68 specialist English-speaking jobs in Hainaut

  • MSI Pharma
  • Tournai
  • June 20
Analytical Systems & Data Integrity Specialist Location: Braine-l'Alleud (hybrid working model) Engagement ... Overview We have partnered with a large global pharmaceutical organisation to appoint a Data Integrity Specialist
  • MSI Pharma
  • Charleroi
  • June 20
Analytical Systems & Data Integrity Specialist Location: Braine-l'Alleud (hybrid working model) Engagement ... Overview We have partnered with a large global pharmaceutical organisation to appoint a Data Integrity Specialist
  • MSI Pharma
  • Hainaut Province
  • June 20
Analytical Systems & Data Integrity Specialist Location: Braine-l'Alleud (hybrid working model) Engagement ... Overview We have partnered with a large global pharmaceutical organisation to appoint a Data Integrity Specialist
  • MSI Pharma
  • Mons
  • June 20
Analytical Systems & Data Integrity Specialist Location: Braine-l'Alleud (hybrid working model) Engagement ... Overview We have partnered with a large global pharmaceutical organisation to appoint a Data Integrity Specialist
  • Vulcain Engineering Group | Belgium
  • Hainaut Province
  • June 14
Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.
  • Vulcain Engineering Group | Belgium
  • Tournai
  • June 14
Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.
  • Vulcain Engineering Group | Belgium
  • Charleroi
  • June 14
Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.
  • Vulcain Engineering Group | Belgium
  • Mons
  • June 14
Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.
  • Lutosa
  • Leuze-en-Hainaut
  • June 4
Designs, develops, and implements cybersecurity policy for two production sites and central offices. Manages security audits for all sites worldwide. Establishes and maintains a comprehensive security program to protect systems, networks, and data.
  • Jefferson Wells Belgium
  • Charleroi
  • June 20
QA CSV Specialist needed for new role within Quality R&D & PV organization. Focus on Business QA oversight of GxP computerized systems used in clinical and pharmacovigilance activities. Ensuring compliance with regulatory standards and business needs. Requires experience in CSV, GCP or PV environments, pharmaceutical R&D, and GxP frameworks. Fluent English required.
  • Jefferson Wells Belgium
  • Tournai
  • June 20
QA CSV Specialist needed for new role within Quality R&D & PV organization. Focus on Business QA oversight of GxP computerized systems used in clinical and pharmacovigilance activities. Ensuring compliance with regulatory standards and business needs. Requires experience in CSV, GCP or PV environments, pharmaceutical R&D, and GxP frameworks. Fluent English required.
  • Jefferson Wells Belgium
  • Mons
  • June 20
QA CSV Specialist needed for new role within Quality R&D & PV organization. Focus on Business QA oversight of GxP computerized systems used in clinical and pharmacovigilance activities. Ensuring compliance with regulatory standards and business needs. Requires experience in CSV, GCP or PV environments, pharmaceutical R&D, and GxP frameworks. Fluent English required.
  • Arcadis
  • Tournai
  • June 20
Regulatory Strategist interprets regulations and supports product registration activities. Authors regulatory submissions (CTD, BLA, NDA) and collaborates with cross-functional teams and global colleagues. Manages responses to regulatory requests and assesses post-approval changes. Requires a Master's degree in Life Sciences and 3+ years of experience in the pharmaceutical sector with regulatory and quality experience.
  • Arcadis
  • Charleroi
  • June 20
Regulatory Strategist interprets regulations and supports product registration activities. Authors regulatory submissions (CTD, BLA, NDA) and collaborates with cross-functional teams and global colleagues. Manages responses to regulatory requests and assesses post-approval changes. Requires a Master's degree in Life Sciences and 3+ years of experience in the pharmaceutical sector with regulatory and quality experience.
  • Arcadis
  • Mons
  • June 20
Regulatory Strategist interprets regulations and supports product registration activities. Authors regulatory submissions (CTD, BLA, NDA) and collaborates with cross-functional teams and global colleagues. Manages responses to regulatory requests and assesses post-approval changes. Requires a Master's degree in Life Sciences and 3+ years of experience in the pharmaceutical sector with regulatory and quality experience.
  • Nalys
  • Mons
  • June 11
QA Specialist / Quality Assurance Officer (CMO oversight) Walloon Brabant, Belgium Introduction Are you ... We are currently recruiting, on behalf of one of our partners in the pharmaceutical industry, a QA Specialist ... engaging recruitment journey: Talent Acquisition Call A first discussion with our Talent Acquisition Specialist
  • Nalys
  • Tournai
  • June 11
QA Specialist / Quality Assurance Officer (CMO oversight) Walloon Brabant, Belgium Introduction Are you ... We are currently recruiting, on behalf of one of our partners in the pharmaceutical industry, a QA Specialist ... engaging recruitment journey: Talent Acquisition Call A first discussion with our Talent Acquisition Specialist
  • Nalys
  • Charleroi
  • June 11
QA Specialist / Quality Assurance Officer (CMO oversight) Walloon Brabant, Belgium Introduction Are you ... We are currently recruiting, on behalf of one of our partners in the pharmaceutical industry, a QA Specialist ... engaging recruitment journey: Talent Acquisition Call A first discussion with our Talent Acquisition Specialist
  • Jefferson Wells Belgium
  • Hainaut Province
  • June 20
QA CSV Specialist needed for new role within Quality R&D & PV organization. Focus on Business QA oversight of GxP computerized systems used in clinical and pharmacovigilance activities. Ensuring compliance with regulatory standards and business needs. Requires experience in CSV, GCP or PV environments, pharmaceutical R&D, and GxP frameworks. Fluent English required.
  • Arcadis
  • Hainaut Province
  • June 20
Regulatory Strategist interprets regulations and supports product registration activities. Authors regulatory submissions (CTD, BLA, NDA) and collaborates with cross-functional teams and global colleagues. Manages responses to regulatory requests and assesses post-approval changes. Requires a Master's degree in Life Sciences and 3+ years of experience in the pharmaceutical sector with regulatory and quality experience.
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