Catalent

Perform inspection and release of materials and products, ensuring GMP compliance, and support process improvements. | High school diploma or GED, 2+ years of GMP experience, strong communication skills, computer proficiency. | Quality Assurance Inspector Position Summary: Work Schedule: Monday – Friday, 8:00am – 4:30pm 100% on-site Catalent’s 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated packaging solutions, including temperature-controlled options for sensitive products. Come and be part of a team that delivers industry-leading quality and innovation. Catalent Pharma Solutions in Philadelphia is hiring a Quality Assurance Inspector and this position reports to the Quality Supervisor. The Quality Inspector is responsible for performing inspection and release of all components, clinical trial and commercial labels, drug products, distribution materials and paperwork as well as materials slated for destruction and associated paperwork, while ensuring SOPs and cGMP are being followed. The Quality Inspector will identify opportunities to improve the processes, raise these to Quality Management and assist in the implementation and improvement of these processes, in partnership with Supply Chain personnel, Project Management, and Operations. The Role Ensure adherence to SOPs and cGMPs during incoming inspection, distribution, label control, returns, and destruction activities, supporting both Commercial and Clinical Operations. Verify and inspect incoming materials and collaborate with Quality and Project Management to resolve discrepancies. Inspect and release clinical and commercial drug products and components per customer specifications and Catalent SOPs, including review of labels and receipt documentation. Inspect and release shipping and distribution materials by verifying paperwork, picked items, and randomized containers for protocol compliance. Inspect and release materials designated for destruction by reviewing associated documentation and materials. Inspect and release clinical labels (open, randomized, booklet, multilingual) by comparing to approved proofs or label copy requests. Review BMS and chart recorder printouts for temperature, humidity, and pressure deviations, and inspect retain samples as needed. Maintain and report departmental metrics and support walkthrough audits of Supply Chain areas for GMP compliance. Review facility, label room, pest control, and sampling logbooks for compliance; update SOPs as needed and support deviation investigations and process improvements. Perform additional sampling or testing as requested, participate in customer audits, complete required documentation, and support other tasks assigned by QA Management. All other duties as assigned The Candidate High school diploma or GED with a minimum of 2 years of quality or manufacturing experience within a GMP environment; Bachelor’s degree preferred with a minimum of 1 year of quality or manufacturing experience within a GMP environment. Strong written and verbal communication skills. Effective interpersonal skills and ability to work collaboratively in a team environment. Proficient computer skills; experience with MS Office and inventory management systems is a plus. Strong analytical thinking and sound judgment. Ability to thrive in a dynamic environment with shifting priorities. Comfortable being on your feet and moving between multiple warehouse areas. Ability to quickly learn and apply QA auditing techniques. Individual will be required to stand and/or sit for long periods of time, occasionally lift 0-25 pounds Willingness to work overtime, frequently in cold environments, and track, monitor and maintain production rates, labor hours and downtime. 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 Several Employee Resource Groups focusing on D&I Dynamic, fast-paced work environment Community engagement and green initiatives Generous 401K match Medical, dental and vision benefits Tuition Reimbursement - Let us help you finish your degree or start a new degree! WellHub- program to promote overall physical wellness Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories 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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Hunt new clients, build relationships, collaborate with sales team, manage CRM, and report sales activities. | Bachelor's degree, 2+ years in sales or related fields, pharma experience preferred, strong communication, and willingness to travel up to 50%. | Business Development Specialist Position Summary: We are seeking a motivated and driven individual to join our team as a Business Development Specialist. As a key member of our sales department, you will be responsible for hunting new clients and opportunities, managing early relationships, building trust with potential customers, and collaborating with colleagues to transfer and close deals. This is a remote, field-based role. The Role: Proactively hunt for new clients and opportunities through various channels such as cold calling, networking, and attending industry events. Build and maintain strong relationships with potential customers by providing exceptional customer service and showcasing the value of our products/services. Collaborate with seasoned colleagues from the West Coast team to transfer opportunities seamlessly and ensure a smooth sales process. Set up appointments with potential clients and work with the current BD team to present product/service offerings and address any queries or concerns. Utilize CRM (Customer Relationship Management) system to track and manage customer interactions, update contact information, and monitor progress on leads and opportunities. Provide regular follow-up reporting on sales activities, including pipeline updates, lead conversion rates, and sales forecasts. Other duties as assigned. The Candidate: Bachelor’s degree; scientific or business degree preferred. Minimum of two years’ experience within sales, project management, supply chain, marketing, recruiting, or related function. Pharma industry experience preferred. Hunting mentality mandatory. Ability and willingness to travel up to 50% of the time to meet with clients and attend industry events. Excellent communication and interpersonal skills, with the ability to build rapport and establish trust with potential clients. Pay: The annual pay range for this position in New Jersey is $76,000-$110,000 Why you should join Catalent: Join a high growth and fast paced organization with a people focused culture Global exposure, defined career path and annual performance review and feedback process Competitive Medical, Dental, Vision and 401K 19 days PTO & 8 paid holidays 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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Transport raw, in-process, and finished goods according to production schedules, manage shipping and receiving processes, and maintain accurate inventory records. | High school diploma or GED, 1+ years warehouse experience, forklift operation skills, ability to lift heavy weights, and familiarity with shipping documentation and inventory systems preferred. | Material Handler Position Summary 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. Our Manassas, Virginia site is a part of the Consumer Health division and provides expanded capabilities in soft chews and lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors available, we can work with complex formulations to help create engaging new products consumers will love. The Material Handler transports raw, in process and finished goods as required by production schedule. Ships and receives materials necessary to meet production goals and requirements. The Material Handler verifies and keeps records on incoming and outgoing product & material movements, accurately. Process daily, weekly cycle counts. This position is 100% based on-site in Manassas, VA and regular working hours are M-F 2PM-10:30PM. The Role • Perform stablished method of order picking (FIFO), finished goods to customers according to specified instructions. • Must be able to read, understand, and interpret shipping documents i.e. BOL, packing list, pro-numbers. • Assembles and inserts product into cardboard containers or selects pre-assembled containers. • Posts weights and shipping charges and affixes necessary postage. • Affixes shipping labels on packed cartons to identifying shipping information on cartons. • Receives raw materials and supplies into warehouse with accordance to our internal receiving SOP. • Obtains Material samples as required by sample orders. • Unpacks and examines all incoming shipments, rejects damaged items, records shortages, and corresponds with shipper to rectify damages and shortages. • Operates tier lift truck and uses electric pallet jack to move, convey, or hoist shipments from shipping and receiving platform to storage or work area. • Other assigned duties The Candidate • High School diploma or GED required • 1+ years of experience working in a warehouse required • Forklift operating experience is required • Shipping and BOL paperwork experience is preferred • 1+ years of experience working with inventory management systems preferred • The employee must regularly lift and /or move up to 50 pounds, frequently lift and/or move up to 100 pounds and occasionally lift and/or move up to 2500 pounds. • While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel and is frequently required to stand, walk, reach with hands and arms, stoop, kneel, crouch, or crawl, and talk or hear. • The employee is occasionally required to sit, climb or balance and taste or smell. Why You Should Join Catalent • Spearhead exciting and innovative projects • Fast-paced, dynamic environment • High visibility to members at all levels of the organization • 152 hours of PTO + 8 paid holidays 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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Inspect, assemble, and package pharmaceutical products following strict quality standards. | High school diploma, 2-3 years production or warehouse experience, ability to follow detailed instructions, physical ability to perform manual tasks, and work in cold environments. | Packaging Technician (2nd shift) Position Summary: Catalent Pharma Solutions in Philadelphia, PA is hiring a Packaging Technician (2nd shift) in the Operations Department. The Operations Department is responsible for providing customized innovative manufacturing and packaging solutions. The department oversees all manufacturing and production aspects of quality packaging and labeling of our customer’s clinical trial projects. 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. This 206,878 square-foot facility, located in the Philadelphia area is Catalent’s global Center of Excellence for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to hold a single product, or multiple products as determined by study requirements. We offer manual patient kit assembly along with semi-automated and automated wallet sealing and high-speed automated carding to meet the needs of studies of all sizes. For temperature sensitive products and those with minimal to zero allowable time out of environment, we can perform secondary packaging in refrigerated and frozen packaging rooms or over dry ice depending upon your project needs. Using our Clinicopia global labeling system with its multi-lingual label phrase library we can design single panel, booklet labels or our unique Peel-ID™ safe storage labels for your studies. Single panel and Peel-ID™ safe storage labels can be conveniently reviewed and approved online via our Fusion portal before being printed and inspected at our facilities. Catalent hires people with a passion to make a difference to the health of millions of people globally. Your expertise, coupled with Catalent’s advanced technologies and collaboration with thousands of innovative pharmaceutical, biotech and healthcare companies, will help bring life-enhancing products to the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. This position must be able to work in a team environment to offer quality packaging and labeling of customer’s clinical trials. Employees will be involved with handling look-alike products and labeling. Clinical operations can be run as a blister fill, bottle fill, pouch, carding, vial/syringe inspection or hand assembly. Employees will also be involved with de-inking of product and capsule manufacturing. These individuals must be detail oriented in order to work with multiple look-alike products at the same time This is a full-time hourly position: Monday – Friday,4:00pm to 12:10am. Please Note: Occasional weekend work is required. This is a union position. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee. The Role: • Inspect blister cavities, bottles, pouches, vials, ampoules, syringes, and sealed clinical cards for defects such as missing product, poor seals, misaligned closures, print errors, or contamination. • Perform hand counts of product using trays and fill tablet, bottle, desiccant, and closure hoppers. • Support manufacturing tasks including de-inking product, tablet breaking, oversized capsule filling, and capsule inspection. • Place blister units into assigned card locations for multi-fill operations, following product assignment requirements on look-alike or multi-fill projects. • Inspect and verify clinical labels, ensuring 100% accountability for both manual and automated applications. • Operate barcode scanners and computers for packaging and assembly work. • Perform cleaning of product contact parts, machine equipment, and production rooms according to SOPs and logbook requirements. • Execute sanitation tasks using the three-bucket mop system for ceilings, walls, and floors. • Work in cold storage environments as required, handling products both inside and outside refrigerated conditions. • Adhere to all SOPs, safety, and quality requirements while ensuring accuracy and compliance in all packaging operations. • Other duties as assigned. The Candidate: • High School Diploma or equivalent. • 2-3 years previous production or warehouse experience preferred. • Ability to read and interpret customer specifications, cGMPs, SOPs, and follow written/oral instructions accurately while communicating effectively. • Demonstrates attentiveness, professionalism, good personal hygiene, and strong teamwork skills in a fast-paced environment. • Able to troubleshoot problems, report issues, and follow all plant safety guidelines. • Physically capable of standing, walking, sitting, and occasionally lifting up to 25 lbs; must meet vision requirements for reading documents and computer use. • Willingness to work overtime, frequently in cold environments, and perform sanitation/cleaning tasks (e.g., mopping walls, floors, ceilings, equipment). • Accessible to both manufacturing floor and office staff, with ability to operate required office equipment. Position Benefits: • Diverse, inclusive culture • Several Employee Resource Groups focusing on D&I • Dynamic, fast-paced work environment • 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 • Competitive salary • Community engagement and green initiatives • Medical, dental and vision benefits effective after 90-day probationary period 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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Transport raw, in-process, and finished goods per production schedules, manage shipping and receiving documentation, operate warehouse equipment, and maintain inventory accuracy. | High school diploma or GED, 1+ years warehouse experience, forklift operation skills, ability to lift heavy items, and familiarity with shipping documents and inventory systems preferred. | Material Handler Position Summary 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. Our Manassas, Virginia site is a part of the Consumer Health division and provides expanded capabilities in soft chews and lozenges. With extensive development and manufacturing expertise and a wide range of flavors, ingredients, and colors available, we can work with complex formulations to help create engaging new products consumers will love. The Material Handler transports raw, in process and finished goods as required by production schedule. Ships and receives materials necessary to meet production goals and requirements. The Material Handler verifies and keeps records on incoming and outgoing product & material movements, accurately. Process daily, weekly cycle counts. This position is 100% based on-site in Manassas, VA and regular working hours are M-F 2PM-10:30PM. The Role • Perform stablished method of order picking (FIFO), finished goods to customers according to specified instructions. • Must be able to read, understand, and interpret shipping documents i.e. BOL, packing list, pro-numbers. • Assembles and inserts product into cardboard containers or selects pre-assembled containers. • Posts weights and shipping charges and affixes necessary postage. • Affixes shipping labels on packed cartons to identifying shipping information on cartons. • Receives raw materials and supplies into warehouse with accordance to our internal receiving SOP. • Obtains Material samples as required by sample orders. • Unpacks and examines all incoming shipments, rejects damaged items, records shortages, and corresponds with shipper to rectify damages and shortages. • Operates tier lift truck and uses electric pallet jack to move, convey, or hoist shipments from shipping and receiving platform to storage or work area. • Other assigned duties The Candidate • High School diploma or GED required • 1+ years of experience working in a warehouse required • Forklift operating experience is required • Shipping and BOL paperwork experience is preferred • 1+ years of experience working with inventory management systems preferred • The employee must regularly lift and /or move up to 50 pounds, frequently lift and/or move up to 100 pounds and occasionally lift and/or move up to 2500 pounds. • While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel and is frequently required to stand, walk, reach with hands and arms, stoop, kneel, crouch, or crawl, and talk or hear. • The employee is occasionally required to sit, climb or balance and taste or smell. Why You Should Join Catalent • Spearhead exciting and innovative projects • Fast-paced, dynamic environment • High visibility to members at all levels of the organization • 152 hours of PTO + 8 paid holidays 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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.

Manage multiple pharmaceutical development and manufacturing projects, ensuring milestone achievement, cross-functional communication, and compliance with industry standards. | Bachelor's in engineering or physical sciences, 3+ years in FDA regulated or pharmaceutical CDMO industry, project management experience, and proficiency with project management software. | Associate Project Manager Position Summary The Associate Project Manager is responsible for managing multiple projects simultaneously. This includes projects for new feasibility, generic program, clinical supplies, transfers or commercial product support. Additionally, the position is responsible to communicate cross-functionally, and with customers, vendors, suppliers, contractors, other sites and upper management on project related activities. St. Petersburg is our primary soft gel development and manufacturing facility in North America with capacity of 18 billion capsules per year.  Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve difficult development and manufacturing challenges. Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee. 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. This position is 100% on-site at the St. Petersburg site. The Role • Facilitate and lead projects that pertain to the following: Product Development for new chemical entity (NCE), generic programs, and early phase feasibilities. Technical Services for commercial product support. Transfer and Business Continuity Programs. • Prepare and manage project plan to meet milestones. • Facilitate the removal of roadblocks and barriers that hinder or delays project progress. • Lead effective cross-functional teams. • Provide notification of milestone completions for billing to finance. • Oversee and manage capital appropriated for a project to ensure funding for the projects goals are obtained, spent and closed in accordance with the project plan. • Prepare project plans and maintains an accurate and up to date project schedule that is readily accessible to management and all team members. • Ensures project requirements embraces current cGMP, EHS, and Financial industry standards. • Other duties as assigned. The Candidate • Bachelors in engineering or physical sciences, including, but not limited to, Chemistry, Biology, Chemical, Mechanical, Electrical, or Civil Engineering, or Pharmacy. • At least 3 years of experience in FDA regulated industry, pharmaceutical CDMO industry preferred. • Working knowledge of project management principles and concepts in a cGMP environment. • At least 2 year of project management experience or other experience that demonstrates successful team leadership and project completion. • PC skills, including training on Microsoft Project & other Catalent software packages are required. • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, and financial reports. • Ability to work effectively under pressure to meet deadlines. • Individual may be required to sit, stand, walk regularly and occasionally lift to 15 pounds; no lifting greater than 44.09 pounds without assistance. • Be accessible to manufacturing floor and office staff and to use required office equipment. • Specific vision requirements include reading of written documents and frequent use of computer monitor. • Individual’s primary workstation is in an office area, where the noise level is low. • Employee will be present on the manufacturing floor where the noise level is low to moderate. Why You Should Join Catalent • Competitive medical benefits and 401K • 19 days of PTO + 8 Paid Holidays • Dynamic, fast-paced work environment • Opportunity to work on Continuous Improvement Processes 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 DisabilityAccommodations@catalent.com. 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 spam@catalent.com for us to investigate with local authorities. California Job Seekers can find our California Job Applicant Notice HERE.