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Stratpharma is a global medical devices and pharmaceutical company specialising in innovative dermatology and medical device solutions.
With an international footprint and a strong commitment to qua...Voir plusDernière mise à jour : il y a 22 jours
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RAQA Assistant - Innovative Dermatology Company, Basel
StratpharmaBasel, BS, CHIl y a 22 jours
Type de contrat
- Quick Apply
Description de posteDegree in Life Sciences or a related scientific discipline Interest in Regulatory Affairs and / or Quality Assurance within pharmaceuticals or medical devices Strong organisational skills with high attention to detail Proficient in Microsoft Word, Excel, and general document management Excellent communication and interpersonal (soft) skills Fluent English (written and spoken) – essential Quality or Regulatory diploma / certification is an advantage Entry-level opportunity with structured learning and development Exposure to international regulatory and quality environments Supportive, professional team culture Modern offices in Basel Opportunity to build a long-term career in RAQA
About Stratpharma
Stratpharma is a global medical devices and pharmaceutical company specialising in innovative dermatology and medical device solutions. With an international footprint and a strong commitment to quality, compliance, and patient safety, Stratpharma offers an excellent environment for learning and professional growth.
The Role
We are looking for a motivated and detail-oriented RAQA Assistant to join our Regulatory Affairs & Quality Assurance team in Basel. This is an entry-level position , ideal for a graduate or early-career professional seeking to develop a career in regulatory affairs and quality within the life sciences sector.
While prior experience in Regulatory Affairs or Quality Assurance would be an advantage, it is not essential . Full training and support will be provided.
Key Responsibilities
- Support Regulatory Affairs and Quality Assurance activities across the product lifecycle
- Assist with preparation, maintenance, and control of regulatory and quality documentation
- Maintain document management systems in line with internal procedures and regulatory requirements
- Support audits, inspections, and internal quality processes
- Assist with data tracking, reporting, and document updates using MS Word and Excel
- Liaise with internal stakeholders and external partners as required
Requirements
Benefits
This is a medium-sized global company with an entrepreneurial spirit, a proactive mindset, and a friendly company culture. Stratpharma enjoys an enviable rate of staff retention and is known as a desirable place to work.