Pharmaceutical Development Technologist

Transpire BIO Inc.•Weston, FL

About The Position

The Pharmaceutical Development Technologist independently conducts, leads, and supervises standard and advanced laboratory activities, including formulation and manufacturing process development, process scale-up, and process transfer across equipment, manufacturing scales, and sites. The role oversees the manufacture of lab-scale R&D, pilot-scale, pivotal-scale, and commercial-scale batches in accordance with written documentation. The position provides practical feedback on study designs, document development, and manufacturing equipment selection. It contributes to equipment installation, maintenance, and troubleshooting; development of orally inhaled and nasal drug products (OINDPs) under applicable regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines; and evaluation of new formulation manufacturing technologies. The technologist initiates investigations and data reviews and coaches and trains junior scientific staff. The role participates in project activities, supports timelines and team objectives, communicates with colleagues and partner companies, and works effectively across functional groups and global respiratory R&D sites. Laboratory work must follow SOPs, safety procedures, and corporate guidelines and policies. The position is based in a laboratory environment involving biological materials and disinfectants. The technologist must be able to stand for extended periods, lift up to 30 lbs, and wear appropriate PPE, including a lab coat, gloves, and eye protection. The company describes itself as a fast-growing pharmaceutical startup and highlights hands-on experience, exposure to various functions, career development opportunities, and a collaborative, supportive work environment.

Requirements

High school diploma and 10 years of work experience.
A relevant degree, certification, or license may be required.
Experience as a technician in the manufacture of pharmaceutical products.
A driver's license.
Ability to multitask and liaise with professionals in different fields.
Ability to explain problems simply and clearly.
Proficiency in MS Office.
Ability to exercise independent judgment and discretion.
Ability to understand verbal and written instructions.
Ability to follow health and safety regulations.
Excellent mathematical and problem-solving skills.
Ability to stand for extended periods.
Ability to lift up to 30 lbs.
Ability to work in a laboratory environment with biological materials and disinfectants and wear appropriate PPE, including a lab coat, gloves, and eye protection.

Nice To Haves

Experience in a regulated laboratory, such as pharma, biotech, or medical device.
Knowledge of GMP, GLP, or ISO standards.

Responsibilities

Independently conduct, lead, and supervise standard and advanced laboratory activities, including formulation and manufacturing process development, scale-up, and process transfer across equipment, scales, and sites.
Conduct, lead, and supervise manufacture of lab-scale R&D, pilot-scale, pivotal-scale, and commercial-scale batches according to written documentation.
Provide practical feedback on study designs, document development, and manufacturing equipment selection.
Contribute to installation, maintenance, and troubleshooting of manufacturing equipment and interface with equipment vendors.
Contribute to development of orally inhaled and nasal drug products (OINDPs) in accordance with regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines.
Contribute to development and evaluation of new formulation manufacturing technologies as needed.
Initiate investigations and data reviews, and coach and train junior scientific staff.
Participate in project activities, support project timelines, and contribute proactively to team objectives.
Communicate effectively with Transpire Bio and partner-company team members and collaborate with other functional groups and global respiratory R&D sites.
Establish and maintain effective relationships with team members.
Conduct laboratory work in accordance with SOPs and follow safety rules and procedures.
Comply with corporate guidelines and policies.