Catalent Pharma Solutions Inc

Senior Program Manager - Program Management

Catalent Pharma Solutions Inc • $100K — $130K *
Madison, WI 53711In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Reposted 1 week ago
Job Overview by Ladders

Qualifications

  • B.S. in Science or Engineering; advanced degree preferred.
  • 7+ years of project management and/or pharmaceutical industry experience.
  • PMP or related certification preferred.
  • Knowledge of Biologics Fermentation, Cell Culture, Purification, and Analytics preferred.
  • Experience in a related field like Biologics or Pharma.

Responsibilities

  • Deliver assigned program objectives on time and within scope and budget.
  • Apply project management practices and coach others.
  • Balance multiple priorities effectively for self and teams.
  • Manage cross-functional, multi-site project teams and share best practices.
  • Develop and oversee project plans and schedules including tech transfer.
  • Maintain open communication with clients, providing updates and progress reports.
  • Monitor program progress to ensure timely completion and high-quality deliverables.
  • Troubleshoot problems independently and promote innovative solutions.

Benefits

  • Defined career path with annual reviews and feedback.
  • Inclusive and diverse workplace culture.
  • Focus on process improvement and innovation.
  • Career growth opportunities within a dedicated team.
  • 152 hours of PTO plus 8 paid holidays.
  • Generous 401K match and immediate health benefits.
  • Tuition reimbursement to support educational advancement.
Full Job Description
Senior Program Manager - Program Management

Position Summary:

  • Work Schedule: M-F 8am-5pm
  • 100% on-site


Catalent Pharma Solutions in Madison, WI is hiring a Senior Program Manager - Program Management I. The Senior Program Manager (SPM) will lead multiple complex client Process Development and GMP Manufacturing projects. The SPM is responsible for managing the client contract and will use organizational, collaboration, influencing and leadership skills to initiate, plan, execute and monitor client projects. The SPM will lead cross-functional, cross-site project teams and partner with internal business and technical leadership together with subject matter experts to deliver project results in an efficient manner consistent with client expectations.

The Role:

  • Delivers on assigned program objectives within agreed upon time, budget, scope, and quality.
  • Applies sound project management practices within assigned projects and coaches others in the same.
  • Demonstrated ability to recognize priority tasks and balance multiple changing priorities both for self and program teams.
  • Manages cross-functional, multi-site project teams, and contributes to best practices of such.
  • Develops and manages the overall project plan and schedule including tech transfer.
  • Maintains open, collaborative and solution focused communication with clients and provides periodic updates & progress reports.
  • Monitors progress of assigned programs to ensure on-time milestone and budget completion while ensuring high quality deliverables are provided to the client.
  • Troubleshoots problems with minimal assistance. Consistently seeks and promotes innovative solutions or approaches to problem solving, from a technical and functional viewpoint in a highly flexible and interactive manner as scientific data reveals new information or requirements evolve or change.
  • Works to continue to develop project management competencies across the company while strengthening the support capabilities of Program Management.
  • Effectively negotiate to settle differences and maintain positive relationships with external and internal clients
  • Other duties as assigned.

The Candidate:

  • B.S. in Science or Engineering, or equivalent combination of education and experience required. Advanced degree (M.S., M.B.A., PhD) is preferred.
  • Approximately 7+ years direct experience in project management and/or pharmaceutical industry.
  • PMP or PM certification or course work preferred.
  • Working knowledge of Biologics Fermentation, Cell Culture, Purification and Analytics preferred.
  • Professional experience in a related field such as Biologics, Biotechnology, Pharma preferred.
  • Experience working across Catalent sites preferred.
  • Experience managing commercial programs preferred.


Why you should join Catalent:
  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Positive working environment focusing on continually improving processes to remain innovative
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • 152 hours of PTO + 8 paid holidays
  • Generous 401K match
  • Medical, dental and vision benefits effective day one of employment
  • Tuition Reimbursement - Let us help you finish your degree or start a new degree!


About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Pharmaceuticals & Biotech
Founded
2007
* Ladders Estimates

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