Introduction

Would you like to work with us on fascinating and challenging projects in the pharma industry? Are you looking for an attractive career with a varied array of activities? At Brunel, you get to accumulate knowledge across different industries, acquiring a broad base of qualifications that keeps you flexible and independent for your future career path. Apply today to join us as head of quality management and join Brunel in discovering the diversity of engineering.

What are you going to do

Responsibility for the quality culture and employee development, planning a long-term quality strategy that aligns with overall business objectives and ensures that quality considerations are integrated into the site's strategic planning and decision-making processes
Developing and implementing quality and compliance strategies and initiatives, ensure full implementation of the Quality Management System in accordance with cGMP compliance and regulatory requirements
Provide leadership and direction on all quality-related aspects and develop the on-site quality organization with a focus on patient safety and product quality
Maintain a state of inspection readiness by staying abreast of regulatory changes and trends, and ensuring that the site's quality systems and processes are robust and compliant with current industry standards and practices
Support in the continuous improvement, development and monitoring of key quality indicators to increase productivity

Essential skills and knowledge

You have successfully completed your university degree in natural sciences or equivalent and have extensive experience in pharmaceutical or biological production environments
Proven leadership skills, with experience in managing large cross-functional teams and complex projects
Strong knowledge of FDA/EU/ICH/CDN/AUS guidelines and the ability to navigate complex regulatory requirements
Strong communication skills and ability to work effectively with stakeholders at all levels
You make autonomous, thoughtful and risk-based decisions that prioritize patient safety and product quality
Driving organizational change and a desire for continuous improvement comes naturally to you
Strong knowledge of good manufacturing practices and data integrity
German language skills are desirable but not essential

What we offer

Brunel's corporate culture is shaped by the diversity of our people and a commitment to mutual respect between colleagues on every level of the company. That includes a varied program of social get-togethers with your team but also regular feedback sessions with your manager to discuss the challenges you face and your prospects for the future. Personally, tailored training and development create ideal conditions to improve your skills and prepare yourself for future projects. At Brunel: permanent contracts, 30 days' leave, flexible working hours and employer-funded company pension programs are business as usual.

Application process

First Contact

We carefully review your application and in the coming weeks, you will be notified for an interview session if you are selected. Only shortlisted candidates will be contacted within 7 days.

Scheduling an Interview

After being shortlisted, you will be contacted via email or telephone to arrange for a date on your availability for the qualification interview.

Phone/ Qualification Interview

During the interview, you will be assessed on your level of experience and skills, work history, availability, and the qualifications the company is seeking for the position.

Meeting in Real Life

After successfully making through the phone interview, a face to face interview will be scheduled between the candidate and recruiter. This session can be a more in-depth interview to review your communication and interpersonal skills.

Application for the Position

Submission of candidates resume for client’s approval and screening.