Technical Program Lead

Piscataway · On-site$120k – $130k

About this role

Description:

Project Planning and Execution: Define and manage the scope of post-approval projects. Develop and track project timelines to ensure timely completion. Set and achieve key milestones throughout the project lifecycle. Stakeholder Communication: Coordinate with R&D, manufacturing, marketing, and other departments. Communicate with regulatory bodies, healthcare professionals, and other stakeholders. Provide updates to internal teams and external partners. Documentation and Record Keeping: Maintain accurate records of compliance activities and changes. Keep thorough records of project plans, progress, and outcomes.


Essential Functions:

  • Introduction and tracking of new post-approval projects when received from SSSM or other cross-functional departments. Tracking of Existing material Inventory and highlight the importance of post-approval project completion. Coordinating with supply chain and procurement department for procurement of API samples, impurities and submission batch qty. Tracking of Vendor qualification and Method Validation and Verification activities on daily basis. Coordinating with CFT’s on documentation, specification, method preparation and revision requirements. Tracking and scheduling the timeline for release of the material and drug product. Coordinating with operations for the submission batch schedule and stability initiation. Tracking of post-approval project throughout the completion of stability, filing and approval. Coordinating with RA and other CFTs for required filing documents and submission timeline. Providing confirmation of grant/approval status and implementation of post-approval project at commercial scale. Providing numerical data on cost-saving/alternate source projects.
  • Project Selection: Actively participates in the supply chain management and forecast meetings. Mentors Senior Manager of Strategic Portfolio Management on the process and target products consistent with the company’s strategic objectives and based on knowledge of Brand and Generic pharmaceutical markets.
  • Business Development: Works closely with Business Development and Corporate Development to identify and evaluate opportunities for alternate source and cost saving projects. Builds financial models to determine value and potential deal structures. Conducts due diligence on BD opportunities.
  • Planning: Works closely with supply chain management, Operations, and Project Management on project timing and projections to ensure a smooth and effective completion of projects from either internal or external facilities. Assesses and provides critical input on timing, market dynamics, etc. that drive near- and long-term forecasts for Finance and Tech Ops.
  • Market Intelligence: Analyzes products, markets, regulatory issues, companies, therapeutic categories, etc. to drive decisions on portfolio and new opportunities.

 


Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at [email protected]. Requests will be handled confidentially and in accordance with applicable laws. 


Company at a glance

Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver.

Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions.

Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam.

Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or [email protected]. If you are currently experiencing a life-threatening event, please immediately contact 911.

Founded2002
Team Size5,001-10,000 employees
WorkspaceOn-site
IndustryPharmaceutical Manufacturing
Location
Piscataway, New Jersey, United States
Websiteamneal.com
LinkedInLinkedIn

Top Benefits

  • Health Insurance
  • Insurance Benefits
  • 401k Matching
  • Short-term Incentive Opportunity
  • Performance-based Award

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