Associate Scientist - Pharma

About the role

A fast-growing pharmaceutical research and manufacturing organization is expanding its R&D operations in Coral Springs, FL. We are seeking motivated Scientists and Associate Scientists (Levels I & II) to support formulation and analytical development for inhalation-based drug products, including MDI, DPI, and nasal spray formulations.

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.
• 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.

Requirements

• 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 strongly preferred.
• Solid understanding of GDP and deviation processes.
• Prior exposure to regulated audits (FDA, EMA, MHRA) is advantageous.
• Experience in method validation or transfer projects a plus.
• Strong analytical thinking, data review, and problem-solving skills.
• Excellent communication and teamwork abilities.
• High attention to detail, organization, and quality compliance.

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 strongly preferred.
• Solid understanding of GDP and deviation processes.

Skills

• Hands-on experience with chromatographic systems (HPLC, UPLC, GC).
• Good documentation practices (GDP).
• Data integrity standards.
• Empower software proficiency.
• Method validation or transfer projects experience.
• Analytical thinking, data review, and problem-solving skills.
• Excellent communication and teamwork abilities.
• Attention to detail, organization, and quality compliance.

Benefits

At ttg, we offer a competitive compensation package including a pay rate of $35 - $36 per hour, along with comprehensive benefits.

Pay

The pay rate for this position is $35 - $36 per hour.

Schedule

This role is available on a 1st Shift & 2nd Shift schedule.