At a Glance
- Tasks: Join our team as a Qualified Person, certifying IMP for clinical trials.
- Company: MAC is a global CRO dedicated to improving human health with integrity.
- Benefits: Enjoy competitive salary, health insurance, 25 days leave, and your birthday off!
- Why this job: Make a positive impact in a supportive environment focused on your growth.
- Qualifications: Must have a degree in Pharmacy, Biological or Chemical Science and relevant experience.
- Other info: Flexible working options available, including remote work and travel between sites.
The predicted salary is between 36000 - 60000 £ per year.
MAC is a full-service global Contract Research Organisation (CRO). We also own a network of research sites. Our mission is to serve with honesty and integrity to make an outstanding contribution to human health.
We are seeking to appoint a Qualified Person to join our team and make a positive impact in a growing and progressive CRO. This is a fantastic opportunity to work with an experienced QA and Production team in an inclusive company that put the needs and wellbeing of their people first, and who deliver exceptional service.
The focus of the job is the certification of IMP under our MIA IMP licence under directive 2001/20/EC Article 13. You will be working primarily from our Leeds site, with regular visits to our Manchester site. You will be expected to attend at site if required, but with some remote working, as appropriate. Some flexibility will be necessary, and out-of-hours working will also apply, on a pre-arranged basis.
KEY SKILLS AND QUALIFICATIONS:
Pharmacy, Biological or Chemical Science degree
Member of recognised professional body (Royal Pharmaceutical Society GB, Royal Society of Chemistry, or Institute of Biology)
Two or more years’ experience of Clinical Trials within the Pharmaceutical industry.
Experience in CRO, Phase 1 Unit or Hospital pharmacy
Eligibility to act as QP and be named on MIA IMP Licence
Responsibilities:
Certification of IMP under MIA IMP licence under directive 2001/20/EC Article 13
Performing the duties of the Qualified Person(s) as described in Article 51 of Directive 2001/83/EC and the applicable UK Statutory Instrument
Release of IMP for use in human Clinical Trials at MAC Clinical Research facilities according to 2001/20/EC article 9 to ensure subject safety
Ensure compliance with MIA IMP
Working with and organising workload of any other contract/trainee QPs employed by MAC
Review and approve Technical Quality Agreements
Review and approve Master Batch Records
Review CTA
Review IMP label according to Annex 13
Review and approve PSF
Review and approve executed Batch Records
Check and sign QP Certification document for each batch
Record batch certification and release in QP Batch register
Act upon product complaints, deviations and recalls
Ensure that the Quality Management System is robust and effectively implemented to support safe IMP manufacture and release
Oversight of the management and maintenance of GMP compliance
Perform GMP audits to monitor compliance
Conduct audits of third party GMP providers as required
Attend regulatory Inspections and GMP Sponsor audits as required
Perform GMP training to staff as required
Interpret, communicate, and ensure that new regulations are incorporated into procedures
Involvement with Incidents, Deviations and CAPAs as required
Undertake Continuing Professional Development as required
Follow QP code of Practice
Maintain Personal training and attend training sessions as required
Compliance with MAC health and Safety policy
Compliance with MAC policy on equality and diversity
To maintain professional qualifications required for the role, including continuous personal development
To work to the requirements of SI 2004 no 1031 and amendments thereof, which includes Good Clinical Practice
To work according to MAC SOPs, guidelines and policies
To work according to current data protection standards and practice good information management. Maintenance of strict confidentiality of patient and business-related data.
To maintain a high level of initiative and personal responsibility, liaising appropriately with team members and managers to ensure your job role is efficiently carried out
To support the aims of MAC and to represent MAC appropriately in a professional way to all our customers
Physical Work Environment and Travel Demands
QP activities may be carried out at other MAC sites or remotely, so travel between sites will be necessary for this role and to participate in inter-site meetings or problem-solving groups.
BENEFITS:
Competitive salary in keeping with pharmaceutical industry standards that will reflect experience
Health Insurance
Free onsite parking
25 days annual leave (increasing in increments to 30 days after 6 years' service)
Your birthday off work
MAC Clinical Research invites applications from highly motivated candidates, with a desire to fulfil their full potential. You will be working with an organisation that sees you as an investment and is keen for you to achieve your career aspirations.
Please email should you require any special arrangements or reasonable adjustments to be made throughout this selection process. This will enable us to accommodate your request as necessary.
QP employer: MAC Clinical Research
Contact Detail:
MAC Clinical Research Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land QP
✨Tip Number 1
Familiarize yourself with the specific regulations and directives mentioned in the job description, such as the MIA IMP licence and directive 2001/20/EC. Understanding these will not only help you in interviews but also demonstrate your commitment to compliance and safety.
✨Tip Number 2
Network with professionals in the CRO and pharmaceutical industry, especially those who are already working as Qualified Persons. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Highlight any experience you have with GMP compliance and audits during your conversations or interviews. This is a crucial aspect of the role, and showcasing your expertise in this area can set you apart from other candidates.
✨Tip Number 4
Be prepared to discuss your approach to continuous professional development. The role emphasizes maintaining qualifications and staying updated with regulations, so showing your proactive attitude towards learning can make a strong impression.
We think you need these skills to ace QP
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in Clinical Trials and your qualifications, such as your Pharmacy or Biological Science degree. Emphasize any previous roles in CROs or hospital pharmacies.
Craft a Strong Cover Letter: In your cover letter, express your passion for contributing to human health and how your skills align with the responsibilities of a Qualified Person. Mention your eligibility to act as QP and your commitment to compliance and quality management.
Highlight Relevant Experience: Detail your experience with IMP certification and any specific knowledge of regulations like 2001/20/EC. Provide examples of how you've ensured compliance and safety in previous roles.
Showcase Professional Development: Mention any continuing professional development activities you have undertaken that are relevant to the role. This could include training sessions, certifications, or workshops related to GMP compliance and clinical trials.
How to prepare for a job interview at MAC Clinical Research
✨Understand the Regulatory Framework
Familiarize yourself with the MIA IMP licence and the relevant directives, especially 2001/20/EC Article 13. Being able to discuss these regulations confidently will demonstrate your expertise and readiness for the role.
✨Highlight Relevant Experience
Prepare to discuss your previous experience in Clinical Trials and any specific roles you've held in CROs or hospital pharmacies. Use concrete examples to illustrate how your background aligns with the responsibilities of a Qualified Person.
✨Showcase Your Commitment to Quality
Emphasize your understanding of GMP compliance and quality management systems. Be ready to share instances where you ensured compliance or improved quality processes in your past roles.
✨Demonstrate Team Collaboration Skills
Since the role involves working with other QPs and various teams, be prepared to discuss how you have successfully collaborated in the past. Highlight your ability to communicate effectively and support team goals.