Project Manager

Posted Yesterday
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Chelsea, MA, USA
In-Office
90K-105K Annually
Junior
Biotech • Pharmaceutical
The Role
Manages customer development and manufacturing projects across their full lifecycle, coordinating technical teams, timelines, budgets, documentation, issue escalation, incident closure, and customer communications. Tracks project progress, ensures deliverables meet requirements, supports customer relationships, and reports status and risks to management. The role is fully onsite, Monday through Friday, in Chelsea, Massachusetts.
Summary Generated by Built In

Project Manager

Catalent’s Chelsea, Massachusetts site—often referred to as the Boston location—is a global Center of Excellence for spray dry dispersion (SDD) and dry powder inhaler (DPI) capsule manufacturing and packaging, supporting inhalation drug products from clinical development through commercial launch. Located at 190 Everett Avenue, the approximately 96,000‑square‑foot GMP facility features ISO 8 production suites, high‑potency containment capabilities, and advanced spray drying equipment, including multiple large‑scale GMP spray dryers. The site offers integrated services such as powder processing, capsule filling, blister packaging, and on‑site quality control and analytical testing, with capacity to produce up to 100 million capsules annually. Strategically positioned just minutes from Boston Logan International Airport and within the Greater Boston life sciences hub, the Chelsea site plays a critical role in Catalent’s global inhalation network and regulatory‑compliant manufacturing operations.

Position Summary

The Project Management function is responsible for managing the non-technical aspects of projects at Catalent Boston which include customer projects for the development and manufacturing of inhalation products and oral spray dried powders.  This includes ensuring on time and on budget delivery of projects and acting as a focal point between customers and our technical team by using project management methodologies and corporate PMO procedures.

This position is responsible for managing activities for a portfolio of projects through leading analytical development and/or manufacturing project teams (and other project teams as designated). This position is the main point of customer contact for project related activities and involves managing the execution of the customer’s requirements as per an agreed upon program of activities. He/she is responsible for overall project knowledge and execution according to the agreed upon deliverables and timeline.

Shift: Monday - Friday, 8:00am to 5:00pm
Location: Chelsea, MA
100% Onsite

The Role

  • Ensure meeting minutes, agendas, timelines, trackers, and other tools are used effectively for customer projects
  • Assist Business Development in maintaining customer relationships and ensuring return business by communicating with customers, coordinating visits, and acting as the customer advocate
  • Develop, coordinate, and track client projects through the entire project life cycle
  • Monitor and report project progress within agreed timelines, ensuring technical and financial goals are met; Consult and advise upper management on project status and report issues that may affect results
  • Evaluate, highlight, and escalate unresolved issues, potential barriers, and resource constraints to the supervisor; Prepare verbal reports and presentations on project progress as needed
  • Coordinate the revision of Standard Operating Procedures, Batch records, and other site-specific documents for clients
  • Follow up to ensure incident reports are closed in a timely manner and notify clients within 24 hours of any incident
  • All other duties as assigned

The Candidate

Minimum Requirements

  • Bachelor’s Degree is required; Life sciences discipline is preferred
  • 2+ years of relevant experience is required; preferably in a Contract Research Organization (CRO) or Contract Development and Manufacturing Organization (CDMO) environment
  • Excellent communication, negotiation, and interpersonal skills are required
  • Proficiency using Microsoft Office Excel, Word, PowerPoint, and Microsoft Project
  • Lifting up to 10 lbs. as needed

Preferred Skills & Background

  • Previous pharmaceutical or biotech industry experience is preferred

Pay

The anticipated salary range for this position in MA is $90,000 – $105,000. 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

Catalent offers rewarding opportunities to further your career!  Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference. 

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [email protected]. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

    

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond— it is a fraudulent request. Please forward such requests to [email protected] for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Skills Required

  • Bachelor's degree
  • Life sciences discipline
  • 2 or more years of relevant experience
  • Excellent communication, negotiation, and interpersonal skills
  • Proficiency with Microsoft Excel, Word, PowerPoint, and Project
  • Ability to lift up to 10 pounds as needed
  • Previous pharmaceutical or biotechnology industry experience
  • Experience in a contract research organization or contract development and manufacturing organization

Catalent, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Catalent, Inc. and has not been reviewed or approved by Catalent, Inc..

  • Leave & Time Off Breadth Paid time off is commonly described as roughly 152 hours per year plus about eight paid holidays for U.S. roles. Eligibility and exact counts vary by location, but the allotment is positioned as competitive.
  • Retirement Support A 401(k) with a company match (often described as dollar‑for‑dollar up to 6%) is part of the package. The match level is commonly referenced as a meaningful component of total rewards.
  • Inclusive Benefits Coverage Medical, dental, vision, life/disability, HSA/FSA, EAP, tuition reimbursement, adoption assistance, commuter and dependent‑care benefits, and wellness programs are offered. Some roles indicate benefits eligibility begins on the first day for direct hires.

Catalent, Inc. Insights

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The Company
HQ: Tampa, FL
13,715 Employees
Year Founded: 2007

What We Do

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. For more information, visit www.catalent.com.

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