Simtra Deutschland GmbH
33790 Halle (Westfalen) - Deutschland
Pharmakant/in
Arbeit
Vollzeit
ab 13.01.2026
Beschreibung
At our plants in Halle/Westphalia we produce drugs for the treatment of various cancers and other life-threatening diseases.
In the role of **Specialist (m/f/x) QA Client Communication**, you will be the QA representative for clinical and commercial transfer projects. You serve as the main QA-contact for clinical and commercial clients and are responsible for managing the QA-relationship with clients, including oversight of QMS-activities between SMEs and clients. You will be empowered to:
- T... weiter lesen
In the role of **Specialist (m/f/x) QA Client Communication**, you will be the QA representative for clinical and commercial transfer projects. You serve as the main QA-contact for clinical and commercial clients and are responsible for managing the QA-relationship with clients, including oversight of QMS-activities between SMEs and clients. You will be empowered to:
- T... weiter lesen
At our plants in Halle/Westphalia we produce drugs for the treatment of various cancers and other life-threatening diseases.
In the role of **Specialist (m/f/x) QA Client Communication**, you will be the QA representative for clinical and commercial transfer projects. You serve as the main QA-contact for clinical and commercial clients and are responsible for managing the QA-relationship with clients, including oversight of QMS-activities between SMEs and clients. You will be empowered to:
- Translate the client’s needs into QA requirements and provide feedback
- Review of product-specific SOPs / documentation
- Review of validation documents
- Monitoring of Stage-Gate Reviews
- Assure compliance with Simtra and cGMP standards
- Accompanying special manufacturing steps
- Supporting client visits in manufacturing area
- Explanation of Simtra quality standards and quality processes -- details are explained by SMEs
- Advocate for Simtra processes to improve the quality of new manufacturing
- Review of specific NCR
- Support process improvements in QA and Pharma Production
- Support client audits and MOH inspections with regard to client products
- Change Control review and communication to client
**What you'll bring:**
- Completed studies in Pharmacy, Chemistry, Biology, Technology or a related field
- 3+ years of experience in the Pharmaceutical or Biotech industry
- Experience in Quality Assurance and Aseptic Manufacturing required
- Strong knowledge of cGMP guidelines and microbiology
- Strong ability to deliver training and feedback
- Decisive and solution-oriented mindset, capable of making clear decisions under pressure
- Excellent communication skills in connection with excellent written and spoken German and English skills
**What we offer:**
- Fair, collectively agreed terms of pay, including social benefits such as a 13th month's salary, vacation pay, company pension plan, and additional nursing care insurance
- Modern in-house cafeteria with attractive subsidies
- 30 days of vacation plus special leave
- 37.5-hour working week
- Job bike leasing
- Corporate benefits: Exclusive employee discounts on numerous well-known brands
- Good transport connections and free employee parking with e-charging stations at favorable conditions
- Job-related relocation? We provide financial support as part of our relocation allowance
- Free company sports, e.g., badminton, soccer, and fitness classes
We offer interesting opportunities to committed and talented people. Gender, age, skin color, origin, sexual orientation and disabilities do not play a role - on the contrary: we promote diversity and believe that diversity is an enrichment.
We look forward to receiving the documents relating to your professional career directly via our online system.
In the role of **Specialist (m/f/x) QA Client Communication**, you will be the QA representative for clinical and commercial transfer projects. You serve as the main QA-contact for clinical and commercial clients and are responsible for managing the QA-relationship with clients, including oversight of QMS-activities between SMEs and clients. You will be empowered to:
- Translate the client’s needs into QA requirements and provide feedback
- Review of product-specific SOPs / documentation
- Review of validation documents
- Monitoring of Stage-Gate Reviews
- Assure compliance with Simtra and cGMP standards
- Accompanying special manufacturing steps
- Supporting client visits in manufacturing area
- Explanation of Simtra quality standards and quality processes -- details are explained by SMEs
- Advocate for Simtra processes to improve the quality of new manufacturing
- Review of specific NCR
- Support process improvements in QA and Pharma Production
- Support client audits and MOH inspections with regard to client products
- Change Control review and communication to client
**What you'll bring:**
- Completed studies in Pharmacy, Chemistry, Biology, Technology or a related field
- 3+ years of experience in the Pharmaceutical or Biotech industry
- Experience in Quality Assurance and Aseptic Manufacturing required
- Strong knowledge of cGMP guidelines and microbiology
- Strong ability to deliver training and feedback
- Decisive and solution-oriented mindset, capable of making clear decisions under pressure
- Excellent communication skills in connection with excellent written and spoken German and English skills
**What we offer:**
- Fair, collectively agreed terms of pay, including social benefits such as a 13th month's salary, vacation pay, company pension plan, and additional nursing care insurance
- Modern in-house cafeteria with attractive subsidies
- 30 days of vacation plus special leave
- 37.5-hour working week
- Job bike leasing
- Corporate benefits: Exclusive employee discounts on numerous well-known brands
- Good transport connections and free employee parking with e-charging stations at favorable conditions
- Job-related relocation? We provide financial support as part of our relocation allowance
- Free company sports, e.g., badminton, soccer, and fitness classes
We offer interesting opportunities to committed and talented people. Gender, age, skin color, origin, sexual orientation and disabilities do not play a role - on the contrary: we promote diversity and believe that diversity is an enrichment.
We look forward to receiving the documents relating to your professional career directly via our online system.
Ref-Nr.: 8702275
Aktualisiert:
14.01.2026
Quelle: Bundesagentur für Arbeit
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
weitere Infos Rechtliche Hinweise zur Nutzung
Ob die Stelle noch verfügbar ist und weitere Informationen findest du direkt auf der Website der Bundesagentur für Arbeit. Bitte beachte: OPROMA ist nicht der Anbieter dieser Stelle und kann keine Auskünfte geben.
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