Quality Control Senior Associate Scientist I

Quality Control Senior Associate Scientist I

Position Summary:

• Work Schedule: Monday – Friday 12:00PM – 8:00PM  

• 100% onsite

Catalent's Kansas City (KCM) facility is a premier site for integrated drug development, manufacturing, and clinical supply services, supporting a wide range of pharmaceutical and biotech products. With cutting-edge technologies and a collaborative work environment, it offers exciting opportunities for professionals across all functions—from science and engineering to operations and logistics.

The Quality Control Senior Associate Scientist I is responsible for performing raw material testing, to support clinical manufacturing.

The Role:

• Executes various laboratory test methods for raw material release testing

• Maintains accurate and high-quality laboratory documentation in accordance with regulatory guidance and site SOPs

• Performs parallel review of laboratory documentation 

• Assists in execution of efficiency improvement projects

• Other duties as assigned

The Candidate:

• Bachelor's degree in chemistry or closely related physical science required

• Minimum 2 years of relatable experience highly preferred

• Prior knowledge of current Good Manufacturing Practices (cGMP's) and Standard Operating Procedures (SOPs) preferred

Why you should join Catalent:

• Career growth with a clear path and regular performance reviews

• Day-one benefits: medical, dental, vision

• 401(k) match, tuition reimbursement, and wellness perks

• Paid time off: 152 hours + 8 holidays

• Inclusive culture with Employee Resource Groups and community initiatives

• Discounts from 900+ merchants via Perkspot

• A mission-driven workplace where your work helps save lives

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 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.

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