Associate Scientist - Pharma

ttg Talent Solutions, Inc.; Fort Lauderdale (FL); On-site; USD 48,000 - 50,000; Full time

Job summary

ttg Talent Solutions, Inc. seeks an Associate Scientist - Pharma to join a fast-growing pharmaceutical research and manufacturing organization in Coral Springs, FL.

The role is on-site and focuses on formulation and analytical development within a GMP-regulated environment. The position involves hands-on laboratory work in pre-formulation, formulation, analytical method development, data interpretation, troubleshooting, and continuous improvement initiatives.

Qualifications

• Minimum 1 year of hands-on GMP laboratory experience.
• Proven 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.

Responsibilities

• Perform routine and advanced analytical testing of materials and products per GMP.
• Support development of formulations for inhalation drug products.
• Operate and troubleshoot analytical instruments (HPLC, UPLC, GC, UV, FTIR) and manage data in Empower.
• Prepare and review protocols, reports, and SOPs to quality standards.
• Ensure documentation complies with GDP and data integrity requirements.
• Collaborate with cross-functional teams on manufacturing trials and scale-up.

Skills

Analytical testing

GDP

Data review

Problem solving

Teamwork

Communication

Education

PhD/MS/BS in Analytical Chemistry

Tools

HPLC

UPLC

GC

UV

FTIR

Empower

Job description

Associate Scientist -Pharma
Location:Coral Springs, FL 33065
Type of Work:On-Site
Schedule: 1st Shift & 2nd Shift
Type of Contract:Temp-to-Perm
Pay Rate:$35 - $36 per hour
Department:Research & Development - Analytical & Formulation
About the Opportunity
A fast-growing pharmaceutical research and manufacturing organization is expanding its R&D operations in Coral Springs, FL. We are seeking motivatedScientists and Associate Scientists (Levels I & II)to support formulation and analytical development for pharmeutical products.
These arehands-on laboratory rolesin a GMP-regulated environment. Successful candidates will demonstratestrong 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 inpre-formulation, formulation, analytical method development, data interpretation, troubleshooting, and continuous improvement initiatives.
Key Responsibilities

• Perform routine and advancedanalytical testingof raw materials, in-process, and finished products in compliance withGMP.
• Support thedevelopment of formulations(solutions, suspensions, propellant-based systems) for inhalation drug products.
• Operate and troubleshootanalytical instruments includingHPLC, UPLC, GC, UV, and FTIR, and manage data throughEmpower (Waters)software.
• Prepare and reviewprotocols, reports, and SOPsin alignment with quality and regulatory requirements.
• Ensure all documentation complies withGood Documentation Practices (GDP)anddata integrity standards.
• Participate inmethod transfer, verification, and validationactivities as assigned.
• Support investigations ofOOS/OOT, deviations, and CAPAwith accurate analytical input.
• Collaborate cross-functionally duringmanufacturing trials and scale-upactivities.
• Mentor junior scientists and contribute to the team's technical development.
• Maintain asafe and compliant laboratory environmentin accordance with EH&S and corporate policies.

Qualifications

• PhD, MS, or BSin 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).
• Provenhands-on experience with chromatographic systems (HPLC, UPLC, GC)and analytical testing.
• Working knowledge ofGMP/GLP, USP, ICH, andFDA regulatory expectations.
• Experience withEmpower softwarefor data acquisition and reporting strongly preferred.
• Solid understanding ofGDP and deviation processes.

Preferred Attributes

• Prior exposure toregulated audits (FDA, EMA, MHRA)is advantageous.
• Experience inmethod validation or transfer projectsa plus.
• Strong analytical thinking, data review, and problem-solving skills.
• Excellent communication and teamwork abilities.
• High attention to detail, organization, and quality compliance.

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.