Oslo, 6. July 2023
Are you a skilled medical and technical writer with expertise in analytical chemistry, API and drug product analysis, and quality control procedures? We are currently seeking a talented individual to join our Pharma Services team as a Medical and Technical Writer specializing in Analytical Chemistry and Quality Control.
In this project-based role, you will be responsible for producing well-written and comprehensive documents related to analytical methods, validation plans, study reports, and quality control procedures. These projects will be sponsored by various national and international external entities.
You will work closely with scientists, researchers, and quality assurance professionals to gather data and information and ensure compliance with EMA, FDA, and ICH guidelines, as well as GMP and GxP standards. Your strong skills in written and spoken English, along with fluency in Norwegian, will enable effective communication with team members and stakeholders from diverse backgrounds.
Key qualifications for this position include:
Proven experience in medical and technical writing, specifically in the field of analytical chemistry, API and drug product analysis, and quality control of biological samples.
Strong understanding of analytical methods, validation processes, and study report requirements.
Familiarity with EMA, FDA, and ICH guidelines related to analytical chemistry and quality control.
Knowledge of GMP and GxP standards and their application in pharmaceutical and biotechnology industries.
Excellent written and spoken communication skills in English, with the ability to effectively translate complex scientific information.
Proficiency in using scientific terminology, creating tables and graphs, and presenting data effectively.
Fluent in Norwegian language for effective communication with team members and stakeholders.
If you are a detail-oriented writer with a passion for analytical chemistry and quality control, and enjoy working on project-based assignments sponsored by national and international entities, this is an exciting opportunity to contribute to the development and documentation of critical processes in the pharmaceutical and biotechnology sectors.
Join our team and make a significant impact on ensuring the safety, efficacy, and quality of API and drug products, as well as the accuracy and reliability of biological sample analysis for diverse sponsors.
To apply, please submit your resume, writing samples demonstrating your expertise in analytical chemistry and quality control, and any relevant certifications or qualifications. We look forward to reviewing your application and discussing how your skills and expertise align with our needs.