Job summary
Job post source
This job is directly from KBI Biopharma
Job overview
The Technical Writer I/II at KBI Biopharma supports the Rapid Analytics group by producing and editing technical documents critical to biopharmaceutical analytical testing and compliance.
Responsibilities and impact
The role involves writing and revising technical reports, test methods, SOPs, and investigations, reviewing documents for accuracy and consistency, assisting with deviation investigations and CAPA plans, managing document routing for approvals, and communicating with teams and clients about priorities.
Compensation and benefits
The salary range is $74,000 to $102,000 with an annual bonus, medical, dental, vision coverage, paid PTO and holidays, 401K matching with full vesting in 60 days, and employee recognition programs.
Experience and skills
Candidates need a bachelor's degree with relevant experience, strong attention to detail, knowledge of cGMP and EDMS systems preferred, a strong biochemistry background in biopharmaceutical analytical testing, critical thinking, troubleshooting, and excellent writing skills.
Work environment and culture
KBI Biopharma values diversity and inclusion, fosters innovation by encouraging diverse perspectives, and maintains a safe and healthy workplace with COVID-19 vaccination policies.
Company information
KBI Biopharma is a global CDMO providing integrated drug development and biologics manufacturing services, supporting over 500 customers and manufacturing ten commercial products across six global locations.
Unique job features
The job offers involvement in a regulated biopharmaceutical environment with opportunities to work on stability studies, analytical method performance, and quality system document management.
Company overview
KBI Biopharma is a contract development and manufacturing organization (CDMO) that specializes in providing comprehensive biopharmaceutical services to biotechnology and pharmaceutical companies. They generate revenue by offering a range of services, including process development, clinical and commercial manufacturing, and analytical testing for biologics. Founded in 1996, KBI Biopharma has grown significantly, establishing multiple facilities in the United States and Europe. The company is known for its expertise in accelerating drug development timelines and ensuring high-quality production standards.
How to land this job
Position your resume to clearly showcase your technical writing skills, especially your ability to produce and revise technical reports, SOPs, and analytical test methods, reflecting the responsibilities at KBI Biopharma.
Emphasize your background in biochemistry and biopharmaceutical analytical testing, along with your critical thinking and data interpretation skills, as these are crucial for this role.
Apply through multiple channels including KBI Biopharma's official corporate career page and LinkedIn to maximize your application visibility and chances.
Connect with current employees in the Rapid Analytics group or technical writing teams at KBI Biopharma on LinkedIn; use ice breakers like commenting on recent company projects, asking about their experience with cGMP documentation, or inquiring about the team’s approach to document standardization.
Optimize your resume for ATS by incorporating keywords such as 'technical writing,' 'SOPs,' 'analytical test methods,' 'cGMP,' 'data review,' and 'biopharmaceutical analytical testing' to ensure it passes initial screenings.
Leverage Jennie Johnson’s Power Apply feature to automate tailored applications, find multiple application portals, and identify LinkedIn contacts, freeing you to focus on preparing for interviews and networking effectively.
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