Quality & Regulatory Affairs Specialist — Roche
- Location
- Taguig City
- Contract
- full-time
- Posted
- 7 days ago
Role overview
At Roche you can show up as yourself, embraced for the unique qualities you bring.
Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come.
- At Roche you can show up as yourself, embraced for the unique qualities you bring.
- Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally.
Application process
- Recommends strategies for earliest possible approvals of applications.
- Manage product licenses during the product life-cycle and ensure license to operate
- Submit and review promo applications and maintain promo permits to make sure seamless business continuity
- Support regulatory activities to meet product sustainability and compliance with chemical registrations Manages Affiliate Notifications;
- Safety Board Notifications (SBN) and Quality Notifications (QN) in a timely manner
- Approve release incoming RBR(Repackaging Batch Record)
- Assist in creating artwork for labelling and suppliers’ work instruction
- Guide and support internal stakeholders to comply with regulatory and quality requirements
Company and context
- Perform various regulatory and quality activities required for organizational operations Who You Are:
- Pharmacy Degree or Bachelor's Degree in relevant field is preferred.
- Ideally minimum of 2 years industry experience in the Medical Devices is preferred. Who we are A healthier future drives us to innovate.
- Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come.
- Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products.
- We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.
- Let’s build a healthier future, together.
- Roche is an Equal Opportunity Employer.
Additional details
- Join Roche, where every voice matters.
- Location : Taguig City, Roche Philippines (Diagnostics Division)
- Support regulatory activities to meet product sustainability and compliance with chemical registrations Manages Affiliate Notifications;
- Perform various regulatory and quality activities required for organizational operations
- Ideally minimum of 2 years industry experience in the Medical Devices is preferred. A healthier future drives us to innovate.
Notes and original content
- The Position
- The Opportunity:
- Support regulatory activities to meet product sustainability and compliance with chemical registrations
- Manages Affiliate Notifications;
- Who You Are:
- Ideally minimum of 2 years industry experience in the Medical Devices is preferred.
- Who we are
- A healthier future drives us to innovate.
Questions about this listing
What salary does Roche offer for this role?
Roche lists CHF 62'000 - 94'000 gross per year for this position in Taguig City. 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 Roche 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 Roche 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 Roche?
Use the "Apply now" button on this page — it links directly to Roche's original listing at roche.wd3.myworkdayjobs.com, so your application goes straight to the employer's own applicant-tracking system. Frontaliere Ticino does not collect or forward applications itself.
