Pharmaceutical Development Scientist I (2nd shift)

Catalent • Kansas City, MO

1d • Onsite

About The Position

Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects. Catalent Pharma Solutions in Kansas City, MO is hiring a Pharmaceutical Development Scientist I. The Kansas City Pharmaceutical Development Scientist I serve as technical representative for formulation design and development of oral solid dosage forms. Design and execute experiments and processes necessary for developing formulations of pharmaceuticals oral solid. Lead clinical trial manufacturing endeavors and ensures that all work is carried out in compliance with regulatory requirements, good manufacturing practices (cGMP) and standard operating procedures (SOPs).

Requirements

• Bachelor's degree in related life science or physical science field required with 6+ years related work experience required

Nice To Haves

• Master’s degree in related life science or physical science field required with 4+ years related work experience preferred
• Doctorate Degree in related life science or physical science field preferred
• Hands on experience in oral solid dosage form development and manufacturing preferred

Responsibilities

• Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics
• Authors technical documents, such as protocols, batch records, test methods, technical reports, and operating procedures
• Review technical documents for accuracy, thoroughness and regulatory compliance
• Trains, coaches or mentors’ others on technical development or business issues
• May direct work (limited) of technical staff, including work assignments
• Supervised customer interaction on team meetings
• Knowledge of high-shear granulation, fluid-bed technology, roller compaction, compression, encapsulation
• Executes efficiency improvement project with moderate guidance
• Identify and recommend business opportunities on a project specific basis
• All other duties as assigned

Benefits

• 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!

What This Job Offers

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