Regulatory affairs Work, Jobs in Wokingham (with Salaries)

Regulatory Affairs Executive
Sandoz —Bracknell
- Full-time
- Project management
- Agile
- Annual leave
1d
Sr. Regulatory Affairs Officer
Milpharm Ltd —Uxbridge
- £30,000 - £37,500 a year
- Full-time
- Maintenance
- Master's degree
- Bachelor's degree
- Life insurance
Quick apply
5d
EMEA Regulatory Affairs Specialist - Cosmetics
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
5d
Senior Regulatory Affairs Officer
Sanofi —Reading
- Hybrid work
- English
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
PV Systems and Processes Lead x2
CSL Seqirus —Maidenhead
- Full-time
- No degree
- Leadership
- Communication skills
Senior Regulatory Affairs Manager
Elanco —Hook
- Full-time
- English
- Master's degree
- Leadership
Regulatory Affairs Manager
Reckitt —Slough
- Management
- Communication skills
- Employee assistance programme
- Life insurance
3d
Global Regulatory Affairs Manager, Pharma Strategy
Karo Healthcare —Maidenhead
- Full-time
- Hybrid work
- Management
- English
- Project management
- Flexible schedule
Quick apply
Head of Spectrum & Regulatory Affairs
Open Cosmos —Didcot
- Hybrid work
- English
Regulatory Compliance Supervisor (m/f/x)
3M —Bracknell
- Full-time
- Management
- Engineering
- Master's degree
- Flexible schedule
4d
Consumer Health Medical Affairs Manager
Bayer —Reading
- £65,000 - £80,000 a year
- Hybrid work
- English
- Communication skills
- Annual leave
- Employee discount
12d
Regulatory CMC strategy manager
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Annual leave
- Employee assistance programme
Head of Global Regulatory Affairs
Karo Healthcare —Maidenhead
- Full-time
- Hybrid work
- Business
- Leadership
- Flexible schedule
Quick apply
12d
Director, Global Affairs & Communications
AALTO —Farnborough
Quick apply
Director of Corporate Governance & Compliance
Frimley Health NHS Foundation Trust —Camberley
- £115,052 - £132,053 a year
- Full-time
- Leadership
4d
Head, PV and Regulatory QA
CSL Seqirus —Maidenhead
- Full-time
- Customer service
- Bachelor's degree
- Organisational skills
Associate Director, CMC Regulatory Affairs (Hematology/Oncology)
Regeneron —Uxbridge
- Bachelor's degree
- IT
- In-person
- Annual leave
1d
Principal Medical Writer
ICON Plc —Reading
- Full-time
- Remote
- Bachelor's degree
- Communication skills
- Employee assistance programme
3d
Governance and Compliance Officer
Buckinghamshire New University —High Wycombe
- £33,951 - £37,694 a year
- University
- Employee discount
9d

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regulatory affairs jobs near wokingham

Regulatory Affairs Executive

Sandoz -
Bracknell

Apply Now

Job details

Full-time
1 day ago

Benefits

Annual leave
Company pension

Qualifications

Project management
Agile

Full job description

The performance of various regulatory activities to ensure timely, accurate and strategic preparation and submission of registration dossiers to obtain and launch new UK Marketing Authorisations whilst also supporting business needs such as re-introductions and portfolio expansion projects.

Your Key Responsibilities:Your responsibilities include, but not limited to:

The execution of business aligned regulatory filing strategies in collaboration with regional and local stakeholders to meet the product launch deadline.
Preparation and submission of the following New Marketing authorisation application (National/DCP/MRP/CP), MA variation, Change of ownership applications and Educational materials and associated risk minimisation measures
Timely execution of launch enabling regulatory activities such as the registration of Risk Management Plans and associated educational materials, the registration and sign off artworks, approval of launch limiting variations.
Engagement with the MHRA to address application queries, liaising with relevant company departments and external sources to ensure full and rapid responses.
Creation, assessment and approval of artwork texts and mock-ups.
License cancellations.
Sunset Clause monitoring and reporting.
Liaising with customers and third-party suppliers concerning regulatory activities such as own label supplier registration, ongoing maintenance, and change of ownerships, to ensure compliance is maintained whilst meeting customer expectations.
Liaising with launch team to input the progress of regulatory application and/ or projects to assist with mapping out product launch activities.
Handling the regulatory activities in relation to the re-introduction of license and coordination with other stakeholder to ensure execution of regulatory strategy in this regard.
Handling labelling changes and associated regulatory applications (e.g. PIQ) as per business or external needs.
Ensuring timely response to Corrective and Preventative Actions (CAPAs) assigned to DRA and other associated quality management activities.
Working in accordance with Global and local Working Instructions, SOPs whilst adhere to compliance.
Maintenance of regulatory archives and record keeping.
Reviewing and updating Summaries of Product Characteristics.
The processing and clear communication of regulatory approvals to internal and external stakeholders within set timelines.
Provision of regulatory support for medical information and patient safety to assist with queries on product information.
Provision of regulatory support for strategic commercial opportunities.
Provision of regulatory support for internal and external audits.
Carrying out other activities which contribute to the effective performance of the Regulatory Affairs Department.

What you’ll bring to the role:Essential Requirements:
Experience (2 to 3 years) in Regulatory Affairs within a Generic or Pharma business.
Experience in supporting new product launch activities.
Ability to be flexible and multi-task within a fast-paced environment.

Desirable Requirements:
Experience in working with new product registration& CMC elements of a dossier.
Experience in project management.
Experience in working with various variation applications.

You’ll receive:
Competitive salary, Annual bonus, Pension scheme, Health insurance, 24 days annual leave, Flexible working arrangements, Employee recognition scheme, learning and development opportunities.

Why Sandoz?
Sandoz is the global leader in Biosimilar and Generic medicines, a segment of the healthcare industry that delivers 80% of the world’s medicines at 30% of the cost, touching the lives of more than 1 billion people across 100+ countries! While we are proud of our achievements, we have an ambition to do more so that everyone can achieve the basic human right of good health.

With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help even more people gain access to low-cost, high-quality medicines, sustainably.

Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful careers, where diversity of thought is welcomed and where personal growth is supported! 
 
Join us, help us make healthcare fairer and faster.

Commitment to Diversity& Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

#Sandoz

Apply Now

Refine Your Search

regulatory affairs jobs in wokingham

Regulatory Affairs Executive

Sr. Regulatory Affairs Officer

EMEA Regulatory Affairs Specialist - Cosmetics

Senior Regulatory Affairs Officer

Senior Regulatory Affairs Specialist

PV Systems and Processes Lead x2

Senior Regulatory Affairs Manager

Regulatory Affairs Manager

Global Regulatory Affairs Manager, Pharma Strategy

Head of Spectrum & Regulatory Affairs

Regulatory Compliance Supervisor (m/f/x)

Consumer Health Medical Affairs Manager

Regulatory CMC strategy manager

Head of Global Regulatory Affairs

Director, Global Affairs & Communications

Director of Corporate Governance & Compliance

Head, PV and Regulatory QA

Associate Director, CMC Regulatory Affairs (Hematology/Oncology)

Principal Medical Writer

Governance and Compliance Officer

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