Company Mission

Company values

• Your key responsibilitiesCollaborate with Subject Matter Experts, stakeholders, and various teams to obtain an in-depth understanding of the process and the documentation requirementsGap analysis: determining where documents need to be created, edited, consolidated, or retiredDocumentation auditDocumentation Architecture set-upCreating and Editing Documents: ensure that all documents comply with internal and external requirementsCoordinate reviews/approvals from clients and manage resulting changes Skills and attributes for successAbility to analyze, organize, structure, and prioritize complex technical information from multiple sources and make them easily understandableAbility to learn quickly and adjust to multiple demands, shifting priorities, ambiguity, and rapid changeMust be able to work independently and with minimal direct supervisionFocused on how to convey information best clearly and conciselyOutstanding communication skillsStrong attention to detail with the ability to proofread and edit wellExperience with coordinating and following tasks, and projects through the completion To qualify for the role, you must have Education:Advanced degree in Technical Communications, Technical and Scientific Writing Experience:Five or more years of relevant experience producing technical documentation, preferably in the Pharmaceutical Industry (GMP)Good time management, organizational, and decision-making skills Ideally, you’ll also haveInformation Mapping Certification and experienceProject Management skillsProcess Improvement experience We strive to achieve the right balance for our people, enabling us to deliver excellent client service while allowing you to build your career without sacrificing your priorities. Our client-facing professionals can be required to travel regularly, and at times be based at client sites. If you can confidently demonstrate that you meet the criteria above, please get in touch with us as soon as possible.