Join Progress - Experts in Life Sciences as a QC consultant
32 - 38 uur | Quality Control | Project Management
Are you ready to take on multiple QC projects with diverse clients? Progress might be your perfect match. Do you thrive in dynamic, fast-paced environments and are passionate about advancing cutting-edge therapies? Progress might be your perfect match.
Your challenges
As a QC Consultant at Progress you will have the unique opportunity to be deployed in various capacities, consisting of larger and smaller projects within the pharmaceutical and biotechnology industries or healthcare sector for example by:
- Setting up and/or performing routine QC testing;
- Support method transfers and method validations;
- Providing training and be the point of contact for lab practices and documentation;
- Supporting GMP compliance, troubleshooting, and continuous improvement projects;
- Drafting and reviewing SOPs and technical instructions;
- Delivering overall expert project management and consultancy services.
Our offer to you
Focus on human capital
Informal work environment
Healthy work-life balance
Short communication lines
Company car
Competitive salary and benefits
Our offer
- A varied job in challenging projects at renowned companies in the life sciences & healthcare industry;
- a healthy growing company with an informal work environment and people centric culture;
- a personal development budget and continuous professional development, both in practice and through courses, trainings and networking events;
- short communication lines, personal commitment, team spirit;
- a healthy work-life balance; work 32-38 hours a week;
- a competitive salary with a bonus on top;
- 25 days of paid annual leave, and the opportunity to build up additional leave;
- a flexible mobility scheme: the choice of various options such as a lease car or travel allowance;
- a contribution to your pension scheme;
- an opportunity to take part in our collective employee participation scheme;
- different social and fun activities, like team events, family day and an end-year weekend.
Your profile
As a people-centric company, your personality is what matters most to us. That is why we expect you to share the same values we hold: integrity, flexibility, customer focus, and expertise.
- Experience: 3-5 years relevant GMP QC experience in Biotech industry, preferably within cell & gene therapy. Experience with method validation and/or method transfer.
- Education: University or Higher Professional Education (HBO) degree in biotechnology, pharmaceutical, chemical of mechanical engineering or similar;
- Project Management: Proven track record on managing multiple projects with a strong stakeholder management, planning and communication skills in Dutch and English.
Our team
The strength of Progress lies in the interaction between highly qualified and motivated colleagues, supported by a robust management team. Colleagues help each other and share their professional know-how by regularly evaluating projects and sharing experiences. After a training period, you will become part of a close-knit and enthusiastic team.
Meet our experts
For more information please contact
Haris Achterberg
Human Resources Manager
Office: +31 (0)235635016
Mobile: +31 (0)6 48 08 91 78
