ytical Researcher I

Who weare

Together were on a mission tomake good health more affordable and accessible to help millionsaround the world enjoy healthier lives. Its a mission that bondsour people across nearly 60 countries and a rich diverse variety ofnationalities and backgrounds. Working here means working with theworlds leading manufacturer of generic medicines and the proudproducer of many of the products on the World Health OrganizationsEssential Medicines List. Today at least 200 million people aroundthe world take one of our medicines every single day. An amazingnumber but were always looking for new ways to continue making adifference and new people to make a difference with.

The opportunity

Finished product testing and analytical methoddevelopment by HPLC GC IC UV etc.

Analyticalmethod validation and transfers analysis of API Finished product RDsamples.

How youll spend your day

• 1. Analysis of Solid oral dosage i.e.Dissolution Assay CU BU and Related substancesetc.
• 2. Analysis of samples received fromFormulation department (samples include inprocess finished productpreformulation study samples and stability samplesetc.).
• 3. To carry out analytical methoddevelopment and method validation inprocess samples and finishedproducts.
• 4. To carry out analytical methodtransfer activity to QC Goa.
• 5. Handling andtesting of hipotent compounds/molecules.
• 6.Trouble shooting of analytical instruments for difficulties facedduring daytoday operations.
• 7. Calibration andmaintenance of analytical instruments. Maintenance includesactivities such as Qualification keeping track of AMC HistorySpares Usage records etc.
• 8. Literature Searchfor development of analytical methods.
• 9. Toensure that all activities undertaken are executed in the frameworkof good laboratory and documentation practices and the existingquality systems are adhered.
• 10. To ensure safepractices are followed during the of activities and strictadherence to the EHS systems of the site.

Your experience andqualifications

• M.Sc./ M. Pharm./Ph.D.
• 48 Years relevantexperience
• Sound knowledge of Chemistry andanalytical method development method validation and transferInstrumental method of analysis and logicalapproach.
• Hands on experience on Instrumentsviz. GC HPLC Ion Chromatography UV and Dissolution apparatusetc.
• Knowledge of regulatory requirements fordifferent markets (US EU Canada etc.)
• Knowledge on ICH guidelines forced degradation studies impurityprofile etc.
• PersonalAttributes
• Basic communicationskills
• Must be honest andtrustworthy.
• Berespectful.
• Possess cultural awareness andsensitivity.
• Outgoing personable responsibleselfmotivated and confident

Tevas Equal Employment OpportunityCommitment

Teva Pharmaceuticalsis committed to equal opportunity in employment. It is Tevas globalpolicy that equal employment opportunity be provided without regardto age race creed color religion sex disability pregnancy medicalcondition sexual orientation gender identity or expression ancestryveteran status national or ethnic origin or any other legallyrecognized status entitled to protection under applicable laws. Weare committed to a diverse and inclusive workplace for all. If youare contacted for a job opportunity please advise us of anyaccommodations needed to support you throughout the recruitment andselection process. All accommodation information provided will betreated as confidential and used only for the purpose of providingan accessible candidateexperience.

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RemoteWork :

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