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Associate Medical Device Labeling Jobs in Minnesota

Collabera

Labeling Specialist

Moundsview, MN

This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Medtronic ...

Collabera

Labeling Specialist

Moundsview, MN

This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Structural ...

Teleflex

Labeling Coordinator 3

Maple Grove, MN · On-site

$54K - $81K/yr

Manage Labeling data collection activities and provide requested reports. Maintain labeling project ... High school diploma or equivalent * 4-7 yrs Experience in Medical Device or related industry

Teleflex

Labeling Coordinator 3

Maple Grove, MN

$54K - $81K/yr

Manage Labeling data collection activities and provide requested reports. Maintain labeling project ... High school diploma or equivalent * 4-7 yrs Experience in Medical Device or related industry

Medtronic

Technical Writer

Moundsview, MN · On-site

This includes labeling for both clinicians and patients that accompany medical device productsthat conform to the Medtronic documentation and quality assurance standards. Projects include R&D new ...

Medtronic

Technical Writer

Moundsview, MN

This includes labeling for both clinicians and patients that accompany medical device productsthat conform to the Medtronic documentation and quality assurance standards. Projects include R&D new ...

Medtronic

Technical Writer

Moundsview, MN · On-site

This includes labeling for both clinicians and patients that accompany medical device products that conform to the Medtronic documentation and quality assurance standards. Projects include R&D new ...

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Associate Medical Device Labeling information

What are some common challenges faced by Associate Medical Device Labeling professionals, and how can they be addressed?

Associate Medical Device Labeling professionals often encounter challenges such as keeping up with evolving regulatory requirements across different countries, ensuring accuracy and clarity in complex technical information, and coordinating input from multiple departments like regulatory affairs, engineering, and marketing. Addressing these challenges involves staying updated on global labeling standards, developing strong attention to detail, and building effective communication and collaboration skills. Leveraging project management tools and regularly participating in training can also help manage these complexities and ensure timely, compliant labeling deliverables.

What are Associate Medical Device Labeling professionals?

Associate Medical Device Labeling professionals are responsible for creating, reviewing, and maintaining the labeling and packaging materials for medical devices. Their work ensures that all product information, instructions, and regulatory warnings are accurate, clear, and compliant with industry regulations. They collaborate closely with regulatory affairs, quality assurance, and product development teams to make sure that labels meet local and international standards. This role is critical in helping ensure patient safety and regulatory approval of medical devices.

What are the key skills and qualifications needed to thrive as an Associate Medical Device Labeling Specialist, and why are they important?

To thrive as an Associate Medical Device Labeling Specialist, you need a strong understanding of regulatory requirements, attention to detail, and experience in technical writing, often supported by a degree in life sciences or a related field. Familiarity with labeling software, document management systems, and knowledge of FDA or EU MDR regulations are typically required. Excellent communication, collaboration, and organizational skills set top performers apart in this position. These skills are crucial to ensure label accuracy, regulatory compliance, and patient safety in a highly regulated industry.
What are the most commonly searched types of Medical Device Labeling jobs in Minnesota? The most popular types of Medical Device Labeling jobs in Minnesota are:
Associate Medical Device Labeling jobs near you
Labeling Specialist

Labeling Specialist

Collabera

Moundsview, MN

Contractor

Posted 27 days ago

Job description

Company Description

About Collabera

Collabera is ranked amongst the top 10 Information Technology (IT) staffing firms in the U.S., with more than $525 million in sales revenue and a global presence that represents approximately 12,000+ professionals across North America (U.S., Canada), Asia Pacific (India, Philippines, Singapore, Malaysia), and Europe (Ireland, Netherlands, Poland, United Kingdom). We support our clients with a strong recruitment model and a sincere commitment to their success, which is why more than 75% of our clients rank us amongst their top three staffing suppliers.

Not only are we committed to meeting and exceeding our customer's needs, but also are committed to our employees' satisfaction as well. We believe our employees are the cornerstone of our success and we make every effort to ensure their satisfaction throughout their tenure with Collabera. As a result of these efforts, we have been recognized by Staffing Industry Analysts (SIA) as the "Best Staffing Firm to Work For" for five consecutive years since 2012. Collabera has over 50 offices across the globe with a presence in ten countries and provides staff augmentation, managed services and direct placement services to global 2000 corporations.

For consultants and employees, Collabera offers an enriching experience that promotes career growth and lifelong learning. Visit www.collabera.com to learn more about our latest job openings.

Awards and Recognitions

--Staffing Industry Analysts: Best Staffing Firm to Work For (2016, 2015, 2014, 2013, 2012)

--Staffing Industry Analysts: Largest U.S. Staffing Firms (2016, 2015, 2014, 2013)

--Staffing Industry Analysts: Largest Minority Owned IT Staffing Firm in the US.

Job Description

Labeling Specialist: This position will be a subject matter expert in Medical Device labeling regulations and standards.

They will be responsible for planning, development and execution of
product labeling for Medtronic Structural Heart Businesses by coordinating and
communicating across functions, as well as across multiple US and international
sites. Key responsibilities include project planning, leading the development
of technical labeling content and navigating the QMS, PDP and PLM workflows to
execute labeling.
Responsibilities:
Plans projects and manages scope, deliverables and timelines using project
management tools, managing communication with stakeholders and managing project
teams to keep deliverables aligned with business objectives and priorities.
Effectively engages with the project team and seeks out support when
appropriate
Fosters a collaborative environment. Gains support and cooperation for ideas,
proposals, projects and solutions to accomplish goals
Is a subject matter expert of labeling regulations and standards
Understands all procedures impacting the design and development of product
labeling
Able to translate customer needs into labeling requirements
Develops and executes labeling documentation and labeling per business
processes and policies
Continuously builds knowledge, keeping up-to-date on the technical or
procedural aspects of the job
Takes into account cause and effect relationships when making decisions.
Aligns one's objectives with the Packaging and Labeling and business strategies
in order to make the best possible judgments. Familiar with continuous
improvement tools such as DMAIC/A3 and root cause
Writes effectively, gathers and compiles data and translates it into easily
understandable documents,
Utilize good documentation practices (i.e. revision control, red lining,
Agile release)

Qualifications

Experience working on multi-disciplinary teams and projects.
Highly detail oriented
Experience working with project management tools, adobe acrobat pro, MS
Office Tools, PLM systems and ERP systems.
Experience with medical device regulations and standards
BS or BA in related fields.

Additional Information

To know more about this opportunity, please contact:

Sagar Rathore

sagar.rathore(at)collabera.com
630-485-2166

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