Philadelphia, Pennsylvania, United States · On-site
Director, Quality Position Summary: 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 cli…
Skills: Quality Assurance, cGMP, Quality Management Systems, Batch Release, Change Control
Muncy, Pennsylvania, United States · On-site
NationsBenefits is recognized as one of the fastest-growing companies in America and a Healthcare Fintech provider of supplemental benefits, flex cards, and member engagement solutions. We partner with managed care organ…
Skills: Hearing Evaluations, Hearing Aid Fitting, Patient Counseling, Clinical Protocols, Patient Education
Edinboro, Pennsylvania, United States · On-site
Overview If you’re a Physical Therapist (PT) who wants to empower patients to achieve meaningful outcomes through compassionate and patient-centered therapy—this is it. In this role, you’ll provide physical therapy servi…
Skills: Speech Therapy, Patient Evaluation, Treatment Planning, Cognitive Rehabilitation, Swallowing Function Therapy
Springfield, Pennsylvania, United States · On-site
Sign-On Bonus! Student Loan Assistance! The responsibilities of this job include, but are not limited to, the following: Obtaining quality x-rays using correct position and radiation exposure;Implementing safety procedur…
Skills: X-ray Positioning, Radiation Safety, Patient Care, Medical Documentation, Keyboarding
Pocono Township, Pennsylvania, United States · On-site
$90k–$130k/yr
Job Title: Statistical Data Scientist - Injectables and Tech Transfer Manufacturing Location: Swiftwater, PA About the Job: As a Statistical data Scientist - Injectables and Tech Transfer. , you'll be on a mission to ena…
Skills: Machine Learning, Statistics, Text-mining, NLP, Forecasting
Philadelphia, Pennsylvania, United States · On-site
Job Details Works under direct supervision and assists research coordinators with organizing, gathering and compiling clinical research data. Tracks and maintains credentialing documentation for staff and all researchers…
Skills: Clinical Research Data Collection, Credentialing Documentation, IRB Regulations, Research Protocol Adherence, Data Reporting
Zug, Zug, Switzerland · Hybrid
Position Summary For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market positioning. Specifically, evidence must be generated and maintaine…
Skills: Real-World Evidence, Health Outcomes Research, Study Design, HTA Submissions, Budget Management
Philadelphia, Pennsylvania, United States · On-site
Manager, Project Management Position Summary: Work Schedule: M-F 8am-5pm100% on-site Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufac…
Skills: Project Management, Line Management, Client Relationship Management, Financial Milestone Management, Budget Tracking
Montgomery County, Pennsylvania, United States · On-site
Job Details The Klein Family Parkinson’s Rehabilitation Center at MossRehab, in conjunction with the Cognitive-Motor Learning Laboratory at the Moss Rehabilitation Research Institute (MRRI) located in Elkins Park, PA, ha…
Skills: Neuroeconomics, Motor Learning, Programming, Data Analysis, Statistics
Pennsylvania, United States · Remote OK
$148k–$204k/yr
By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice an…
Skills: Territory Planning, Strategic Account Management, Data Interpretation, Consultative Selling, Matrix Collaboration
Philadelphia, Pennsylvania, United States · On-site
$21/hr–$26/hr
SHIFT: Evening (United States of America) Seeking Breakthrough Makers Children’s Hospital of Philadelphia (CHOP) offers countless ways to change lives. Our diverse community of more than 20,000 Breakthrough Makers will i…
Skills: Specimen Processing, Data Entry, Customer Service, Medical Laboratory Equipment Maintenance, Inventory Management
Mechanicsburg, Pennsylvania, United States · On-site
FOX Rehabilitation is hiring a Fitness Specialist to lead group exercise and personal training for older adults at a Senior Living Community in Hanover, PA. This role is ideal for a personal trainer, exercise science gra…
Skills: Group Exercise Leadership, Personal Training, Fall Prevention, Functional Fitness, Relationship Building
Chambersburg, Pennsylvania, United States · On-site
FOX Rehabilitation is hiring a Fitness Specialist to lead group exercise and personal training for older adults at a Senior Living Community in Chambersburg, PA . This role is ideal for a personal trainer, exercise scien…
Skills: Group Exercise Leadership, Personal Training, Functional Fitness, Fall Prevention, Relationship Building
Philadelphia, Pennsylvania, United States · On-site
Job Details The Registered Respiratory Therapist administers respiratory therapy procedures to examine, diagnose, and treat patients with respiratory and pulmonary disorders. The Respiratory Therapist assesses patient co…
Skills: Respiratory Therapy, Mechanical Ventilation, Patient Assessment, PFTs, ABGs
Stevenage, England, United Kingdom · Hybrid
$151k–$252k/yr
Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicin…
Skills: Diagnostic Strategy, Clinical Trial Design, IVD Development, Translational Biomarkers, Regulatory Compliance
Philadelphia, Pennsylvania, United States · On-site
$19/hr–$29/hr
Job Summary Produces precision-machined components by programming, setting up, and operating computer numerical control (CNC) equipment and conventional machining tools. Ensures adherence to quality, safety, and operatio…
Skills: CNC Programming, Manual Machining, CAD/CAM Software, Technical Instruction, Blueprint Reading
Philadelphia, Pennsylvania, United States · On-site
About Exponent Exponent is the only premium engineering and scientific consulting firm with the depth and breadth of expertise to solve our clients’ most profoundly unique, unprecedented, and urgent challenges. We are co…
Skills: Mechanical Engineering, Cell and Molecular Biology, Medical Device Development, Laboratory Test System Design, Cardiopulmonary Physiology
Wilkes-Barre, Pennsylvania, United States · On-site
Location: Geisinger Wyoming Valley (GWV) Shift: Evenings (United States of America) Scheduled Weekly Hours: 40 Worker Type: Regular Exemption Status: No Job Summary: Join our team at Geisinger Medical Laboratories. You c…
Skills: Communication, Computer Literacy, Laboratory Equipment Operation, Laboratory Information Systems (LIS), Laboratory Services
Philadelphia, Pennsylvania, United States · On-site
$22/hr–$36/hr
University Overview The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks amo…
Skills: Surgical Nursing, Aseptic Technique, Patient Positioning, Sterilization, Instrument Processing
Wexford, Pennsylvania, United States · On-site
Company :Allegheny Health NetworkJob Description : GENERAL OVERVIEW: Optimizes patient care by promoting rational, safe and cost effective pharmaceutical care including drug dispensing, intravenous admixture program and …
Skills: Drug Dispensing, Intravenous Admixture, Drug Therapy Monitoring, Prescription Review, Compounding
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The Director of Quality provides leadership and management for quality systems, finished product batch release, and regulatory compliance within Clinical Specialty Services. This role oversees quality disposition, validation, and the implementation of quality improvement programs and CAPAs.
Requires a Bachelor's degree in Chemistry, Biological Sciences, or a related scientific field. Candidates must have 10+ years of experience in pharmaceutical quality assurance, with a strong understanding of cGMPs and clinical trials.
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.
The Quality function is to build, monitor, and sustain a robust and effective quality system that delivers reliable, high-quality products that meet all customer and regulatory agency requirements and expectations. Components of the quality system establish the requirements for and measure how Catalent complies with all applicable regulations and guidance world-wide, including but not limited to, good manufacturing practice/quality system requirements of the Food and Drug Administration, state boards of pharmacy, European, South American, Japanese, and Australian agencies and other international and/or local health authorities.
The Director of Quality is responsible for providing leadership and Quality Management support within each of the Clinical Specialty Services divisions. This individual will have responsibility for Quality aspects related to Quality Systems, Finished Product Batch Release, Change Control, and Customer relations.
Provides direction and guidance to the Quality Disposition, Materials Sampling Quality Assurance, Regulatory and Compliance Quality Assurance, and Validation Quality Assurance.
Management responsibilities include professional development, performance appraisals, and employee counselling for direct reports. Assigns work and reviews workload for all direct reports. Supervises staff by establishing goals that will increase knowledge and skill levels, and by delegating tasks commensurate with skill level.
Recommends courses of action on all management/human resources’ matters, including salary administration, transfers, hiring, terminations, and position description preparation.
Promotes, implements, and maintains quality initiatives of processes and programs to assess compliance with regulations, Global and Site SOPs, and client requirements.
Provides to the Operational CDS and Quality organization consultation, and interpretation of regulations/guidelines related to GXPs focused mainly on good clinical trials, as applicable.
Writes and approves Quality unit SOPs and Forms, as needed. Approves Operational CDS SOPs and Forms. Supports harmonization of worldwide Quality operating procedures as needed.
Provides leadership for Data Integrity and Computer System Validation documentation review and approval for instruments, equipment, and systems used in GXP Operations throughout the system life cycle.
Assist with Client Audit and Regulatory Agency inspections.
Provides direction in identification and implementation of quality improvement programs.
Provides leadership for the investigation, root cause analysis, and CAPAs association with Deviations, Non-conformances, Complaints, Client Audits, and Internal Audit Reports.
Other duties as assigned
BS or BA in Chemistry, Biological Sciences, or other related scientific discipline or equivalent experience.
10 + years of Scientific or Pharmaceutical Quality Assurance, preferring clinical supply services, in addition to commercial packaging.
Clear understanding of cGMPs including clinical trials.
Communicates clearly with internal and external clients, both verbal and written.
Cooperates with co-workers; is a team player. Willingness to contribute to team activities.
Demonstrates flexibility in organizing work and priorities.
Good organizational skills relating to management of associates’ daily activities.
Good problem-solving skills and decision-making skills to identify and solve work related issues.
Good change management skills and strategic thinking
Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
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
Dynamic, fast-paced work environment
Community engagement and green initiatives
Generous 401K match and Paid Time Off accrual
Medical, dental and vision benefits effective day one of employment
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.
Championing the missions that matter™. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) and trusted partner to pharma, biotech, and consumer health companies worldwide. We put patients first in everything we do, helping people live better and healthier lives through every product we help develop, manufacture and deliver. With over 1,000 active development programs at any given time, we launch over 100 new products and line extensions annually. Catalent has supported half of all FDA approvals over the past decade, and our teams working at over 40 global sites help us produce over 60 billion doses every year. Our strength lies in our people: teams across our more than 40 sites and thousands of passionate scientists and technicians who bring expertise in development sciences, delivery technologies, and multi-modality manufacturing. What unites us is our commitment to championing our partners’ missions as our own, anticipating customer needs, solving complex challenges and ultimately making a difference in the lives of patients across the globe. At Catalent, you will be able to directly have an impact, solving problems and ensuring excellence for our customers. Our focus on delivering meaningful outcomes alongside our customers means your work directly impacts millions of people around the world. Join us in championing the missions that matter. Catalent is headquartered in Tampa, Florida, with over 40 global sites. Visit www.catalent.com to learn more.
Offices: 101 E Kennedy Blvd, Tampa, Florida 33602, US · 14 Schoolhouse Road, Somerset, NJ 08873, US · Frankland Road, Blagrove, Swindon, Wiltshire SN5 8YG, GB · 4-9-17 Akasaka, Minato-ku, Tokyo 107-0052, JP · 160 Pharma Dr, Morrisville, NC 27560, US
Based on 1198 listings with disclosed salaries, most science & research jobs in Pennsylvania pay between $72k–$220k per year. Individual offers vary with seniority, company size, and specialization.
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