Staff Specialist - Global Labelling (m/f/d) — Stryker
- Location
- Selzach
- Contract
- full-time
- Posted
- 2 days ago
Role overview
Work Flexibility: Hybrid Purpose of Job
Serves as the global subject matter expert and strategic leader for Product Use Information and labeling, driving compliance, governance, and transformation initiatives that support market access, business continuity, and the safe and effective use of medical devices throughout their lifecycle.
Acts as a strategic partner to global business functions and serves as a key liaison between cross-functional stakeholders, customers, and regulatory authorities.
- Work Flexibility: Hybrid Purpose of Job:
- Serves as the global subject matter expert and strategic leader for Product Use Information and labeling, driving compliance, governance, and transformation initiatives that support market access, business continuity, and the safe and effective use of medical devices throughout their lifecycle.
Company and context
- Demonstrates a strong commitment to patient safety, product quality, and regulatory compliance, consistently upholding the organization's Quality Policy, ethical standards, and company values while fostering a culture of continuous improvement and operational excellence What You'll Do:
- Lead the development, maintenance, and lifecycle management of compliant product labeling in accordance with global regulatory requirements, international standards, and quality system requirements.
- Partner closely with cross-functional stakeholders, including Regulatory Affairs, Risk Management, Packaging, Medical/Clinical Affairs, and Quality, from concept through regulatory release.
- Represent the Labeling function during internal and external audits and inspections, ensuring regulatory compliance and effective resolution of audit observations.
- Drive investigation and resolution of non-conformances by identifying root causes, implementing corrective and preventive actions (CAPAs), and ensuring sustainable compliance improvements.
- Support Mergers & Acquisitions (M&A) due diligence activities by assessing labeling, regulatory, and quality system impacts and identifying integration requirements and risks.
- Assess and interpret emerging regulations, standards, guidance documents, and quality agreements to define compliant implementation strategies for both legacy product portfolios and New Product Introduction (NPI) programs.
- Serve as Division Process Owner (DPO) for the Product Use Publications Quality Management System landscape, overseeing governance, periodic reviews, continuous improvement initiatives, and the development of best-practice guidance.
- Maintain ownership of DQP 16-001, the overarching procedure governing both Labels and Labeling processes.
- Develop and deliver training programs to ensure effective adoption of labeling processes, systems, and compliance requirements across the organization.
Additional details
- Work Flexibility: Hybrid
- Demonstrates a strong commitment to patient safety, product quality, and regulatory compliance, consistently upholding the organization's Quality Policy, ethical standards, and company values while fostering a culture of continuous improvement and operational excellence
- Drive digital transformation and process modernization initiatives to improve scalability, automation, quality, and efficiency of global labeling operations.
Notes and original content
- Purpose of Job:
- What You'll Do:
- What You'll Need:
Questions about this listing
What salary does Stryker offer for this role?
Stryker lists CHF 68'500 - 104'000 gross per year for this position in Selzach. 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 Stryker 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 Stryker 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 Solothurn?
EU/EFTA residents living in the border zone of the country adjoining Canton Solothurn 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 Solothurn's cantonal migration office or with HR during the application.
How do I apply for this position at Stryker?
Use the "Apply now" button on this page — it links directly to Stryker's original listing at stryker.wd1.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
