Pharma Lab Scientist I - HPLC/UPLC, 2nd Shift (Temp)

Transpire Bio Inc.; 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

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.