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 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 4 days ago

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Research Associate - FD Piramal Finance

0.0 - 1.0 years

2 - 3 Lacs

Ahmedabad

Work from Office

Formulation development of NCE projects, generic projects and line extension projects Preparation/review of literature summary and development report to the assigned product. Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product. Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP. Representation in departmental audit Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same. Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition. Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required. Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS Communication with cross-functional team and client via mails, meetings and oral communication Qualifications M. Pharm (Pharmaceutics)

Posted 2 months ago

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