QA/QC Manager (m/w/d) at Semdor Pharma Group GmbH
berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

21 Dec, 26

Salary

90000.0

Posted On

22 Sep, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

Your tasks

  • As a Quality Manager, you are looking for responsible tasks and independent work in an open and honest team.
  • You enjoy optimizing systems and being the point of contact for other departments regarding QA topics assigned to you.
  • You are familiar with deviations, measures, complaints and change control, and SOPs and management review are not foreign concepts to you.
  • You communicate internally and externally with suppliers, service providers and cooperation partners.
  • Furthermore, you will evaluate batch-related documents from the areas of manufacturing and quality control.
  • You participate in various projects and carefully document project progress and results.
  • You enjoy creating and reviewing documents such as contracts or instructions. Analyzing key performance indicators is something you are familiar with and handle with ease.
  • You are interested in internal and external audits, in English as well as in German, and therefore have no problem with travel.

Your profile

  • Completed pharmaceutical studies / Pharmacist
  • Qualifications in the areas of responsible person for wholesale, MedCanG responsible person or as a qualified person according to §14 AMG are desirable.
  • Experience in a highly regulated environment (GMP/GDP/MedCanG/medical devices) is desirable.
  • You are detail-oriented and results-driven. You are characterized by strong organizational skills and a high level of self-motivation.
  • You have the ability to juggle multiple tasks without losing track or prioritizing them.
  • You are characterized by a structured, independent and self-reliant work style.
  • Knowledge of MS Office products.
  • Excellent German and English skills are required, as we operate internationally.

Your tasks

  • As a Quality Manager, you are looking for responsible tasks and independent work in an open and honest team.
  • You enjoy optimizing systems and being the point of contact for other departments regarding QA topics assigned to you.
  • You are familiar with deviations, measures, complaints and change control, and SOPs and management review are not foreign concepts to you.
  • You communicate internally and externally with suppliers, service providers and cooperation partners.
  • Furthermore, you will evaluate batch-related documents from the areas of manufacturing and quality control.
  • You participate in various projects and carefully document project progress and results.
  • You enjoy creating and reviewing documents such as contracts or instructions. Analyzing key performance indicators is something you are familiar with and handle with ease.
  • You are interested in internal and external audits, in English as well as in German, and therefore have no problem with travel.

Your profile

  • Completed pharmaceutical studies / Pharmacist
  • Qualifications in the areas of responsible person for wholesale, MedCanG responsible person or as a qualified person according to §14 AMG are desirable.
  • Experience in a highly regulated environment (GMP/GDP/MedCanG/medical devices) is desirable.
  • You are detail-oriented and results-driven. You are characterized by strong organizational skills and a high level of self-motivation.
  • You have the ability to juggle multiple tasks without losing track or prioritizing them.
  • You are characterized by a structured, independent and self-reliant work style.
  • Knowledge of MS Office products.
  • Excellent German and English skills are required, as we operate internationally.


Responsibilities

Your tasks

  • As a Quality Manager, you are looking for responsible tasks and independent work in an open and honest team.
  • You enjoy optimizing systems and being the point of contact for other departments regarding QA topics assigned to you.
  • You are familiar with deviations, measures, complaints and change control, and SOPs and management review are not foreign concepts to you.
  • You communicate internally and externally with suppliers, service providers and cooperation partners.
  • Furthermore, you will evaluate batch-related documents from the areas of manufacturing and quality control.
  • You participate in various projects and carefully document project progress and results.
  • You enjoy creating and reviewing documents such as contracts or instructions. Analyzing key performance indicators is something you are familiar with and handle with ease.
  • You are interested in internal and external audits, in English as well as in German, and therefore have no problem with travel.

Your profile

  • Completed pharmaceutical studies / Pharmacist
  • Qualifications in the areas of responsible person for wholesale, MedCanG responsible person or as a qualified person according to §14 AMG are desirable.
  • Experience in a highly regulated environment (GMP/GDP/MedCanG/medical devices) is desirable.
  • You are detail-oriented and results-driven. You are characterized by strong organizational skills and a high level of self-motivation.
  • You have the ability to juggle multiple tasks without losing track or prioritizing them.
  • You are characterized by a structured, independent and self-reliant work style.
  • Knowledge of MS Office products.
  • Excellent German and English skills are required, as we operate internationally.


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