Experienced CQV Engineer for Pharmaceutical Engineering Projects

At PHARMENG TECHNOLOGY PTE. LTD., we're seeking an experienced Commissioning / Qualification and Verification (CQV) Engineer to join our team in Singapore.About the RoleThis is a fantastic opportunity for a skilled CQV professional to leverage their expertise in pharmaceutical engineering, equipment qualification, and pharmaceutical solutions in the Life...

Roles & ResponsibilitiesCommissioning / Qualification and Verification (CQV) Engineer (Singapore)PharmEng 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,...

Roles & ResponsibilitiesResponsibilities: Develop and execute Commissioning, Qualification, and Validation (CQV) protocols (IQ/OQ/PQ) for pharmaceutical manufacturing facilities, equipment, and systems. Collaborate with project teams to ensure compliance with regulatory standards (e.g., FDA, EMA, GMP). Perform risk assessments, gap analysis, and prepare...

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification, and Automation services to our clients in the pharmaceutical, nutritional, and related sectors.With offices across Europe, Asia, and the US, our core focus is on consistently delivering high quality outcomes for our multinational...

At ANTER CONSULTING PTE. LTD., we are seeking a skilled Pharmaceutical Validation Professional to join our team. This exciting opportunity is ideal for an experienced professional with a strong background in Commissioning, Qualification, and Validation (CQV) processes.About the Role:The successful candidate will be responsible for developing and executing...

At IPS, we are seeking a highly experienced Regional CQV Director to lead our growth efforts in APAC. This role reflects our dedication to delivering exceptional solutions while solidifying our position as a global industry leader. As a Regional CQV Director, you will be responsible for performing cGMP compliance-based services, including commissioning,...

Company OverviewAnter Consulting PTE. LTD. is a renowned consulting firm specializing in pharmaceutical and biotechnology industry services.About the RoleWe are seeking an experienced Principal Validation Specialist to join our team in Singapore. The successful candidate will be responsible for leading Commissioning, Qualification, and Validation (CQV)...

About the RoleWe are seeking a skilled Pharmaceutical Process Engineer to join our team at NO DEVIATION PTE. LTD.Job DescriptionSupport and lead projects as an Engineering Technical Lead or Subject Matter Expert for process equipment in new product introductions, change controls, and other qualifications activities.Provide technical expertise in site...

Roles & ResponsibilitiesPosition: CQV / Validation LeadJob DescriptionWe are currently expanding our team and are looking for a CQV / Validation Lead for our project on site with our client.You will be responsible for overseeing, planning, writing, implementing and reviewing Validation protocols in place within highly regulated environments. Your expertise...

Process Engineering Specialists is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors. With offices across Europe, Asia and US, our core focus is on consistently delivering high quality outcomes...

Company OverviewNo Deviation Pte. Ltd., a provider of patient-centric solutions for the pharmaceutical industry, is seeking individuals passionate about joining our team. With expertise in engineering consultancy, Commissioning Qualification Validation (CQV), and Quality, Compliance, and Regulatory services, we strive to create a collaborative, innovative,...

Roles & ResponsibilitiesResponsibilities: Develop and execute Commissioning, Qualification, and Validation (CQV) protocols (IQ/OQ/PQ) for pharmaceutical manufacturing facilities, equipment, and systems. Collaborate with project teams to ensure compliance with regulatory standards (e.g., FDA, EMA, GMP). Perform risk assessments, gap analysis, and prepare...

Senior CQV Engineer RolesWe are seeking experienced Senior CQV Engineers to join our team at Process Engineering Specialists Pte. Ltd.The ideal candidate will have a strong background in process engineering, quality assurance, and validation of biopharmaceutical GMP plants.About the Role:Lead the development and implementation of C&Q plans and...

CQV Manager – Singapore – 2 Year Contract Location: Singapore Contract: 2 Years possible extension Start Date: ASAP Company: A huge multinational Pharmaceutical company with a big presence in Singapore. This company is home to some advanced technology using state-of-the-art systems. Roles and Responsibilities This person will need to lead the overall...

About No Deviation PTE. LTD.No Deviation PTE. LTD. is a patient-centric solutions provider for the pharmaceutical industry, specializing in engineering consultancy, Commissioning Qualification Validation (CQV), Quality, Compliance, and Regulatory services. Our team upholds core values of Empathy, Integrity, and Transparency, fostering a collaborative work...

Job DescriptionSUNWARD PHARMACEUTICAL PRIVATE LIMITED is seeking a skilled Maintenance Engineer - Pharmaceutical Manufacturing to join our team. This role will be responsible for ensuring the smooth operation of our manufacturing equipment, maintaining high standards of quality and productivity.Responsibilities:Equipment Maintenance: Supervise and maintain...

About UsProcess Engineering Specialists Pte. Ltd. is a global services company delivering high-quality outcomes for pharmaceutical clients worldwide.Sales Consultant OpportunityWe are seeking a skilled Sales Consultant to support our business development executive and contracts recruiter in the China/Japan/Korea region, based in Singapore.Job DescriptionThe...

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...

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...

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...