Quality Assurance Advisor (GLP/GCP)
Quality Assurance Advisor (GLP/GCP)

Quality Assurance Advisor (GLP/GCP)

Full-Time 30000 - 40000 £ / year (est.) No home office possible
Pharmaron

At a Glance

  • Tasks: Ensure compliance with GLP/GCP regulations and conduct audits for quality assurance.
  • Company: Join Pharmaron, a global leader in biopharmaceutical research and development.
  • Benefits: Be part of a collaborative culture with opportunities for growth and innovation.
  • Other info: Exciting career opportunities in a supportive and inclusive environment.
  • Why this job: Make a real impact in drug discovery while working with a dynamic team.
  • Qualifications: Degree in Chemistry preferred; strong attention to detail and communication skills required.

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

Pharmaron is a global CRO helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

Pharmaron is currently looking to recruit a Quality Assurance Advisor who is enthusiastic and highly motivated to work at their Rushden facility in the GLP/GCP QA Team. In this role you will be responsible for monitoring the status and reporting of studies and other programmes, ensuring compliance with the appropriate GLP/GCP regulations and requirements.

Key Responsibilities
  • To assure that regulatory studies are performed in compliance with the appropriate GLP/GCP regulations.
  • To conduct timely and effective GLP/GCP Inspections, according to authorised documents/Company Standard Operating Procedures and as directed by the Line Manager.
  • To conduct accurate and timely audits of the draft Reports according to company Standard Operating Procedures and as directed by the Line Manager.
  • To perform Process, System and Facility inspections to determine that Plans and SOPs are being followed.
  • To promptly report findings following audits and inspections to the Scientific Staff and Management.
  • To investigate deviations from Plans or SOPs (including the review of any corrective and preventative actions required) and to advise scientific staff and Management accordingly.
  • To demonstrate an understanding of the requirements and expectations of GLP/GCP principles and pragmatically apply them in discussions in order that consistent guidance and advice can be provided to staff as appropriate.
  • To resolve (with minimal supervision) with Scientific Staff as necessary, apparent inaccuracies and irregularities, arising out of observations made during inspection/audit.
  • To support continuous Quality improvement and advise Scientific Staff and Management accordingly.
  • To write, review and authorise SOPs and Policies.
Candidate Profile
  • Degree in Chemistry is advantageous.
  • Good knowledge of current GLP/GCP guidelines.
  • High attention to detail with the ability to process data accurately.
  • Good communication skills with the ability to communicate effectively at all levels within a large organization.
  • Excellent planning and organization skills – ability to multi-task, manage time and work to tight deadlines.
  • Strong interpersonal and relationship-building skills with the ability to influence and encourage a quality mindset.
  • Ability to work within and effectively contribute to multidisciplinary scientific teams and environments.
  • Ability to work with minimum supervision and as part of a team.
  • Proven ability to problem solve.
  • Willing to get involved with new ideas and initiatives.

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

Quality Assurance Advisor (GLP/GCP) employer: Pharmaron

Pharmaron is an exceptional employer, offering a collaborative culture that values teamwork and innovation at its Rushden facility. With a strong commitment to employee development and a focus on quality improvement, you will have the opportunity to grow within a dynamic environment that prioritises your contributions and fosters a sense of belonging. Join us to be part of a leading global CRO dedicated to advancing biopharmaceutical research and making a meaningful impact in the industry.
Pharmaron

Contact Detail:

Pharmaron Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Quality Assurance Advisor (GLP/GCP)

✨Tip Number 1

Network like a pro! Reach out to current employees at Pharmaron on LinkedIn or other platforms. Ask them about their experiences and any tips they might have for landing a role in the GLP/GCP QA Team.

✨Tip Number 2

Prepare for interviews by brushing up on GLP/GCP regulations. We recommend creating a cheat sheet of key points to discuss, so you can show off your knowledge and enthusiasm during the interview.

✨Tip Number 3

Practice your communication skills! Since this role requires effective communication at all levels, consider doing mock interviews with friends or family to get comfortable discussing your qualifications and experiences.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re serious about joining the Pharmaron team and contributing to our collaborative culture.

We think you need these skills to ace Quality Assurance Advisor (GLP/GCP)

GLP/GCP Compliance
Quality Assurance Auditing
Attention to Detail
Data Processing Accuracy
Effective Communication
Planning and Organisation
Interpersonal Skills
Problem-Solving
Team Collaboration
SOP Writing and Review
Regulatory Knowledge
Continuous Quality Improvement
Multidisciplinary Teamwork
Adaptability to New Ideas

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Quality Assurance Advisor role. Highlight your experience with GLP/GCP guidelines and any relevant audits you've conducted. 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 biopharmaceutical field. Share specific examples of how you've contributed to compliance and quality improvement in past roles.

Show Off 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 application is polished and professional.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets to us quickly and efficiently. Plus, you'll find all the info you need about the role and our company culture there!

How to prepare for a job interview at Pharmaron

✨Know Your GLP/GCP Inside Out

Make sure you brush up on the latest GLP and GCP guidelines before your interview. Being able to discuss these regulations confidently will show that you're not just familiar with them, but that you can apply them in real-world scenarios.

✨Showcase Your Attention to Detail

Prepare examples from your past experiences where your attention to detail made a significant impact. Whether it was catching an error in a report or ensuring compliance during an audit, these stories will highlight your suitability for the role.

✨Communicate Effectively

Practice articulating your thoughts clearly and concisely. Since the role requires good communication skills, be ready to demonstrate how you can convey complex information to different stakeholders, from scientific staff to management.

✨Emphasise Teamwork and Collaboration

Pharmaron values a collaborative culture, so be prepared to discuss how you've successfully worked within multidisciplinary teams. Share specific instances where your interpersonal skills helped foster a quality mindset among colleagues.

Quality Assurance Advisor (GLP/GCP)
Pharmaron

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