At a Glance
- Tasks: Manage regulatory affairs and ensure compliance for life-saving medicines.
- Company: Join SERB, a fast-growing specialty pharmaceutical company making a global impact.
- Benefits: Competitive salary, benefits, and a supportive team culture.
- Other info: Dynamic work environment with opportunities for professional growth.
- Why this job: Be part of a mission-driven team that saves lives through innovative medicines.
- Qualifications: Experience in regulatory roles within the pharmaceutical industry preferred.
The predicted salary is between 50000 - 60000 £ per year.
SERB is a fast-growing specialty pharmaceutical company that equips healthcare providers worldwide with life-saving medicines for patients facing rare conditions and emergencies. For over 30 years we have consistently provided emergency medicines, medical countermeasures, and the world’s leading portfolio of antidotes. Today SERB has over 500 employees in 18 countries and group revenue in excess of €400m. With a strong presence in the US, Europe, and the Middle East, along with a global network of trusted distribution partners, we make a broad range of essential medicines available in over 100 countries.
Broad Function
To manage all aspects of regulatory affairs and regulatory compliance for the Company’s licensed products. To ensure that the Company is at a high level of regulatory compliance through continual review of published information from relevant Regulatory Authorities. To support Director, Group Regulatory Affairs and provide Regulatory support to Qualified Persons, Operations and Quality Directors and Managers.
Principle Responsibilities
- Manage the preparation, collation and review the relevant information for timely submission to Regulatory Authorities in accordance with local requirements.
- Manage the evaluation of the regulatory impact of proposed manufacturing changes and to ensure continued compliance with regulatory licences.
- Represent the Regulatory function on multi-disciplinary teams for licensed products with regard to proposed post-marketing changes.
- Ensure that the regulatory strategy is aligned with project and business objectives and that deliverables are on time.
- Manage the preparation and maintenance of submission documents in support of licensed products (e.g. supplements, variations, annual reports, general correspondence, responses to inquiries from regulatory agencies).
- Involves the collection, review and assembly of scientific, medical, manufacturing, and other supporting documentation into submission documents.
- Manage revisions to artwork and labelling.
- Manage document control activities as applicable to Regulatory Affairs.
- Support Quality Assurance in the generation of the Annual Product Quality Reviews in line with global procedures for licensed pharmaceutical products.
Education and Experience
- A relevant level of experience within the pharmaceutical industry in a quality or regulatory role.
- Demonstrated knowledge of MHRA, EMA, Health Canada and FDA regulations.
- Educated to degree or equivalent level in a life science subject preferred, but not mandatory.
Skills and Attributes
- Excellent verbal, written and interpersonal skills with ability to articulate views clearly.
- Ensure SERB's regulatory interactions with Competent Authorities are of the highest calibre.
- Proven ability to make recommendations to effectively resolve problems or issues, by using judgement that is consistent with standards, practices, policies, regulation or guidance from governmental bodies.
- Performance driven, customer-focused and cost-conscious dynamic operations professional with a strong influential personality who is comfortable working closely within a multi-disciplinary team across setting.
- Excellent verbal and written communication with the ability to communicate effectively in a multicultural multinational, matrix environment.
- Excellent negotiation skills in dealing with third parties and internal stakeholders.
- Demonstrated ability to interpret information and present salient issues to internal management.
- Commercial acumen and first class analytical and problem solving skills focused on identifying areas within the organisation for which maximum benefit can be obtained.
- Skilled in organisation and prioritisation with a strong attention to detail and a commitment to quality.
- Must be self-motivated with the ability to handle multiple tasks simultaneously.
- Demonstrated advanced computer skills – Microsoft Office preferred.
- Demonstrated success working in a team environment.
- Dynamic Regulatory professional and diligent in all matters of compliance.
Serb Pharmaceuticals is an equal opportunity employer. We offer competitive compensation & benefit packages, challenging opportunities and a culture of working together in a supportive way built on our strong foundation of values.
Regulatory Affairs Manager employer: Meeveem Limited
At SERB, we pride ourselves on being a dynamic and supportive employer, dedicated to providing our employees with competitive compensation and comprehensive benefits. Our collaborative work culture fosters professional growth and development, allowing you to thrive in your role as a Manager in Regulatory Affairs while contributing to the vital mission of delivering life-saving medicines globally. Join us in making a meaningful impact in the healthcare sector, where your expertise will be valued and your contributions recognised.