Supervisor Quality Engineering - Technical Operations

Prothya Biosolutions Belgium BV; Netherlands; Remote; EUR 52,000 - 75,000; Full time

Benefits offered by this job

Flexible working hours

Competitive salary

Holiday allowance 16.66%

13th month

30 holidays

Training budget

Travel expense support

Parking/public transport

Pension plan

Job summary

Prothya Biosolutions BV in the Netherlands seeks a Supervisor Quality Engineering within Technical Operations. You will lead a team of Quality Engineers to support manufacturing, drive robust processes, and ensure timely batch releases.

The role focuses on deviations, CAPA, Change Control, Training, data analysis, and risk assessment within a cGMP framework, with opportunities to grow in a dynamic, fast-growing company.

Qualifications

• Bachelor qualification in Science, Technology, or Pharmacy.
• Demonstrable people management experience with strong leadership skills.
• Technical quality engineering experience within the pharmaceutical sector, with history of leading complex investigations.
• In-depth knowledge of pharmaceutical manufacturing processes, cGMP, and quality system use.
• Knowledge of risk analysis tools, data analysis, automation, and engineering.
• Experience with deviation management is a plus.
• Fluency in English.

Responsibilities

• Team Results: Timely handling of production issues and deviations to ensure timely batch release and prevent compliance gaps.
• Establish new and improve current KPIs to identify gaps and drive improvement.
• Support in training of operators and handling of quality records for Production Operations.
• Align with Production Support Manager to improve processes based on data.
• Work in matrix organization to support timely batch releases and on-time-in-full targets.

Skills

People management

Leadership

Data analysis

Quality engineering

English fluency

Education

Bachelor in Science/Technology/Pharmacy

Tools

Quality systems

Deviation management

Job description

Supervisor Quality Engineering- Technical Operations

Prothya Biosolutions makes life-saving plasma medicines and is proud of that! Every day, Prothya colleagues take the extra mile to improve the health of millions of patients worldwide. Are you looking for a position at a dynamic and fast-growing company with an exciting history? Then the position of Supervisor Quality Engineeringwithin our Technical Operations department might be something for you! You will be responsible for the leadership of a dedicated team of Quality Engineers who support the needs of the manufacturing departments in the drive to ensure robust and efficient manufacturing processes within Prothya Biosolutions BV.

Your responsibilities:

1) Team Results

• Timely handling of production issues and deviations to ensure timely batch release and the prevention of compliance gaps.
• Establish new and improve current KPIs which help identify gaps and drive improvement.
• Provide support in the training of operators and in the handling of quality issues and records for the whole of Production Operations.
• Alignment with the Production Support Manager to improve processes based on data.
• Working in matrix organization within the value streams to ensure the team supports timely batch releases and on time in full targets.

2) Effective and efficient business processes

• Data driven improvements to ensure the performance of manufacturing departments is efficient and yields high quality, right first-time product batches.
• Key business processes supported will include Deviations, CAPA, Change Control, Training, and all production processes.

3) Timely availability of the product

• To ensure we serve our external and internal customers it is vital that all processes are continuously improved and that all potential compliance gaps are addressed on time and in full. Where required the team will also support deviation handling as SMEs to ensure timely batch release.

4) Team management

• Hire, lead, coach and appraise employees, and develop (the cooperation between) employees of your team using the relevant HR instruments, service and procedures.

Your profile:

• Bachelor qualification in Science, Technology, or Pharmacy.
• Demonstrable people management experience, strong leadership skills.
• Technical quality engineering experience within the pharmaceutical sector, demonstrating a successful history of leading complex investigations and enacting meaningful quality enhancements.
• In depth knowledge of pharmaceutical manufacturing processes, cGMP, and quality system use.
• Knowledge of risk analysis tools and processes, data analysis, automation, and engineering.
• Experience with deviation management is a plus.
• Fluency in English

What We Offer

• Full-time employment (40h) with flexible working hours in consultation.
• A salary between€ 4.702,26 and € 6.759,41 gross per month (based on full-time employment).
• A budget of 16,66% (holiday allowance and 13th month) on top of your gross salary, yours to spend or to save monthly
• 30 holiday days (based on fte).
• A personal training budget of €2,100 every three years to foster professional growth and development.
• Contribution to travel expenses from the first kilometer.
• Excellent accessibility by public transport and private parking available.
• A pension plan with Zorg & Welzijn, providing security for your future.
• A dynamic, safe, and challenging working environment with ample opportunities to grow, innovate, and learn, all while making a meaningful impact on the health of millions.