Job description

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:

• General duties include, but not limited to material handling and coordination of raw materials, review of experiment bill of materials, and collaborating with supply chain partners to facilitate material requisitions.
• Other responsibilities include; performing goods receipt, transport & stocking of materials, pulling and kitting of materials, and routine inventory cycle counts.
• Must be able to lift up to 50lbs and push/pull heavy loads using material handling equipment.
• Performs routine preventative maintenance and standardization of benchtop analytical devices to such as automated cell counter, metabolic analyzers, and solution meters.
• Carries out laboratory tasks per plan and procedure in a team environment.
• Documents data and process information in accordance to good documentation practices.
• Performs laboratory safety evaluations.
• Performs daily cleaning and sanitization of the laboratory.
• May support various experiment preparation and execution as directed to include, but not limited to; execution of cell culture, harvest and downstream purification process studies using 500 L scale pilot equipment including bioreactors, chromatography skids and filtration systems.
• Additional routine tasks may include 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 to good documentation practice
• Perform inventory management processes for pilot scale process development biopharmaceutical laboratory.

Qualifications:

• Bachelor's degree in engineering or science
• Prior hands-on experience with SAP and/or similar electronic inventory software.
• Knowledge in 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 and Demonstrated equipment troubleshooting skills.
• Excellent problem-solving capabilities and attention to detail.
• Experience collaborating within and across functional areas and outstanding customer focus
• Excellent written and verbal communication skills.
• 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.
• Availability for 1st shift (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: Full-time, Temporary

Schedule:

• Weekend availability

Ability to commute/relocate:

• West Greenwich, RI: Reliably commute or planning to relocate before starting work (Required)

Education:

• Bachelor's (Preferred)

Experience:

• Cell culture: 1 year (Preferred)
• SAP: 1 year (Preferred)
• pharmaceutical: 1 year (Preferred)
• Chemistry, manufacturing & controls: 1 year (Preferred)

Shift availability:

• Day Shift (Required)

Work Location: In person

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