Associate Scientist

Transpire Bio; Florida; On-site; USD 50,000 - 70,000; Part time

Job summary

Transpire Bio Inc. in the United States is seeking an Associate Scientist I to conduct laboratory testing and manufacturing support on second shift, on-site. This entry-level temp/contract role offers exposure to cGMP practices, drug product analysis, and collaboration with a growing team.

The position emphasizes HPLC/UPLC analysis, data documentation, and participation in method transfers and equipment qualification, with potential conversion to full-time based on performance.

Qualifications

• BSc in Chemistry, Pharmacy or related field; 0–2 years of experience.
• Computer literacy and familiarity with analytical equipment such as HPLC, IR/FTIR, UV-Vis; etc.
• Effective English written and oral communication skills.

Responsibilities

• Conduct basic laboratory activities and analyze raw materials, in-process materials and finished products for quality, safety, purity, strength and identity following applicable guidelines.
• Set up and operate lab equipment; prepare reagents and samples; document tests in lab notebooks.
• Process analytical data on lab equipment and support manufacture of drug products; assist with blend sampling as needed.
• Participate in project team activities; support timelines and team objectives.
• Maintain effective relationships with team members and follow SOPs and safety rules.
• Comply with corporate guidelines and policies.

Skills

Lab testing

Documentation

English communication

Team collaboration

Education

BSc in Chemistry/Pharmacy or related

Tools

HPLC/UPLC

IR/FTIR

UV-Vis

Empower

Laboratory equipment

Job description

The Associate Scientist I is responsible for conducting laboratory testing and manufacturing support activities with limited supervision, including analysis of raw materials, in-process materials, and finished pharmaceutical products in accordance with cGMP, FDA, EH&S, SOP, and corporate requirements. The role requires strong HPLC/UPLC, Empower, documentation, and analytical problem-solving skills, along with the ability to maintain accurate laboratory records, support method transfers and equipment qualification, contribute to project timelines, and collaborate effectively with team members. Candidates must be eligible to work in the United States without visa sponsorship or transfer and must be willing to work on-site during 2nd shift.

NOTE: This role does NOT offer sponsorship for work authorization.

External applicants must be eligible to work in the US without visa sponsorship or visa transfer. These are 1-year Temp/Contract roles. Roles may offer possibility to convert to full-time based on performance, contribution and other factors.

Essential Duties and Responsibilities

• Conduct basic laboratory activities including for example analyzing raw materials, in process materials and finished pharmaceutical products for quality, safety, purity, strength and identity using applicable methods or manufacturing drug product, following the cGMP, EH&S and other relevant guidelines of Corporate, FDA and other governing bodies.
• Set up and operate lab equipment. Prepare reagents, solvents and solutions for analytical and formulation activities. Prepare and maintain accurate records in lab notebooks of all tests performed. Process analytical data on lab equipment such as HPLC/UPLC, enter data in spreadsheets and conduct routine calculations. Support the manufacture of inhalation drug products. Prepare samples for blend uniformity as required.
• Participate in project team activities and support project timelines and proactively contribute to meeting team objectives.
• Establish and maintain effective relationships with team members.
• Conduct lab work in accordance with SOPs & STPs; follow corporate health & safety rules and procedures.
• Comply with Corporate guidelines and policies.

Qualification Requirements

• BSc in Chemistry, Pharmacy or related fields with 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, powder blender etc.
• Effective English written and oral communication skills.

Physical & Work Environment Requirements

• Ability to stand for extended periods
• Ability to lift up to 30 lbs
• Work in a laboratory environment with biological materials and disinfectants
• Wear appropriate PPE including lab coat, gloves, and eye protection

Why Join Us?

We are a fast-growing pharmaceutical startup dedicated to innovation and improving patient outcomes. Join us to gain hands‑on experience in a growing pharmaceutical business, get exposure to various functions with opportunities for career development and work in a collaborative and supportive work environment.

We are required by law to provide equal employment opportunity to qualified people with disabilities. We are also required to measure our progress toward having at least 7% of our workforce be individuals with disabilities. To do this, we must ask applicants and employees if they have a disability or have ever had a disability. Because a person may become disabled at any time, we ask all of our employees to update their information at least every five years.

Identifying yourself as an individual with a disability is voluntary, and we hope that you will choose to do so. Your answer will be maintained confidentially and not be seen by selecting officials or anyone else involved in making personnel decisions. Completing the form will not negatively impact you in any way, regardless of whether you have self-identified in the past. For more information about this form or the equal employment obligations of federal contractors under Section 503 of the Rehabilitation Act, visit the U.S. Department of Labor’s Office of Federal Contract Compliance Programs (OFCCP) website at www.dol.gov/ofccp.