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For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.
General Information:
Start date: 01.01.2025
End date: 31.07.2025
Workplace: Neuchâtel
Workload: 100%
Tasks and responsibilities:
Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.
Responsible for compliance and quality oversight related to activities throughout the manufacturing and release process of bulk drug substance (BDS).
Representative for both routine GMP (Good Manufacturing Practices) activities as well as for all improvement projects for the site
Ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements.
Participation in GMP zone audits as well as internal and external regulatory inspection
Accountable for the promotion of continuous improvement and involved related initiatives.
Understand and apply EHS guidelines and commitments policy, take care of its own safety, report risk situations and improvement opportunities to supervisory personnel.
Can act as back up of other QA Senior experts and QA Lead as requested.
Your profile:
At least 3 years of experience in an GMP environment
University degree in Engineering, Biotechnology, Pharmacy or Quality Management applied to industrial process or equivalent experience in pharmaceutical and /or biotechnological companies
Knowledge or experience in bulk drug substance (BDS).
Fluent French and a good command of English
Good knowledge of FDA, EMA, ICH regulations, Pharmacopeias and Quality system standards
Knowledgeable in auditing and inspection against regulatory / Quality standards
Knowledge/Experience with Quality tools such as Trackwise
Good analytical skills and ability to simplify the complex
Solution oriented and team spirit
Good listener and communication skills
Good organizational skills and continuous improvement mindset
For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.
General Information:
Start date: 01.01.2025
End date: 31.07.2025
Workplace: Neuchâtel
Workload: 100%
Tasks and responsibilities:
Responsible for Quality Assurance in the frame of activities all along the manufacturing and release process.
Responsible for compliance and quality oversight related to activities throughout the manufacturing and release process of bulk drug substance (BDS).
Representative for both routine GMP (Good Manufacturing Practices) activities as well as for all improvement projects for the site
Ensure the quality of information reported within the various systems and documentation with respect to current guidelines, compliance and regulatory requirements.
Participation in GMP zone audits as well as internal and external regulatory inspection
Accountable for the promotion of continuous improvement and involved related initiatives.
Understand and apply EHS guidelines and commitments policy, take care of its own safety, report risk situations and improvement opportunities to supervisory personnel.
Can act as back up of other QA Senior experts and QA Lead as requested.
Your profile:
At least 3 years of experience in an GMP environment
University degree in Engineering, Biotechnology, Pharmacy or Quality Management applied to industrial process or equivalent experience in pharmaceutical and /or biotechnological companies
Knowledge or experience in bulk drug substance (BDS).
Fluent French and a good command of English
Good knowledge of FDA, EMA, ICH regulations, Pharmacopeias and Quality system standards
Knowledgeable in auditing and inspection against regulatory / Quality standards
Knowledge/Experience with Quality tools such as Trackwise
Good analytical skills and ability to simplify the complex
Solution oriented and team spirit
Good listener and communication skills
Good organizational skills and continuous improvement mindset
nous sommes à ta disposition pour toute question.
Découvre comment se déroule la procédure de candidature et comment nous pouvons t'aider à trouver un emploi.
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.
Si tu n'as jamais travaillé avec nous auparavant, nous aurons besoin d'informations de base supplémentaires pour confirmer ton éligibilité à travailler en Suisse.
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.
Nous veillerons à ce que tu sois parfaitement préparé avant ton entretien et que tu saches exactement à quoi t'attendre – bonne chance!
Félicitations, tu es prêt à commencer ton nouvel emploi. L'équipe veillera à ce que tu sois parfaitement préparé pour ton premier jour.
Après avoir commencé ta nouvelle mission, nous te contacterons pour avoir de tes nouvelles et t'apporter notre soutien dans ton nouveau rôle.
Nous te tiendrons informé lorsque nous aurons des offres d'emploi similaires.
Merci de t'être abonné à tes alertes emploi personnalisées.