דרושים טבע תעשיות פרמצבטיות

Perform experiments for the development and implementation of biological and immunological assays and related tasks including but not limited to samples analysis, data analysis, documentation, archive and SOP preparation.
Review scientific literature and relevant pharmaceutical regulatory guidelines to plan and perform the development of bioassays.
Draft and review protocols and reports in compliance with pharmaceutical regulations and Teva internal guidelines.
Ensures lab notebooks and documents are complete, signed and stored appropriately.
Work with the Team Leader in identifying, studying, communicating and solving problems in biological assays development and sample analysis
Work with interfaces within Teva.
Track each project milestones to ensure deliverables needed on Time.
Work under pressure to meet projects timelines.
Participate in laboratory maintenance.

Manage and lead RA team.
Key Responsibilities / Deliverables:
Manage and lead RA team in preparing submissions for US, EU and CA markets and responding to deficiency letters.
Review submission files and deficiency letter responses.
Provide regulatory guidance, support and resolve issues raised during product development and review period.
Ensure teams regulatory activities are carried out and tracked on a timely manner.
Support pre-launch activities.

Define & maintain a long term strategy for the api networks as a whole. Build and maintain a long term strategy for each individual site.
General duties and responsibilities.
Work with pillar leadership to define the design principals for the api Network (Capacity & technology siting, product allocation framework).
Support pillar and site functions in the development of long range site plans through clear communication of site strategy, portfolio requirements & network assumptions. Work with global, pillar & site functions to facilitate identification of key initiatives & capabilities required to execute the site plan.
Build and implement Governance Processes for the execution and maintenance of the agreed strategy.
Prepare analysis and recommendations on strategic topics to support discussion & decision making by Senior Management.

Responsibilities include scheduling, coordinating and performing internal audits in assigned areas to determine the effectiveness of internal controls, efficiency of operations, and compliance with company policies and procedures and the legislations.

This position will assist the audit team leaders in establishing and implementing a Global Integrated Audit Program that is consistent with Teva's Guidelines and Policies, Tevas Code of Business Conduct, and Global Anti-bribery/Anti-corruption Laws and Regulations.

Mission and roles:
Support the review of 3rd party Batch Manufacturing Records and analytical data.
Support review of stability studies.
Data consolidation and organization to enable statistical analysis.
Support data entry into different data base platforms.
Support statistical and trend analysis.
Support the preparation of regulatory documentation prior and post submission /approval.
Support with review, harmonization and alignment of specifications documents for commercial and pipeline products prior and post submission /approval.
Facilitate collaboration with other functions and individuals in Teva's Bio Operation teams.
Participate and contribute to cross-functional meetings.
Part time position in our Tel Aviv HQ.