Associate Scientist

Transpire BIO Inc. • Weston, FL

9d • $28 - $38 • Onsite

About The Position

The Associate Scientist I conducts laboratory testing and manufacturing support activities with limited supervision. The role analyzes raw materials, in-process materials, and finished pharmaceutical products in accordance with cGMP, FDA, EH&S, SOP, and corporate requirements. It supports manufacture of inhalation drug products, method transfers, equipment qualification, project timelines, and team objectives. The position requires accurate laboratory documentation, analytical problem-solving, and effective collaboration. It is a one-year temporary/contract role, with a possibility of conversion to full-time based on performance, contribution, and other factors. The position is on-site during second shift. Applicants must be eligible to work in the United States without visa sponsorship or transfer.

The company is a fast-growing pharmaceutical startup focused on innovation and improving patient outcomes. The role offers hands-on experience in a growing pharmaceutical business, exposure to various functions, career-development opportunities, and a collaborative and supportive work environment.

Requirements

• BSc in Chemistry, Pharmacy, or a related field.
• 0–2 years of experience.
• Computer literacy and familiarity with analytical and/or process equipment used in laboratories, such as HPLC, IR/FTIR, UV-Vis AA, or powder blenders.
• Effective written and oral English communication skills.
• Eligibility to work in the United States without visa sponsorship or visa transfer.
• Willingness to work on-site during second shift.

Responsibilities

• Analyze raw materials, in-process materials, and finished pharmaceutical products for quality, safety, purity, strength, and identity using applicable methods, following cGMP, EH&S, corporate, FDA, and other governing-body requirements.
• Set up and operate laboratory equipment; prepare reagents, solvents, and solutions for analytical and formulation activities.
• Maintain accurate laboratory notebook records of tests performed.
• Process analytical data using laboratory equipment such as HPLC/UPLC, enter data in spreadsheets, and perform routine calculations.
• Support the manufacture of inhalation drug products and prepare samples for blend uniformity as required.
• Participate in project team activities, support project timelines, and contribute to team objectives.
• Establish and maintain effective relationships with team members.
• Conduct laboratory work in accordance with SOPs and STPs and follow corporate health and safety rules and procedures.
• Comply with corporate guidelines and policies.
• Support method transfers and equipment qualification.

Benefits

• Hands-on experience in a growing pharmaceutical business.
• Exposure to various functions.
• Opportunities for career development.
• Collaborative and supportive work environment.
• Possibility of conversion to full-time based on performance, contribution, and other factors.

What This Job Offers

• Career Level: Entry Level