QA/QC Document Controller

QA/QC Document Controller

Sunderland Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as a QA/QC Document Controller, ensuring high-quality documentation standards.
  • Company: Onyx Scientific is a leading analytical services provider focused on quality and compliance.
  • Benefits: Enjoy perks like company events, health programs, life insurance, and private medical coverage.
  • Why this job: Be part of a dynamic environment where your attention to detail makes a real impact.
  • Qualifications: A degree in chemistry or analytical chemistry is preferred; strong communication skills are essential.
  • Other info: Flexible hours and opportunities for personal development in a supportive team.

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

Overview

Onyx Scientific are currently looking for a QA/QC Document Controller to join our analytical services department. The successful candidate will report to the Senior QA/QC Document Controller or Analytical Team Leader on day-to-day issues.

The successful candidate will ideally have a degree which is chemistry or analytical chemistry based.

The ideal candidate will be self-motivated and able to work with minimal supervision. Good interpersonal skills, both verbal and written, are essential for working with both customers and colleagues.

The QA/QC Document Controller will be expected to work within the GMP and safety guidelines set by the company. They will ensure the company Quality Management System (QMS) is maintained and complies with the requirements of Good Manufacturing Practice (GMP) as described in the current EU and ICH guidelines.

Alongside the benefits listed, we offer a competitive salary, dependent upon skills and experience.

Key Responsibilities

  • Timely review of the following documentation review to a consistently high standard:

> RTID reference standard proformas

> Non-key raw material proformas

> In-process proformas

> Analytical training documents (ATT/AST)

  • Level 1 trained in change controls, analytical non-conformance reposts and out of specification procedures.
  • Maintain GMP documentation standards at all times.
  • Liaise with senior staff within analytical and other departments where required.

Key Skills and Qualities

  • Familiar with analytical techniques, their applications, and interpretation of results
  • Basic understanding of GMP requirements.
  • Demonstrates problem-solving skills and competency in identifying potential issues
  • Able to communicate appropriately and effectively with colleagues
  • Positive can-do attitude with a sense of urgency in a fast-paced environment
  • Good attention to detail
  • Adherence to the highest quality standards of precision, accuracy, and record keeping for a wide range of methods
  • Able to use initiative, multi-task and plan work effectively to meet strict deadlines
  • A flexible approach to working additional hours when required
  • Computer literate, familiar with Microsoft Word and Excel
  • Strong verbal and numerical aptitude skills
  • Strong team player with the ability to work independently
  • Good organisational, interpersonal, and time management skills
  • Enthusiastic, flexible, conscientious and proactive in approach
  • Takes a positive approach to own training and development
  • Good decision making skills

Benefits:

  • Company events
  • Cycle to work scheme
  • Free parking
  • Health & wellbeing programme
  • Life insurance
  • On-site parking
  • Private medical insurance

QA/QC Document Controller employer: Onyx Scientific

Onyx Scientific is an exceptional employer that fosters a collaborative and innovative work environment, ideal for a QA/QC Document Controller. With a strong commitment to employee growth, we offer comprehensive training programs and opportunities for advancement within our analytical services department. Our competitive benefits package, including health and wellbeing programs, private medical insurance, and company events, ensures that our team members feel valued and supported in their professional journey.
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Contact Detail:

Onyx Scientific Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA/QC Document Controller

✨Tip Number 1

Familiarize yourself with GMP guidelines and the Quality Management System (QMS) relevant to the role. Understanding these frameworks will not only help you in interviews but also demonstrate your commitment to maintaining high standards.

✨Tip Number 2

Brush up on your analytical techniques and their applications. Being able to discuss specific methods and how they relate to the documentation you'll be handling can set you apart from other candidates.

✨Tip Number 3

Showcase your problem-solving skills by preparing examples of past experiences where you've identified and resolved issues. This will highlight your competency and proactive approach, which are key qualities for this position.

✨Tip Number 4

Demonstrate your ability to work independently and as part of a team. Be ready to share instances where you've successfully collaborated with colleagues or taken initiative on projects, as this aligns with the expectations of the role.

We think you need these skills to ace QA/QC Document Controller

Analytical Techniques
Good Manufacturing Practice (GMP)
Quality Management System (QMS)
Documentation Review
Attention to Detail
Problem-Solving Skills
Effective Communication
Time Management
Organisational Skills
Microsoft Word
Microsoft Excel
Ability to Work Independently
Team Collaboration
Flexibility in Working Hours
Initiative and Proactivity

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in QA/QC and analytical chemistry. Emphasize your familiarity with GMP requirements and any specific analytical techniques you have worked with.

Craft a Strong Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention your self-motivation and ability to work independently, as well as your strong interpersonal skills that will help you collaborate effectively with colleagues.

Showcase Problem-Solving Skills: Provide examples in your application of how you've demonstrated problem-solving skills in previous roles. This could include situations where you identified potential issues and implemented solutions.

Highlight Attention to Detail: Since the role requires high standards of precision and accuracy, make sure to mention specific instances where your attention to detail made a difference in your work, especially in documentation or compliance with quality standards.

How to prepare for a job interview at Onyx Scientific

✨Show Your Knowledge of GMP

Make sure to familiarize yourself with Good Manufacturing Practice (GMP) guidelines before the interview. Be prepared to discuss how you have adhered to these standards in your previous roles, as this will demonstrate your understanding and commitment to quality.

✨Highlight Your Analytical Skills

Since the role requires familiarity with analytical techniques, be ready to talk about your experience with these methods. Provide specific examples of how you've applied these skills in past positions, especially in relation to documentation and quality control.

✨Demonstrate Attention to Detail

Attention to detail is crucial for a QA/QC Document Controller. During the interview, share instances where your meticulous nature helped prevent errors or improved processes. This will show that you take quality seriously.

✨Communicate Effectively

Good interpersonal skills are essential for this position. Practice articulating your thoughts clearly and concisely. Be prepared to answer questions about how you handle communication with colleagues and clients, especially in challenging situations.

QA/QC Document Controller
Onyx Scientific
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  • QA/QC Document Controller

    Sunderland
    Full-Time
    36000 - 60000 £ / year (est.)

    Application deadline: 2027-01-29

  • O

    Onyx Scientific

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