Senior Quality Engineer
Lotusworks
Cork
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 LotusWorks as a Senior Quality Engineer, you will be responsible for leading current project compliancy requirements and project completions. The project teams will require influencing, supporting, and monitoring to ensure targets are met and communicate to the LT (Leadership team. Responsibilities. Point of contact for Global Supply Chain for a supplier labelling compliancy project. Point of contact for supplier agreements project. Provide leadership to improve present project structures. 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 and deployed. Provide technical guidance in developing, negotiating and closing supplier agreements. Provide technical guidance in developing, negotiating and supplier labelling solutions. 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. Know and follow all laws and policies that apply to one’s job, and maintain the highest levels of professionalism, ethics and compliance always. Requirements. A minimum of a bachelor’s Degree is required. A Degree in Engineering, Life Science, or related discipline is preferred. Minimum 5-6 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. Strong in Regulations, agreements, labelling, MRP ERP IT Systems. Strong communication, teamwork, and problem-solving skills are required. Benefits. Life Assurance. Pension Contribution. Training & Educational Assistance (Engineers Ireland CPD Members. Healthcare Contribution. Annual GP Check-Up. Extra Annual Leave. Healthcare Screening. Refer someone you know for this role and if we hire them you will receive a €250 voucher. (T’s & C’s apply) Click on the following link to Refer Your Friend today! http://www.lotusworks.com/en-ie/refer-a-friend. Not ready to apply, or have some questions? Call our Talent Specialist’s on +3537191-69783 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 29 years. LotusWorks is an Equal Opportunity Employer. This job originally appeared on RecruitIreland.com.
2128 days ago