Catalent Pharma Solutions Inc

Scientist 1, Analytical Development

Catalent Pharma Solutions Inc • $78K — $85K *
San Diego, CA 92154In-Person
Pharmaceuticals & Biotech
Less than 5 years of experience
Today
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Job Overview by Ladders

Qualifications

  • Bachelor's degree in Science required; Master's degree considered with no prior industry experience
  • Minimum 1 year of experience in analytical development, or 2 years preferred with a Master's degree
  • Proficiency with HPLC, UPLC, GC, and other analytical techniques
  • Experience with physical characterization methods such as TGA, DSC, and PXRD
  • Familiarity with GMP regulations and technical writing skills

Responsibilities

  • Independently perform laboratory experiments related to analytical methods
  • Train others in various analytical techniques and laboratory practices
  • Develop and execute cleaning verification methods and compatibility studies
  • Troubleshoot and optimize methods for characterizing drug products
  • Conduct qualification studies with some complexity requiring supervisor assistance
  • Interact with clients to discuss project-related technical topics
  • Maintain accurate records and review colleagues' work for compliance

Benefits

  • Engaging employee activities including fitness programs and team events
  • Eco-friendly initiatives and community engagement opportunities
  • Defined career advancement pathways with feedback processes
  • Employee Resource Groups promoting diversity and inclusion
  • Comprehensive benefits starting from day one, including health insurance
  • Generous PTO policy including holidays
  • Tuition reimbursement program
  • Wellness initiatives through WellHub program
  • Discounts through Perkspot for various merchants
Full Job Description
Scientist 1, Analytical Development

Position Summary:

  • Work Schedule: Monday-Friday, core hours 8am-4:30pm
  • 100% on-site (San Diego)


The Scientist 1 in our Analytical Development group will independently plan and execute simple laboratory experiments and clearly communicate the status of projects to cross-functional team members, management, and clients. This individual will support the qualification of analytical test methods for Active Pharmaceutical Ingredients (API), intermediates, and final drug products using a variety of chromatography techniques (H/UPLC, GC), physical characterization techniques (TGA, DSC, PXRD, GVS, SEM) and dissolution/water content methods. You will be a key member of a multi-site mission to deliver unparalleled service to our clients and quality drug products to the patients.

The Role:

  • Perform and train others on a variety of analytical techniques including, but not necessarily limited to: analytical balances, pH meters, high performance liquid chromatography (HPLC/UPLC), UV/Vis spectroscopy, Gas Chromatography (GC), USP dissolution testing apparatus, moisture analysis by Karl Fischer, disintegration, Pion µdiss, DSC, TGA, PSD, PXRD, SEM, hardness, and friability testing
  • Develop cleaning verification methods and execution of excipient compatibility and forced degradation studies, under supervision
  • Troubleshoot and optimize analytical methods for characterization of drug products and intermediates
  • Perform qualification studies to determine if methods are suitable for transfer to Quality Control. Simple experimental design and execution will be performed independently. Complex design may need supervisor assistance
  • Data interpretation should be conducted with limited guidance. Individuals will be able to identify key factors from data and understand the importance of the findings. Clear and accurate record keeping in laboratory notebooks and some secondary review of other colleagues' work for scientific accuracy and compliance
  • Increase in client interaction will be a focus. Individuals may lead discussions with clients on technical topics relating to their project
  • Individuals should have a good general foundation of scientific principles, chemistry concepts, and be proficient in core analytical scientific techniques, GMPs, and technical writing
  • Other duties as assigned.


The Candidate:

  • Bachelor's of Science degree is required plus a minimum of one (1) year of analytical development experience
  • We will also accept a Master's of Science without any formal industry experience, but highly preferred to have two (2) years of experience in analytical development
  • The individual must have demonstrated proficiency in the qualification of analytical test methods for API, intermediates, and final drug products, particularly HPLC and UPLC stability-indicating assays, GC, dissolution methods, and water content methods. The individual should also have experience in physical characterization techniques such as TGA, DSC, PXRD, GVS, and SEM. The individual will be responsible for developing product-specific cleaning methods to support use of GMP manufacturing equipment
  • Physical Requirements: Individual needs to be accessible to lab and office staff and able to use required office equipment. Specific vision requirements include reading of written documents and use of computer monitor screen frequently


Pay:

  • The anticipated salary range for this role in California is $78,000 to $85,000 annually. The final salary offered to a successful candidate may vary, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a multi-state employer, and this salary range may not reflect positions that work in other states.


Why you should join Catalent:

  • Awesome employee activities: Movie Day, Monthly Birthday Celebrations, Friday Bagel Breakfast, On-site Fitness Center with machines, Sponsored Sports Teams, and several other company-sponsored events that encourages positive employee comradery, which contributes to effectively building positive employee relationships, overall creating a positive work environment.
  • Environmentally friendly green initiatives with on-site practices as well as regularly participating in Beach Clean-up activities for community engagement.
  • Defined career path and annual performance review and feedback process. Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
  • Several Employee Resource Groups focusing on Diversity and Inclusion.
  • Competitive salary with bonus potential. Generous 401K match and Paid Time Off accrual. Medical, dental and vision benefits effective day one of employment.
  • 152 hours of PTO + 10 paid holidays.
  • Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic.
  • Tuition Reimbursement - Let us help you finish your degree or earn a new one!
  • WellHub program to promote overall physical wellness.
  • Perkspot - offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.


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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