• Executing recruitment activities which involve screening candidates, setting up interviews and corresponding with prospective employees
• Preparing candidates on-boarding, induction procedures, job descriptions, employment contracts and other departmental documents such as confirmations of employment, visas etc.
• Arranging in-house trainings, registering staff for external trainings following CEO approval and preparing HRDA documents
• Prepare reports and presentations as per team needs
• Updating departmental databases (eg. HRIS, training records) and maintaining accurate electronic and paper records, issuing and filing company documentation
• Support the organization and participation in company-related events and activities
• Executing and/or assisting in the implementation of HR policies, procedures and schemes

• BSc in Human Resources or related field
• Previous experience in a similar role 2-3 years
• Proficient in MS Office (Word, Excel, PowerPoint)
• Keen attention to detail and strong organizational skills
• Excellent verbal and written communication skills in both Greek and English
• Familiarity with HRIS systems will be considered an advantage

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Initiating change requests impacting the GMP of the manufacturing facility
• Evaluating and monitoring change requests
• Preparing or assisting in the preparation of technical reports, documents and reports
• Providing training to new employees on how to submit CRFs (Change Request Form) requests through the electronic system
• Communicating with relevant internal stakeholders to collect feedback needed for the potential implementation of changes to specific products
• Ensuring that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), Good Documentation Practices (cGDP) and the current Good Manufacturing Practices (cGMP)

• Degree in Pharmacy, Chemical Engineering or any other relevant field
• Any relevant experience will be considered an advantage
• High attention to detail
• Organized and methodical way of thinking
• Ability to work collaboratively in a team
• Excellent written and verbal communication skills
• Excellent command of the English Language
• Knowledge of Microsoft Office

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Performing the necessary tests for raw materials, and the products’ intermediate, final and under stability studies, according to written procedures and specifications. Proceeding with the completion of the required documentation
• Ensuring that all analysis conducted follow the procedures of the analytical methods
• Checking the documentation and results of the analysis prepared by the QC Department, as and when requested to ensure the validity of the analysis/conformity with regulations
• Monitoring equipment maintenance needs, keeping the working area clean and tidy and promptly informing Laboratory Engineers of any equipment troubleshooting needed
• Reporting updates about the status of analysis to Supervisors, conducting relevant investigations when necessary

• University degree in Chemistry, Chemical Engineering or any other relevant field
• MSc will be considered as an advantage
• Excellent knowledge of English language
• Previous experience within pharma industry will be considered an advantage (HPLC, GC/MS, ICP, TLC, LC/MS, LC/MS/MS, XRD, PSD)
• Excellent organizational skills
• Ability to work on multiple projects at the same time
• Ability to work as part of a team and individually
• Excellent time management and prioritization skills

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Performing the necessary tests for raw materials, intermediates, and finished products to ensure compliance with specifications and then complete the required documentation according to the relevant specifications.
• Checking the documentation and results of the analysis to ensure the validity of the analysis and its conformity with specifications. Preparing laboratory documents such as reports and analytical protocols
• Providing guidance and supervision to Junior Analysts and Assistants in conducting their work as and when needed
• Evaluating new and updated analytical methods and procedures
• Monitoring equipment maintenance needs, keeping the working area clean and tidy and promptly informing of any equipment troubleshooting needed
• Reporting updates as regards the status of analysis to supervisors and conduct the relevant investigation when necessary
• Ensuring that tasks and analysis are completed according to established regulations and guidelines such as Standard Operating Procedures (SOPs), current Good Laboratory Practices (cGLP), and the current Good Manufacturing Practices (cGMP)

• University degree in Chemistry, Chemical Engineering or any other relevant field
• Previous experience in Junior Analyst position
• Excellent knowledge of English language
• Good command of Microsoft Office
• Previous experience within pharma industry will be considered an advantage (HPLC, GC/MS, ICP, TLC, LC/MS, LC/MS/MS, XRD, PSD)
• Excellent organizational skills
• Ability to work as part of a team and individually
• Excellent time management and prioritization skills

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Preparing regulatory submissions (new registrations, renewals, variations) according to the requirements of each country
• Communicating with internal and external stakeholders responding to queries and requests following the approval of Supervisor
• Updating departmental databases, ensuring regulatory compliance
• Notifying all departments when approvals and withdrawals are received and when registration/renewal submissions have been sent
• Compiling and/or assisting in the preparation of dossier sections and the updating of dossier sections and document versions
• Preparing dispatch of samples, original documents and declarations to customers
• Ensuring that tasks and processes are executed according to established regulations and guidelines such as Standard Operating Procedures (SOPs) and the current Good Manufacturing Practices (cGMP)

• Degree in Pharmacology, Pharmacy, Biology, and any other relevant science field
• Accuracy and close attention to detail
• Strong analytical skills
• Time management skills
• Problem-solving and organizational skills
• Strong written communication skills to provide concise and clear documentation
• Must be able to work in a fast-paced environment
• Good computer skills
• Excellent knowledge of English language

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Preparing regulatory submissions (new registrations, renewals, variations) according to the requirements of each country following guidance from Supervisor
• Communicating with internal and external stakeholders responding to queries and requests following guidance from Supervisor.
• Updating departmental databases and reviewing of RIM records to ensure regulatory compliance.
• Assessing Change Requests following feedback from Supervisor for potential regulatory impact
• Informing all departments when approvals and withdrawals are received, registration/ renewal submissions have been sent.
• Compiling and/or preparing dossier sections, updating dossier sections and document versions, ensuring the validity of information to be submitted for all regulatory submissions.
• Monitoring regulations and guidelines relating to products and registration procedures, informing the relevant departments when necessary
• Assisting in the preparation of departmental documents such as procedures and/or SOPs

• University degree in, Pharmacology, Pharmacy, Biology and any other relevant science field
• Previous experience as a Junior RA Officer considered an advantage
• Accuracy and close attention to detail
• Time management skills
• Organisation skills
• Strong written communication skills to provide concise and clear documentation
• Must be able to work in a fast-paced environment.
• Good computer skills
• Excellent knowledge of English language

• Suggest clinical trial designs, provide input to CROs and finalize designs
• Review and approve the BE/pK study protocols
• Analyze data, review/evaluate and approve study reports
• Liaise with pK experts for the assessment of data and reports
• Collaborate cross-functionally, working closely with R&D for pK data needed for formulation development
• Provide feedback advice on strategies for establishing IVIVC
• Manage the BE Study monitoring activities ensuring compliance with Good Clinical Practices (GCP) and applicable regulations
• Track and obtain approval of clinical operations expenses

• BSc in Pharmacy, Pharmacology
• PhD with concentration on Pharmacology or Pharmacokinetics will be considered an advantage
• At least two years’ experience in the generic pharmaceutical industry, preferably clinical trial experience
• Knowledge of Pharmaceutical legislation, Knowledge of GCP, ICH guidelines and regulatory requirements for clinical trial management are mandatory
• High attention to detail
• Analytical thinking
• Scientific writing experience
• Excellent written and verbal communication skills
• Excellent command of the English Language
• Strong clinical study management skills

• Organize and monitor equipment maintenance
• Fill in related documents taking into consideration relevant legislation, guidelines, company procedures and regulations
• Plan and coordinate engineering processes on daily basis
• Execute personally troubleshooting of the equipment and assists his team in this activity
• Collaborate to the development of production equipment operating SOPs
• Communicate and liaises with any relevant department such as Production, R&D, QA and QC Departments

• Bachelor in Electrical, Mechanical or Chemical Engineering, or any other relevant field
• Master Degree will be considered as an advantage
• Accuracy and close attention to detail
• Demonstrated ability to work in both independent and team environments
• Ability to work under pressure with minimum supervision

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Εκτέλεση διαδικασιών αντιμετώπισης προβλημάτων των μηχανών Παραγωγής και Συσκευασίας προκειμένου να διασφαλίζεται η συνεχής λειτουργία και η βέλτιστη απόδοση
• Εκτέλεση και διεκπεραίωση προγραμματισμένων εργασιών/καθηκόντων συντήρησης όπως ορίζονται από τις ανάγκες του λογισμικού και σύμφωνα με τις προκαθορισμένες διαδικασίες
• Συμμετοχή σε διαδικασίες εγκατάστασης και λειτουργίας νέου εξοπλισμού και νέων συστημάτων και συντονισμός με τα αρμόδια τμήματα για τον έλεγχο των εγκαταστάσεων, υπό την επίβλεψη του Ανώτερου Μηχανικού Παραγωγής
• Προετοιμασία, αλλαγή εξαρτημάτων/εργαλείων μηχανών και ρύθμιση των μηχανών Παραγωγής και Συσκευασίας
• Τήρηση αρχείων σχετικά με τη συντήρηση του εξοπλισμού παραγωγής σε έντυπα όπως απαιτείται.

• Απολυτήριο Λυκείου ή Τεχνικής Σχολής
• Σχετικό πιστοποιητικό Ηλεκτρολογία, Αυτοματισμοί
• Προηγούμενη εμπειρία θα θεωρηθεί επιπρόσθετο προσόν
• Τεχνικές δεξιότητες Ηλεκτρολογίας
• Μεθοδικές δεξιότητές
• Προσοχή στη λεπτομέρεια
• Ικανότητα συνεργασίας σε ομάδα
• Δεξιότητες γραπτής και προφορικής επικοινωνίας
• Καλή γνώση της Αγγλικής και Ελληνικής Γλώσσας

• 13ος και 14ος μισθός
• Ταμείο Προνοίας
• Ιατρική Κάλυψη
• Εκπτωτικό πακέτο
• Πρόσβαση στο γυμναστήριο

• Λειτουργεί μηχανήματα φαρμακευτικής παραγωγής και εκτελεί διαδικασίες παρασκευής και συσκευασίας όπως ζύγισμα και / ή ανάμιξη και / ή επικάλυψη και / ή δισκιοποίηση και / ή κοκκοποίηση κ.α.
• Χειρίζεται της φαρμακευτικής μηχανής, ρύθμιση των παραμέτρων της και αντιμετώπιση προβλημάτων όπου και όταν χρειάζεται
• Εκτελεί τις διαδικασίες που χρησιμοποιούνται για τον καθαρισμό εξοπλισμού και εγκαταστάσεων φαρμακευτικής παραγωγής βάση των SOP
• Εξετάζει και επιθεωρεί τα δοχεία, υλικά και προϊόντα προκειμένου να διασφαλιστεί ότι πληρούνται οι προδιαγραφές συσκευασίας
• Εκτελεί και συμπληρώνει τα Μητρώα Παραγωγής καθώς και το βιβλίο καταγραφής με λεπτομέρεια και ακρίβεια
• Διασφαλίζει ότι όλες οι λειτουργίες του τμήματος συμμορφώνονται με τους καθιερωμένους κανονισμούς και οδηγίες όπως τις τυπικές διαδικασίες λειτουργίας (SOP) και τις τρέχουσες καλές πρακτικές παρασκευής (cGMP)
• Εκτελεί οποιαδήποτε άλλα καθήκοντα του ανατίθενται από τον, IPC, Υπεύθυνο της Γραμμής Παραγωγής, τον Επικεφαλή Παραγωγής ή/και τον Chief Operating Officer

• Απολυτήριο Λυκείου ή Τεχνικής Σχολής
• Προσοχή στη λεπτομέρεια
• Ικανότητα συνεργασίας σε ομάδα

• 13ο και 14ο μισθο
• Ιατρική κάλυψη
• Εκπτωτικό πακέτο
• Πρόσβαση στο γυμναστήριο
• Ταμείο Προνοιας

• Χειρισμός, τροφοδοσία, επίβλεψη, καθαρισμός μηχανής συσκευασίας
• Έλεγχος της ποιότητας και της ποσότητας των προϊόντων σε όλα τα στάδια της παραγωγικής διαδικασίας
• Εκτύπωση πληροφοριών του προϊόντος σε χαρτονάκια και ετικέτες
• Καθαρισμός των δωματίων συσκευασίας και των κοινόχρηστων χώρων. Καθαρισμός εξαρτημάτων
• Γενικός έλεγχος και καθαριότητα των χώρων εργασίας και των μηχανών καθώς και κλείσιμο φώτων, πριζών, παροχών αέρα/νερού και άλλων μηχανημάτων στο τέλος της ημέρας
• Ενεργή συμμετοχή σε διάφορα εκπαιδευτικά προγράμματα
• Πλήρης και συνεχής ενημέρωση και συμμόρφωση προς όλους τους κανονισμούς της εταιρείας
• Συνεχής ενημέρωση, κατανόηση και εφαρμογή των γραπτών τυποποιημένων διαδικασιών λειτουργίας (SOPs). Σε καμία περίπτωση δεν παραβιάζονται γραπτές διαδικασίες/οδηγίες χωρίς γραπτή εντολή από εξουσιοδοτημένο άτομο
• Εκτέλεση άλλων σχετικών εργασιών οι οποίες ανατίθενται από τον προϊστάμενο

• Απολυτήριο Λυκείου ή Τεχνικής Σχολής
• Προσοχή στη λεπτομέρεια
• Ικανότητα συνεργασίας σε ομάδα

• 13ος και 14ος μισθός
• Ταμείο Προνοίας
• Ιατρική Κάλυψη
• Εκπτωτικό πακέτο
• Πρόσβαση στο γυμναστήριο

• Executing the development and validation of analytical methods according to ICH guidelines
• Executing stability studies
• Carrying out of Method Transfer procedures
• Carrying out analysis during process validation activities
• Testing materials and products under development
• Assisting in the preparation of quality reports and other analytical documents
• Ensuring data integrity and proper documentation of experimental data
• Executing calibration activities for pH metres and balances
• Executing cleaning activities of instruments used during analysis

• Degree in Chemistry, Pharmacy or any other relevant field
• Previous experience with HPLC mandatory
• Excellent attention to detail
• Verbal and written communication skills
• Good teamwork skills
• Ability to keep detailed records
• Ability to work under pressure
• Willingness to adjust on a full schedule
• Good command of English language and computer

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Assisting in the development and validation of analytical methods according to ICH guidelines
• Assisting in the execution of stability studies
• Assisting in the execution of Method Transfer/Process validation procedures
• Testing materials and products under development
• Assisting in the preparation of quality reports and other analytical documents
• Ensuring data integrity and proper documentation of experimental data
• Executing calibration activities for pH metres and balances
• Executing cleaning activities of instruments used during analysis

• Degree in Chemistry, Pharmacy or any other relevant field
• HPLC hands on experience is preferred and considered an advantage
• Excellent attention to detail
• Verbal and written communication skills
• Good teamwork skills
• Ability to keep detailed records
• Ability to work under pressure
• Willingness to adjust on a full schedule
• Good command of English language and computer

• Defining the scope of the project and communicating it within R&D and to other stakeholders
• Setting up the project plan
• Following-up with R&D scientists for day to day tasks and project milestones
• Monitoring Contract Research Organisations’ (CRO) progress, have a constant update on the process and raising flags where necessary
• Monitoring the progress of analytical method development and method transfer activities in order to ensure that these are executed within the timelines given
• Maintaining accurate records of the development evolvement and communicating results to Head of R&D Project Management
• Compiling project progress reports
• Maintaining/updating departmental databases and project management software
• Identifying risks/opportunities involved in each project and managing them
• Writing and/or assisting in the write-up of documents related to project management timelines and procedures

• Bachelor in Chemical Engineering, Chemistry, Pharmacy or any other relevant field
• Master’s degree in pharmaceutical sciences or MBA preferred
• Project Management certification preferred
• Knowledge and certification on Microsoft Project an added benefit
• Accuracy and close attention to detail
• Strong analytical skills and mind-set
• Demonstrated ability to work in both independent and team environments
• Ability to work under pressure with minimum supervision
• Excellent communication skills
• Organization skills
• Time management skills and ability to prioritize and manage multiple tasks
• Fluency in English writing and speaking
• Good MS skills (Word, PowerPoint, Excel)

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Defining the scope of the project and communicating it within R&D and to other stakeholders
• Setting up the project plan
• Following-up with R&D scientists for day to day tasks and project milestones
• Monitoring Contract Research Organisations’ (CRO) progress, have a constant update on the process and raising flags where necessary
• Monitoring the progress of analytical method development and method transfer activities in order to ensure that these are executed within the timelines given
• Maintaining accurate records of the development evolvement and communicating results to Head of R&D Project Management
• Compiling project progress reports
• Maintaining/updating departmental databases and project management software
• Identifying risks/opportunities involved in each project and managing them
• Writing and/or assisting in the write-up of documents related to project management timelines and procedures
• Preparing and/or reviewing organizational and departmental documents, reports, policies, and procedures

• Bachelor in Chemical Engineering, Chemistry, Pharmacy or any other relevant field
• Master’s degree in pharmaceutical sciences or MBA preferred
• Previous experience within an R&D Department 3-4 years’ minimum
• Project Management certification preferred
• Knowledge and certification on Microsoft Project an added benefit
• Accuracy and close attention to detail
• Strong analytical skills and mind-set
• Demonstrated ability to work in both independent and team environments
• Ability to work under pressure with minimum supervision
• Excellent communication skills
• Good leadership skills are essential
• Organization skills
• Time management skills and ability to prioritize and manage multiple tasks
• Fluency in English writing and speaking
• Good MS skills (Word, PowerPoint, Excel)

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Leading a team of analysts, giving support and guidance during their daily work
• Reviewing and evaluating the development and validation of analytical methods and procedures
• Reviewing and evaluating stability study results
• Designing and/or overviewing dissolution method development experiments
• Preparing laboratory documents such as SOPs, protocols and reports.
• Reviewing the documentation and results of the analysis to ensure the validity of the analysis and its conformity with specifications and approve the audit trail, managing out of specification/out of trend procedures if and when needed
• Evaluating deficiencies received by the registration department and providing scientific explanations

• Degree Chemistry, Pharmacy or any other relevant field
• Previous experience with HPLC systems, GC, UV mandatory, Previous experience with method validation an advantage
• Previous experience on pharmaceutical analysis of 4-6 years in QC or R&D roles mandatory
• A Senior Analyst must be obedient organized, cooperative and willing to adjust on a full schedule
• Good time-task allocation and ability to meet project deadlines
• Good leadership skills are of essence
• Attention to Detail
• Analytical Thinking
• To be able to work under pressure
• Good command of English language

• Evaluation of the product technical suitability at Remedica, especially for the critical and complex molecule/product
• Conducting literature research on the originator drug product (RLD)/drug substance prior to the initiation of lab activities, including Product & API patents (if applicable)
• Technical aspects: Designing of the formula & process as per QbD, evaluate equipment feasibility, API physical characterisation, DEC study, feasibility/prototype trials/scale up trials including the optimization of process and process parameters, stability testing in accordance to the specifications
• Works closely with IP and reviews patents and proposes non-infringing strategies for active pharmaceutical ingredients, compositions and manufacturing processes.
• Planning, organising, follow-ups must be made to achieve target timelines among technical teams as per the guidance from the supervisor/Head
• Compiling/reviewing formal documentation required for product registration purposes

• Bachelor in Chemical Engineering, Chemistry and Pharmacy
• Master’s degree in pharmaceutical sciences preferred
• Minimum 5 – 7 years of previous Job experience in pharma sector
• Attention to detail, accurate and precise in recording data and batch information
• Strong analytical skills and mindset
• Good leadership skills are of essence.
• Timely decision making to avoid delays
• Demonstrated ability to work in both independent and team environments
• Ability to work under pressure with minimum supervision. Multi-tasking as per departmental requirement with minimum supervision
• Excellent communication skills
• Good organization skills
• Fluency in English writing and speaking
• Good MS skills (Word, PowerPoint, Excel)

• Visit doctors, dentists and other health professionals to promote (scientifically update) products assigned to him/her according to schedule
• Develops relationships of trust with health professionals
• Keeps track of product sample for doctors, dentists and other healthcare professionals
• Provides a daily report about schedule, activities and/or other issues related to his/her duties work done
• Collects information, data and other material about competitors, conferences and other events of interest for Remedica, including relevant laws / regulations
• Keeps a record with data of doctors, dentists and other health professionals
• Actively participates in scientific conferences related to the health sector

• Medical Representative Diploma or bachelor’s degree in pharmacy, Biology, Chemistry or related field
• Proven experience in the health sector (preferably in a pharmaceutical company) for a minimum of 3 years and ideally as a Medical Representative
• Registered to the Registry of Medical Representatives of the Cyprus Medical Representatives Registration Council, operating under the auspices of the Ministry of Health
• Excellent level of knowledge of the Greek and the English language
• Strong negotiation skills
• Excellent communication and organizational skills
• Exceptional customer service skills

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

• Promotion of Oncology Medicines: Drive sales growth by effectively promoting our oncology products to healthcare professionals, including oncologists, gynaecologists, and other specialists.
• Product Knowledge: Develop a deep understanding of our oncology medicines, including their mechanism of action, indications, contraindications, and side effects, to provide accurate information to healthcare professionals.
• Customer Relationship Management: Build and maintain strong relationships with key opinion leaders, physicians, pharmacists, and other healthcare professionals within the assigned territory.
• Market Analysis: Continuously monitor market trends, competitor activities, and healthcare developments to identify opportunities and threats within the oncology market.
• Strategic Planning: Develop and implement effective sales strategies and tactics to achieve sales targets and maximize market penetration for oncology products.
• Training and Education: Conduct product training sessions and educational programs for healthcare professionals to enhance their understanding of our oncology medicines.
• Collaboration: Work closely with cross-functional teams, including marketing, medical affairs, and sales, to ensure alignment of strategies and initiatives in the oncology therapeutic area.
• Compliance: Adhere to all relevant regulations, guidelines, and company policies, including compliance with the Code of Ethics, during all interactions with healthcare professionals.

• Bachelor’s degree in pharmacy, Medicine, Life Sciences, or related field.
• Minimum of 3 years of experience in pharmaceutical sales, with a focus on oncology products preferred.
• Proven track record of achieving sales targets and building strong customer relationships.
• Excellent communication, presentation, and negotiation skills.
• Strong understanding of oncology therapeutic area and related market dynamics (Preferred).
• Ability to work independently and as part of a team in a fast-paced environment.
• Valid driver’s license and willingness to travel within the assigned territory.

• 13th and 14th salary
• Provident Fund
• Group Medical Plan
• Discount scheme
• Gym access

Εάν δεν υπάρχουν θέσεις εργασίας που σας ενδιαφέρουν, μπορείτε να υποβάλετε το βιογραφικό σας στη βάση δεδομένων μας, στην οποία και θα ανατρέξουμε όταν ανοιχθεί νέα αντίστοιχη θέση εργασίας. Το βιογραφικό σας, θα αποθηκευτεί για περίοδο 6 μηνών στην εσωτερική βάση δεδομένων μας, σύμφωνα πάντα με τον Γενικό Κανονισμό Προστασίας Δεδομένων. Η ομάδα Ανθρώπινου Δυναμικού μας θα επικοινωνήσει μαζί σας σε περίπτωση που προκύψει η οποιαδήποτε ευκαιρία η οποία ταιριάζει το προφίλ σας.