Job Description
*Job Title: Scientist / Associate Scientist – Formulation & Analytical *
*Location:* Coral Springs, FL
*Type of Work:* On-Site
*Schedule:* Second Shift (2:00 p.m. – 11:00 p.m.)
*Type of Contract:* Temp-to-Perm
*Pay Rate:* Competitive – commensurate with experience and technical proficiency
*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 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.
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 strongly preferred.
* Solid understanding of *GDP. *CAPA and deviation processes is a PLUS but not required.
*Preferred Attributes*
* 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.
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.
At ttg, ‘We believe in making a difference One Person at a Time,’ ttg OPT.
#INDR
Job Type: Full-time
Pay: From $30.00 per hour
Expected hours: 40 per week
Benefits:
* 401(k)
* Dental insurance
* Health insurance
* Paid time off
* Vision insurance
Application Question(s):
* Please, write your email here to complete your application:
Education:
* Bachelor's (Preferred)
Experience:
* hands-on GMP regulated laboratory environment: 2 years (Required)
* operating analytical instruments (HPLC or GC): 2 years (Preferred)
Location:
* Coral Springs, FL (Required)
Shift availability:
* Night Shift (Preferred)
Work Location: In person
Job Tags
Hourly pay, Permanent employment, Full time, Contract work, Temporary work, Shift work, Night shift, Afternoon shift,