Quality Assurance - Cardiff, United Kingdom - Molecular Devices

Molecular Devices
Molecular Devices
Verified Company
Cardiff, United Kingdom

2 weeks ago

Tom O´Connor

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Tom O´Connor

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Description
Do you want to help advance scientific discovery, improving quality of life around the world? We do, too.


Molecular Devices makes innovative, high-performance life science technology that enables academia, pharma and biotech customers to accelerate research breakthroughs and new therapeutic discoveries.

Guided by our diverse leadership team and female president, you'll grow your career alongside best-in-class teams around the globe, and within a culture of collaboration, engagement, diversity, and inclusion.

Molecular Devices is proud to work alongside a community of nine fellow Danaher Life Sciences companies.

Together, we're pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.

Do you want to work in an innovative team in the life science business? Do you enjoy overseeing the Quality of manufacturing practices, in-process analytics and batch release testing of Cellesce's organoid products, to ensure that product quality requirements are met at all times?


We are currently seeking a Quality Assurance (QA) Officer who will be responsible to help foster a strong Quality culture throughout the business and may be required to deliver training to other staff members.


As a core member of the Quality team, the main focus of this role will be the development, promotion and continuous improvement of the Quality Management System.

As such, the post holder should have a very solid working knowledge of Quality Management Systems and be able to review quality systems documentation, including deviations, change controls and Corrective and Preventative Actions (CAPAs)


What we'll get you doing:

Foster a strong Quality culture throughout the business
Develop, promote, and continuously improve the Quality Management System
Review and approval of Quality systems documentation
Review and approval of Manufacturing and batch release documentation
Participation in customer inspections/audits
Performing Quality investigations and root cause analysis, identifying CAPAs
Ensure a safe working environment by complying with all health and safety policies and procedures
Occasionally travel to attend conferences or to meet with customers


The essential requirements of the role include:
A minimum of 3 years' experience working within scientific or pharmaceutical QA
First (Bachelors) Degree in a scientific or technical discipline or equivalent technical experience
Solid working knowledge of validation and Pharmaceutical Quality Management Systems
Working knowledge of GMP & Quality-related pharmaceutical regulations and standards


It would be a plus if you also possess previous experience in:
Regulatory or customer-led inspections/audits
Quality investigations and root cause analysis


When you join us, you'll also be joining Danaher's global organization, where 80,000 people wake up every day determined to help our customers win.

As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System tools and the stability of a tested organization.


At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve.

Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

If you've ever wondered what's within you, there's no better time to find out.
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