Technical Document Coordinator
Job Description
JOB DESCRIPTION:
Nourish the world and your career as part of the Nutrition team at Abbott.
Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow, to keeping adult bodies strong and active. Millions of people around the world count on our leading brands - including Similac®, PediaSure®, Pedialyte®, Ensure®, Glucerna® and ZonePerfect® - to help get the nutrients they need to live their healthiest life.
WHAT WE OFFER
At Abbott, you can have a good job that can grow into a great career. We offer:
- A fast-paced work environment where your safety is our priority
- Production areas that are clean, well-lit and temperature-controlled
- Training and career development, with onboarding programs for new employees and tuition assistance
- Financial security through competitive compensation, incentives and retirement plans
- Health care and well-being programs including medical, dental, vision, wellness and occupational health programs
- Paid time off
- 401(k) retirement savings with a generous company match
- The stability of a company with a record of strong financial performance and history of being actively involved in local communities
WHAT YOU'LL DO
Responsible for writing and editing technical documents including requirements documents, specifications, design history files, verification and validation protocols, etc.
- Reviews Contractor GMP Design Control documentation to assess compliance to processes and procedures and works with teams to address and correct deficiencies.
- Technical Writing: Write and edit technical documents including requirements documents, specifications, verification and validation documents, Failure Modes and Effects Analysis (FMEA) documents, Design Planning documents, Design Review records. etc. in a manner which will achieve accuracy and avoid errors.
- Convert relevant product data and information into a form that meets Quality and submission requirements.
- The output provided by the incumbent/candidate is subject to external audit (e.g. FDA, ISO). The lack of accuracy and timeliness will impact the Quality system at site and division levels.
- Ability to use a number of engineering and design packages to create and edit files (e.g. SolidWorks, Altium, Adobe Photoshop, MS Office suite)
- Perform Administrative duties and project management as required
EDUCATION
- HS Diploma or GED Required
- Associate Degree preferred
EXPERIENCE
- Minimum 2 years relevant experience in a related area such as Operations, Technical Services, in a food manufacturing industry.
- 2 years developing spreadsheets or databases for the capture, assembly, and graphical presentation of metrics is required.
- 1-year technical writing and editing experience.
Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. Abbott is an Equal Opportunity Employer, committed to employee diversity.
Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.
The salary for this role is between:
N/A
JOB FAMILY:
Operations Quality
DIVISION:
ANSC Nutrition Supply Chain
LOCATION:
United States > Casa Grande : Plant
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous walking for prolonged periods (more than 2 hours at a time in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
Date Posted
01/07/2023
Views
21
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