Qms - 1,286+ job offers

Job Title: QMS Executive Engineering Department: Engineering / Technical Services Industry: Pharmaceutical Formulation Location: Harohalli, Bangalore Experience: 2–5 years (Pharma formulation plant preferred) Qualification: B.E./B.Tech (Mechanical / Electrical / Instrumentation) or Diploma with rele

IAFT 16949, ISO 14001, ISO 45001. QMS Documents and format preparation. Conducting internal process and product audits. Co-ordination with customer audit. Supporting for new project on QA and QMS activity. Conduct MSA Study and NC Follow up.

Writing procedures and processes to support the QMS development. Lead and undertake audits across all areas of the business as well as across the supply chain. Location - Talegaon, Pune. Walking Interview Contact - Ashwini Mam 7057469892

Implement, maintain, and continuously improve the Quality Management System (QMS). Ensure compliance with ISO 9001 and other applicable standards. Handle complete responsibility of IATF documentation and compliance requirements. Develop, review, and control documentation including SOPs, Work Instruc

Job Description Purpose To ensure the smooth and compliant transfer of pharmaceutical formulations from R&D to manufacturing, ensuring scalability, consistency, and regulatory compliance for successful product commercialization. Position / Job Title Assistant Manager Department Technology Transf

Responsibilities \* Ensure compliance with ISO standards \* Coordinate QMS activities across departments \* Maintain accurate records and reports \* Develop and implement QMS procedures \* Conduct regular audits and assessments *Perks and benefits** Health insurance

raw materials,in-process,finished goods testing Manage deviation, OOS ,OOT investigations,implement capa and change control actions.Monitor calibration, preventive maintenance,troubleshooting of analytical instruments HPLC, GC, UV, and Karl Fischer.

Job Description Description At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Governme

<\/p> Position: <\/span><\/span><\/b> QMS Engineer<\/span><\/span> <\/div> ​<\/span> <\/span><\/div> <\/span> Job Summary:<\/span><\/span><\/b> <\/span><\/div> <\/p> We are seeking a highly skilled

Key Responsibilities A. Quality Management System (QMS) Develop, implement, and maintain the QMS to ensure compliance with ISO and customer-specific requirements. Lead internal and external audits (ISO, customer audits, supplier audits). Ensure documentation, procedures, SOPs, and quality manuals ar

Company Description SAHI HR Services provides comprehensive human resource solutions tailored to enhance business operations. The company specializes in manpower supply, HR management systems, and conducting reliable background verification checks. Additionally, SAHI HR Services offers professional

Zensar Technologies

Job Description Job Description Zensar is seeking an experienced Computer System Validation (CSV) Expert to join its Hleathcare and Life Sciences team. This is a senior role responsible for leading the validation of GxP-regulated computerised systems, including infrastructure, clinical, and business

merck group

Job Description Work Your Magic with us! Ready to explore, break barriers, and discover more We know you've got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics.

Philips

Job Description Job Title Product Risk Management Specialist Job Description Job title: Product Risk Management Specialist Your Role The Product Risk Management Specialist is responsible for contributing expertise in the development and deployment of the central Philips product safety risk managemen

JOB DESCRIPTION – QMS LEAD Standards: ISO 9001 & IATF 16949 ROLE OBJECTIVE Lead independent implementation and enforcement of a robust Quality Management System ensuring audit readiness, system discipline, and continuous improvement across manufacturing operations. CRITICAL ROLE EXPECTATIONS Ind

Minimum Requirement : Minimum 7+ years of experience in Quality Assurance / Accreditation / QMS ISO 9001:2015 Lead Auditor Certification (Mandatory ) Proven experience in audits, compliance, and process improvement Strong understanding of industry standards and regulatory frameworks Role & respo

Implement and maintain the Quality Management System (QMS) across the organization.Ensure alignment with:ISO 9001:2015 ,AS9100D (where applicable)Standardize and deploy:SOPs, procedures, work instructions, and policies Required Candidate profile Strong knowledge of ISO 9001:2015 clauses ,AS9100D req

Maintain and update QMS documentation (SOPs, procedures, manuals) Ensure compliance with ISO standards (e.g., ISO 9001) Conduct internal audits and support external audits Monitor process quality and drive continuous improvement initiatives Handle customer complaints and implement corrective & p

We are partnering with our customers across the complete semiconductor value chain spectrum that includes Hardware design and development, Supply chain management, Quality management, Product Management, Reliability, Data Science, ML/AI and many more. We are enabling our customers to develop technol

Job Profile: Familiar with Investigation Methods and Tools like Fish Bone. 5 Why/WHY-WHY analysis. Responsible for Issuance, Log-in and Review of Deviation/ Incident Responsible for Issuance, Log-in and Review of Change Control Responsible for Issuance, Log-in and Review of CAPA. Handling of Market