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Pharma Associate Jobs in Florida (NOW HIRING)

Pharmacy Contract Consultant

Tampa, FL · On-site

$79K - $98K/yr

This role requires associates to be in-office 1-2 days per week, fostering collaboration and ... The role is responsible for the review, red-lining, and documentation of pharma contract language ...

This role requires associates to be in-office 1-2 days per week, fostering collaboration and ... The role is responsible for the review, red-lining, and documentation of pharma contract language ...

Pharmacy Contract Consultant

Tampa, FL · On-site

$79K - $98K/yr

This role requires associates to be in-office 1-2 days per week, fostering collaboration and ... The role is responsible for the review, red-lining, and documentation of pharma contract language ...

This role requires associates to be in-office 1-2 days per week, fostering collaboration and ... The role is responsible for the review, red-lining, and documentation of pharma contract language ...

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Showing results 1-20

Pharma Associate information

What does a Pharma Associate do?

A Pharma Associate typically supports pharmaceutical operations, which may include working in research, development, quality assurance, regulatory affairs, or sales. Their responsibilities can involve assisting with clinical trials, ensuring compliance with regulations, preparing documentation, and collaborating with various teams to help bring pharmaceutical products to market. The specific duties of a Pharma Associate can vary depending on the department and company, but the role generally requires attention to detail and strong organizational skills. This position is often an entry-level step into the pharmaceutical industry, offering the opportunity to learn about drug development and regulatory processes.

What are the key skills and qualifications needed to thrive as a Pharma Associate?

To thrive as a Pharma Associate, you need a solid understanding of pharmaceutical products, regulatory compliance, and sales or customer service, often supported by a degree in pharmacy, life sciences, or a related field. Familiarity with CRM software, pharmaceutical databases, and knowledge of industry regulations such as FDA or EMA guidelines are typically required. Strong communication, relationship-building, and organizational skills help you effectively engage clients and manage multiple tasks. These skills are crucial for ensuring accurate information delivery, regulatory adherence, and successful client partnerships in a competitive industry.

What degree do I need for pharmaceutical associate jobs?

Pharmaceutical associate jobs typically require at least a high school diploma or equivalent; however, many employers prefer candidates with a bachelor's degree in pharmacy, chemistry, biology, or a related field. Relevant certifications or training in pharmaceutical procedures and good manufacturing practices can also be beneficial.

What are the most commonly searched types of Pharma jobs in Florida?

The most popular types of Pharma jobs in Florida are:

What job categories do people searching Pharma Associate jobs in Florida look for?

The top searched job categories for Pharma Associate jobs in Florida are:

What cities in Florida are hiring for Pharma Associate jobs?

Cities in Florida with the most Pharma Associate job openings:

Infographic showing various Pharma Associate job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 26% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Associate Scientist - Pharma

ttg Talent Solutions

Coral Springs, FL

$35 - $36/hr

Other

Posted 28 days ago


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 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 and deviation processes.

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.
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