Quality Engineer

Westbrook, Maine

GTT, LLC
Job Expired - Click here to search for similar jobs
Quality Engineer
Contract Duration 3 Months

Job Role:
Manufacturing Line Quality Engineers operate as an independent Quality resource partnered with Production to facilitate GMP, GDP, and Client quality standard compliance.
Responsible for assisting in the implementation and maintenance of an effective Quality System for the site.

Job Responsibilities:
Quality Engineer will be responsible for performing line clearance, shift change activities, set-up verification, and label verification.
Independently contribute to Quality System processes manufacturing, corrective action & preventive action (CAPA) activities, equipment maintenance, product and process planning, quality audits, and validation.
Coach and reinforce quality attributes and requirements. May provide technical assistance.
Independently utilize quality management techniques to perform investigations and facilitate solutions.
Quality Engineer will be responsible for Independently completing documentation promptly and by business standards.
Responsible for maintaining the effectiveness of the Quality System.
Understand and comply with applicable EHS policies, procedures, and guidelines.
Works under the general supervision of more experienced staff who review results for overall accuracy, completeness, and sound judgment;
Identifies and quantifies technical risks and their consequences relative to the success of part of a project; recommends appropriate action; decisions or recommendations would typically achieve department/project objectives; drives functional performance to ensure that cross-functional standards and expectations are met; may assist in the training of personnel as directed by management; may mentor others.
Consult with Manufacturing, Information Management, Research Development & Engineering, Quality Assurance Operations, and Product Performance Analysis teams to ensure compliance with client software development procedures and industry regulations.
Review and approve deliverables of the software development lifecycle.
Lead teams in performing Hazard Analysis.
Occasionally assist teams in developing Standard Operating Procedures and Work Instructions for software development activities that meet their specific needs.
Occasionally provide training for select software development activities.
Occasionally write and execute test protocols and reports.
Other tasks and duties as assigned.

Experience
0-3 years of experience.

Note:
This position is Non-Exempt.
Hours over 40 will be paid at Time and a Half.

Benefits:
Medical, Vision, and Dental Insurance Plans
401k Retirement Fund

About The Company:
Our client is a globally diversified healthcare company with a central purpose to help people live their healthiest possible lives. They offer a broad portfolio of market-leading products that align with favorable long-term healthcare trends in both developed and developing markets. Working with this company, you'll tackle a wide array of problems including some of the world's greatest healthcare challenges while experiencing myriad cultures, geographies, and technologies. They are creating the future of healthcare through life-changing technologies and products that make you healthier and stronger, quickly identify when you have a medical need, and treat conditions to help you get back to doing what you love. It serves people in more than 160 countries with leading medical devices, diagnostics, nutrition products, and branded generic medicines.
If you are looking for a great company to work for, look no further because our client has received an average of a four-star rating from its thousands of employees that have written positive reviews on Glassdoor and Indeed.

24-05962
Date Posted: 16 May 2024
Job Expired - Click here to search for similar jobs