JT519 - SENIOR MANUFACTURING PROCESS TECHNICIAN NS

New Albany, OH

Temporary

Biopharmaceutical

Mid Level

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:

Under limited supervision, perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency.
Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment.
Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions.
Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records).
Assist as training resource on manufacturing tasks and equipment use.
Use human machine interfaces (HMIs) to identify alarms and correct line stoppages.
Ensures components and products are available for a continuous operation.
Carries out equipment inspections and generates emergency, corrective, or preventative work orders as needed in the Maximo system.
Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes.
Partner with cross-functional teams to help drive improvement opportunities.
Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.
Oversight of equipment/process validation protocols independently.
Safely follow standardized operating procedures including material handling, record keeping, assembly and packaging.
Must follow Good Manufacturing Practices (GMPs).
Reports to Team Leader or Production Supervisor of any discrepancies to ensure quality standards and safety of operations are always maintained.

Qualifications:

Associate's degree and 6 months work experience
1–2 years of hands-on manufacturing or packaging experience
Technical & Mechanical Aptitude (Machine Operation & Troubleshooting)
GMP & Regulatory Compliance Knowledge
Attention to Detail & Quality Control, Team collaboration, communication skills, computer literacy.
Shift: 3rd shift starting at 10:30 PM – 7:00 AM, transitioning to 6:00 PM – 6:00 AM in the future (possibly October)

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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