Cache of job #13721767

Job Title

Quality Engineer

Employer

Lotusworks

Location

Limerick, Cork

Description

About Us. A valued and trusted partner to the world’s leading companies. We are committed to service excellence through our talented people who are empowered to be innovative and best in class. Location. Based at Ireland’s southwest coast, Cork is home to a large university with pharmaceutical and medical device hubs across the county. From sports, culture and activities Cork has so much to offer! Join us and work with us to deliver the excellent service we are renowned for with our clients. Be part of something great. Your Job Purpose. Working with the LotusWorks team as a Quality Engineer you will be responsible for influencing, negotiating, and executing on the Finished Goods Date of the Manufacturing program. You will do this through the creation of baseline IT requirements, onsite travelling to suppliers and execution of collaborated IT interfaces. You will ensure compliance to a harmonised Date of Manufacture (DoM) approach, whilst using strong quality assurance leadership to manage key Suppliers. Responsibilities: Point of contact for Global Supply Chain for DoM project. Provide leadership to improve the DoM requirement across the Finished Goods Suppliers. Influence the Senior Leadership teams of the ASL to ensure strategic focus on completing supplier harmonisation. Liaise with internal stakeholders to ensure that supplier agreements are adequately assessed. Provide technical guidance in developing, negotiating and closing supplier agreements. Lead the resolution of problems & eliminate constraints to ensure project targets are met. Maintain standards of housekeeping & GMP requirements. Represent the Supply Process Quality Assurance function as required by management. Ensure that all Health, Safety and Environmental requirements are fulfilled. Requirements. Bachelor`s Degree is required. A Degree in Engineering, Life Science, or related discipline is preferred. Minimum 5+ years’ experience in a Quality or Engineering Function within a Medical Device Company. Experience in the medical device, biotech and/or pharmaceutical industry is preferred. Both, FDA and ISO (International Organization for Standardization) regulations knowledge is required FDA CFR Part 820 and ISO 13485 knowledge is preferred. Negotiation skills. Knowledge in international contract management. Willingness to travel (average 2/month. Strong in MRP ERP IT Systems and the labelling requirements. Auditing background is preferred. Possess knowledge of statistical analysis tools (Minitab SAS preferred. Benefits. Life Assurance. Pension Contribution. Training & Educational Assistance (Engineers Ireland CPD Members. Healthcare Contribution. Annual GP Check-Up. Extra Annual Leave. Healthcare Screening. Not ready to apply, or have some questions? Call our Talent Specialist’s on 07191-69783 or Email jobs@lotusworks.com and we will be happy to help! LotusWorks is proud to be listed in the Best workplaces 2017. Empowering talent we care about for over 27 years. LotusWorks is an Equal Opportunity Employer. This job originally appeared on RecruitIreland.com.

Date Added

2530 days ago

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