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Pharmaceutical Research Associate, Product Development

Catalent Pharma Solutions

San Diego, CAOnsitePosted 11 days ago$31.25 - $32.21/hour
InternshipInternResearch & ScientistCDMO
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Summary

Work Schedule: Monday-Friday between 8am-5pm, 100% on-site (San Diego). Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic, offering services that support oral and injectable dosage forms including preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution.

Job description

Position Summary

Work Schedule: Monday-Friday between 8am-5pm, 100% on-site (San Diego). Catalent's San Diego facility focuses on early-stage development of small molecule and peptide drug candidates from the bench to the clinic, offering services that support oral and injectable dosage forms including preformulation testing, formulation and analytical development, cGMP manufacturing and clinical packaging, labeling, and worldwide distribution.

Catalent Pharma Solutions is hiring a Lab Assistant (Intern) for multiple departments on our San Diego, CA team. Through guided mentorship, the Student Lab Intern program offers students a fun and stimulating environment to gain lab experience and exposure to pharmaceutical chemistry development. Lab Assistants will have the opportunity to learn analytical chemistry techniques such as volumetric analysis, spectroscopy, and liquid chromatography.

An individual at the level of Pharmaceutical Research Associate will be expected to understand and execute basic formulation and characterization procedures in order to develop preclinical and human clinical drug products under supervision. This candidate is expected to have attained experience in solid state characterization techniques necessary for the development of oral solid dosage form drug products. This is a student internship.

The Role

  • Conduct physical characterization activities of solid-state materials for the purpose of downstream drug development activities.
  • Leverage previous experience in polymer science to conduct formulation development and drug product characterization activities under supervision.
  • Prepare reports, summaries, protocols, batch records, and quantitative analyses.
  • Clear and accurate record keeping in laboratory notebooks.
  • Impact of decisions limited to their personal workload.
  • Limited client interaction will be supported by supervisor.
  • Development of problem-solving skills for experimental outcomes.
  • Experimental design and execution will be under a supervisor's direction.
  • Training on scientific techniques, CMC strategy, GMPs, and ICH Guidance is emphasized.
  • Comply with good housekeeping and safety practices.
  • Personnel management is not expected.
  • Other duties as assigned.

The Candidate

  • Must be currently enrolled in a Graduate program.
  • Requires a Bachelors degree in Chemical, Physical, Pharmaceutical or Biological and at least one year of experience with basic formulation or laboratory techniques.

Physical Requirements

On an average day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk and hear, smell and lift up to 25 pounds. Specific vision requirements including reading of written documents, visual inspection of materials and use of computer monitor screen frequently.

Requirements

  • Currently enrolled in a Graduate program
  • Bachelors degree in Chemical, Physical, Pharmaceutical or Biological
  • At least one year of experience with basic formulation or laboratory techniques
  • Experience in solid state characterization techniques
  • Experience in polymer science

Benefits

  • On-site Fitness Center
  • Yoga Classes
  • HIIT Classes
  • Sponsored Sports Teams
  • Employee Resource Groups
  • Diversity & Inclusion Programs
  • Movie Day
  • Monthly Birthday Celebrations
  • Friday Bagel Breakfast
  • Beach Clean-up Activities

Company overview

Catalent Pharma Solutions, now known as Catalent, Inc., is a leading global contract development and manufacturing organization (CDMO) headquartered in Tampa, Florida. Founded in 2007 as a spin-off from Cardinal Health's pharmaceutical technologies segment, the company has grown into a major player in the pharmaceutical services industry. Catalent provides comprehensive drug development and manufacturing solutions including drug delivery technologies, formulation development, analytical testing, clinical and commercial manufacturing, clinical packaging, and supply chain services. The company operates over 50 facilities across four continents and has supported more than half of all FDA-approved products over the past decade. With approximately 16,900 employees, Catalent produces over 70 billion doses annually for more than 8,000 products, serving major pharmaceutical companies like Pfizer, Moderna, Novo Nordisk, and Bristol-Myers Squibb. In 2024, the company was acquired by Novo Holdings A/S for $16.5 billion, further strengthening its position in the global pharmaceutical manufacturing landscape.

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