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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.
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As Associate Director Legal Ix, you will:
Senior Director General Counsel Europe Commercial Ix
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 Associate Director Legal Ix, you will:
Senior Director General Counsel Europe Commercial Ix
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
These jobs might be a good fit

Share
As Associate Director Legal Ix, you will:
Senior Director General Counsel Europe Commercial Ix
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 design, implementation and stabilization of advanced analytics' solutions in Global Supply chain.
- Relevant university degree- bachelor's or master's degree
- High level of analytical capabilities
- 10 years of experience in supply chain functions (preferably with both market and site supply chain)
- Experience with advanced analytics projects and self-service tools is an advantage
- Project management capabilities
- Ability to work in a changing and dynamic environment
- Excellent level in English - reading, writing, speaking
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
- Relevant university degree- bachelor's or master's degree
- 10+ years' experience in pharmaceutical or related industry
- Strong knowledge of backup technologies (e.g., Veeam, Commvault, NetBackup, Azure Backup).
- Expertise in storage technologies (EMC, NetApp, Hitachi, etc.)
- Familiarity with cloud storage solutions (AWS, Azure, Google Cloud)
- Leadership Skills: Experience in managing and mentoring IT teams.
- Problem-Solving: Ability to troubleshoot backup failures and optimize recovery processes.
- Communication: Strong verbal and written communication skills for reporting and collaboration.
- Certifications: Relevant certifications such as Microsoft Certified: Azure Administrator Associate, VMware Certified Professional, or Commvault Certified Engineer are a plus.
- Proven global experience in leading large scale IT units
- Proven experience in project planning, methodology, budget and AOP
- Experience in managing IT Operations & Infrastructure teams
- Proven ability to lead a large, diverse, global team (~17+ employees) of operators managing 24x7 operations covering multiple data centers and regional sites
- Strong understanding of data integrity, security, and availability principles
- Experience in developing automated solutions for storage management
- Project management capabilities
- Ability to work in a changing and dynamic environment
- Readiness for international travels as needed- about 20 to 30%
- Excellent level in English - reading, writing, speaking
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
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