MSAT Engineer (CPV) – Frankfurt, Germany

Optimus Life Sciences; Frankfurt; On-site; EUR 65,000 - 90,000; Full time

Job summary

Optimus Life Sciences in Frankfurt is seeking an MSAT Engineer to support Continued Process Verification (CPV) activities on a long-term GMP project. The role targets professionals with 2–5 years in pharmaceutical manufacturing, MSAT, or process validation, focusing on CPV strategy development and documentation.

German language skills are essential with a good command of English. You will collaborate with cross-functional teams across Manufacturing, Quality, and Validation to monitor processes

Qualifications

• Approximately 2–5 years of experience within pharmaceutical manufacturing, MSAT, process validation or a closely related function.
• Practical understanding of Continued Process Verification (CPV) and its application in a GMP environment.
• Experience preparing or contributing to CPV strategies, plans and technical documentation.
• Understanding of pharmaceutical manufacturing processes and GMP requirements.
• German language skills are essential, alongside a good working level of English.
• Ability to work collaboratively with cross-functional technical teams.

Responsibilities

• Support the local MSAT Lead with the development and implementation of Continued Process Verification (CPV) strategies.
• Prepare and maintain CPV plans, protocols and supporting GMP documentation.
• Review manufacturing process data to identify trends, variability and potential process improvements.
• Support ongoing process monitoring and verification activities to maintain a state of control.
• Collaborate with Manufacturing, Quality, Validation and other technical stakeholders.
• Contribute to technical investigations and continuous improvement activities where required.

Skills

German language skills

English language skills

Cross-functional collaboration

Job description

MSAT Engineer – Continued Process Verification (CPV)

Pharmaceutical Manufacturing | Frankfurt, Germany | Long-Term Project

We are supporting an engineering consultancy delivering a major pharmaceutical project in Frankfurt and are looking for an MSAT Engineer with experience in Continued Process Verification (CPV) to join the team.

This opportunity would suit someone with approximately 2–5 years of experience in pharmaceutical manufacturing, process validation or MSAT who is looking to develop their technical expertise on a significant GMP project.

Responsibilities

• Support the local MSAT Lead with the development and implementation of Continued Process Verification (CPV) strategies.
• Prepare and maintain CPV plans, protocols and supporting GMP documentation.
• Review manufacturing process data to identify trends, variability and potential process improvements.
• Support ongoing process monitoring and verification activities to maintain a state of control.
• Collaborate with Manufacturing, Quality, Validation and other technical stakeholders.
• Contribute to technical investigations and continuous improvement activities where required.

Requirements

• Approximately 2–5 years of experience within pharmaceutical manufacturing, MSAT, process validation or a closely related function.
• Practical understanding of Continued Process Verification (CPV) and its application in a GMP environment.
• Experience preparing or contributing to CPV strategies, plans and technical documentation.
• Understanding of pharmaceutical manufacturing processes and GMP requirements.
• German language skills are essential, alongside a good working level of English.
• Ability to work collaboratively with cross-functional technical teams.