Quality Assistant (m/f/d) (Pharmaceutical-technical Assistant)

For a renowned client at the Frankfurt am Main location, we are looking for the earliest possible date for:

Quality Specialist (m/f/d) Pharma | Frankfurt | Homeoffice

Your tasks:

• Inspection and processing of incoming goods documents as well as quality defects

for the Sanofi domestic market in close coordination with the external warehouse

• Procurement, assignment, and control of batch documentation (CoA, CoC)

as well as packaging materials for correctness and compliance with requirements

• Execution of the compliance check of incoming goods documents according to

applicable SOPs as well as subsequent release in the SAP system and in the Batch

Market Release Tool

• Evaluation and tracking of quality-relevant incidents of the external

service provider within the framework of Sanofi Quality Oversight

• Inspection and evaluation of transport temperatures in case of limit violations

as well as preparation of the legal release according to § 16 AMWHV

• Creation and review of SOPs; representation of the Quality Release area during

audits and authority inspections

• Processing and documentation of returns as well as creation of

Distribution Complaints

• TOR management: Maintenance of warm times for chilled goods in the PLE of the external

service provider

• KPI tracking as well as active participation in continuous

improvement measures in the areas of quality, occupational safety, and environmental protection

Your profile:

• Have you completed training in the pharmaceutical or scientific

field, such as as Pharmazeutisch-technische Assistentin (m/f/d),

Chemisch-technische Assistentin (m/f/d) or as Pharmakant (m/f/d) and bring

several years of professional experience in the pharmaceutical industry? Then

you fulfill the essential requirement for this position.

• Several years of experience in a GMP/GDP-regulated environment, ideally in

drug manufacturing or quality assurance

• Very good SAP knowledge (especially QM module / PLE) as well as confident

handling of MS Office

• Very good English skills in spoken and written form

• Independent, responsible, and team-oriented way of working with

high flexibility and resilience

• Strong communication skills and reliability – even under

time pressure

Your advantages:

• Remuneration according to Equal Pay, fair and transparent pay at eye level

with permanent staff

• Flexible working hours through flextime regulations

• Homeoffice possibility after successful induction and by arrangement

• Employment in an internationally oriented, pharmaceutical

corporate environment with high quality standards

• Long-term assignment with a predictable perspective until July 2027

Additional information: Homeoffice: Scope: By arrangement Requirements for the applicant: Basic knowledge: Process analysis, Standard Operating Procedure (SOP), GMP (Good Manufacturing Practice), International pharmaceutical standards (e.g., GLP, GMP), Documentation (technical) Expert knowledge: SAP module QM (Quality Management), Quality inspection, Quality assurance