Regulatory Affairs Manager
- Remote
- Contract
- Drug Safety / Pharmacovigilance
This vacancy has now expired
Our client, a globally recognised pioneer in Biotechnology, are recruiting for the position of Regulatory Affairs Manager. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to join them on their global mission to better the lives of those effected by disease and illness.
Responsibilities include:
- Contributes for the filing plan (MA and Lifecycle maintenance), advising and discussing with the local cross-functional team.
- With minimal supervision, executes the filing plan (MA and Lifecycle maintenance) for their country(ies), where applicable.
- Ensures regulatory submissions are made on time and meet the corporate and local regulatory requirements.
- Creates, reviews and approves source text for country labelling, and owns the country artwork based on source text.
- Collaborates with Regional and Global Study Operations (GSO) teams to support local planning and execution for clinical studies in accordance with national legal and regulatory requirements (where appropriate).
- Reviews and approves the promotional and non-promotional materials.
- Monitors changes in the local Trade Associations /national legislation and forwards information to local/regional groups communicating the impact to the client.
- Monitors the external regulatory environment to help inform/advise in the regulatory decision making.
- Ensures/supports regulatory product compliance (e.g. IMR, PMCs, pediatric and other agency commitments).
- Knowledge of Regulatory principles.
- Working with policies, procedures and SOP’s.
- Good knowledge of national legislation and regulations relating to medicinal products.
- Awareness of the registration procedures/challenges in the country(ies) for CTAs, MAs and all lifecycle management activities.
- Knowledge and experience in the local regulatory environment relevant for product area and development stage.
- Good negotiation and Influencing skills.
- Ability to anticipate and prevent potential issues.
- Ability to resolve conflicts and develop a course of action leading to a beneficial outcome.
- Degree and in-depth regulatory experience and/or related to the country(ies).
- Depth knowledge of country(ies) legislation and regulations relating to medicinal products.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
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