Quality Assurance Employee (m/f/d) Full-time at Chiracon 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

Skills

Industry

Pharmaceutical Manufacturing

Description

Full-time Quality Assurance Employee

Requirements:

Successfully completed studies or training in natural sciences, pharmacy or a comparable field
At least 2 years of professional experience in quality assurance in the pharmaceutical industry.
basic knowledge of analytical methods (e.g. HPLC)
Ideally, experience in conducting audits.
good knowledge of GMP regulations
good English skills
good knowledge of MS Office
Flexibility and team orientation
Problem-solving and conflict-solving skills
proactive, structured and independent work style

Processing, monitoring, maintenance and optimization of the central quality assurance systems (change control, deviations, CAPA, OOS, complaints)
Creation, review, monitoring and approval of standard operating procedures (SOPs)
Review of quality-relevant documents (qualification and validation reports, risk analyses, specifications, batch documentation, manufacturing and testing instructions)
Creating Product Quality Reviews
Review and creation of Quality Agreements
Conducting self-inspections and supplier audits
Support in the qualification of production facilities/equipment and suppliers/service providers
Answering customer inquiries (e.g. processing questionnaires)

Responsibilities

Full-time Quality Assurance Employee

Requirements:

Successfully completed studies or training in natural sciences, pharmacy or a comparable field
At least 2 years of professional experience in quality assurance in the pharmaceutical industry.
basic knowledge of analytical methods (e.g. HPLC)
Ideally, experience in conducting audits.
good knowledge of GMP regulations
good English skills
good knowledge of MS Office
Flexibility and team orientation
Problem-solving and conflict-solving skills
proactive, structured and independent work style

Processing, monitoring, maintenance and optimization of the central quality assurance systems (change control, deviations, CAPA, OOS, complaints)
Creation, review, monitoring and approval of standard operating procedures (SOPs)
Review of quality-relevant documents (qualification and validation reports, risk analyses, specifications, batch documentation, manufacturing and testing instructions)
Creating Product Quality Reviews
Review and creation of Quality Agreements
Conducting self-inspections and supplier audits
Support in the qualification of production facilities/equipment and suppliers/service providers
Answering customer inquiries (e.g. processing questionnaires)