Specialist I - Quality Assurance Systems, Deviations/CAPAs

Posted 12 Days Ago
Be an Early Applicant
Madison, WI, USA
In-Office
Entry level
Biotech • Pharmaceutical
The Role
Manage Investigation and CAPA systems for deviations, OOS investigations, and quality system improvements. Lead cross-functional teams for process and system enhancements, develop metrics, provide training, maintain controlled documents, and ensure FDA/regulatory compliance.
Summary Generated by Built In

Specialist I - Quality Assurance Systems, Deviations/CAPAs

Position Summary:

  • Work Schedule: M-F 8am-5pm
  • 100% on-site

Working  for  Catalent  Biologics  is  an  opportunity  to  join  an  entrepreneurial  team.   Catalent  Biologics  is  making significant investments in people and capabilities.  This is a unique opening to join a small, fast-growing business, backed by a global public company.  People joining our team will have the opportunity for career development as our  business  continues  to  grow  and  expand.   Catalent-Madison  employees  are  helping  to  improve  future  patient outcomes by working on products that are designed to treat COVID-19, cancer, various autoimmune, fibrotic and blood disorders, HIV, diabetes, heart and lung diseases as well as Alzheimer’s. 

Catalent Pharma Solutions in Madison, WI is hiring a Specialist I - Quality Assurance Systems, Deviations/CAPAs.
The Quality Assurance department is responsible for all aspects of the quality assurance functions at Catalent, Madison. The department’s primary function is to ensure compliance with FDA and other regulatory agency requirements as well as  internal quality systems requirements.    This includes systems implementation and maintenance, documentation management, site-wide systems training, internal and external auditing, project review actions to ensure regulatory compliance, which is essential in providing high quality drug products for our clients and their patients.

The Role:

  • Accountable for the Investigation and CAPA Management Systems.
  • Responsible for managing complex and high-level deviations, supporting OOS investigations, and collaboration with internal Catalent stakeholders to support the effective execution of the Investigation and CAPA systems.
  • Maintains and enhances effectiveness of the Quality System, including developing and reporting metrics, identification, and implementation of improvement opportunities for established Quality Systems, processes, procedures, and training to support Deviation, Out-of-Specification and CAPA processes.
  • Drives alignment and improvement initiatives, leading cross function teams, to address process improvement, system improvement, and new regulations/expectations.
  • Provides technical assistance and training for personnel.
  • Files and maintains controlled documents.
  • Other duties as assigned

The Candidate:

  • Doctorate Degree in STEM discipline with minimum of 0 years related experience.
    OR
  • Master's Degree in STEM discipline with minimum of 4 years related experience.
    OR
  • Bachelor's Degree in STEM discipline with minimum of 6 years related experience.
    OR
  • Associates Degree in STEM discipline with minimum of 10 years related experience.
     

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
  • 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!

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

  • Doctorate Degree in STEM (0 years related experience)
  • Master's Degree in STEM (minimum 4 years related experience)
  • Bachelor's Degree in STEM (minimum 6 years related experience)
  • Associate's Degree in STEM (minimum 10 years related experience)
  • Experience managing investigations, deviations, OOS investigations, and CAPA processes/systems
  • Knowledge of FDA and other regulatory agency requirements and quality systems (GxP)
  • Experience leading cross-functional teams and driving process/system improvement initiatives
  • Experience developing and reporting quality metrics and implementing improvement opportunities
  • Experience maintaining controlled documents and providing site training
  • Able to work M-F 8am-5pm; 100% on-site in Madison, WI

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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