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For Companies At a Glance
- Tasks: Lead regulatory activities and collaborate on innovative product development projects.
- Company: Join a diverse and inclusive team at Olympus, a leader in healthcare innovation.
- Benefits: Enjoy competitive salary, generous leave, private medical cover, and wellness perks.
- Other info: Dynamic environment with opportunities for personal and professional growth.
- Why this job: Make a real impact in healthcare by ensuring compliance and supporting patient-focused innovations.
- Qualifications: Experience in Regulatory Affairs and strong communication skills are essential.
The predicted salary is between 50000 - 65000 £ per year.
Responsibilities
- Lead coordination of regulatory activities across the product portfolio, to ensure alignment with global regulatory strategies.
- Collaborate with regulatory counterparts to ensure consistency and standardisation across regions.
- Facilitate the development of regulatory plans for new product development projects, novel technologies, and emerging market segments.
- Support responses to regulatory authority requests and inquiries.
- Contribute to both internal and external regulatory audits, ensuring preparedness and compliance.
- Monitor and interpret evolving global regulatory requirements and assess business impact.
- Support resolution of internal and external audit findings, including oversight of regulatory CAPAs.
- Develop and maintain regulatory procedures to support consistent and compliant operations.
- Provide regulatory support to cross‑functional initiatives, including manufacturing engineering, quality assurance, product development, and clinical affairs.
Qualifications
- Experience in Regulatory Affairs within the medical device or healthcare industry.
- Strong understanding of global regulatory frameworks.
- Demonstrated experience supporting product development or regulatory strategy.
- Experience supporting audits and regulatory authority interactions.
- Ability to manage multiple programs and stakeholders simultaneously.
- Strong communication and cross‑functional collaboration skills.
Highly Desirable
- Experience within complex medical device portfolios.
- Familiarity with global regulatory submissions and lifecycle management.
- Experience managing CAPAs and regulatory compliance programs.
Competencies
- Patient Focus – We put patients at the heart of everything.
- Integrity – We do the right thing.
- Innovation – We look for new ways to make things better.
- Impact – We take accountability and get things done.
- Empathy – We care for one another and work together.
Benefits
- Competitive salary and generous annual leave entitlement.
- Private medical cover.
- Comprehensive company pension scheme.
- Annual health check with BUPA, funded by the company.
- Employee Assistance Program to support health, mental and emotional wellbeing.
- Subsidised staff restaurant and free parking at HQ.
- Discounts on gym and wellness memberships, cashback and discounts with major UK retailers.
Additional Information
We value the diversity of individuals, perspectives, and lifestyles, and prioritise inclusion and mutual respect. We are committed to fostering a non‑discriminatory, inclusive work environment where everyone feels a sense of belonging. If you would like to bring your talents to this role at Olympus, please apply.
Regulatory Affairs Program Manager in Southend-on-Sea employer: Olympus Corporation
Contact Detail:
Olympus Corporation Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Program Manager in Southend-on-Sea
✨Tip Number 1
Network like a pro! Reach out to folks in the regulatory affairs space, especially those who work with medical devices. A friendly chat can open doors and give you insights that job descriptions just can't.
✨Tip Number 2
Prepare for interviews by brushing up on global regulatory frameworks. Be ready to discuss how you've navigated these in past roles. We want to see your experience shine through!
✨Tip Number 3
Showcase your collaboration skills! Think of examples where you've worked cross-functionally. Highlighting your ability to work with teams like quality assurance and product development will set you apart.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Regulatory Affairs Program Manager in Southend-on-Sea
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight your experience in Regulatory Affairs, especially within the medical device or healthcare industry. We want to see how your skills align with our needs!
Showcase Your Collaboration Skills: Since this role involves working with various teams, emphasise your cross-functional collaboration experience. Share examples of how you've successfully worked with different stakeholders to achieve regulatory goals.
Highlight Your Regulatory Knowledge: Demonstrate your understanding of global regulatory frameworks and your experience with audits and compliance. We’re looking for someone who can navigate these complexities with ease, so don’t hold back!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at Olympus Corporation
✨Know Your Regulatory Stuff
Make sure you brush up on global regulatory frameworks, especially those relevant to the medical device industry. Be ready to discuss how your experience aligns with the responsibilities of the role, like managing CAPAs and supporting audits.
✨Showcase Your Collaboration Skills
This role requires strong communication and cross-functional collaboration. Prepare examples of how you've worked with different teams in the past, particularly in developing regulatory plans or responding to authority inquiries.
✨Stay Updated on Regulations
Familiarise yourself with the latest trends and changes in global regulatory requirements. Being able to discuss recent developments will show that you're proactive and can assess their impact on business operations.
✨Prepare for Scenario Questions
Expect questions that ask how you'd handle specific regulatory challenges or audit findings. Think through potential scenarios and how you would approach them, demonstrating your problem-solving skills and integrity.