About us
Our Business Unit Pharmaceutical Systems is one of the world’s leading manufacturers of drug containment solutions and delivery systems for injectable drugs. More than 600 production lines in 14 countries worldwide produce more than 10 billion syringes, vials, ampoules, cartridges and special articles of tubing glass or polymer.Your Contribution
Environmental Monitoring
 

Implementation and provision of monitoring activities for clean rooms, technological media and products in accordance with the provisions of relevant guidelines

Provision of basic data for environmental monitoring reports

Participation in the monitoring and processing of deviations occurring in the scope of responsibility (initiation of CAPA for OOS & deviations in clean/ controlled areas), as well as in supporting CAPA measures and investigations in cooperation with other departments

Participation or lead investigations for OOS and deviations

Order nutrient media

Hygiene concept: participation in monitoring of the implementation of the hygiene concept at the site

Organization: general laboratory organization and administration (e.g. inventory management, orders, ensuring the calibration status of the devices used)

Management the pest control process, keeping contact with external company, review external reports and initiates CAPAs as per the internal process/ limits

Responsible for the light intensity measurements, planning of external measures, address local actions if needed

 
Clean & controlled room qualification
 

Participation in the qualification and validation processes of the infrastucture (clean room, controlled area, WFI, compressed air), responsible for the control and compliance with the required standards

Participation in the validation of microbiological process and test methods, preparation of reports

Preparation/ support of URS of clean/ controlled rooms

 
GMP concept & training
 

Participation in the implementation/ establishment and maintenance of the hygiene concept, its monitoring, dress code and clothing requirements and implementation of clean room check

Initial GMP training for new employees (if necessary)

Support assessments, projects and developments with knowledge/ experience of GMP

Follow GMP and GDP rules and make others keep the rules; support the employees with training and technical instructions in consultation with their supervisors

 
Projects & developments
 

Support of process and product development through preparing risk analyzes related to bioburden, endotoxins and particle measurements, as weel as during sterilization processes and procedures

 Your Profile

BSc in natural science, microbiology, chemistry or biology

Min. 2 years of experience in microbiological laboratory and clean room environment

Experience in environmental monitoring

Experience in bioburden test

Knowledge of ISO 15378/ ISO 13485 / ISO 14644 standard, GMP

Good command of English

Problem solving skills (OOS & deviation management)

 Your Benefits
SCHOTT’s openness to promote your further development is just as great as our additional benefits. Ranging from active health management via flexible working hours and hybrid work all the way to corporate pension plans: everything geared to suit your goals and needs. Discover a special corporate culture where everyone has the opportunity to develop their entire potential.
At SCHOTT, you can expect a unique corporate culture where we emphasize equity, diversity, and inclusion. We know: motivated and committed employees are the precondition for the success of our company.
 
Flexible working hours; Further training and education; Multiple career opportunities; Talent developmentPlease feel free to contact us
You can expect interesting tasks and challenging projects, as well as motivated and friendly teams in fields that influence our future. Do you want to be successful with us? Then, please send us your application: SCHOTT Hungary Kft., Human Resources, Ilona Mosonyi+3694568484
 

At SCHOTT, it’s your personality that counts – not your gender, your identity, or origin.