14 beste Stellen als quality gcp in basel bs – aktuell auf Personalsuche

Senior Manager, GCP Inspection Lead
BeiGene —Basel, BS
- CHF 141’800 - CHF 177’300 pro Jahr
- 100%
- Englisch
- Microsoft Office
- PC-Kenntnisse
Regional Clinical Compliance Optimization Lead
BeiGene —Basel, BS
- CHF 156’200 - CHF 195’200 pro Jahr
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
4 Tage
Associate Director, Good Clinical Practice (GCP) Audit and Vendor Management
BeiGene —Basel, BS
- CHF 105’800 - CHF 186’100 pro Jahr
- 100%
- Homeoffice
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
Regional Clinical Compliance Inspection Manager
BeiGene —Basel, BS
- CHF 156’200 - CHF 195’200 pro Jahr
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
4 Tage
Regional Clinical Compliance Inspection Lead
BeiGene —Basel, BS
- CHF 187’400 - CHF 234’200 pro Jahr
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
4 Tage
Associate technical program manager
Swiss Biotech Association —Basel, BS
- Datenanalyse
- Master
- AWS
Regional Clinical Compliance Lead
BeiGene —Basel, BS
- CHF 156’200 - CHF 195’200 pro Jahr
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
4 Tage
Sr GVP QA
Santhera —Pratteln, BL
- Schreibfähigkeiten
- Englisch
- Erfahrung mit Netzwerken
Clinical Trials Expert
Roche —Basel, BS
- 100%
- Management-Erfahrung
- Bachelor
- Ohne Hochschulabschluss
6 Tage
Software Engineer, Data Infrastructure & Acquisition - Basel, Switzerland
Speechify —Basel, BS
- CHF 30’000 - CHF 160’000 pro Jahr
- Homeoffice
- Doktorat
- Master
- Scripting
1 Tag
Senior Associate - Bioanalytical LC-MS Assay Developer
Roche —Basel, BS
- 100%
- Master
- Bachelor
Senior Drug Safety Physician (m/f/d)
Viatris —Allschwil, BL
- 100%
- Hybrides Arbeiten
- Englisch
- Kommunikationsfähigkeit
Global Product Safety Science Lead
Sobi —Basel, BS
- 100%
- Homeoffice
- Microsoft Excel
- Doktorat
- Schreibfähigkeiten
Direkt bewerben
(Senior) Medical Director - Cardiology, EMEA
Thermo Fisher Scientific —Reinach, BL
- 100%
- Englisch
- Kommunikationsfähigkeit

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Regional Clinical Compliance Optimization Lead
BeiGene —Basel, BS
Collaborate closely with RBQM teams to integrate findings into process risk assessment and risk mitigation strategies. Travel: up to 10% travel.
CHF 156’200 - CHF 195’200 pro Jahr
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Digital Marketing Specialist
Sentec —Therwil, BL
Collaborate cross-functionally with sales, marketing, clinical, and content teams to develop impactful messaging tailored to key regions.
Direkt bewerben

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Senior Manager, GCP Inspection Lead

BeiGene -
Basel, BS

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%
CHF 141’800 - CHF 177’300 pro Jahr

Qualifikationen

Englisch
Microsoft Office
Qualitätssicherung
PC-Kenntnisse
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

Reporting to the Senior Director, Global GCP Inspection Management, R&D Quality, the Senior Manager, Inspection Management serves as an inspection lead with primary responsibility for Health Authority GCP inspection readiness across cross‑functional clinical study teams. This role oversees end‑to‑end inspection planning and execution, including inspection logistics, stakeholder coordination, and continuous process improvements, to ensure research and development activities comply with applicable global regulatory requirements, guidelines, laws, and internal standards and practices.

Essential Functions of the job:

Lead and oversee GCP Inspection readiness activities and serve as inspection lead for regulatory Health Authority inspections, including but not limited to FDA, MHRA, EMA, CFDI, MFDS, PMDA, TGA, and TFDA.
Collaborate with cross-functional clinical study teams to develop and execute an integrated, risk‑based inspection readiness strategy, ensuring consistent alignment across functions.
Manage end‑to‑end inspection readiness activities, including development and maintenance of inspection storyboards with subject matter experts (SMEs), proactive identification and mitigation of inspection‑related risks, and planning, facilitation, and leadership of mock inspections and Health Authority inspections.
During regulatory inspections, coordinate and assign inspection requests to appropriate SME), providing oversight and guidance to ensure accurate, timely, and effective responses.
Create/revise appropriate SOPs and tools for inspection readiness and management.
Implement and maintain key QA systems, including investigations, Significant Quality Events (SQEs), Deviations, and CAPAs.
Demonstrate ability to solve complex problems requiring in-depth evaluation of various factors.
Fulfill all inspection commitments, respond to inspections, and carry out post-inspection activities, corrective and preventative actions, and resolve any issues for timely closure.
Manage a central repository of global inspection status and updates.
Meticulous attention to detail, excellent reviewing skills, and ability to independently manage multiple tasks in a fast-paced environment.
Support/manage Site Inspection Preparation Visit (SIPV) at investigative sites.
Lead and facilitate post-inspection lessons learned sessions to trends, share best practices, and drive sustainable process improvements.
Demonstrate the ability to define strategic direction and lead initiatives that enhance quality systems, inspection readiness, and overall operational excellence.
Exhibit strong leadership capabilities, including the ability to mentor, coach, and develop team members and cross‑functional partners.
Possess a thorough understanding of global regulatory requirements and guidelines governing the conduct of clinical trial operations across multiple regions.

Supervisory Responsibilities:

Not Applicable

Computer Skills: All basic Microsoft Office Programs

Other Qualifications:

+7 years of experience in GCP-related Quality Assurance function of the pharmaceutical, biotechnology or related health care industry.
High level of understanding of international GCP requirements and standards in the pharmaceutical, medical device and biotech industries.
Excellent English language skills, and additional language depending on locations and need.
Excellent verbal and written communication skills
Ability to effectively collaborate in a dynamic environment.

Travel:

Flexible to travel, including international.
May require up to 35% travel, sometimes with short notice time.

Salary Range Switzerland: 141,800.00 CHF - 177,300.00 CHF

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
Self-Awareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
Results-Oriented
Analytical Thinking/Data Analysis
Financial Excellence
Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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Erweiterte Suche

quality gcp Jobs in basel bs

Senior Manager, GCP Inspection Lead

Regional Clinical Compliance Optimization Lead

Associate Director, Good Clinical Practice (GCP) Audit and Vendor Management

Regional Clinical Compliance Inspection Manager

Regional Clinical Compliance Inspection Lead

Associate technical program manager

Regional Clinical Compliance Lead

Sr GVP QA

Clinical Trials Expert

Software Engineer, Data Infrastructure & Acquisition - Basel, Switzerland

Senior Associate - Bioanalytical LC-MS Assay Developer

Senior Drug Safety Physician (m/f/d)

Global Product Safety Science Lead

(Senior) Medical Director - Cardiology, EMEA

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