Η DEMO Α.Ε. αναζητά απόφοιτους/ες για τις θέσεις :
- «Production Shift Supervisor-On-site»,
- «Quality Assurance Validation Engineer- On-site»
Περισσότερα στις αγγελίες:
«1. Production Shift Supervisor-On-site
As part of our continuous development, our company is looking for a talented candidate for the position of Production Shift Supervisor in Kryoneri. The position reports to Production Manager.
Responsibilities
Ensures the smooth operation of the production wing during the shift hours.
Follows and controls the implementation of written procedures and instructions cGMP’s ensuring the quality of the product.
Monitors the execution of production program in an efficient manner.
Creates the standard or ad hoc reports including the shift performance indicators.
Takes initiatives or participates in actions aimed at improving productivity and reducing production costs.
Proposes corrective and improvement actions related to production processes.
Requirements
Degree in Chemical Engineering or Chemistry. Postgraduate degree will be considered as an asset.
Ideally 1 year of experience in a similar role in pharmaceutical industry.
Very good PC skills (MS Office) and ERP knowledge (SAP).
Excellent knowledge of English.
Ability to work on shifts.
Problem solving skills.
Ability to manage multiple tasks and set priorities.
Flexibility and adaptability.
Commitment to achieving qualitative and quantitative goals.
Excellent communication and team management skills.
Benefits
The company offers competitive compensation, continuous training & career development opportunities and a friendly working environment.
14 workdays per month with compensation equivalent to full monthly employment! DEMO Pharmaceutical Industry SA introduces a new pioneering work program.
Και οι αιτήσεις θα θέλαμε να αποστέλλονται στο Production Shift Supervisor – Demo S.A. https://careers.demo.gr/_/j/6A1D60FC18/
2. Quality Assurance Validation Engineer- On-site
Responsibilities
Prepares or/and executes the URS documentation, the qualification, validation protocols and the reports and any other procedures related to the new facilities quality system’s design, the credibility of which must be validated due to their criticality.
Issuance/revision of QA procedures related to planned activities.
Confirmation that the production areas as well as the rest of the supporting areas in a new facility, comply fully with the current legislation, the standards, and the internal Procedures, reviewing the Corrective/Preventive Actions that refer to Internal Audits.
Ensures projects are managed in conjunction with all regulatory requirements (FDA, Part 11).
Ensures the validation status of equipment and systems are always following cGMPs.
Execution of requalification for all critical equipment according to VMP.
Execution of calibration of all critical instruments according to CMP.
Requirements
Bachelor’s degree in Engineering, Physics or a related scientific discipline. MSc degree would be considered a plus.
At least 1 year of relevant work experience in industrial production. Relevant experience in Validation of pharmaceutical production in injectables is preferred.
Experience in risk management tools. (FMEA, FMECA, FTA, HACCP)
Experience in Cleaning Validation, Process Validation and Facility design.
Experience in Qualification of pharmaceutical equipment (IQ, OQ, PQ etc.)
Good understanding of FDA regulations, Part 211 regulations and pharmaceutical industry standards.
Very good knowledge of MS Office.
Excellent verbal and written communication in Greek and English.
Ability to manage multiple tasks and set priorities to meet manufacturing deadlines.
Benefits
The company offers competitive compensation, continuous training & career development opportunities and a friendly working environment.
Και οι αιτήσεις θα θέλαμε να αποστέλλονται στο Quality Assurance Validation Engineer – Demo S.A. https://careers.demo.gr/_/j/4DB303BC5B/ »
Κατηγορία: Γενικές Ανακοινώσεις Εργασίας,Θέσεις εργασίας Χημικών Μηχανικών,Θέσεις εργασίας Μηχανολόγων Μηχανικών,Θέσεις εργασίας Εφαρμοσμένων Μαθηματικών & Φυσικών Επιστημών
Ημερομηνία Λήξης Προβολής: 26 Μαΐου 2025