Quotient Sciences · 1 day ago
Staff Formulator
Garnet Valley, PA
Full-time
Onsite
Senior Level, Lead/Staff
1+ years expQuotient Sciences is a leading drug development and manufacturing accelerator, helping biotech and pharma companies bring new medicines to patients faster. The Staff Formulator will be responsible for formulating oral solid dosage forms for clinical trials, developing various formulations, and collaborating with clients to ensure high-quality results.
Clinical TrialsCommercialConsultingHealth CareManufacturingMedicalPharmaceutical
Hiring Manager
Katrina Simpson
Responsibilities
Formulate oral solid dosage forms in a dynamic contract manufacturing setting
Develop a wide array of formulations, including both immediate and modified release, for Phase I–III clinical trials
Conduct pre-formulation, formulation, and manufacturing process development and optimization for various solid dosage forms
Collaborate directly with clients to deliver high-quality results within ambitious project timelines
Author essential documentation including product specifications, process validation protocols, batch records, and developmental reports
Work cross-functionally with QA and Analytical Development teams to ensure seamless product delivery
Manufacture and package clinical supplies under CGMP standards for Phase I–III trials
Train and mentor manufacturing scientists and technicians
Qualification
Required
Hands-on experience with immediate release, modified release, solid oral dosage forms, and high-potency formulations
Solid understanding of federal and state regulations including FDA, EPA, OSHA, and DEA
Strong grasp of chemical components, theories, and solid oral production processes
Proficiency in Microsoft Office Suite
Ability to interpret safety rules, operating procedures, and SOP manuals
Skilled in writing reports, business correspondence, and SOPs
Competence in applying mathematical operations to tasks such as frequency distribution, test reliability, analysis of variance, and sampling theory
Analytical mindset to define problems, collect data, and draw valid conclusions
Ability to interpret technical instructions and manage abstract and concrete variables
Commitment to safety in hazardous environments, with effective use of instruments, equipment, and technology
Preferred
Master's degree in Pharmaceutical Science, Chemical Engineering, or a related field with 1–2 years of industry experience preferred
Alternatively, a Bachelor's degree in Chemistry or a related field with 3 years of relevant experience
Benefits
Impactful Work: Play a key role in developing life-changing medications for clinical trials across Phases I–III.
Innovation-Driven Culture: Work on diverse and challenging formulations, from immediate to modified release, using cutting-edge technologies.
Client-Facing Opportunities: Build strong relationships with industry-leading clients and contribute to high-profile projects.
Professional Growth: Benefit from ongoing training, mentorship, and opportunities to expand your skills and advance your career.
Cross-Functional Collaboration: Partner with experts in QA, Analytical Development, and Manufacturing to deliver high-quality products.
Commitment to Excellence: Operate in a CGMP-compliant environment with a strong focus on safety, quality, and regulatory standards.
Company
Quotient Sciences
Quotient Sciences provides formulation development, clinical pharmacology, clinical & commercial manufacturing services.
1001-5000 employees
Funding
Current Stage
Late StageTotal Funding
$35MKey Investors
TA Associates
2019-07-18Acquired
2008-09-03Private Equity· $35M
Leadership Team
Thierry Van Nieuwenhove
Chief Executive Officer
Recent News
FierceBiotech
2025-12-20
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