QA Associate - CAPA, Audits & Inspections UST

4.0 - 8.0 years

0 Lacs

karnataka

On-site

Role Overview: As a Quality Assurance (QA) Associate specializing in Corrective and Preventive Actions (CAPA), Audits, and Inspections, you will play a critical role in ensuring compliance and continuous improvement within GMP-regulated environments in the Life Sciences industry. Your primary focus will be managing CAPA processes, supporting audits, and preparing for regulatory inspections to maintain adherence to standards such as GMP, ISO, and ICH guidelines. Key Responsibilities: - Manage Corrective and Preventive Actions (CAPA) by initiating, tracking, and closing CAPA records in alignment with quality objectives. - Conduct root cause analysis using tools like 5 Whys, Fishbone, or Six Si...

Posted 3 weeks ago

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Manager -2 SUN PHARMA

7.0 - 9.0 years

0 Lacs

vadodara, gujarat, india

On-site

Job Title IT- Manager(Trackwise) Job Grade (refer to JE) G10A Function IT Location: Tandalja(Baroda) Areas Of Responsibility 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 Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Job Summary To lead the end-to-end implementation of...

Posted 2 months ago

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PMO Team Member - Tool Validation & QMS Automation Olympus Medical Systems India Pvt Ltd

5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

You will be joining the Engineering Operations team in the Digital Unit as a PMO Team Member specializing in Tool Validation & QMS Automation. Your primary focus will be on driving tool validation projects, automating validation processes, QMS documentation automation, and researching productivity-enhancing tools. Your role will play a crucial part in ensuring compliance with regulatory standards such as FDA, ISO 13485, IEC 62304, and IEC 82304-1, while also fostering innovation and operational efficiency within engineering and quality processes. The ideal candidate should have a strong understanding of software validation in regulated environments. Your responsibilities will include: - Mana...

Posted 4 months ago

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