Mylan is a global pharmaceutical company committed to setting new standards in healthcare and providing 7 billion people access to high quality medicine. We offer a growing portfolio of more than 7,500 products, including prescription generic, branded generic, brand-name and biosimilar drugs, as well as over-the-counter (OTC) remedies. We market our products in more than 165 countries and territories, and every member of our approximately 35,000-strong workforce is dedicated to creating better health for a better world.
Vacancy Details
Assistant – EHS
Roles and Responsibilities:
- Competent Knowledge of Environment with appropriate experience in OSD Tablet Manufacturing Unit.
- To Assist in operation and Maintenance of effluent treatment plant as per procedure.
- Maintain training of workers and Operators for safety awareness and use of PPE.
- Receive the hazardous waste and maintain the records.
- Maintain ETP lab & hazardous storage area & chemical storage area.
- Daily Monitoring of Unsafe act, Unsafe conditions and unsafe equipments.
- Regular Monitoring of EMS system.
- Perform Risk Assessment and Risk Management by conducting activity-based risk assessment.
- Documentation of ISO 14001 & OHSAS 18001.
- Perform analysis for effluent treatment plant sample such as pH, TDS & COD and maintain the records as per procedure.
Desired Candidate Profile: B.Sc. / M.Sc. (Environment) With 1 – 4 Years of Experience
Chemist / Sr. Chemist – QC
Roles and Responsibilities:
- Review of Daily records like balance verification, pH calibration, cleaning records.
- Review of Analytical reports.
- Preparation of Trends.
- Culture receipt and maintenance.
- Change control, Cleaning validation, CAPA
- Equipment qualifications
- Identification of inhouse isolate by monitoring the day to day plates and co-ordination with external laboratory.
Desired Candidate Profile: B. Sc. / M. Sc. (Biotech./ Micro.) With 1-4 Years of Experience
Deputy Manager – AQA
Roles and Responsibilities:
- Competent knowledge of QC Analytical Review in Tablet Manufacturing.
- Review and Approval of LIR (Out of Specification, Out of Trend, Atypical), QIA, Invalid, Out of Calibration events etc.
- Review of Standard Testing procedure, Specification and Analytical Work Record and Certificate of Analysis (COA) and other Master document related to Quality Control Department.
- To ensure Qualification, Calibration and Preventive maintenance of instruments/ equipment is performed as per the schedule and review relevant documents.
- To monitor cGMP, GLP in quality control department.
- To ensure adherence to the SOPs, Specifications and Standard Testing procedures, General Test procedures.
- Responsible for Preparation and review of Trend report for Out of Specification, Out of Trend, and Incident of Quality Control department.
- Review of Stability Summary / Analytical Report, Stability Protocols, Annual challenging study of stability chamber.
- Review of Quality Control Related SOPs.
- 9. To ensure compliance of the analytical raw data and verification of electronic records.
- Responsible for Approval of User Creation /Removal, Archival and Retrieval of Empower projects.
- To review & monitor of CSV of QC instruments.
Desired Candidate Profile: B.Pharm / M.Pharm with 10 – 14 years experience
Chemist- Microbiology
Roles and Responsibilities:
- Review of Daily records like balance verification, pH calibration, cleaning records.
- Review of Analytical reports.
- Preparation of Trends.
- Culture receipt and maintenance.
- Change control, Cleaning validation, CAPA
- Equipment qualifications
- Identification of inhouse isolate by monitoring the day to day plates and co-ordination with external laboratory.
Desired Candidate Profile: B. Sc. / M. Sc. (Biotech./ Micro.) With 1-4 Years of Experience
E-mail ID – ajay.mekhiya@viatris.com
Contact: Mylan Laboratories Ltd, Plot No. 1606-09 GIDC, Sarigam, Tal- Umbergaon, Dist- Valsad, Gujarat – 396155