DO WORK THAT MATTERS.
At Abbott, diverse ideas, perspectives, and expertise allow us to create the 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.
Abbott Rapid Diagnostics (formerly Alere) is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies. Our in-vitro Diagnostic Assay manufacturing site in Dundee has an exciting opportunity for 2 Technical Writers to join the team on a fixed term basis until the end of December 2020.
Directly participating in a Quality Systems Improvement program on site (certified to ISO13485), you will play a key part in the creating and/or update of Standard Operating Procedures, work/testing instructions, Validation Documentation (IQ / OQ / PQ), Design History Documentation including Design Inputs & Specifications, Verification Studies and Risk Management Dossiers. This is an exciting opportunity to join a team in a period of change and future-shaping, and offers the incumbent a challenging work package of creating of high-quality written content to a pre-defined project timelines.
The ideal candidate will be educated to degree level, preferably in a Science or similar field, and bring demonstrable experience from within GMP / Biotech / Pharma / Regulated Industry. You will be adept at preparing and writing technical documentation, with added exposure of creating and delivering associated training materials. You will be a natural communicator, whether this be written or verbal, and be comfortable working in a fast paced and dynamic environment.
As you’d expect from an innovative global healthcare company, we offer an excellent starting salary, and a competitive range of benefits including a defined contribution pension scheme and private healthcare.