
Endo
Job Description Summary Responsible for Quality Assurance activities, reviewing documentation, and implementing quality measures to ensure compliance with Good Manufacturing Practices (GMP) and other relevant standards
Job Description
Job Description:
- Good hands-on calibration & maintenance of Analytical instruments like Balance, pH meter, Conductivity meter, Auto titrator, UV, chromatographic technique IR, HPLC, etc.
- Good technical knowledge of finished product/stability/Raw material samples and execution of analytical activities, instrument calibrations.
- Review of analytical data.
- Implement and maintain quality assurance systems and procedures to ensure the integrity and reliability of data.
- Knowledge on pharmacopeial guidelines.
- Preparation of SOP’s, review of analytical documents
- Knowledge on document management ( issuance, archival & retrieval etc) procedure.
- Maintain good documentation practices.
- Preparation of investigation reports/ summaries for QA related incidents.
- Maintain accurate and detailed records of all quality assurance activities.
- Timely execution of Assigned Task.
- To upkeep laboratory for All Time Readiness.
- Collaborate with cross-functional teams to drive continuous improvement initiatives.
Education & Experience
Master’s degree in Pharmacy, Chemistry, or a related field, 1-3 years of experience in quality assurance in the pharmaceutical industry.
Commitment to Diversity, Equity, and Inclusion:
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person’s unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.