. Create validation plans aligned with client strategic goals and ensure timely, compliant delivery. Commissioning and qualification of equipment, including small QC Equipment and benchtop equipment, like fridges and freezers. Participate in investigations of deviations, conduct analyses, and assess changes. Collaborate with multiple functions to organize, plan, and facilitate smooth qualification activities. Lead change control management. We are currently looking for candidates in Singapore. If you'd like to find out about this opportunity, please forward your CV to Nelson Anthony ( ). PES International operates as an equal opportunity employer. We confirm that we are happy to accept applications from persons of any background for this role. #J-18808-Ljbffr
-
Process Equipment Validation Specialist
3 weeks ago
Singapore PROCESS ENGINEERING SPECIALISTS PTE. LTD. Full timeAbout 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...
-
Senior Validation Lead
4 days ago
Singapore COALESCE MANAGEMENT CONSULTING PTE. LIMITED Full timeWe are currently seeking a skilled Senior Validation Lead to join our team at Coalesce Management Consulting PTE. Limited.Job DescriptionThe successful candidate will be responsible for overseeing and implementing validation protocols within highly regulated environments. They will work closely with our client to ensure that all validation activities are...
-
Biopharmaceutical Validation Lead
3 weeks ago
Singapore COALESCE MANAGEMENT CONSULTING PTE. LIMITED Full timeCQV / Validation Lead Job DescriptionAs a CQV / Validation Lead, you will be responsible for overseeing, planning, writing, implementing, and reviewing validation protocols in highly regulated environments. Your technical expertise will contribute to tactical problem-solving, effective communication, and a progressive growth culture.Key...
-
Validation Specialist
2 weeks ago
Singapore QUASAR MEDICAL (SINGAPORE) PTE. LTD. Full timeJob Summary:The Validation Engineer plays a pivotal role in ensuring the quality of medical devices and manufacturing processes. The position is responsible for leading and executing validation activities, including equipment, process, and software validation. This ensures that products are manufactured consistently and reliably in accordance with Good...
-
Validation Specialist
3 weeks ago
Singapore RECRUIT EXPRESS PTE LTD Full timeJob 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,...
-
Validation Engineer
4 days ago
Singapore QUASAR MEDICAL (SINGAPORE) PTE. LTD. Full timeRoles & ResponsibilitiesJob Summary:The Validation Engineer is responsible for ensuring that medical devices and manufacturing processes meet required quality standards and regulatory requirements. It includes lead and/or execute validation activities, including equipment, process, test method and software validation, to ensure that products are manufactured...
-
Singapore ROYAL EQUIPMENT (PTE.) LTD. Full timeJob Title: Mechanical Engineer AssistantAbout the Role:A highly skilled and experienced Mechanical Engineer Assistant is required to join our team at ROYAL EQUIPMENT (PTE.) LTD. in $3000 - $4700 per annum.Key Responsibilities:To lead a team of service technicians, arranging daily work schedules with a focus on safety.To perform equipment installations,...
-
QA Specialist
2 months ago
Singapore PHARMAGEND GLOBAL MEDICAL SERVICES PTE. LTD. Full timeRoles & ResponsibilitiesKEY DUTIES AND RESPONSIBILITES:• Preparation and review of qualification documents e.g., User requirement specification, DQ, IQ, OQ and PQ protocol for equipment, utilities & facility in compliance with the regulatory guidelines.• Execution of qualification and validation activities including process, cleaning, computer system,...
-
Validation Engineer
3 weeks ago
Singapore T0SS-EX S PTE. LTD. Full timeRoles & 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...
-
Computer System Validation Expert
3 weeks ago
Singapore PHARMENG TECHNOLOGY PTE. LTD. Full timeComputer 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...
-
Computer System Validation Consultant
2 months ago
Singapore PHARMENG TECHNOLOGY PTE. LTD. Full timeRoles & ResponsibilitiesWe 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 solutions for our clients—both nationally and...
-
Validation Engineer
3 weeks ago
Singapore NES GLOBAL PTE. LTD. Full timeRoles & ResponsibilitiesJob Title: Validation EngineerLocation: SingaporeStart Date: January 2025Duration: 1 year (Renewable contract)NES Fircroft has partnered with our client, a leading pharmaceutical company dedicated to innovation and quality in healthcare, to seek a Validation Engineer to join the team.POSITION RESPONSIBILITIES:-· Ensure equipment for...
-
Manufacturing Validation Specialist
4 days ago
Singapore NES GLOBAL PTE. LTD. Full timeRole OverviewNES Global PTE. LTD. is seeking a Manufacturing Validation Specialist to join their team in Singapore.Job SummaryThis is an exciting opportunity for a highly skilled and motivated individual to work on validating equipment and ensuring compliance with safety and quality standards in the pharmaceutical industry.Responsibilities:Develop,...
-
CSV Validation Specialist
3 weeks ago
Singapore NUSANTARA PRIME CONSULTING PTE. LTD. Full timeJob 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...
-
Senior Validation/Validation Engineer
4 days ago
Singapore ESCO ASTER PTE. LTD. Full timeRoles & ResponsibilitiesThe OpportunityEsco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in...
-
CQV / Validation Engineer
3 weeks ago
Singapore COALESCE MANAGEMENT CONSULTING PTE. LIMITED Full timeRoles & ResponsibilitiesPosition: CQV / Validation LeadJob DescriptionWe are currently expanding our team and are looking for a CQV / Validation Lead for our project on site with our client.You will be responsible for overseeing, planning, writing, implementing and reviewing Validation protocols in place within highly regulated environments. Your expertise...
-
Pharmaceutical Validation Specialist
3 weeks ago
Singapore Wood Full timeAt 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...
-
Validation and Quality Expert
3 weeks ago
Singapore MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD Full timeQuality Assurance Validator RoleAs a Quality Assurance Validator at MANPOWER STAFFING SERVICES (SINGAPORE) PTE LTD, you will partner with cross-functional teams to ensure quality oversight of commissioning, qualification, and validation lifecycle activities. This includes providing quality oversight to validation/qualification and continued verification of...
-
Computer System Validation Engineer
2 months ago
Singapore PHARMENG TECHNOLOGY PTE. LTD. Full timeRoles & 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...
-
Junior Validation Engineer
4 days ago
Singapore ANTER CONSULTING PTE. LTD. Full timeRoles & ResponsibilitiesWe are seeking a Junior Validation Engineer with 0-3 years of experience to support validation activities, ensuring compliance with regulatory and quality standards, especially GMP. The role involves collaboration with cross-functional teams to meet project goals.Key Responsibilities: Develop, review, and execute validation protocols...