QA Specialist M/F (30500)

At Guerbet, we build lasting relationships so that to enable people to live better. This is Our Purpose.

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95 years ,we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.

Achieve, Cooperate, Care and Innovate are the values that we share and practice on a daily basis.

Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.

For more information on Guerbet, go to www.guerbet.com and follow Guerbet on Linkedin, Twitter, Instagram and Youtube

WHAT WE ARE LOOKING FOR

We are looking for a dynamic QA Specialist to work within a cross functional environment to foster an ethos and culture of cGMP & Quality awareness.

YOUR ROLE

Ensure that all Deviations are investigated and resolved, and that associated CAPAs are completed
Compile and/or review all GMP Procedures
Manage Change Controls
Participate and/or lead Internal Audits
Review and approve completed Production Batch Records
Ensure Quality related complaints are investigated and resolved
Perform Annual Product Quality Reviews
Release and Rejection of API and other production materials and labels
Manage and/or lead External Audit program
Ensure an effective Supplier Management program
Ensure Manufacturing batch record is in compliance with relevant Marketing Authorisation.
Ensure that EHS roles and responsibilities are complied with as per the requirements of the site Safety Statement
Perform other related duties as assigned from time to time based on company needs.

YOUR BACKGROUND

Minimum of a Bachelor Degree in Science or related pharmaceutical discipline
Minimum 3 years’ experience within the pharmaceutical industry.
Desirable evidence of Continuous Professional Development.
Understanding of EU GMP Complexity.
A proven identifiable track record of success in a similar environment.
Good organizational skills and attention to detail.
Requires good written, verbal and interpersonal communication skills and the ability to effectively interact cross functionally.
Ability to prioritize, manage multiple tasks, and meet deadlines
Ability to learn and utilize computerized systems for daily performance of tasks.

Reason to join US

Much more than a Competitive salary,

We offer continued personal development. When you join Guerbet, you :

Are choosing a global leader with recognized expertise in diagnostic and interventional imaging,
Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient’s life all over the world,
Are joining a company where we value diversity of talents coming from various horizon.

We # Innovate # Cooperate # Care #Achieve at Guerbet.

Guerbet is an Equal Opportunity Employer. As an organization, we believe that no individual should be discriminated against because of their differences, which includes the following: age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, or any other basis as protected by federal, state, or local law. Guerbet is committed to diversity, equity, and inclusion.

Guerbet provides accommodations to applicants and employees with disabilities. If you need an accommodation to apply for a position please send an email to careers@guerbet.com or you can also call this number +19843443717

QA Specialist M/F (30500)

Benefits

Job Description