JT932 - ASSOCIATE PILOT PLANT
About The Position
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.
Requirements
- Bachelor's or associate degree in related are preferred
- 1+ year of related 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.
- Dayshift (start time and end time can be flexible)
- Must have the ability to support WEEKEND work
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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
Associate degree
Number of Employees
51-100 employees
