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Support production pharmaceuticals [f/m/x]

Wavre
MANTU GROUP SA
EUR 30’000 - EUR 80’000 pro Jahr
Inserat online seit: 15 April
Beschreibung

Mission Description
As a Production Supervisor, you will support our client's supervision team across four critical operational pillars:

1. Production Team Performance Optimization

Team Leadership Development: Coach team leads on effective team management methodologies

Performance Management: Establish and monitor team KPIs, driving continuous improvement

Best Practice Implementation: Guide team leads in optimizing their leadership approach and team dynamics

2. Production Variability Analysis

Variation Detection: Identify and analyze production variability patterns across manufacturing lines

Trend Analysis: Support teams in trending variability data and developing actionable insights

Resolution Support: Partner with production teams to implement corrective measures for identified variations

3. Problem Resolution & Continuous Improvement

Root Cause Analysis: Lead DMAIC methodology application for production issues and deviations

CAPA Development: Create and implement Corrective and Preventive Actions (CAPAs)

Field Support: Provide hands‑on assistance to production teams during problem resolution

Documentation: Ensure proper VQD (Verification, Qualification, Documentation) compliance

4. Process Optimization & Simplification

Documentation Management: Streamline documentation processes, reviews, and archival systems

Process Fine‑tuning: Optimize ancillary production activities and support processes

Efficiency Gains: Identify and implement simplification opportunities in non‑core production workflows

Profile Requirements
Experience & Education

4-6 years proven experience in production supervision within manufacturing environments

Bachelor's degree in Engineering, Industrial Management, or related field

Experience in regulated industries (pharmaceutical, food processing, or automotive preferred)

Technical Competencies

Strong knowledge of: Lean manufacturing, Six Sigma (DMAIC methodology)

Proficiency in: Production KPI development and monitoring

Experience with: CAPA processes and VQD documentation standards

Tools: MS Office, ERP systems, statistical analysis software

Soft Skills

Leadership: Ability to coach and develop team leads

Analytical Thinking: Strong problem‑solving and data analysis capabilities

Communication: Excellent verbal and written skills in English and Spanish

Collaboration: Proven ability to work effectively with cross‑functional teams

Preferred Qualifications

Six Sigma Green Belt or Black Belt certification

Experience with pharmaceutical GMP environments

Knowledge of Spanish labor regulations and safety standards

Amaris Consulting is proud to be an equal‑opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

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