Team Leader IPI - Quality Operations — Thermo Fisher Scientific (Schweiz) AG
- Location
- Allschwil
- Contract
- full-time
- Posted
- 49 days ago
Role overview
Work Schedule Standard (Mon-Fri) Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, helping customers in finding cures for cancer, protecting the environment, and making sure our food is safe.
- Work Schedule Standard (Mon-Fri) Environmental Conditions
- Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description
- Your Responsibilities Operations & Inspection Management
- Ensure smooth daily IPI operations within Press Manufacturing
- High School Diploma or GED required Associate Degree preferred
- 2+ years of inspection and/or proofreading experience required
Main responsibilities
- Your Responsibilities Operations & Inspection Management
- Ensure smooth daily IPI operations within Press Manufacturing
- Coordinate inspection activities across multiple operational areas, including flexographic and digital press production + folding machines
- Monitor daily production schedules and proactively address operational constraints or delays
- Ensure timely completion of inspection activities aligned with manufacturing priorities
- Support inspection execution when operationally required
- Provide visibility on inspection status and operational priorities to management
- Ensure effective shift handover and continuity between teams
- Support manufacturing coverage planning, including overtime coordination when needed Team Management
- Lead, supervise, and support IPI inspectors in daily operations
Key requirements
- High School Diploma or GED required Associate Degree preferred
- 2+ years of inspection and/or proofreading experience required
- 2+ years of pharmaceutical, clinical, packaging, labeling, or related GMP experience preferred
- Previous leadership or supervisory experience preferred
- Experience in QA/QC, manufacturing, packaging, or clinical operations is considered an asset
- Strong knowledge of GMP and regulatory requirements
Company and context
- Strong organizational and prioritization skills
- Ability to manage multiple tasks in a fast-paced environment
- Strong communication and interpersonal skills
- Strong attention to detail and documentation accuracy
- Ability to work effectively with confidential information
- Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, Outlook) Key Competencies
- Strong leadership and team collaboration skills High level of accountability and ownership
- Ability to make decisions and solve operational challenges effectively Strong problem-solving mindset
- Flexibility and adaptability in a changing operational environment
- Ability to work under pressure and meet tight timelines Strong customer and quality focus Strong engagement and shop floor presence
Additional details
- Environmental Conditions
- Adherence to all Good Manufacturing Practices (GMP) Safety Standards
- We are leaders in providing clinical supply chain management services and clinical supplies distributed to patients worldwide. Your Responsibilities Operations & Inspection Management
- Support manufacturing coverage planning, including overtime coordination when needed
- Support conflict resolution and day-to-day team management activities Training & People Development
- Establish and support annual development objectives for team members Quality, Safety & Compliance
- Promote a strong quality culture within the department Support investigations related to: Audit observations
- Cross-functional Coordination & Communication Coordinate activities with: Planning / Administration Other operational departments
- Support implementation and revision of SOPs, WIs, and Master Forms Reporting & Operational Support High School Diploma or GED required Associate Degree preferred
- Proficiency with Microsoft Office tools (Word, Excel, PowerPoint, Outlook)
Notes and original content
- Work Schedule
- Standard (Mon-Fri)
- Job Description
- We are leaders in providing clinical supply chain management services and clinical supplies distributed to patients worldwide.
- Position Summary
- Your Responsibilities
- Operations & Inspection Management
- Team Management
- Support conflict resolution and day-to-day team management activities
- Training & People Development
Questions about this listing
What salary does Thermo Fisher Scientific (Schweiz) AG offer for this role?
Thermo Fisher Scientific (Schweiz) AG lists CHF 62'000 - 94'000 gross per year for this position in Allschwil. This is the salary published in the original listing (or, when the employer omits a figure, a realistic estimate for the role and sector) — the calculator on this site converts it to your actual net take-home once cross-border tax and social contributions are applied.
Is this a full-time role, and what type of contract does Thermo Fisher Scientific (Schweiz) AG offer?
This listing is a full-time position. The contract type shown here comes directly from the employer's original posting; always confirm exact hours, notice period and probation length with Thermo Fisher Scientific (Schweiz) AG during the application process, since these details can vary by role even within the same contract category.
Do I need a cross-border work permit for a role in Basel?
EU/EFTA residents living in the border zone of the country adjoining Canton Basel can apply for a G permit; the Swiss employer files it with that canton's migration office after the contract is signed. Border-zone rules and processing times vary by neighbouring country and canton, so confirm the specifics with Basel's cantonal migration office or with HR during the application.
How do I apply for this position at Thermo Fisher Scientific (Schweiz) AG?
Use the "Apply now" button on this page — it links directly to Thermo Fisher Scientific (Schweiz) AG's original listing at jobs.thermofisher.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
