Quality Assurance(QARA) Administrator in Sunbury-on-Thames

Quality Assurance(QARA) Administrator in Sunbury-on-Thames

Sunbury-on-Thames Full-Time 28000 - 30000 £ / year (est.) No working from home possible
Job Search Place Limited

At a Glance

  • Tasks: Maintain and update the Quality Management System and support regulatory submissions.
  • Company: Leading pharmaceutical manufacturer with a commitment to quality and innovation.
  • Benefits: Competitive salary, career development opportunities, and a supportive work environment.
  • Other info: Equal opportunity employer dedicated to workplace equality.
  • Why this job: Join a dynamic team and ensure the highest standards in healthcare products.
  • Qualifications: Bachelor's degree and experience in a regulated environment preferred.

The predicted salary is between 28000 - 30000 £ per year.

Proactive Global is looking for a Quality Assurance Administrator (QARA) for a leading pharmaceutical products manufacturer based in Sunbury, TW16. This is a permanent position. Salary - £28-30K Per annum.

Key Responsibilities

  • Maintain and update the Quality Management System (QMS) in accordance with ISO 13485 and internal procedures.
  • Administer document control processes, ensuring timely revision, approval, and distribution of controlled documents.
  • Support CAPA, non-conformity (NC), complaint handling, and change control processes.
  • Assist with internal and external audits (Notified Bodies, FDA, suppliers).
  • Ensure training records are accurate, complete, and up to date.
  • Monitor calibration, equipment maintenance, and environmental controls as required.

Regulatory Affairs

  • Assist in preparing documentation for the filing of regulatory submission.
  • Manage registration activities for products in various markets (MHRA, EUDAMED, etc.).
  • Support with keeping up to date with regulatory landscape changes by identifying and documenting gaps.

Qualifications and Experience

  • Bachelor's degree in a relevant field (e.g., Quality Management, Engineering, or related discipline).
  • Experience in a regulated environment (preferably medical devices or pharmaceuticals).
  • Understanding of ISO 13485, EU MDR, and/or FDA QSR requirements.
  • Strong organisational and administrative skills.
  • Excellent attention to detail and accuracy.
  • Proficiency in MS Office (Word, Excel, Outlook, Teams).

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.

Quality Assurance(QARA) Administrator in Sunbury-on-Thames employer: Job Search Place Limited

Proactive Global is an exceptional employer, offering a dynamic work environment in the heart of Sunbury-Upon-Thames. With a strong commitment to employee development and a culture that values quality and compliance, we provide our team with opportunities for growth within the pharmaceutical industry. Our focus on equality and inclusivity ensures that every employee feels valued and empowered to contribute meaningfully to our mission.

Job Search Place Limited

Contact Details:

Job Search Place Limited Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Assurance(QARA) Administrator in Sunbury-on-Thames

Tip Number 1

Network like a pro! Reach out to people in the pharmaceutical industry, especially those who work in quality assurance. A friendly chat can lead to insider info about job openings that aren't even advertised yet.

Tip Number 2

Prepare for interviews by brushing up on ISO 13485 and other relevant regulations. We want you to show off your knowledge and how it applies to the role. Practice common interview questions and have examples ready that highlight your experience in a regulated environment.

Tip Number 3

Don’t forget to follow up after interviews! A quick thank-you email can keep you fresh in the interviewer’s mind. It shows your enthusiasm for the role and gives you another chance to reiterate why you’re the perfect fit.

Tip Number 4

Apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy to navigate and keeps everything in one place.

We think you need these skills to ace Quality Assurance(QARA) Administrator in Sunbury-on-Thames

Quality Management System (QMS)
ISO 13485
Document Control
CAPA
Non-Conformity (NC) Management
Complaint Handling
Change Control

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the Quality Assurance role. Highlight your experience with ISO 13485 and any relevant regulatory knowledge. We want to see how your skills match what we're looking for!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in the pharmaceutical industry. Let us know how your background makes you a great fit for our team.

Showcase Your Attention to Detail:In QA, attention to detail is key. When filling out your application, double-check for any typos or errors. We appreciate candidates who take the time to ensure their submissions are polished and professional.

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’s super easy to do!

How to prepare for a job interview at Job Search Place Limited

Know Your ISO Standards

Familiarise yourself with ISO 13485 and other relevant regulations before the interview. Be ready to discuss how you've applied these standards in your previous roles, as this will show your understanding of the quality management system.

Showcase Your Organisational Skills

Prepare examples that highlight your organisational and administrative skills. Discuss specific instances where you successfully managed document control processes or supported audits, as this will demonstrate your capability to handle the responsibilities of the role.

Be Ready for Regulatory Talk

Brush up on the regulatory landscape, especially regarding MHRA and EUDAMED. Be prepared to discuss how you've kept up with changes in regulations and how you’ve contributed to regulatory submissions in the past.

Attention to Detail is Key

During the interview, emphasise your attention to detail. You might be asked to review a sample document or process, so be ready to showcase how you ensure accuracy and completeness in your work.