Timişoara

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Fișa jobului

Team Leader _Audit Management Department_ SC STADA Hemofarm SRL Timisoara

Qualification And Experience
  • University Degree in Pharmacy, Chemistry, Microbiology, Biochemistry or another related science preffered with technical background;
  • More than 2 years experience as a team leader ideally in pharmaceutical industry or quality oriented environment (. ISO 9001);
Skills And Attributes
  • Ability to define and monitor processes for own team as a part of an international collaboration with a global organization;
  • Good interpersonal skills, ability to work with all levels of personnel and management;
  • Good problem solving and risk assessment abilities;
  • Good organizational and in time management skills;
  • English language fluency in speaking and writing;
Knowledge about Microdoft office word and excel is a muct and ability to learn and become proficient with appropiate software like SAP.

Key Responsibilites
  • Management of an Audit Management Team in the Audit Management Department as a functional superior;
  • Responsability and coordination of corporate GMP-related auditing processes(organisation, management, execution, closure) and continuous improvement of the overall process executed in teams.
  • Responsability for Cost efficient audit planning and reporting of key performance indicators related with this task;
  • Responsability for creation and maintenance of documents related with processes for own team;
  • Creation and maintenance of the annual corporate audit planning list for API and key intermediates manufacturers, CMO’s, testing laboratories and suppliers to assure compliance of manufacturing/supply process for API and medicinal products with EU-GMP-Guideline and local Medicines / Pharmaceutical Acts;
  • Responsibility for process definition regarding correspondence with and coordination of internal and external auditors as well as global contract partners;
  • Responsibility and maintenance of contracts with external auditors / auditor companies and reporting of key performance indicators related with this task;
  • Implementation of new global or local requirements related with auditing and qualification process in compliance with EU-GMP-Guideline and local Medicines / Pharmaceutical Acts;
  • Willingness to travel.
Benefits
  • Attractive salary package;
  • The opportunity to develop a career in a multinational industrial group;
  • Trainings performed abroad.
Please send your CV in English.
Nivel de vechime

Asociat

Tip de angajare

Full-time

Ocupație

Contabilitate/Audit

Sectoare de activitate

Chimie

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