Job summary
Job post source
This job is from a recruiting firm hiring for a separate company.
Job overview
The Supplier Quality Engineer role at cGxPServe focuses on ensuring quality and compliance in supplier processes, impacting product reliability and regulatory adherence.
Responsibilities and impact
The candidate will conduct root cause analysis, validations, FMEAs, and manage supplier quality in a regulated environment, contributing to product quality and compliance.
Experience and skills
Requires a minimum of four years relevant experience, production line validation experience, knowledge of NC/CAPA, FMEAs, NPI, Design Control, and supplier quality in medical devices; experience with J&J is preferred.
Company overview
cGxPServe operates in the engineering and information technology sectors, specializing in research services with a focus on manufacturing, process control systems, and clinical data management. The company provides expertise in areas such as supplier quality, regulatory affairs, clinical project management, and data programming, serving clients in highly regulated industries, including medical devices and pharmaceuticals, as indicated by references to ISO 13485 and 21 CFR 820 compliance. cGxPServe generates revenue through professional services and staffing solutions, supporting roles like manufacturing engineers, clinical data managers, and regulatory specialists. With locations in California and North Carolina, the company is positioned to address complex compliance and operational needs for clients. Its history and growth reflect a commitment to supporting quality and regulatory standards in life sciences and advanced manufacturing.
How to land this job
Position your resume to emphasize at least four years of relevant experience in supplier quality engineering, especially highlighting hands-on production line validations and familiarity with medical device regulations.
Focus on showcasing your expertise in NC/CAPA root cause analysis, FMEAs, New Product Introduction (NPI), Design Control, and supplier quality management, as these are core to this role at cGxPServe.
Apply through multiple platforms including cGxPServe’s corporate website and LinkedIn to maximize your application visibility and opportunities.
Connect with current employees in the supplier quality or medical device divisions at cGxPServe on LinkedIn; start conversations with ice breakers like asking about their experience with supplier quality challenges or recent projects involving design control improvements.
Optimize your resume for ATS by incorporating keywords from the job description such as 'NC/CAPA,' 'root cause analysis,' 'FMEAs,' 'NPI,' 'Design Control,' and 'medical device,' ensuring your resume passes automated screening effectively.
Utilize Jennie Johnson’s Power Apply feature to automate tailoring your resume, applying through multiple channels, and identifying LinkedIn contacts, so you can focus your energy on preparing for interviews and networking.
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