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Pharma jobs in Germany

Project Director and Operations Head

Project Director and Operations Head
Novartis
Nürnberg
EUR 60,000 - 100,000
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Pharmaberater (m/w/d) Diabetologie

Pharmaberater (m/w/d) Diabetologie
Careforce24
Rheda-Wiedenbrück
EUR 45,000 - 75,000

Hardware developer (m/f/d)

Hardware developer (m/f/d)
GULP – experts united
Mannheim
EUR 50,000 - 80,000

Pharmazeutisch-technischer Assistent (m/w/d)

Pharmazeutisch-technischer Assistent (m/w/d)
BBS 2 Aurich
Aurich
EUR 20,000 - 40,000

Sachbearbeiter:in Medizinischer Einkauf (m/w/d)

Sachbearbeiter:in Medizinischer Einkauf (m/w/d)
Gesundheitsverbund Landkreis Konstanz
Konstanz
EUR 35,000 - 55,000
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Pflegefachfrau, Pflegefachmann oder Gesundheits- und Krankenpfleger (m/w/d)

Pflegefachfrau, Pflegefachmann oder Gesundheits- und Krankenpfleger (m/w/d)
medius KLINIKEN gemeinnützige GmbH
Ruit
EUR 30,000 - 50,000

Projektleiter Elektrotechnik (m/w/d)

Projektleiter Elektrotechnik (m/w/d)
Hays
Leipzig
EUR 45,000 - 75,000

PTA (m/w/d) Apotheken- oder Arzt-Außendienst Direktvermittlung

PTA (m/w/d) Apotheken- oder Arzt-Außendienst Direktvermittlung
Careforce24
Köln
EUR 40,000 - 80,000
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Validation Expert (Qualifizierung) (m/w/d)

Validation Expert (Qualifizierung) (m/w/d)
绿叶制药集团有限公司
Miesbach
EUR 45,000 - 75,000

Mitarbeiter Qualitätssicherung (m/w/d)

Mitarbeiter Qualitätssicherung (m/w/d)
Neo Temp GmbH
Dresden
EUR 40,000 - 70,000

Mitarbeiter:in Patiententransport (m/w/d)

Mitarbeiter:in Patiententransport (m/w/d)
Gesundheitsverbund Landkreis Konstanz
Konstanz
EUR 30,000 - 50,000

Quality Engineers(w/m/d)

Quality Engineers(w/m/d)
PCC Solutions GmbH
Mannheim
EUR 40,000 - 80,000

Strategy Insights & Planning Consultant - R&D Drug Development / Clinical Trials

Strategy Insights & Planning Consultant - R&D Drug Development / Clinical Trials
ZS
Berlin
EUR 60,000 - 100,000

Key Account Manager Onkologie (m/w/d)

Key Account Manager Onkologie (m/w/d)
Inizio Engage
Germany
EUR 60,000 - 100,000

QA Manager Mikrobiologie (m/w/d) (Außertarifliche Bezahlung nach Chemietarif)

QA Manager Mikrobiologie (m/w/d) (Außertarifliche Bezahlung nach Chemietarif)
BS Wutow GmbH
Frankfurt
EUR 50,000 - 90,000

Mitarbeiter MSAT Technology Transfer Scientist (m/w/d) (Außertarifliche Bezahlung nach Chemietarif)

Mitarbeiter MSAT Technology Transfer Scientist (m/w/d) (Außertarifliche Bezahlung nach Chemietarif)
BS Wutow GmbH
Frankfurt
EUR 80,000 - 100,000

Laborleiter (m/w/d)

Laborleiter (m/w/d)
BS Wutow GmbH
Frankfurt
EUR 60,000 - 100,000

Chemikant (m/w/d)

Chemikant (m/w/d)
BS Wutow GmbH
Frankfurt
EUR 40,000 - 70,000

Compliance Expert (m/w/d) Schwerpunkt Trainingssystem

Compliance Expert (m/w/d) Schwerpunkt Trainingssystem
BS Wutow GmbH
Frankfurt
EUR 45,000 - 75,000

Quality Assurance Manager (m/w/d)

Quality Assurance Manager (m/w/d)
BS Wutow GmbH
Frankfurt
EUR 40,000 - 70,000

Quality Control Technician (m/w/d)

Quality Control Technician (m/w/d)
BS Wutow GmbH
Frankfurt
EUR 40,000 - 70,000

Quality Assistant (m/w/d)

Quality Assistant (m/w/d)
BS Wutow GmbH
Frankfurt
EUR 40,000 - 65,000

Projektverantwortlicher Manufacturing Science Technology and analytics (m/w/d) Bezahlung nach C[...]

Projektverantwortlicher Manufacturing Science Technology and analytics (m/w/d) Bezahlung nach C[...]
BS Wutow GmbH
Frankfurt
EUR 45,000 - 75,000

Lab Head & Key Expert (m/w/d) Bezahlung nach Chemietarif

Lab Head & Key Expert (m/w/d) Bezahlung nach Chemietarif
BS Wutow GmbH
Frankfurt
EUR 60,000 - 100,000

Quality Assurance Experte (m/w/d) Bezahlung nach Chemietarif

Quality Assurance Experte (m/w/d) Bezahlung nach Chemietarif
BS Wutow GmbH
Frankfurt
EUR 40,000 - 70,000

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Pharmareferent jobs

Project Director and Operations Head

Novartis
Nürnberg
EUR 60.000 - 100.000
Job description
Summary
Responsabile delle funzioni di produzione
Dirige l'organizzazione delle funzioni di produzione (MF) del sito, che
assicura che le apparecchiature, le infrastrutture e gli edifici siano pienamente operativi, soddisfino la conformità normativa, GMP e HSE e siano ulteriormente sviluppati per soddisfare i requisiti futuri e le esigenze aziendali.
mantiene e migliora la supervisione scientifica dei processi di produzione e delle modifiche tecniche, le conoscenze e le capacità tecniche pertinenti e garantisce il prodotto e la gestione tecnica, in tutte le unità di produzione e le funzioni del sito.

Testa Unità Produttiva Medio/Piccolo Sito
Guidare il team dell'unità di produzione per produrre e consegnare prodotti farmaceutici di alta qualità e convenienti in tempo, ogni volta, in modo sicuro ed efficiente. Guidare il percorso di trasformazione basato sull'eccellenza operativa dell'unità di produzione per migliorare le prestazioni, la produttività e la qualità al fine di garantire la competitività del sito.

Responsabile del team di processo per siti di grandi e medie dimensioni
Supervisiona le operazioni quotidiane all'interno dell'unità di produzione, in modo coerente con una cultura di auto-direzione (responsabilizzazione e responsabilità), per produrre e fornire prodotti di alta qualità ai clienti in modo conforme, efficiente ed economico.

Responsabile dell'unità di supporto al processo per siti di grandi e medie dimensioni
Guidare il team dell'unità di processo nel coordinamento e nella pianificazione di tutte le attività con responsabilità di produzione end-to-end (logistica, project work, eccellenza operativa, risorse e budget/costi) in modo coerente con una cultura di auto-direzione (empowerment e accountability). Garantisce la piena conformità ai requisiti di qualità, salute, sicurezza e ambiente (HSE), buone pratiche di fabbricazione (GMP), servizio clienti, statutari, normativi e Novartis.

Responsabile senior dei sistemi di produzione
Esperto MES che fornisce competenze tecniche a supporto di tutte le questioni legate ai registri elettronici dei lotti (eBR). Gestisci grandi team di esperti interfunzionali (automazione/produzione/background IT) >15 persone. Gestire sistemi di esecuzione della produzione complessi e integrati (MES/SAP/LIMS...)
About the Role

Possible locations: Halle, Dresden, Leipzig.

Major Accountabilities

  • Direct and manage Production, HSE (Safety), Engineering, Supply Chain and Manufacturing Science & Technology activities.
  • Lead the site leadership team comprised of department heads from each function, monitoring team performance to company goals and objectives through use of established metrics, driving cross-site collaboration within their respective functions.
  • Ensure the site, people, operations, and processes are compliant with cGMP, safety rules and other applicable regulations.
  • Coordinate site activities through planning to ensure the overall manufacturing objectives are accomplished in a timely and cost-effective manner.
  • Collaborate with other Site Heads to determine processes and procedures, which can be used across sites and where variances are needed to meet the unique needs of the site.
  • Develop and communicate the site strategic plan to achieve company short-term and long-term objectives.
  • Provide leadership to site employees including appropriate direction, mentoring and development opportunities. Maintain a positive work environment that supports positive team relations and teamwork.
  • Plan and lead site meetings to ensure compliance with site policies, safety regulations, procedures, and processes. Also ensures compliance with company policies and provides a forum for questions and discussion about impact to the site of company initiatives.
  • Investment projects and project management from construction to product launch.

Obligatory requirements:

  • Bachelor's degree in chemical engineering, chemistry, pharmacy, or related field (or equivalent experience).
  • Minimum 10 years of experience in the pharmaceutical industry, with at least 5 years in leadership roles, including experience with sterile manufacturing operations or relevant experience as site head or large scale PU.
  • Experience as a Project Director / extensive project management background, especially in capital project execution.
  • Strong strategic thinking with an enterprise focus.
  • Excellent collaboration skills with experience working in a matrix organisation and solid communication skills.
  • In-depth knowledge of cGMP regulations.
  • Demonstrated ability to communicate effectively and inspire a large organization to achieve shared objectives.
  • Fluent English and German, written and spoken.

Desirable requirements:

  • Experience with Health Authorities and inspections is highly desirable.

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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