Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
Key Responsibilities:
Create and update
labels and box prints
in alignment with current procedures, regulatory expectations, and market needs.
Ensure documentation complies with
QSR, ISO
, and other internal quality and regulatory standards.
Maintain adherence to company
style guides
, templates, and quality management systems (QMS).
Collaborate cross-functionally with teams such as
Product Development, Regulatory Affairs, Quality Assurance, Marketing, and Global Operations
to gather information and validate technical accuracy.
Drive and manage activities within the assigned area of responsibility.
Contribute to the
continous improvement
of documentation standards, templates, and processes.
Support
Deviation, CAPA, and complaint investigations
by providing documentation expertise and contributing to corrective action processes.
Qualifications & Experience:
University degree
in the life science field and/or relevant work experience.
Excellent English,
including speaking, writing, and editing skills.
2-3 years of label creation experience
in the life sciences, medical devices, or in vitro diagnostics (IVD) industry.
Familiarity with
visual and multimedia tools (e.g., Adobe InDesign, Illustrator)
for creating clear, user-friendly illustrations.
Proven ability to manage multiple documentation projects in a
global, fast-paced, and regulated environment
.
Experience with
EU IVDR
documentation requirements.
Preferred Skills:
Multilingual skills
(e.g., Swedish, German, French, Spanish) to support localization and translation processes.
Strong
cross-cultural communication and collaboration skills
, with flexibility to work in a dynamic, global team setting.
Attention to detail,
accuracy, and a commitment to continuous improvement.
Demonstrated
technical curiosity and interest
in understanding complex products and systems.
Good collaborator with clear communication skills.
Ability to work both independently and in collaboration with others, as well as the ability to handle both small and large tasks.
Experience with
EU MDR
is an advantage.
