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Formulation Scientist; Largo, FL

Job in Largo, Pinellas County, Florida, 34640, USA
Listing for: Cedent Consulting Inc.
Full Time position
Listed on 2026-01-02
Job specializations:
  • Engineering
    Quality Engineering, Research Scientist
Salary/Wage Range or Industry Benchmark: 70000 - 90000 USD Yearly USD 70000.00 90000.00 YEAR
Job Description & How to Apply Below
Position: Formulation Scientist (Largo, FL)

PRIMARY PURPOSE

The I&D Formulator III will have responsibilities for the design, development, testing and implementation of new formulations from initial concept through production; troubleshooting/resolving, adjusting or reformulating existing formulas as needed. This individual must have extensive cGMP experience and FDA and ICH Guidance experience. Must be able to provide leadership and mentoring to I&D Interns, Associates, and Formulator I(s).

MAJOR DUTIES AND RESPONSIBILITIES
  • Supports efforts to brainstorm new customer concepts based on personal experience, market insights, competitive position, online research, technology/market trends, etc.
  • Develops new products to meet customer requirements per assigned projects.
  • Works to proactively prioritize multiple projects/workload, effectively anticipate/manage resource gaps, and deliver on agreed‑to timelines.
  • Develops new product ideas for presentation to Marketing for future consideration in customer innovation events.
  • Prepares samples for customer evaluation or for use by Marketing, Project Management, Engineering, QC/QA.
  • Actively assists in the troubleshooting of off‑target batches in the I&D Lab.
  • Prepares protocols for both formal and informal stability testing.
  • Accurately records raw data and analyzes, as well as calculates and interprets the results. Ensures all documentation produced is in compliance with cGMP standards.
  • Communicates effectively in verbal and written form on research results and plans.
  • Demonstrates initiative in handling responsibilities.
  • Attends project meetings and prepares project updates.
  • Develops working relationships with vendors and attends vendor meetings.
  • Maintains raw material supply in I&D laboratory including but not limited to: vendor sample inventory, in-house sample inventory.
  • Promotes cGMP and safety practices throughout the facility.
  • Promotes continuous improvement and customer satisfaction.
  • Recognizes OOS or out of trend results and assists in the completion of lab investigations.
  • Reads and understands SDSs for all raw materials they will be working with.
  • Responsible and accountable for compliance with all aspects of the company's Health and Safety policies, and Safe Work Procedures.
  • Works to identify more efficient ways of working and shares ideas with management.
  • Prepare and present technical presentations
  • Participates in other activities as assigned by the I&D Manager or VP of I&D.
QUALIFICATION
  • Responsible for contributing to audit readiness and for assisting in quality audits with FDA, other Regulatory Agencies, and customers, as needed.
  • Working knowledge of FDA regulation for drug/device especially for the lab.
  • Ability to use a personal computer and peripheral equipment to accurately enter and analyze data and produce reports.
  • Knowledge of chemical safety and personal protective equipment.
  • Proficient in approaches to aerosol and/or emulsion blending, chemistry and troubleshooting.
  • Advanced knowledge of various analytical equipment and techniques utilized in an analytical laboratory including but not limited to pH, viscosity, specific gravity, infrared spectroscopy, HPLC, GC, atomic absorption.
  • Demonstrated ability to represent the I&D technical function in cross‑functional team meetings.
  • Ability to establish priorities, work independently, productively and proceed with objectives without supervision.
  • Ability to handle and resolve recurring problems.
  • Communicates effectively in verbal and written form on projects and research results.
  • Ability to work in a dynamic fast‑paced—sometimes rapidly shifting environment and quickly establish priorities. Ability to concentrate in such an environment and perform quality work.
  • Contributes to overall lab safety, organization, cleanliness, calibration, and maintenance.
  • Strong leadership and mentoring skills.
  • Must be able to lift up to 15 pounds.
Preferred Additional
  • Aerosol formulation experience strongly preferred.
  • Regulated products formulation experience strongly preferred.
CRITICAL

SKILLS AND ABILITIES
  • Advanced knowledge of benchtop and production scale emulsion chemistry.
  • Familiarity with aerosol chemistry and delivery systems.
  • Ability to independently generate formulas for experimental blending.
  • Demonstrated ability to work both independently and in a team environment.
COMPUTER SKILLS
  • Familiarity with the use of MS Word, MS Excel, MS Access.
EDUCATION AND/OR TRAINING
  • Bachelor’s degree in Chemistry or appropriate discipline with 5+ years related experience in the personal care or pharmaceutical industry.
  • OR MS in Analytical Chemistry or equivalent with 3+ years related experience in a pharmaceutical industry a strong plus.
Environmental Demands
  • Exposure to chemicals and/or other potential hazards.
  • Exposure to loud noises.
  • Moving machines and robots.
  • Self‑starting machinery.
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