Pharmaceutical Development Senior Associate Scientist II

Catalent; Kansas City (MO); On-site; USD 65,000 - 90,000; Full time

Job summary

Catalent is seeking a Pharmaceutical Development Senior Associate Scientist II for our Kansas City, MO site to support formulation design and development of oral solid drug products. This onsite role emphasizes GMP compliance and training others in clinical trial manufacturing operations.

You will draft technical docs, perform lab testing, and lead efficiency projects in a collaborative team environment. The ideal candidate has a Bachelors (4+ years) or a Master’s degree (2+ years) in a life or

Qualifications

• Bachelor's or Master’s degree in a life or physical science with related experience.
• Strong understanding of pharmaceutics principles and GMP practices.
• Ability to apply math and scientific reasoning; good communication skills.

Responsibilities

• Execute laboratory work plans with input from supervisor or senior team member.
• Draft batch records, technical reports, and SOPs with limited guidance.
• Train others on procedures and laboratory techniques.
• Lead efficiency improvement projects and review manufacturing documentation for regulatory compliance.
• Maintain high-quality laboratory documentation per regulatory guidance and site procedures.
• Perform physical testing (bulk/tap density, flow analysis, sieve analysis) as needed.
• Execute moderately complex procedures with high quality.
• Work in GMP areas under minimal supervision.
• Perform all other duties as assigned.

Skills

Pharmaceutics knowledge

GMP knowledge

Education

Bachelor's degree

Master's degree

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 II 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. You will ensure all work complies with regulatory requirements, good manufacturing practices and standard operating procedures.
Shift: M-Th or Tues-Fri 12pm-10:30pm
Location: Kansas City, MO
100% Onsite

The Role

• Execute laboratory work plans and schedules with input from supervisor or senior team member
• Draft technical documents such as batch records, technical reports and standard operating procedures with limited guidance
• Train others on procedures and laboratory techniques
• Execute efficiency improvement projects with limited guidancePerform parallel review of manufacturing documentation and may qualify to perform technical review for accuracy, thoroughness and regulatory compliance
• Maintain high-quality laboratory documentation in accordance with regulatory guidance and site procedures
• Perform physical testing as needed, including bulk/tap density, flow analysis (FT4) and sieve analysis
• Execute procedures or methods of moderate complexity with high quality
• Conduct work in GMP area under minimal supervision
• Perform all other duties as assigned

The Candidate

Minimum Requirements

• Bachelor's degree in a related life science or physical science field with 4+ years of related work experience preferred, or a Master’s degree in a related life science or physical science field with 2+ years of related work experience preferred
• Strong knowledge of the principles and concepts of pharmaceutics
• Ability to apply mathematical and scientific reasoning
• Advanced understanding of equipment and instrument operations and troubleshooting skills in multiple techniques
• Excellent written and verbal communication skills with internal and external customers
• Understanding of current Good Manufacturing Practices and ability to work in GMP space with supervision

Preferred Skills & Background

• Not applicable

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 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.

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

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.