Gestern veröffentlicht

Senior Expert / GMP Officer (m/f/d)

Senior Expert / GMP Officer (m/f/d)

Senior Expert / GMP Officer (m/f/d)

Senior Expert / GMP Officer (m/f/d)

Novartis AG

Pharmazeutische Produkte, Arzneimittel

Österreich

  • Art der Anstellung: Vollzeit
  • 65.500 € – 91.500 € (von XING geschätzt)
  • Vor Ort
  • Zu den Ersten gehören

Senior Expert / GMP Officer (m/f/d)

Über diesen Job

Senior Expert / GMP Officer (m/f/d)

Job ID
REQ-10058967
Juli 29, 2025
Österreich

Summary

About the role:
#LI-Hybrid

We are seeking a highly motivated and experienced GMP Officer to support compliance activities and quality assurance processes across the Analytical Operations team in Austria (AO AT). As the GMP Officer you are coordinating and preparing inspections, assuring GMP compliance of all activities in the department and providing expert guidance on GMP compliance aspects including state-of-the art analytical technology and Data & Digital solutions. In addition, you lead quality-related strategic initiatives in alignment with the global Analytical Operations team.

About the Role

Key responsibilities

  • Act as first point of contact for all GMP/compliance related aspects for team members and stakeholders.
  • Assure audit readiness of the department and facilitate audits and inspections, including self-inspections, global audits and Health Authority visits and manage Corrective & Preventive Actions (CAPAs) resulting from inspections.
  • Lead local and global quality related strategic initiatives in alignment with the global Analytical Operations team.
  • Provide GMP/compliance guidance on documentation, systems use, SOPs/WPs/Guidelines, including state-of-the art analytical technology (e.g. lab automation systems, mass spectrometry) and Data & Digital solutions (e.g. ELN).
  • Track updates and manage the review/implementation of global and local SOPs in collaboration with Subject Matter Experts (SMEs).
  • Train new team members on general GMP topics and Standard Operating Procedures (SOPs).
  • Act as an investigator for quality related incidents and create trending reports for investigations, including OOX and deviations.
  • Conduct regular spot-checks for lab systems, instrumentation, and processes. Author and review SOPs.

Essential Requirements:

  • Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry or similar with at least 4 years relevant industry experience or PhD in relevant field or equivalent and 2+ years of work experience within the pharmaceutical industry in a GMP regulated environment.
  • Thorough knowledge of GMP, compliance regulations and quality assurance principles.
  • Experience participating in audits and inspections.
  • Certifications and hands-on experience with deviations, Data Integrity (DI), and CAPA processes are an advantage.
  • Strong matrix leadership skills.
  • Strong organizational and exceptional communication skills.

Desirable requirements:

  • Proficiency in laboratory systems and reporting (e.g., 1QEM system, trending reports).
  • Knowledge in SAP and LIMS application.

You’ll receive:

You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development opportunities as well as worldwide career possibilities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 65,605.54 a year (on a full-time basis). The actual salary will be significantly higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies.

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive working environment and diverse teams, representative of the patients and communities we serve.

Adjustments for Applicants with Disabilities

If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to disabilities.austria@novartis.com and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. If you would like to request this, please let us know in advance as a note on your CV.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network

Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Division
Development
Business Unit
Universal Hierarchy Node
Standort
Österreich
Site
Schaftenau
Company / Legal Entity
AT33 (FCRS = AT033) Novartis Pharmaceutical Manufacturing GmbH
Functional Area
Research & Development
Job Type
Full time
Employment Type
Regular
Shift Work
No
Apply to Job

Adjustments for Applicants with Disabilities

If because of a medical condition, physical disability or a neurodiverse condition you require an adjustment during the recruitment process, please reach out to disabilities.austria@novartis.com and let us know the nature of your request as well as your contact information. The support which we can provide will include advice on suitable positions as well as guidance at all stages of the application process. Austrian law provides candidates the opportunity to involve the local disability representative, Behindertenvertrauensperson (BVP), in the application process. If you would like to request this, please let us know in advance as a note on your CV.

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

Job ID
REQ-10058967

Senior Expert / GMP Officer (m/f/d)

Apply to Job

Ähnliche Jobs

QC Analytical Development Manager (m/w/d)

Schorndorf

Catalent

66.000 €86.000 €

Vor über 30 Tagen veröffentlicht

QC Analytical Development Manager (m/w/d)

Schorndorf

Catalent

66.000 €86.000 €

Vor über 30 Tagen veröffentlicht

Expert (m/w/d) Product Compliance

Halle (Westfalen)

Simtra Biopharma Solutions

62.500 €84.000 €

Vor über 30 Tagen veröffentlicht

Expert (m/w/d) Product Compliance

Halle (Westfalen)

Simtra Biopharma Solutions

62.500 €84.000 €

Vor über 30 Tagen veröffentlicht

Manager Project Engineering (m/w/d)

Bubendorf

CARBOGEN AMCIS AG

96.500 CHF127.000 CHF

Vor 6 Tagen veröffentlicht

Manager Project Engineering (m/w/d)

Bubendorf

CARBOGEN AMCIS AG

96.500 CHF127.000 CHF

Vor 6 Tagen veröffentlicht

Manager (m/w/d) REACH

Waldenburg

expertum GmbH

52.000 €67.000 €

Vor 14 Stunden veröffentlicht

Manager (m/w/d) REACH

Waldenburg

expertum GmbH

52.000 €67.000 €

Vor 14 Stunden veröffentlicht

Gehalts-Prognose

Unternehmens-Details

company logo

Novartis AG

Pharmazeutische Produkte, Arzneimittel

10.001 oder mehr Mitarbeitende

Basel, Schweiz

Bewertung von Mitarbeitenden

Vorteile für Mitarbeitende

Flexible Arbeitszeiten
Home-Office
Kantine
Restaurant-Tickets
Kinderbetreuung
Betriebliche Altersvorsorge
Barrierefreiheit
Gesundheitsmaßnahmen
Betriebsarzt
Training
Parkplatz
Günstige Anbindung
Vorteile für Mitarbeitende
Firmenwagen
Smartphone
Gewinnbeteiligung
Veranstaltungen
Privat das Internet nutzen
Hunde willkommen

Unternehmenskultur

Unternehmenskultur

412 Mitarbeitende haben abgestimmt: Sie bewerten die Unternehmenskultur bei Novartis AG als ausgeglichen zwischen traditionell und modern.Dies stimmt ungefähr mit dem Branchen-Durchschnitt überein.

Mehr Infos anzeigen

Wir benachrichtigen Dich gern über ähnliche Jobs in Österreich:

Ähnliche Jobs

QC Analytical Development Manager (m/w/d)

Schorndorf

Catalent

66.000 €86.000 €

Vor über 30 Tagen veröffentlicht

QC Analytical Development Manager (m/w/d)

Schorndorf

Catalent

66.000 €86.000 €

Vor über 30 Tagen veröffentlicht

Expert (m/w/d) Product Compliance

Halle (Westfalen)

Simtra Biopharma Solutions

62.500 €84.000 €

Vor über 30 Tagen veröffentlicht

Expert (m/w/d) Product Compliance

Halle (Westfalen)

Simtra Biopharma Solutions

62.500 €84.000 €

Vor über 30 Tagen veröffentlicht

Manager Project Engineering (m/w/d)

Bubendorf

CARBOGEN AMCIS AG

96.500 CHF127.000 CHF

Vor 6 Tagen veröffentlicht

Manager Project Engineering (m/w/d)

Bubendorf

CARBOGEN AMCIS AG

96.500 CHF127.000 CHF

Vor 6 Tagen veröffentlicht

Manager (m/w/d) REACH

Waldenburg

expertum GmbH

52.000 €67.000 €

Vor 14 Stunden veröffentlicht

Manager (m/w/d) REACH

Waldenburg

expertum GmbH

52.000 €67.000 €

Vor 14 Stunden veröffentlicht

Team Lead Regulatory Affairs (Division Pharma) (m/w/d)

Ladenburg

Jungbunzlauer Ladenburg GmbH

Vor 29 Tagen veröffentlicht

Team Lead Regulatory Affairs (Division Pharma) (m/w/d)

Ladenburg

Jungbunzlauer Ladenburg GmbH

Vor 29 Tagen veröffentlicht

Senior Compliance Specialist (m/w/d) | Biopharma

Biberach, Baden

Modis Deutschland

67.000 €86.000 €

Vor 21 Stunden veröffentlicht

Senior Compliance Specialist (m/w/d) | Biopharma

Biberach, Baden

Modis Deutschland

67.000 €86.000 €

Vor 21 Stunden veröffentlicht

Supervisor GMP Compliance (m/w/d)

Schorndorf

Catalent

64.500 €85.000 €

Vor 15 Tagen veröffentlicht

Supervisor GMP Compliance (m/w/d)

Schorndorf

Catalent

64.500 €85.000 €

Vor 15 Tagen veröffentlicht

​​Production Supporter Logistic (m/w/d)]

Bubendorf

CARBOGEN AMCIS AG

80.500 CHF101.500 CHF

Vor 6 Tagen veröffentlicht

​​Production Supporter Logistic (m/w/d)]

Bubendorf

CARBOGEN AMCIS AG

80.500 CHF101.500 CHF

Vor 6 Tagen veröffentlicht

Spezialist für GMP-Compliance (m/w/d)

Bensheim

engineering people GmbH

50.500 €74.000 €

Vor 23 Stunden veröffentlicht

Spezialist für GMP-Compliance (m/w/d)

Bensheim

engineering people GmbH

50.500 €74.000 €

Vor 23 Stunden veröffentlicht

Specialist Engineering (m/w/d) - Regulatory Affairs

Lemgo

Gebr. Brasseler GmbH & Co. KG

57.500 €70.500 €

Vor 19 Tagen veröffentlicht

Specialist Engineering (m/w/d) - Regulatory Affairs

Lemgo

Gebr. Brasseler GmbH & Co. KG

57.500 €70.500 €

Vor 19 Tagen veröffentlicht

Regulatory Affairs Manager (m/w/d)

Lübeck

Drägerwerk AG & Co. KGaA

56.500 €74.500 €

Vor 12 Tagen veröffentlicht

Regulatory Affairs Manager (m/w/d)

Lübeck

Drägerwerk AG & Co. KGaA

56.500 €74.500 €

Vor 12 Tagen veröffentlicht

Regulatory Manager Specialty Fertilizers (m/w/d) 80-100 %

Binningen

Ameropa AG

Vor 9 Tagen veröffentlicht

Regulatory Manager Specialty Fertilizers (m/w/d) 80-100 %

Binningen

Ameropa AG

Vor 9 Tagen veröffentlicht

QK-Manager (m/w/d) für Stabilitätsstudien und Entwicklung

Trittau

PANPHARMA GmbH

49.000 €64.000 €

Vor 5 Tagen veröffentlicht

QK-Manager (m/w/d) für Stabilitätsstudien und Entwicklung

Trittau

PANPHARMA GmbH

49.000 €64.000 €

Vor 5 Tagen veröffentlicht