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For one of our client, a pharmaceutical company specialized in aseptic manufacturing, we are looking for a
Team Leader Compliance PQS
Location: Jura canton
Contract: Permanent
Please note that French and English (fluent level) are mandatory for this vacancy.
Your Tasks:
Overseeing a small team within the Quality Assurance department to ensure compliance.
Managing sub-processes related to deviations, Corrective and Preventative Actions (CAPA), and Change Control.
Collaborating on investigations and approving investigation reports for minor and major deviations.
Representing the company in dealings with clients regarding deviations or Change Control.
By fulfilling these responsibilities, you will significantly contribute to the high quality of the services offered by our client.
Your Profile:
To be successful in this role, the following qualifications are required:
A scientific degree.
A minimum of 3 years experience in Quality Assurance, including investigations related to deviations, CAPA, and Change Control.
5 years of experience in an environment compliant with cGMP standards.
Fluency in French and English (C1 level) with excellent writing skills.
Proficient in MS Office and Visio.
Preferred, but not required skills include:
Experience with eQMS (Trackwise or similar).
Experience as a QP or QP substitute.
Experience in regulatory Affairs
For one of our client, a pharmaceutical company specialized in aseptic manufacturing, we are looking for a
Team Leader Compliance PQS
Location: Jura canton
Contract: Permanent
Please note that French and English (fluent level) are mandatory for this vacancy.
Your Tasks:
Overseeing a small team within the Quality Assurance department to ensure compliance.
Managing sub-processes related to deviations, Corrective and Preventative Actions (CAPA), and Change Control.
Collaborating on investigations and approving investigation reports for minor and major deviations.
Representing the company in dealings with clients regarding deviations or Change Control.
By fulfilling these responsibilities, you will significantly contribute to the high quality of the services offered by our client.
Your Profile:
To be successful in this role, the following qualifications are required:
A scientific degree.
A minimum of 3 years experience in Quality Assurance, including investigations related to deviations, CAPA, and Change Control.
5 years of experience in an environment compliant with cGMP standards.
Fluency in French and English (C1 level) with excellent writing skills.
Proficient in MS Office and Visio.
Preferred, but not required skills include:
Experience with eQMS (Trackwise or similar).
Experience as a QP or QP substitute.
Experience in regulatory Affairs
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Postuler avec nous, c'est facile. Nous examinerons ta candidature et verrons si tu corresponds au poste et à l'entreprise.
Notre consultant t'appellera au moment qui te convient pour discuter de ta candidature et de tes aspirations professionnelles.
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Ensuite, nous devrons simplement vérifier quelques éléments – nous effectuerons les contrôles de conformité appropriés et te tiendrons informé.
Notre équipe d'experts organisera un entretien pour le poste pour lequel tu as postulé ou, si elle pense qu'il existe une meilleure opportunité, elle te proposera également des options alternatives.
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