Quality Assurance Assistant Manager

Posted 10 Days Ago
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Digha, Purba Medinipur, West Bengal
1-3 Years Experience
Healthtech • Pharmaceutical • Telehealth
The Role
The Quality Assurance Assistant Manager is responsible for supporting the Analytical Laboratory by preparing and reviewing SOPs, ensuring compliance with safety precautions and cGMP, maintaining calibration schedules, participating in audits, and reviewing various reports and documents. They are also part of the investigation team for incidents in the Analytical lab.
Summary Generated by Built In

Job Description Summary

To Support the Analytical Laboratory, Preparation and review of SOP and its updation, Review of all QMS documents. Review of ROA, Calibration reports, IQ, OQ, PQ reports. Review of Tech transfer, Analytical validation document. Review of Stability Protocol, Stability reports and stability trend data. To ensure Compliance of Safety precaution & cGMP in Analytical Laboratory. Maintaining all Calibration & preventive maintenance Schedule. Assists in audits & preparations of Audit compliance reports. Handling and maintaining of all training records. Responsible for review of OOS, OOT, Incidents, Deviations, CAPA and Change control.
Part of investigation team for investigation of OOS, OOT, Incidents of Analytical lab

Job Description

Job Description :-

  • SOP preparation & its Updation.
  • Reviewing of all QMS documents like change control and investigation for OOS/OOT, incident/deviation.
  • Reviewing of Tech transfer and Analytical Validation/verification data. 
  • Responsible for conducting the Internal Audit as per schedule and Audit compliance reports.
  • Ensuring compliance of all SOP and system implementation
  • Reviewing of Stability Protocol, Reports & Trends data, Responsible for review of all analytical instrument (HPLC, LCMS, GCMS, GC, UPLC, UV, IR etc.) calibration records.
  • Basic understanding of GMP, Review of standard testing procedure, specification and record of analysis.
  • Experience on Risk assesment and Gap assesment.
  • SOP , QMS and issuance of formats,& documentation for Analytical Laboratory
  • Maintaining Documentation room.
  • Documentation support for Analytical Lab.
  • Technical support for Analytical Lab

Education & Experience :-

  • Bachelors/Masters in relevant stream
  • 8 to 12 years of Experience

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.

The Company
Montreal, Quebec
1,722 Employees
On-site Workplace
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs.

Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward.

Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life.

Endo has global headquarters in Malvern, Pennsylvania.

Community Guidelines:
1. Be respectful. Everyone who visits our page should feel comfortable and respected.
2. If we see a comment that violates anything in the following list, it may be removed.
• Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional.
• Comments that are excessively repetitive and/or disruptive to the community.
• Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter.
• Comments that appear to be medical advice.
We reserve the right to remove a reply for any reason at any time.
3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088.

Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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