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For Companies At a Glance
- Tasks: Lead and support Quality Assurance, Control, and Validation teams in a dynamic environment.
- Company: Join Almac Group, a global leader in advancing human health through innovative drug development services.
- Benefits: Enjoy flexible working hours, competitive salary, annual bonus, 34 days leave, and healthcare perks.
- Why this job: Be part of a mission-driven team making a real impact in clinical trials and patient care.
- Qualifications: Degree in Life Sciences or related field; significant experience in Quality Management within Pharma.
- Other info: Open to both internal and external applicants; apply by 5pm on 26th January 2025.
The predicted salary is between 48000 - 72000 £ per year.
Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.
Skills and Attributes
- cGMP practices
- Cross Functional Team Building
- Proactive Solutions
Description
Quality Manager
Hours: 40 per week. Monday – Friday. Flexible working hours.
Business Unit: Almac Sciences
Open To: Internal & External applicants welcome to apply
The Role
Almac Sciences is seeking a dedicated and experienced Quality Manager to join our team at Edinburgh, Technopole. The team at Technopole manufacture peptides at small scale in accordance with cGMP, for clinical trial supply.
The successful candidate will provide leadership, management and support to our Quality Assurance, Quality Control and Quality Validation teams, ensuring the implementation and maintenance of GMP compliant operations, supporting small scale Peptide Manufacturing operations for Clinical Trials.
They are responsible for ensuring that cGMP compliance is maintained in accordance with regulatory and client expectations for Clinical Supply, whilst delivering to a varied operational portfolio and associated challenging timelines.
Key Requirements
- Degree (or equivalent) in relevant Life Sciences or Analytical discipline.
- Significant experience in a Quality Management Role with responsibilities for Quality Assurance, Control & Validation within the Pharmaceutical Industry.
- Strong understanding of cGMP principles and regulatory requirements and significant, proven experience in a cGMP environment.
- Excellent communication, management and leadership skills of the wider Quality Team, Cross-Functional Stakeholders and Clients.
- Ability to manage multiple tasks and projects effectively, whilst facilitating the identification and deployment of creative solutions, as necessary.
Apply Now
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.
Closing Date
We will no longer be accepting applications after 5pm on Sunday 26th January 2025.
Reward
For the successful candidate, we offer an attractive benefits package which will include a competitive salary, annual bonus, employer pension contributions, 34 days paid annual leave, healthcare benefits and much more.
Almac Group is an Equal Opportunity Employer.
Quality Manager employer: OASIS Group
Contact Detail:
OASIS Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Manager
✨Tip Number 1
Familiarise yourself with cGMP practices and regulations. Understanding these principles is crucial for a Quality Manager role, so consider brushing up on the latest guidelines and industry standards to demonstrate your expertise during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical industry. Attend relevant conferences or webinars where you can meet people who work in quality management. Building connections can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your leadership style and experiences. As a Quality Manager, you'll need to lead teams effectively, so think of examples where you've successfully managed cross-functional teams or resolved conflicts.
✨Tip Number 4
Research Almac Group's values and recent projects. Tailoring your conversation to align with their mission and demonstrating your knowledge about their work can set you apart from other candidates during the interview process.
We think you need these skills to ace Quality Manager
Some tips for your application 🫡
Understand the Role: Read the job description thoroughly to understand the key requirements and responsibilities of the Quality Manager position. Highlight your relevant experience in Quality Assurance, Control, and Validation within the Pharmaceutical Industry.
Tailor Your CV: Customise your CV to reflect how your skills and experiences align with the role criteria. Emphasise your understanding of cGMP principles and any leadership roles you've held in quality management.
Craft a Strong Cover Letter: Write a compelling cover letter that showcases your passion for advancing human health and your proactive approach to problem-solving. Mention specific examples of how you've successfully managed quality teams or projects in the past.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a Quality Manager role.
How to prepare for a job interview at OASIS Group
✨Showcase Your cGMP Knowledge
Make sure to highlight your understanding of cGMP principles during the interview. Be prepared to discuss specific examples from your past experience where you ensured compliance and how you handled any challenges that arose.
✨Demonstrate Leadership Skills
As a Quality Manager, you'll need to lead teams effectively. Share instances where you've successfully managed a team or project, focusing on your communication and management style. This will show your potential employer that you can inspire and guide others.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving abilities in real-world situations. Think of scenarios where you had to implement proactive solutions in a cGMP environment and be ready to explain your thought process and outcomes.
✨Tailor Your CV and Experience
Before the interview, ensure your CV is tailored to the job description. Highlight relevant experiences in Quality Assurance, Control, and Validation, and be ready to discuss how these experiences align with the role at Almac Group.
