Urwah Admin

Zimmer Biomet

<div><p>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.</p><p>
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.</p><div><div><div><h2 class="jobSectionHeader"><b><br>
What You Can Expect</b></h2>
</div><div><p>
Paragon 28, a Zimmer Biomet Company is hiring a Sr Supplier Quality Engineer. The Sr. Supplier Quality Engineer is a quality engineering position that has emphasis on developing and maintaining Paragon 28&rsquo;s supplier quality system and related quality activities specifically relating to product development, manufacturing, and supply chain of Paragon 28 orthopedic products for the Foot and Ankle. This is hybrid position located at our Englewood, Colorado location.</p></div></div><div><div><h2 class="jobSectionHeader"><b>
How You'll Create Impact</b></h2>
</div><div><ul><li>Process Owner for Key Quality Processes: Supplier Management</li><li>Lead supplier qualification process. Interface with suppliers to ensure product compliance to specification and perform supplier audits as needed.</li><li>Develop measurement techniques for product release at suppliers.</li><li>Participating on project teams as a contributing member by providing supplier quality engineering support in the development of new suppliers and processes, and continuously improving company&rsquo;s products and suppliers.</li><li>Provide support for the manufacturing areas (external). Work with production personnel and supervision to determine and monitor quality metrics, samples plans and address non-conforming product issues. Lead corrective and preventive action investigations to resolve the root cause of problems.</li><li>Auditing suppliers on time and per schedule</li><li>Writing audit plans and audit reports for suppliers to all applicable standards and regulations</li><li>Writing and reviewing of procedures, plans, protocols and reports to ensure regulatory compliance.</li><li>Perform Mechanical Inspections and use typical equipment used in inspection.</li><li>Assist with Design Transfer for release of new product development projects.</li><li>Author and/or assist in the development and execution of process validations at suppliers</li><li>Perform statistical analysis for testing requirements and develop MSAs, TMQs, and inspection correlations.</li><li>Assist suppliers in completion of Supplier Corrective Actions per appropriate timelines</li><li>Assisting project teams on compliance with purchasing requirements per FDA QSR, European MDD/MDR, ISO 13485 and other applicable ISO/EN standards</li><li>Capture and calculate supplier metrics on a regular basis</li><li>Develop relationships with employees and suppliers to ensure team-oriented operation.</li><li>Accurately represents quality processes to 3rd party auditors (FDA, ISO 13485, MDSAP, etc.)</li><li>Other duties as assigned</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><ul><li>Bachelor&rsquo;s degree in Engineering or technical discipline</li><li>4+ years in related field, preferably medical device or manufacturing</li><li>Auditing experience, ISO 13485 preferred</li><li>Proficient in Machining methodologies (Titanium and Stainless-Steel experience best), knowledge of hardness, passivation, surface treatments, cleaning techniques etc. for communication with Suppliers and Engineers.</li><li>Familiarity with 21 CFR 820 and ISO 13485 and other Government / ISO Standards</li><li>Technical writing skills that include Quality Management Systems (QMS) and procedures</li><li>Proficient in Geometric Dimensioning and Tolerancing (GD&amp;T) preferable</li><li>Process Validation experience</li><li>Basic Computer Skills (MS Office)</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Compensation Data</b></h2>
</div><div><p>
Salary Range: $90,000 - $110,000 USD annually based on skills and experience</p></div></div><div><div><h2 class="jobSectionHeader"><b>
Travel Expectations</b></h2>
</div><div><p>
Travel should not exceed 50% of total time. Supplier travel will be needed for on-site audits and/or trouble shooting.</p></div></div></div><p><br>
EOE</p></div>

Sr. Supplier Quality Engineer

<div><p>At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient&rsquo;s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.</p><p>
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.</p><div><div><div><h2 class="jobSectionHeader"><b><br>
What You Can Expect</b></h2>
</div><div><p>
Zimmer Biomet is a world leader in musculoskeletal health solutions. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world. We are seeking a highly skilled and detail-oriented professional to manage and maintain a large dataset of deidentified patient information. This role is critical in ensuring data integrity, security, privacy, and compliance with all applicable regulations. The ideal candidate will have strong technical expertise in data management, policy development, and advanced analytics, as well as the ability to collaborate with internal teams and external partners.</p><p><b>
This is a hybrid position, 2 days on site per week required in Warsaw, IN.</b></p></div></div><div><div><h2 class="jobSectionHeader"><b>
How You'll Create Impact</b></h2>
</div><div><ul><li>Oversee the storage, organization, and maintenance of large-scale deidentified patient datasets.</li><li>
Develop, implement, and maintain policies and procedures to ensure compliance with privacy, security, and regulatory requirements (e.g., HIPAA)</li><li>
Manage expert determinations and documentation for deidentification processes.</li><li>
Collaborate with external partners to acquire supplemental datasets.</li><li>
Negotiate and manage data-sharing agreements and ensure compliance with contractual obligations.</li><li>
Perform SQL queries to extract, transform, and analyze data.</li><li>
Utilize advanced Excel functions, including Power Query, for data manipulation and reporting.</li><li>
Leverage tools such as GitHub Copilot, Microsoft Azure, and other advanced analytical platforms for data analysis and automation.</li><li>
Work with other data management systems and platforms to ensure interoperability and efficiency.</li><li>
Identify opportunities to improve data workflows and implement best practices.</li><li>
Document data analysis activities with internal protocols and reports, and lead publishing activities to share findings with the broader scientific community</li></ul><p><i>
This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.</i></p></div></div><div><div><h2 class="jobSectionHeader"><b>
What Makes You Stand Out</b></h2>
</div><div><ul><li>Excellent problem-solving and analytical skills.</li><li>
Ability to communicate complex technical concepts to non-technical stakeholders.</li><li>
Strong organizational skills and attention to detail.</li><li>
Strong time management skills to navigate competing priorities.</li><li>
Proven experience with SQL (e.g. BigQuery) and advanced Excel (including Power Query).</li><li>
Familiarity with cloud platforms (e.g., Microsoft Azure) and version control tools (e.g., GitHub).</li><li>
Strong technical writing and written and oral communication skills</li><li>
Strong understanding of data privacy and security regulations.</li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Your Background</b></h2>
</div><div><ul><li>Bachelor&rsquo;s degree required in Data Science, Computer Science, Information Systems, Public Health, or related field (Master&rsquo;s preferred).</li><li>
3+ years in data management, governance, or analytics roles required.</li><li><b>
Preferred Qualifications:
</b><ul><li>Experience with expert determination processes and privacy compliance frameworks.</li><li>
Experience with cybersecurity assessments and adherence to current standards.</li><li>
Experience with healthcare data or clinical research datasets.</li><li>
Knowledge of additional data management systems or ETL tools.</li><li>
Familiarity with machine learning or advanced statistical analysis.</li><li>
Working knowledge of Python for data analytics.</li></ul></li></ul></div></div><div><div><h2 class="jobSectionHeader"><b>
Travel Expectations</b></h2>
</div><div><p>
5%</p></div></div></div><p><br>
EOE</p></div>

Data Sr Analyst

Join Zimmer Biomet and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Zimmer Biomet

ABOUT_COMPANY

Sr. Supplier Quality Engineer

Data Sr Analyst