0.0 years

0 Lacs

chennai, tamil nadu, india

On-site

About ValGenesis ValGenesis is a leading digital validation platform provider for life sciences companies. ValGenesis suite of products are used by 30 of the top 50 global pharmaceutical and biotech companies to achieve digital transformation, total compliance and manufacturing excellence/intelligence across their product lifecycle. Learn more about working for ValGenesis, the de facto standard for paperless validation in Life Sciences: https://www.youtube.com/watchv=tASq7Ld0JsQ About the Role: We are looking for a great Module Lead, to join our Validation team. You will coordinate with the rest of the team working on different layers of the infrastructure. Therefore, a commitment to collabo...

Posted 3 months ago

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Coordinator - Batch Review & Release (Aurangabad) ACG World

2.0 - 6.0 years

0 Lacs

maharashtra

On-site

Job Description: You will be a member of the ACG Associated Universal Capsules team, with your primary responsibility being to ensure that the Plant complies with the Quality Management System (QMS) guidelines. Your role will involve: - Strengthening the review mechanism of batch records - Conducting effective reviews of batch records - Releasing batches according to the daily plan in a timely manner - Ensuring compliance during internal, external, and regulatory audits To excel in this role, you should hold a degree in B. Pharmacy or B.E. Mechanical with relevant Quality Assurance (QA) experience. Your competencies in these areas will be critical to successfully fulfilling the responsibilit...

Posted 3 months ago

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Assistant Chemist - Production Comed Chemicals Ltd

2.0 - 6.0 years

0 Lacs

vadodara, gujarat

On-site

Job Description: You will be responsible for providing production schedules and necessary guidelines to production operators. Your role will involve reviewing documentation and ensuring all in-process checks are carried out as per the standard operating process. It will be your duty to maintain good manufacturing practices & conditions as per GMP & WHO standards. Additionally, you will need to communicate any equipment breakdown to the maintenance team and follow SOP to improve efficiency. Facilitating audits as a production team member and coordinating with the shift supervisor, cross-functional teams, and within the team will also be part of your responsibilities. You should have knowledge...

Posted 3 months ago

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