Stryker Laboratory Analyst in Limerick, Ireland
Requisition ID 22722BR
Job Title Laboratory Analyst
Group Global Quality and Ops
Division SGS Quality Assurance
Business Unit QA Ireland
Business Function Quality Assurance
Employment Category Full Time
Percent Travel Required None
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 medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. Stryker products and services are available in over 100 countries. All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.
Job Description / Information
6 month fixed term contract role in Stryker, Limerick
The Laboratory Analyst will be responsible for completing day to day operations of the laboratories, with responsibility, which includes, but not limited to the following:
Sampling / testing of raw materials, intermediate and finished products. Testing includes physical and chemical testing , (e.g.: PSA, FTIR, ATR, XRD, Mechanical Strength Testing)
Routine verification activities.
Ordering and control of consumables and testing chemicals.
Documentation review / storage - verification and GMP checks on all raw data / logbooks / records.
Control of documentation associated with Raw Material Receiving Inspection, Traceability and other Quality Records that are to be maintained.
Control of Retain Sample areas (on-site and off-site) and overall process.
Co-ordination of testing and liaise with Contract Laboratories.
Execute Laboratory Equipment Qualifications and Test Method Validations.
Own “out of specification” investigations and perform relevant testing.
Progress updates through the QMS..
Support to Laboratory training program and initiatives including cost savings projects
Participate in both Internal and External Audits.
Diploma or higher in Chemistry or related subject
Experience in a Quality/Regulatory Affairs environment desirable.
Ability to build knowledge and understanding of US and International Medical Device Regulations and standards in area of expertise (Chemistry)
Must possess strong communication skills as well as have the ability to manage multiple tasks simultaneously.
Strong interpersonal skills.
Demonstrated ability to work independently.
Ability to be proficient in statistical techniques, data review and analysis.
High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages
All qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.
Stryker is an EO employer – M/F/Veteran/Disability