zusammenfassung.

Beschleunige die Bewerbung, indem du dein Profil teilst

Job Details

For our client, an international company based in Neuchâtel, we are looking for a QA Senior Expert.

General Information:

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:

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

mit randstad bewerben.
Wir werden deine Bewerbung überprüfen und sehen, ob du zu diesem Job und Unternehmen passt.
Wir werden dich kontaktieren.
Unser Consultant wird dich zu einer passenden Zeit anrufen und mit dir deine Bewerbung und deine Karriereziele besprechen.
deine registrierung.
Falls du noch nie mit uns zusammengearbeitet hast, brauchen wir ein paar Informationen um herauszufinden, ob du in der Schweiz arbeitsberechtigt bist.
background check.
Um sicherzustellen, dass du der perfekte Kandidat für diese Rolle bist, werden wir alle relevanten, von dir zur Verfügung gestellten Referenzen kontaktieren.
der perfekte job für dich.
Unser Expertenteam wird entweder ein Vorstellungsgespräch für die Stelle arrangieren, auf die du dich beworben hast oder passende alternativen vorschlagen.
das interview.
Wir werden sicherstellen, dass du vollständig für dein Interview vorbereitet bist und weisst, was dich erwartet. Viel Glück!
dein start im neuen job.
Gratulation! Du bist bereit für deinen neuen Job. Unser Team wird sicherstellen, dass du vollständig vorbereitet für deinen ersten Arbeitstag bist.
beginne deinen neuen job.
Nachdem du deine neue Herausforderung begonnen hast, werden wir dich kontaktieren und sehen, wie es dir geht und wie wir dich in deiner neuen Rolle unterstützen können.

Danke für die Anmeldung zu persönlichen Job-Benachrichtigungen.

QA Senior Expert.

Job Details