QC Validation Specialist

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...

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...

We are seeking a qualified QC Validation Expert to join our team at No Deviation PTE. LTD.The ideal candidate will have a strong understanding of qualification and validation processes in a GMP/GLP environment.Key Responsibilities:Provide guidance and direction on commissioning/qualification activitiesAssist in change control assessments and reviewsConduct...

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...

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...

Roles & Responsibilities Perform analytical equipment lifecycle management as per current regulatory requirements / SOP. Involve in equipment qualification, writing URS, reporting and implementing SOP’s for system operation and maintenance, monitoring performance of the equipment and decommissioning of equipment. Ensure real time documentation,...

Highly skilled & experienced laboratory professional who contributes by performing analytical release testing, investigational support, research support, and stability testing. About the Role Position Title: QC Specialist I - Raw Materials Key Responsibilities Maintain QC Raw Materials laboratory in full c GMP compliance. Lead raw material method...

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...

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 & 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 & ResponsibilitiesLIMS QC Specialist (Pharmaceutical/ GxP/ 21 CFR Part 11)9 Months ContractLocation: TuasUp to $7,000 depending on experienceIndustry: PharmaceuticalResponsibilities: Implementation of LIMS (Laboratory Information Management System) in QC, alongside with the following activities: Master Data Collection Write and execute LIMS IQ...

Why OCBC?At OCBC, we're committed to building a robust data-driven culture that underpins everything we do. As a key member of our team, you'll play a crucial role in ensuring our data compliance processes are aligned with industry best practices and regulations.What You'll DoAs a Data Validation Specialist, you'll be responsible for certifying that OCBC and...

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...

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...

Why OCBC?At OCBC, we're committed to building a robust data-driven culture that underpins everything we do. As a key member of our team, you'll play a crucial role in ensuring our data compliance processes are aligned with industry best practices and regulations.What You'll DoAs a Data Validation Specialist, you'll be responsible for certifying that OCBC and...

Why OCBC?At OCBC, we're committed to building a robust data-driven culture that underpins everything we do. As a key member of our team, you'll play a crucial role in ensuring our data compliance processes are aligned with industry best practices and regulations.What You'll DoAs a Data Validation Specialist, you'll be responsible for certifying that OCBC and...

No 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 strongly uphold our core...

About the Role:We are seeking a highly skilled and experienced QC Biologics Lab Supervisor to join our team at 825 Glaxo Wellcome Manufacturing Pte Ltd.As a QC Biologics Lab Supervisor, you will be responsible for managing the biological laboratory activities to ensure timely availability and accuracy of results. You will review and approve all required...

Roles & ResponsibilitiesResponsibilities: Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and CSV system) Responsible for overseeing execution of but not limited to IQ, OQ, PQ and ERES Test Scripts of QC laboratory...

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...