Pharmaceutical Development Senior Associate Scientist I

Catalent Pharma Solutions; Kansas City (MO); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Paid time off

8 paid holidays

Benefits from day one (medical, dental

Vision benefits

Tuition reimbursement

Job summary

Catalent Kansas City is seeking a Pharmaceutical Development Senior Associate Scientist I to support formulation design and development of oral solid drug products. You will train others in clinical trial manufacturing operations and ensure compliance with GMP, regulatory requirements, and SOPs.

This onsite role offers opportunities to contribute to meaningful projects impacting patients worldwide. The role emphasizes scientific rigor, documentation quality, and collaboration with

Qualifications

• Master’s degree with 0+ years or Bachelor’s with 2+ years of related work experience preferred.
• Maintain high‑quality laboratory documentation per regulatory guidance and SOPs.
• Draft technical documents such as notebooks, protocols, and batch records.

Responsibilities

• Train others on procedures and laboratory techniques.
• Execute efficiency improvement projects with guidance.
• Apply knowledge within the discipline on projects and assignments.
• Perform work in GMP areas under minimal supervision.

Skills

Laboratory techniques

GMP compliance

Documentation

Written and verbal communication

Problem solving

Multitasking

Education

Master’s degree in life/physical science

Bachelor’s degree in life/physical science

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 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.

Physical Demands

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.

Equal Opportunity Employer

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 [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.

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.

Security Notice

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 [e-mail] for us to investigate with local authorities.

California Job Seekers Notice

California Job Seekers can find our California Job Applicant Notice HERE.

Volunteer Work Disclosure

Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice

Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

About Catalent

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.