Catalent Pharma Solutions Inc

Pharmaceutical Development Senior Associate Scientist II

Catalent Pharma Solutions Inc • $75K — $95K *
Kansas City, MO 64118In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Reposted 2 weeks ago
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life or physical science with 4+ years relevant experience, or Master's degree with 2+ years experience.
  • Ability to interpret complex instructions in various formats.
  • Proficiency in laboratory documentation and regulatory compliance.

Responsibilities

  • Maintain high-quality lab documentation per regulatory guidance and SOPs.
  • Draft technical documents including lab notebooks and batch records.
  • Train colleagues on procedures and lab techniques.
  • Execute efficiency improvement projects with support.
  • Perform parallel reviews of GMP documents and lab notebooks.
  • Develop procedures and manufacturing processes for simpler projects.
  • Lead small team projects while fostering collaborative environments.

Benefits

  • Competitive medical benefits and 401K.
  • 152 hours PTO plus 8 paid holidays.
  • Dynamic and fast-paced work environment.
  • Opportunities for Continuous Improvement processes.
Full Job Description
Pharmaceutical Development Senior Associate Scientist II

Position Summary
  • Shift: Tuesday - Friday 12pm-10pm
  • 100% on-site


The Senior Associate Scientist II 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


The candidate:
  • Bachelor's degree in related life science or physical science field required with 4+ years related work experience
  • Master's degree in related life science or physical science field required with 2+ years related work experience
  • Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form
  • Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds;


Why you should join Catalent:
  • Competitive medical benefits and 401K
  • 152 hours PTO + 8 Paid Holidays
  • Dynamic, fast-paced work environment
  • Opportunity to work on Continuous Improvement Processes


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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