Pharmaceutical Regulatory Affairs Specialist in Falkirk, Grangemouth
Pharmaceutical Regulatory Affairs Specialist

Pharmaceutical Regulatory Affairs Specialist in Falkirk, Grangemouth

Falkirk +1 Full-Time 36000 - 60000 £ / year (est.) No home office possible
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Piramal Pharma Solutions

At a Glance

  • Tasks: Ensure quality and compliance in the pharmaceutical industry while supporting regulatory registrations.
  • Company: Join a global pharmaceutical leader dedicated to safety and excellence.
  • Benefits: Competitive salary, career growth, and the chance to make a real impact.
  • Other info: Dynamic role with opportunities to grow your expertise in GxP compliance.
  • Why this job: Be part of a team that drives quality improvements and compliance in healthcare.
  • Qualifications: Passion for quality assurance and knowledge of regulatory standards.

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

Join Our Team as a QA Compliance Officer at Piramal Grangemouth! Are you passionate about quality and compliance in the pharmaceutical industry? Do you thrive in a role where your work ensures safety, integrity, and excellence?

As a QA Compliance Officer, you’ll play a key role in supporting the governance and compliance of our Pharmaceutical Quality Management System (PQS) and helping maintain Regulatory Registrations, Licenses, and Certifications.

  • Support key quality system elements, including QMS monitoring, vendor qualification, and audits (self-inspections, vendor & customer audits).
  • Assist with regulatory agency registrations and maintain site compliance commitments.
  • Collaborate with site functions to reduce compliance issues and drive quality improvements.
  • Monitor regulatory findings and trends to prepare for inspections and audits.
  • Lead Quality Management Review meetings, highlighting GxP areas of concern and tracking actions.
  • Support quality investigations and help develop effective CAPAs to resolve issues.
  • Assist with pre-audit preparation and post-audit follow-up for customer audits and regulatory inspections.
  • Escalate any significant breaches of quality or regulatory compliance.

Be part of a global pharmaceutical company making a real impact. Grow your expertise in GxP compliance and quality management. Ready to ensure excellence and drive compliance at the heart of our operations?

Locations

Falkirk Grangemouth

Pharmaceutical Regulatory Affairs Specialist in Falkirk, Grangemouth employer: Piramal Pharma Solutions

Piramal Grangemouth is an exceptional employer that prioritises quality and compliance in the pharmaceutical industry, offering a dynamic work environment where your contributions directly impact safety and excellence. With a strong focus on employee growth, we provide opportunities for professional development in GxP compliance and quality management, all while fostering a collaborative culture that values innovation and integrity. Join us in a location that not only supports your career aspirations but also allows you to be part of a global team dedicated to making a meaningful difference.
Piramal Pharma Solutions

Contact Detail:

Piramal Pharma Solutions Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Pharmaceutical Regulatory Affairs Specialist in Falkirk, Grangemouth

✨Tip Number 1

Network like a pro! Reach out to professionals in the pharmaceutical industry, especially those in regulatory affairs. Attend industry events or webinars to make connections and learn about potential job openings.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of GxP compliance and quality management systems. We recommend practising common interview questions and scenarios related to audits and regulatory inspections.

✨Tip Number 3

Showcase your passion for quality and compliance during interviews. Share specific examples of how you've contributed to quality improvements or resolved compliance issues in previous roles.

✨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 genuinely interested in joining our team.

We think you need these skills to ace Pharmaceutical Regulatory Affairs Specialist in Falkirk, Grangemouth

Quality Management System (QMS)
Regulatory Compliance
Pharmaceutical Quality Management System (PQS)
Vendor Qualification
Auditing Skills
Regulatory Agency Registrations
GxP Compliance
Quality Investigations
Corrective and Preventive Actions (CAPA)
Data Monitoring and Analysis
Communication Skills
Collaboration Skills
Problem-Solving Skills
Attention to Detail

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the role of a QA Compliance Officer. Highlight your experience in quality management systems and regulatory compliance, as these are key areas for us at Piramal.

Craft a Compelling Cover Letter: Your cover letter should reflect your passion for quality and compliance in the pharmaceutical industry. Share specific examples of how you've contributed to quality improvements or compliance initiatives in your previous roles.

Showcase Relevant Skills: Don’t forget to showcase skills that align with the job description, like your ability to monitor regulatory findings and lead quality reviews. We want to see how you can contribute to our team!

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It’s the best way for us to receive your application and get you on board with our mission of ensuring excellence in the pharmaceutical industry.

How to prepare for a job interview at Piramal Pharma Solutions

✨Know Your Regulations

Familiarise yourself with the key regulations and guidelines relevant to the pharmaceutical industry, such as GxP, FDA, and EMA standards. Being able to discuss these confidently will show your commitment to compliance and quality.

✨Showcase Your Experience

Prepare specific examples from your past roles that demonstrate your experience with quality management systems, audits, and regulatory compliance. Use the STAR method (Situation, Task, Action, Result) to structure your responses effectively.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's quality management practices and how they handle compliance challenges. This not only shows your interest but also helps you gauge if the company aligns with your values.

✨Demonstrate Team Collaboration

Highlight your ability to work collaboratively with different teams to drive quality improvements. Share examples of how you've successfully partnered with others to resolve compliance issues or enhance quality processes.

Pharmaceutical Regulatory Affairs Specialist in Falkirk, Grangemouth
Piramal Pharma Solutions
Location: Falkirk
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