Sr Associate Engineering

Posted 10 Days Ago
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Indore, Madhya Pradesh
1-3 Years Experience
Healthtech • Pharmaceutical • Telehealth
The Role
Responsible for all Engineering activities related to Production, Utility, HVAC, Water system, and other Departments at the Indore SEZ plant. Ensures compliance with organization policies and codes of conduct, prepares SOPs, executes maintenance activities, ensures safety procedures, plans and executes project activities, maintains critical spares, coordinates calibration activities, and manages QMS activities. Collaborates with external vendors and agencies for support as needed. Responsible for all Qualification and Validation activities at the Indore site.
Summary Generated by Built In

Job Description Summary

Candidate will be responsible for Process, HVAC & Electrical maintenance activities.

Job Description

  • To take care of all Engineering activity related to Production, Utility, HVAC, Water system and other Departments at Indore SEZ plant.
  • To ensure and follow Organization Policies and Code of conduct.
  • Responsible for preparation and implementation of procedures related to qualification, preventive maintenance and other maintenance related activity for Injectable facility.
  • Responsible for performing and documenting the break down maintenance of Process equipment’s for Injectable facility.
  • To prepare, review of all engineering SOP and QMS documents for Injectable equipment’s installed at facility.
  • To execute and ensure the scheduled preventive maintenance activities.
  • To ensure safety procedures are followed during operation and maintenance of equipment’s and calibration of measuring devices.
  • To prepare, review and execute qualification and requalification protocols (IQ, OQ, PQ) & other activity for Maintenance and process equipment’s and systems in accordance with approved procedures.
  • To provide technical support and review for qualification and requalification / PPV (IQ, OQ, PQ) for Process equipment’s and systems in accordance with approved procedures.
  • To ensure planning and executing the project related activities of equipment’s for Injectable facility.
  • To ensure the stock of critical spares required for trouble free operation of Injectable equipment is maintained.
  • To prepare & execute calibration schedules, calibration records, SOPs in accordance with approved procedures and coordinate the calibration activity with the Internal / external agencies.
  • Responsible for executing and review of QMS activities (change control, incident, deviation and CAPA).
  • Co-ordination with External vendors, Agencies wherever required for support to Process equipment’s maintenance & other activities.
  • Responsible for all Qualification and Validation activity at Indore site.

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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