Quality Validation Officer

Quality 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...

Roles & ResponsibilitiesKey Responsibilities: Act as an integral member of the Quality Systems team, ensuring effective quality oversight for validation activities with an emphasis on Data Integrity. Collaborate with Subject Matter Experts to support the validation team in conducting gap analyses and risk assessments prior to qualification activities,...

Roles & 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...

Job 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...

Roles & ResponsibilitiesMain Responsibilities：1. Assist Quality and Validation Manager Asia to complete the tasks in time with good quality.2. Responsible for successful execution the Validation functions for customer project, as required – Quality, Cost, Time.3. Responsible to drive and support project team for projects where validation is required and...

Roles & ResponsibilitiesJob Info: Monday to Friday 830 - 630 Location: Tai SengResponsibilities: Assist Quality and Validation Manager Asia to complete the tasks in time with good quality. Responsible for successful execution the Validation functions for customer project, as required – Quality, Cost, Time. Responsible to drive and support project team...

Roles & 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...

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...

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...

Role OverviewPSC Biotech Corporation is a leading biotechnology consultancy firm with a global presence, serving clients in over 23 countries worldwide. We provide cloud-based software solutions for quality management and regulatory inspections.We are committed to creating high-performing teams that exceed client expectations in terms of quality,...

Roles & Responsibilities Work closely with project team to assist Quality and Validation Manager Asia region to the tasks on schedule and within quality standard compliance. Responsible completion of the Quality, Cost, and Time validation functions for customer projects. Create and maintain qualification/validation documentation for mechanical, software,...

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,...

Roles & 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...

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...

Roles & ResponsibilitiesValidation Engineers are recognized as a strong quality presence and technical resource. This position is responsible for developing, reviewing, and managing the execution of validation activities for the facility utilities, equipment and processes used in the manufacture and testing of cGMP products.In the role of Validation...

About the Role:The Process Validation Engineer will be responsible for providing process validation support for Takeda vaccines manufacturing operations located in internal and CMO manufacturing locations. This includes overseeing process validation activities, developing and authoring process validation strategies, and ensuring compliance with cGMP...

Roles & 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,...

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. ...

Role 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,...

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...