QA Officer in Essex

QA Officer in Essex

Essex Full-Time 30000 - 40000 € / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure quality and compliance in pharmaceutical operations while supporting audits and investigations.
  • Company: Join a growing organisation in the healthcare distribution sector.
  • Benefits: Gain valuable experience in a regulated environment with potential for career advancement.
  • Other info: Dynamic role with opportunities to work closely with various teams.
  • Why this job: Make a real impact on quality standards and compliance in healthcare.
  • Qualifications: Attention to detail and collaborative skills are essential.

The predicted salary is between 30000 - 40000 € per year.

We’re supporting a growing organisation in the pharmaceutical and healthcare distribution sector to recruit a QA Officer. This role offers the opportunity to play a key part in maintaining quality and compliance across regulated operations, supporting a robust Quality Management System and ensuring adherence to GDP and GMP standards.

Working closely with Responsible Persons (RP) and Qualified Persons (QP), you’ll help investigate quality events, manage CAPAs, support audits, and maintain critical compliance documentation. This role would suit someone with strong attention to detail who enjoys working collaboratively to uphold high quality standards in a regulated environment.

Role Overview

The QA Officer will support the effective operation of the Quality Management System, ensuring processes, documentation, and compliance activities align with regulatory expectations. The role involves coordinating quality events such as deviations, CAPAs, audits, and training records, while working closely with internal teams including warehouse operations.

Key Responsibilities

  • Investigate deviations and support root cause analysis
  • Write and manage Corrective and Preventative Actions (CAPAs) and monitor completion timelines
  • Support the development, implementation, and maintenance of the Quality Management System (QMS)
  • Maintain registers for deviations, CAPAs, change controls, and risk assessments
  • Prepare and draft change controls and risk assessments for review
  • Organise and support Quality Management Review (QMR) meetings and maintain minutes
  • Maintain the internal audit schedule and support follow-up CAPAs
  • Coordinate external audits and documentation preparation
  • Maintain approved customer, supplier, and outsourced GDP supplier lists
  • Support product recalls and mock recall exercises
  • Maintain training records and ensure SOP training completion
  • Work closely with warehouse teams regarding quarantine, temperature monitoring, calibration, cleaning logs, and returns
  • Maintain accurate and compliant GDP/GMP documentation and records
  • Assist with investigations relating to product or distribution complaints
  • Ensure electronic quality records are stored securely and remain easily retrievable

QA Officer in Essex employer: Cranleigh Scientific Ltd

As a leading organisation in the pharmaceutical and healthcare distribution sector, we pride ourselves on fostering a collaborative work culture that prioritises quality and compliance. Our employees benefit from comprehensive training opportunities, a supportive environment for professional growth, and the chance to make a meaningful impact in a regulated industry. Located in a vibrant area, we offer a dynamic workplace where attention to detail is valued and rewarded.

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Contact Detail:

Cranleigh Scientific Ltd Recruiting Team

StudySmarter Expert Advice🤫

We think this is how you could land QA Officer in Essex

Tip Number 1

Network like a pro! Reach out to people in the pharmaceutical and healthcare sectors, especially those already working in QA roles. A friendly chat can lead to insider info about job openings or even a referral.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of GDP and GMP standards. We recommend creating a list of common interview questions related to quality management and practising your answers with a friend.

Tip Number 3

Showcase your attention to detail during interviews. Bring examples of how you've successfully managed CAPAs or supported audits in the past. This will demonstrate your hands-on experience and commitment to quality.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search.

We think you need these skills to ace QA Officer in Essex

Attention to Detail
Quality Management System (QMS)
Good Distribution Practice (GDP)
Good Manufacturing Practice (GMP)
Root Cause Analysis
Corrective and Preventative Actions (CAPAs)
Auditing Skills

Some tips for your application 🫡

Tailor Your CV:Make sure your CV is tailored to the QA Officer role. Highlight your experience with quality management systems, compliance activities, and any relevant certifications. We want to see how your skills align with our needs!

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 sector. Share specific examples of how you've maintained high standards in previous roles.

Showcase Attention to Detail:As a QA Officer, attention to detail is key. In your application, make sure to demonstrate this trait. Whether it's through your writing or by mentioning specific projects where you ensured compliance, we want to see that you take pride in your work!

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 at StudySmarter!

How to prepare for a job interview at Cranleigh Scientific Ltd

Know Your Quality Standards

Familiarise yourself with GDP and GMP standards before the interview. Be ready to discuss how these regulations impact quality management systems and share examples of how you've adhered to them in past roles.

Showcase Your Attention to Detail

Prepare to demonstrate your strong attention to detail. Bring specific examples of how you've successfully managed CAPAs or investigated deviations, highlighting your methodical approach to problem-solving.

Collaborate Like a Pro

Since this role involves working closely with various teams, be prepared to discuss your collaborative experiences. Share stories that illustrate your ability to work effectively with others, especially in high-pressure situations.

Be Audit-Ready

Understand the audit process and be ready to talk about your experience with internal and external audits. Discuss how you’ve prepared documentation and supported audit activities, showcasing your organisational skills.