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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 of the ideal conditions for the working of equipment, including their calibrations, inspections, and maintenance schedule. GMP training, knowledge of documentation as per GMP & QMS guidelines, audits, importance of documentation, basics of production data analysis, process safety analysis, handling hazards, and basic knowledge of production planning, supervising, and delegating are also required. Qualifications Required: - Education: B.Pharm/ M.Pharm - Experience: 2-3 years in the Pharma Industry - Licence: Possession of a certificate approved by FDA for Tablets/Capsules Additional Details: The job type is Full-time, Permanent with benefits such as Cell phone reimbursement, Health insurance, and Provident Fund. The work location is in person. Note: The application method is via email. A resume is required for application. The application updates will be sent to hrmanager613@gmail.com. Candidates can contact you via email.,

Posted 3 days ago

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