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Technical Writer
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A leading biotechnology firm is advertising a vacancy for a Technical Writer position. The organization is seeking for a driven and talented individual to join its North Carolina-based office. This world renowned and highly respected pharmaceutical company is currently setting up a brand-new, large scale sterile packaging operation. The technical writer will play an integral part in getting the new operations up and running and compliant with FDA regulations.
Job Responsibilities:
- Collaborating
- Leading the creation and editing of a variety of Standard Operating Procedures (SOPs), covering Manufacturing, operational, maintenance, and cleaning procedures.
- Getting the new manufacturing line up to speed and fully FDA compliant.
Skills and Requirements:
- At least 5 of years technical writing experience.
- Track record of writing Manufacturing SOPs within the Pharmaceutical Industry.
- Strong knowledge of Good Manufacturing Practices (GMP).
- Ability to write, edit and format documents to exacting requirements.
- Demonstrable project management skills.
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Max Kelly at +312-270-1613or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
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