quality control analyst

Pharco Corporation

<div>
 
 
 We're Hiring | Quality Control Chemists
 
 
 
 
 
 
 We are looking for candidates with
 
 at least 2 years of experience
 
 in one or more of the following Quality Control areas:
 
 
 
 
 
 
 Raw Materials Quality Control
 
 
 
 
 Finished Product Quality Control
 
 
 
 
 Stability Studies
 
 
 
 
 Microbiology
 
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 
 
 Perform routine and non-routine testing in accordance with approved specifications, analytical methods, and GMP requirements.
 
 
 
 
 
 Execute laboratory activities while ensuring compliance with internal procedures, pharmacopoeial standards, and regulatory expectations.
 
 
 
 
 
 Accurately document analytical results and maintain data integrity in all laboratory records.
 
 
 
 
 
 Support laboratory investigations, OOS/OOT assessments, deviations, and CAPA activities as required.
 
 
 
 
 
 Participate in method verification, validation, equipment qualification, and laboratory continuous improvement initiatives.
 
 
 
 
 
 Ensure compliance with cGMP, EHS requirements, and corporate quality standards.
 
 
 
 
 
 Contribute to maintaining inspection and audit readiness at all times.
 
 
 
 
 
 
 Qualifications &amp; Experience
 
 
 
 
 
 
 
 Bachelor's degree in Pharmacy, Science, Biotechnology, Chemistry, or a related discipline.
 
 
 
 
 Minimum 2 years of experience in a pharmaceutical Quality Control environment.
 
 
 
 
 
 
 
 Hands-on experience in at least one of the following areas:
 
 
 
 
 Raw Materials Analysis
 
 
 
 
 Finished Product Testing
 
 
 
 
 Stability Testing
 
 
 
 
 Microbiological Testing
 
 
 
 Good understanding of pharmaceutical GMP requirements and quality systems.
 
 
 Strong analytical, technical, and problem-solving skills.
 
 
 Effective communication and teamwork capabilities.
 
 
 Ability to work within a rotational shift system.
 
</div>

Quality Control Analyst

Meso Scale Diagnostics

<div>POSITION SUMMARY:

Under general supervision, the Quality Analyst I performs routine quality control inspection, testing and data analysis for various incoming materials, in-process samples, and final products within MSD&rsquo;s protein-based immunoassay catalog. This role requires application of scientific principles and laboratory techniques to evaluate product performance against established specifications. The Quality Analyst I is also responsible for executing laboratory support activities, including equipment maintenance, reagent preparation, and cleaning tasks, to ensure compliance with quality standards and support the overall operations of the Quality Control laboratories.

DUTIES AND RESPONSIBILITIES:
<ul><li>Complete testing of incoming, manufactured, and in-process materials using analytical characterization and/or immunoassay testing techniques (e.g. ELISA).</li></ul>
<ul><li>Interpret analytical data to evaluate product quality, assess trends, and determine compliance with established specifications.</li></ul>
<ul><li>Create and/or maintain quality documentation and data summaries in compliance with ISO standards.</li></ul>
<ul><li>Operate standard laboratory equipment including micropipettes, plate washers, automated liquid handling systems, analytical instrumentation, and plate readers.</li></ul>
<ul><li>Adhere to organizational and laboratory safety standards including the proper use of personal protective equipment in BSL-1 and BSL-2 laboratories.</li></ul>
<ul><li>Contribute to the development and refinement of standard operating procedures (SOPs).</li></ul>
<ul><li>Complete scheduled work daily while working in a fast-paced environment with a minimum of deviations.</li></ul>
<ul><li>Specific duties may vary depending upon departmental requirements.</li></ul>

EXPERIENCE AND QUALIFICATIONS:
<ul><li>Bachelor&rsquo;s degree in Biology, Chemistry, Biochemistry, or a closely related scientific discipline is required.</li></ul>

o High School Diploma and additional experience may be substituted for Bachelor&rsquo;s degree. 


KNOWLEDGE, SKILLS AND ABILITIES:
<ul><li>Understanding of molecular biology techniques.</li></ul>
<ul><li>Precision pipetting techniques to ensure accurate measurements for quantitative analytical assays..</li></ul>
<ul><li>Ability to multi-task and work productively in a demanding environment with changing priorities.</li></ul>
<ul><li>Solid interpersonal skills</li></ul>

o Ability to effectively communicate issues/problems and results that impact timelines, accuracy and reliability of laboratory data.
<ul><li>Attention to detail with demonstrated commitment to excellence and performance.</li></ul>
<ul><li>Ability to work independently and as an effective team member.</li></ul>
<ul><li>Proficiency in MS Office suite.</li></ul>

o Experience with standard data analysis tools and databases (Excel, Access, SharePoint).
<ul><li>Ability to work outside of normal business hours to include long hours, weekends and shift schedules.</li></ul>

PHYSICAL DEMANDS:
<ul><li>There are aspects of this position that may require a person in this role be able to work at heights up to four (4) feet on occasion and with objects weighing up to 50 lbs.</li></ul>
<ul><li>Up to 100 % of the day may be spent sitting or standing at a desk/lab bench working with a computer or other items that will require fine motor manipulation.</li></ul>

WORK ENVIRONMENT:
<ul><li>Laboratory environment working with chemical reagents and performing some Biosafety Level 2 work.</li></ul>

o May involve handling of BSL-2 or BSL-2+ materials and organisms including human blood and/or blood products.
<ul><li>Standard office environment</li></ul>

COMPENSATION SUMMARY:

The annual base salary for this position ranges from $52,400 to $76,000. This salary range represents a general guideline as MSD considers other factors when presenting an offer of employment, such as scope and responsibilities of the position, external market factors, and the candidate&rsquo;s knowledge, skills, abilities, education and experience. Employees may qualify for a discretionary or non-discretionary bonus in addition to their base salary. These annual bonuses are intended to recognize individual performance and enable employees to benefit from the Company's overall success.

BENEFITS SUMMARY:

At MSD, we offer a comprehensive benefits package to support our employees' well-being and financial security. In addition to competitive salaries, our benefits include medical, dental, and vision coverage, along with prescription benefits. We provide a 401(k) plan with company matching, flexible spending accounts, and company-paid short- and long-term disability insurance as well as group life and accidental death and dismemberment insurance. Our offerings also encompass paid vacation, paid sick leave, paid holidays, and paid parental leave, along with an employee assistance program. Additional voluntary perks include a fitness club membership contribution, pet insurance, identity theft protection, home and auto insurance discounts, and optional supplemental life insurance.

EEO/AA STATEMENT:

MSD is an Equal Opportunity/Affirmative Action Employer. We are committed to fostering a diverse and inclusive workplace where all individuals are treated with respect and dignity. We welcome applications from all qualified candidates, making employment decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, genetic information, marital status, national origin, age, protected veteran status, pregnancy, disability status, or any other protected characteristic. For our full EEO/AA and Pay Transparency statement, please click on the following link: https://www.mesoscale.com/en/our_company/careers/equal_employment_opportunity_statement (https://www.mesoscale.com/en/our_company/careers/equal_employment_opportunity_statement).

Meso Scale Diagnostics uses E-Verify to validate the work eligibility of candidates.<h4 class="jobSectionHeader"> 
Education</h4>
Preferred<ul><li>
Bachelors or better in Biology or related field</li></ul>
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities 
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.</div>

Quality Control Analyst I

ELECTRIC MACHINERY COMPANY INC

<div>Electric Machinery Company. a division of WEG Electric Corp.
Minneapolis, Minnesota
Position: Quality Analyst / WMS
Team: Quality 
Primary Objective of Position:
This position will be responsible for WMS Office; analyzing end-to-end processes to identify waste, bottlenecks, variation, rework, and implement data-driven improvements. Establishes and maintains process standardization through work instructions, procedures, and control of critical administrative process parameters. Monitors, analyzes, and reports KPI performance, including efficiency, rework, lead time in WMS Office.
Major Areas of Accountability:<ul><li>
Identifies steps in an administrative process to separate those that do not add value; rework, and excess paperwork | documents, transporting physical documents, excessive emails, unnecessary processing, and searching for files</li><li>
Implements RPA (Robotic Process Automation) configuring software &quot;robots&quot; to perform repetitive and rule-based tasks</li><li>
Audits paper forms and manual approvals with digital systems and automated workflows, and updates as needed</li><li>
Reviews different software (such as TOTVS ERP or CRMs) to prevent employees from having to re-enter information from one platform to another</li><li>
Encourages a mindset of daily improvement; encourages everyone to identify waste and suggest solutions</li><li>
Gathers and analyzes data to measure the efficiency of new automated processes; ensure technology is delivering the expected return in time and quality</li><li>
Analyzes data, reports findings to Team; recommends process improvements to enhance efficiency</li><li>
Collaborates with other departments to solve any issues</li><li>
Fosters a culture of continuous improvement and excellence</li><li>
Other duties may be assigned by management to meet business needs</li></ul>
Qualifications/Knowledge/Skills/Abilities:<ul><li>
Bachelor&rsquo;s degree (Information Technology, Information Systems, or Project Management preferred); equivalent professional experience will also be considered</li><li>
5+ years of experience in data analysis and modeling</li><li>
Knowledge of digital transformation and Industry 4.0 concepts applied to manufacturing and administrative processes (data analytics, process automation, MES/ERP, VBA, RPA, RDA, Power BI or Tableau)</li><li>
Proficiency in MS Office Suite, Internet, e-Mail and SAP</li><li>
Demonstrate exceptional written and verbal communication skills including active listening is essential</li><li>
Strong attention to detail and excellent analytical skills</li><li>
Ability to prioritize multiple tasks, and shift work activities in order to meet business needs and goals</li><li>
Demonstrated ability to analyze, manipulate, and interpret data</li><li>
Demonstrated ability to propose, plan, and implement creative solutions</li><li>
Advanced problem-solving and root cause analysis skills</li><li>
Proven ability to lead projects by example</li><li>
Emotional intelligence to handle resistance</li><li>
Self-starting, results-oriented, flexible, and team player</li></ul>
Physical Requirements:<ul><li>
Work is performed in both an office and manufacturing environment. Requires the ability to routinely move throughout the office and manufacturing facility to perform work</li><li>
Requires the ability to routinely lift up to 25 pounds</li><li>
Requires the ability to ascend and descend stairs daily to reach all areas in the manufacturing facility</li></ul>
 Benefits<ul><li>
Medical, Dental &amp; Vision Insurance eligible your 1st day on the job</li><li>
401K with Match 1st of the month following hire</li><li>
Quarterly Bonus Program payout potential</li><li>
Company paid Holidays (13)</li><li>
Paid Time Off (PTO) accrued</li><li>
Company paid Short &amp; Long Term Disability</li><li>
Company paid Life Insurance</li><li>
Paid Birthday (use anytime throughout the year)</li><li>
$6,000 annual Tuition Reimbursement program</li><li>
Company provided tools</li><li>
Uniforms (laundered), Safety Shoes &amp; Glasses</li><li>
Secure, onsite free parking</li></ul>
Company cannot provide sponsorship for this position
Please, no agencies</div>

Quality Analyst / WMS Office

Novartis

<div><div><h3 class="jobSectionHeader">Summary
</h3><div>#LI-Onsite 
Location: Amiria, Egypt 
Relocation Support: This role is based in Amiria, Egypt. Novartis is unable to offer relocation support: please only apply if accessible. 
 
If you thrive in fast-paced environments where your expertise keeps production moving, this role is for you. As a QC Specialist, you will ensure raw materials meet the highest quality standards before reaching production. You&rsquo;ll apply advanced analytical techniques, handle real-time challenges, and play a key role in maintaining compliance and data integrity in a high-demand environment.</div>
</div><div><h3 class="jobSectionHeader">About the Role
</h3><div>Key Responsibilities<ul><li>
Perform raw material testing and analysis using chromatography and related laboratory techniques.</li><li>
Support compliant material release decisions to ensure production readiness and uninterrupted supply.</li><li>
Maintain accurate documentation and strong data integrity across testing and quality records.</li><li>
Ensure full compliance with Good Manufacturing Practices and site quality standards.</li><li>
Support investigations and quality issue resolution in a high-pressure manufacturing environment.</li><li>
Collaborate with production, procurement, and suppliers to prevent delays and resolve risks.</li><li>
Contribute technical expertise to inspection readiness and continuous improvement initiatives.</li></ul>
Essential Requirements<ul><li>
Bachelor&rsquo;s degree in Pharmacy or a related scientific field.</li><li>
At least two years of experience in pharmaceutical quality control.</li><li>
Hands-on experience in raw material testing, including chromatography-based analysis.</li><li>
Strong knowledge of Good Manufacturing Practices and quality compliance requirements.</li><li>
High attention to data integrity, documentation accuracy, and reliable execution.</li><li>
Ability to manage complexity, solve problems quickly, and collaborate across teams.</li></ul>
Desirable Requirements<ul><li>
Experience in environmental monitoring</li><li>
Exposure to quality control, analytical science and technology, or quality assurance environments.</li></ul>
Commitment to Diversity &amp; Inclusion
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Novartis is a proud member of the ILO Global Business and Disability Network and the Valuable 500, promoting the inclusion of people with disabilities in workplaces around the world. We also collaborate with international partners, such as Disability: IN, Purple Space, and Business Disability Forum to identify and develop best practice solutions to enable people with disabilities to participate as equal members of our organization.</div>
</div><div><div>Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients&rsquo; lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Learn about all the ways we&rsquo;ll help you thrive personally and professionally. 
Read our handbook (PDF 30 MB)</div></div></div>
 <div><div>Division
<div>Operations
</div></div><div>Business Unit
<div>Quality
</div></div><div>Location
<div>Egypt
</div></div><div>Site
<div>Amiria
</div></div><div>Company / Legal Entity
<div>EG02 (FCRS = EG002) Novartis Pharma S.A.E
</div></div><div>Functional Area
<div>Quality
</div></div><div>Job Type
<div>Full time
</div></div><div>Employment Type
<div>Regular
</div></div><div>Shift Work
<div>No</div></div></div><div></div>

QC Specialist (m/f/d)

CBC Mortgage Agency

<div>About CBC Mortgage Agency
CBC Mortgage Agency (CBCMA) focuses on personal and professional development as the core value of the Company that has established a record of success and growth. Take your career to the next level in a comfortable workplace with an environment that encourages networking and team socializing. As well as great perks and benefits the position offers competitive wages, depending on experience, as well as full benefits, including medical, dental, and vision insurance coverage, short- and long-term disability, and a 401(k)-plan retirement investment. In addition to these great benefits, we offer 11 company holidays a year and paid time off (PTO). If this is the opportunity that you&rsquo;ve been waiting for, apply today!
Summary 
CBC Mortgage Agency is seeking a detail-oriented, efficient, and knowledgeable Quality Assurance Specialist with good time management and organizational skills, and the ability to effectively resolve problems and issues involving agency and investor guidelines arising from due diligence reviews and investor audits as well as the Company&rsquo;s third-party quality control vendor.
Compensation: $28.00 to $33.00 per hour DOE, Full-time, Remote, fully eligible for Company comprehensive benefits suite.
Essential Functions 
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This position includes but is not limited to the following additional duties:<ul><li>
Supervises monthly Post Purchase QC reporting.</li><li>
Ensures timely delivery of Investor Post Purchase QC orders and timely management responses to all audit findings resulting from monthly Investor Post Purchase QC orders.</li><li>
Submits final reports to President, EVP and Credit Quality Committee.</li><li>
Works together with the Purchase Clearing, QC and Compliance teams to ensure quick resolution of due diligence and investor audit findings.</li><li>
Reviews items that are a variation of an actual condition required to determine if the acceptance of a condition is in line with guidance and will be acceptable to the investor.</li><li>
Assists in all tasks necessary to ensure quality control standards are met pursuant to HUD, FHA, and Fannie Mae requirements for Quality Control Plans.</li><li>
Participates, inter-departmentally, in identifying and developing strategies for process improvements designed to meet service level and productivity objectives and goals.</li><li>
Validates findings on loans post-purchase.</li><li>
Capacity and competency to perform other duties as assigned by management.</li><li>
Conduct and perform audits of Third-party QC vendors.</li><li>
Other duties and tasks as assigned by management.</li></ul>
Competencies<ul><li>
Results Driven &amp; Professionalism.</li><li>
Proficient communication and follow-through skills.</li><li>
Willingness to help both internal and external customers.</li><li>
Able to work independently as well as in a team environment.</li><li>
Strong analytical, organizational, and time management skills.</li><li>
Excellent computer skills as well as analytical and problem-solving skills.</li><li>
Able to maintain a professional image and adhere to standards consistent with company policies and procedures.</li><li>
Ability to adapt to a rapidly changing environment.</li></ul>
Work Environment 
This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets, and fax machines.
Physical Demands 
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms.
Position Type/Expected Hours of Work 
This is a full-time position, working Monday through Friday with consistent hours.
Travel 
No travel is expected.
Required Education and Experience<ul><li>
Two years or more experience working in Quality Control and/or Assurance in mortgage, banking, or another closely related industry field.</li><li>
High School Diploma/GED or higher education degree or certificate.</li><li>
3. Use of Microsoft products and Quality Control systems and procedures.</li></ul>
Work Authorization/Security Clearance 
Must be authorized to legally work within the United States of America.
Other Duties 
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.</div>

Mortgage Loans - Quality Assurance Specialist

NielsenIQ

<div>
 
 Join GfK and help us shape tomorrow. As an NIQ company, we are the world's leading consumer intelligence firm, delivering the Full View&trade; on consumer behavior. We work to enable manufacturers and retailers better understand what consumers really want. Our name has inspired trust for over 89 years because we take pride in discovering new pathways to sustainable growth for our clients, our people, and our planet.
 
 
 
 
 
 
 Job Description
 
 
 
 <ul>
 <li>
 Execute low to medium complexity quality control tasks under supervision
 </li>
 <li>
 Ensure accurate setting of QC Ratings as a quality benchmark and foundation for further analysis
 </li>
 <li>
 Maintain compliance with global quality standards as defined by the MI OPS framework
 </li>
 <li>
 Identify and report quality issues, inconsistencies, or process gaps
 </li>
 <li>
 Collaborate with cross-functional teams to support continuous improvement initiatives
 
 
 </li>
 </ul>
 
 Qualifications
 
 
 
 <ul>
 <li>
 Ability to complete assigned tasks on time with high accuracy and attention to detail
 </li>
 <li>
 Strong technical skills to perform quality checks effectively, including deeper knowledge of tools and systems used
 </li>
 <li>
 Solid written and verbal communication skills for clear documentation and collaboration
 </li>
 <li>
 Good analytical and problem-solving abilities to assess data and identify root causes
 </li>
 <li>
 Sound judgment in handling ambiguous or complex situations
 </li>
 <li>
 Product knowledge in a limited set of Product Groups
 </li>
 <li>
 Proficiency in MS Office (Excel, Word, Outlook, etc.)
 </li>
 <li>
 A collaborative mindset and strong interpersonal skills to work effectively in a team environment
 </li>
 <li>
 Should have a bachelors degree
 
 
 </li>
 </ul>
 
 Additional Information
 
 
 
 
 
 Our Benefits
 
 
 
 
 <ul>
 <li>
 Flexible working environment
 </li>
 <li>
 Volunteer time off
 </li>
 <li>
 LinkedIn Learning
 </li>
 <li>
 Employee-Assistance-Program (EAP)
 </li>
 </ul>
 
 NIQ may utilize artificial intelligence (AI) tools at various stages of the recruitment process, including r&eacute;sum&eacute; screening, candidate assessments, interview scheduling, job matching, communication support, and certain administrative tasks that help streamline workflows. These tools are intended to improve efficiency and support fair and consistent evaluation based on job-related criteria. All use of AI is governed by NIQ&rsquo;s principles of fairness, transparency, human oversight, and inclusion. Final hiring decisions are made exclusively by humans. NIQ regularly reviews its AI tools to help mitigate bias and ensure compliance with applicable laws and regulations. If you have questions, require accommodations, or wish to request human review were permitted by law, please contact your local HR representative. For more information, please visit NIQ&rsquo;s AI Safety Policies and Guiding Principles: https://www.nielseniq.com/global/en/ai-safety-policies.
 
 
 
 
 
 
 About NIQ
 
 
 
 
 
 NIQ is the world&rsquo;s leading consumer intelligence company, delivering the most complete understanding of consumer buying behavior and revealing new pathways to growth. In 2023, NIQ combined with GfK, bringing together the two industry leaders with unparalleled global reach. With a holistic retail read and the most comprehensive consumer insights&mdash;delivered with advanced analytics through state-of-the-art platforms&mdash;NIQ delivers the Full View&trade;. NIQ is an Advent International portfolio company with operations in 100+ markets, covering more than 90% of the world&rsquo;s population.
 
 
 
 
 For more information, visit NIQ.com
 
 
 
 
 Want to keep up with our latest updates?
 
 
 
 
 Follow us on: LinkedIn | Instagram | Twitter | Facebook
 
 
 
 
 
 
 Our commitment to Diversity, Equity, and Inclusion
 
 
 
 
 
 At NIQ, we are steadfast in our commitment to fostering an inclusive workplace that mirrors the rich diversity of the communities and markets we serve. We believe that embracing a wide range of perspectives drives innovation and excellence. All employment decisions at NIQ are made without regard to race, color, religion, sex (including pregnancy, sexual orientation, or gender identity), national origin, age, disability, genetic information, marital status, veteran status, or any other characteristic protected by applicable laws. We invite individuals who share our dedication to inclusivity and equity to join us in making a meaningful impact. To learn more about our ongoing efforts in diversity and inclusion, please visit the https://nielseniq.com/global/en/news-center/diversity-inclusion
 
 
 
</div>

Quality Associate Data OPS

Stellar Consulting Solutions, LLC

<div>
 
 
 Role: Supplier Quality Analyst
 
 
 
 
 Location: Irvine, CA(Onsite)
 
 
 
 
 Duration: 6+Months(Contract#w2)
 
 
 
 
 Client: Medical
 
 
 
 
 
 
 Education Bachelor Engineering or Quality
 
 
 Windchill / PLM Will red line Doc's
 
 
 Doc control , Validating systems , Updating supplier change request , reveiwing Quality Agreements
 
 
 
 Job Summary
 
 
 
 The Supplier Quality Analyst is responsible for ensuring that suppliers of materials, components, and services used in medical devices consistently meet quality, regulatory, and risk requirements. This role supports compliance with FDA Quality System Regulation (21 CFR 820), ISO 13485 through supplier performance monitoring, corrective action management, and risk-based supplier controls.
 
 
 
 Key Responsibilities
 
 
 <ul>
 <li>
 Manage and maintain supplier qualification, monitoring, and re-evaluation activities in accordance with 21 CFR 820.50 (Purchasing Controls) and ISO 13485.
 </li>
 <li>
 Monitor supplier quality performance using KPIs such as defect rates, corrective action trends, and supplier risk levels.
 </li>
 <li>
 Maintain approved supplier lists (ASL) and supplier quality records per document control requirements.
 </li>
 <li>
 Issue, track, and evaluate Supplier change requests.
 </li>
 <li>
 Escalate supplier quality risks and support remediation and improvement plans.
 </li>
 <li>
 Review and support supplier-initiated or internally driven changes that may impact product quality or compliance (materials, processes, manufacturing location).
 </li>
 <li>
 Collaborate with Engineering and Regulatory Affairs to assess supplier changes requiring validation, verification, or regulatory impact evaluation.
 </li>
 <li>
 Provide supplier quality input for management reviews and quality metrics.
 </li>
 <li>
 Ensure supplier quality documentation is accurate, complete, and maintained in the electronic Quality Management System (eQMS).
 </li>
 <li>
 Ensure supplier activities comply with internal procedures, regulatory requirements, and quality system expectations.
 </li>
 </ul>
 
 
 Required Qualifications
 
 
 <ul>
 <li>
 Bachelor&rsquo;s degree in Engineering, Quality, or a related field; or equivalent experience.
 </li>
 <li>
 2&ndash;5 years of experience in Supplier Quality, Quality Assurance, or Manufacturing within a medical device or other regulated environment.
 </li>
 <li>
 Working knowledge of 21 CFR 820, ISO 13485, and supplier control requirements.
 </li>
 <li>
 Proficiency in Microsoft Excel and data analysis.
 </li>
 </ul>
 
 
 Key Skills &amp; Competencies
 
 
 <ul>
 <li>
 Strong understanding of regulated quality systems
 </li>
 <li>
 Analytical, detail-oriented problem-solving mindset
 </li>
 <li>
 Clear written and verbal communication
 </li>
 <li>
 Ability to influence suppliers and internal stakeholders
 </li>
 <li>
 Strong organizational and time-management skills.
 </li>
 </ul>
 
 
 
 
 kindly share resume at gaurav@stellarconsulting.com or call me at 678-935-7045 to discuss more!
 
</div>

Supplier Quality Assurance

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