Job Description

Job Description

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:

• Set up, clean, and sanitize manufacturing equipment.
• Cell culture and GMP Operations will be performed according to Standard Operating Procedures (SOPs).
• Prepare buffers and media per defined Manufacturing Procedures (MPs) and SOPs.
• Perform and monitor critical processes, including basic troubleshooting.
• Conduct in-process sampling and operate analytical equipment.
• Execute washroom activities, including cleaning small- and large-scale equipment.
• Maintain an organized, clean, and compliant workspace.

Qualifications:

• Associate’s Degrees or Bachelors Degree
• Soft skills, biology and biochemistry background, aseptic or lab experience.
• Must be flexible to work various shifts, including day, swing, graveyard, weekends, holidays, and rotating schedules.
• Perform rigorous, repetitive tasks, including lifting up to 35 lbs. and pushing/pulling objects requiring up to 50 lbs. of force.
• Stand for long durations and execute various physical movements, including bending, reaching, climbing, kneeling, squatting, and stooping.
• Work around high-pressure systems and occasionally heavy equipment.

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.

Powered by JazzHR

hufsiO8PKy

Job Tags

Similar Jobs