Catalent Pharma Solutions Inc

Sr Program Manager

Catalent Pharma Solutions Inc$160K — $170K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Science or Engineering; advanced degree preferred.
  • 7+ years direct experience in project management or pharmaceutical industry.
  • Project Management Professional certification or relevant coursework preferred.
  • Familiar with Biologics Fermentation, Cell Culture, Purification, and Analytics.
  • Experience in Biologics, Biotechnology, or Pharma roles preferred.
  • Exposure to working across multiple Catalent sites is beneficial.
  • Experience in managing commercial programs is a plus.

Responsibilities

  • Lead Deviation, CAPA, and Change Control programs to ensure compliance and quality.
  • Manage full lifecycle of investigations and CAPAs including risk assessments and root cause analysis.
  • Act as the Subject Matter Expert for Quality Systems, providing support and training.
  • Monitor quality metrics, drive process improvements, and lead governance forums.
  • Support regulatory inspections and audits while promoting a culture of operational excellence.

Benefits

  • Defined career path with annual performance review and feedback.
  • Diverse and inclusive company culture.
  • Potential for career growth on an expanding team focused on improving lives.
  • Competitive paid time off with 8 additional paid holidays.
  • Community engagement and sustainability initiatives.
  • Immediate medical, dental, and vision benefits upon employment.
  • Tuition reimbursement offered.
Full Job Description

Sr Program Manager

Position Summary:


  • Shift: M-F 8am-5pm
  • Location: Princeton, NJ
  • 100% Onsite

We have an opportunity for a Sr Program Manager to join our team and deliver on program objectives within agreed timelines, budgets, and quality standards. In this role, you will apply strong project management practices and lead cross-functional teams to achieve success. You will maintain open communication with clients, provide updates, and ensure milestones are met. This position requires a solutions-oriented mindset and the ability to adapt in a dynamic environment.

The Role
  • Lead and oversee Deviation, CAPA, and Change Control programs to ensure compliance with regulatory requirements, quality standards, and customer expectations.
  • Manage the full lifecycle of investigations, CAPAs, and change controls, including risk assessments, root cause analysis, impact evaluations, and effectiveness checks.
  • Serve as the site Subject Matter Expert for Quality Systems, providing guidance, training, and support on compliance, investigations, and continuous improvement initiatives.
  • Monitor quality metrics and trends, drive process improvements, and lead cross-functional governance forums to ensure accountability and timely resolution of issues.
  • Support regulatory inspections, customer audits, and internal audits while fostering a culture of quality, compliance, and operational excellence.

 

The Candidate
Minimum Requirements
  • Bachelor of Science in Science or Engineering, or equivalent combination of education and experience required. Advanced degree (Master of Science, Master of Business Administration, Doctor of Philosophy) is preferred.
  • Approximately 7+ years of direct experience in project management and/or pharmaceutical industry.
  • Project Management Professional or Project Management certification or coursework preferred.
  • Working knowledge of Biologics Fermentation, Cell Culture, Purification and Analytics preferred.
  • Professional experience in a related field such as Biologics, Biotechnology, or Pharma preferred.
  • Experience working across Catalent sites preferred.
  • Experience managing commercial programs preferred.

Preferred Skills & Background
  • Project Management Professional or Project Management certification or coursework preferred.
  • Working knowledge of Biologics Fermentation, Cell Culture, Purification and Analytics preferred.
  • Professional experience in a related field such as Biologics, Biotechnology, or Pharma preferred.
  • Experience working across Catalent sites preferred.
  • Experience managing commercial programs preferred.

Pay

The anticipated salary range for this position in NJ is $160,000 – $170,000 Plus Bonus. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.


Why You Should Join Catalent
  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
  • Competitive paid time off plus 8 paid holidays
  • Community engagement and green initiatives
  • Medical, dental and vision benefits effective day one of employment
  • Tuition Reimbursement

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
Founded
2007

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