Require Executive or Sr officer with minimum 5 years experience in QC to handle HPLC

5 years

0 Lacs

Posted:3 days ago| Platform: Linkedin logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Company Description

Rusan Pharma Ltd. is a globally integrated pharmaceutical company that specializes in the treatment of addiction and pain management, with a diverse product portfolio serving countries such as Europe, the UK, Russia, South Africa, and others. Established in 1994, Rusan Pharma has worked to make Opioid Substitution Treatment (OST) a widely accepted practice in India, collaborating with key stakeholders. Rusan is committed to values such as quality, research, customer-focused solutions, personal growth, and fostering diversity, ensuring high ethical standards in its pursuit of innovation and excellence.

Role Description

This is a full-time, on-site role based in Dehradun for an Executive or Senior Officer in Quality Control (QC) with expertise in handling High-Performance Liquid Chromatography (HPLC). Responsibilities include conducting routine analysis using HPLC techniques, ensuring compliance with regulatory standards, performing documentation and record-keeping, and adhering to standard QA/QC procedures. The role may also involve troubleshooting and calibrating laboratory equipment and actively coordinating with production teams to ensure quality benchmarks are met and exceeded.

Qualifications

  • Proficiency in Quality Control processes with a strong understanding of HPLC techniques and related instrumentation.
  • Experience in conducting testing, analysis, and ensuring compliance with pharmaceutical regulatory standards.
  • Skills in documentation, data management, and maintaining detailed and accurate records.
  • Excellent problem-solving skills with the capability to troubleshoot and calibrate laboratory equipment.
  • Bachelor’s or Master’s degree in Pharmaceutical Sciences, Chemistry, or a related field. A minimum of 5 years of relevant experience in QC or HPLC handling is required.
  • Effective communication, teamwork, and time-management abilities.
  • Knowledge of current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP) will be an asset.

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