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Catalent · 4 days ago

Associate Scientist I, Product Development

St. Petersburg, FL

Full-time

Onsite

New Grad, Entry Level

0+ years exp

Catalent is a global leader in drug development and delivery, and they are seeking an Associate Scientist I within Production Development. This role involves executing formulation and process development activities for new pharmaceutical products, ensuring timely completion of laboratory activities and supporting compliance with operational standards.

BiotechnologyHealth CareManufacturingPharmaceutical

H1B Sponsor Likely

Responsibilities

Conduct pre-formulation, formulation preparation, testing, and analytical work within the Production Development (PD) laboratory

Plan, schedule, and execute laboratory activities to ensure timely completion of assigned development work

Perform formulation and material studies, including solubility, compatibility, drying studies, gel swatches, laboratory fill mixes, and air-filled capsules

Execute physical, chemical, and performance testing, including fill moisture, water activity, hardness, rheology, burst strength, impact/drop testing, disintegration, dissolution, and related analyses

Perform HPLC analysis and prepare buffers, mobile phases, and dissolution media as required

Document experimental procedures and results in approved notebooks, batch records, reports, and logbooks; prepare samples for animal PK studies

Support lab operations and compliance, including training personnel, following SOPs and departmental guidance, maintaining training records, and adhering to Health, Safety, and Environmental requirements

Other duties as assigned

Qualification

Softgel formulationHPLC analysisGMP laboratory experienceScientific documentationScientific principlesComputer software proficiencyAttention to detailOrganizational skills

Required

Associate in Science (AS) degree in scientific field with 5 years of experience in GMP laboratory or Bachelor of Science (BS) in a scientific field with 0 year of experience

Strong scientific skills required

Working knowledge and application of scientific principles and techniques

Exposure to computer software associated with word processing and spreadsheets required

Must have accurate and legible documentation skills

Attention to detail and high-level of organizational skills required

Individuals are required to sit, stand, walk, stoop, kneel, crouch regularly and lift to 15 pounds; no lifting greater than 44.09 pounds without assistance

Vision requirements include ability to differentiate color, have 20/30 vision with or without corrective lenses, read written documents and frequent use of a computer monitor

Benefits

Tuition reimbursement to support educational goals

WellHub program to promote physical wellness & Access to Perkspot discounts from over 900 merchants

152 hours of PTO plus 8 paid holidays

Medical, dental, and vision benefits effective day one

Defined career path with annual performance reviews & strong potential for career growth within a mission-driven organization

Inclusive culture with active Employee Resource Groups & Community engagement and green initiatives

Company

Catalent

Catalent - Blow-Fill-Seal Sterile CDMO Business is focusing on complex clinical to commercial stage formulation and manufacturing. It is a sub-organization of Catalent Pharma Solutions.

Founded in 2007

Somerset, New Jersey, USA

10001+ employees

https://www.catalent.com

H1B Sponsorship

Catalent has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)

Distribution of Different Job Fields Receiving Sponsorship

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Trends of Total Sponsorships

2022 (1)