logo

JobNob

Your Career. Our Passion.

Research Associate III


Abbott Laboratories


Location

South Portland, ME | United States


Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.

The Opportunity

At Abbott, diverse ideas, perspectives, and expertise allow us to create life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Abbott offers you enormous opportunities to explore your interests and help you achieve your career and personal goals.

We have an exciting opportunity for a Research Associate III, focused on technical documentation, within the Research & Development team at our Abbott Rapid Diagnostics business located at Scarborough, ME. In this role, you will help support on market products for the ID NOW platform by supporting the development and creation of high-quality written content for internal and external audiences.

Abbott Rapid Diagnostics is part of Abbott's Diagnostics family of businesses, bringing together exceptional teams of experts and industry-leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.

What You'll Do

* Daily interaction with technical documentation, documentation tasks to be performed with high-throughput and attention to detail
* Required to proofread, prepare, create, review, edit, and/or update Quality and Technical Documents including, but not limited to: SOPs, Design Control Documentation (Design and Development Plan, Customer Requirements, Product Requirements, Design Outputs, Design Verification Protocol and Reports), Technical Reports, Risk Management Documentation including FMEAs
* Understands and is aware of the quality consequences which may occur from the improper product performance; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing, and testing activities
* Demonstrate technical proficiency in general laboratory techniques
* Conduct experiments of a varied nature in support of on-market products
* Works with multidisciplinary team including other scientists, researchers, and technicians.
* Analyze experimental results and provide written reports and oral presentations to executives
* Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships
* Carries out duties in compliance with established business policies
* Adapt rapidly to a changing industry and be able to adjust responsibilities, time and objectives accordingly
* Perform other duties & projects as assigned

Required Qualifications

* Bachelor's degree in Biology, Biochemistry or Chemistry, or related technical field
* Minimum of 3 years of laboratory and technical writing experience working under design control and developing human in vitro diagnostic tests for commercialization in the U.S and OUS
* Ability to work as part of a team with excellent communication skills
* Problem-solving skills combined with analytical skills and attention to detail
* Experience owning the end-to-end documentation creating process
* Proficiency with Microsoft Office, specifically in Word, Excel, and PowerPoint
* Must be able to productively generate quality documentation to meet program timelines

Competencies

* Comprehension of scientific literature and terminology
* Practical laboratory skills
* Ability in mathematics and computer literacy
* Good communication skills, capable of communicating ideas to colleagues and customers
* Problem-solving skills and good organizational skills
* Understanding of the commercial value of their work
* Firm knowledge of science and the ability to apply basic principles and techniques.

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

* Career development with an international company where you can grow the career you dream of .
* Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
* Health care and well-being programs including medical, dental, vision, wellness and occupational health programs, Medical Benefits start day 1
* Vacation - 3 weeks of accrued vacation (1st yr is prorated) + vacation buy program + 3 personal days + 10 paid holidays
* An excellent retirement savings plan with high employer contribution
* Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
* A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
* A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The base pay for this position is $52,000.00 - $104,000.00. In specific locations, the pay range may vary from the range posted.


Job tags

Holiday work


Salary

All rights reserved