Biopharmaceuticals Validation Expert

**Responsibilities:**As a Biopharmaceutical Laboratory Expert, you will be responsible for:Performing chemical analysis using advanced instrumentation and techniques.Compiling and recording data for documentation and technical reports.Interpreting test data and providing insights to process scientists and engineers.You will also be responsible for working...

About the RoleWe are seeking a highly skilled Biopharmaceutical Clinical Trials Expert to join our team in Singapore, covering South East Asia, A&NZ and India. This is an exciting opportunity to leverage your technical expertise and industry knowledge to drive sales growth and customer success.

At Lonza Group Ltd., we are committed to delivering high-quality products and services that make a meaningful difference in people's lives.Job DescriptionAs a Biopharmaceutical Expert, you will play a key role in our virus reduction team. Your primary responsibility will be to design and execute specific virus clearance studies that demonstrate the...

Job DescriptionWe are seeking a skilled Biopharmaceutical Process Engineering Specialist to contribute to our Life Science projects for Antaes Asia clients.Main Responsibilities:Perform and review process engineering drawings and calculations, including heat exchanger sizing, pump selection, piping design, control valve sizing, heat and mass balances, and...

About Us:Recruit Express Pte Ltd is a leading recruitment agency providing top talent to the pharmaceutical and biotechnology industries.Job Overview:We are seeking a highly skilled Validation Expert to join our team and support our clients' validation needs.About the Role:Support Validation Projects: Assist with qualification and validation activities,...

Job Overview:At Antaes Consulting SA, we are seeking a highly skilled Biopharmaceutical Process Specialist to join our team. In this role, you will play a critical part in contributing to the success of our Life Science projects for clients across Asia. As a key member of our process engineering team, you will be responsible for performing and reviewing...

Job OverviewWe are seeking a highly skilled Validation Expert to join our quality assurance team. As a key member of our team, you will be responsible for ensuring the compliance of our products with regulatory requirements and maintaining high standards of quality and safety in our operations.About the RoleThis is an exciting opportunity to work in a...

Job SummaryThis role is part of GSK's Career Conversion Programme, aimed at developing skilled manpower for the biopharmaceutical industry.The selected candidate will undergo 15 months of training with our local attachment in Jurong, Singapore.Key ResponsibilitiesEnsure data accuracy and take corrective actions when necessary.Contribute to implementing new...

Job PurposeThe Product Validation Expert will be responsible for ensuring that TRUST RECRUIT PTE. LTD.'s products meet all relevant product validation requirements. The ideal candidate will have extensive knowledge of product validation protocols and industry standards.Key Responsibilities:Develop and implement product validation protocols.Conduct product...

About Private AdvertiserJob OverviewWe are seeking an experienced QA Validation Engineer to join our team in Singapore.This role is responsible for ensuring compliance with regulatory standards and quality specifications in our manufacturing processes, systems, and equipment.The incumbent will work collaboratively with cross-functional teams to develop and...

Roles & ResponsibilitiesResponsibilities:Review of qualification documents such as URS, DQ, IQ, OQ and PQ protocol for automation systems and equipment in compliance with the cGMP and site SOPs. Preparation and review of automation systems, process, and cleaning validation protocols and reports. Perform Quality Risk Assessment to determine criticality of...

Roles & ResponsibilitiesResponsibilities:Review of qualification documents such as URS, DQ, IQ, OQ and PQ protocol for automation systems and equipment in compliance with the cGMP and site SOPs. Preparation and review of automation systems, process, and cleaning validation protocols and reports. Perform Quality Risk Assessment to determine criticality of...

About Nd Incorporated in 2007, we are a patient-centric solution provider for the pharmaceutical industry. We are experts in engineering consultancy, commissioning, qualification and validation services, and regulatory quality/compliance in Asia and Europe. We offer personalized focused solutions for the pharmaceutical industry in engineering consultancy...

Job DescriptionWe are seeking a highly skilled Biopharmaceutical Manufacturing Specialist to join our team at Antaes Consulting SA. As a key member of our engineering department, you will play a crucial role in contributing to the success of our Life Science projects.Contribute to the development and implementation of process engineering designs for...

Roles & ResponsibilitiesWe are seeking highly skilled Commissioning, Qualification, and Validation (CQV) Engineers to provide risk-based CQV services for pharmaceutical and biopharmaceutical clients. This role offers opportunities to work across various areas, including process equipment, CIP/SIP (Clean-In-Place/Sterilize-In-Place), and process manufacturing...

**Validation Engineer / Validation Manager**: At Genetic Design and Magic Corporation (GDMC), our mission is to exponentially increase the availability of genetic medicines and change millions of patients' lives. We achieve this by partnering and supporting early-stage companies and investigators with innovative therapeutic modalities such as gene therapies...

Job DescriptionThe Biopharmaceutical Process Specialist will be responsible for supporting and leading the troubleshooting of manufacturing operations process/product issues, serving as a technical subject matter expert to resolve process issues, perform root cause analysis and impact assessment for process investigations. The role also involves evaluating...

**Responsibilities**: - Monitor day-to-day Validation activities in accordance with approved SOPs / Plan / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility - Participate in review and approval of Validation Protocols / Reports including site discrepancies and deviations investigation / closure - Support / participate in...

**Responsibilities**: - Monitor day-to-day Validation activities in accordance with approved SOPs / Plan / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility - Participate in review and approval of Validation Protocols / Reports including site discrepancies and deviations investigation / closure - Support / participate in...

About UsGSK is a global biopharma company dedicated to uniting science, technology, and talent to get ahead of disease together. We focus on preventing and treating diseases with vaccines, specialty, and general medicines. Our four core therapeutic areas are infectious diseases, HIV, respiratory/immunology, and oncology. The Manufacturing Science &...