Quality Control Specialist

Akkodis; Eigenbrakel; On-site; EUR 52,000 - 78,000; Full time

Benefits offered by this job

Permanent contract

Competitive salary package

Job summary

Akkodis is seeking a Quality Control Engineer to join our client-driven pharma team in Belgium. You will coordinate all quality actions and ensure GMP compliance, handling materials, packaging and finished products.

The ideal candidate holds a scientific engineering degree or pharmacy background, has GMP training, English proficiency, and familiarity with LIMS/SAP/TrackWise; bilingual French/English or Dutch/English is required.

Qualifications

• Scientific background: engineer (chemist/biologist) or pharmacist.
• Experience in the pharmaceutical industry.
• GMP training and good English level.
• Knowledge of LIMS, SAP and TrackWise is an advantage.
• Organisational, interpersonal and rigour are essential assets.
• Bilingual in French and English or Dutch and English.

Responsibilities

• Coordinate all quality actions.
• Follow the GMP associated with the products/processes.
• Ensure the control of raw materials, packaging items and/or finished products.
• Plan the analyses to be carried out.
• Validate the specifications.
• Examine returned products and complaints.
• Control the application of protocols and regulations.
• Write quality control procedures and reports.

Skills

Scientific background

Pharmaceutical experience

GMP training

English proficiency

LIMS knowledge

SAP knowledge

TrackWise knowledge

Organizational skills

Interpersonal skills

Rigour

Bilingual French-English

Education

Engineering degree (chemist/biologist) or pharmacist

Tools

LIMS

SAP

TrackWise

Job description

AKKODIS is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation.

As part of the development of the activities at one of our clients, we are looking for a Quality Control Engineer.

YOUR RESPONSIBILITIES:

• You coordinate all quality actions.
• You follow the GMP associated with the products/processes you work on.
• You ensure the control of raw materials, packaging items and/or finished products.
• You plan the analyses to be carried out.
• You validate the specifications.
• You examine returned products and complaints.
• You control the application of protocols and regulations.
• You write quality control procedures and reports.

YOUR PROFILE:

• You have a scientific background such as an engineer (chemist, biologist...) or pharmacist.
• You have experience in the pharmaceutical industry.
• You are trained in GMP and have a good level of English.
• Good knowledge of material qualification, transfer and validation of analytical methods is required.
• Knowledge of LIMS, SAP and/or Trackwise is an advantage.
• Your organisational skills, your interpersonal skills and your rigour are essential assets to succeed and evolve within our group.
• Bilingual in French and English OR Dutch and English

What’s the offer you can’t refuse?

As an Akkodis Team Member, you will be:

• Onboarded in your position via a buddy process
• Supported in your career by your Business Manager
• Actor of your training plan and your personal and professional development
• Benefiting from a permanent contract
• Benefiting from a competitive salary package including several extra-legal benefits