QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:

• Lead management of materials including oversight of sample requests, test submission, storage, and shipping coordination.
• Support execution of cell culture and purification processes to include, but not limited to: aseptic processes, bioreactor operations, chromatography, and filtration.
• Perform additional routine tasks including, but not limited to:
• In-process sampling
• Operation of laboratory analyzers
• Scientific data collection via electronic laboratory notebook(s)
• Compounding media and buffer solutions
• Clean-In-Place (CIP) and Steam-In-Place (SIP)
• Equipment assembly and disassembly
• Routine maintenance of benchtop analyzers
• Escorting and providing oversight of vendors
• General lab organization, cleaning, and inventory-related tasks
• Utilize scientific principles in execution of experiments and analysis of experimental data.
• Carry out laboratory tasks per plan and procedure in a team environment.
• Document data and process information in accordance with good documentation practices.
• Perform laboratory safety evaluations.
• Perform minor equipment maintenance.
• Help maintain laboratory standards with a focus on safety, quality, and compliance.

Qualifications:

• Bachelor's or associate degree in related are preferred
• Science based recent grad or 3 years of experience
• Prior hands-on experience in pilot- or large-scale cell culture or downstream purification process development or manufacturing.
• Experience with automated computer-controlled biopharmaceutical equipment.
• Knowledge of process data compilation and analysis.
• Demonstrated problem-solving capabilities and excellent attention to detail.
• Well organized with excellent written and verbal communication skills.
• Ability to work fully onsite.
• Ability to support weekend work.
• Willingness to work hard, learn, and be self-motivated.
• 7:30am - 4:30pm Standard hours

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.