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Team Lead, GPM Quality Assurance (Hybrid - Acton, MA)
full-timeActon$65k - $98k

Summary

Location

Acton

Salary

$65k - $98k

Type

full-time

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About this role

Position Overview:

 

The Team Lead, Quality Assurance is a hands-on technical leader serving as a post-market surveillance quality assurance subject matter expert and representative.  This role will provide direction to individuals who are responsible for the review of documented files ensuring the files meet quality compliance standards, regulatory requirements, technical accuracy, and conformity to company policies and procedures. The role involves system level comprehension, attention to detail, organization, and constant interaction within the business to the accomplishment of the company goals. 

 

Responsibilities:

  • Mentor and help develop direct reports through yearly/quarterly reviews, weekly meetings, and daily interactions.

  • Support a positive culture with clear communication regarding goals and objectives

  • Provide leadership to team members, including but not limited to, training support on process and procedures.

  • Provide coaching and feedback in accordance with company SMART goals.

  • Review complaint files to ensure proper complaint coding and accurate complaint reportability assessment. 

  • Support database development and reporting capabilities related to the complaint / reliability department needs.

  • Participate in calibration sessions with leadership to ensure consistency in assessments.

  • Identify and assess trends in Quality Monitoring results.

  • Deliver monthly presentations of Quality Monitoring results to the team.

  • Suggest process improvements or enhancements to monitoring programs, internal processes, and procedures.

  • Provide coaching support to staff based on Quality Monitoring findings.

  • Coordinate with the training team to provide feedback on training opportunities identified through quality analysis.

  • Lead projects that enhance and support the QA function within GPM.

  • Lead or contribute to departmental non-conformances, events, and CAPAs.

  • Perform other duties as required.

 

Education and Experience: 

  • BS degree, preferably in a technical or scientific discipline; and/or equivalent combination of education and experience. 

  • 2-3 years Complaint handling experience, Quality Assurance, or Regulatory Affairs.

  • Minimum of 3 years’ experience in data management, record keeping, and trouble shooting in the Medical Device field, or other transferable experience related to organization, technical aptitude and data management. 

Preferred Skills and Competencies:        

  • Proven leadership skills to engage, coach, mentor, and develop the team, inspire high quality and timely work

  • Proven experience to organize, prioritize and follow through on multiple tasks with minimal supervision

  • Working knowledge/experience with global, multi-country vigilance reporting requirements for medical devices and demonstrated knowledge of country-specific differences and requirements

  • Ability to generate, verify, and maintain accurate records

  • Excellent verbal, written, and interpersonal communication skills.

  • Exceptional listening and analytical skills

  • Experience in CAPA, root cause analysis, or analytics

  • Solid time management skills

  • Must be able to work independently while contributing to the goals of the team.

  • Must be proficient with Microsoft Office (intermediate Word, Excel)

  • Willingness to pursue additional learning and build qualifications in a professional field, as required

  • The ability to rapidly learn and take advantage of new concepts and adjust priorities as needed

  • Experience with Corrective Action/Preventive Action preferred

  • Experience with TrackWise

Physical Requirements (if applicable):  

  • This position is a desk job and requires sitting for extended periods of time.

  • This position requires extensive computer use

NOTE: This position is eligible for hybrid working arrangements and requires on-site work from an Insulet office. #LI-Hybrid

Additional Information:

Compensation & Benefits: For U.S.-based positions only, the annual base salary range for this role is $65,600.00 - $98,450.00 This position may also be eligible for incentive compensation. We offer a comprehensive benefits package, including: • Medical, dental, and vision insurance • 401(k) with company match • Paid time off (PTO) • And additional employee wellness programs Application Details: This job posting will remain open until the position is filled. To apply, please visit the Insulet Careers site and submit your application online. Actual pay depends on skills, experience, and education.

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.

We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!

At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Other facts

Tech stack
Leadership,Quality Assurance,Complaint Handling,Data Management,Record Keeping,Technical Aptitude,Communication,Analytical Skills,Time Management,Process Improvement,Training,CAPA,Root Cause Analysis,Microsoft Office,Vigilance Reporting,Coaching

About Insulet Corporation

Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Omnipod products are offered in 25 countries around the globe.

HIRING SCAM ALERT
Recently, individuals impersonating Insulet Human Resources members have offered fraudulent interviews and job offers to unsuspecting candidates. To help protect you from these scam artists, please be aware that:

• Insulet will never interview a candidate over RingCentral, similar messaging apps or social media (i.e. Google Hangouts, WhatsApp, Facebook Messenger, etc.), or via text message.
• Insulet will never send a company check or ask an applicant to pay a fee or purchase at home work/training materials in connection with an application for employment.
• Insulet will never provide excess money to an applicant and ask the applicant to write a check for repayment.

If you have any doubt about a job offer or any other communication purporting to come from Insulet, please reach out to us directly at 978-600-7000.
If you receive any type of communication on behalf of Insulet that seems inappropriate or suspicious, please report this activity to: www.iC3.gov or www.stopfraud.gov.

Team size: 1,001-5,000 employees
LinkedIn: Visit
Industry: Medical Equipment Manufacturing
Founding Year: 2000

What you'll do

  • The Team Lead will mentor and develop direct reports while ensuring compliance with quality standards and regulatory requirements. Responsibilities also include reviewing complaint files, supporting database development, and leading projects to enhance the QA function.

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Frequently Asked Questions

What does Insulet Corporation pay for a Team Lead, GPM Quality Assurance (Hybrid - Acton, MA)?

Insulet Corporation offers a competitive compensation package for the Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) role. The salary range is USD 66k - 98k per year. Apply through Clera to learn more about the full compensation details.

What does a Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) do at Insulet Corporation?

As a Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) at Insulet Corporation, you will: the Team Lead will mentor and develop direct reports while ensuring compliance with quality standards and regulatory requirements. Responsibilities also include reviewing complaint files, supporting database development, and leading projects to enhance the QA function..

Why join Insulet Corporation as a Team Lead, GPM Quality Assurance (Hybrid - Acton, MA)?

Insulet Corporation is a leading Medical Equipment Manufacturing company. The Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) role offers competitive compensation.

Is the Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) position at Insulet Corporation remote?

The Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) position at Insulet Corporation is based in Acton, Massachusetts, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) position at Insulet Corporation?

You can apply for the Team Lead, GPM Quality Assurance (Hybrid - Acton, MA) position at Insulet Corporation directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Insulet Corporation on their website.