At a Glance
- Tasks: Lead regulatory compliance and quality systems in a dynamic pharmaceutical environment.
- Company: Rapidly growing UK pharmaceutical manufacturer with a focus on innovation.
- Benefits: Competitive salary, 25 days holiday, free parking, and pension scheme.
- Why this job: Make a real impact and shape operations from day one in a pivotal role.
- Qualifications: Previous Pharma RP experience and strong understanding of QMS and compliance.
- Other info: Join a diverse team and enjoy excellent career development opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Lead and Junior level roles available. (Previous Pharma RP experience is essential). On site, Monday to Friday. Base location Knowsley with responsibility of two more sites (Southport & Widnes).
Are you ready to step into a role where your expertise genuinely drives business decisions, shapes operations, and ensures regulatory excellence? We are partnering with a rapidly growing UK pharmaceutical manufacturer to recruit TWO Responsible Persons. This is not just a job, it’s an opportunity to make a visible, lasting impact on a business that is modernising, expanding, and setting new standards for quality and compliance.
Whether you’re already a seasoned RP or a newly qualified RP ready to take the next step, these positions offer autonomy, visibility, and the chance to influence real change from day one.
Why this is an exciting opportunity:- Two positions available, allowing flexibility depending on your experience and ambition.
- Take ownership of regulatory compliance, quality systems, and operational excellence.
- Be part of a business that acts fast, values ideas, and rewards initiative.
- Shape the processes of a new warehouse and help standardise best practice across multiple sites.
- Visibility and influence; your work will directly affect operational success and regulatory outcomes.
- Opportunities for progression as the business continues to grow.
- Act as the Responsible Person for the site, ensuring compliance with MHRA, EMA, and GDP requirements.
- Lead and maintain the Quality Management System (QMS), ensuring continuous improvement.
- Manage audits, deviations, CAPA, complaints, recalls, and risk assessments.
- Collaborate across teams to improve processes, training, and operational standards.
- Analyse trends, identify risks, and implement preventative actions.
- Provide leadership, coaching, and support to quality colleagues.
- Ensure operational activities comply with ISO standards and internal benchmarks.
- Established Responsible Persons ready to take ownership.
- Strong understanding of QMS, audits, compliance, and quality tools.
- Experience in manufacturing pharmaceuticals.
- Someone proactive, confident, and ready to drive improvement.
- Strong communicator with the ability to influence colleagues and leadership.
- Must be confident and capable to make formal decisions independently.
This is ideal for candidates who want visibility, impact, and real responsibility, as well as those who are looking for a step up in influence and leadership.
What’s on offer:- Salary: £45,000-£70,000 depending on experience.
- 25 days holiday per year plus Bank Holidays.
- Free on-site parking.
- Auto-enrolment pension scheme.
- Join a business at a pivotal stage, help shape processes, lead improvement initiatives, and influence culture.
- Long-term stability, visibility, and career development.
This is a rare chance to join a business where your role matters, your decisions have impact, and your expertise is genuinely valued. Even if you’re happy in your current role, this is the kind of opportunity worth exploring. Apply now for a confidential conversation and take the first step towards a role that offers influence, growth, and real responsibility.
At Morgan Ryder we can provide you with a full range of employment opportunities from short term and fixed term temporary vacancies to permanent positions.
Our commitment: Equal opportunities are important to us. We believe that diversity and inclusion at Morgan Ryder Associates are critical to our success as a DE&I positive company, so we want to recruit, develop, and keep the best talent. We encourage applications from everyone, regardless of background, gender identity, sexual orientation, disability status, ethnicity, belief, age, family or parental status, and any other characteristic.
Please note that calls to and from the offices of Morgan Ryder Associates Ltd. may be monitored or recorded. This is to ensure compliance with regulatory procedures, record business transactions and for training purposes.
Responsible Person in Knowsley employer: Morgan Ryder Associates
Contact Detail:
Morgan Ryder Associates Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Responsible Person in Knowsley
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry and let them know you're on the lookout for a Responsible Person role. You never know who might have the inside scoop on an opportunity that’s not even advertised yet!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of MHRA, EMA, and GDP requirements. Show us you’re not just familiar with these regulations but can also discuss how you've applied them in past roles. Confidence is key!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds and shows your proactive attitude.
✨Tip Number 4
Apply through our website! We’ve got some fantastic opportunities waiting for you, and applying directly can sometimes give you an edge. Plus, it’s super easy and straightforward – just a few clicks and you’re in!
We think you need these skills to ace Responsible Person in Knowsley
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that match the Responsible Person role. Highlight your previous Pharma RP experience and any relevant achievements to show us you’re the right fit.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about this opportunity and how your background aligns with our needs. Be genuine and let your personality come through!
Showcase Your Regulatory Knowledge: Since compliance is key for this role, make sure to mention your understanding of MHRA, EMA, and GDP requirements. We want to see that you can take ownership of regulatory compliance from day one.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on this exciting opportunity to join our team!
How to prepare for a job interview at Morgan Ryder Associates
✨Know Your Regulations
Make sure you brush up on your knowledge of MHRA, EMA, and GDP requirements. Being able to discuss these regulations confidently will show that you're not just familiar with the role but also understand the critical compliance aspects that come with it.
✨Showcase Your QMS Experience
Prepare specific examples of how you've led or improved Quality Management Systems in your previous roles. Highlighting your hands-on experience with audits, CAPA, and risk assessments will demonstrate your capability to manage the responsibilities of a Responsible Person.
✨Communicate Effectively
Since strong communication is key for this role, practice articulating your thoughts clearly. Be ready to explain how you've influenced colleagues and leadership in past positions, as well as how you plan to foster collaboration across teams in the new role.
✨Demonstrate Proactivity
Employers are looking for someone who can drive improvement. Prepare to discuss instances where you've taken initiative to solve problems or implement changes. This will show that you're not just reactive but can also lead proactive efforts in quality and compliance.