Process Engineer - Manufacturing, cGMP, French

RM IT Services GmbH; Neuenburg; Hybrid; CHF 85’000 - 115’000; Vollzeit

Zusammenfassung

A leading company in the pharma sector is seeking a Process Engineer for a hybrid contract position in Neuchatel. Ideal candidates will have a degree in biotechnology and 3-5 years of relevant experience. The role encompasses protocol development and cross-functional collaboration to ensure compliance and efficiency in manufacturing processes.

Qualifikationen

• 3-5 years of experience in FF area for recombinant protein.
• Fluency in English and French.

Aufgaben

• Create and standardize Engineering Runs and PPQ Runs protocols.
• Collaborate with the Manufacturing team on validation runs.
• Author comprehensive final validation reports.

Kenntnisse

Process Validation

Problem-solving

Attention to detail

Technical writing

Collaboration

Ausbildung

Engineering or university degree in biotechnology

Tools

Kneat software

Jobbeschreibung

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Location:

Job Category:

Manufacturing

Job Reference:

BBBH23054_1749465098

Job Views:

2

Posted:

09.06.2025

Expiry Date:

24.07.2025

Job Description:

Process Engineer - Manufacturing, cGMP, French contract opportunity to join our Neuchatel-based client in the Pharma sector.

Your tasks:

• Protocol Development: Create and standardize Engineering Runs and PPQ Runs protocols in compliance with applicable regulations, quality standards, and project scopes.
• Execution Support: Collaborate with and guide the Manufacturing team to ensure smooth execution of validation runs, addressing technical challenges, and ensuring adherence to protocols.
• Documentation & Reporting: Author comprehensive final validation reports, ensuring accuracy, compliance, and integration of all relevant data (e.g., deviations, observations).
• Cross-Function Collaboration: Liaise with Quality Assurance, Process Engineering, and other relevant teams to align validation activities with manufacturing goals and timelines.
• Continuous Improvement: Focus on optimizing validation processes, leveraging best practices to ensure regulatory compliance and efficiency.

Your experience/knowledge:

• Minimum 3-5 years of experience in FF area for recombinant protein.
• Engineering or university degree in biotechnology.
• Language skills: Fluent in English and French.
• Experience using Kneat software for validation documentation and processes.
• Proven expertise in process validation within pharmaceutical or biotech manufacturing.
• Strong knowledge of Process Validation and Performance Qualification, GMP regulations, and risk management.
• Exceptional technical writing skills for clear, compliant documentation.
• Ability to work collaboratively and communicate effectively in a high-paced environment.
• Problem-solving mindset with attention to detail and quality.

Your soft skills:

• Excellent comprehension and attention to detail.
• Strong self-organization and time management skills.
• Analytical and solution-oriented thinking.

Location: Neuchatel

Work setting: Hybrid

Sector: Pharma

Start: 07/2025

Duration: 6+ months

Workload: 100%

Ref.Nr.: BH 23054

Take the next step and send us your resume along with a daytime phone number where we can reach you.

Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens, and current Swiss work-permit holders.

Ukrainian refugees are warmly welcomed, and we will support you throughout the process.

We welcome applications from individuals of all genders, ages, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. There is no requirement to provide gender information or a photo in your application.

As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our client.