Associate Scientist I - Quality Control, AQC

Posted 3 Days Ago
Be an Early Applicant
Madison, WI, USA
In-Office
Entry level
Biotech • Pharmaceutical
The Role
Perform entry-level cGMP quality control testing and documentation for raw materials, operate basic QC equipment, enter data into LIMS, conduct inbound material inspections, perform routine maintenance and 5S lab housekeeping, and follow SOPs under supervision.
Summary Generated by Built In

Associate Scientist I - Quality Control, AQC

Position Summary: 

  • Work Schedule: M-F 8am-5pm 

  • 100% on-site 

Catalent Biologics is a fast-growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients.  The business includes our proprietary GPEx cell line engineering platform, our new state-of-the-art biomanufacturing facility in Madison, WI, and our leading biologics analytical services in Kansas City, MO and Research Triangle Park, NC, as well as SMARTag Antibody Drug Conjugate technology in Emeryville, CA.  Leveraging our growing differentiated technology portfolio, world class manufacturing capability, and other integrated services across the Catalent network, Catalent Biologics is positioned to drive significant growth for Catalent. 

Catalent Pharma Solutions in Madison, WI is hiring an Associate Scientist I - Quality Control, Raw Materials.  This position requires a variety of skills necessary for biotech company operations. The position is an entry level laboratory role with the expectation that the candidate can be trained in technical procedures and once trained, execute them consistently and reliably. Additionally, this position may support preventative maintenance and basic laboratory maintenance activities while maintaining a GMP quality system. 

The Role: 

  • Executes and properly documents cGMP Quality Control testing with supervision.  

  • Operates basic cGMP Quality Control equipment. 

  • Performs self-review of analytical data for accuracy and consistency with SOP.  

  • Enters data into Laboratory Information Management System (LIMS) or laboratory reports.  

  • Frequently lift and/or move up to 10 pounds and occasional lifting and/or moving up to 50 pounds. 

  • Handles products using material handling equipment. 

  • Conducts inspections on inbound single use manufacturing materials in a warehouse environment. 

  • Performs general lab housekeeping in adherence to 5S standards. 

  • Accurately completes routine and preventive maintenance on basic equipment. 

  • Actively participates in team meetings and/or training sessions. 

  • Other duties as assigned. 
     

The Candidate: 

  • Bachelor’s Degree in Biology, Biotechnology, Chemistry, or related life sciences field. 

  • Associate Degree in Biology, Biotechnology, Chemistry, or related life sciences field with a minimum of 1 year of industry experience. 

  • High School Diploma or equivalent with a minimum of 4 years of industry experience. 

  •  Preferred: 

  • Basic understanding of analytical chemistry and simple lab equipment. 

  • Familiarity with clean room procedure, aseptic technique, and general lab equipment experience. 

  •  cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP) knowledge. 

  • Experience following standard operating procedures (SOP). 

  • General laboratory equipment experience, including micropipettes. 

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 

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

  • Bachelor's degree in Biology, Biotechnology, Chemistry, or related life sciences field.
  • Associate degree in Biology, Biotechnology, Chemistry, or related field plus minimum 1 year industry experience.
  • High school diploma or equivalent plus minimum 4 years industry experience.
  • Execute and properly document cGMP Quality Control testing.
  • Operate basic cGMP Quality Control equipment.
  • Perform self-review of analytical data for accuracy and consistency with SOPs.
  • Enter data into Laboratory Information Management System (LIMS) or laboratory reports.
  • Frequently lift/move up to 10 pounds and occasionally up to 50 pounds; handle material handling equipment.
  • Conduct inspections on inbound single use manufacturing materials in a warehouse environment.
  • Perform general lab housekeeping in adherence to 5S standards.
  • Accurately complete routine and preventive maintenance on basic equipment.
  • Experience following standard operating procedures (SOP).
  • Knowledge of cGMP, Good Documentation Practices (GDP), or Good Laboratory Practices (GLP).
  • Basic understanding of analytical chemistry and simple lab equipment.
  • Familiarity with clean room procedure and aseptic technique.
  • General laboratory equipment experience, including micropipettes.

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: Somerset, NJ
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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