Pharmaceutical Development Senior Associate Scientist I

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 Pharmaceutical Development Senior Associate Scientist I to join our team. In this role, you will support formulation design and development of oral solid drug products. You will train others in clinical trial manufacturing operations using sound pharmaceutical principles and ensure all work complies with regulatory requirements, good manufacturing practices, and standard operating procedures. This position offers the chance to contribute to meaningful projects that impact patients worldwide.

Shift: M-F 8am-5pm
Location: Kansas City, MO
100% Onsite

The Role

• Train others on procedures and laboratory techniques.
• Execute efficiency improvement projects with guidance.
• Apply knowledge of principles and concepts within the discipline.
• Use technical and functional knowledge to perform duties on most projects or assignments within the team.
• Conduct work in a Good Manufacturing Practice (GMP) area under minimal supervision.

The Candidate

Minimum Requirements

• Master’s degree in a related life science or physical science field with 0+ years of related work experience preferred, or Bachelor’s degree in a related life science or physical science field with 2+ years of related work experience preferred.
• Maintain high-quality laboratory documentation in accordance with applicable regulatory guidance and site standard operating procedures.
• Draft technical documents such as laboratory notebook writeups, protocols, and batch records.
• Proactively address work issues at the individual level.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Perform parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.
• Execute procedures, methods, and manufacturing processes with minimal complexity, high quality, and limited supervision.
• Propose deviations from established procedures and methods based on sound judgment.
• Lead by example according to Catalent's values and culture.
• Client interactions are very limited and supervised.
• Recognize unmet needs within the department.
• Ability to learn and retain technical information.
• Demonstrate mathematical and scientific reasoning ability.
• Basic understanding of manufacturing equipment operations and troubleshooting skills in multiple techniques.
• Intermediate written and verbal communication skills with internal customers.
• Assist with process efficiency under significant supervision.
• Well organized with the ability to multitask.
• Ability to work effectively under pressure to meet deadlines.
• May contribute material to publications and/or external presentations.
• Stand, walk, sit, use hands to manipulate, and reach with hands and arms for up to 8 hours per day.
• Frequent sitting, standing, walking, reading of written documents, and use of computer monitor screen.
• Able to work with respirator (P100, PAPR, etc.).
• Occasional lifting and/or moving up to 50 pounds.

Preferred Skills & Background

• Previous solids development 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.

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 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.

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