Opening For Production Injection Dept. @ Rusan Pharma Ltd.

from 1 to 5 year(s) of Experience
₹ 50,000 - 3,00,000 P.A.

Job Description

Roles and Responsibilities

  • Responsible for all production activities with respective to cGMP with various guidelines of CDSCO, WHO, ANVISA & ISO.
  • Completion of BPR, BMR, equipment log sheet and all GMP records.
  • Coordinating with warehouse, QA, QC and engineering people to run production activity without any hiccups.
  • Prepration of daily production report and man power allocation as per production plan.
  • In process checking on various intermediates stages.
  • Good working experience in Packing of injectable products Blister machine , Shrink machine.
  • Deftly handling Dry Heat Sterlization (DHS, TUNNELS), Steam Heat Sterilization (Autoclave) & bung washing machine.
  • Responsible for taking precaution for aseptic work to prevent contamination.

Desired Candidate Profile



Perks and Benefits



Role:Regulatory Affairs Manager

Salary: 50,000 - 3,00,000 P.A.

Industry:Pharmaceutical & Life Sciences

Functional Area:Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology

Role Category:Drug Regulatory Affairs/Documentation

Employment Type:Full Time, Permanent

Key Skills

Education-

UG:B.Pharma in Any Specialization,B.Sc in Any Specialization

Company Profile

Rusan Pharma Ltd

Rusan is a research driven pharmaceutical company having its Manufacturing Units in India and Worldwide Marketing of Pharmaceutical Formulation, Active Pharmaceutical Ingredients and Intermediates. The company has its own Research & Development centre at Kandivli (west), Mumbai, state of the art, Bulk Manufacturing Plant at Ankleshwar and Formulation plant at Dehradun and SEZ, Kandla having approval of MHRA (UK), MCC (SA) and other International Health Authorities. March 2008 - 82 Crs., Expected by March 2009 €“ 150 Crs.
Company Info
View Contact Details+

Contact Company:Rusan Pharma Ltd

Address:58-D,GOVT INDUSTRIAL ESTATE, CHARKOP,KANDIVALI WEST, MUMBAI, Maharashtra, India