Principal Representative, QA

Posted 12 Hours Ago
Be an Early Applicant
Bloomington, MN
7+ Years Experience
Biotech • Pharmaceutical
The Role
The Principal Representative, QA will implement and maintain the Data Integrity program, manage System and Validation Lifecycle Documentation, and ensure compliance with GxP standards. Responsibilities include reviewing validation documents and SOPs, performing data integrity assessments, and participating in audit trail reviews.
Summary Generated by Built In

We're hiring for a Principal Representative, QA in Bloomington, IN to implement and maintain the Data Integrity program.

Catalent is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients worldwide. Your talents, ideas, and passion are essential to our mission: to help people live better, healthier lives. 

This Principal Representative, QA's primary role is to support the data integrity program, and compliance initiatives. This is a full-time, salaried position and is 100% site based. The schedule is Monday – Friday, 1st shift.

Catalent Biologics in Bloomington, Indiana is a state-of-the art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better, healthier lives.

The Role

  • Responsible to implement and maintain the Data Integrity Program.

  • Assist with the development, execution and approval of System and Validation Lifecycle Documentation for site GxP systems, including specifications, test protocols, traceability matrices, and various assessments.

  • Complete review and approval of Computer System Validation documents in the EDMS system.

  • Develop and implement administrative procedures for individual systems or family of systems through the creation, revision, and approval of SOPs.

  • Review & approve Actions, Change Controls, and Deviations in the TrackWise.

  • Participate in audit trail reviews with System Owners, ensuring completion on time.

  • Complete Data Integrity Assessments.

  • Other duties as assigned. 

The Candidate

  • Bachelor’s Degree with 8+ of relatable experience.

  • Bachelor’s degree in a STEM disciple highly preferred.

  • 12+ years of relatable experience, or demonstrated excellence in role, with justification.

  • Minimum of 4 years GxP experience, or other regulated industry.

  • Prior experience supporting data integrity initiatives, in a cGMP environment, highly preferred.

  • A strong working knowledge of quality systems and processes, preferred.

  • Must be able to read and understand English-written job instructions and safety requirements.

Why you should join Catalent

  • Medical, dental, vision, and wellness benefits are effective on the first day of employment.

  • Potential for career growth on an expanding team and organization.

  • 152 hours of paid time off annually plus 8 paid holidays.

  • Community engagement and green initiatives.

  • Engaging D&I Employee Resource Groups.

  • Tuition reimbursement program.

  • Generous 401K match.

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

Gxp
The Company
HQ: Somerset, NJ
13,715 Employees
On-site Workplace
Year Founded: 2007

What We Do

Catalent Inc. (NYSE: CTLT), an S&P 500® company, is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. With broad and deep scale and expertise in development sciences, delivery technologies, and multi-modality manufacturing, Catalent is a preferred industry partner for personalized medicines, consumer health brand extensions, and blockbuster drugs.

Catalent supports our partners in introducing 200 new products and manufacturing over 70 billion doses each year. Since becoming a publicly traded company in 2014, we have grown to become a community of approximately 19,000+ workers who support over 7,000 products for over 1,000 customers around the world. We share a common goal: to put patients first and help people around the world live better and healthier lives.

Catalyst + Talent. Our name combines these ideas. From drug and biologic development services to delivery technologies to supply solutions, we are the catalyst for your success. We have the deepest expertise, the broadest offerings, and the most innovative technologies to help you get more molecules to market faster, enhance product performance, and provide superior, reliable manufacturing and packaging results.

more products. better treatments. reliably supplied.™

Your talents, ideas, and passion are essential to our mission: to develop, manufacture, and supply products that help people live better, healthier lives. Join us!

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 life.

Grow with us. Be challenged. Make a personal impact.

Visit https://careers.catalent.com/us/en to explore career opportunities

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