Jobs at Teva in India, Greater Noida

• Excellent communication and with hands on experience.

• Having working experience of analytical method development/ validation for HPLC/GC test methods, from different markets.

• Troubleshooting/OOS investigations during validations.

• Having a good knowledge of HPLC, IR, UV, KF Titrator, Halogen Moisture analyzer, Polarimeter and wet analysis

• Having good knowledge of HPLC trouble shooting.

• Sound knowledge of Organic Chemistry & Spectroscopy.

• Having a good knowledge of HPLC Method development of API/RM/KSM and SM using various detector like Mass, IR, CAD, ELSD, UV-PDA and UV.

• Structure elucidation and Identification and characterization of APIs, known and unknown impurities

• and intermediates by various spectroscopy techniques.

• Data interpretation by NMR, Mass Spectrometer, DSC, TGA & FTIR

• Having a sound knowledge of Analytical method validation.

• Hands on experience of various Analytical Instruments-Coulometer, FT-IR, UV, Karl Fisher, Halogen Moisture Analyzer etc., >sound knowledge of Organic Chemistry & Spectroscopy.

• MSc (Organic chemistry/Analytical chemistry)

• 4- 7 years

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.

Leadership and Strategy:

• Develop and execute a comprehensive logistics strategy aligning with the organization’s global goals
• Lead and mentor a team of logistics managers (Imports, Exports) and professionals to achieve operational excellence
• Drive cross-functional collaboration to ensure seamless integration of logistics with production, warehousing, and procurement team

Import and Export Operations Management:

• Oversee the entire import and export lifecycle, including raw materials, finished goods, and capital equipment
• Ensure compliance with local and international regulations, including customs laws, drug laws, and export control standards

Regulatory and Compliance Management:

• Build and maintain strong relationships with customs officials, government agencies, and other regulatory authorities
• Ensure adherence to Export Oriented Unit (EOU) protocols, Free Trade Warehousing Zone (FTWZ) regulations, and duty exemption schemes
• Stay updated on regulatory changes and implement process adjustments to maintain compliance

Management of Government Incentive Schemes:

• Identify, interpret, and leverage government incentive programs applicable to export-oriented businesses, including MEIS, RoDTEP, and duty drawback schemes
• Expedite applications and claims for financial incentives and tax refunds under applicable government policies

Stakeholder and Vendor Management:

• Collaborate with suppliers, freight forwarders, and third-party logistics (3PL) providers to ensure seamless operations
• Negotiate contracts and service agreements to achieve optimal costs and service quality

Continuous Improvement and Technology Implementation:

• Drive process improvements to enhance logistics efficiency and reduce lead times
• Implement advanced logistics software & other digital initiatives, including ERP and freight management systems, for tracking, planning, and reporting

• Bachelor’s degree in Supply Chain Management, International Business, or a related field (MBA preferred)
• Minimum 15 years of logistics experience, with at least 5 years in leadership roles in the pharmaceutical industry
• Proven track record in managing large-scale import and export operations and multi-location supply chains
• Certifications in Logistics or Supply Chain Management (e.g., CSCP, CILT)

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.

• Do Literature search for a given step(s)/molecule (STN/Sci finder)
• Organize for relevant patents and papers from literature
• Develop a most economical/eco-friendly commercially viable technology at bench scale
• Co-ordinate with Analytical members and prepare reports like safety
• Upscale developed technology at Kilo Lab/Pilot /Plant Scale and to take care of up-scaling problems

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.

• To work as part of team
• Do Literature search for a given step(s)/molecule
• Organize for relevant patents and papers from literature and to organize/ order raw materials /chemicals from different vendors/Plant etc.
• Develop a most economical/eco-friendly commercially viable technology at bench scale
• Co-ordinate with Analytical members
• To prepare reports like safety
• Upscale developed technology at Kilo Lab/ Pilot /Plant Scale and to take care of up-scaling problems
• Develop own skill by way of reading/attending seminars etc. and to maintain discipline and dignity of the organization
• Contribute novel ideas by way of participation during technical discussion
• To meet the EHS and compliance expectations

• PhD/M.Sc. - Organic Chemistry
• 6 -10 yrs of work exp into R&D (For M.Sc.)
• 2.5 - 5 yrs of exp (PhD)

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.

Policy & Regulatory Research:

• Research support on various regulatory and policy matters such as upcoming policies, new regulations and notifications & prepare recommendations on draft policy/regulations for submission directly or through industry associations
• Include research from journals/newsletters/online research/social media such as twitter, and other relevant platforms & tracking of news/notifications/union budget/election results/political & economic updates etc., and preparation of its related summary communication for dissemination to concerned internal stakeholders
• Tracking national/international developments related to TAPI business
• Timely coordination with team for preparation and circulation of Monthly reports to leadership, documents for important and other meetings
• Preparation of monthly policy and regulator monitors, annual policy report,whitepapers, reports, leadership advisories etc.
• Engagement support in policy outreach with relevant external stakeholders

Partnering with Sites & BU leads:

• Support the unit location teams on projects, government communications, monthly reports, trackers, strategy documents, stakeholder mapping, briefing books etc.
• Coordinate for projects including business transfer, major approvals, special projects etc.
• Timely support to the international business team for meeting with external stakeholders, pending payment issues, information on FTAs etc.
• Extend support for coordination with personnel involved in liaison/dealing with authorities from site

Engagement with External stakeholder and Industry Associations:

• Ensuring positive external stakeholder engagement on relevant business matters and regular engagement with Industry Associations
• Engage in policy outreach for key policy/regulatory matters with relevant external stakeholders - Industry associations, government officials
• Track and ensure participation in key industry events/forums/state level investment summits. It will include identification of thought leadership forums and evaluation of same (for Teva leadership and relevant businesses) with a focus on Teva's priority areas
• Providing support in management of critical legal issues in conjunction with the legal team

Community Development Programs/Corporate Social Responsibilities:

• Identifying the initiatives for community development as part of the overall strategy and within the purview of the applicable laws and norms
• Partner with NGOs/agencies and implementation partners for program effectiveness
• Validate, qualify and propose projects to the committee for approvals and implementation
• Administer the progress of key performance indicators and publish periodic reports
• Guide the site teams on the overall strategy and ensure adherence with the global donation policy
• Conduct periodic audits to ensure effectiveness of the programs and utilization of the funds
• Ensure adequate documentation and process governance
• Single point of contact for all community development related queries and solutions

• Masters in Mass Communication/Business Administration/Economics or any other Master Degree
• 15 to 20 years (Corporate Affairs)in Pharmaceutical industry and Manufacturing business

Sr Director Head of Develop API R&D, Global R&D

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 available in our state-of-the-art R&D center in Greater Noida.

Validation of a new global ELN system for the R&D organization. It is starting from building the system and implementation in all the R&D sites. Once implemented completely, then to manage the system validation maintenance and change management of further enhancements. Support with some additional CSV activities for TAPI sites.

• Software Validation - Validation Plan definition, URS/FS/DS, Risk Assessment, Testing Plan and Scrips, Testing Execution, PQ / User Acceptance testing guidance and support, Validation Summary Report, system WI/SOP.
• Validation state maintenance. Periodic Reviews of Laboratory Applications Systems with respect to compliance to SDLC, User permissions and data integrity controls.
• Activities and Documentation of Data Integrity controls, Back-Up/Restore processes, Disaster Recovery processes and User Management processes on Laboratory Application Systems.
• Understanding system requirements, discussing business process / proposals / implementation issues / data security / data integrity / compliance to application guidelines, etc.
• Documenting the changes and new developments as per the documentation standards.
• Compliance with GxP Guidelines, Good Documentation practices & activities.

• Background in computer science or similar IT background, or a background in chemistry or related scientific field
• 2-5 years of experience working with CSV within the pharmaceutical or biotech industry.
• Expertise in Pharma Laboratory Application Systems - User Management, BackUp/Restore processes, Data Integrity Controls as per GxP Compliance.
• Experience in software validations.
• Experience with HP gALM system & understanding of SDLC structure.
• Documentation related to Quality processes such as Change Controls, CAPA, Deviations and Investigations.
• Knowledge of GAMP5 and regulatory guidelines such as 21 CFR Part 11, EU Annex 11, etc.
• OS: Windows
• Basic knowledge of LAN / WAN
• Basic knowledge of Servers / Switches / Routers
• Strong experience with Microsoft Office application
• Exposure to File Server/Network Shared Drives/Shared Multifunction Devices

TAPI IT QA & R&D Lead

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.

• Perform Polymorph screening as per guideline & follow cGMP Documentation and EHS compliance at workplace
• Perform Virtual and Experimental Screen and evaluate all literature that relates to solid-state issues & screen new forms by performing stress tests and File ASAP new forms in patent application
• Analyze laboratory samples by XRD, DSC, TGA and other characterization techniques
• Assess kinetic stability and interconversions and produce scheme of all polymorphic transitions
• Produce solubility curves of different polymorphs and assess thermodynamic stability relationships
• Develop detection methods to assess polymorphic purity and monitor in the laboratory samples
• Support the development of the crystallization process with full characterization
• Monitoring stability and physical properties of micronized/milled materials
• Perform calibration, method development, method validation, and troubleshooting using various instruments like PXRD, DSC, TGA and Particle size analyzer
• Knowledge of various regulatory guidelines w.r.t. method development, product development, and documentation

• M.Sc. Chemistry/B Tech (Chemical Engineer) with 1-5 years of experience in relevant industry and profile

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.