Laboratory Analyst

Work Flexibility: Onsite Laboratory Analyst Location: Limerick

Position requirements The Laboratory Analyst will be responsible for completing day to day operations of the laboratories, in accordance with relevant regulatory requirements and lab standards for medical devices. The Laboratory Analyst will adhere to sustained levels of product quality, manufacturing and chemistry compliance.

What you will do:

• Complete sampling / testing of raw materials, intermediate and finished products. Testing includes physical and chemical testing , (e.g.: PSA, FTIR, ATR, XRD, Mechanical Strength Testing)
• Complete routine verification activities.
• Provide business support, as applicable
• Understands role and the importance of meeting the requirements of the Laboratory. Understands the business requirements and potential implications owning to any failures to deliver products and services within the agreed timeframe / standard to Production and support functions.
• Complete ordering and control of consumables and testing chemicals.
• Complete documentation review / storage - verification and GMP checks on all raw data / logbooks / records. Filing and archiving of records.
• Control of documentation associated with Raw Material Receiving Inspection, Traceability and other Quality Records that are to be maintained by the Laboratory.
• Control of Retain Sample areas (on-site and off-site) and overall process.
• Co-ordination of the testing which is out-sourced and liaises 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.
• Own related changes.
• Complete the Originator task for change control.
• Support to Laboratory training programme.
• Provide recommendations to support the business, continuous improvements in test methodologies / Laboratory systems
• Support Company and laboratory initiatives.
• Participate in both Internal and External Audits within Stryker.
• Own and drive identified cost savings.

What you will need:

• 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

Pay Ranges:

Ireland: €40,000 - €67,000 EUR Annual At Stryker, we believe transparency helps candidates make confident decisions about their next career step. Compensation is an important part of that process and we want to be clear about how pay is determined. The compensation information posted for this role may be presented as a salary range or a fixed amount depending on the role.

In addition to base salary, this role may be eligible for incentive compensation (such as bonus and/or commissions where applicable), along with Stryker’s comprehensive benefits package.

Travel Percentage: 0%

Stryker is one of the world’s leading medical technology companies and, together with its 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!

For more information, visit: www.stryker.com

Work Flexibility

Remote – Role allows you to work the majority to 100% of time from an alternate workplace. These roles could have travel expectations, and you must work within the country of the job requisition location.

Field-based – You can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Almost all sales roles would likely be qualified as field-based.

Onsite – Role is 100% located at a Stryker facility. Some ad hoc flexibility may be available depending on role, level, and job requirements. Manufacturing roles and any role that requires physical presence at the office would qualify under this category.

Hybrid – You can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager/supervisor.

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