Dr.Reddys Laboratories Ltd Walk-in Interview.Dr.Reddys Laboratories Ltd Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue.
Important Details :
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
- Job Location: Hyderabad
Vacancy details:
- Department: Chemist-Production/Team Member – AQA/Team member – MSAT
- Qualification: B.Sc Chemistry, M.Sc Chemistry & Diploma in Chemical engineering/A Bachelor’s/Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related field
Job Description : Greeting from Dr.Reddys Laboratories Ltd..!!!!
Chemist-Production
Roles & Responsibilities
- You will be responsible for Equipment Operations of Reactors (GL, SS & All Glass), Mobile Receivers & tanks, ANFD, PNF & VTD, Isolators (Reactor Charging, ANFD Discharge, Dispensing/packing, sifter & multimill), Air jet mill, Multimill, Blender & Sifter, Spray dryer, TCU, Vacuum Pumps, AODD Pumps, centrifugal pumps & peristatic pumps, VNS sealing machine, RLAF & dispensing booth, Refrigerators and Deep freezers etc.
- You will be responsible to Execution of Batches, Equipment product change over & General cleaning of equipment. Batch production record filling as per SOP & as per Good documentation practices.
- You will be responsible for Filling of Equipment Logs, daily production monitoring records like Temperature, Humidity & RH, weighing balance calibrations, reviewing of house keeping records, Printing Data logger records and Updating status boards etc as per site SOPs. Collection of Records/books, submission of completed BPRs/Records to QA.
- You will be responsible for In process sample collection from Reactors, ANFD & VTD etc. Raw Material, Solvents handling, material moments & dispensing and maintaining records as per SOP.
- You will be responsible to reduce the accidents in the plant by following safety principles, install earth rods to remove static electricity from material, Handling different chemicals with appropriate PPE & following SHE Norms. Monitor adherence of behavioral safety of contract persons.
- You will be responsible to meet the production schedules and reduce breakdowns by planning the equipment for idle condition to prepare for preventive maintenance, issue work order to maintenance to carry on with maintenance, follow up with maintenance on problem rectification.
- You will be responsible for Handling of Production waste & Detoxification batches execution.
- Support the engineering team in equipment qualification activities to meet the batch planning.
- You will be responsible for handling, initiation of deviations, incidents and support for closure of deviation & Incident reports
2-6 years of experience in Pharma industry
Team Member – AQA/Team member – MSAT
Roles & Responsibilities
- Review and approval of all analytical test data of Quality control.
- Review and usage decision of analytical reports in LIMS, Empower and SAP.
- Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments.
- Review the Analytical test report in LIMS.
- Review the reported results against specification and trends.
- Review the method validation and method transfer documents.
- Review the instrument calibrations and working standard qualification records.
- Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure.
- Monitoring of analytical activities in Quality control laboratory.
- Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval.
- Verification and review of the audit trails for Standalone, Empower and LIMS.
- Ensure cGMP / cGLP compliance.
- To follow Safety, Health and Environmental procedures and practices.
- Review and approval of excel sheet validations.
- Review results acceptance for API and Excipients and Packing material.
- Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols.
- Handling of Robotic Process Automation of Chromatography Data review (RPACD)
- To carry any other activities assigned by upward reporting staff.
Qualifications
Educational qualification: A Bachelor’s/Master’s degree in Pharmacy, Chemistry, Chemical Engineering, or a related field
Minimum work experience: 3 to 7 years of experience in pharmaceutical manufacturing or a similar role
ABAC
