Stryker is one of the world’s leading medical technology companies and, together with our customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces and a Best Workplace for Diversity by Fortune Magazine. Learn more about our award-winning organization by visiting stryker.com
Initial 12 month FTC with possibility of extension
The technical writer will work as a member of a project team liaising with Process Development, Quality, Engineering and Operations to complete required documentation. Working within the Engineering Project Team, responsible for validation and process qualification related activities with regards document generation.
Main Duties & Responsibilities
Processing of Change Requests for the support group.
Under direction, will draft up the required specification/procedure.
Responsibility for compiling raw data for support group (protocols, reports, etc.) and deliver to Doc Services for archiving.
Maintaining a central database of all work.
Responsible for the "Redlining" of documents from current PLM system.
Deliver BOM, Parts and Router updates and training as required
Will understand the system integrations and complete work related to these integrations accordingly.
SME for document standards and documentation processes.
Create/execute and complete validation protocols - VP, EQ, OQP, URS, FAT, SAT, etc.
Build quality into all aspects of work by maintaining compliance to all quality requirements
Travel may be required as part of this role for project related activities within travel policy guidelines
Skills & Experience Required
Level 8 Degree in Engineering, Science or related discipline
Has 2-4 years' experience in a similar role within manufacturing environment.
Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.
Must be willing to work as part of a multi-functional team
Excellent communication and organizational skills. Ability to liaise internally and with relevant personnel in other sites.
Ability to work independently with minimal assistance, with attention to detail.
Experience working with documentation systems and possess a good knowledge of GMP and ISO90001/EN46001.
Previous experience of working in an FDA regulated manufacturing environment an advantage.
Stryker is one of the world's leading medical technology companies and, together with our customers, we are driven to make healthcare better. The Company offers a diverse array of innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. Stryker is active in over 100 countries around the world.
Together with our customers, we are driven to make healthcare better.
At Stryker, quality is first in everything we do. We are driven to make healthcare better for our customers by
providing innovative products and services that meet regulatory requirements through our effective quality system.
The Company was founded in 1941 by Dr. Homer Stryker and incorporated in 1946 as the Orthopedic Frame Company. In 1964, the Company’s name was changed to Stryker Corporation.
• $13.6 billion in annual sales in 2018; annual revenue has grown for 39 straight years
• 17.1% CAGR (compound annual growth rate) in sales over 39 years
• ~36,000 employees globally in 2018
• 43 manufacturing and research & development locat...ions worldwide
• Included in the Standard & Poor’s 500 Index
• Ranked # 233 on Fortune Magazine’s “FORTUNE 500” list for 2019
• Ranked # 3 on Fortune Magazine’s “World’s Most Admired Companies” list for the “Medical Equipment” industry for 2019
• Ranked # 11 on Fortune Magazine’s “100 Best Companies to Work For” list (U.S.) for 2019
• Spent $862 million on R&D in 2018
• 7,784 patents owned globally in 2018
• Initial public offering of stock was in 1979
• Listed on the New York Stock Exchange under ticker SYK