Operator - Tapi jobs at Teva in India

• Carrying out dispensing activities as per applicable procedure.

Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards.

• Responsible for recording the observations of reaction parameters on the batch card as per approved procedure.
• Filling of all the batch cards (production cleaning) as per approved instructions.
• Ensure verification of pH meters and weigh balances as per applicable procedures.
• Maintain work procedure, safety precaution and cGMP.

Ensure housekeeping of plant and cleanliness of the equipments, update the equipmentReport accidents and irregularities at the work station to the Shift Officer.
• Knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives

2 to 3 years – Msc. ( Chemical) 0 to 2 years - B.Tech / B.E / Diploma(Chemical)

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.

• Carrying out dispensing activities as per applicable procedure.
• Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards.
• Responsible for recording the observations of reaction parameters on the batch card as per approved procedure.
• Filling of all the batch cards (production cleaning) as per approved instructions.
• Ensure verification of pH meters and weigh balances as per applicable procedures.
• Maintain work procedure, safety precaution and cGMP.
• Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards .
• Coordination of production tasks to meet assigned schedule
• Knowledge of Liquide chromatography Operations.

• 3-5 Years – M.SC
  0.5 to 3 years - B.Tech / B.E (Chemical)
• 24/7 Shift

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.

• Carrying out dispensing activities as per applicable procedure.

Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards.

• Responsible for recording the observations of reaction parameters on the batch card as per approved procedure.
• Filling of all the batch cards (production cleaning) as per approved instructions.
• Ensure verification of pH meters and weigh balances as per applicable procedures.
• Maintain work procedure, safety precaution and cGMP.

Ensure housekeeping of plant and cleanliness of the equipments, update the equipmentReport accidents and irregularities at the work station to the Shift Officer.

• Extensive equipment knowledge to perform trouble shooting and root cause analysis. Develops solutions to complex problems requiring resourcefulness and creativity/innovation and ensures solutions are consistent with organization’s objectives.

• 2-4 Years - Diploma (Chemical)3-5 Years – M.SC
  0.5 to 3 years - B.Tech / B.E (Chemical)
• 24/7 Shifts

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.

• 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.

Regularly generate and deep-dive analyze Costing processes, variance analysis, Annual Operating Plan (AOP), Latest Best Estimation (LBE), month-end reporting & presentation, monitor Cost of Raw Materials and Production, Diagnose the Cause of Inventory Variance, Stock take variance analysis (PV), Create and Archive Monthly Journal Entries. Responsible for review and analysis of inventory transactions to ensure integrity of inventory value, COGS, and inventory adjustments & provisioning. Developed analysis tools to enhance review of changes to part cost, purchase price variance, to ensure accurate financial reporting of inventory.

Communication and (internal) stakeholder management with higher management levels within the Global Teva organization is required in this process.

• Technical/functional knowledge in Costing, Inventory, Accounting and closing & reporting process area, with strong background of USGAAP
• Managing all Costing & inventory related activities including accounting policies and memos, cost accounting and write offs, their reporting and balance sheet reconciliations.
• Full responsibility for the initial set-up and carve in of all Costing & inventory accounting activities into the Global Business Services. Therefore tight communication and collaboration with local, regional and global accounting teams where needed
• Supervise and oversee the group’s Costing / Inventory and cost of goods sold journal entries
• Be fully accountable for all the Costing processes & Inventory accounting activities- plan, report, ageing, provisions, monitor and analyze
• Responsible for tight alignment with local accounting and operations as well as procurement and supply chain
• Coordination of SOX compliance work for all entities and create further awareness of importance of SOX compliance
• Driving Standardization of processes and implementing of Best practices
• Support of external and internal audit requests by providing inventory analyses
• Management of day-to-day operations and coaching of the team members
• Support and lead of complex and international ad-hoc projects and ad-hoc reporting
• Support systems implementation and modification to existing system and ensure timely delivery of all system testing and validation.
• Process documentations and certifications – will have to ensure that all process are appropriately documented and periodically certified by team members on regular basis.
• Build and strengthen client relationships to achieve long-term partnerships
  

• Qualified CMA with minimum 10+ years of experience in Costing and Inventory.
• Minimum 4 years as people management experience is must
• Manufacturing experience is must
• Strong knowledge of US-GAAP and SOX
• SAP & excel experience is must
• IT Literacy- SAP, Oracle or any other ERP, Microsoft Office, Hyperion
• Well versed with latest trends, technology & best practices in the industry
• Experience in fast-paced multinational matrix organization
• Strong change management, communication and influencing skills
• Excellent listening, negotiation and presentation skills
• Fluent verbal and written communication in English
• Hands-on and proactive; strong organizational skills
• Results driven and service oriented to internal and external customers

Associate Director Finance Operations

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.

• Responsible for issuance of raw material from warehouse as per production requirement. Storage and labeling as per applicable procedure
• Assisting the Team leader in ensuring proper storage of raw materials, intermediates and finished goods in designated areas and labeling as per applicable procedures
• Carrying out dispensing activities as per applicable procedure & carrying out process and sampling activities during the production of Intermediate/API’s according to the approved batch cards
• Filling of the batch cards (production & cleaning) as per approved instructions and recording the observations & parameters in the batch card
• Ensure verification of weigh balances and all daily documents as per applicable procedures & carrying out the pH analysis & performing the verification of the pH meter as per applicable procedures
• Follow Standard operating procedure (SOP), Safety and cGMP guideline
• Ensure housekeeping of plant and cleanliness of the equipment/area, update the equipment status board, use logbook, other documents as per applicable procedure
• Complete knowledge of clean area standards, specifically adhering to ISO Class 8 requirements & expertise in operating powder processing equipment, including Micronizer, Sifter, Fitz Mill, and others
• Preparation of batch card, qualification protocol, report & other GMP related documents and adding batch details in ERP system
• Preparation of safety work permits to carry out maintenance activities in shift & report accidents and irregularities at the workstation to the Shift Officer

• B.Sc./M.Sc./Diploma (Chemical)/B.Tech (Chemical)/B.E (Chemical)

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.

1. Analysis of stability samples & working standard qualification activity as per defined procedure & monograph.
2. Maintaining a set of procedure supporting to ATS department for (GMP & GLP) techniques implementation.
3. Maintaining a system of methods and specification for all materials and products.
4. Data filling and maintaining the log books, certificate, stability report and stability data in archive.
5. Monitoring of stability studies with respect to ICH Q-1 and conducting analytical method validation activity according to ICH Q-2.
6. To initiate the LIR / OOS if any procedural gap related with SOP / monograph during routine activity.
7. Qualifications of all analytical instruments should be maintained in stability Section.
8. Follow the defined safety procedure during day to day activity in laboratory.
9. Any other job assigned by Manager Quality Control.

Bachelor/Master of Science/ B. Pharmacy

One Years Experience

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.