Quality Systems Expert

TN Switzerland; Neuenburg; Vor Ort; CHF 80’000 - 120’000; Vollzeit

Zusammenfassung

An established industry player is seeking a Quality Systems Expert to manage documentation and quality systems integration at their Neuchâtel site. This role involves ensuring compliance with global cGMP requirements, collaborating with business partners for system improvements, and providing user support and training. The ideal candidate will have a degree in life sciences, extensive experience in quality systems, and excellent organizational and communication skills. Join this innovative firm to enhance site efficiency and drive continuous improvement in quality management systems.

Leistungen

Great compensation packages

Hybrid role (2 days a week remote)

Participation in health insurance premiums

Financial participation in employee sports activities

Support for local public transport passes

Free parking

Car sharing program

Qualifikationen

• 5+ years of experience in quality systems, preferably in cGMP manufacturing.
• Strong knowledge of good document practices and data integrity.

Aufgaben

• Implement and update Quality Systems documentation and processes.
• Collaborate with cross-functional teams and provide user training.

Kenntnisse

Organizational Skills

Communication Skills

Stakeholder Management

Data Integrity

Problem Solving

Ausbildung

Degree in Life Sciences

Advanced Degree (Preferred)

Tools

Quality Management Systems

CAPA

Change Control

Deviation Management

Jobbeschreibung

As a Quality Systems Expert at our Neuchatel site, you will report to the Quality Systems Manager. Your responsibilities will include managing documentation and quality systems integration to align with Takeda's policies and global cGMP requirements.

Our mission is:

Management of Quality Systems You will promote and guarantee the compliant use and implementation of Quality Management Systems and ensure implementation of any changes in system/process or operational modes.

Collaboration and Improvement Work closely with business partners on site and at other Takeda locations to implement system changes and improvements. Proactively assist business partners in expressing their needs to provide adapted solutions and collaborate with global teams.

User Support and Capability Building Process user account requests for various systems, train superusers, and manage the associated training toolkits.

QMS Performance Monitor QMS performance and ensure escalation to management.

Key Responsibilities:

1. Implement and update Quality Systems (Documentation, deviation, CAPA, change control, etc.).
2. Support end-users and provide first-level support.
3. Collaborate with cross-functional teams and global partners.
4. Train users and manage training toolkits.
5. Participate in audits and continuous improvement initiatives.

What you bring to Takeda:

1. Degree in life sciences (biotechnology, (bio)chemistry, engineering); advanced degree preferred.
2. 5+ years of experience, with at least 3 years in cGMP manufacturing.
3. Strong knowledge of good document and data practices, including data integrity.
4. Excellent organizational, communication, and stakeholder management skills.
5. Fluency in French and English (B2 level or higher).
6. Knowledge of other Quality Systems (such as deviation, change control, complaint, CAPA, risk management, training) is preferred.

What Takeda offers you (this list is non exhaustive):

1. Great compensation packages
2. Hybrid role (2 days a week in remote)
3. Participation in health insurance premiums
4. Financial participation in employee sports activities
5. Transport: support for local public transport passes, free parking, car sharing program

Takeda Neuchâtel offers its employees an attractive working environment and conditions. The well-being, safety, development and career advancement of its employees are at the heart of our vision and our Human Resources, Health, Environment and Safety policies.

Takeda Neuchâtel is an employer committed to its employees and to future generations.

Recruitment process:

1. Round 1 with Recruiter (1h)
2. Round 2 with HM manager (45mn) + test (30mn)
3. Round 3 with Business Partners (45mn)

Join us to enhance site efficiency, ensure compliance, and drive continuous improvement in our quality systems.