דרושים ב-Teva ב-Chile, Santiago

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.

This position will be responsible for several site wide EHS programs and processes to safeguard employees and surrounding communities and to ensure that all facilities are in compliance with regulations. Responsibilities are within the EHS function as a generalist or in a combination of disciplines.

TRAVEL REQUIREMENTS:

• Uses best practices and knowledge of internal or external business issues to improve products/services or processes
• Often leads the work of project teams
• Requires in-depth knowledge and experience in general safety, occupational health and environmental regulations
• Solves complex problems independently; takes a new perspective using existing solutions
• Works independently; receives minimal guidance
• EHS training presentation skills
• Assists in emergency response and preparedness 24/7
• Responsible for OHSA related Programs
• Responsible for the occupational health programs including:
o Industrial hygiene
o Medical surveillance
o Hearing conservation
o Chemical management program
o Process containment
• Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
• Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
• Responsible for performing additional related duties as assigned.

Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered.

Education/Certification/Experience:
• Requires Bachelor’s degree in Science, Engineering or equivalent from an accredited college or university and a minimum of 3-5 years relevant progressive experience in the pharmaceutical industry.
• Requires a minimum of 7 year of experience in an environmental or safety and regulatory compliance experience, preferably in food, drug or cosmetic industry.
• CIH or CSP preferred
• Requires experience with Federal, state, and local regulations relative to environment, health, and safety (OSHA, EPA, FL DEP, etc.).
o General Safety
o Occupational Safety
o Process Safety
o Environmental Regulation
• Knowledge of Current Good Manufacturing Practices (cGMP) a plus

Skills/Knowledge/Abilities:
• Implementing goals, objectives and practices for effective, efficient and cost effective management of allocated resources.
• Writing, preparing and presenting safety related regulatory programs.
• Preparing clear and concise reports and/or proposals related to safety and regulatory compliance programs.
• Communicating clearly and concisely, both orally and in writing, with all levels personnel.
• Establishing and maintaining cooperative working relationships with those contacted in the course of work.
• Operating a personal computer, including working knowledge of Microsoft Office.
• Ensuring compliance with all Company policies and procedures, including safety rules and regulations.
• Developing and delivering training of all levels of personnel in the areas of safety and regulatory compliance.
• Self-starter; Results driven; Anticipate/initiates and implements solutions.
• Adheres to professional standards and company code of conduct.
• Must be comfortable in a fast paced environment
• Ability for scheduling flexibility to cover different work shifts (24 hours a day/7 days a week).
• Required to be on call 24 hours for emergency response needs.
• Training and presentation skills, techniques, applications and practices.

Problem Solving:
• Analyzing problems, identifying alternative solutions, and implementing recommendations in support of Company safety goals and objectives.

We offer a competitive benefits package, including:

Comprehensive Health Insurance: Medical, Dental, Vision, and Prescription coverage starting on the first day of employment, providing the employee enrolls.

Time Off: Paid Time Off including vacation, sick/safe time, caretaker time and holidays.

The total compensation may also include restricted stock units and discretionary awards, depending on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

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.

• Serve as an IT liaison and business process expert in the areas of supply chain, operations, inventory management, lab systems and quality. Analyzing the business needs, validating solutions with the client, and working with local and regional IT to support the critical aspects of the business.
• Maintain focus on process analysis and re-engineering with an understanding of technical problems and solutions and the relationship to the business and technical environment.
• Collaborate with customers, staff, regional IT colleagues, and other stakeholders to support existing processes and technologies in the supply chain, operations and quality areas. Identify customer requirements; assess impacts to the delivery and development of applications and other IT functions. This may involve some or all lab systems, engineering systems, or both, depending on the site(s) supported and other resources supporting the site(s).
• Administer and support all laboratory computer systems – LIMS (Labware), CDS (Empower), standard-alone computerized instruments and other applications identified by laboratory management. Support interfaces to these systems and troubleshoot as required.
• Develop and support appropriate administration and master data maintenance processes and procedures to ensure efficient day-to-day laboratory system operation.
  Develop, maintain and deliver appropriate training modules for laboratory systems. Act as a key site expert of laboratory processes to provide appropriate knowledge to laboratory system implementations.
• Support the implementation and ongoing use of MES, serialization, and OEE systems. Knowledge of ERP systems such as SAP is required to understand the key interfaces for MES and Batches / Dispensing systems.
• Administer local systems as necessary. Work to a local / global support model for day-to-day administration; not compromising the data integrity of these systems.
• Maintain the integrity of global and local systems and ensuring backup up solutions are in place by the global or local ITMUs using standardized solutions.
  Consider all regulatory compliance requirements for system implementation and maintenance including GMP, computer systems validation, SOX, security and risk. Assist in the generation and execution of validation deliverables.
• Ensure appropriate service levels are developed and monitored for support of global and local systems working with the global team, external partners and providers of software. Ensure support partners perform

• Careers IT related or engineerings
• 4+ years of experience in pharmaceutical or related manufacturing industry and Supply Chain, Operations, Quality, Enterprise Asset Management, and Costing functions is a plus.
• English is a plus
• Experience in systems related to the pharma industry

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.

• E2E Supply Chain Execution:
• Forecasting & Inventory Optimization: Drive forecasting accuracy and demand planning excellence through close collaboration with Commercial, Finance, and Global Supply Chain teams. Lead initiatives to optimize inventory levels and replenishment cycles.
• Cost Management & Budget Oversight: Own and manage the local supply chain and logistics cost base. Lead budget planning, execution, and monitoring to ensure fiscal responsibility and cost efficiency.
• 3PL & Logistics Partner Management: Oversee the selection, performance, and continuous improvement of third-party logistics providers (3PLs). Ensure service levels and contractual obligations are met through robust KPI monitoring.
• KPI & Operational Excellence: Define and track key performance indicators (KPIs) across all supply chain functions. Lead continuous improvement initiatives to enhance efficiency, agility, and service quality.
• External Supplier Management: Collaborate closely with the Import Hub to ensure a reliable, efficient, and agile supply chain for imported products.

• Strategic Leadership & Alignment: Develop and implement a best-in-class local supply chain strategy aligned with Teva Chile's Commercial goals and the broader LATAM cluster and Global Supply Chain strategy.
• Cross-Functional Collaboration: Collaborate with Commercial, Regulatory, Quality, Finance, and Global Supply Chain teams to ensure integrated planning and responsive execution.

• Bachelor’s degree in Supply Chain, Engineering, Business Administration, or related field; MBA or Master’s preferred
• Minimum 8–10 years of experience in supply chain management, with significant leadership responsibilities in the pharmaceutical or healthcare industry
• Strong knowledge of demand planning, inventory control, S&OP processes, and logistics
• Proven ability to manage complex supply networks and external partners
• Strong financial acumen and experience managing supply chain budgets
• Fluent in Spanish; English proficiency required

Sr Dir of SC, LATAM Region

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.

• E2E Supply Chain Execution:
• Forecasting & Inventory Optimization: Drive forecasting accuracy and demand planning excellence through close collaboration with Commercial, Finance, and Global Supply Chain teams. Lead initiatives to optimize inventory levels and replenishment cycles.
• Cost Management & Budget Oversight: Own and manage the local supply chain and logistics cost base. Lead budget planning, execution, and monitoring to ensure fiscal responsibility and cost efficiency.
• 3PL & Logistics Partner Management: Oversee the selection, performance, and continuous improvement of third-party logistics providers (3PLs). Ensure service levels and contractual obligations are met through robust KPI monitoring.
• KPI & Operational Excellence: Define and track key performance indicators (KPIs) across all supply chain functions. Lead continuous improvement initiatives to enhance efficiency, agility, and service quality.
• External Supplier Management: Collaborate closely with the Import Hub to ensure a reliable, efficient, and agile supply chain for imported products.

• Strategic Leadership & Alignment: Develop and implement a best-in-class local supply chain strategy aligned with Teva Chile's Commercial goals and the broader LATAM cluster and Global Supply Chain strategy.
• Cross-Functional Collaboration: Collaborate with Commercial, Regulatory, Quality, Finance, and Global Supply Chain teams to ensure integrated planning and responsive execution.

• Bachelor’s degree in Supply Chain, Engineering, Business Administration, or related field; MBA or Master’s preferred
• Minimum 8–10 years of experience in supply chain management, with significant leadership responsibilities in the pharmaceutical or healthcare industry
• Strong knowledge of demand planning, inventory control, S&OP processes, and logistics
• Proven ability to manage complex supply networks and external partners
• Strong financial acumen and experience managing supply chain budgets
• Fluent in Spanish; English proficiency required

Portal de carrera interno está disponible en tu red doméstica. Si tienes dificultades para acceder a tu cuenta de EC, contacta con tu RRHH/ IT locales.

• To be the local medical contact point for the Therapeutic Areas (Therapeutic Areas), responsible for the medical and scientific support to current and future commercialized products, and management of problems of current medications.
• Close collaboration with the Regional Medical Directors (Therapeutic Area) to support them in the coordination and execution of the general medical strategy from the start of the pre-launch activities until several years after the launch.
• Interconnect effectively with other Local functions, including Commercial, Regulatory Affairs, R & D and Pharmacovigilance, among others.
• Integrate equipment with the Product Managers of the assigned therapeutic areas, giving medical-scientific support at a strategic and tactical level, and contributing in the elaboration of the marketing plans.
• Participate in making strategic decisions in their area and in their implementation, taking into account global, regional and local product strategies.
• Collaborate with the development of clinical research (if any), ensuring alignment to business needs and company policies.
• To be the medical-scientific contact in your area for clients and other external partners, as well as to act as liaison between the company and opinion leaders, medical societies, the scientific community and the academic community in general.
• Participate in the training of the Medical Prompting, Sales and Marketing team of their assigned therapeutic area.

• University degree in health careers such as Medicine.
• Experience of at least one year in relatable roles in pharmaceuticals (Desirable) or as MSL.
• Possess advanced level of English (A must)

Sr Dir Medical Affairs

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.