• 3
  • Active Jobs Found
    (Last Updated: Mar 29, 2024)
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Asst. Manager / Sr Executive - Microbiology

Acme Generics LLP

Full time
  • 6+ years
  • Not Disclosed
  • Baddi, India
  • Post Date: Mar 01, 2024
  • End Date: May 01, 2024
  • 6+ years
  • Not Disclosed
  • Baddi, India
  • Post Date: Mar 01, 2024
  • End Date: May 01, 2024

Responsibilities To ensure gowning/ De-gowning procedure during Entry/Exit of Quality Control Lab and microbiology lab. Conducting the Investigation of incident, OOS, OOT, Change control, OOC & OOE and take an appropriate CAPA to prevent the incident in future. To do the review of Environmental monitoring trends and water trends of microbiological analysis. To prepare/review SOP of microbiology department. Allotment of daily work to the Microbiologists and monitoring their routine working. Daily verification and calibration of all instruments in Microbiology department wherever applicable. Update the Head QC after the end of each shift regarding routine working. To Co-ordinate for inter-departmental activities for continuous improvement. Responsibility to follow compliance as per GLP and GDP during routine activity.   Qualification & Experience Qualification- MSc (Micro) Experience - 6 to 9 Years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"    

  • pharma
  • Quality control
  • Compliance
  • Management

Plant Head & Compliance Officer

Unichem Laboratories Limited

Full time
  • 10+ years
  • Not Disclosed
  • Baddi, India
  • Post Date: Feb 27, 2024
  • End Date: Apr 27, 2024
  • 10+ years
  • Not Disclosed
  • Baddi, India
  • Post Date: Feb 27, 2024
  • End Date: Apr 27, 2024

Responsibilities Ensure achievement of budgeted targets on a monthly and yearly basis. Ensure site is in state of compliance for multiple authorities’ inspections and guide / coordinate during inspections and local statutory authorities. Work out areas of improvement in product cost, engineering cost and implement the same. Create and maintain an environment of mutual trust, respect, and customer centricity. Build and maintain a high performing team and culture. Ensure manpower management and engagement. Brand ambassador of Unichem for any internal and external stakeholders at the plant.   Qualification & Experience Experience - 20 to 25 Years B. Pharm/M. Pharm

  • pharma
  • bpharm
  • mpharm
  • Compliance

Head Quality Control (OSD Facility)

Acme Generics LLP

Full time
  • 10+ years
  • Not Disclosed
  • Baddi, India
  • Post Date: Feb 21, 2024
  • End Date: Apr 21, 2024
  • 10+ years
  • Not Disclosed
  • Baddi, India
  • Post Date: Feb 21, 2024
  • End Date: Apr 21, 2024

Responsibilities To manage QMS activity like change control, Deviation, CAPA, OOS, OOT, Lab events etc. To Conduct Risk Assessment& SOP reviews; investigating& supporting in the grievances. Responsible for Document & review Specification, SOPs, Review of Test Data Sheet, Analytical Test Report & Masters. Responsible for review of Method Validation Protocols & Method Validation Reports. To Monitor the Review of calibration/Preventive maintenance schedule. Responsibilities to Initiate for Procurement of impurity standard/reference standard, chemicals/reagents, columns, Laboratory glasswares etc. To Develop and implement Site Policies & Procedures (SOPs) to assure compliance with regulatory requirements, and corporate policies Responsibilities to Supervising deviation review and managing the CAPA review, approval and implementation reviews To Create goals, objectives and measures to drive continuous improvement of the QC operations Responsible for implementing the CAPA Parameters after investigation. Responsibilities assign to check the effectiveness of CAPA. To ensure Co-ordination for IQ, OQ, PQ and qualification plan of the instruments. Responsible for Coordinate & present all relevant documents to external auditors and to ensure that corrective measures are taken on any non-compliance finding. To Review method transfer protocols & reports & stability protocols. Responsible for rendering technical support to the Section in charges and managers. To Review various submissions to General Export and other regulatory markets related to quality control. Responsible for Review of comparison protocol & report of multimedia DRP & Dose dumping between RLD & exhibit batches. To complete quality projects within time by proper planning & execution of planning. To ensure the Implementation of several measures to identify deformities, malfunctions or other abnormalities such as Periodic verification of instruments/Equipment / components / products, Trending of failures. To Coordinate with various cross functional groups for timely availability of API/RM, PM , manufacturing area (Production), Analytical documents (Like Method Transfer, Specifications, Analytical Testing procedures etc.) & Quality control facility (Like column, critical chemicals working standard & impurities).   Qualification & Experience M.sc B. pharma, M. pharma Experience: 16-20 Years   Note: Please ensure you include this in the EMAIL Subject line: "medbots.in: YourName: Years  of Experience"  

  • Quality control
  • Operations
  • Inspection

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