In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.
We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.
The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.
About the role
The primary responsibility of the Commercial Quality Manager & QP Israel is to provide leadership for excellence in Quality and Compliance of all Reckitt products and processes within the Israelian Commercial Business Unit. Youll:
Ensure a robust Quality Management system is in place and fit for purpose to comply with current regulations such as relevant GMP and GDP and Israelian Health Authorities requirements
Lead and facilitate quality continuous improvement activities
Implement processes and procedures and observe/audit for compliance
Provide feedback to the Commercial Quality SE manager on performance
Serve as a resource for information relative to all aspects of products and process quality
Implement and enhance culture of Quality
Final batch certification and release to the Israelian market
Maintain the validity of the GMP license
Ensure product safety and regulatory compliance
Co-ordinate and host external inspections by External Authorities, third parties and Reckitt.
Requirements: BSc. in Pharmacy
Valid Pharmacist License
At least 2 years' experience as QP in the pharmaceutical industry
Experience in developing and maintaining a robust QMS in a Pharma or Medical Device related industry
Clear understanding and assessing upon product safety, quality, efficacy and compliance risks
Good understanding of relevant requirements e.g.: EU GMP, EU GDP, WHO, PIC/S, CFR 21 Part 210/211
Strong interpersonal and communication skills
Experienced Auditing, appropriate qualifications in auditing an advantage
Language skills appropriate to the assigned country and/or regional cluster
QP should be approved by the Ministry of Health via the importer license
This position is open to all candidates.