Sr. Specialist / Technical Writer

Job#: 3043861 Job Description: Title: Sr. Specialist / Technical Writer Client: Biotechnology company Contract/Perm & duration: 12-month contract (possibility of extension/conversion) Location: Toronto (remote, occasional onsite days if needed) Pay Rate: $35-45/hr Description of Position: Our innovative biotechnology client is seeking a talented Sr. Specialist / Technical Writer to join the growing Manufacturing Science & Technology (MS&T) group. The preferred location for the role is Toronto, Ontario to facilitate engagement with the broader Technical Operations organization. With the scope of leading technology transfers and broader technology implementation initiatives, the MS&T team has a need for a dedicated role that interfaces with adjacent functions including Research, Non-clinical, Analytical Development, Manufacturing, Quality Control, and Quality Assurance. As a key contributor within the function, this role will drive revisions to internal procedures while developing templates that can be applied to a variety of source documents such as protocols and technical reports. In addition, this role will be trained in the Quality Management System to ensure appropriate reviews and assessments are documented for relevant Change Controls, Deviations, etc. We are seeking individuals who are collaborative, thrive in a fun and dynamic culture, and are steadfast in the commitment to contribute to innovate cellular therapies that have the potential to impact patients’ lives. Responsibilities: Accountable for key internal procedures related to technology transfers and annual reports Developing, revising, and implementing suitable templates for cross-functional use Creating and revising standard operating procedures Supporting the management and timely closure of quality events Facilitating comment resolution and driving cross-functional discussions to ensure alignment, timely decision-making, and document progression Taking charge of various technical documents including protocols and reports with appropriate support from technical experts Proactively establishing standards and procedures for accurate and timely drafting of technical content Driving preparation of Information Requests, Briefing Books, and other regulatory submissions with support from subject matter experts Developing reporting tools in partnership with Quality Assurance and CMC Strategy Minimum Requirements: MSc. degree in a Biological Science, such as Biochemistry, Immunology, Molecular Biology, or similar 5+ years of experience in technical writing with relevant certifications and affiliations Experience working with Quality Management Systems Knowledge of ICH guidelines and eCTD formatting Expertise in technical writing as it pertains to regulatory submissions and scientific writing for publications Strong English written and verbal communications skills Ability to work in a fast-changing environment Strong project management skills, with the ability to collaborate effectively with cross-functional teams and deliver high-quality documents on time Collaborative team player with proactive approach to work Continuous improvement mindset, with the ability to identify and implement initiatives that increase efficiency and drive progress Everforth Apex is a world-class IT services company that serves thousands of clients across the globe. When you join Everforth Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRateds Best of Staffing® in Talent Satisfaction in the United States and Great Place to Work® in the United Kingdom and Mexico. Everforth Apex Benefits Overview: In terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. © 2026 Everforth, Inc. All rights reserved. Everforth Apex Systems is part of the Commercial Segment of Everforth, Inc. NYSE: EFOR 4400 Cox Road Suite 200 Glen Allen, Virginia 23060 Everforth Apex is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Everforth Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Benefits Department at [email protected] or 804-523-8228. (Do not submit resumes or solicit consultants to this email address). UnitedHealthcare creates and publishes the Transparency in Coverage Machine-Readable Files on behalf of Everforth Apex.

The role is responsible for leading technical writing efforts for technology transfers, including the creation of SOPs, protocols, and technical reports. It also involves managing quality events and driving the preparation of regulatory submissions and briefing books.

Requires an MSc in a Biological Science and over 5 years of experience in technical writing, specifically within regulatory and scientific contexts. Candidates must have knowledge of ICH guidelines, eCTD formatting, and experience with Quality Management Systems.

• On-demand training program • Certification prep • Technical and leadership courses/books/seminars • Certification discounts

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Technical Writing
• Quality Management Systems
• Regulatory Submissions
• Project Management
• Scientific Writing
• ICH Guidelines
• eCTD Formatting
• Cross-functional Collaboration
• Standard Operating Procedures
• Technology Transfer
• Change Control
• Deviation Management

Formation minimale

Autre formation

Expérience minimale

5+ ans

Postuler avant le

26 août 2026