Home Production Sr Manager QC | Sun Pharmaceuticals | Guwahati

Sr Manager QC | Sun Pharmaceuticals | Guwahati

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Sun Pharma has grown to become the 5th largest generic pharmaceutical company in the world and No. 1 in India. Our passion for research has enabled us to develop over 2000 products that are sold in more than 100 countries worldwide. Our global presence is supported by over 40 manufacturing facilities spread across six continents and R&D centers across the globe. Innovation is at the core of the Sun.

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¬†We have nearly 2000 scientists working in six research centers across India, Israel, and the USA who have a passion for innovation and longing to provide better healthcare to humanity at large. Our multi-cultural workforce, comprising over 30,000 employees from 50 nationalities, is our biggest strength. We recognize our employee’s passion for growth and empower them to achieve their aspirations. We owe our success to our passionate and skilled workforce. At Sun, one can work with an inspiring, approachable, and visionary leadership. Our open, enabling and trust-based culture will offer you an exciting environment to work and excel in your chosen career.

Position: Sr Manager Quality Control

Location: Guwahati, Assam, India

Job Description:

  • To monitor and ensure that In-process/ Finished product samples are tested and released in time to meet market/customers requirements.
  • Accountable for the Quality of intermediates and finished products, which are released as per the specification.
  • Responsible for productivity improvement by optimization of instrument utilization, troubleshooting of analytical methods, and resource planning for responsible sections.
  • Responsible to participate and implement laboratory continuous improvement/ Lean lab programs
  • Co-ordination for technology transfer products during new product manufacturing/ launches for analytical method transfers and timely releases.
  • To review the laboratory investigations and to ensure the timely decision for further actions w.r.t. the extended investigation, timely escalation of OOS/OOT findings to QA and Plant Management.

  • Review & Approve protocol/report for Analytical method validation, Analytical method transfer, Process validation, Cleaning validation, Qualification, Continued process verification, and additional sampling/activity or any study required by the Validation master plan.
  • Ensure compliance to cGMP/GDP/ cGLP at all operational activities and participate in internal/ external audits
  • To ensure the harmonization and consistent implementation of Quality Systems and Good Laboratory Procedures at the site, in alignment with Global Quality Policies and Standards.
  • To ensure the implementation of CAPA to address the internal/external audit findings in QC labs within a stipulated time frame.
  • To participate in risk assessment and Appropriate action in co-ordination with QA department
  • To review & monitor training calendar, on-job training completion, reconciliation, and compliance.
  • To review and approve the activities under contract lab testing (External lab).
  • To Co-ordinate of Instrument maintenance, Calibration, Qualification, and Troubleshooting.
  • To Coordinate and ensure the procurement of Standards, Impurities, Lab consumables are of good standards and are managed with full records of receipt, storage, issuance and disposal

Qualification: B.Pharma, M.S/M.Sc

Experience: 13-15 Years

Salary: Negotibale

Contact Details:

hrd@sunpharma.com, vignesh.iyer@sunpharma.com

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