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Job Details

Regulatory Affairs Lead

Company: i-Pharm Consulting
Location: Netherlands
Reference: RQA-AN 2
Closing Date: 25 Jul 18
Type: Permanent
Salary (£): Negotiable

Job Summary:

Regulatory Affairs and Quality Assurance Lead, NetherlandsAn exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products. ...


Regulatory Affairs and Quality Assurance Lead, Netherlands

An exciting opportunity has arisen to join this global company and manage their regulatory activities. You will be involved in the entire life-cycle of medical device products.

Job Title: Regulatory Affairs and Quality Assurance Lead
Location: Netherlands

Benefits: Above market rate salary + fantastic benefits package

Permanent position

Job Responsibilities:

* Determine appropriate regulatory strategy for proposed new products and initiate necessary activities.
* Collaborate with sales and marketing teams to define market priorities
* Responsible for leading regulatory affairs and quality responsibilities.
* Review promotional material and labeling
* Interface with regulatory agencies and certifying bodies
* Manage EU country registrations
* Maintain regulatory records.
* Work with other departments about the regulatory requirements

Ideal Candidate:

Minimum of 8 years of related experience with a Bachelor’s degree.

Preferred Qualifications

* In depth understanding of Regulatory Affairs as it applies throughout the product lifecycle.
* Oversee various department processes to achieve department goals
* Demonstrate leadership abilities within team and with internal customers
* Must be detail oriented
* Must possess interpersonal communication, teamwork and organizational skills.
* Ability to prioritize workload for self & direct reports
* Ability to work collaboratively with peers in & outside department to achieve goals

To apply:
If you would like to discuss this vacancy further, please call Alisha Nandhe on +44 (0)20 3326 4123, or email If this role is not suitable, Alisha is also available to discuss other possible positions or answer any general questions regarding your career and the current market.

About i-Pharm

i-Pharm Regulatory is a specialist Recruitment team working wholly within the Regulatory Affairs market. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm Regulatory is a team within the larger organisation i-Pharm Consulting which provides candidates in areas such as: Clinical Operations, Pharmacovigilance, Biometrics, Project Managements, Quality Assurance and Health Economics. Visit our website to see our extensive current vacancies:


Regulatory Affairs / Reg Affairs / RA / Regulatory Affairs Officer / Reg Affairs Officer / RA Officer / systems / variations / dossier / labelling / registrations / renewals / submissions / CMC / Medical Device / ISO 13485 / Central Europe / Netherlands / The Hague / Amsterdam

Apply for this job: Regulatory Affairs Lead

Contact Information:

Address:  Head Office
212 New King’s Road London
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

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