Vaccine Production Specialist: GMP & Process Improvement

Merck Gruppe - MSD Sharp & Dohme; Boxmeer; Remote; EUR 55,000 - 75,000; Full time

Job summary

Merck Gruppe - MSD Sharp & Dohme in Boxmeer is seeking a Production Specialist Inactivated Vaccines and Pharmaceuticals to join a global animal health manufacturing environment. You will lead site-wide projects, serve as SME on quality issues, and drive investigations and improvements in GMP-compliant production.

The role requires a degree in biomedical/life sciences or process, 3-5 years of relevant production experience, and strong analytical and project management skills, with fluency in

Qualifications

• Academic degree in biomedical, life sciences or process.
• 3-5 years of relevant experience in a production organization, preferably pharma/biological/chemical.
• Proven analytical and problem-solving skills.
• Knowledge of project management.
• Preferably knowledge of GMP standards and pharmaceutical regulatory requirements.
• Excellent command of Dutch and English.

Responsibilities

• Leading business unit-/site-wide projects/product transfers
• Serving as Subject Matter Expert on product quality related issues
• Actively leading and participating in cross-functional investigations
• Developing proposals and business cases for improvement projects
• Monitoring and analyzing data, and evaluating the consequences of external guidelines

Skills

Capacity Analysis

Data Analysis

Data Modeling

Performing Statistical Analysis

Process Engineering

Process Improvement Initiatives

Process Improvements

Process Standardization

Production Engineering

Production Support

Quality Control Management

Education

Biomedical / life sciences / process degree

Job description

Merck Gruppe - MSD Sharp & Dohme in Boxmeer is seeking a Production Specialist Inactivated Vaccines and Pharmaceuticals to join a global animal health manufacturing environment. You will lead site-wide projects, serve as SME on quality issues, and drive investigations and improvements in GMP-compliant production.

The role requires a degree in biomedical/life sciences or process, 3-5 years of relevant production experience, and strong analytical and project management skills, with fluency in