JT519 - SENIOR MANUFACTURING PROCESS TECHNICIAN NS bei Quality Consulting Group
Quality Consulting Group · New Albany, Vereinigte Staaten Von Amerika · Onsite
- Professional
- Optionales Büro in New Albany
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:
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)
