Equipment Qualification - 48+ job offers

Roles Responsibilities Accountable for technology transfer and process validation Translate design inputs into manufacturing processes Conduct risk assessments and mitigation planning Manage validation across manufacturing and CMOs Support equipment qualification and pilot runs Ensure documentation

Cyient Inc

Lead and execute qualification test programs. Perform and execute testing in compliance with quality assurance and safety requirements. Prepare test reports using data and results obtained during testing. Work with project managers and subsystem/component leads to develop and maintain project schedu

We are looking for a detail-oriented IPQA Executive to ensure quality and compliance in our manufacturing operations. Key responsibilities. Ensure adherence to procedures at critical production stages Perform Equipment Qualifications activities (IQ, OQ, PQ) Prepare and review qualification protocals

Amneal

Plan, coordinate and execute mechanical engineering activities for projects (greenfield/brownfield)  Review BOQs, layouts, specifications and ensure installation of HVAC, utilities and cleanroom systems as per cGMP & FDA norms.  Collaborate with cross-functional teams – QA, QC, Production, EHS, Ma

MSN Laboratories

Experience Level : 2 to 6 years Experienced in downstream manufacturing for cell culture based products , specifically Monoclonal antibodies production Equipment qualification & lifecycle management QMS documentation - Change control, deviation, Risk assessment, CAPA Sterilization Buffer preparation

Job Title Manager - 2 Business Unit Sun Global Operations Job Grade G11A Location : Halol At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to C

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We‘re looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We‘re looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We‘re looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Job Description QUALITY COMPLIANCE AND SYSTEM: 1.1 Documentation 1.1.1 To ensure online documentation related to current good manufacturing practices (cGMP). 1.1.2 Continuous improvement and review for upgrading existing SOP's with respect to compliance to global standards. 1.2 Quality Management Sy

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We‘re looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for

Quascenta

Are you a pharma validation professional who knows your way around IQ/OQ/PQ protocols, qualification lifecycle management, and GxP documentation? We're looking for a subject matter expert to help us demonstrate the power of ValDoc Pro — our qualification management application built specifically for