Pharmaceutical Development Senior Associate Scientist I

The International Society for Pharmaceutical Engineering, Inc.; Kansas City, Northern (MO, KY); Hybrid; USD 85,000 - 110,000; Full time

Benefits offered by this job

152 hours PTO + holidays

Generous 401K match

Medical, dental and vision benefits

Tuition Reimbursement

Job summary

Catalent's Kansas City site is a premier facility for integrated drug development, manufacturing, and clinical supply services. The Pharmaceutical Development Senior Associate Scientist I supports formulation design of oral solid drugs, trains others, and ensures work complies with regulatory requirements, cGMPs, and SOPs.

The role emphasizes maintaining quality lab documents, drafting technical records, and leading small team projects while contributing to process improvement and compliance

Qualifications

• Bachelor's or Master's in life/physical/physical science with related experience.
• Ability to interpret instructions furnished in multiple formats.
• Physical requirements: stand/walk, respirator use, lift up to 50 lbs.

Responsibilities

• Maintain high quality laboratory documentation in accordance with regulatory guidance and site SOPs.
• Draft technical documents such as laboratory notebook writeups, protocols and batch records.
• Train others on procedures and laboratory techniques.
• Executes efficiency improvement projects with guidance.
• Has applied knowledge of discipline principles and concepts.
• Applies technical knowledge to duties on projects within own group.
• Perform parallel review of GMP documents and notebooks; may conduct compliance reviews.
• Develop and execute procedures and manufacturing processes with minimal complexity; high quality.
• Demonstrated ability to lead small team projects.

Skills

Lab documentation

Training others

Regulatory understanding

Team leadership

Education

Bachelor's degree in life/physical science

Master's degree in life/physical science

Job description

Pharmaceutical Development Senior Associate Scientist I

Position Summary:

• Work Schedule: 2nd shift Monday - Thursday, 12pm-10pm

• 100% on-site

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 Pharmaceutical Development Senior Associate Scientist I supports formulation design and development of oral solid drug products. Trains others in clinical trial manufacturing operations using sound pharmaceutical principles. Ensures that all work is carried out is in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs).

The Role:

• Maintain high quality laboratory documentation in accordance with applicable regulatory guidance and Site SOPs.

• Draft technical documents such as laboratory notebook writeups, protocols and batch records.

• Trains others on procedures and laboratory techniques.

• Executes efficiency improvement project with guidance.

• Has applied knowledge of the principles and concepts of a discipline.

• Applies technical and functional knowledge to job related duties on most projects/ assignments within own group/project team.

• Performs parallel review of GMP documents and laboratory notebooks and may become qualified to conduct compliance technical reviews.

• Develop and executes procedures, methods, manufacturing processes with minimal complexity, with high quality.

• Demonstrated ability to lead small team projects.

• All other duties as assigned.

The Candidate:

• Bachelor's degree in a related life science or physical science field with a minimum of 2 years of related experience, or a Master's degree in a related life science or physical science field; prior experience preferred but not required with an MS.

• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

• Physical Requirements: Ability to stand, walk, sit, use hands for manipulation, and reach with hands and arms for up to 8 hours per day; frequent sitting, standing, walking, reading written documents, and use of computer monitors; ability to wear a respirator (e.g., P100, PAPR); and occasional lifting and/or moving of up to 50 pounds.

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

• Generous 401K match

• Medical, dental and vision benefits effective day one of employment

• Tuition Reimbursement - Let us help you finish your degree or start a new degree!

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.

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.

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