Technical Writer, R&D Analytical

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

JOB SUMMARY

The Technical Writer is responsible for the creation of protocols and reports and is able to present complex and technical information in a clear and concise manner. They will work together with the validation scientists to ensure accuracy of protocols and reports by following Standard Operating Procedures (SOP). The environment is fast paced and requires the flexibility to adjust to changing priorities and timelines.

Duties & Responsibilities:

• The on-site position involves preparing scientific documents in collaboration with R&D validation scientists. The technical writer prepares and finalizes validation, transfer, and verification protocols and reports following SOPs and other guidance documents.
• Management of document flow from generation of documents to final approvals from quality assurance and client.
• The technical writer will refer to SOPs and scientists to implement any changes or improvements required for documents.
• The technical writer will work closely with quality assurance to ensure the integrity of all documents and processes and maintain compliance with cGDP and cGMP guidelines.
• Execution of administrative activities as related to the technical writing department, which include compiling and filing documents, maintaining the

on-site archive and working with the offsite archive center.

Requirements:

• Bachelor's degree in a life science (biology/chemistry/pharmacy) or communications/English with at least 3 years' experience in pharmaceutical company
• Detail oriented
• Quality driven
• Excellent writing and communication skills; ability to effectively communicate problems and solutions applicable to analytical activities
• Strong Collaborative skills working with cross functional teams.
• Self-started with the ability to work independently on assigned tasks.
• Thoroughness in preparing and reviewing documents
• Management of workload to accommodate and meet department deadlines and client commitments
• Follow-up with scientists, project managers, and clients to manage document flow
• Experience with risk assessment writing preferred

The pay range for this role is $68,800 - $123,800. Job-related, non-discriminatory factors used to determine the actual offered rate include qualifications and experience, geographic location, education, external market data, and consideration of internal equity.As part of the total rewards package, Jabil offers benefits to enhance your health, wealth, and resilient self. These include medical, dental, and vision insurance plans; paid time off; paid parental leave; company-paid holidays subject to change yearly; 401(k) retirement plan; and employee stock purchase plan.

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Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identity, age, disability, genetic information, veteran status, or any other characteristic protected by law.

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