Commercial Quality Intern
Sign up free to see how well your resume matches this role.
What you'll do
- Consumer Quality Management System (QMS) & continuous improvement: Ensure that all local or Cluster Standard Operating Procedures (SOPs) that describe all GxP related processes are established ensuring adequacy and continuous improvement.
- New Product Introduction (NPI) & Product Lifecycle: quality approval of all new products to be marketed in Iberia through the relevant procedures (Finished Product, FAI, Incoming Control, etc.), as well as managing product returns and interaction with warehouse and distribution center.
- Training: Local monitoring and oversight of Training as per Cluster Training Matrix.
- Change Controls: ensure that any changes affecting the distribution related activities are appropriately controlled and supervised.
- Document & Data Management: ensure that a document and data management system is accurately implemented according to Kenvue and local regulatory requirements and that quality records are properly handled, stored and maintained.
- Non-Conformances (NC) & Corrective/ Preventive Actions (CAPA): processing of NCs and CAPAs via the current systems and according to applicable Kenvue processes and on time closure.
- Kenvue CQ Community: Participation in workshops and projects, task forces at NSE&F Cluster and EMEA Regional level on Quality related topics.
What they're looking for
- University Scientific degree preferably in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar.
- Fluency in English
- Up-to-date knowledge of relevant pharmaceutical legislation and GDP regulations.
Nice to have
- Intermediate in Portuguese
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Kenvue is currently recruiting for a:
What we do
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent.
Who We Are
Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.
Role reports to:
Commercial Quality Specialist SPLocation:
Europe/Middle East/Africa, Spain, Community of Madrid, MadridWork Location:
HybridWhat you will do
This is an exciting opportunity to join the Commercial Quality team of a world leading company in healthcare, in Spain!
The Commercial Quality (CQ) Intern is responsible for maintaining the appropriate Quality Standards and Systems for the operation of the Spanish Consumer Health organization. It will also support the Northen and Southern European & CQ Cluster team in implementing departmental strategies and services to optimize and harmonize processes and find opportunities to collaborate in the Cluster.
Key Responsibilities:
Consumer Quality Management System (QMS) & continuous improvement: Ensure that all local or Cluster Standard Operating Procedures (SOPs) that describe all GxP related processes are established ensuring adequacy and continuous improvement.
New Product Introduction (NPI) & Product Lifecycle: quality approval of all new products to be marketed in Iberia through the relevant procedures (Finished Product, FAI, Incoming Control, etc.), as well as managing product returns and interaction with warehouse and distribution center.
Training: Local monitoring and oversight of Training as per Cluster Training Matrix.
Change Controls: ensure that any changes affecting the distribution related activities are appropriately controlled and supervised.
Document & Data Management: ensure that a document and data management system is accurately implemented according to Kenvue and local regulatory requirements and that quality records are properly handled, stored and maintained.
Non-Conformances (NC) & Corrective/ Preventive Actions (CAPA): processing of NCs and CAPAs via the current systems and according to applicable Kenvue processes and on time closure.
Kenvue CQ Community: Participation in workshops and projects, task forces at NSE&F Cluster and EMEA Regional level on Quality related topics.
Experience and Skills:
Required:
University Scientific degree preferably in Pharmaceutical Sciences, Chemistry, Chemical Engineering or similar.
Fluency in English
Up-to-date knowledge of relevant pharmaceutical legislation and GDP regulations.
Preferred:
Intermediate in Portuguese
What��s in it for you
Competitive Benefit Package
Flexible work policy
Learning & Development Opportunities
Canteen
If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.
Company
Company facts come from this company's own listings. We only show what the postings themselves carry.