Pharmaceutical Development Senior Associate Scientist I

Catalent • Kansas City, MO

6d • Onsite

About The Position

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).

Requirements

• 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.

Responsibilities

• 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.

Benefits

• 152 hours of PTO + 8 paid holidays
• Generous 401K match
• Medical, dental and vision benefits effective day one of employment
• Tuition Reimbursement

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level