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Danaher Corporation QMS Training Specialist in Marlborough, Massachusetts

Be part of something altogether life-changing

Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.

At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term.

Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

What you'll do

  • Provide comprehensive support to the Cytiva eLMS administration for the Global QARA and Global Business teams.

  • Accountable for formulating the QMS specific training plans for QARA and Product Governance and Compliance teams.

  • In collaboration with the line management support establishing the priorities for training plans roll out.

  • Lead the development and revisions of selected training content in support of deploying standard and consistent QMS training across Cytiva

  • Working with the training manager and sites training representatives, lead and develop the training content and delivery mechanisms and methods for different types & segments of training.

  • Support the Training Leader in maintaining the Global QMS procedures related training and communication on the training across the sites and functions.

  • Support the sites training admin and training plans roll out.

  • Work closely with the leadership within the QARA organization to ensure their training needs are being met.

  • Coordinate the training approach and standard practices for QMS procedures across all sites and global functions

Who you are

  • Bachelor's Degree and minimum of 10 years working in a regulated pharmaceutical, medical device or life science industry in the area of QMS training or equivalent

  • QMS 9001, 13485 or pharmaceutical(drug) QMS experience in the LiveScience medical device industry or pharmaceutical industry

  • Experience of administration of electronic LMS and developing training content. Exceptional analytical, problem solving & root-cause analysis skills

  • Excellent communication skills (written and oral)

  • Experience in administration of electronic LMS and developing training content

  • Exceptional analytics problem solving and root cause analysis skills

When you join us, you’ll also be joining Danaher’s global organization, where 68,000 people wake up every day determined to help our customers win. As an associate, you’ll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) tools and the stability of a tested organization.

Danaher is committed to a diverse and inclusive culture where everyone feels they belong and all voices are heard. We believe in our associates and the unique perspectives they bring to every challenge, which is why we’ll empower you to push the boundaries of what’s possible.

If you’ve ever wondered what’s within you, there’s no better time to find out.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here (http://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf) .

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