Scientist, Quality Control

Catalent Pharma Solutions; Saint Petersburg (FL); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Tuition Reimbursement

Paid time off + holidays

Career development opportunities

Wellness programs

Job summary

Catalent in St. Petersburg, FL, is seeking a Scientist, Quality Control to join our team.

You will perform microbiological and analytical testing of finished products, raw materials, and validation samples, ensuring GMP compliance and accurate documentation. This onsite role requires a BA/BS in a related science, 5+ years in an analytical lab, and experience with HPLC/GC, infrared, and atomic absorption instrumentation.

Qualifications

• Bachelor of Arts or Bachelor of Science with college coursework in related sciences.
• 5+ years of experience in an analytical laboratory.
• Experience with Infrared and Atomic Absorption instrumentation.
• High-Performance Liquid Chromatography and Gas Chromatography instrumentation experience.
• Vision requirements and ability to work extended hours as needed.

Responsibilities

• Perform microbiological and analytical testing of finished products, raw materials, in-process materials, and validation samples.
• Conduct environmental and utility testing, including water, gases, and cleaning/process validation support.
• Maintain microbial cultures and prepare reagents and materials for testing.
• Interpret, document, and enter analytical results into notebooks, reports, logbooks, and the LIMS database.
• Support equipment qualification and preventive maintenance, calibration, and repairs.
• Follow GMP, safety, and environmental requirements, including hazardous/DEA waste handling.

Skills

Analytical laboratory experience

HPLC/GC instrumentation

IR spectroscopy

Atomic Absorption instrumentation

Interpersonal skills

Education

BA or BS in related sciences

Tools

Infrared spectroscopy

Atomic Absorption instrumentation

Job description

Scientist, Quality Control

About Site

St. Petersburg in the primary softgel development and manufacturing facility in North America. The site has the capability to develop lipid formulations in a dedicated pilot plant which supports rapid transition from laboratory scale to clinical supply. Liquid in bottle, as well as Liquid fill Hard shell capabilities at the facility provide diversification and offerings that increase the speed to clinic. Within the Catalent network, we offer a broad range of integrated formulation and analytical services to solve your most difficult development and manufacturing challenges. Our analytical laboratory provides a full service offering from development of analytical methods to routine QC testing, supporting commercial and development stability studies. With capacity to generate over 18 billion softgels per year and servicing over 100 markets globally, the St. Petersburg site can handle any Over the Counter (OTC), Prescription (Rx), Medical Device, Controlled Substance, or Dietary Supplement manufacturing needs. The facility also contains a segregated hormone manufacturing area that meets current regulatory requirements. In addition to the manufacturing of traditional animal based gelatin softgels, St. Petersburg site manufactures products in non-gelatin based OptiShell® and Vegicaps® to expand the range of molecules that can be encapsulated.

Position Summary

We have an opportunity for a Scientist, Quality Control to join our team. In this role, you will perform microbiological and analytical testing of finished products, raw materials, and validation samples. You will also conduct environmental and utility testing, maintain microbial cultures, and prepare necessary reagents and materials. This position involves interpreting and documenting results, supporting laboratory equipment activities, and ensuring compliance with GMP and safety requirements.

Shift: Standard Hours, Monday through Friday Location: St. Petersburg, FL 100% Onsite

The Role

• Perform microbiological and analytical testing of finished products, raw materials, in-process materials, and validation samples according to approved methods, protocols, and compendia.
• Conduct environmental and utility testing, including water, compressed gases, manufacturing environments, moisture, and cleaning/process validation support.
• Cultivate, isolate, and identify microorganisms using selective and non-selective media, Gram staining, API, and other identification techniques.
• Maintain microbial cultures in accordance with ATCC requirements and departmental Standard Operating Procedures.
• Prepare reagents, standards, media, and other materials required for laboratory testing.
• Interpret, document, and enter analytical results into approved notebooks, reports, logbooks, and the LIMS database.
• Support laboratory equipment activities, including qualification (Installation Qualification/Operational Qualification/Performance Qualification), training, preventive maintenance, calibration, troubleshooting, and repairs.
• Follow Good Manufacturing Practices, safety, regulatory, and environmental requirements, including hazardous/DEA waste handling and working with potent or teratogenic compounds; serve as Senior Scientist Designee when needed.
• Other duties as assigned.

The Candidate Minimum Requirements

• Bachelor of Arts or Bachelor of Science with college coursework in related sciences.
• 5+ years of experience in an analytical laboratory.
• Good interpersonal skills.
• Ability to effectively communicate with co-workers.
• Strong organizational skills.
• Experience with Infrared and Atomic Absorption instrumentation.
• High-Performance Liquid Chromatography and Gas Chromatography instrumentation experience.
• Individual may be required to sit, stand, walk regularly and occasionally lift up to 15 pounds; no lifting greater than 44.09 pounds without assistance.
• Be accessible to manufacturing, laboratory, and office staff.
• Ability to use required office equipment.
• Vision requirements include ability to differentiate color (Pass the Ishihara Color Vision Screening) and obtain 20/30 acuity in both far and near vision with or without corrective lenses.
• For Catalent’s in-house screening, the acceptable score is to identify at least 4 of 6 numbers in the circles.
• Ability to work extended hours or off-hours as required.

Preferred Skills & Background

• Experience with Ultraviolet spectroscopy.
• Experience with Infrared and Atomic Absorption instrumentation.
• High-Performance Liquid Chromatography and Gas Chromatography instrumentation experience.
• Experience with autoclave.

Why You Should Join Catalent

• Positive and fast-paced working environment focusing on continually improving processes to remain innovative and dynamic.
• Competitive Paid Time Off plus 8 paid holidays.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition Reimbursement – support to finish your degree or earn a new one.
• Employee Resource Groups focusing on Diversity and Inclusion.
• Environmentally friendly, community engagement green initiatives including regularly participating in Beach Clean-up.
• Defined career path and annual performance review and feedback process with potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
• WellHub program to promote overall physical and mental wellness.
• Perkspot offers exclusive or private discounts from approximately 900+ merchants in a wide array of categories.
• Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world.
• Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market.
• Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
• Join us in making a difference. personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer, including disability and veterans. If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to [e-mail]. This option is reserved for individuals who require accommodation due to a disability.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life‑cycle supply. With time-tested experience in development sciences, delivery technologies, and multi‑modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life‑enhancing and life‑saving treatments for patients annually.