Senior Associate Scientist I, Quality Control

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Competitive PTO and holidays

Benefits from day one (medical, dental

Tuition reimbursement

Job summary

Catalent Kansas City is seeking a Sr. Associate Scientist I to maintain analytical laboratories and support GMP-driven project activities. The role emphasizes clean, organized workspaces and accurate documentation, with a Monday–Friday 12pm–8:30pm shift and 100% on-site location.

You will communicate with internal/external customers and ensure training is current on SOPs, mentoring peers as needed, and handling sample pickup/delivery.

Qualifications

• Master's degree in a science discipline, or Bachelor's with 2+ years of related work experience.
• Familiarity with GMP and documentation practices is expected.

Responsibilities

• Maintain analytical laboratories and ensure cleanliness and organization.
• Assist project activities and ensure compliance with GMP and proper documentation.
• Train or mentor peers and manage sample pickup/delivery.

Education

Master's degree in a relevant science discipline

Bachelor's degree in a relevant science discipline with 2+ years of related work experience

Job description

About Site

Catalent's Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses.

Position Summary

We have an opportunity for a Sr. Associate Scientist I to join our team. In this role, you will help maintain analytical laboratories and ensure a clean, organized work environment. You will support project activities through effective communication and adherence to Current Good Manufacturing Practices. This position also involves performing assigned tasks and maintaining accurate documentation.
Shift: Monday - Friday, 12pm - 830pm
Location: Kansas City, MO 100% Onsite

The Role

• Maintain analytical laboratories, including cleanliness, glassware cleaning, ordering supplies, and minor documentation.
• Communicate effectively with internal and external customers, peers, and supervisors to support project activities.
• Maintain awareness of Current Good Manufacturing Practices, industry standards, and modern techniques relevant to pharmaceutical sciences.
• Keep training current on all applicable standard operating procedures, ensuring records are up to date in the internal system.
• Train or mentor peers as needed.
• Ensure a clean and organized laboratory work environment is maintained.
• Perform basic Good Manufacturing Practice documentation and testing in accordance with assigned tasks, including sample pickup and delivery.
• Perform tasks as assigned.

Candidate Minimum Requirements

• Master's degree in a relevant science discipline; OR Bachelor's degree in a relevant science discipline with 2+ years of related work experience preferred.

Why You Should Join Catalent

• Defined career path and annual performance review and feedback process.
• Diverse, inclusive culture.
• Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
• Competitive paid time off plus 8 paid holidays.
• Community engagement and green initiatives.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition reimbursement.
• Personal initiative.
• Dynamic pace.
• Meaningful work.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 an Equal Opportunity Employer, including disability and veterans.

Important: 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 [e-mail]. 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.