Regulatory affair Manager - Medical devices at Approach People Recruitment

Position	Regulatory affair Manager - Medical devices
Veröffentlicht	08 Aug 2026
Abgelaufen	07 Sep 2026
Unternehmen	Approach People Recruitment
Standort	Lausanne \| CH
Anstellungsart	Full Time

Stellenbeschreibung:

Aktuelle Karriere-Informationen von Approach People Recruitment für die Position als Regulatory affair Manager - Medical devices. If the Regulatory affair Manager - Medical devices Stellenangebot in Lausanne Ihren Qualifikationen entspricht, reichen Sie Ihre Bewerbung bitte direkt über das aktualisierte Jobkos-Portal ein.

Bitte beachten Sie, dass eine Bewerbung Qualifikationen erfordert, die vom Arbeitgeber festgelegt wurden. Wir hoffen, dass diese Karrierechance bei Approach People Recruitment für die Position als Regulatory affair Manager - Medical devices unten zu Ihrem Profil passt.

Stellenbeschreibung: As a Regulatory Affairs Manager, you will be responsible for ensuring compliance with regulatory requirements related to the development, approval, and marketing of pharmaceutical, medical device, or other healthcare products. You will work closely with cross-functional teams to navigate the complex regulatory landscape and to ensure that products meet all applicable regulations and standards.

Responsibilities:

Develop and implement regulatory strategies for product development, registration, and commercialization.
Prepare and submit regulatory submissions, including Investigational New Drug (IND), New Drug Application (NDA), 510(k), Pre-Market Approval (PMA), or other regulatory filings, as required.
Liaise with regulatory agencies, such as the FDA, EMA, or other regulatory authorities, to facilitate the review and approval process for new products or product changes.
Provide regulatory guidance and support to cross-functional teams, including R&D, Clinical Affairs, Quality Assurance, and Marketing, to ensure compliance with regulatory requirements throughout the product lifecycle.
Monitor and interpret changes in regulations and guidelines and communicate potential impact to relevant stakeholders.
Manage regulatory documentation and maintain regulatory compliance records.
Participate in regulatory audits and inspections as needed.
Represent the Unternehmen in regulatory interactions and meetings with regulatory agencies.

Qualifications:

Bachelor's degree in a scientific or healthcare-related field; advanced degree (e.g., Master's or PhD) preferred.
Minimum of (X) years of experience in regulatory affairs within the pharmaceutical, medical device, or healthcare industry.
Strong understanding of regulatory requirements and guidelines, including FDA regulations (21 CFR), ICH guidelines, and other applicable regulations.
Experience with regulatory submissions, including INDs, NDAs, 510(k)s, PMAs, or other regulatory filings.
Excellent communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and regulatory agencies.
Detail-oriented with strong analytical and problem-solving skills.
Ability to manage multiple projects simultaneously and prioritize tasks in a fast-paced environment.
Regulatory Affairs Certification (RAC) preferred.

Job-Informationen:

Unternehmen: Approach People Recruitment
Position: Regulatory affair Manager - Medical devices
Arbeitsort: Lausanne
Land: CH

So bewerben Sie sich:

Nachdem Sie die Kriterien und Mindestanforderungen in der Stellenanzeige gelesen und verstanden haben, Regulatory affair Manager - Medical devices at the office Lausanne bereiten Sie bitte umgehend Ihre Bewerbungsunterlagen (Anschreiben, Lebenslauf, Zeugnisse) vor. Senden Sie diese über den Link 'Nächste Seite' unten ein.

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Regulatory affair Manager - Medical devices at Approach People Recruitment

Stellenbeschreibung:

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