Associate Pilot Plant

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:

• Perform inventory management processes for pilot scale process development biopharmaceutical laboratory.
• Material handling and coordination of raw materials, review of experiment bill of materials, and collaborating with supply chain partners to facilitate material requisitions.
• Perform goods receipt, transport & stocking of materials, pulling and kitting of materials, and routine inventory cycle counts.
• Performs routine preventative maintenance and standardization of benchtop analytical devices to such as automated cell counter, metabolic analyzers, and solution meters.
• Documents data and process information in accordance with good documentation practices.
• Performs laboratory safety evaluations.
• Performs daily cleaning and sanitization of the laboratory.
• Execution of cell culture, harvest and downstream purification process studies using 500 L scale pilot equipment including bioreactors, chromatography skids and filtration systems.
• Equipment preparation such Clean-In-Place and Steam-In-Place, compounding media and buffer solutions, and sampling.
• Utilizes scientific principles in execution of experiments and analysis of experimental data.
• Documents data and process information in accordance with good documentation practice

Qualifications:

• Bachelor's degree in related area
• Electronic inventory management experience
• Laboratory and/or pharmaceutical manufacturing experience
• Must be able to lift up to 50lbs and push/pull heavy loads using material handling equipment.
• Prior hands-on experience with SAP and/or similar electronic inventory software.
• Pilot-scale or large-scale cell culture or downstream purification process development or manufacturing operation.
• Experience with automated and computer-controlled biopharmaceutical process equipment.
• Knowledge of process data compilation and analysis Demonstrated equipment troubleshooting skills.
• Availability for Standard Work Hours (8:30am - 5:00pm)

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.

Job Types: Temporary, Contract, Full-time

Salary: $25.00 - $28.00 per hour

Schedule:

• 8 hour shift
• Day shift
• Monday to Friday

Ability to commute/relocate:

• Cambridge, MA: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• Manufacturing: 1 year (Preferred)
• pharmaceutical industry: 1 year (Preferred)

Shift availability:

• Day Shift (Preferred)

Work Location: In person

Salary : $25 - $28