QA Associate Cover Letter

I am excited to be applying for the position of QA associate. Please accept this letter and the attached resume as my interest in this position.

In my previous role, I was responsible for guidance and support to departments with respect to procedures, equipment, testing, documentation, and other GMP requirements.

Please consider my experience and qualifications for this position:

• Able to “multi task”, to balance multiple priorities to meet targets
• Knowledge MS Office, VB, VC++, SQL
• Working in a laboratory known to contain potentially harmful chemicals
• Long terms of standing to watching methods being done
• Relevant experience within a Pharmaceutical Quality Assurance / GMP background
• Prior experience of batch release activities (preferable)
• Shows strong drive to resolve issues taking the lead in problem solving
• Tenacious and persistent in follow through

In response to your job posting for QA associate, I am including this letter and my resume for your review.

Previously, I was responsible for guidance for GMP product quality and compliance, including resolution of product quality investigations and quality issues of a significant nature.

My experience is an excellent fit for the list of requirements in this job:

• Provide timely feedback to line management on audit lifecycle system status as appropriate
• Provide administrative support for Customer Audits and Regulatory Inspections in the QRTP office
• Excellent analytical skills, familiarity with basic statistical analysis, and proficiency in utilizing PC based applications
• Working knowledge of C# and/or JavaScript
• Excited to learn new technology
• Trained in Rapid Software Testing methodologies
• Manage product inquiries and follow-ups on retrieved consumer complaints
• Maintain issue data within internal system(s) and provide summary reports and/or status updates, as needed

Please consider me for the QA associate opportunity. I am including my resume that lists my qualifications and experience.

In the previous role, I was responsible for oversite and guidance to Product Development areas mentioned above with respect to current GMP regulations.

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:

• Create and maintain deliverables including test plans, test cases and test data
• Set up test environments and build out interdependent test beds
• Planning and execution of functional, system and performance testing of products across all platforms to test various features at various phases of product development and release cycles
• Assist developers in reproducing problems and getting them resolved
• Experience in Defect Life cycle, STLC, SDLC, Gap Analysis, Impact Analysis
• Should be ready to incorporate the automation requirement and maintaining scripts
• Good in communication and team player
• Agile project experience preferred

I submit this application to express my sincere interest in the QA associate position.

In my previous role, I was responsible for expertise and guidance in interpreting governmental regulations, agency guidelines and internal procedures to assure continued GMP compliance at the Warren facility.

My experience is an excellent fit for the list of requirements in this job:

• Experience with unit testing frameworks (ex
• Plans and directs creation of quality assurance processes and procedures, test methods, and fixtures for clinical simulation utilizing clinical and engineering knowledge
• Designs, develops and executes test protocols for clinically-based surgical simulation, automated testing, and functional verification
• Participate in the product development lifecycle, including the design review process
• Evaluates instrument designs using measurement devices and inspection tools
• Identifies, reproduces, and escalates new or persistent software or hardware related failure modes to management and appropriate Engineering teams
• Troubleshoots, diagnoses, and documents all findings in the ISI bug-tracking database
• Complete documentation of test protocols, results and reports

Please consider me for the QA associate opportunity. I am including my resume that lists my qualifications and experience.

In the previous role, I was responsible for qA oversight of commissioning, qualification and validation activities to deliver Moderna’s new early phase GMP manufacturing facility which includes raw material, Drug Substance, Formulation, Drug Product, Finished Goods and personalized medicine capabilities.

Please consider my qualifications and experience:

• Looking for someone to join immediately
• Basic black, gray, and white box testing design and testing skills
• Experience working on an Agile development team with rapid iterations
• Exposure in working with commercial or open-source testing tools
• Exposure in working in an Agile methodology
• Understanding of all phases of SDLC
• Understand software quality assurance
• Familiar/Basic exposure to Operating systems and basic DOS/Unix commands