Find Jobs
Find Jobs Near You – Available Work in Your Location
Associate Scientist - Pharmaceutical Industry
Career Insights for Quality Control Analyst
See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.
Scorecard
Based on Florida data
Review key factors to help you decide if this role fits your goals. How is this calculated?
What they do
A Quality Control Analyst, in the biotech and medical device industries, works in laboratories performing biological, microbiological, and chemical tests on products and materials. Responsible for calibrating equipment, inspecting products, processing and testing materials, and reporting results. May work in other production environments to monitor and improve quality and efficiency in production systems and products.
$64,742 / year median in Florida
-13% projected decline
Job Description
Pharmaceutical Industry Location:
Broward County, FL Type of Work:
In Office Schedule:
1st Shift & 2ndShift Type of Contract:
Temp toPerm Pay Rate:
$30/h - $35/h depeding of experience Description ttg Talent Solutions is seeking an Associate Scientist to support a pharmaceutical company. This is a hands-on laboratory opportunity within a GMP-regulated pharmaceutical environment. The ideal candidate will have recent experience in the pharmaceutical industry, supporting analytical testing, documentation, data review, and laboratory activities related to raw materials, in-process samples, finished products, or stability samples. This role is best suited for junior to mid-level candidates with pharmaceutical laboratory experience. Please note that relocation assistance is not provided; candidates must be local or able to commute/relocate independently. Responsibilities and Duties Perform routine analytical testing of raw materials, in-process samples, finished products, and/or stability samples. Support laboratory testing using instruments such as HPLC, UPLC, GC, UV-Vis, FTIR, or similar analytical equipment. Follow approved SOPs, test methods, protocols, and laboratory procedures. Maintain accurate and complete laboratory documentation in compliance with GDP and data integrity requirements. Support sample preparation, testing execution, data entry, and basic data review. Assist with troubleshooting laboratory testing issues, instrument issues, or unexpected results. Support investigations related to deviations, OOS/OOT results, CAPA, or testing abnormalities as needed. Participate in method verification, method transfer, or validation activities when assigned. Collaborate with Quality, Manufacturing, Regulatory, and R D teams to support compliant laboratory operations. Maintain a clean, safe, and compliant laboratory environment according to GMP and company procedures. Requirements Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biochemistry, Biology, or a related scientific field. Recent experience working in the pharmaceutical industry is required. Hands-on experience with Empower chromatography data system is required. Hands-on laboratory experience in a GMP or regulated environment. Experience with analytical testing and laboratory documentation. Experience with HPLC, UPLC, GC, UV-Vis, FTIR, or similar instruments preferred. Experience testing raw materials, in-process samples, finished products, or stability samples preferred. Knowledge of GMP, GLP, GDP, SOPs, and data integrity principles. Must be authorized to work in the United States. Skills Empower chromatography data systemHPLC / UPLC / GC GMP
laboratory documentation Analytical testing Raw material, in-process, finished product, and stability testing Data integrity and GDP 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.Tipo de puesto:
Tiempo completoSueldo:
$30.00 - $35.00 la hora Horas previstas: 40.0 por semana Pregunta(s) de postulación: Have you used Empower chromatography data system in a professional laboratory setting? Which instruments have you used hands-on: HPLC, UPLC, GC, UV-Vis, FTIR? Please specify which ones and how recently. Have you tested raw materials, in-process samples, finished products, or stability samples in a pharma environment? Do you have recent hands-on experience working in a pharmaceutical GMP laboratory? How many years?Lugar de trabajo:
Empleo presencialBenefits
- Dental Insurance