Catalent Pharma Solutions Inc

Project Manager

Catalent Pharma Solutions Inc$85K — $115K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Life Sciences, Engineering, Pharmacy, or related field (advanced degree preferred).
  • 5+ years of experience in pharmaceutical manufacturing, biotech, or CDMO operations.
  • Proven experience managing complex technical projects in a Good Manufacturing Practices environment.
  • Deep understanding of drug development, technology transfer, validation, and commercial manufacturing.
  • Strong financial acumen, including budget management and commercial awareness.
  • Excellent communication, stakeholder management, and negotiation skills.

Responsibilities

  • Lead end-to-end project planning, execution, and governance for multiple concurrent projects.
  • Develop integrated project plans covering technical, quality, regulatory, supply chain, and operational workstreams.
  • Drive project reviews, risk management, stage-gate decisions, and change control.
  • Ensure compliance with Good Manufacturing Practices, regulatory, and client expectations.
  • Manage site capital expenditure budgets, forecasts, and cost tracking.
  • Support regulatory submissions, client audits, and authority inspections as required.
  • Identify risks, bottlenecks, and drive mitigation plans across the project portfolio.

Benefits

  • Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)
  • Group Retirement Savings - Registered Pension Plan (RPP) with employer contributions
  • Employee Reward & Recognition programs
  • Opportunities for professional and personal development & growth including tuition reimbursement
Full Job Description
Project Manager

Position Summary

We have an opportunity for a Project Manager to join our team and lead a portfolio of complex, cross-functional business projects within Catalent Adair - Zydis®. You will ensure successful delivery of projects such as infrastructure upgrades, equipment acquisitions, technical transfer, process development, validation, and scale-up. This role involves managing timelines, resources, budgets, and stakeholder expectations while meeting quality, regulatory, and EH&S standards. You will play a key role in ensuring compliance with Catalent policies and driving project success in a cGMP-regulated CDMO environment.

Shift: Typical Working Hours will be Monday-Friday 8 AM - 4:30 PM
Location: Adair, ON
100% Onsite

The Role
  • Lead end-to-end project planning, execution, and governance for multiple concurrent projects.
  • Develop integrated project plans covering technical, quality, regulatory, supply chain, and operational workstreams.
  • Drive project reviews, risk management, stage-gate decisions, and change control.
  • Ensure all activities comply with Good Manufacturing Practices, regulatory, and CDMO client expectations.
  • Manage expectations, provide regular status updates, and ensure transparency of risks and milestones.
  • Manage site capital expenditure budgets, forecasts, and cost tracking.
  • Support regulatory submissions, client audits, and authority inspections as required.
  • Identify risks, bottlenecks, and process inefficiencies within the project portfolio and drive mitigation plans.
  • Manage cross-functional teams and set expectations based on project timelines.
  • Lead internal and external project team meetings, facilitate decision-making, and drive execution to ensure key milestones and deliverables are achieved.
  • Foster accountability by monitoring progress, communicating expectations, and ensuring timely completion of assigned deliverables.
  • Other duties as assigned.


The Candidate

Minimum Requirements
  • Bachelor's degree in Life Sciences, Engineering, Pharmacy, or a related field (advanced degree preferred).
  • 5+ years of experience in pharmaceutical manufacturing, biotech, or CDMO operations.
  • Proven experience managing complex technical projects in a Good Manufacturing Practices environment.
  • Deep understanding of drug development, technology transfer, validation, and commercial manufacturing.
  • Strong financial acumen, including budget management and commercial awareness.
  • Excellent communication, stakeholder management, and negotiation skills.


Preferred Skills & Background
  • Formal project management training (Project Management Professional, PRINCE2, Agile) is an advantage.


Pay

The final salary offered to a successful candidate may vary within this range $85,000 - $115,000, 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 global employer, and this salary range does not reflect positions that work in other countries.

Why You Should Join Catalent
  • Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance)
  • Group Retirement Savings - Registered Pension Plan (RPP) with employer contributions
  • Employee Reward & Recognition programs
  • Opportunities for professional and personal development & growth including 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

Similar Jobs

More Jobs at Catalent Pharma Solutions Inc

More Pharmaceuticals & Biotech Jobs

Find similar Project Manager jobs: