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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.
Learn more at .
Learn more at .
• Actively participate in meetings related to registration procedures or when CMC expertise is needed.
• Collect and critically evaluate data for inclusion in marketing authorization dossiers.
• Compile module 3 and corresponding module 2.3 Quality Overall Summary (QoS) for presentation to regulatory authorities or clients, taking all necessary measures to ensure that dossiers meet relevant, current requirements and trends.
• Critically evaluate the content of module 2.3 and module 3 in terms of completeness and relevance for supporting a new registration and respond to queries.
• Actively participate in the change control system and work in line with established processes.
• Prepare the variation packages and other necessary documents as required by the variation process
• Perform regulatory evaluation and assessment of technical documentation
• Contribute to renewal applications or annual reports
• Keep up to date with regulatory and other developments in the pharmaceutical industry, including relevant legislation and guidelines (EU, US and International markets) and pharmacopoeias.
• Support strategic projects such as technical transfers.
• Ensure that all documents and records pertaining to the RA CMC Lifecycle Department are archived properly. Keep departmental database or other tracking systems up to date.
• University degree, preferably be in possession of a master level of education in ‘Regulatory Disciplines’ or in other area, but pertinent with the field.
• 2-5 years of experience in CMC Regulatory Affairs or in another scientific role in the pharmaceutical industry.
• Knowledge on registration procedures and pharmaceutical regulation.
• Working independently with a moderate level of guidance and direction.
• Very good command of English, speaking and writing.
• Good IT skills.
• Ability to work in team.
• Communication skills with internal and external customers.
• Organisation skills.
• Accuracy in practice and attention to detail.
• 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
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

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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
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
As a Data Author, you will play a key role in maintaining the accuracy and consistency of master data across our supply chain systems. You’ll work closely with cross-functional teams to gather, validate, and manage data that supports operational efficiency and reliable reporting.
• Create, update, and maintain master data records in line with governance policies and data standards
• Ensure data completeness, accuracy, and timeliness across enterprise systems
• Collaborate with stakeholders to gather and validate data inputs
• Identify data inconsistencies and support cleansing and quality initiatives
• Provide structured data for reports and dashboards
• Escalate data issues to stewards or relevant teams for resolution
• University degree (preferably in science or business-related fields)
• Strong written and verbal English communication skills
• Understanding of master data standards and governance principles
• Basic knowledge of supply chain or business process flows
• Experience with enterprise data systems (e.g., ERP, MDM platforms)
• Analytical mindset with attention to detail and data accuracy
• Strong time management and organizational skills
• Team player with the ability to work in a multicultural, cross-functional environment
• 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
• Championing data accuracy in analytical tools
• Conducting regression tests to validate changes and updates
• Ensuring timely resolution of user service tickets
• Supporting users through guidance, training, and troubleshooting
• Creating ad-hoc reports using self-service capabilities for complex requests
• Managing user access rights and licenses for analytical platforms
• Tracking and reporting success measures of analytical tools
• Communicating tool improvements, known issues, and disruptions to users
• University Degree
• Very strong analytical skills
• Good collaboration and communication abilities
• Experience in supply chain or related operational environments
• Proficiency in Excel and PowerPoint
• Experience with SAP is an advantage
• Ability to work independently and manage multiple priorities
• Strong attention to detail and commitment to data quality
• 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
• 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
• 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

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.
Learn more at .
Learn more at .
• Actively participate in meetings related to registration procedures or when CMC expertise is needed.
• Collect and critically evaluate data for inclusion in marketing authorization dossiers.
• Compile module 3 and corresponding module 2.3 Quality Overall Summary (QoS) for presentation to regulatory authorities or clients, taking all necessary measures to ensure that dossiers meet relevant, current requirements and trends.
• Critically evaluate the content of module 2.3 and module 3 in terms of completeness and relevance for supporting a new registration and respond to queries.
• Actively participate in the change control system and work in line with established processes.
• Prepare the variation packages and other necessary documents as required by the variation process
• Perform regulatory evaluation and assessment of technical documentation
• Contribute to renewal applications or annual reports
• Keep up to date with regulatory and other developments in the pharmaceutical industry, including relevant legislation and guidelines (EU, US and International markets) and pharmacopoeias.
• Support strategic projects such as technical transfers.
• Ensure that all documents and records pertaining to the RA CMC Lifecycle Department are archived properly. Keep departmental database or other tracking systems up to date.
• University degree, preferably be in possession of a master level of education in ‘Regulatory Disciplines’ or in other area, but pertinent with the field.
• 2-5 years of experience in CMC Regulatory Affairs or in another scientific role in the pharmaceutical industry.
• Knowledge on registration procedures and pharmaceutical regulation.
• Working independently with a moderate level of guidance and direction.
• Very good command of English, speaking and writing.
• Good IT skills.
• Ability to work in team.
• Communication skills with internal and external customers.
• Organisation skills.
• Accuracy in practice and attention to detail.
• 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
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