Reagent Labeling Writer Intern - Miami, FL
Reagent Labeling Writer Intern - Miami, FL
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Job Description
Reagent Labeling Writer Intern
Accelerating answers
Are you ready to accelerate your potential and make a real difference within life sciences diagnostics and biotechnology
At Beckman Coulter Life Sciences one of Danahers 15 operating companies our work saves livesand were all united by a shared commitment to innovate for tangible impact.
Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers system of continuous improvement you help turn ideas into impact innovating at the speed of life.
Working at Beckman Life Sciences 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 Beckman Life Sciences 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. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible.
The Reagent Labeling Writer Intern will gain hands-on experience and exposure in the critical area of regulatory labeling within the medical device and Life Sciences industry. Interns will work closely with cross-functional teams including R&D Quality/Regulatory Assurance and Technical Support.
This position reports to the Senior Manager of Global Service Compliance Technical Publications and Digital Solutions in Beckman Coulter Life Sciences located in Miami FL and will be an on-site role.
What will you do:
Assist in drafting editing and reviewing artwork content for consumables product labeling.
Manage new labeling projects to meet FDA EU IVDR ISO CLP/GHS and other countries regulatory requirements.
Support the management of labeling change control processes including document version control and archival.
Coordinate time with graphic designers and technical writers to assist with proofreading and formatting documents to ensure consistency and adherence to style guides.
Work with different project teams to coordinate labeling markup and approval process to meet product release timelines by participating in labeling review meetings providing input and recording feedback.
Learn and utilize document management systems and other relevant software tools.
Who are you:
Currently pursuinga Bachelors or Masters degree in a relevant field such as Technical Communication Professional Writing English Regulatory Affairs or a related discipline.
0-2 years experience or coursework in technical writing regulatory affairs or scientific communication.
Proficiency in Microsoft Office Suite (Word Excel PowerPoint).
Strong written and verbal communication skills with an exceptional eye for detail and accuracy.
Eagerness to learn about regulatory affairs quality systems and the diagnostics industry.
Ability to work independently and in a team environment
It would be a plus if you also possess previous experience in:
Document control systems or content management systems.
The hourly range for this role is $28.00. This is the rate that we in good faith believe is the rate of compensation for this role at the time of this posting
Join our winning team today. Together well accelerate the real-life impact of tomorrows science and technology. We partner with customers across the globe to help them solve their most complex challenges architecting solutions that bring the power of science to life.
For more information visit .
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race color national origin religion sex age marital status disability veteran status sexual orientation gender identity or other characteristics protected by law.
The U.S. EEO posters are available here.
We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process to perform essential job functions and/or to receive other benefits and privileges of employment please contact:1- or .
Required Experience:
Intern
Employment Type
Full-Time
