Job Title: Technical Writer
Location: Pearl River, NY
About the Job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
The Technical Writer will be responsible for creating and finalizing comprehensive technical documentation related to the manufacturing process of Flublok Drug Substance. Working with a high degree of autonomy, the Technical Writer will draft and complete a wide range of documents essential to the manufacturing process, including Change Controls, CAPAs, protocols, standard operating procedures, formal memos, and other technical materials.
The Technical Writer will also be responsible for inputs to completion and status data of work assignments in applicable software for reporting purposes, which will require strong Project Management skills.
We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?
Main Responsibilities:
Documentation: Initiate, draft, and finalize documentation related to the manufacturing process, including change controls, CAPAs, protocols, standard operating procedures, and other technical documents.
Collaborate: Work cross-functionally to ensure accurate descriptions of processes, equipment, procedures, and all other technical aspects. Maintain a high degree of awareness of Deviation Reports generated by Manufacturing Principal Investigators to assist in rework of verbiage as requested by Quality Assurance.
Problem Solving: Collaborate effectively across functions. Proactively address and resolve issues, and escalate appropriately if problems cannot be resolved independently to ensure timely resolution.
Communication: Provide status updates on all documents under your control. Attend check-ins as necessary and provide accurate, concise, and complete updates on work status.
Context of the Job/Major Challenges
The Technical Writer is expected to complete all documents prior to agreed-upon deadlines and with minimal need for additional edits or revisions.
Dimensions/Scope
The Technical Writer collaborates closely with cross-functional teams, including Quality, R&D, Engineering, and Operations, to fully understand the scope and requirements of documents and assignments. While not expected to serve as a subject matter expert (SME), they should possess strong communication skills, a solid technical background, and the ability to gather necessary information to produce accurate and comprehensive documentation.
About You
Requirements
Education/Experience
Minimum bachelor’s degree (preferably in Science or Life Sciences) AND at least 1 year of experience in a cGMP controlled/pharmaceutical industry.
Certifications
None required, but certifications relevant to the position are preferred.
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs, and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital, domestic partnership or civil union status, sex, gender, gender identity or expression, affectional or sexual orientation, disability, veteran or military status or liability for military status, domestic violence victim status, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other characteristic protected by law.
The salary range for this position is $67,500.00 to $97,500.00 USD Annually. All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the link, www.benefits.sanofiusallwell.com.
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