Catalent Pharma Solutions Inc

Pharmaceutical Development Senior Associate Scientist I

Catalent Pharma Solutions Inc • $70K — $95K *
Kansas City, MO 64118In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor's degree in a related life science or physical science field; a Master's degree is a plus
  • Minimum 2 years of relevant experience with a Bachelor's; prior experience preferred but not required with a Master's
  • Strong ability to interpret complex instructions in various formats
  • Familiarity with regulatory compliance and good manufacturing practices (cGMP)
  • Physical capability to handle laboratory and manual tasks as specified.

Responsibilities

  • Maintain high quality documentation per regulatory guidance and SOPs
  • Draft technical documents, including protocols and batch records
  • Train colleagues on laboratory techniques and standard procedures
  • Lead efficiency improvement projects with supervision
  • Conduct parallel reviews of GMP documents and laboratory records
  • Develop and execute manufacturing processes with a focus on quality
  • Perform other assigned duties as needed.

Benefits

  • Defined career path and annual performance reviews
  • Diverse and inclusive workplace culture
  • Focus on innovation and process improvement
  • Opportunities for advancement within an expanding team
  • 152 hours of PTO plus 8 paid holidays
  • Generous 401K match available
  • Immediate medical, dental, and vision benefits on day one
  • Tuition reimbursement for educational advancement.
Full Job Description
Pharmaceutical Development Senior Associate Scientist I

Position Summary:

  • Work Schedule: 2nd shift Tuesday - Friday, 12pm-10pm
  • 100% on-site


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).

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.
  • All other duties as assigned.


The Candidate:
  • 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.
  • Physical Requirements: Ability to stand, walk, sit, use hands for manipulation, and reach with hands and arms for up to 8 hours per day; frequent sitting, standing, walking, reading written documents, and use of computer monitors; ability to wear a respirator (e.g., P100, PAPR); and occasional lifting and/or moving of up to 50 pounds.


Why You Should Join Catalent:
  • 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!


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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