דרושים Analytical Scientist E & L R&d ב-טבע ב-Croatia, Zagreb

Data Governance & Backbone Enrichment

• Lead and manage data governance activities for the R&D analytical backbone.
• Support enrichment efforts across both backend and frontend layers of the analytical backbone.

Digital Platform Ownership

• Be assigned to relevant digital platforms and areas of need, including tools within the Microsoft 365 suite (e.g., Power BI, SharePoint, Power Automate) and AI-related platforms.
• Ensure platforms are effectively deployed, adopted, and maintained to meet business requirements.

Stakeholder Collaboration

• Collaborate closely with SHMs, Digital Leads, and cross-functional stakeholders to ensure alignment, adoption, and usability of digital tools and platforms.
• Act as a liaison between IT and business units to translate strategic needs into actionable digital solutions.

Within the scope of responsibilities:

• Drive implementations and continuous improvement of digital capabilities across R&D.
• Excels at cross-functional coordination – Working with IT, business units, vendors, and leadership.
• Maintain and enhance digital assets such as dashboards, SharePoint sites, and automation workflows.
• Facilitate knowledge sharing and training to promote digital literacy and platform usage.
• Participate in strategic planning and intake processes for new digital initiatives.
• Familiarity with Jira, Confluence & Sprints agile methodology

• Bachelor’s degree in Business or Software Engineering, or equivalent combination of education and related experience
• 2-3 years of experience as a business analyst managing multiple small to mid-sized projects with an understanding of digital offerings, including Power Platform, RPA and ML / AI capabilities
• Computer skills, especially with Project management software (Planisware, Jira, and/or Confluence), Excel, Powerpoint
• Must demonstrate ability to solve moderately complex problems and analyze and apply appropriate solutions. Identifies and solves problems by gathering and applying information from a variety of sources
• Project management skills in planning, milestone tracking & reporting
• Delivery oversight skillset mindset
• Stakeholder Management capabilities and customer facing approach.

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.

• Support the management of patient safety throughout different lifecycle stages of assigned Teva products, including retrieving and analyzing data to assist the review and evaluation of safety information (in collaboration with a Safety Physician, when applicable).
• Review and evaluate safety information associated with Teva products and provide medical and scientific input for (including but not limited to) Health Authority requests, signal evaluation documents and health hazard assessments.
• Participate in Product Safety Group (PSG) and coordinate all PSG related activities; support major safety issues escalations to senior safety governance committees as well as other forums attended by Teva’s senior management.
• Perform signal management activities related to assigned Teva products, including authoring of signal evaluations.
• Support risk management activities for assigned products globally and contribute to the preparation of Risk Management Plans (RMPs), REMS, design of additional risk minimization measures (ARRMs) as well as management of these plans throughout the product’s lifecycle. Contribute to measuring effectiveness of ARRMs.
• Author safety analysis and responses to HA requests.
• Take part in preparing and providing training to newcomers or other MSU/PV members in different topics as required.
• Take part in and/or lead internal and/or cross-functional working groups, projects, and/or forums.
• Review portions of, and contribute to, the writing of periodic reports (PSUR, PADER, AR) involving assigned products.
• Consult and work with other functional teams both within and outside of PV to help define strategies and plans for important milestones and activities in assigned products.
• Support of data analytics related activities within MSU, including contributing to improving data quality in PV database and supporting data retrieval activities (e.g., generation of reports, QC support, modification of line listings/tables)
• Develop and maintain expertise in the relevant therapeutic area and assigned Teva products.

• Bachelor’s degree in pharmacy, biology, veterinary medicine, nursing, paramedical studies degree or Pharm D
• Experience in patient safety/pharmacovigilance: solid knowledge in pharmacovigilance concepts, regulations and procedures
• Solid medical or pharmacological knowledge
• Advanced knowledge of Microsoft Office platforms
• Ability to work cross-functionally with an international team across multiple time-zones.
• Flexible to adapt to shifting team priorities
• Advanced communication skills in speaking and writing English

Temporary, 1-year contract

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.

• Design and execution of Extractable and Leachable (E&L) studies, incorporating LC/UV/MS or GC/FID/MS analytical techniques.
• Development and validation of analytical methods incorporating Mass Spectrometry detection (LC/MS or GC/MS).
• Support the characterisation of polymer materials used in medical devices and packaging, including inhalation and injectable drug products, for both small molecules and biopharmaceuticals.
• Assist in the interpretation of Mass Spectrometry (MS) data as part of compound identification studies.
• Instigate and drive scientific and technical investigations developing multidisciplinary approaches to solve wide ranging and complex problems.
• Compilation and review of detailed technical documents.
• Deliver high levels of customer service (both internal & external)

• Temporary (maternity leave cover)

• Degree, Masters or PhD qualification in Chemistry (or related discipline), with minimum 3 year’s work experience with analytical method development and validation.
• Experience in analytical method development and validation with mass spectrometry is highly desirable.
• Experience with Empower and MassHunter software is highly desirable.
• Excellent communicator (both oral and written).
• Experience of working to current Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) and implementing policies and procedures in line with regulatory guidelines.
• Knowledge of regulatory and compliance requirements.
• Good planning and organising skills, adaptable to changing priorities.

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.

Join Teva’s Combination Products & Devices (CPD) R&D Team – Shaping the Future of Drug Delivery. At Teva’s CPD team, we’re pioneering the development of advanced needle-based injection devices and cutting-edge technologies to deliver our portfolio of Small Molecule and Generic medicines. From Pre-Filled Syringes (PFS) to Autoinjectors and Pen Injectors, our diverse device portfolio supports both generic and specialty products across key therapeutic areas including Neuroscience, Immunology, and Endocrinology. Our work is organised into three product technology clusters, each broadly focused - though not exclusively - on a specific subset of injection devices:

• Cartridges & Pen Injectors
• Autoinjectors (AI)
• Pre-Filled Syringes & Safety Systems (PFS)

As Senior Device Engineer, reporting to one of the Engineering Team Leaders or to a Project Technical Lead, you’ll play a key role in ensuring our combination products are safe, effective, and compliant with global standards. You’ll apply best-practice engineering principles, Design Controls, and Safety Risk Management to guide products from concept through to production.

Your expertise in manufacturing technologies - such as plastic injection moulding - will be vital in preparing device designs for seamless transfer into production. You’ll bring creativity and problem-solving skills to tackle complex engineering challenges, while also contributing to the evolution of our departmental systems and influencing best practices across the team.

• Support the engineering design and development of drug delivery devices across various stages of development, including early research, design verification and validation, and life-cycle management.

• Ensure that products in your care are:
  • Engineered to be reliable and robust through the application of appropriate design, analysis, and testing methodologies.
  • Comprehensively specified, ready to be verified, and provide our submissions with objective evidence of compliance.
  • Documented in compliance with CPD’s Quality Management System.
• Lead or support Safety Risk Management activities, including:
  • Hazard identification.
  • Risk analysis and evaluation through the conduct of design Failure Modes and Effects Analyses (FMEAs).
  • Support to the Manufacturing, Science & Technology (MS&T) function in conducting process risk assessments.
• Lead or support technical design reviews to assess design robustness, safety, and documentation quality compliance.
• Lead or support investigations to identify root causes of device-related issues using established techniques such as Fault Tree Analysis and Design of Experiments.
• Contribute to the continuous improvement of departmental processes, including the development and maintenance of Standard Operating Procedures, guidelines, templates, and the introduction of new software tools.
• Mentoring and coaching capabilities, with the ability to support and guide junior colleagues as required.
• Responsible for the management of externally sourced engineering services, including oversight of associated budgets, timelines, and risk.
• Domestic and international travel may be required (approximately 10%) to support project activities, including visits to suppliers, Teva manufacturing sites, and other stakeholders.

• Bachelor’s degree (or higher) in Engineering, Scientific, or other relevant Technical discipline.
• Proven experience in the design, manufacture, and life-cycle management of medical devices or combination products from concept through to commercialisation (preferred), or equivalent expertise from a relevant regulated industry.
• A demonstratable high level of independence in executing engineering tasks, with minimal supervision. Proactively identifies additional activities required and exercises sound judgement in seeking peer support when appropriate.
• Training in Design Controls, medical device Safety Risk Management, and European Medical Device Directive/Regulations (preferred).
• Familiarity with statistical methods relevant to design input definition, verification and validation testing, including the determination of sample sizes proportionate to risk.
• Strong 3D spatial awareness and ability to visualise concepts, mechanisms, and assemblies.
• Working knowledge of SolidWorks 3D CAD software (preferred).
• Able to influence and educate peers and stakeholders; confident in professional judgement and decision-making.
• Bringing strong analytical skills with the ability to assess mechanisms and systems from a first-principles engineering perspective.
• Comfortable operating in dynamic environments, with the ability to adapt to change, manage uncertainty, and respond flexibly to evolving conditions.
• An effective verbal and written communication skills, including the ability to produce high-quality engineering documentation.

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.

• Provide legal counsel research and development activities, data privacy, and data transfer matters.
• Draft, review, and negotiate a wide range of R&D-related agreements, including
  • Consultancy and service agreements
  • Research collaborations and MTAs
  • Investigator-initiated studies
  • Licensing agreements
  • academic collaborations and research consortiums.
• Advise on regulatory compliance, transparency, pharmacovigilance, and inspection readiness.
• Collaborate with internal legal, IP, compliance, and privacy teams to ensure alignment with applicable laws, regulations, and internal policies.
• Contribute to continuous improvement of legal processes and templates.
• Support other legal projects and initiatives as needed.

• Master of Law or equivalent European / International legal degree; bar admission required.
• 3–8 years of relevant legal experience, ideally in a law firm, pharmaceutical company, or academic research setting.
• Solid understanding of legal and regulatory frameworks related to clinical research and drug development.
• Strong contract drafting and negotiation skills.
• Ability to assess complex legal issues and provide clear, actionable advice.
• Excellent communication and interpersonal skills with the ability to work effectively with stakeholders in different time zones;
• Team-oriented with a proactive, solution-focused mindset.
• Strong organizational skills and ability to manage multiple priorities in a fast-paced environment.
• High level of integrity, professionalism, and commitment to ethical conduct.

• Strong business acumen
• Techniques to work effectively under pressure, meet deadlines, and adjust to changing priorities.
• Ability to think strategically and tackle complex problems
• Ability to identify, advise on, minimize business risks, and propose practical solutions
• Strong customer-orientation; an ability to see issues from the point of view of others
• Ability to work successfully and cooperatively with colleagues across multiple cultures and time-zones
• Substantive experience in Word, Excel, and PowerPoint

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.

• Develop and deploy TPM methodologies, including Autonomous Maintenance and Focused Improvement
• Align TPM rollout with TLMS principles and site maturity levels
• Design and implement global reliability tools (e.g., FMEA, RCM, Root Cause Analysis)
• Lead cross-site benchmarking and best practice sharing for both technical and operational excellence solutions
• Support collaboration with Global TLMS Pillar leaders and drive proper synergies and integration with the rest of the journey
• Support cultural change and capability building in maintenance and engineering teams
• Collaborate with site teams to implement TPM pillars and measure impact on Overall Equipment Effectiveness and downtime
• Define (in coordination with global Key performance Indicators program), align and track TPM-specific Key performance indicators and improvement program/roadmaps
• Conduct reliability assessments and develop action plans to address identified gaps
• Facilitate workshops and training sessions to build TPM capabilities across sites
• Provide on the floor, hands-on support to tackle major losses for the sites. Coaching the team on how to tackle losses using the TLMS tools
• Monitor and report on the progress of TPM initiatives and their impact on operational performance
• Establish good engineering practices related to maintenance as well as building community of practices and knowledge hubs
• Co-design TPM roadmap and TPM steps evolution for advanced problem solving tools like Work point analysis, Advanced condition based analysis tools, In depth analysis on recurrent breakdown, etc.
• Support in person and remote Pillar assessment as key enable for site phase progression
• The role requires more than 30% travel time

You are

• A leader with demonstrated success in leading reliability improvement initiatives across all sites
• Someone with an analytical mindset and ability to interpret data and drive decisions
• Strong facilitator with coaching skills for cultural and behavioral change trough remote and on site support
• Experienced in conducting training sessions and workshops for engineering teams
• Fluent in English

You have

• Bachelor’s or Master’s degree in Mechanical, Electrical, Industrial Engineering, or related field
• More than 10 years of experience in maintenance, reliability, Operational excellence or continuous improvement roles in a manufacturing environment in pharma, food, or automotive industry
• Hands-on experience with Total Productive Maintenance implementation and Lean Manufacturing systems and related pillars
• Deep knowledge of maintenance strategies and reliability engineering principles
• Experience with tools such as Failure Mode and Effects Analysis, Reliability-Centered Maintenance, Root Cause Analysis, and Overall Equipment Effectiveness analysis
• Experience in implementing predictive maintenance strategies using SAP PM
• Proven track record in managing global spare parts inventory and optimization project
• Lean Manufacturing or Total Productive Maintenance certification (i.e. from Japan institute of Plant Maintenance or Black belt); Certified Maintenance & Reliability Professional (CMRP) or equivalent is preferred
• Proven experience in management of change for organizational and technical initiatives

VP, Head of Engineering Center of Excellence

Miha Pongrac
Human Resources

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.

• Provide legal counsel on clinical trials, data privacy, and data transfer matters.
• Draft, review, and negotiate a wide range of R&D-related agreements, including:
  • Clinical trial agreements
  • Informed consent forms
  • Consultancy and service agreements
  • Investigator-initiated studies
  • Research collaborations and MTAs
• Support academic collaborations and research consortiums.
• Advise on regulatory compliance, transparency, pharmacovigilance, and inspection readiness.
• Collaborate with internal legal, IP, compliance, and privacy teams to ensure alignment with applicable laws, regulations, and internal policies.
• Contribute to continuous improvement of legal processes and templates.
• Support other legal projects and initiatives as needed.

• Advantage - experience interacting with U.S. clinical sites and applying legal guidance on FDA regulations related to clinical trials obligations and ensuring alignment with FDA expectations in global R&D activities.

• Master of Law or equivalent European / International legal degree; bar admission required
• 3–8 years of relevant legal experience, ideally in a law firm, pharmaceutical company, or academic research setting
• Solid understanding of legal and regulatory frameworks related to clinical research and drug development
• Experience supporting U.S.-based clinical trials and regulatory related submissions is a strong advantage
• Strong contract drafting and negotiation skills
• Ability to assess complex legal issues and provide clear, actionable advice
• Excellent communication and interpersonal skills with the ability to work effectively with stakeholders in different time zones, especially in the US
• Team-oriented with a proactive, solution-focused mindset
• Strong organizational skills and ability to manage multiple priorities in a fast-paced environment
• High level of integrity, professionalism, and commitment to ethical conduct

• Strong business acumen
• Techniques to work effectively under pressure, meet deadlines, and adjust to changing priorities
• Ability to think strategically and tackle complex problems
• Ability to identify, advise on, minimize business risks, and propose practical solutions
• Strong customer-orientation; an ability to see issues from the point of view of others
• Ability to work successfully and cooperatively with colleagues across multiple cultures and time-zones
• Substantive experience in Word, Excel, and PowerPoint

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.