regulatory affairs specialist Work, Jobs in ruislip (with Salaries)

Regulatory Affairs and Pharmacovigilance Specialist
Ferring Pharmaceuticals, Inc. —West Drayton
- Full-time
- Hybrid work
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Specialist, Sustainability Regulatory Strategy & Execution
The Bank of New York Mellon Corporation —London
- Full-time
- Microsoft Powerpoint
- Bachelor's degree
4d
Senior Regulatory Specialist EU/UK, International Regulatory Affairs Prime Air
Amazon Business EU Sarl, UK Branch - P97 —London
- Full-time
- Doctoral degree
- Engineering
- Master's degree
Regulatory Affairs Scientist (Chemical Compliance)
Thermo Fisher Scientific —London
- £2,625.00 - £3,937.50 a month
- Full-time
- Hybrid work
- Master's degree
- Project management
- Bachelor's degree
Quality Assurance & Regulatory Affairs Specialist
Pangaea Data —London
- Communication skills
- Flexible schedule
- Life insurance
Regulatory and Scientific Affairs Senior Manager | Leatherhead Food Research
Sagentia Regulatory —Epsom
- Full-time
- Management
- Mentoring
- Organisational skills
Quick apply
Governance and Compliance Officer
Buckinghamshire New University —High Wycombe
- £33,951 - £37,694 a year
- University
- Employee discount
2d
Government Relations Specialist II
Honeywell —Bracknell
- Full-time
- Hybrid work
- Master's degree
- Administrative experience
- Analysis skills
- Work from home
Head of Legal Risk & Compliance
Splendid Hospitality Group —Watford
- £80,000 - £100,000 a year
- Full-time
- Hybrid work
- Hospitality
- Contracts
- Employee assistance programme
- Employee discount
Specialist, GPV Performance Excellence - Monitoring Team (18-month FTC)
Kyowa Kirin International plc —Marlow
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Policy Advisors
Public Sector Resourcing —London
- Full-time
- Communication skills
Senior Regulation Specialist
ESB —London
- £61,450 - £76,813 a year
- Full-time
- Communication skills
- Negotiation
12d
Senior Manager – ESG and Sustainability Regulatory Legal
Pwc UK —London
- Full-time
- Hybrid work
- Analysis skills
- Presentation skills
Regulatory Engagement & Advocacy Manager – UK and France
Nadara —London
- Full-time
- Analysis skills
- Communication skills
Senior Counsel - Regulatory Law
Visa Europe Limited —London
- Doctoral degree
- English
- Financial services
13d
South & EE Team Regulatory Affairs Lead
Shell Energy —London
- Full-time
- Engineering
- English
- Supervising experience
Clinical Data & Device Specialist
SAVA —London
- Maths
Quick apply
South & EE Team Regulatory Affairs Lead
Shell —London
- Full-time
- Engineering
- English
- Supervising experience

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Regulatory Affairs and Pharmacovigilance Specialist

Ferring Pharmaceuticals, Inc. -
West Drayton

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Job details

Full-time

Full job description

Job Description:

At Ferring Pharmaceuticals, we help people around the world build families and live better lives. We are entrepreneurial and innovative, with a global team focused on scientific advances in the areas of reproductive and women’s health, gastroenterology and urology. Ferring + You is all about working together and sharing ideas, so that we can bring science to life for patients around the world.

Our Commercial teams collaborate as trusted partners with patient groups, clinicians, policy makers and the scientific community to identify and develop new opportunities to help patients. Customer centric, we offer an empowering, entrepreneurial culture – and a place to thrive and grow.

Ferring+You

You will take responsibility for a range of tasks across Regulatory Affairs, Compliance, and Good Distribution Practice (GDP) as well as Good Pharmacovigilance Practices (GVP), working closely with your regulatory, quality, and safety colleagues. In this role, you will be expected to bring an innovative, solutions‑driven mindset, demonstrating curiosity, entrepreneurial spirit, and a strong desire to create opportunities while confidently challenging established norms. We will support you and ensure you have the learning support you need.

Your day at Ferring

Prepare, review and submit variations, renewals, new product authorisations and other regulatory filings, including packaging material.
Maintain and update the local UK Pharmacovigilance System Master File (PSMF).
Monitor and update data in the Regulatory Information Management System (RIMS).
Manage the assessment and response process for Parallel Trade Import Notifications for the UK and Ireland.
Handle requests for Certificates of Pharmaceutical Products (CPP) and special statements.
Monitor regulatory changes for the UK and Ireland, assess impact and record updates in internal systems.
Contribute to monthly Regulatory Affairs and Pharmacovigilance reports.
Act as Document Owner for assigned SOPs, policies and regulatory/PV documentation.
Provide backup support for Regulatory Affairs, Pharmacovigilance, and the reporting of adverse events and product quality complaints.
Ensure full compliance with GDP, GVP and all applicable regulatory requirements.

Behind our innovation…There’s you

Life Science degree or equivalent.
Minimum of 3 years Regulatory experience in a pharmaceutical company (ideally 5 years experience).
Knowledge of the UK Regulatory environment is mandatory (this should include the current post-Brexit requirements).
Preferable to have experience or knowledge in the UK Pharmacovigilance environment (ideally to have some work experience in Pharmacovigilance).
Preferable to have direct experience of communicating with the UK Health Authority (the MHRA).

People come first at Ferring

Get inspired from our commitment to advocate for everyone’s right to build a family, no matter who you are, where you live or who you love.
Our inclusive support package – “Building Families at Ferring” provides equal and accessible policies for all employees who wish to start their family journey, ensuring a global standard, irrespective of location and role. Subject to a minimum period of employment at Ferring.
Parental leave for both birthing and non-birthing parents.
Extended support on family building journey.

Making a difference in the life of millions of people means we succeed by working together. Our diverse backgrounds, experiences, expertise, and perspectives enable us to find solutions to even the most challenging problems, and our success is tied to each team member’s contributions. Imagine the power of your career when it’s Ferring + You.

Behind our purpose… There’s you

If our mission and your vision are aligned, please apply!

We strive to build and maintain an inclusive and diverse workplace with equal opportunities and mutual respect for all employees regardless of their backgrounds and socioeconomic status.

We operate a hybrid working arrangement with employees expected to work from the office for a minimum of 3 days each week – for this reason you should live within a reasonable commutable distance.

Note to agencies: this search is being managed by Ferring’s Talent Acquisition team. Kindly do not send us spontaneous profiles

Location:

Ferring UK

Apply Now

Refine Your Search

regulatory affairs specialist jobs in ruislip

Regulatory Affairs and Pharmacovigilance Specialist

Senior Regulatory Affairs Specialist

Sr. Specialist, Regulatory Affairs

Specialist, Sustainability Regulatory Strategy & Execution

Senior Regulatory Specialist EU/UK, International Regulatory Affairs Prime Air

Regulatory Affairs Scientist (Chemical Compliance)

Quality Assurance & Regulatory Affairs Specialist

Regulatory and Scientific Affairs Senior Manager | Leatherhead Food Research

Governance and Compliance Officer

Government Relations Specialist II

Head of Legal Risk & Compliance

Specialist, GPV Performance Excellence - Monitoring Team (18-month FTC)

Policy Advisors

Senior Regulation Specialist

Senior Manager – ESG and Sustainability Regulatory Legal

Regulatory Engagement & Advocacy Manager – UK and France

Senior Counsel - Regulatory Law

South & EE Team Regulatory Affairs Lead

Clinical Data & Device Specialist

South & EE Team Regulatory Affairs Lead

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