The Client is looking for a technical writing with labeling and advertising and promotional material experience that can write and work through the approval process new SOPs for the review and approval of labeling/advertising material. The consultant would work with the various subject matter experts and team members to obtain the necessary technical information, write the SOP based off of general templates, lead review workshops for the team members and work the documents through the final review and approval process. The consultant must have significant regulatory, labeling and ad/promo experience, have strong technical writing experience and have biotech and/or pharma experience.
10 years of Biotech and/or pharmaceutical industry regulatory technical writing
Experience in Labeling & ad/promo
Small to mid-sized biotech and/or pharma company experience
Project management/leadership skills
Ability to guide and work documents through the approval process