Quality Manager Nordics at Reckitt Benckiser
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Quality Manager Nordics at Reckitt Benckiser
Are GMP and GDP in your DNA and do you like to be in charge of your own work day?
Your new company
Reckitt Benckiser Group plc, is a British multinational consumer goods company headquartered in Slough, England. Reckitt operates under three business units (BU) - Health, Hygiene and Nutrition. This position is within the Health BU. Each BU is dedicated to building sustainable solutions that will help Reckitt address the challenges presented by global mega-trends like sustainability, urbanization, climate change and digital transformation. At Reckitt you fight to make access to the highest quality hygiene, wellness and nourishment a right and not a privilege because this is what inspires and motivates us!
Your new role
The primary responsibility is to provide leadership for excellence in "Quality and Compliance" of all health products and processes within the supply/distribution chain, including embellishment.
Work tasks:
- Lead and facilitate quality continuous improvement activities
- Assure proper quality systems are developed to comply with current regulations such as relevant GMP and GDP
- Implement and maintain processes and procedures and observe/audit for compliance
- Establish objectives for Quality improvement within the region; provide feedback to the region on performance against relevant internal and external quality, regulatory/statutory requirements
- Serve as a resource for information relative to all aspects of products and process quality
- Facilitate the ‘right first-time’ approach and implementation of new products and processes;
- Support and integrate continuous improvement principles within the region through proactive communication, partnering, training and education
- Work effectively with internal parties, manufacturing sites, third parties, external bodies, and corporate personnel
- Co-ordinate and host external inspections by External Authorities, third-parties, and Reckitt.
What you'll need to succeed
- At least 5 years of experience working in a quality compliance function in Healthcare, Pharmaceutical, or Medical Device related industry.
- Experience in developing and maintaining a robust QMS in a Healthcare, Pharmaceutical, or Medical Device related industry.
- Clear understanding and ability to assess and act upon product safety, quality, efficacy, and compliance risks.
- Good understanding of regulatory, GMP, and GDP requirements relevant to a regulated product e.g. EU GMP, EU GDP, WHO, PIC/S, CFR 21 Part 210/211.
- Clear understanding to ensure operations do not compromise the quality of products and can demonstrate compliance with GDP.
- Strong interpersonal and communication skills.
- Auditing skills, appropriate qualifications in auditing an advantage
- Experience as GDP RP is an advantage
What you'll get in return
This is a great chance to advance your career, taking a more holistic, strategic view of different brands ant to gain experience in working in a multi-functional/multi-national environment
As this is a new position in the Nordics, you can shape and develop this role according to your own ambitions. No "norms" exist and you are the one who decides how to apply the standards and requirements.
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV incl a short section of your motivation for applying for this job..
If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career.
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Information og data
Denne ledige stilling har jobtypen "Kvalitetskoordinator", og befinder sig i kategorien "Kontor, handel og service".
Arbejdsstedet er beliggende i København
Jobbet er oprettet på vores service den 27.5.2021, men kan have været deaktiveret og genaktiveret igen.
- Kvalitetskoordinator
- København
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