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Jobs in the Netherlands, in English.
10,000+ live jobsQualified Person - Alloga
On-site in Veghel·Full-time·Added 1 month ago
Still open when we checked on 8 Oct
Overview
Job details
Full-time
Per the ad.
Requirements
Dutch
The ad asks for Dutch, or counts it in your favour.
Skills
This job advert was originally written in Dutch.
Requirements
What we're looking for
· A completed university degree in Pharmacy (or equivalent).
· Registered as a Qualified Person according to European guidelines (2001/83/EC).
· Excellent knowledge of quality and regulatory requirements within the pharmaceutical industry and 3PL.
· Strong analytical skills and a problem-solving mindset.
· Communicatively skilled and a team player.
· Good command of the Dutch and English languages, both spoken and written.
Nice to have
· Registration as a Responsible Person is a plus.
The role
Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!
What you'll do
· Developing and maintaining internal quality standards to ensure that processes and procedures are compliant with GxP laws and regulations;
· Reviewing and approving complaints, deviations, changes, and CAPAs;
· Contributing to the maintenance of the quality system, including drafting, reviewing, and approving new and amended procedures and work instructions;
· Monitoring the internal training plan related to the quality system;
· Reviewing and approving service providers as part of the supplier program;
· Responsible for leading audits by customers and inspecting authorities and ensuring that self-inspections are carried out;
· Performing audits at third parties where outsourced GxP activities are carried out;
· Advising management and department managers regarding the implementation of and compliance with GxP regulations.
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Job Details
As a Qualified Person (QP), you are responsible for the release of medicinal products and ensuring they comply with applicable laws and regulations, such as GMP (Good Manufacturing Practice). You play a key role in the production process and are involved in quality controls, audits, and solving complex challenges.
What will you do?
What you bring
We are looking for a driven professional with a sharp eye for quality and detail. You have strong knowledge of the pharmaceutical industry and possess excellent communication skills.
Your profile:
What Cencora offers
Benefit offerings outside the US may vary by country and will be aligned to local market practice. The eligibility and effective date may differ for some benefits and for team members covered under collective bargaining agreements.
Full timeAffiliated CompaniesAffiliated Companies: Alliance Healthcare Management Services (Nederland) BVEqual Employment Opportunity
Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.
The company's continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned
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