Senior Validation Specialist

Job Title: Senior System Validation SpecialistAmaris Consulting is a leading provider of consulting services in the pharmaceutical and biotech industries.Estimated Salary: $120,000 - $180,000 per yearAbout the Role:We are seeking an experienced Senior System Validation Specialist to join our team. The ideal candidate will have a strong background in system...

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,...

Company Overview: Thermo Fisher Scientific is a leading biotechnology company that enables customers to make the world healthier, cleaner, and safer.Salary: $120,000 - $150,000 per yearJob Description: We are seeking an experienced Senior Molecular Biologist and Validation Specialist to join our team. As a key member of our V&V function, you will play a...

Job Description:Amaris Consulting is seeking a highly skilled CSV Validation Specialist to join our team. As a CSV Validation Specialist, you will be responsible for developing and implementing CSV strategies and validation plans for computerized systems, including LIMS, MES, eBR, and other relevant software.Key Responsibilities:Validation Planning: Develop...

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...

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,...

About the RoleWe are seeking a highly skilled Process Validation Specialist to join our team at Snaphunt. As a Process Validation Specialist, you will be responsible for ensuring the safety and purity of products by validating processes in accordance with GMP and cGMP regulations.ResponsibilitiesLead cleaning validation efforts to ensure robust and...

Job Overview:We are seeking a skilled Technical Validation Specialist to join our team at NNIT. This role will involve providing Computerized System Validation (CSV) consulting services to pharmaceutical and medical device manufacturing clients.Estimated Salary: $90,000 - $120,000 per yearAbout the Role:In this position, you will be responsible for managing...

OCBC Bank, one of Singapore's longest established banks, is seeking a skilled Model Validation Specialist to join its Market Risk Management team. This permanent, full-time role offers a competitive base salary and a range of benefits to support your career and wellbeing.About the RoleThe Model Validation Specialist will be responsible for validating pricing...

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...

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...

• Job Summary:The client, a renowned semiconductor company from the USA, is seeking a skilled Validation Engineer to join their team in Singapore. As a leading employer, they offer a supportive and dynamic work environment.• Key Responsibilities:Execute thorough testing of SSDs on test systems, utilizing Protocol Analyzers and oscilloscopes to ensure...

Job OverviewAmaris Consulting is seeking a highly skilled Certified Pharmaceutical Cleaning Validation Specialist to join our team in Singapore.Estimated Salary:$85,000 - $110,000 per annum, depending on experience.About the RoleWe are looking for a talented individual with experience in cleaning validation within the pharmaceutical or biotech industry. As a...

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...

Company OverviewMicron Technology, Inc. is a leading global developer and manufacturer of advanced memory and storage solutions. Our vision is to transform how the world uses information to enrich life for all.About the RoleWe are seeking a highly skilled NAND Product Validation Specialist to join our Non-Volatile Engineering (NVE) Product Engineering...

Posted Job Advert Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas,...

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. ...

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,...