Technical Writer

Proclinical is partnering with a leading biotechnology firm to advertise a vacancy for a Technical Writer position. The organization is seeking for a driven and talented individual to join its Greater Philadelphia-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:

• Writing equipment Standard Operating Procedures (SOPs)
• Creating User Requirement Specifications (URS) as well as Technical and Functional specifications.
• Becoming involved with Pre-validation and Validation activities.

Skills and Requirements:

• 1 - 2 years pharmaceutical industry experience.
• 1 - 2 years technical writing experience.
• Track record of writing documentation and SOPs within a pharmaceutical environment.
• Strong knowledge and exposure to Good Manufacturing Practices (GMP).
• Validation experience attractive, but not essential.
• 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.

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 +312-270-1613 or 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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