QA Officer - Pharmaceutical
QA Officer - Pharmaceutical

QA Officer - Pharmaceutical

Buxton Full-Time 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join a friendly team ensuring quality and compliance in a fast-paced lab environment.
  • Company: A contract testing lab supporting healthcare, committed to high standards.
  • Benefits: Enjoy a full-time role with pension contributions and statutory sick pay.
  • Why this job: Make an impact in quality assurance while developing your skills in a supportive culture.
  • Qualifications: Attention to detail and experience in QA within a regulated lab are essential.
  • Other info: Private transport is necessary unless you're local; some overtime may be required.

The predicted salary is between 30000 - 42000 £ per year.

My client is a contract testing laboratory supporting the healthcare and related industries. We are looking for a highly motivated and detail-oriented QA Officer to join a small and friendly team based in Tideswell, UK. This is an exciting opportunity to work in a fast-paced environment, ensuring the quality and compliance of laboratory work in line with ISO 17025 and GMP standards.

Key Responsibilities:

  • Ensure compliance with company policies and procedures, including Health and Safety, ISO 17025, and GMP.
  • Review, write, and amend documentation such as SOPs.
  • Manage controlled documentation and maintain its circulation and availability.
  • Audit GMP data, including reviewing raw data prior to releasing GMP CoA or CoP.
  • Coordinate quality issues, investigations, and CAPA.
  • Assist with OOS, NC, NTF, CMP, RA, and CAPA investigations.
  • Participate in the change control process to ensure changes maintain GMP compliance.
  • Track, trend, and gather data for meetings as per procedures.
  • Conduct staff training on quality matters when required.
  • Liaise with customers or regulatory representatives.
  • Host and manage external audits by customers or regulatory bodies.
  • Respond to external audit report findings and plan corrective actions.
  • Release and obtain necessary documentation in a controlled manner.
  • Plan and conduct internal audits.
  • Maintain the archives.

The Ideal Candidate:

  • Strong attention to detail and commitment to compliance with industry standards.
  • Experience in a QA role within a laboratory or regulated environment.
  • Knowledge of ISO 17025 or GMP, and controlled documentation.
  • Strong communication skills and the ability to liaise with internal and external stakeholders.
  • Ability to work independently and manage multiple priorities.

Other Information:

  • Please note - private transport is essential to access the site unless you live in the immediate area.
  • Full-time role, 37.5 hours per week (some overtime may be required).
  • Statutory Sick Pay.
  • Auto-enrolment into a pension scheme with a 6% employer contribution after probation.

If you're interested in the above role then please click apply or get in touch to discuss further. Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.

QA Officer - Pharmaceutical employer: Consult

As a QA Officer at our Tideswell location, you will join a supportive and close-knit team dedicated to maintaining the highest standards of quality in the pharmaceutical industry. We offer a dynamic work environment with opportunities for professional growth, competitive benefits including a pension scheme with employer contributions, and a commitment to employee well-being through a focus on health and safety. Our culture encourages collaboration and continuous learning, making it an ideal place for those seeking meaningful and rewarding employment.
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Contact Detail:

Consult Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA Officer - Pharmaceutical

✨Tip Number 1

Familiarise yourself with ISO 17025 and GMP standards. Understanding these regulations will not only help you in the interview but also demonstrate your commitment to quality assurance in a laboratory setting.

✨Tip Number 2

Network with professionals in the pharmaceutical QA field. Attend industry events or join relevant online forums to connect with others who can provide insights or even refer you to opportunities at companies like ours.

✨Tip Number 3

Prepare to discuss specific examples of how you've handled quality issues or compliance challenges in previous roles. This will showcase your problem-solving skills and your ability to manage multiple priorities effectively.

✨Tip Number 4

Research our company culture and values. Understanding what we stand for will help you tailor your approach during interviews and show that you're genuinely interested in being part of our team.

We think you need these skills to ace QA Officer - Pharmaceutical

Attention to Detail
Knowledge of ISO 17025
Knowledge of GMP
Document Control
Audit Management
Data Analysis
Problem-Solving Skills
Communication Skills
Training and Development
Regulatory Compliance
Change Control Management
Quality Assurance
Ability to Work Independently
Time Management

Some tips for your application 🫡

Understand the Role: Before applying, make sure you fully understand the responsibilities of a QA Officer in a pharmaceutical setting. Familiarise yourself with ISO 17025 and GMP standards, as well as the specific requirements mentioned in the job description.

Tailor Your CV: Highlight your relevant experience in quality assurance, particularly in laboratory or regulated environments. Emphasise your attention to detail and any specific knowledge of ISO 17025 or GMP compliance that you possess.

Craft a Strong Cover Letter: Write a compelling cover letter that showcases your motivation for the role and how your skills align with the company's needs. Mention your ability to manage multiple priorities and your strong communication skills, as these are key for liaising with stakeholders.

Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial for a QA Officer.

How to prepare for a job interview at Consult

✨Know Your Standards

Familiarise yourself with ISO 17025 and GMP standards before the interview. Be prepared to discuss how your experience aligns with these regulations, as they are crucial for the QA Officer role.

✨Showcase Your Attention to Detail

Prepare examples that demonstrate your strong attention to detail. Discuss specific instances where your meticulousness has positively impacted quality assurance processes in previous roles.

✨Communicate Effectively

Practice articulating your thoughts clearly and confidently. Since the role involves liaising with various stakeholders, showcasing your communication skills will be key during the interview.

✨Prepare for Scenario Questions

Anticipate questions related to quality issues, investigations, and CAPA. Think of scenarios from your past experiences where you successfully managed similar challenges and be ready to share those stories.

QA Officer - Pharmaceutical
Consult
C
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