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Mgr Quality Assurance

Covance 4/8/2019 3:21:51 PM
JOB ID: 29552 Category: Quality Assurance
Maidenhead, United Kingdom

   

 

Job Overview

Get ready to redefine what's possible and discover your extraordinary potential at Covance. Here, you'll have the opportunity to personally advance healthcare and make a difference in peoples' lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose, you'll be empowered to own your career journey with mentoring, training and personalized development planning.

Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow's drug development challenges, creating new possibilities for our clients—and your career.

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries. We have an exciting opportunity available to join our team.

We are looking to recruit QA Manager - full time, permanent role

This position provides management support to the Global Clinical Quality Assurance & Compliance Department, with duties primarily focused on quality system, compliance, Inspection and audit related tasks and responsibilities. These may include (but will not be limited to) management of tasks related to Client audits and regulatory inspections;

* Corrective / Preventive Actions (CAPA);
* Quality data analysis, trending and reporting;
* Quality Improvement initiatives;
* Quality oversight and risk management.

Education / Qualifications

* University Degree in a biomedical or related life science, nursing or engineering qualification required

Experience

Minimum requirements

* Previous GCP Experience within a CRO/Pharmaceutical organisation, or an equivalent combination of education and Experience to successfully perform the key

Experience

* Proven ability to understand, analyze and communicate the impact of global regulatory issues affecting the drug development process
* Thorough knowledge, understanding and Experience applying ICH Guidelines, GCPs including applicable regulatory requirements for the conduct of clinical development programs
* Knowledge of the drug development process from the perspective of a contract research organisation


Position Type: Full-Time

Location: Maidenhead, UK - United Kingdom



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Covance Recruiting Process

Below is a general Overview of Our Recruiting Process

If you’d like to work for us, please submit your resume/CV online. If your ability to use or access our electronic application is limited due to a disability, please visit www.gettinghired.com or call 1-800-978-4473 for help.

We consider applications from everyone who is interested in a position with us and who meets the required criteria and qualifications.

If your application is selected, someone from our recruiting team will contact you to arrange an initial screen. We may carry this out over the phone or at a face-to-face meeting. You must complete the screen to be considered for the position.

Based on the results of the initial screen, we may invite you to an interview. One of our recruiting team members will contact you to arrange this. The process may involve several interviews, initially over the phone, and then face-to-face with different members of the hiring team.

Our interviews follow a behavioral-based format. This means we’ll ask you to give us information that’s specific to your professional and educational experiences.

Hiring team members will share and discuss their input and then make their decision.

If you’re the person who best meets the requirements of the position, a member of the hiring team will get in touch to make you an offer of employment. Covance is an eVerify employer (United States only).