Technical Writer - Fully Remote Working

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Manage the controlled document approval process (author, review, approval).

Assist project teams in updating global and local controlled documents.

Manage high volume of document updates from multiple regions and projects.

Coordinate procedure editing and review activities across global sites.

Assist document authors with alternative wording, presentation, and style to ensure clarity of content.

Assist project teams with harmonizing document update feedback from multiple reviewers.

Edit draft procedural documents to ensure the technical material in a clear, concise, and effective to global users.

3+ years of experience in technical writing, specializing in Standard Operating Procedures (SOPs) and Work Instructions for the Pharmaceutical industry, including:

A minimum of 3 years' experience with the entire documentation development life cycle from procedure design, authoring, and approval workflow management.Excellent written and spoken English.

Experience using electronic document management systems. Veeva experience is a plus.

Highly proficient in MS Office products, such as Word, PowerPoint, and Excel.

Expertise in SOP writing techniques.

Able to work flexible hours when needed to accommodate global project teams.

Able to work effectively with other professionals, such as Quality Assurance specialists, pharmacovigilance specialists, and information technology specialists.

Ability to work independently with minimal supervision.

Ability to work on multiple simultaneous projects with tight deadlines.

AS or BS degree in a related field.

Experience Requirements

~ Minimum 3 years relevant experience

We are committed to diversity, equity, and inclusion. We do not rely on AI screening tools to support our hiring process. Whilst ProPharma supports remote working, we also recognise the value that comes from in person collaboration. As such, we encourage any new hires that are based within a reasonably short commute of one of our offices to work on a hybrid basis and spend some time working from that office location, as agreed with your manager. All applications will be treated on their own merit and candidates will not be at any advantage or disadvantage based on their proximity to an office.

• **ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.*** For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

Manage the controlled document approval process (author, review, approval).

Assist project teams in updating global and local controlled documents.

Manage high volume of document updates from multiple regions and projects.

Coordinate procedure editing and review activities across global sites.

Assist document authors with alternative wording, presentation, and style to ensure clarity of content.

Assist project teams with harmonizing document update feedback from multiple reviewers.

Edit draft procedural documents to ensure the technical material in a clear, concise, and effective to global users.

3+ years of experience in technical writing, specializing in Standard Operating Procedures (SOPs) and Work Instructions for the Pharmaceutical industry, including:

A minimum of 3 years' experience with the entire documentation development life cycle from procedure design, authoring, and approval workflow management.Excellent written and spoken English.

Experience using electronic document management systems. Veeva experience is a plus.

Highly proficient in MS Office products, such as Word, PowerPoint, and Excel.

Expertise in SOP writing techniques.

Able to work flexible hours when needed to accommodate global project teams.

Able to work effectively with other professionals, such as Quality Assurance specialists, pharmacovigilance specialists, and information technology specialists.

Ability to wo