Project Manager Documentation (m/f/d)

Belimed Life Science AG is a globally active company headquartered in Sulgen, Switzerland. Belimed Life Science AG develops, produces, distributes, installs, modifies, and optimizes systems for cleaning and sterilization in the application areas: Pharma, Biopharma, Life Science, and Cosmetics for laboratory and production applications. With retrofit solutions for existing systems, the development of accessories, and extensive qualification activities, we complete our service portfolio.

We meet the current new challenges of the industry for rapid development of vaccines and medicines and the necessary assurance of the quality of these pharmaceutical end products with new, innovative solutions at the highest level. After the spin-off on 01.04.2019 from Belimed AG, we currently have more than 150 specialists at two locations in Sulgen (CH) and Grosuplje (SI).

Interested in working with hot steam and purest water? Then apply with us as

Project Manager Documentation (m/f/d)

Your tasks

Direct contact person for customers regarding all matters related to the system documentation of our steam sterilizers for the pharmaceutical industry

Ensuring that the system documentation complies with regulatory requirements and GMP principles of pharmaceutical systems

Creation of project-specific design, manual, test, and qualification documents. Coordination and control of technical documents from experts in the fields of design, process engineering, electrical engineering, and software

Compilation of the entire "document package" of system projects and provision for internal factory acceptance with the customer

Execution of internal test instructions that prove that the built system complies with the agreed technical specifications and design regulations

Active participation and support in factory acceptance with the customer

Support of sales in customer inquiries for technical order clarification

Your profile

Technical basic training preferably in mechanical engineering/automation

Further training in technical editing desirable

Several years of professional experience in plant engineering, preferably in technical documentation

Linguistic precision and joy in writing, combined with very good technical understanding

Very good MS Office skills and structured approach in "document management"

Good knowledge in the application of GMP and GAMPx guidelines in the pharmaceutical industry

Structured approach in handling customer projects

Confident appearance and strong communication skills

Reliability and accuracy

Customer orientation (recognizing and responding to customer needs)

Teamwork skills

Flawless communication possible in German and English

Our offer

Take on a central role in a dynamic international company. With us, you can expect a varied and exciting activity in a complex field. Interested in this challenge? Then we look forward to receiving your application documents (CV, cover letter, and certificates) via our career page.

We are happy to review dossiers from recruitment agencies, provided that the business terms for the placement are individually negotiated in each case. General conditions will not be accepted.