QA Specialist - Artwork Management
QA Specialist - Artwork Management

QA Specialist - Artwork Management

Temporary Home office possible
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At a Glance

  • Tasks: Manage artwork changes for pharmaceutical products and ensure quality compliance.
  • Company: Join a leading multi-national Pharma client based in Milton Keynes.
  • Benefits: Enjoy fully remote work with competitive pay ranging from £17.79 to £29.33 per hour.
  • Why this job: Be part of a dynamic team impacting global healthcare through quality assurance.
  • Qualifications: Bachelor’s degree in science and 3 years of experience in Quality/GMP or Regulatory environments required.
  • Other info: This is a 12-month contract role; candidates must have the right to work in the UK.

Overview

PE Global is currently recruiting for a Quality Specialist – Artwork Manager for a leading multi-national Pharma client based in Milton Keynes. The role is fully remote. This is a 12-month contract paying £17.79ph – £29.33ph PAYE depending on experience.

Responsibilities

  • Manage the operational implementation of artwork changes for several small and large molecule external Contract Manufacturing Organizations (CMOs) in the EU, covering finished product packaging and quality as well as supply chain related adaptations.
  • Be the EMQ Site Point of Contact (SPOC).
  • Maintain close contact with the central Reliance QRD SPOC and with the global Artwork department (GRA Operations).
  • Coordinate with the responsible project contact at the CMO.
  • Act as the change task owner in Reliance (quality management system for change controls).
  • Participate in stakeholder meetings and ensure timely execution and closure of identified tasks.
  • Develop new technical specifications with follow-up actions where applicable.
  • Execute the Quality Representative role.
  • Develop an artwork switch plan with the global artwork department, the QRD Reliance Manager, the Global Supplier Management (GSM) contact and the CMO project contact for impacted products.
  • Escalate challenges and risks related to project timelines and resources to CMO Governance.

Qualifications

  • You have a Bachelor’s degree in science (Pharmacist, Engineer or equivalent) or an equivalent field.
  • 3 years of experience in Quality/GMP or Regulatory environment.
  • Experience with artwork management.
  • Solid working knowledge of Good Manufacturing Practices (GMP) in the pharmaceutical industry.
  • Solid working knowledge of compliance, regulatory, or quality requirements in the pharmaceutical industry.

How to apply

Interested candidates should submit an updated CV. Please click the link below to apply, or send an up-to-date CV to anett@peglobal.co.uk.

Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in the UK.

Job details

  • Seniority level: Associate
  • Employment type: Contract
  • Job function: Quality Assurance
  • Industries: Staffing and Recruiting; Pharmaceutical Manufacturing

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QA Specialist - Artwork Management employer: PE Global

PE Global is an exceptional employer, offering a fully remote role as a QA Specialist - Artwork Management for a leading multi-national Pharma client in Milton Keynes. With competitive pay rates and a strong focus on employee growth, the company fosters a collaborative work culture that values quality and compliance, providing opportunities to engage with global teams and enhance your expertise in the pharmaceutical industry.
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Contact Detail:

PE Global Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA Specialist - Artwork Management

✨Tip Number 1

Familiarise yourself with the specific artwork management processes used in the pharmaceutical industry. Understanding the nuances of how artwork changes are implemented and managed will give you an edge during interviews.

✨Tip Number 2

Network with professionals in the pharmaceutical quality assurance field, especially those who have experience with Contract Manufacturing Organizations (CMOs). Engaging with them can provide insights and potentially lead to referrals.

✨Tip Number 3

Stay updated on the latest regulations and compliance standards related to Good Manufacturing Practices (GMP) and artwork management. This knowledge will not only help you in interviews but also demonstrate your commitment to the role.

✨Tip Number 4

Prepare to discuss specific examples from your past experience where you successfully managed artwork changes or quality assurance tasks. Being able to articulate your contributions clearly will make a strong impression on the hiring team.

We think you need these skills to ace QA Specialist - Artwork Management

Artwork Management
Good Manufacturing Practices (GMP)
Regulatory Compliance
Quality Assurance
Project Coordination
Stakeholder Engagement
Change Control Management
Technical Specification Development
Risk Management
Communication Skills
Attention to Detail
Problem-Solving Skills
Time Management
Collaboration with Cross-Functional Teams

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in Quality/GMP or Regulatory environments, particularly focusing on any artwork management roles you've held. Use keywords from the job description to align your skills with what the company is looking for.

Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities and qualifications mentioned in the job description. Explain how your background in science and your experience with GMP and artwork management make you a suitable candidate for this role.

Highlight Relevant Experience: In your application, emphasise your 3 years of experience in Quality/GMP or Regulatory environments. Provide specific examples of how you've managed artwork changes or worked with CMOs to demonstrate your capability.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in the pharmaceutical industry.

How to prepare for a job interview at PE Global

✨Know Your Artwork Management

Make sure you brush up on your knowledge of artwork management processes, especially in the pharmaceutical industry. Be prepared to discuss specific examples from your past experience that demonstrate your understanding of Good Manufacturing Practices (GMP) and how they relate to artwork changes.

✨Familiarise Yourself with Quality Systems

Since the role involves using a quality management system for change controls, it’s crucial to understand how these systems work. Be ready to explain your experience with similar systems and how you’ve successfully managed quality-related tasks in previous roles.

✨Prepare for Stakeholder Interaction

This position requires coordination with various stakeholders, including CMOs and global departments. Think of examples where you effectively communicated and collaborated with different teams to achieve project goals, and be ready to share these during the interview.

✨Showcase Problem-Solving Skills

The job involves escalating challenges and risks related to project timelines. Prepare to discuss situations where you identified potential issues and how you addressed them. Highlight your proactive approach to problem-solving and your ability to manage risks effectively.

QA Specialist - Artwork Management
PE Global

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