Singapore, Singapore · On-site
🔹 Role: CQV Lead / CQV Engineer 📍 Location: Singapore / Global Pharma Projects 🧪 Industry: Pharmaceutical / Biotech / Life Sciences 💼 Experience: 5+ years (CQV/Validation mandatory) / CQV Lead - Team Handling Experie…
Skills: Commissioning, Qualification, Validation, cGMP, GAMP
Singapore, Singapore · On-site
Job Description – IP21 Engineer (Pharma, Singapore) Position Overview We are seeking an experienced IP21 Engineer to support pharmaceutical manufacturing operations in Singapore. The role focuses on OSIsoft PI / AspenTec…
Skills: Aspen IP21, OSIsoft PI, DeltaV, MES, PLC/DCS Integration
Barceloneta, Puerto Rico · On-site
A leader in Life Sciences Manufacturing Technology solutions, AMTSOL partners with global pharmaceutical and biotechnology organizations to deliver Automation, MES, CSV, CQV, and Digital Transformation solutions across S…
Skills: Process Engineering, Biopharma Manufacturing, Process System Design, Equipment Specification, GxP Compliance
Barceloneta, Puerto Rico · On-site
A leader in Life Sciences Manufacturing Technology solutions, AMTSOL partners with global pharmaceutical and biotechnology organizations to deliver Automation, MES, CSV, CQV, and Digital Transformation solutions across S…
Skills: Project Management, Stakeholder Management, Budget Ownership, GxP Compliance, Vendor Management
Barceloneta, Puerto Rico · Hybrid
A leader in Life Sciences Manufacturing Technology solutions, AMTSOL partners with global pharmaceutical and biotechnology organizations to deliver Automation, MES, CSV, CQV, and Digital Transformation solutions across S…
Skills: Automation Delivery, Project Management, System Integration, GxP Compliance, GAMP5
Singapore, Singapore · On-site
Job Title: Siemens MES – Opcenter Engineer Location: Singapore Employment Type: Full‑time About the Role We are looking for experienced professionals with 5+ years of pharmaceutical industry experience to join our team i…
Skills: Siemens Opcenter, MES Implementation, Computer System Validation, GMP Compliance, Deviation Handling
Singapore, Singapore · On-site
QA Engineer – MES, DeltaV, HBV Key Responsibilities & Requirements: Ensure quality oversight of MES, DeltaV, and HBV systems in pharma manufacturing.Develop and execute validation protocols (IQ/OQ/PQ) in compliance with …
Skills: MES, DeltaV, HBV, Validation Protocols, IQ/OQ/PQ
Dundalk, Leinster, Ireland · On-site
Automation Engineer – DeltaVLevel : Mid level (3 – 6 yrs)Location: Ireland, Dundalk, Onsite role.Industry: Biopharmaceutical Manufacturing About the Role AMTSOL is seeking a motivated Automation Engineer with hands-on Em…
Skills: Emerson DeltaV, Automation Engineering, GMP Compliance, Functional Design Specifications, Change Control
Singapore, Singapore · On-site
Job Title: IT Helpdesk Support Specialist - Laboratory IT (Pharmaceutical Manufacturing) Overview: We are seeking an experienced IT Helpdesk Support Specialist to join our team and provide technical assistance for Labora…
Skills: Laboratory Operations, Equipment Qualification, GxP Compliance, GMP Regulations, IQ OQ PQ
Dundalk, Leinster, Ireland · On-site
Advanced Manufacturing Tech Solutions (AMTSOL) is a specialist provider of Life Sciences Manufacturing Technology solutions. We support global pharmaceutical and biopharmaceutical clients with automation, digitalization,…
Skills: Emerson DeltaV, DCS Configuration, ISA-88 Standards, Batch Recipes, FDS/SDS Documentation
Dublin, Leinster, Ireland · On-site
Advanced Manufacturing Tech Solutions (AMTSOL) is a specialist provider of Life Sciences Manufacturing Technology solutions. We support global pharmaceutical and biopharmaceutical clients with automation, digitalization,…
Skills: Emerson DeltaV, ISA-88, DCS Configuration, GMP, CSV
Singapore, Singapore • On-site
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Lead and execute CQV activities, including the development of validation strategies and protocols for pharmaceutical facilities. Manage the commissioning of HVAC, cleanrooms, and automation systems while ensuring compliance with regulatory standards.
Requires over 5 years of CQV experience in the pharma or biotech industry with mandatory team handling experience for lead roles. Candidates must possess strong knowledge of GAMP, 21 CFR Part 11, and GMP compliance.
🔹 Role: CQV Lead / CQV Engineer
📍 Location: Singapore / Global Pharma Projects 🧪 Industry: Pharmaceutical / Biotech / Life Sciences
💼 Experience: 5+ years (CQV/Validation mandatory) / CQV Lead - Team Handling Experience mandatory
We are looking for experienced Commissioning, Qualification & Validation (CQV) professionals to join our growing team.
📩 Interested candidates can share their CVs at [email protected]
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Delivering innovation through technology for Life Science manufacturing!
We are Delivering Innovation through Technology for Life Science Manufacturing. With focus on Pharma 4.0 and Digitalization, helping regulated manufacturers to increase speed to market and operating efficiency. Life Science Manufacturing Systems expert with end to end implementation and support capability of GMP Manufacturing systems and solutions for Automation, Manufacturing Execution Systems (MES), OT Networking and Digital Technologies.
Offices: Singapore, SG · Cork, IE · Pune, IN · Dover, DE, US
Delivering innovation through technology for Life Science manufacturing!
We are Delivering Innovation through Technology for Life Science Manufacturing. With focus on Pharma 4.0 and Digitalization, helping regulated manufacturers to increase speed to market and operating efficiency. Life Science Manufacturing Systems expert with end to end implementation and support capability of GMP Manufacturing systems and solutions for Automation, Manufacturing Execution Systems (MES), OT Networking and Digital Technologies.
Offices: Singapore, SG · Cork, IE · Pune, IN · Dover, DE, US
