Manufacturing Associate Purification Process

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)

Job Types: Contract, Temporary

Pay: $32.00 per hour

Schedule:

• 12 hour shift
• Day shift
• Monday to Friday
• Morning shift
• Night shift
• Overnight shift
• Rotating weekends
• Weekends as needed

Education:

• Associate (Preferred)

Shift availability:

• Day Shift (Preferred)
• Overnight Shift (Preferred)
• Night Shift (Preferred)

Work Location: In person

Salary : $32