product manager medical device

AEG Consulting

<p><b>Position Overview</b></p><p>The Manager of Quality Control (QC) &amp; Quality Assurance (QA) leads the factory&rsquo;s quality function for medical devices and disposables (bandages, masks, medical tapes, and related products). This role ensures full compliance with Drug Regulatory Authority of Pakistan (DRAP) Medical Device Rules 2017, Good Manufacturing Practices for Medical Devices (GDPMD), and ISO 13485 Quality Management Systems. The position oversees quality testing, assurance systems, audits, regulatory compliance, and continuous improvement of product quality and safety.</p><p><b>Key Responsibilities</b></p><p><b>1. Regulatory &amp; Compliance Oversight:</b></p><ul><li>Ensure all quality systems comply with DRAP Medical Device Rules 2017 and ISO 13485 requirements.</li><li>Maintain valid DRAP certifications, licenses, and product registrations for all manufactured devices.</li><li>Prepare and manage documentation required for DRAP audits, GMP/GDPMD inspections, and ISO audits.</li><li>Liaise with regulatory bodies (DRAP, MoH) during inspections, ensuring timely responses to observations.</li></ul><p><b>2. Quality Assurance (QA):</b></p><ul><li>Develop, implement, and maintain SOPs for all production and quality processes.</li><li>Oversee validation and qualification activities (equipment, processes, and cleanrooms).</li><li>Ensure all raw materials, in-process checks, and finished goods comply with quality and regulatory requirements.</li><li>Lead Corrective and Preventive Actions (CAPA) for deviations and non-conformities.</li><li>Ensure proper implementation of Document Control and Change Control systems.</li></ul><p><b>3. Quality Control (QC):</b></p><ul><li>Oversee laboratory and in-process QC testing for raw materials, intermediates, and finished products.</li><li>Monitor and report number of quality issues per month and ensure corrective actions.</li><li>Validate and maintain testing methods for accuracy, reliability, and compliance with device standards.</li><li>Ensure calibration and maintenance of laboratory instruments.</li><li>Review and approve Certificates of Analysis (CoA) and release of finished goods.</li></ul><p><b>4. Risk Management &amp; Safety:</b></p><ul><li>Implement risk-based quality management in line with ISO 14971 (Risk Management for Medical Devices).</li><li>Ensure hygienic, contamination-free production environments through audits and inspections.</li><li>Work with the Operations Manager to maintain a Zero Total Recordable Incident Rate (TRIR) and maximize safe man-hours.</li></ul><p><b>5. Audits &amp; Inspections:</b></p><ul><li>Lead internal quality audits to ensure compliance with GDPMD, ISO 13485, and DRAP requirements.</li><li>Coordinate management reviews and ensure continuous improvement of the QMS.</li><li>Lead preparation for DRAP and ISO surveillance audits, ensuring audit readiness across departments.</li></ul><p><b>6. Team Leadership &amp; Training:</b></p><ul><li>Manage and mentor QC/QA staff to build strong technical and compliance capabilities.</li><li>Conduct regular training sessions for production and QC/QA teams on GDPMD, GMP, ISO 13485, hygiene, and quality standards.</li><li>Foster a culture of quality, accountability, and regulatory compliance across the organization.</li></ul><p><b>7. KPI Monitoring &amp; Reporting:</b></p><ul><li>Track and report the following KPIs regularly:</li><li>Number of quality issues per month in QC checks.</li><li>CAPA closure rate and lead time.</li><li>Audit observations vs. compliance closures.</li><li>Planned vs. Actual product release timelines.</li><li>% of batches released without deviation.</li><li>Material rejection rate &le;1% (in line with wastage targets).</li><li>Submit quality performance reports to senior management and regulatory bodies where required.</li></ul><p><b>Education &amp; Experience Requirements:</b></p><ul><li>Bachelor&rsquo;s or Master&rsquo;s in Pharmacy, Microbiology, Biomedical Engineering, or related field.</li><li>Minimum 8&ndash;12 years&rsquo; experience in QC/QA within medical devices or pharmaceutical manufacturing, including at least 3 years in a leadership role.</li><li>In-depth knowledge of DRAP Medical Device Rules 2017, GDPMD, ISO 13485, and ISO 14971.</li><li>Strong background in laboratory management, audits, and regulatory compliance.</li></ul><p><b>Key Skills &amp; Competencies:</b></p><ul><li>Expertise in quality systems (QMS), validation, and compliance.</li><li>Strong leadership in audit handling (internal &amp; external).</li><li>Proficiency in CAPA, deviation handling, and root cause analysis.</li><li>Excellent documentation, reporting, and regulatory communication skills.</li><li>Analytical and problem-solving skills with a focus on continuous improvement.</li></ul><p>Job Type: Full-time</p><p>Pay: Rs125,000.00 - Rs175,000.00 per month</p><p>Work Location: In person</p>

Manager of QA/QC – Medical Devices Manufacturing (DRAP Compliance)

Arthrex

<div><div><div><div><div><div><div><div><div><div><div><b>Requisition ID</b>:</div> <div>63725</div>
</div><br>
<div><div><b>Title</b>:</div> <div>Associate Product Manager, Global Endoscopy</div>
</div><br>
<div><div><b>Division</b>:</div> <div>Arthrex, Inc. (US01)</div>
</div><br>
<div><div><b>Location:</b></div> <div>Naples, FL</div>
</div><br>
<div><div><b>Salary Range:</b></div>
<div><div><div><div><div><b>Salary Minimum:</b></div> <div>$79,001.00</div>
</div><br>
<div><div><b>Salary Maximum:</b></div> <div>$120,000</div>
</div><br>
</div></div></div></div><br>
</div></div><p><b><i>*This position is based in Naples, FL or Santa Barbara, CA.*</i></b></p><br>
<p></p>
<p>
Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Associate Product Manager - Global Endoscopy to manage and lead our initiatives. The successful candidate will be responsible for supporting our multi-speciality product solutions, clinical training and fluorescence imaging - focusing on general surgery, assisting marketing and sales opportunities, product performance, training and other activities. This position is based in Naples, FL or Santa Barbara, CA and does require travel. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better&trade;.</p><br>
<p></p>
<p><b>
Essential Duties and Responsibilities:</b></p>
<ul>
<li>Support field sales opportunities with expert support material and education</li>
<li>Train and educate sales teams on fluorescence, general surgery</li>
<li>Provides leadership and guidance to other Product / Project Managers</li>
<li>Participates in overall product strategy, research and development requirements, development, and manufacturing coordination for new and emerging products.</li>
<li>Manages technical product development, estimates of potential profits, and release to production.</li>
<li>Manages day-to-day progress of product.</li>
<li>Provides technical expertise and training to other departments in support of product development.</li>
<li>Conducts marketing analysis to develop product definitions.</li>
<li>Collaborates with a wide variety of functional areas such as sales, engineering, marketing, manufacturing, and operations to develop and provide product definitions responsive to customer needs and market opportunities.</li>
<li>Develops and maintains a prioritized list of customer and market requirements for product.</li>
<li>Conducts market research and identifies and tracks market trends in company's industry.</li>
<li>Produces competitive analysis materials comparing product with its key competitors.</li>
<li>Identifies partnering opportunities for complementary third-party products to broaden company's product line.</li>
<li>Participates in key sales situations for the product.</li>
<li>Maintains communications and contacts to collect and analyze technical, financial, schedule, and sales information for product line.</li>
<li>Identifies market potential, establishes pricing and market strategies, estimates potential sales, introduces market, distribution/channel issues, and manages mature product through phase-out.</li>
<li>Defines promotional activities, publicizing the product through the press, sales force, and alternate distribution channels.</li>
<li>Provides expertise in particular product area and develops strategies and applicable portions of the company business plan.</li>
<li>Plans, organizes, and coordinates assigned programs to ensure accomplishment of financial/budgetary goals and optimum allocation of resources.</li>
<li>Manages resources to execute assigned programs.</li>
<li>Coordinates details of program within the organization with a wide range of functions and individuals.</li>
<li>Coordinates product introduction and market exploitation with marketing and sales organizations to ensure maximum penetration of market segment.</li>
<li>Provides continuing product surveillance and management of established products to obtain financial objectives.</li>
<li>Must be able to be in operating rooms during surgery.</li>
<li>Must be able to work with cadaveric and porcine specimens.</li>
<li>Naples based or Santa Barbara based</li>
<li>Travel to customer sites for sales opportunities is required.</li>
<li>Up to 60% travel required.</li></ul><br>
<p></p>
<p><b>
Education and Experience:</b></p>
<ul>
<li>Bachelor&rsquo;s degree required, preferably in business, engineering or clinical.</li>
<li>One or more years&rsquo; experience in medical device product management, sales, engineering, clinical OR a master&rsquo;s degree is required.</li>
<li>General surgery/clinical experience is preferred.</li>
<li>Understanding of all functions involved in development, production, and marketing of product.</li>
<li>Travel to customer sites for sales opportunities is required.</li></ul><br>
<p></p>
<p><b>
Knowledge and Skill Requirements/Specialized Courses and/or Training:</b></p>
<ul>
<li>Knowledge of general surgery anatomy and procedures and fluorescence imaging.</li>
<li>Skilled in working with different functions and effectively coordinates their activities to achieve desired results.</li>
<li>Excellent listening skills, including the ability to identify and isolate customers' concerns or objections, in addition to excellent written and oral communication skills.</li>
<li>Proven ability to travel for past positions.</li>
<li>Ability to work with cadaveric and porcine specimens is required.</li></ul><p></p><div><b><br>
Arthrex Benefits</b></div>
<ul>
<li>Medical, Dental and Vision Insurance</li>
<li>Company-Provided Life Insurance</li>
<li>Voluntary Life Insurance</li>
<li>Flexible Spending Account (FSA)</li>
<li>Supplemental Insurance Plans (Accident, Cancer, Hospital, Critical Illness)</li>
<li>Matching 401(k) Retirement Plan</li>
<li>Annual Bonus</li>
<li>Wellness Incentive Program</li>
<li>Gym Reimbursement Program</li>
<li>Tuition Reimbursement Program</li>
<li>Trip of a Lifetime</li>
<li>Paid Parental Leave</li>
<li>Paid Time Off</li>
<li>Volunteer PTO</li>
<li>Employee Assistance Provider (EAP)</li></ul><br>
<div></div>
<div><b>
All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.</b></div></div></div></div></div></div></div></div><p></p>

Associate Product Manager, Global Endoscopy

Sehat Medical Devices Pvt Ltd

<div>
 <p>
  <strong>
   QC Manager
  </strong>
 </p>
 <p>
  <strong>
   Location:
  </strong>
  Sundar Industrial Estate, Lahore, Pakistan
 </p>
 <p>
  <strong>
   Department:
  </strong>
  Quality Control
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Position Overview
  </strong>
 </p>
 <p>
  The QC Manager will be responsible for overseeing all quality control operations at Sehat Medical Devices Pvt Ltd (SMD), ensuring products meet international quality standards, regulatory requirements, and customer specifications. This role requires deep technical expertise in medical device manufacturing, particularly syringes, infusion sets, and other disposables, as well as leadership skills to manage a multidisciplinary QC team.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities
  </strong>
 </p>
 <p>
  <strong>
   Quality Control Operations
  </strong>
 </p>
 <ul>
  <li>
   Lead all QC activities from raw material inspection to final product release.
  </li>
  <li>
   Implement and maintain quality control procedures in compliance with
   <strong>
    ISO 13485, ISO 10993, ISO 9001, GMP, WHO PQ
   </strong>
   and
   <strong>
    DRAP Medical Device Rules 2017
   </strong>
   .
  </li>
  <li>
   Ensure inspection and testing are carried out at all stages&mdash;incoming, in-process, and final&mdash;according to
   <strong>
    ISO 7886-1, ISO 8536, ISO 7864
   </strong>
   , and other relevant standards.
  </li>
  <li>
   Oversee microbiological, chemical, and mechanical testing in accordance with SMD&rsquo;s validated protocols.
  </li>
  <li>
   Manage product traceability systems, including
   <strong>
    batch number verification, retention samples, and documentation
   </strong>
   .
  </li>
 </ul>
 <p>
  <strong>
   Compliance &amp; Regulatory
  </strong>
 </p>
 <ul>
  <li>
   Ensure full compliance with
   <strong>
    DRAP regulations, ISO standards, and international customer requirements
   </strong>
   .
  </li>
  <li>
   Prepare and maintain QC records for regulatory audits, customer inspections, and internal reviews.
  </li>
  <li>
   Support certification processes for
   <strong>
    ISO 13485 Notified Body audit, WHO Prequalification, CE Marking, and FDA 510(k)
   </strong>
   .
  </li>
  <li>
   Liaise with regulatory bodies for inspections, queries, and product approvals.
  </li>
 </ul>
 <p>
  <strong>
   Lab Management
  </strong>
 </p>
 <ul>
  <li>
   Supervise QC laboratory operations, ensuring calibration and maintenance of equipment such as Universal Testing Machines, Leak Testers, UV-Vis spectrophotometers, GC, AAS, and microbiology lab instruments.
  </li>
  <li>
   Oversee procurement and qualification of new QC instruments.
  </li>
  <li>
   Establish lab safety protocols and training for staff.
  </li>
 </ul>
 <p>
  <strong>
   Team Leadership
  </strong>
 </p>
 <ul>
  <li>
   Manage, train, and mentor the QC team, including inspectors, lab technicians, and microbiologists.
  </li>
  <li>
   Set departmental KPIs and monitor performance against targets.
  </li>
  <li>
   Foster a culture of continuous improvement and root cause problem-solving.
  </li>
 </ul>
 <p>
  <strong>
   Investigation and Continuous Improvement
  </strong>
 </p>
 <ul>
  <li>
   Lead product non-conformance investigations, CAPA (Corrective and Preventive Actions), and deviation handling.
  </li>
  <li>
   Work closely with Production, QA, and R&amp;D teams to resolve quality issues.
  </li>
  <li>
   Implement statistical process control (SPC) and other data-driven quality improvement tools.
  </li>
  <li>
   Recommend process changes to reduce defects, improve yields, and ensure zero-compromise on product safety.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   <strong>
    QUALIFICATIONS
   </strong>
  </li>
  <li>
   Bachelor&rsquo;s or Master&rsquo;s degree in Biomedical Engineering, Pharmacy, Bio Technology etc
  </li>
  <li>
   8+ years of experience in QC, preferably in medical device manufacturing.
  </li>
  <li>
   In-depth knowledge of ISO 13485, ISO 10993, ISO 7886-1, ISO 7864, and relevant product standards.
  </li>
  <li>
   Experience with GMP, regulatory audits, and third-party certifications.
  </li>
  <li>
   Strong analytical skills with hands-on experience in laboratory testing and inspection methods.
  </li>
  <li>
   Proficiency in MS Office, ERP/Quality Management Systems
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Interested candidates are encouraged to apply at hr@sehat.ltd or through the easy apply button on linkedin
 </p>
</div>


QC Manager - Medical Devices

One97 Communications Limited

<div>
 <p>
  <strong>
   Senior Product Manager (Devices)
  </strong>
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About Paytm
  </strong>
 </p>
 <p>
  Paytm is India's leading mobile payments and financial services distribution company. Pioneer of the mobile QR payments revolution in India, Paytm builds technologies that help small businesses with payments and commerce. Paytm&rsquo;s mission is to serve half a billion Indians and bring them to the mainstream economy with the help of technology.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Experience:
  </strong>
  - 5+ years
 </p>
 <p>
  <strong>
   Location
  </strong>
  : Noida (WFO)
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About the Role-
  </strong>
 </p>
 <p>
  As a Senior Product Manager (Devices), you will own and lead the device charter across Soundbox, EDC, and emerging AI-enabled devices. You will set the strategy, define the roadmap, and work closely with CXOs to drive merchant experience, operational efficiency, and business impact.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Key Responsibilities-
  </strong>
 </p>
 <p>
  - Define and own the device roadmap &amp; vision aligned to Paytm&rsquo;s growth strategy.
 </p>
 <p>
  - Lead end-to-end device lifecycle management: activation &rarr; monitoring &rarr; predictive health &rarr; refurb/replacement &rarr; end-of-life.
 </p>
 <p>
  - Drive AI-powered device innovation (merchant-facing AI device, multilingual bot integration).
 </p>
 <p>
  - Influence leadership and cross-functional priorities with data-backed recommendations.
 </p>
 <p>
  - Mentor PMs/Associate PMs and build a strong device product culture.
 </p>
 <p>
  - Track industry benchmarks and competitive landscape to position Paytm devices ahead of peers.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What You&rsquo;ll Contribute To
  </strong>
 </p>
 <p>
  - Large-scale of AI adoption strategy.
 </p>
 <p>
  - Cross-device predictive health models to reduce downtime and false positives.
 </p>
 <p>
  - Proactive merchant engagement through Device and CLM.
 </p>
 <p>
  -Sustainability &amp; cost efficiency through smart refurb and replacement policies.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Skills &amp; Qualifications-
  </strong>
 </p>
 <p>
  - 5+ years of product experience, with at least 2 years owning device/IoT/fintech hardware products.
 </p>
 <p>
  - Strong leadership &amp; roadmap ownership skills, with CXO-level exposure.
 </p>
 <p>
  - Experience in driving cross-functional programs (engineering, business, operations).
 </p>
 <p>
  - Strategic thinker with execution excellence.
 </p>
 <p>
  - Ability to influence stakeholders and mentor junior PMs.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   &ZeroWidthSpace;Why join us?&nbsp;A
  </strong>
 </p>
 <p>
  collaborative output driven program that brings cohesiveness across businesses through technology Improve the average revenue per use by increasing the cross-sell opportunities&nbsp;A
 </p>
 <p>
  solid 360 feedback from your peer teams on your support of their goals&nbsp;R
 </p>
 <p>
  espect, that is earned, not demanded from your peers and manager&nbsp;C
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   ompensation:&nbsp;I
  </strong>
 </p>
 <p>
  f you are the right fit, we believe in creating wealth for you with enviable 500 mn+ registered users, 25 mn+ merchants and depth of data in our ecosystem, we are in a unique position to democratize credit for deserving consumers &amp; merchants &ndash; and we are committed to it. India&rsquo;s largest digital lending story is brewing here. It&rsquo;s your opportunity to be a part of the story
 </p>
</div>


Product Management- Sr. PM- Device Product

FujiFilm

<div>Position Overview:
<div>
We are hiring a Senior Counsel to be an integral part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas Corporation and FUJIFILM SonoSite, Inc., wholly-owned subsidiaries of FUJIFILM Holdings America Corporation (HLUS). The Senior Counsel, reporting to the Division General Counsel, Medical Devices, will be an experienced commercial transactions lawyer, responsible for working independently and collaboratively on legal issues affecting the Medical Device businesses to minimize risks of legal liability and ensure maximum legal rights of the company. The right candidate will be excited to join a growing company with a diverse portfolio of businesses. This attorney will be a senior legal resource and valued business partner for HLUS and its Medical Device businesses.</div><div></div><div><br>
Please include cover letter and resume indicating your interest and expertise in this position.</div>
Company Overview:
<p>
At FUJIFILM Holdings America Corporation, we&rsquo;re redefining innovation across the industries we touch&mdash;from healthcare and photography to semiconductors and data storage. With roots in photosensitive materials and a legacy of groundbreaking technology, we now lead 23 diverse affiliate businesses across the Americas.</p><br>
<p>We&rsquo;re looking for mission-driven talents eager to join us to help create, market, and support a vast portfolio of products. At Fujifilm you&rsquo;ll have the opportunity to explore and grow your skills in new, exciting ways. Whether you&rsquo;re shaping tomorrow&rsquo;s tech or redefining today&rsquo;s processes, we&rsquo;ll provide a flexible work environment and dynamic culture where innovation thrives.</p><br>
<p><br>
Our Americas HQ is nestled in Valhalla, New York, a charming town known for its excellent schools, beautiful parks, and easy access to the vibrancy of New York City.</p><br>
<p><br>
Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of &ldquo;giving our world more smiles.&rdquo; Visit: https://www.fujifilm.com/us/en/about/region/careers</p>
Job Description:
<div><b>
Responsibilities</b></div><ul><li>
Manage and support the day-to-day legal affairs of assigned Medical Device businesses or operating divisions, under the general supervision of, and in consultation and collaboration with, the Division General Counsel.</li><li>
Manage outside counsel supporting designated Medical Device businesses and operating divisions as assigned by the Division General Counsel.</li><li>
Coordinate and provide strategic legal advice to business partners with respect to a variety of legal matters affecting the Medical Device businesses, including commercial contracts, advertising and marketing, competitor interactions, and other matters.</li><li>
Draft, review and negotiate a variety of complex commercial contracts, including customer, distributor and vendor agreements; development, manufacturing and service agreements; clinical trial agreements; group purchasing agreements; and distributor agreements, among others. Work with internal colleagues and outside counsel on a regular basis to review and handle a large volume of contracts, to ensure agreements mitigate legal risk and support business objectives.</li><li>
Advise, counsel and report to Division General Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare regulatory compliance, anti-kickback statutes, the False Claims Act, U.S. government programs and contracting compliance requirements, antitrust laws, and other applicable laws.</li><li>
Keep abreast of legislative and regulatory changes with respect to healthcare and other relevant regulations that may affect HLUS&rsquo; Medical Device businesses.</li><li>
Provide training to HLUS&rsquo; Medical Device businesses on substantive legal topics relevant to healthcare regulatory compliance, as assigned by Division General Counsel.</li><li>
Contribute to, and help drive, the Legal Department&rsquo;s commitment to continuous operational improvement and achievement of efficiency, consistency, and alignment of contracting practices and best-in-class contract terms across the Legal Department and the HLUS Group organization to support the evolving needs and growth and expansion of HLUS Group companies.</li><li>
Perform other duties as assigned.</li></ul><div></div><div><b><br>
Required Skills/Education</b></div><ul><li>
Juris Doctor from accredited law school. Academic honors preferred.</li><li>
Admitted to practice law and in good standing under the Bar of at least one U.S. state.</li><li>
Minimum 10+ years of relevant legal experience with at least 3 years with an in-house corprorate legal department preferred.</li><li><b><i>
5+ years recent experience advising medical device, pharmaceutical or life science companies</i></b></li><li>
Experience with the federal antikickback statue desired</li><li>
Solid commercial contract background with extensive drafting and negotiation experience in fast-paced business environment. Experience in legal matters involving tariffs and other trade compliance issues would be a plus.</li><li>
Strong work ethic and ability to timely, effectively and autonomously manage multiple complex projects, to collaborate with internal and external stakeholders and to drive contracts and other legal projects to completion.</li><li>
Quickly grasps organizational objectives and applies them to commercial contracts or other work product in a way that is succinct and practical.</li><li>
Skill in providing regulatory advice in a complex business environment.</li><li>
Strong ability to produce clear, concise, and professional written work product, including business communications with senior leadership.</li><li>
Adept at partnering across business divisions, functions, and geography, with a skill for engaging resources at all levels in projects and processes while continuing to own and drive them.</li><li>
Ability to manage junior-level counsel, paralegals, or non-attorney administrative staff.</li><li>
Ability to use, or quickly acquire skill necessary for using, legal technology platforms and applications such as Microsoft Office and Microsoft Teams.</li><li>
Maintains professional demeanor, including when working under pressure.</li></ul><div></div><div><b><br>
Desired Skills</b></div><ul><li>
Strong organization, communication, and interpersonal skills</li><li>
Ability to complete time-sensitive projects under pressure</li><li>
Analytical ability</li><li>
Proactive and responsive</li><li>
Budget conscious</li></ul><div></div><div><b><br>
Salary and Benefits</b></div><ul><li>
Up to $180,000- $190,000 depending on experience.</li><li>
Medical, Dental, Vision</li><li>
Life Insurance</li><li>
401k</li><li>
Paid Time Off</li><li>#LI-REMOTE</li></ul>
EEO Information:
<div>
Fujifilm is committed to providing equal opportunities in hiring, promotion and advancement, compensation, benefits, and training regardless of nationality, age, gender, sexual orientation or gender identity, race, ethnicity, religion, political creed, ideology, national, or social origin, disability, veteran status, etc.</div>
ADA Information:
<div>
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to our HR Department (hlushrteam@fujifilm.com).</div></div>

Senior Counsel (Medical Device)

Breg, Inc

<p></p><div><p><b>Join Our Team and Keep Moving Forward with Breg!</b></p>
<p>
At Breg, we are dedicated to advancing orthopedic solutions that enhance the lives of patients and support healthcare professionals. As a leader in the orthopedic industry, we provide innovative products, consulting, technology, and services that help people move forward with confidence.</p>
<p>
We are currently seeking a <b>Product Manager</b> to join our team. If you thrive in a dynamic environment where innovation and impact go hand in hand, this is the opportunity for you.</p>
<p><b>
Who You Are</b></p>
<p>
You are a forward-thinking professional who values collaboration, innovation, and making a meaningful difference. You bring expertise in the ability to lead and influence others effectively and impart knowledge efficiently through various methods of training and are committed to delivering exceptional patient outcomes.</p>
<p><b>
What You&rsquo;ll Do</b></p>
<p><b>
As a Product Manager, you will:</b></p>
<ul>
<li>Demonstrates expertise over assigned products, services and/or software and conveys credibility on category both internally and externally</li>
<li>Seeks to understand and listen with humility (curiosity)
<ul><li>Acquires multiple perspectives from customers, internal stakeholders and key opinion leaders</li>
<li>Effectively leverages market and financial data to guide recommendations</li>
<li>Understands Breg&rsquo;s overall value proposition, and how assigned category fits and supports growth</li>
<li>Evaluates new product ideas and proposed changes</li>
<li>Conducts field trials to evaluate product/service/software design effectiveness throughout development</li>
</ul></li><li>Translates feedback and complexity into strategic recommendations to drive growth (strategy)
<ul><li>Guides portfolio strategies, product development opportunities and life cycle plans for category</li>
<li>Develops specifications and requirements for new and sustaining product development projects</li>
<li>Leads targeting, positioning and pricing for products in assigned categories</li>
<li>Develops channel level strategies to drive product sales through Breg services/solutions</li>
<li>Makes decisions with acute focus on driving customer loyalty and growth</li>
</ul></li><li>Drives revenue and profitability results through cross-functional team collaboration with
<ul><li>Product development: to bring innovation to market that solves customer pain points</li>
<li>Field sales teams: to provide technical and market expertise, co-travel on customer visits and support tradeshows and events</li>
<li>Operations: to guide product level forecasts, demand planning and category optimization</li>
<li>Regulatory, Compliance, and Legal: to develop and support labels and claims</li>
<li>Marketing Communications: to execute communications plan and materials</li>
</ul></li><li>May manage Associate Product Managers, Technical Specialists or other supporting roles
<ul><li>Leadership responsibilities include the selection, development, performance management and continuous recalibration of staff; ensures appropriate staffing levels and resource allocation; performs administrative tasks associated with timekeeping, pay, performance, policy administration and other matters related to employment.</li>
<li>Assesses staff and provides timely and consistent feedback regarding technical proficiency and effectiveness. Provides constructive feedback, guidance, and reinforcement to employees regarding job performance. Works with staff to identify work goals and create individual development plans. Evaluates training programs to ensure content meets staff needs.</li>
</ul></li><li>Collaborate with cross-functional teams to drive excellence in patient care and business solutions.</li>
</ul>
<p><b>What You Bring</b></p>
<ul>
<li>Four year college degree required. Degree focus in marketing or a related field is preferred but not required.</li>
<li>Master&rsquo;s degree or MBA is preferred.</li>
<li>4+ years of product marketing experience within the medical device or orthopedic industries or equivalent knowledge and experience.</li>
<li>Sales experience or prior orthopedic industry experience is preferred.</li>
<li>Athletic trainer certificate, Certified Orthotic Fitter, or other related industry certification or experience is preferred.</li>
<li>A passion for innovation and a commitment to Breg&rsquo;s mission to <i>Keep Moving Forward</i>.</li>
</ul>
<p><b>Why Breg?</b></p>
<p>
At Breg, we invest in our people and culture. We offer:</p>
<ul>
<li>Comprehensive Benefits: Medical, dental, vision, disability, and life insurance, effective the first of the month after hire.</li>
<li>Work-Life Balance: Paid Time Off (PTO) and company-paid holidays.</li>
<li>Growth &amp; Development: Opportunities for professional advancement within a company that values your contributions.</li>
<li>Commitment to Diversity &amp; Inclusion: Breg is proud to be an Equal Employment Opportunity employer, fostering a diverse and inclusive workplace.</li>
<li>For more information regarding Company benefits, please see https://www.breg.com/benefits</li>
</ul>
<p><b>Work Schedules include&hellip;.</b></p>
<ul>
<li>May include variable start/end times outside of the company&rsquo;s standard business hours of 8:00 a.m.&ndash; 5:00 p.m.</li>
</ul>
<p><b>Compensation</b></p>
<p>
Salary Range: $89,300-$125,900 per year. Actual compensation is determined by factors such as experience, skills, and business needs. This range reflects the minimum and maximum target range for new hire base salary/pay across all US locations. Actual pay is based on many factors unique to each candidate, including but not limited to geographical location, work experience, skill set, relevant trainings and certifications, and business needs. The base pay range is subject to change and may be modified in the future. This role may also be eligible for bonus.</p>
<p><b>
Ready to Move Forward?</b></p>
<p>
If you&rsquo;re ready to be part of a company that is redefining orthopedic care, apply today at www.breg.com/careers.</p>
<p>
Breg is an Equal Employment Opportunity Employer and dedicated to a diverse work force and Drug Free work environment. EOE/Minorities/Females/Vet/Disabled are encouraged to apply.</p>
<p>
Applicants must be currently authorized to work in the United States on a full-time basis. The Company will not sponsor applicants for work visas for this position.</p>
<p>
#LI-KB1</p><p></p><p>
Equal Opportunity Employer<br>
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 notice from the Department of Labor.</p></div>

Product Manager (DME/Orthopedic)

Stryker

<div><h3 class="jobSectionHeader"><b>Why join Stryker?</b></h3>
Looking for a place that values your unique talents? Discover Stryker's award-winning culture.<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<h3 class="jobSectionHeader"><b>
Job description</b></h3>
We are excited to be named one of the World&rsquo;s Best Workplaces by Fortune Magazine!
<br>
We are proud to offer you our total rewards package which includes bonuses, healthcare, insurance benefits, retirement programs, wellness programs, as well as service and performance awards &ndash; not to mention various social and recreational activities, all of which are location specific.<div><p><br>
We are seeking a dynamic <b>Product Manager </b>in <b>Duba&iuml;</b> to drive the growth of our <b>Joint Replacement</b> portfolio across the <b>MEA</b> region.</p><p></p><p><b><br>
What you will do</b></p><ul><li><p>
Conduct competitive analysis and gather insights to inform product strategy.</p></li><li><p>
Develop and maintain strong networks for obtaining competitive information.</p></li><li><p>
Collaborate with stakeholders to understand and articulate customer needs.</p></li><li><p>
Create and implement marketing plans, including strategic and annual plans.</p></li><li><p>
Manage budget forecasts and provide supporting information for financial decisions.</p></li><li><p>
Develop value propositions and segmentation based on customer insights.</p></li><li><p>
Lead the development of marketing messages and materials to support sales efforts.</p></li><li><p>
Analyze customer satisfaction data to enhance strategic planning and improve engagement.</p></li></ul><p></p><p><b><br>
What you will need</b></p><p><i>
Required:</i></p><ul><li><p>
Bachelor's Degree in Business, Marketing or related field</p></li><li><p>
Minimum 4 years of experience in marketing/product management</p></li><li><p>
Prior experience in Medical Devices industry</p></li><li><p>
Proficiency in English
</p></li><li><p>Excellent presentation and interpersonal communications skills</p></li><li><p>
Strong analytical and problem-solving skills</p></li><li><p>
Proficiency in Microsoft Office suite (Excel, Outlook and Powerpoint)</p></li></ul><p></p><p><i>
Preferred:</i></p><ul><li><p>
MBA (Master&rsquo;s in Business Administration) or equivlalent advance degree</p></li><li><p>
Experience in Joint Replacement or related Orthopaedic sepcialty is highly valued</p></li></ul></div><p></p>
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.</div>

Product Manager, Joint Replacement, MEA

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