Sr Analyst, Quality Control

Posted 2 Days Ago
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Pudupakkam, Marakkanam, Viluppuram, Tamil Nadu
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
The Sr Analyst, Quality Control is responsible for conducting analytical testing of samples, including in-process and finished products. The role involves maintaining compliance with good laboratory and documentation practices, performing method verification and validation, and ensuring safety and quality standards in the lab. The analyst prepares reports, maintains records, and participates in training activities as needed.
Summary Generated by Built In

To perform the analysis of In-process sample, Hold Time, Finished product samples, WRS Qualification, Instrument Calibration and any other analytical testing based on routine requirement. 
• Reporting and documenting the analytical data as per good laboratory practices and Good documentation practices.
• To perform the analytical method transfer, method verification/validation as per requirement.
• To maintain respective working area, documents, and records in auditable manner.
• To follow the safety, cGLP and cGDP in work area.
• To attend and complete the training activities whenever assigned.
• To ensure lab compliance during daily routine activities.
• Initiating events/change requests based on daily lab activities.
• Maintain a high standard of 5S practices at our workplace, through teamwork and self-discipline.
• Follow safety instructions at all times at the workplace. Should follow safety guidelines in the interest of self, environment and property and community at large.

To perform the analysis of In-process sample, Hold Time, Finished product samples, WRS Qualification, Instrument Calibration and any other analytical testing based on routine requirement. 
• Reporting and documenting the analytical data as per good laboratory practices and Good documentation practices.
• To perform the analytical method transfer, method verification/validation as per requirement.
• To maintain respective working area, documents, and records in auditable manner.
• To follow the safety, cGLP and cGDP in work area.
• To attend and complete the training activities whenever assigned.
• To ensure lab compliance during daily routine activities.
• Initiating events/change requests based on daily lab activities.
• Maintain a high standard of 5S practices at our workplace, through teamwork and self-discipline.
• Follow safety instructions at all times at the workplace. Should follow safety guidelines in the interest of self, environment and property and community at large.

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.

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