Regulatory Affairs Technical Writer — CERs & Submissions in Keele
Regulatory Affairs Technical Writer — CERs & Submissions

Regulatory Affairs Technical Writer — CERs & Submissions in Keele

Keele Full-Time 36000 - 60000 £ / year (est.) No home office possible
Biocomposites

At a Glance

  • Tasks: Create and revise clinical evaluation reports for regulatory submissions.
  • Company: Leading international medical devices company in Keele.
  • Benefits: Competitive salary, pension, and employee discounts.
  • Why this job: Join a dynamic team and contribute to impactful medical innovations.
  • Qualifications: 5 years of medical writing experience and a degree in life sciences.
  • Other info: Exciting opportunities for career growth in a supportive environment.

The predicted salary is between 36000 - 60000 £ per year.

A leading international medical devices company in Keele is seeking a Regulatory Affairs Specialist. This role focuses on creating and revising clinical evaluation reports (CER) to support regulatory submissions.

The ideal candidate should have at least 5 years of medical writing experience, particularly with clinical evaluations and regulatory submissions, and a degree in a life science.

The company offers a competitive salary and benefits including a pension and employee discounts.

Regulatory Affairs Technical Writer — CERs & Submissions in Keele employer: Biocomposites

As a leading international medical devices company based in Keele, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we offer numerous growth opportunities and a comprehensive benefits package, including competitive salaries, pensions, and employee discounts, making us an excellent employer for those seeking meaningful and rewarding careers in regulatory affairs.
Biocomposites

Contact Detail:

Biocomposites Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Affairs Technical Writer — CERs & Submissions in Keele

Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how personal connections can open doors for you.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of clinical evaluation reports and regulatory submissions. We recommend practising common interview questions and having examples ready to showcase your experience.

Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest checking out our website for tailored job listings that fit your expertise in medical writing.

Tip Number 4

Follow up after interviews! A simple thank-you email can leave a lasting impression. We believe it shows your enthusiasm and professionalism, which can set you apart from other candidates.

We think you need these skills to ace Regulatory Affairs Technical Writer — CERs & Submissions in Keele

Medical Writing
Clinical Evaluation Reports (CER)
Regulatory Submissions
Life Science Degree
Attention to Detail
Technical Writing
Research Skills
Communication Skills
Project Management
Analytical Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your medical writing experience, especially in clinical evaluations and regulatory submissions. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs and how your skills can benefit us. Keep it concise but impactful – we love a good story!

Showcase Your Attention to Detail: As a Regulatory Affairs Technical Writer, precision is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to ensure their documents are polished and professional.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications better and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at Biocomposites

Know Your Stuff

Make sure you brush up on your knowledge of clinical evaluation reports (CERs) and regulatory submissions. Familiarise yourself with the latest guidelines and standards in the medical devices sector, as this will show your expertise and commitment to the role.

Showcase Your Experience

Prepare specific examples from your past work that highlight your medical writing experience. Be ready to discuss how you've successfully created or revised CERs and navigated the regulatory submission process. This will help demonstrate your suitability for the position.

Ask Insightful Questions

Think of thoughtful questions to ask during the interview. Inquire about the company's approach to regulatory challenges or how they support their writers in staying updated with industry changes. This shows your genuine interest in the role and the company.

Dress the Part

Even if the company has a casual dress code, it's always best to err on the side of professionalism for an interview. A smart outfit can boost your confidence and make a great first impression, showing that you take the opportunity seriously.

Regulatory Affairs Technical Writer — CERs & Submissions in Keele
Biocomposites
Location: Keele

Land your dream job quicker with Premium

You’re marked as a top applicant with our partner companies
Individual CV and cover letter feedback including tailoring to specific job roles
Be among the first applications for new jobs with our AI application
1:1 support and career advice from our career coaches
Go Premium

Money-back if you don't land a job in 6-months

>