137 specialist English-speaking jobs in East Flanders

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

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

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

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

About the role As a Regulatory Affairs Specialist, you will be part of our global Regulatory Affairs ... Regulatory Affairs & Intellectual Property department we are currently looking for a Regulatory Affairs Specialist

Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.

Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.

Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.

Vulcain Engineering Belgium is looking for an HSE Fire Safety Specialist to join its consulting team.

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.

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.

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.

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.

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.

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.

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

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

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

EHS Specialist (m/f/d) – Europe Region About the Role We are looking for an experienced and proactive ... EHS Specialist to support multiple sites across Europe in driving excellence in Environment, Health

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.