Catalent Pharma Solutions Inc

Pharmaceutical Development Senior Scientist I

Catalent Pharma Solutions Inc • $90K — $120K *
Kansas City, MO 64118In-Person
Pharmaceuticals & Biotech
8 - 10 years of experience
3 weeks ago
Job Overview by Ladders

Qualifications

  • Bachelor's, Master's, or Doctorate in life or physical sciences required with specific years of relevant experience
  • Proven ability to lead team projects and identify unmet needs
  • Advanced knowledge in pharmaceutics and related disciplines
  • Basic to moderate understanding of manufacturing equipment operations
  • Proactive approach to addressing work issues on both individual and team levels

Responsibilities

  • Develop and execute independent laboratory work plans according to customer milestones
  • Author and review technical documents such as protocols and reports
  • Train and mentor others on technical development and business issues
  • Lead clinical trial manufacturing efforts while ensuring compliance
  • Recommend business opportunities on a project-specific basis
  • Execute efficiency improvement projects under moderate guidance
  • Apply technical knowledge to assist in experiment/project design

Benefits

  • Defined career path with annual performance reviews
  • Diverse and inclusive workplace culture
  • Generous PTO and paid holidays
  • Dynamic and fast-paced working environment
  • Opportunities for career growth in an expanding team
  • Community engagement and sustainable initiatives
  • Robust medical, dental, and vision benefits starting day one
  • Tuition reimbursement and wellness programs
Full Job Description
Pharmaceutical Development Senior Scientist I

Position Summary
  • Work Schedule: Monday to Friday 8am-5pm
  • 100% based on-site in Kansas City


The Kansas City Pharmaceutical Development Senior Scientist I serves as Technical Lead for formulation/process 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).

The Role
  • Develop and execute laboratory work plans/schedules independently, using customer milestones and Division/site performance standards and metrics
  • Authors/Reviews technical documents, such as protocols, batch records, test methods, technical reports, and operating procedures
  • Trains, coaches or mentors' others on technical development or business issues
  • Knowledge of high-shear granulation, fluid-bed technology, roller compaction, compression, encapsulation, coating technology
  • Executes efficiency improvement project with moderate guidance
  • Identify and recommend business opportunities on a project specific basis
  • Has advanced knowledge of the principles, theories and concepts applicable to a limited range of work in pharmaceutics and knowledge of principles and concepts in other disciplines.
  • Applies technical and functional knowledge to assist in experiment/project design that will enable department to meet goals.
  • All other duties as assigned


The Candidate
  • Bachelor's degree in related life science or physical science field required with 11+ years related work experience or Master's degree in related life science or physical science field required with 9+ years related work experience or Doctorate Degree in related life science or physical science field required with 8+ years related work experience required.
  • Proactively address work issues at both an individual level and a team level
  • Propose deviations from established procedures and methods based upon sound judgment.
  • Develop and executes procedures, methods, manufacturing processes with minimal complexity, with high quality.
  • Demonstrated ability to lead small team projects and recognizes unmet needs within department.
  • Basic/Moderate understanding of manufacturing equipment operations and troubleshooting skills in multiple techniques.


Why you should join Catalent
  • Defined career path and annual performance review and feedback process
  • Diverse, inclusive culture
  • 152 hours of PTO + 8 paid holidays
  • Several Employee Resource Groups focusing on D&I
  • Dynamic, fast-paced work environment
  • 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
  • Competitive salary with quarterly bonus potential
  • Community engagement and green initiatives
  • Generous 401K match and Paid Time Off accrual
  • Medical, dental and vision benefits effective day one of employment
  • Tuition Reimbursement
  • GymPass program to promote overall physical wellness

About Catalent Pharma Solutions Inc

Catalent Pharma Solutions Inc is a global provider of advanced delivery technologies, development, and manufacturing solutions for drugs, biologics, gene therapies, and consumer health products. The company operates in four segments: Softgel and Oral Technologies, Biologics, Oral and Specialty Delivery, and Clinical Supply Services. Catalent Pharma Solutions serves customers in various industries, including pharmaceuticals, biotechnology, and consumer health. The company was founded in 2007 and is headquartered in Somerset, New Jersey.
Learn more about Catalent Pharma Solutions Inc
Size
14,000 employees
Industry
Pharmaceuticals & Biotech
Founded
2007
* Ladders Estimates

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