CSV Validation Specialist

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 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...

Amaris Consulting is seeking a skilled Validation Engineer to join our team. As a Senior Validation Specialist, you will play a crucial role in ensuring the accuracy and compliance of our computerized systems.Job Summary:We are looking for a highly experienced professional with around 3-7 years of experience in computer systems validation (CSV) engineering....

Job Description We are currently seeking a skilled CSV Engineer with expertise in Delta-V automation systems to join our team in Singapore's pharmaceutical industry. The ideal candidate will play a crucial role in designing, implementing, and optimizing computerized systems validation (CSV) processes to ensure compliance with regulatory requirements 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...

Roles & ResponsibilitiesThis role is responsible for handling mainly DeltaV and BAS changes due to tech transfer, upgrades, and routine change, able to independently handle the validation of the mini projects so relevant experience is required.Responsibilities: Manage Computer System Validation Lifecycle from design to execution phases, Including relevant...

Here's the job de ion for CSV CONSULTANT / SENIOR CONSULTANT: Location: Tuas, Singapore Mode of Employment: Permanent position Schedule: Dayshift (8am - 5pm) Work Setup: Onsite Note: Candidates with Singapore PR/Citizenship only will be considered for this position. Candidate must have experience in the Pharmaceutical industry . Responsibilities:...

Responsibilities:Provide Computerized System Validation (CSV) consulting services for pharmaceutical and medical device manufacturing companies.Manage SDLC (system design life cycle) including risk, deviation, and change management.Ensure Good Documentation Practices, working with policy and procedural governance.Develop and execute FAT/SAT test scripts,...

Job DescriptionIn this role as an Automation Validation Expert, you will be responsible for devising automation solutions that improve productivity and business operations. Your primary focus will be on supporting the development of DeltaV systems architecture, specifications, controls strategies, and sequence of operations through all design stages.Key...

About the Role:Amaris Consulting is seeking a skilled Computer Systems Validation Professional to join our team. As a key member of our team, you will be responsible for maintaining accurate validation documentation for computerized systems, training staff members, and ensuring compliance with regulatory requirements.Key Responsibilities:Write, review, and...

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...

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,...

About the RoleAs an Automation Specialist - DeltaV Systems, you will play a key role in devising automation solutions that improve productivity, business operations, and safety/quality standards.Key ResponsibilitiesSupport the development of automation solutions that improve productivity, business operations, and safety/quality standards.Assist lead...

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...

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...

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...

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 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...