Job ID: TM9770801113
Location: Midland, GA
Category: Engineering
Employment Type: Permanent
Join our client's Midland, Georgia organization dedicated to safety, quality, and customer satisfaction. Lead their operations with a winning attitude and drive for excellence.
WHAT IS GREAT ABOUT THIS OPPORTUNITY?
- Competitive salary of $80,000/year – $105,000/year annually, reflecting your expertise and technical skills
- Direct Hire opportunity: Enjoy stability, growth opportunities, and direct access to client’s benefits
- Onsite position: Be at the forefront of change and collaborate with a dedicated team onsite
- Join their team to embark on a career journey with ample room for growth and professional growth
DO YOU ALIGN WITH THESE KEY QUALIFICATIONS?
- 5+ years in a regulated environment, ideally within medical devices or pharmaceuticals, focusing on Validation, CAPA, and Supplier Management.
- Strong knowledge of Quality Management Systems and regulatory requirements (CFR 820, ISO 13485 preferred)
- Project management skills, with the ability to adapt to shifting priorities.
- Excellent written and verbal communication skills and a collaborative approach.
- Proficiency in Microsoft Office, as well as eQMS and WMS systems.
- Bachelor’s degree in a scientific field, biomedical engineering, or quality management, or equivalent experience
WHAT WILL YOUR SUCCESS LOOK LIKE?
As the Quality Engineer, supports the validation, quality systems, and supplier management programs for our client’s global operations. This position ensures that processes and equipment meet validation and regulatory standards, while driving continuous improvement and compliance throughout the organization.
WHAT WILL YOU DO?
- Lead the Validation Program to ensure compliance with all processes and equipment, implementing updates and remediation where necessary.
- Oversee validation activities for new processes and equipment, including authoring IQ/OQ/PQ protocols.
- Facilitate risk assessments, update pFMEA evaluations, and lead CAPA initiatives, including coordinating the CAPA Review Board.
- Monitor supplier quality through surveys, annual reviews, tracking metrics, audits, and managing SCARs.
- Conducted audits as assigned, monitored, and reported on quality metrics, ensuring accurate documentation.
- Work cross-functionally to conduct process walk-throughs, verifying adherence to procedures and identifying improvement opportunities.
- Oversee and prioritize assigned projects, ensuring alignment with global quality standards.
- Provide backup coverage for other quality roles when needed.
WHAT WILL YOU RECEIVE?
Gain access to The Reserves Network Team:
- Partnership with experienced recruiters that will advise you on all aspects of your job search and career aspirations
- Our network has direct access to hiring managers, and we will get your resume to the top of the pile of submissions for this opportunity and many more like this
- Long-term career partner who will provide you with market intelligence and guidance
Client Benefits:
- Industry competitive salary based on your experience/qualifications
- Health, Vision, and Dental Insurance
- 401(k) plan
- PTO
And much more!
DO YOU WANT TO KNOW MORE?
If you have a background that aligns well with the description of Director of Plant Operations and would like to learn more about this opportunity, please apply below NOW!
Studies have shown that people are likely to only apply for jobs if they meet every qualification. At The Reserves Network, we strive to provide the best experience and opportunities for everyone, so if you are excited about this role but your experience doesn’t align perfectly with every qualification listed, we still encourage you to apply. You may be the right candidate for this or other available roles.
As an equal opportunity employer, we value our employees and foster an environment of respect, integrity, and trust in every aspect of employment. However you identify, and whatever your background, we encourage you to apply today.
