Associate Project Manager

Catalent Pharma Solutions; Greenville (NC); In loco; USD 60.000 - 90.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive PTO

Medical, dental, vision

Tuition reimbursement

Employee engagement activities

Diversity & Inclusion ERGs

Wellness program

Discount programs

Descrizione del lavoro

Catalent’s Greenville, NC site is seeking an Associate Project Manager to support inventory tracking, project billing and forecasting for scheduling and quotes. You will serve as a key contact for development project activities and help drive on-time milestones.

The role involves managing multiple projects from pre-formulation through process validation, coordinating meetings, and ensuring timely delivery of deliverables in a regulated CDMO environment. Onsite work is required.

Competenze

• High school diploma or equivalent with at least 4 years of coordination or management experience (preferably in the CDMO industry).
• Experience in a regulated industry; PMP certification desired.
• Proficiency in Microsoft Word, Excel, Project, and PowerPoint desired.

Mansioni

• Perform meticulous data entry in the ERP system to enable contract billing and forecasting.
• Generate reports from the ERP system or process ERP data in Excel or other software to create various reports.
• Process forward billing work orders to generate invoices for project-specific items and services.
• Assist the Project Management team as needed to ensure group goals and deliverables are met.
• Manage and oversee the delivery of multiple projects from pre-formulation through process validation, including all phases of clinical development.
• Facilitate effective team meetings to track deliverables and timelines; distribute meeting notes, action items, and project timelines.
• Track material setup/release, batch record issuance, and disposition.
• Assist in tracking analytical method transfers, analytical testing, and raw material specifications.
• Coordinate sample shipments with Safety, Warehouse, and Project Managers.
• Work with Project Managers on assembling and tracking invoices and billing.
• Review forecasting and scheduling against quotes.
• Manage project scope changes and generate QARs as needed.
• Manage customer expectations, project risks, and escalations.
• Maintain project information for corporate site reporting mechanisms.
• Facilitate on-site and virtual customer meetings.
• Assist with project kick-off and close-out activities.

Conoscenze

ERP systems

Project coordination

PMP

MS Excel

MS Word

PowerPoint

Formazione

High school diploma or equivalent

Bachelor’s degree in related field

Associate degree in related field

Strumenti

ERP software

MS Project

Billing software

Descrizione del lavoro

About Site Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus, delivering end‑to‑end, turnkey solutions from formulation development through commercial manufacturing and packaging. The site specializes in oral solid dosage forms, supported by integrated formulation expertise, comprehensive analytical services, and scalable manufacturing capabilities designed to support both commercial products and potent or targeted therapies, including orphan drugs. Backed by more than $100 million in recent investments, the Greenville operation features fit‑for‑scale infrastructure, potent handling capabilities, and a strong regulatory track record, making it a critical part of Catalent’s global network for advancing complex oral drug programs from development to market.

Position Summary

We have an opportunity for an Associate Project Manager to join our team. In this role, you will work closely with the site project management team to support inventory tracking, project billing, and forecasting related to scheduling and approved quotes. You will also assist with improvement projects and serve as a key point of contact for development project activities. This position focuses on managing the execution of customer requirements to achieve established goals, milestones, and deliverables.

Shift: Monday to Friday 8am‑5pm

Location: Greenville, NC 100% Onsite

The Role

• Perform meticulous data entry in the ERP system to enable contract billing and forecasting
• Generate reports from the ERP system or process ERP data in Excel or other software to create various reports
• Process forward billing work orders to generate invoices for project‑specific items and services
• Assist the Project Management team as needed to ensure group goals and deliverables are met
• Manage and oversee the delivery of multiple projects from pre‑formulation through process validation, including all phases of clinical development
• Facilitate effective team meetings to track deliverables and timelines; distribute meeting notes, action items, and project timelines
• Track material setup/release, batch record issuance, and disposition
• Assist in tracking analytical method transfers, analytical testing, and raw material specifications
• Coordinate sample shipments with Safety, Warehouse, and Project Managers
• Work with Project Managers on assembling and tracking invoices and billing
• Review forecasting and scheduling against quotes
• Manage project scope changes and generate QARs as needed
• Manage customer expectations, project risks, and escalations
• Maintain project information for corporate site reporting mechanisms
• Facilitate on‑site and virtual customer meetings
• Assist with project kick‑off and close‑out activities
• Other duties assigned

Candidate Minimum Requirements

High school diploma or equivalent with at least 4 years of coordination or management experience (preferably in the CDMO industry) Experience in a regulated industry PMP certification desired Proficiency in Microsoft Word, Excel, Project, and PowerPoint desired

Preferred Skills & Background

Bachelor’s degree with at least 1 year of project coordination or management experience (preferably in the CDMO industry) Associate degree with at least 2 years of project coordination or management experience (preferably in the CDMO industry) ERP experience preferred

Why You Should Join Catalent

• Positive and fast‑paced working environment focusing on continually improving processes to remain innovative and dynamic
• Competitive Paid Time Off plus 8 paid holidays
• Medical, dental, and vision benefits effective day one of employment
• Tuition Reimbursement – support to finish your degree or earn a new one
• Site‑based Employee Engagement activities such as Music Bingo, Puppy Supply Donation Program, Halloween Costume Contests, and more
• Employee Resource Groups focusing on Diversity and Inclusion
• Environmentally friendly initiatives including regular participation in Highway Clean‑up
• Defined career path and annual performance review process with potential for career growth
• WellHub program promoting physical and mental wellness, including onsite fitness center
• Perkspot offers exclusive discounts from approximately 900+ merchants in various categories

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 [e-mail]. 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.

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.

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.