Recruitment for Pharmacy graduates as Chemist at HLL Lifecare Limited - Government of India

 

HLL Lifecare Limited, a Government of India Public Sector Enterprise under the Ministry of Health & Family Welfare is a global provider of high quality healthcare products & services. HLL Lifecare Limited, a Mini Ratna Central Public Sector Enterprise under the Ministry of Health & Family Welfare is India's leading manufacturers and marketers of Contraceptive, Health Care and Pharma products. The company is now looking for Manufacturing Chemist and Quality Control Chemist on fixed term contract basis for it’s manufacturing facility at Manesar, District- Gurgaon (Haryana).

Manufacturing Chemist

Qualification & Experience : Graduate in Science (Chemistry / Biochemistry) / Pharmacy from a recognized university with minimum 2 years or Diploma in Engineering(Biotechnology) / Pharmacy from a recognized institute with minimum 4 years experience in manufacturing or testing of Medical Devices (In-Vitro diagnostic kits). Shall be approved as manufacturing chemist for In- vitro diagnostics and preference will be given to those are approved Manufacturing Chemist by Haryana State FDA.

Job Responsibility :
• Production planning & execution of orders in time bound manner
• Compliance to regulatory protocols, SOP for manufacturing of IVDs.
• Documentation as per ISO 13485 including Batch Manufacturing Records, Calibration, Validation Records
• Maintenance of manufacturing records complying to regulatory requirements
• Managing shop floor activities for manufacturing of IVDs,
• Handling regulatory & statutory audits

QC Chemist

Qualification & Experience : Graduate in Science (Chemistry/ Biochemistry) / Pharmacy with minimum 2 years or Diploma in Engineering (Biotechnology) / Pharmacy from a recognized institute with minimum 4 years experience in testing of Medical Devices (In-Vitro diagnostic kits). Shall be approved as Q.C. chemist for In-vitro diagnostics and preference will be given to those are approved Q.C. Chemist by Haryana State FDA.

Job Responsibility :
• Plan and control QA/QC activities, quality supervision and in process quality control (IPQC)
• Compliance to SOP, STP, Specification of materials and finished products
• Method validation, Qualification and Calibration of Instruments
• Quality testing of incoming materials and finished products and stability study
• Maintenance of QC records complying to regulatory requirements, ISO 13485, CE
• Development of marketing support material including product design and development
• Handling customer complaints including corrective and preventive action (CAPA), Handling Deviation, OOS
• Maintaining licenses, ISO, CE mark certification; Handling regulatory & statutory audits.

Age: Maximum 37 years as on 01.10.2019

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