What are the responsibilities and job description for the Report Writer 1 position at MilliporeSigma?
Work Your Magic with us!
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
At MilliporeSigma, as a Report Writer 1, you will prepare and write routine reports (GMP, GLP and non-GLP) for laboratories within the Biologics Department using templates and customized text. You will produce reports that meet relevant quality regulatory standards and practices, such as GLP/GMP.
Minimum Qualifications:
OR
OR
Apply now and become a part of our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
At MilliporeSigma, as a Report Writer 1, you will prepare and write routine reports (GMP, GLP and non-GLP) for laboratories within the Biologics Department using templates and customized text. You will produce reports that meet relevant quality regulatory standards and practices, such as GLP/GMP.
- Review lab data/ workbooks and accurately represent data final reports
- Identify and/or resolve issues with study raw data and information
- Monitor department's reporting metrics including tracking deadlines ON Time Delivery (OTD) and Document Error Rate (DER)
- Coordinate and plan work within the technical team to meet and improve deadlines
- Obtain required signatures and transfer study reports to assigned team members
- Communicate with other departments to resolve outstanding issues
- Assist in the preparation of Event Records
- Generate, control and track revisions to study documentation and statements
- Track status of laboratory testing and update Excel study tracking files with data trends
Minimum Qualifications:
- Associate's Degree in a scientific discipline (e.g., Biology, Chemistry, Microbiology, etc.)
OR
- High school diploma or GED with 6 months hands on laboratory experience
OR
- High school diploma or GED with 6 months report writing experience
- 1 years' experience in an FDA regulated environment
- 1 years' experience technical writing
- Basic knowledge of GLP/GMP
- Ability to write routine reports professionally with proper grammar and language
- Intermediate technical knowledge and ability to analyze complex scientific data
- Basic knowledge of Microsoft Office and applicable systems (e.g., Excel, Word, PowerPoint, LIMS, BRIQS, etc.)
- Ability to perform and understand scientific calculations
Apply now and become a part of our diverse team!
If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html
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