Quality Engineer

Forummolding; Watertown (CT); On-site; USD 80,000 - 110,000; Full time

Job summary

Forum Contract Manufacturing in Watertown, CT is seeking a dedicated Quality Engineer to support quality systems, manufacturing processes, and customer requirements in a fast-paced medical device environment.

The role emphasizes analytical thinking, collaboration with Quality, Engineering, Production and Customer Service, and a commitment to regulatory compliance, continuous improvement, and data accuracy on the shop floor.

Responsibilities

• Support quality systems, manufacturing processes, and customer requirements.
• Collaborate with Quality, Engineering, Production and Customer Service teams.
• Assist in investigations, root-cause analysis and corrective actions.
• Ensure compliance with regulatory requirements in a fast-paced medical device setting.
• Maintain documentation and data integrity across processes.

Job description

Quality Engineer

Forum Contract Manufacturing is seeking a motivated and detail-oriented Quality Engineer to support our quality systems, manufacturing processes, and customer requirements. The ideal candidate will be analytical, organized, and comfortable working closely with Quality, Engineering, Production, and Customer Service teams in a fast-paced medical device manufacturing environment.

We are looking for someone who is:

• Hard-working, dependable, and accountable
• Detail-oriented with a strong commitment to quality and accuracy
• A strong communicator who can confidently interact with customers and internal teams
• Comfortable working on the manufacturing floor and collaborating directly with production personnel
• Analytical and able to identify problems, determine root causes, and develop effective solutions
• Comfortable asking questions, investigating issues, and seeking assistance when needed
• Organized and skilled at managing multiple projects, priorities, and deadlines
• Able to work with urgency while maintaining attention to detail
• Comfortable working independently while also contributing effectively as part of a team
• Willing to tackle challenges head-on and take ownership of problems through resolution
• Interested in continuous improvement and finding ways to improve processes, efficiency, and product quality
• Committed to following established quality systems, procedures, and regulatory requirements
• Able to work effectively in a fast-paced manufacturing environment
• Motivated to learn and grow within the medical device manufacturing industry