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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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Applying with us is easy. We will review your application and see if you are a good fit for the job and the company.
Our consultant will call you at a suitable time to discuss your application and further career aspirations.
If you’ve never worked with us before, we’ll need some basic additional pieces of information to confirm your eligibility to work in Switzerland.
Next, we just need to verify a few things - we’ll make the relevant compliance checks and and in ensuring you’re perfect for the role, we’ll make contact with any relevant references you’ve provided and will keep you posted.
Our expert team will either arrange an interview for the role you’ve applied for, or if they believe there’s a better opportunity, they’ll suggest alternative options too.
We’ll ensure that you’re fully prepared ahead of your interview and know exactly what to expect - good luck!
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