Quality Assurance Manager*in - GMP (m/w/d)
at
Axolabs GmbH
BERLIN, Berlin, Germany
-
Full Time
Start Date
Immediate
Expiry Date
03 Jan, 27
Salary
90000.0
Posted On
05 Oct, 26
Experience
4 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
No
Skills
Industry
Pharmaceutical Manufacturing
Description
This is what you can do with us
Responsible for quality assurance in the GMP control laboratory and overseeing the GMP-compliant release of therapeutic molecules.
Check documents and data for quality and compliance and support validations and qualifications.
Actively participate in the continuous improvement of processes and the quality management system.
Provide support with OOS cases, deviations, CAPAs and change control processes.
Accompany internal, external and supplier audits and conduct training for employees.
That's what we want.
Completed training in a natural science subject (e.g. biochemistry, biology, biotechnology, chemistry, pharmacy), in the pharmaceutical-medical field or a comparable qualification
Professional experience in a GLP, GCP, GMP or ISO 13485 regulated environment, e.g. quality control laboratory, pharmaceutical industry, MedTech, accredited laboratory
Independent, structured and committed work style as well as strong communication skills
Reliability, teamwork and a sense of responsibility
Proficient use of standard software and very good German and English skills
What we offer you
Structured onboarding and mentoring for a successful start
A full-time position (40 hours/week) with a flexible flextime system
Permanent employment contract and centrally located workplace in Kulmbach
Responsible tasks and individual development and career opportunities in an innovative, international company
Company pension scheme, subsidies such as JobRad (bike leasing) and access to corporate benefits
100% reimbursement of the cost of the job ticket (Deutschlandticket) or free parking in the adjacent parking garage
30 days of annual leave
Relocation support for applicants from outside the region
Responsibilities
This is what you can do with us
Responsible for quality assurance in the GMP control laboratory and overseeing the GMP-compliant release of therapeutic molecules.
Check documents and data for quality and compliance and support validations and qualifications.
Actively participate in the continuous improvement of processes and the quality management system.
Provide support with OOS cases, deviations, CAPAs and change control processes.
Accompany internal, external and supplier audits and conduct training for employees.
That's what we want.
Completed training in a natural science subject (e.g. biochemistry, biology, biotechnology, chemistry, pharmacy), in the pharmaceutical-medical field or a comparable qualification
Professional experience in a GLP, GCP, GMP or ISO 13485 regulated environment, e.g. quality control laboratory, pharmaceutical industry, MedTech, accredited laboratory
Independent, structured and committed work style as well as strong communication skills
Reliability, teamwork and a sense of responsibility
Proficient use of standard software and very good German and English skills
What we offer you
Structured onboarding and mentoring for a successful start
A full-time position (40 hours/week) with a flexible flextime system
Permanent employment contract and centrally located workplace in Kulmbach
Responsible tasks and individual development and career opportunities in an innovative, international company
Company pension scheme, subsidies such as JobRad (bike leasing) and access to corporate benefits
100% reimbursement of the cost of the job ticket (Deutschlandticket) or free parking in the adjacent parking garage
30 days of annual leave
Relocation support for applicants from outside the region
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