Quality Control Manager / Sr Manager

Posted 5 Days Ago
Be an Early Applicant
Indore, Madhya Pradesh
Mid level
Healthtech • Pharmaceutical • Telehealth
The Role
The Quality Control Manager will manage laboratory operations, including workforce planning, supervising testing activities, training analysts, investigating non-conformances, and participating in quality management discussions. The role also involves reviewing laboratory documents and managing materials necessary for testing activities.
Summary Generated by Built In

Job Description Summary

To handle Laboratory Operations:
- Workforce planning and allocation of work
- Facilitating the required materials, document/records for laboratory testing
- Supervising the testing activity and troubleshooting on need basis
- Providing training/coaching to the analysts in a proactive manner to avoid laboratory errors/Analyst errors
- Attending the meetings w r t batch planning and further deliverables
- To report and investigate the non-conformances reported in the lab
- To take part in the QMS discussions esp in the laboratory events, Change records and CAPA implementations
- Escalating the atypical results, excursions, discrepancies identified in the laboratory
- Review and approve laboratory documents and records

Job Description

To handle Laboratory Operations:
- Workforce planning and allocation of work
- Facilitating the required materials, document/records for laboratory testing
- Supervising the testing activity and troubleshooting on need basis
- Providing training/coaching to the analysts in a proactive manner to avoid laboratory errors/Analyst errors
- Attending the meetings w r t batch planning and further deliverables
- To report and investigate the non-conformances reported in the lab
- To take part in the QMS discussions esp in the laboratory events, Change records and CAPA implementations
- Escalating the atypical results, excursions, discrepancies identified in the laboratory
- Review and approve laboratory documents and records  

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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