Quality Specialist, Quality Management Systems

Posted 4 Days Ago
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Malvern, PA
Mid level
Biotech • Pharmaceutical
The Role
The Quality Specialist manages quality assurance standards and procedures, leads training programs, interacts with divisions for documentation, and ensures compliance for regulatory inspections.
Summary Generated by Built In

Quality Specialist, Quality Management Systems

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.

Catalent Pharma Solutions is hiring a Quality Specialist, Quality Management Systems. The Quality Specialist, Quality Management Systems must be flexible and have well-developed organizational skills and have the ability to interact with all levels of personnel. The Quality Specialist, Quality Management Systems must be a self-starter, results oriented individual with ability to articulate, receive, disseminate and analyze data. The Quality Specialist, Quality Management Systems is responsible for assisting in managing the development, implementation and maintenance of quality assurance standards and procedures as well as quality systems to ensure the precision, accuracy and reliability of company products in accordance with quality specifications, government, company and GMP standards

This is a full-time role position: Monday-Friday 8:00am-5:00pm. Salary Role, Onsite

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  

  • Lead Document Management site program (hardcopies, EDMS). Interact with other divisions of Catalent in regard to record retention policies and document management and control.

  • Leads  the  Training  Program  for GMP  Training,  Procedural  based  training,  and  other  training  need  for  performing tasks. Site administrator for Trackwise, EDMS and ComplianceWire

  • Lead the revisions and implementation of Catalent Global standard updates for the site. Lead completion of Annual Product Quality Review documents on schedule, as required. Schedule, prepare for and lead customer audits through response and audit closure.

  • Assist in preparing, supporting and closure of the site for inspection by regulatory authorities.

  • Develop new procedures, and review and update existing procedures. Represent QA on project teams and other internal forums. Use and extract information from the following systems: EDMS, TrackWise, and ComplianceWire

  • Work closely with site on Trackwise compliance and timeliness of responses. Site Pathwise representative. Completion of QMR presentation and minutes

  • Reporting of monthly Quality metrics. Lead Supplier program (qualification, requalification, complaints, technical agreements). Lead Internal Audit program. Lead Quality Technical Agreements for the site with client. Manage Iron Mountain and record retention

  • Backup for DEA and State Licensing program

  • All other duties as assigned; 

The Candidate 

  • Required a High School Diploma with Five years of experience working in a regulated environment, such as, food, aero, automotive, pharma.

  • Bachelors Degree highly preferred

  • Candidate must have computer skills with MS Office and capable of quickly learning other software including EDMS, TrackWise and ComplianceWire.

  • Individual may be required to sit, stand, walk regularly and occasionally lift up to 40 pounds

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 effective day one of employment 

  • 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 [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.

Top Skills

Compliancewire
Edms
MS Office
Trackwise
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The Company
HQ: Somerset, NJ
13,715 Employees
On-site Workplace
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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