What are the responsibilities and job description for the Senior Supplier Quality Engineer position at Stark Pharma?
Hi,
My name is Karthik Mutyala and I m a Recruitment Manager with Stark Pharma, specializing in pharmaceutical, biotechnology, and medical device roles. I came across your profile and wanted to see if you are open to new opportunities.
If interested, please send me your updated resume along with the best number and time to reach you.
Job Title: Senior Supplier Quality Engineer
Location: Bothell, WA (100% Onsite)
Duration: 6 Month Contract
Job Summary
We are seeking a Senior Supplier Quality Engineer to support supplier quality operations within a medical device manufacturing environment. This role will focus on driving supplier quality improvements, resolving non-conformance issues, and ensuring compliance with regulatory and quality standards across the supply chain.
The ideal candidate will have strong experience in supplier quality engineering, supplier audits, and manufacturing process improvements within FDA-regulated medical device environments.
Key Responsibilities
My name is Karthik Mutyala and I m a Recruitment Manager with Stark Pharma, specializing in pharmaceutical, biotechnology, and medical device roles. I came across your profile and wanted to see if you are open to new opportunities.
If interested, please send me your updated resume along with the best number and time to reach you.
Job Title: Senior Supplier Quality Engineer
Location: Bothell, WA (100% Onsite)
Duration: 6 Month Contract
Job Summary
We are seeking a Senior Supplier Quality Engineer to support supplier quality operations within a medical device manufacturing environment. This role will focus on driving supplier quality improvements, resolving non-conformance issues, and ensuring compliance with regulatory and quality standards across the supply chain.
The ideal candidate will have strong experience in supplier quality engineering, supplier audits, and manufacturing process improvements within FDA-regulated medical device environments.
Key Responsibilities
- Investigate, resolve, and prevent supplier-related non-conformances impacting manufacturing operations
- Drive supplier corrective and preventive actions to improve product quality and process performance
- Support implementation of design and manufacturing process changes at supplier sites
- Conduct and document part qualification and process validation activities
- Partner cross-functionally with Engineering, Manufacturing, Supply Chain, and Quality teams to prevent supplier-driven shortages and quality issues
- Lead supplier quality system and process audits to ensure compliance with company and regulatory requirements
- Monitor supplier performance metrics and identify opportunities for continuous improvement
- Support evaluation, qualification, and onboarding of new suppliers
- Participate in departmental meetings, training sessions, and continuous improvement initiatives
- Bachelor s degree in Engineering, Life Sciences, or related technical field
- Minimum 5 years of experience in Supplier Quality, Quality Engineering, or related roles within the medical device industry
- Strong knowledge of FDA 21 CFR Part 820 and ISO 13485:2016 requirements
- Experience conducting supplier audits and managing supplier quality systems
- Strong communication, documentation, and problem-solving skills
- Excellent organizational skills and attention to detail