QA-Supplier Cover Letter

Please consider me for the qa-supplier opportunity. I am including my resume that lists my qualifications and experience.

In the previous role, I was responsible for continuous re-enforcement of the respective requirements for medical device law and regulation and standards to all associates on site and provide guidance and recommendations involving the implementation of regulatory requirements (e.g., Quality System Regulation, EU MDD, ISO standards, etc.).

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Good knowledge of medical device development and life-cycle management
• Experience in working with suppliers/customer for quality related issues specifically in Analog High-Power Radio-Frequency generators and matches, OEM (Original Equipment Manufacturer) and COTS (Commercial off-the Shelf) parts
• Design understanding of radio frequency systems
• Knowledge of Quality Systems – Statistics, DOE, FMEA, FRACAS, problem solving
• Effective working knowledge of quality tools and concepts such as
• Communication and interpersonal savvy
• Problem solving skills including 5W, 8D
• Experience with Minitab, MS Access or Excel

In response to your job posting for qa-supplier, I am including this letter and my resume for your review.

Previously, I was responsible for professional expertise, guidance and strong leadership in Computer System Validation and applicable regulatory requirements (21 CFR Part 11/Annex 11/ GAMP 5) as applicable to the Global R&D GxP requirements (GLP, GCP, GPvP, GDP) to proactively identify compliance issues/risks in all functions within the organization and its external partners.

Please consider my qualifications and experience:

• Design for Six Sigma and Critical to Quality (CTQ) experience
• Trained at a minimum as a Certified Auditor with working knowledge of Good Manufacturing Practices (GMP’s), Quality Systems standards and regulatory requirements such as 21 cfr 820, 21 CFR Part 600, ISO 13485 and IVDD
• Strong organizational, planning, lean, problem solving and reporting skills
• Knowledge of Good Manufacturing Practices (GMPs), Quality System standards and regulatory requirements such as 21 CFR 820
• Trained in auditing techniques
• Fluent English and add
• Applying all elements of the External Sourcing Supplier Standard and External Supplier Management Standard
• Managing all associated risk, governance and compliance activities within the Deal QA team

Please consider me for the qa-supplier opportunity. I am including my resume that lists my qualifications and experience.

In my previous role, I was responsible for quality Assurance input to the development and clinical manufacturing of medical devices, and ensure that all activities are conducted in compliance with the lab’s regulatory requirements.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Experience working in an industry with high levels of manufacturing environmental controls (medical devices, drugs, electronics etc)
• Experience with manufacturing or kit assembly
• Experience with chemicals, excipients, media components
• Demonstrated experience and results in the areas of transactional lean and identifying areas of process design and improvement, especially as applied to Supplier Quality and related processes
• Proficiency with of personal computers and the Moog mainframe operating systems
• NADCAP preferred
• Demonstrated experience completing CAPAs preferred
• Open to challenging assignments requiring creative solutions

In response to your job posting for qa-supplier, I am including this letter and my resume for your review.

In my previous role, I was responsible for expert interpretation and application of regulatory guidelines to ensure operations, facilities and documentation meet Bayer standards and regulatory requirements.

Please consider my experience and qualifications for this position:

• Process improvement oriented mindset
• Previous experience in conducting internal and external audits and demonstrated auditing skills is preferred
• Prior experience in a FDA regulated industry or ISO certified organization is preferred
• CQE (Certified Quality Engineer) or CQA (Certified Quality Auditor) is desirable
• Fluent in Korean and English (both writing and verbal)
• BS in Mechanical or Plastics Engineering
• Awareness of regulatory requirements for Consumer Products, specifically toys and infant feeding
• Demonstrated understanding of NPD process and practices

In response to your job posting for qa-supplier, I am including this letter and my resume for your review.

Previously, I was responsible for qA direction to the validation team during document review to ensure the organization is complying with local and global quality standards, regulatory requirements and partner commitments.

I reviewed the requirements of the job opening and I believe my candidacy is an excellent fit for this position. Some of the key requirements that I have extensive experience with include:

• Accountable for the strategic alignment of Barclays and managed suppliers by establishing common goals and objectives
• Where appropriate provide active support across the wider Procurement community to enable effective team performance
• Works collaboratively with the broader Supplier Management community and leadership
• Engage with internal colleagues and participate in and deliver control environment discussions across key stakeholders in particular, Barclays Supplier Risk (1LOD, 2LOD and 3LOD) Chief Controls Office (CCO) and Global Supplier Assurance (GSA)
• Ensure the Supplier Management team maintains positive relationships with all relevant internal and external colleagues and agencies connected with the successful delivery of a well governed business
• Track record in improving Supplier Management Governance in a services related organization
• Knowledge and experience of Sourcing standards and policies
• This leader will play a key role in influencing a change in direction for supplier quality, moving from site focus to a commodity community focus