Process engineer (m / f / d)

GULP – experts united; Singen (Hohentwiel); Vor Ort; EUR 40.000 - 60.000; Vollzeit

Zusammenfassung

A leading recruitment agency is looking for an experienced Process Engineer in Singen, Baden-Württemberg. The successful candidate will manage technology transfers and improve biopharmaceutical manufacturing processes. Applicants should have a university degree in biotechnology and significant experience in GMP compliance. Excellent German and English skills are required, along with strong teamwork and organizational abilities. This role offers a performance-oriented salary and opportunities for further training.

Leistungen

Performance-oriented salary package

Vacation and Christmas bonuses

Up to 30 days vacation per year

Good chances of being taken on by client

Individual training programs

Wide range of employee benefits

Potential for remote work by arrangement

Qualifikationen

• Several years of experience in technology transfer and cGMP-compliant processes.
• Experience in writing validation documents, protocols, and reports.
• Good knowledge of biological drug manufacturing.

Aufgaben

• Perform change control and continuous process improvements.
• Manage work packages for capital projects.
• Support qualification of new vaccine manufacturing facilities.

Kenntnisse

Interdisciplinary teamwork

GMP knowledge

Technical documentation writing

Statistical analysis tools

DoE

Problem-solving

Organizational skills

Bilingual (German and English)

Ausbildung

University degree in biotechnology or related field

Jobbeschreibung

We create lasting connections : Thanks to our trusting contacts with local HR decision-makers, we can offer you attractive jobs with successful companies in the pharmaceutical sector . We are currently looking for an experienced Process Engineer in Singen . Are you a biotechnologist looking for a secure job with fair pay and long-term prospects? You'll find what you're looking for with us - apply now! Our working atmosphere and the openness of our teams promote equal opportunities for all people - including those with disabilities, whose applications we welcome.

Here’s what we offer

• Performance-oriented salary package depending on qualifications and professional experience
• Attractive social benefits, for example vacation and Christmas bonuses
• Vacation entitlement of up to 30 days per year
• Good chances of being taken on by our client company
• Individual training with renowned partners
• A wide range of employee benefits
• Possibility of predominantly working from home by arrangement

Your tasks

• Perform change control, investigations, CAPAs and continuous process improvements during validation / manufacturing activities
• Manage work packages for capital projects in compliance with timelines, policies and procedures
• Support qualification of new vaccine manufacturing facilities and equipment in compliance with cGMP requirements and global regulatory requirements
• Assist in the planning, execution and reporting of validation activities, including analyzing data and determining results and conclusions
• Collaborate with QA, Quality Control and other support functions to ensure the smooth flow of technology transfer and validation
• Responsibility for recipes and recipe lists
• Coordination of technology transfer as representative of the Receiving Unit
• Troubleshooting and improvements during technology transfer
• Responsibility for the creation and content of bills of materials (BOM) for raw materials and single-use materials
• Support in setting up the practical process in production

Your profile

• University degree in biotechnology or a related field
• Several years of experience in supporting start-ups, technology transfer and maintaining cGMP-compliant biopharmaceutical manufacturing processes
• Sound knowledge of GMP
• Ideally experience in working with live viruses
• Experience in writing technical documents, including validation documents, protocols and reports
• Experience in the use of statistical analysis tools and Design of Experiments (DoE) an advantage
• Technical knowledge within biological drug manufacturing
• Very good written and spoken German and English skills
• Enjoy interdisciplinary and cross-functional teamwork
• Organizational talent and a goal-oriented way of working