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Teva Pharmaceuticals has been developing and producing medicines for more than 120 years. Along with our established presence in generics, we have significant research and operations supporting our growing portfolio of innovative medicines and biopharmaceutical products.
· Bachelor Degree or equivalent (preferably in business management discipline)
· Minimum 2 years of experience in an international business environment
· Excellent communication skills in English
· Knowledge of MS Word, MS Excel, MS Outlook
· ERP experience - SAP or other business management system
· Understanding of pharmaceutical business and/ or knowledge of PowerPoint and Visio would be an advantage
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.
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This position is based in Sofia. Its main purpose is to check the accuracy of the provided by the suppliers print ready files (prepress and quality checks) and to coordinate the workflow of Supplier`s Print Proofs between the Global Artwork Studio, global markets and suppliers. Record data for quality measures, reports and continuous improvement
• Check Supplier Printers Proofs for anomalies
• Co-ordinate the workflow between suppliers and markets to ensure required deadlines are met
• Chase markets/suppliers where required
• Investigate and report to Team Leader, Production and Print Proof Team Sofia errors or issues with Print Proofs
• Record and trend data to be fed into the Quality Management System for quality measures and continuous improvement
• Support and assist other QC roles when required
• Relevant professional degree level
• Fluent in English (both written and spoken)
• Copy checking/Proof reading skills – 2 years
• Experience with Adobe Creative Suite
• Experience in prepress and/or printing / packaging industry
• Experienced computer user
• Knowledge of Pharmaceutical industry Quality process
• Excellent communication skills
• Goal focused
• Structured and systematic
• Customer oriented
• Enthusiastic and flexible
• Confident and thorough, conscientious
Additionally, we will consider as an advantage any of the following
• Experience of working within Pharmaceutical packaging environment
• Experience of working to deadlines
• Dynamic and challenging work environment in one of the world leading pharmaceutical company and the biggest pharmaceutical company in Bulgaria
• Competitive remuneration bound with performance
• Additional healthcare insurance
• Transportation allowance and other flexible benefits
• Flexible working hours and option to work from home as per the company policy
• Opportunity for development
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This position is ultimately organizationally and functionally subordinated to the Global Head of Compliance Audit within the Global Internal Audit Group and is designed to provide for optimum independence and objectivity.
• Responsible for assisting the overall Global Internal Audit department in the establishment of a program for compliance and financial auditing based upon direction from Global Head of Compliance Audit.
• Responsible for the performance of audit procedures in accordance with the annual compliance internal audit work plan or at the direction of the Global Head of Compliance Audit or Compliance Audit team leaders.
• Responsible for the design and delivery of meaningful, accurate and effective presentations to local, regional and global senior management and ensure follow-up on any areas that require corrective action. This role is also responsible for the performance of ongoing follow-up of the implementation of the recommendations of the auditor’s reports and shall draw the attention of the general management of the country being audited for delays in the rectification of deficiencies that have been found in the past.
• Serve as subject matter expert and provide expertise and advice to regional business partners regarding compliance and financial issues. Partner with regional Legal, Finance, and Global Compliance, in carrying out compliance and financial audit activities.
• Maintain all organizational and professional ethical standards and ensures internal audit activities are carried out in compliance with the IIA’s International Standards for the Professional Practice of Internal Auditing (Standards) and department and company policies and procedures.
• Works independently with extensive latitude for initiative and independent judgment.
• Bachelor’s degree in Accounting or related business discipline (i.e. law, criminal or forensic sciences, IT, etc.).
• Minimum of three (3) years of full-time experience in internal audit, external audit, law or Compliance.
• Big 4 Accounting Firm, and/or international Compliance experience with emphasis on Compliance specific to PhRMA Code and FCPA including Anti-Corruption and Anti-Bribery, and experience within Pharmaceutical/Life Sciences industry.
• Professional certification (i.e. CPA, CMA, CIA, CFE, CISA, CRMA, CRISC, CSA, etc.) Other certifications in related field are also a plus.
• Advanced skills in collecting and analyzing complex data, evaluating risk, drawing logical conclusions and presentation of results.
• Knowledge of and skill in applying audit principles and practices, preferred business practices and concepts, and common indicators of fraud; in global operations within the pharmaceutical industry.
• Ability to travel extensively internationally (approx. 25%)
• Advanced level of English – both written and spoken
• Dynamic and challenging work environment in one of the world leading pharmaceutical company and the biggest pharmaceutical company in Bulgaria
• Competitive remuneration bound with performance
• Additional healthcare insurance
• Transportation allowance and additional flexible benefits
• Flexible working hours and option to work from home as per the company policy
• Opportunity for development
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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• Planning, preparing, submitting post-approval variations in line with the corporate procedures
• Provide input into regulatory strategies and process improvement/compliance activities within defined areas of scope.
• Analyse regulatory issues and communicate with key stakeholders.
• Maintaining of the relevant regulatory tools
• Keeping up to date with regulatory legislation
• Maintaining communication pathways with all relevant internal stakeholders and external contacts Regulatory Affairs, Local Affiliates, Business Development, Contract Management, IP, Marketing, Core Teams, Portfolio, Manufacturing sites, QA, Authorities, consultants, etc.
• MSc/PhD in Life Science, Pharmaceutical or equivalent university degree
• Experience in regulatory or pharmaceutical industry
• Solution and result oriented attitude
• Good organizational and good communication skills
• High level of written and spoken English
• Dynamic and challenging work environment in one of the world leading pharmaceutical company and the biggest pharmaceutical company in Bulgaria
• Competitive remuneration bound with performance
• Additional healthcare insurance
• Transportation allowance and other flexible benefits according to the company policy
• Flexible working hours and option to work from home as per the company policy
• Opportunity for development
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
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Responsible for designing, implementing, and optimizing enterprise-wide IT infrastructure solutions.
- Develop and maintain enterprise infrastructure architecture strategies and roadmaps.
- Writing documents High-Level Design (HLD), Low-Level Design (LLD) - Overview of the system or architecture, outlining the major components, their relationships, and high-level functionality.
- Design and implement scalable, secure, and high-performance infrastructure solutions.
- Lead the evaluation and integration of cloud technologies (AWS, Azure) with on-prem environments.
- Oversee network architecture, storage solutions, and virtualization strategies.- Ensure compliance with security policies, regulatory standards, and industry best practices.- Drive automation and modernization efforts, including Infrastructure as Code (IaC).
- Conduct performance analysis and capacity planning to ensure optimal system efficiency.
- Manage vendor relationships and negotiate contracts for enterprise IT solutions.
Qualifications
- 10+ years' experience in pharmaceutical or related industry
- A bachelor's or master's degree
- Expertise in cloud platforms (AWS, Azure, GCP) and hybrid environments.
- Strong knowledge of networking, security, virtualization, and storage technologies.
- Experience with DevOps, CI/CD, and automation tools (Terraform, Ansible, Kubernetes).
- Excellent analytical and problem-solving skills.
- Effective communication and leadership abilities in a large enterprise setting.
- Strategic thinker
- Strong leadership capabilities
- Project management capabilities
- Ability to work in a changing and dynamic environment
- Stakeholder management orientation
- Planning and execution capabilities
- Structured and organized
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.
Sr Dir Cloud, On-Premises Compute, Security, and DC Services
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• Lead the monthly development of a replenishment plan for each allocated 3rd Party Manufacturing site that supports customer service and inventory metrics for all countries and global business units across the defined product portfolio
• Lead the development and agreement of constrained replenishment plans for existing and new products
• Support the Global and Regional S&OP process through relevant metric reporting and summary of key supply/capacity decisions required
• Evaluate changes requested in the frozen window to best response to market and the companies business needs
• Manage customer service issues and facilitate discussions to resolve with the 3rd Party Manufacturing sites and markets. Perform management reporting on customer service issues
• Analyze and maintain the consistency of data in the information systems
• Support KPI and management reporting
• Previous Supply Chain experience in an international business environment
• At least 2 years’ experience in planning
• Experience in a GxP environment is considered an advantage
• Experience with planning, MPS, RCCP software is preferred
• Ability to utilize technology to improve efficiency and performance including advanced knowledge in Excel, PowerPoint and Word
• Ability to deal with complexity and manage relationships across a diverse range of stakeholders
• Excellent analytical skills, ability to see the big picture while paying attention to details
• Advanced level of English – both written and spoken
• Dynamic and challenging work environment in one of the world leading pharmaceutical company and the biggest pharmaceutical company in Bulgaria
• Competitive remuneration bound with performance
• Additional healthcare insurance
• Transportation allowance and additional flexible benefits
• Flexible working hours and option to work from home as per the company policy
• Opportunity for development
Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
These jobs might be a good fit

Share
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
These jobs might be a good fit