JT702 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN

Quality Consulting Group, LLC; New Albany (OH); On-site; USD 35,000 - 55,000; Full time

Job summary

An established industry player in the pharmaceutical and biotech sectors is seeking a motivated Associate Manufacturing Process Technician. This entry-level role offers an exciting opportunity to work in a dynamic manufacturing environment, where you will be responsible for equipment setup, operation, and troubleshooting. Collaborating with cross-functional teams, you'll contribute to continuous improvement initiatives while ensuring compliance with Good Manufacturing Practices. Join a passionate team dedicated to quality and efficiency, and take the first step in your career within a world-class manufacturing setting.

Qualifications

• Experience in manufacturing or operations is essential.
• Ability to safely follow standardized operating procedures.

Responsibilities

• Perform equipment setup, operation, and troubleshooting.
• Maintain machine uptime and assist in documentation review.

Skills

Troubleshooting

Equipment Setup

Basic Analytics

Material Handling

Good Manufacturing Practices (GMP)

Education

Associate degree

High school/GED + 1 year of related work experience

Tools

SAP

Maximo system

Job description

JT702 - ASSOCIATE MANUFACTURING PROCESS TECHNICIAN

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic individual 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.

Qualifications:

• Associate degree or High school/GED + 1 year of related work experience.
• Experience in manufacturing or operations.
• Able to use computer systems to support material inventory system (SAP transactions) and electronic batch records.
• Knowledge 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).
• Day shift 6am - 6:30pm.
• 3 days on week 1 Mon, Thurs, Friday - 4 days on week 2 Tues, Wed, Sat, Sun.
• Must work every other weekend.

Seniority level: Entry level

Employment type: Temporary

Job function: Management and Manufacturing

Industries: Pharmaceutical, Biotech, Medical Devices, and Manufacturing