Master Data Builder

4 weeks ago

Madison, Wisconsin, United States Catalent Pharma Solutions Full time

We're hiring for a LIMS Master Data Builder – Quality Control to support laboratory information management systems (LIMS) administration at our facility in Madison, Wisconsin

Catalent is a global, high-growth 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.

The LIMS Master Data Builder – Quality Control is responsible for supporting various functions with laboratory information management systems (LIMS) administration. This is a full-time, salaried position and is 100% site based. The schedule is Monday – Friday 1st shift.

Catalent's Madison, Wisconsin site is a state-of-the-art biomanufacturing facility specializing in integrated formulation and analytical services. Our site features our proprietary Gene Expression Technology (GPEx) cell line engineering platform, and biomanufacturing capabilities utilizing single-use systems. Our 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 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

  • Support QC, AD and PD departments in the build and/or revision, review and approval of master data, including but not limited to products, specifications, and methods in LIMS, per global and local LIMS procedures.
  • First-line support for end-user LIMS template and data entry issues.
  • Assist in the development, implementation, enhancement of the overall process for requesting, creating/revising, and reviewing of LIMS master data at the Madison facility.
  • Assist in the development and implementation of a site process for the scheduling and status tracking of all site LIMS master data, including needs for raw material, finished goods, and stability testing.
  • Work with the site LIMS Administrator to maintain site and Catalent Global requirements of LIMS.
  • Participate in the development and/or revision of site and/or Catalent Global Standard Operating Procedures (SOPs).
  • Other duties as assigned.

The Candidate

  • Master's Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 1 years of industry experience, or Bachelor's Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 4 years of industry experience, or Associate Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 8 years of industry experience.
  • Prior experience with Laboratory Information Management Systems (LIMS) preferred.
  • Experience writing technical documents preferred.
  • cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP) knowledge preferred.
  • Experience following standard operating procedures (SOP) preferred.
  • Demonstrated excellence in prior roles can be a substitute for the minimum years of experience.

Why you should join Catalent

  • Defined career path and annual performance review and feedback process.
  • Medical, dental and vision 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.
  • Competitive salary with bonus potential.
  • Tuition reimbursement program.
  • Diverse, inclusive culture.
  • 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.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

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 . 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 for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE ) .


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