

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.
משרות נוספות שיכולות לעניין אותך

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.

As an, you will oversee a team responsible for managing the end-to-end regulatory artwork process for pharmaceutical and non-pharmaceutical products across Europe. In addition to your leadership responsibilities, you’ll remain actively involved in daily operations—ensuring high-quality service delivery and compliance with regulatory standards.
• Lead and support a team of Artwork Coordinators Markets, ensuring effective workload distribution and team development
• Oversee the end-to-end regulatory artwork process, including initiation, review, and approval of packaging artworks
• Actively contribute to daily operations (approx. 50% of the role), maintaining hands-on expertise and supporting peak periods
• Collaborate with internal stakeholders across markets, artwork studios, and regulatory teams to ensure timely and compliant delivery
• Monitor team performance, identify improvement opportunities, and contribute to process optimization initiatives
• Higher education in Life Sciences, Healthcare, Business Administration, or a related field
• 3+ years of relevant experience, including 1–2 years in a leadership role
• Strong organizational, communication, and stakeholder management skills
• Proficiency in Microsoft 365 and experience with document management systems
• Advanced English; additional languages are a plus
• Strong compliance awareness
• 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.

The Cyber Security Solutions Architect has the expertise and hands-on experience in multiple technical areas across various IT domains. He or she has broad industry knowledge, stakeholder engagement experience and can deliver complex tasks or solutions.
• Hands-on Integration of various security tools and technology.
• Planning and executing multi-faceted large scale and enterprise-wide security projects in accordance with established policies, regulations, and cycle best practices.
• Translate business requirements into secure, scalable, and cost-effective technical solutions.
• Develop and maintain security architecture blueprints, standards, and guidelines.
• Perform security assessments of new technologies, tools, and integrations.
• Act as a trusted advisor to senior stakeholders, providing guidance on risk, threats, and remediation strategies.
• Provides recommendations to the various business units regarding current and future cyber security policy considerations and technologies, based on ongoing requirement and the evolving threat environment.
• Work with different departments in the company to reduce risk. Plans and conducts consultation with users, management, vendors, and technical staff to assess computing needs and system requirements that may affect the client’s cyber security posture.
• Establishing clear roles, responsibilities, lines of authority, communications, and accountability among staff.
• Utilization of program and project management best practices. Identifying staff development and training needs and ensure that training, mentoring, and hands-on assistance is available to raise the talent/skill level of staff as appropriate.
• Assist with collecting customer business and technical requirements and determining recommended solution(s).
• Build and review Statement of Work (SOWs), RFI, RFP and ensuring quality and accuracy.
• 7+ Years of experience as a Senior Security Engineer/Security Architect, or 10+ years of Security oriented sys admin experience.
• Deep understanding of information security principles, concepts, and best practices.
• Understanding of network architecture, protocols, and security measures.
• Project management skills for leading large-scale, cross-functional security initiatives.
• Familiarity with a wide range of security technologies, tools, and platforms, such as firewalls, PAM, ITDR, IPS, DNS Security, SSE, SIEM systems, and encryption technologies.
• Strong background in designing secure architectures for enterprise-scale systems.
• Understanding of cloud security principles.
• 5+ years of experience with installation integration and deployment of enterprise applications in client environment.
• Understanding of identity and access management solutions.
• Knowledgeable with 3 or more of the following domains: Firewalls\IPS, Web content, endpoint protection, PAM, CDR, ITDR, SSE.
• Ability to document architectures and technical solutions in a clear, structured manner.
• Knowledge of Zero Trust principles and security frameworks (NIST, CIS, ISO 27001).
• Proficiency in threat modeling, risk analysis, and security assessments.
• Experience with Cybersecurity Operations, policy, procedures, and processes.
• Strong communication and stakeholder management abilities.
• One or more of the following or similar domain certifications: CCSA, CCSE, MCITP, CISSP – Advantage
• +3 years of experience working with account management on various platforms such a Windows Active Directory, Entra ID, network devices, databases and storage systems.
• Experience troubleshooting applications and scripts by accessing and analyzing logs on UNIX and Windows servers.
• Experience working with GxP frameworks and methodologies – Advantage.
• Hard working, motivated, self-learner with strong inter-personal and out-of-the-box thinking.
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.

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.
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.

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
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.

ESSENTIAL AREAS OF RESPONSIBILITY
The following areas of responsibility are essential to the satisfactory performance of this position by any incumbent, with reasonable accommodation if necessary. Any nonessential functions are assumed to be included in other related duties or assignments.
Proactively share knowledge, ideas, and best practices with cross-functional partners and demonstrate openness to others' ideas
POSITION REQUIREMENTS
Any equivalent combination of education, training, and/or experience that fulfills the requirements of the position will be considered.
Education/Certification/Experience
Skills/Knowledge/Abilities
TRAVEL REQUIREMENTS
Regular travel, which may include air travel and weekend or overnight travel
The annual starting salary for this position is between $88,000 – $170,000 annually. Factors which may affect starting salary within this range and level of role may include geography/market, skills, education, experience and other qualifications of the successful candidate.
We offer a competitive benefits package, including:

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.
משרות נוספות שיכולות לעניין אותך