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Job at Merck Group in Glasgow, G20
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23 jobs at Merck Group

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Validation Manager by Agreement in Livingston, West Lothian, EH54
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Quality Specialist - Computer Systems Validation

Job at Merck Group in Glasgow, G20

Work Your Magic with us! Start your next chapter and join EMD Electronics.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimaginable with us.

Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers.

Your Role: As a Quality Specialist - Computer Systems Validation, you will be an integral part of the Global Systems Audit team within the Quality Assurance department. Your role will impact a range of important customer, operational, project, or service activities within your team and related teams. You will guide and influence peers or management regarding technical issues and challenges, contributing to the technical or strategic direction and operational decision making in your specialization.

Who You Are:

Degree level or equivalent, preferably in a science or technical area 4+ years of experience in validation, QA validation, validation testing, or related technical field within a pharmaceutical, life sciences, or biotechnology GXP environment Thorough knowledge of FDA and EU computer systems validation, including IT system development life cycle and software quality assurance in a regulated environment and associated regulations (cGMP, GLP, ICH, GAMP, Data Integrity, and Part11) Strong problem-solving, organizational, and communication skills Ability to work with agility and implement change on local and global scales Collaborates with various teams to identify and implement improvements Willingness to travel occasionally

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of our diverse team!

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html

ID 978689 Sectors:
in Glasgow, Scotland, G20
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