What are the responsibilities and job description for the JT758 - MANUFACTURING ASSOCIATE position at Quality Consulting Group?
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:
- Works in a dynamic production environment at the client's plant, supporting development, clinical, and launch activities.
- Under general supervision, employee will perform operations in the Manufacturing area, specifically for Purification processes.
- Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment
- Preparing buffers/media per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)
- Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance
- Performing and monitoring critical processes with the ability to perform basic troubleshooting
- Initiating quality deviation reports
- Drafting and revising documents (SOPs, MPs)
- Identifying, recommending, and implementing improvements related to routine functions.
- Assisting in the review of documentation for assigned functions (equipment logs, batch records)
- Performing in-process sampling of equipment and operating analytical equipment.
- Working around high-pressure systems and work around heavy equipment.
- Maintaining an organized and clean workspace
- Able to work in teams to complete operational tasks and create a positive work environment through interactions with team members
- Ability to take direction well, follow documents and policies at all times
- Performing activities that include periods of rigorous, repetitive work
- Working in a clean room environment wearing steel toe shoes, full clean room gowning, hairnet and gloves when performing all work.
Qualifications:
- Associate degree or Bachelor’s Degree.
- The ideal candidate has experience with large-scale purification processes, including chromatography, filtration, and pressurized equipment.
- Able to follow strict GMP documentation procedures.
- Must be able to work various shifts (day, swing, graves, weekends, holidays, 5x8hrs, 4x10hrs, 3 or 4x12hrs)
- Able to regularly lift up to 35lbs, push and pull objects that require up to 50lbs of force, and work on your feet for long durations.
- Able to perform the list of physical movements that may be necessary to perform daily functions on the production floor: bending, reaching above the head, climbing, kneeling, squatting, stooping, walking upstairs, and standing on portable stairs or ladders up to 6 feet off of the ground.
- Works well in a fast-paced environment while complying with GMP standards
- Able to work in teams and maintain a positive work environment.
- Primary Shift: 7:00 AM – 8:00 PM to start
Rotating Shift: 7:00 AM – 8:00 PM and 7:00 PM – 8:00 AM (6-month rotations)
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.
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