Associate Scientist

ttg Talent Solutions; Fort Lauderdale (FL); On-site; USD 65,000 - 95,000; Full time

Job summary

ttg Talent Solutions is seeking motivated Associate Scientists to support formulation and analytical development for inhalation drug products in Coral Springs, FL. These are hands-on GMP-regulated lab roles demanding strong documentation and attention to detail.

Candidates will perform analytical testing (HPLC/UPLC/GC/UV/FTIR), develop formulations, manage data in Empower, prepare protocols and reports, and contribute to method transfer, validation, and CAPA investigations.

Qualifications

• Hands-on GMP laboratory experience required; academic-only work not eligible.
• Experience with chromatographic systems (HPLC/UPLC/GC) and analytical testing.
• Knowledge of GMP/GLP, USP, ICH, and FDA expectations.
• Experience with Empower data acquisition and reporting.
• GDP and deviation processes understanding.
• Excellent communication and teamwork skills.

Responsibilities

• Perform routine and advanced analytical testing of materials, in-process, and finished products in GMP.
• Support the development of formulations for inhalation drug products (solutions, suspensions, propellant-based systems).
• Operate and troubleshoot analytical instruments including HPLC, UPLC, GC, UV, and FTIR; manage data through Empower software.
• Prepare and review protocols, reports, and SOPs per quality and regulatory requirements.
• Ensure documentation complies with GDP and data integrity standards.
• Participate in method transfer, verification, and validation activities.

Skills

Analytical testing

Documentation

Attention to detail

Communication

Education

PhD/MS/BS in Analytical Chemistry/Pharmaceutics/Pharmaceutical Sciences/Biochemistry

Tools

HPLC

UPLC

GC

UV

FTIR

Empower software

Job description

Pay Rate: Competitive – commensurate with experience and technical proficiency

About the Opportunity

A fast-growing pharmaceutical research and manufacturing organization is expanding its R&D operations in Coral Springs, FL. We are seeking motivated Associate Scientists to support formulation and analytical development for inhalation-based drug products.

These are hands-on laboratory roles in a GMP-regulated environment. Successful candidates will demonstrate strong documentation skills (GDP), attention to detail, and the ability to perform and review analytical work with minimal supervision.

This is an excellent opportunity to be involved in pre-formulation, formulation, analytical method development, data interpretation, troubleshooting, and continuous improvement initiatives.

Key Responsibilities

• Perform routine and advanced analytical testing of raw materials, in-process, and finished products in compliance with GMP.
• Support the development of formulations (solutions, suspensions, propellant-based systems) for inhalation drug products.
• Operate and troubleshoot analytical instruments including HPLC, UPLC, GC, UV, and FTIR, and manage data through Empower (Waters) software.
• Prepare and review protocols, reports, and SOPs in alignment with quality and regulatory requirements.
• Ensure all documentation complies with Good Documentation Practices (GDP) and data integrity standards.
• Participate in method transfer, verification, and validation activities as assigned.
• Support investigations of OOS/OOT, deviations, and CAPA with accurate analytical input.
• Collaborate cross-functionally during manufacturing trials and scale-up activities.
• Mentor junior scientists and contribute to the team’s technical development.
• Maintain a safe and compliant laboratory environment in accordance with EH&S and corporate policies.

Qualifications

• PhD, MS, or BS in Analytical Chemistry, Pharmaceutics, Pharmaceutical Sciences, Biochemistry, or related discipline.
• Minimum 1 year of hands-on GMP laboratory experience (academic-only exposure will not be considered).
• Proven hands-on experience with chromatographic systems (HPLC, UPLC, GC) and analytical testing.
• Working knowledge of GMP/GLP, USP, ICH, and FDA regulatory expectations.
• Experience with Empower software for data acquisition and reporting
• Solid understanding of GDP and deviation processes.
• Prior exposure to regulated audits (FDA) is advantageous.
• Experience in method validation or transfer projects a plus.
• Excellent communication and teamwork abilities.
• High attention to detail, organization, and quality compliance.

ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees.