Project Management Senior Manager

Posted 10 Days Ago
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Pudupakkam, Marakkanam, Viluppuram, Tamil Nadu
Senior level
Healthtech • Pharmaceutical • Telehealth
The Role
The Senior Project Management Manager is responsible for leading project teams, managing cross-functional activities for new launches and site transfers, and ensuring timely progress through risk identification and resolution. This includes building relationships with clients and teams, tracking project progress, and coordinating with production for timely filing and compliance.
Summary Generated by Built In

Job Description Summary

The Project Management, Senior Manager is responsible for leading project teams and managing cross-functional activities essential for new launches, site transfers, alternate API vendor development programs, and R&D projects and exhibiting the batches and deficiency management program at Chennai/ Indore location. Based out of Chennai/Indore, this role will be responsible for working with Tech ops, R&D, Regulatory, Manufacturing, Quality, and SCM to ensure end to end management of NPL/Site transfer projects and handoff to the site.
The project manager tracks and reports progress, identifies risks, and escalates concerns and challenges to the broader project team for resolution. The role builds effective client and team relationships, with demonstrated competence managing the project plan, the assigned resources, reviewing financial forecasts, and the project activities.

Job Description

Job Description:-

  • Track and report site additions / transfer and project progress, identifies risks, and actively participate in resolving project difficulties to meet project timelines.
  • Interface with a cross-functional team including R&D, Tech Services, Quality Operations, Production, SCM, Regulatory affairs and US stakeholders
  • Preparing and updating the project trackers
  • Ensure that key milestones are achieved and the project is progressed in a timely manner for successful on time product filing
  • Evaluate volumes of commercial projects in discussion with central planning team
  • Track availability of API, RM, PM, tooling, change parts on time for submission / validation batches. Also to ensure licensing and compliances for the projects
  • Build effective relationship with all internal and external stakeholders / cross functional team
  • Conduct team meetings/teleconferences provide agendas, issue minutes with follow-up actions identified.
  • Coordinating with the production planner to plan and prioritize the batches at commercial sites for timely filing

Education & Experience

  • M. Pharm / B. Pharm
  • Prior technical site transfer / launch / R&D development experience 

5+ years of Pharmaceutical project management experience, 10+ yrs of Industry 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.

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