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Catalent Pharma Solutions Sr LIMS Administrator in Massachusetts

Job Description

Position Overview:

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 the people you know and love. Your talents, ideas and passion are essential to our mission; to develop, manufacture and supply products that help people live better, healthier lives. Interested in learning more about life at Catalent? Start here (http://www.catalent.com/index.php/about-us/Catalent-Careers2)

Job Title

Senior Quality Control Systems Administrator

Position Summary

The Senior Quality Control System Administrator is responsible for maintaining compliance and building electronic content for the Quality Control GMP systems. Responsibilities include management of Laboratory Execution System (LES) and the Laboratory Information Management System (LIMS) for executing QC testing and related analytical activities. The System Administrator leads the creation of new content as needed in support of product development, release and stability. This individual conducts routine maintenance and Administrator responsibilities of the electronic laboratory system per the standard operating procedures.

This role will be located at our site in Chelsea, MA.

This 90,000 square-foot Boston-area facility is Catalent’s global Center of Excellence for spray dry dispersion and Dry Powder Inhaler (DPI) capsule manufacture and packaging. The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America.

The Role

  • Performs System Administrator responsibilities for Electronic Laboratory Notebook and Empower enterprise systems.

  • Coordinates with SME team to write and develop new method content.

  • Creates electronic methods with outline of User Acceptance Testing for method Implementation.

  • Creates new Specification documents for any new Content.

  • Trains End users on new functions.

  • Facilitates and coordinates with IT and business owner to resolve any maintenance and enhancement requests.

The Candidate

  • Bachelor’s Degree in Physical, Chemical, Computer Sciences or related field required.

  • Minimum of 4+ years of experience in and/or supporting a cGMP regulated environment required.

  • Experience managing a LIMS system required. Experience with BIOVIA (VelQuest) preferred.

  • Experience with QC test methods and generating electronic content to follow validated SOP’s in a 21 CRF Part 11 compliant system.

  • Familiarity with executing Standard Operating Procedures in a GMP setting required.

  • Critical understanding of the importance of documentation and data traceability required.

  • Experience with method development and validation preferred.

  • Experience with Empower software at an administrator level

  • Experience building electronic content for a LIMs or ELN LES

  • Strong interpersonal and communication skills

Catalent’s standard leadership competencies that are used to interview and for Performance & Development:

  • Leads with Integrity and Respect

  • Delivers Results

  • Demonstrates Business Acumen

  • Fosters Collaboration and Teamwork

  • Champions Change

  • Engages and Inspires

  • Coaches and Develops

Position Benefits

  • Competitive medical benefits and 401K

  • 19 days of PTO + 8 paid holidays

  • Exposure to a wide array of systems

  • Opportunity to expand skillsets through training courses

  • State of the art facility and equipment

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 www.catalent.com/careers to explore career opportunities.

C atalent is an Equal Opportunity / Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, sexual orientation or gender identity. 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 DisabilityAccommodations@catalent.com . 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.

Catalent = Catalyst + Talent

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!

personal initiative. dynamic pace. meaningful work.

Catalent is the perfect place to grow your career if…

  • You enjoy the fast pace of a start-up, but want the opportunities and stability of a growing, publicly traded company (Listed on NYSE: CTLT).

  • You want meaningful work. From cough treatments to cancer-fighting drugs, biologics, and vitamins, we help develop, launch, and supply over 200 new products each year – more than any branded drug maker in the world!

  • You want to plant your career in a growing company. Over the last five years, Catalent has re-invested more than $2 billion back into the company and its people.

  • You are excited about learning, collaborating, and growing alongside a global diverse team. Our team of more than 11,000 comes to work every day ready to overcome new challenges with teamwork, advanced technologies, and a passion to deliver by putting patients first.

  • You want to make a global impact! From North America to Europe, Asia to Latin America, we have innovative science and manufacturing teams who are looking (https://catalent.wd1.myworkdayjobs.com/External) for YOU!

  • See how our teams are making a difference, while growing their careers and fulfilling our mission by putting patients first every day here (https://www.youtube.com/playlist?list=PLuUGqEwwnH7hBwFlrsfSOH_raQHu4hOBK) .

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