Quality Assurance Manager

Quality Assurance Manager - 345921 GH

Come and join this innovative Medical Device company as their new QA Manager.

You will be joining an international organisation with a divers multicultural environment. You will be working hands on as well as in a team environment. In this role you will bring your experience in EU as well as U.S. regulations to the table as you will be the first point of contact with QA for their internal as external partners. You will be working with Medical Devices that have Liquids involved. This is a great role in a niche industry that will give you the chance to become even more of an expert than you already are. Giving you the opportunity to get a step ahead on the competition.

Benefits:

• Great work/life balance
• More opportunity to take a break
• Great for spending time with family, friends and hobbies

• Receive training
• Great for development
• Good for your profile

Responsibilities:

• You will be ensuring that products under the company's responsibilities are released and recorded will be meeting all specifications
• You are going to be leading and executing various investigations into quality issues and
• You will be maintaining and improving the part of the QMS specific to the portfolio of your scope
• You will be supporting the expansion into new markets and provide support in registration activities;
• You will be providing various updates regarding quality to senior management on the performance of processes and products related to your portfolio;
• You will also be providing training and advising on various QA aspects .

Requirements:

• You have experience with problem solving skills in a pharmaceutical process - including
• You are and expert in steam sterilisation;
• You are fluent in English in word as well as writing
• You have experience in supporting pharmacovigilance, regulatory and other relevant functions in relation to medical questions concerning the use of relevant products;
• You have knowledge of the practical application of GMP
• You know how to effectively communicate, with internal and external stakeholders in an international environment
• You can coach and train people on QA and compliance;
• You have a great understanding of regulatory expectations in medical device and pharmaceutical markets regarding to manufacturing, distribution and design
• You have 3 years of working experience in this market and industry

If this job appeals to you please apply here or on the NonStop Consulting website or send it to me, Gilson Heitinga, on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland, Romania, Luxembourg, US and the Czech Republic and we hold labour leasing licences for all EU8 countries. Please visit our website for a full list of the niche markets we cover.