Jobs at Teva in India, Gwalior

• 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 equipment
• Report 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.
• Work is performed without appreciable direction while exercising considerable latitude in determining objectives and approaches to assignment
• Good organizational skills, basic first-line management skills for daily operation, situational Leadership and decision-making skills
• 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.

2 to 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.

• Carrying out dispensing activities as per applicable procedure
• Responsible for recording the observation of reaction parameters on the batch card as per approve procedure
• Filling of all the batch card (production cleaning) as per approved instruction
• Ensure verification of pH meters and weigh balances as per applicable procedures & to maintain work procedure, safety precaution and cGMP
• Ensure housekeeping of plant and cleanliness of the equipment, update the equipment
• Report accident and irregularities at the workstation to the Shift Officer. To prepare the production batch card, protocol and other relative document of production
• ERP operation related to Production activities
• Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production
• Coordinating with QA for Online compliance of GMP at shop floor
• All other Production related activities advised by the Superiors from time to time

• B.Sc./M.Sc. (Chemistry)/Diploma (Chemical Engineering)
• Minimum 5+ years of experiene required

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 Collection, compilation, analysis, and review of all data for APQR.
• Responsible for Processing and oversight of changes through the generation, justification, impact assessment, modification, review, approval, and implementation workflow.
• Responsible for Review/approval of all documentation associated with the process validation ,CPV & cleaning validation.
• Responsible for processing of documents through the generation, modification, review, and approval and archival of records.
• Responsible for review/approval of all documentation associated with the GMP equipment. This includes any Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documents.
• Responsible for tracking, trending, and reporting of Quality Metrics for site, regional, and global review. Trending as required by SOP, Corp. Standards, and/or regulations.
• Responsible for Review/approval of all documentation associated with the establishment and configuration of a GMP computerized system. This includes all lifecycle documents.
• Responsible for Review of regulatory and quality compliance requirements and divisional policy, performance of gap assessments, and establishment or improvement of SOPs covering all areas of applicability.
• Quality support to Regulatory Affairs as it relates to updates/changes to Market Authorizations.
• Responsible for Management, tracking, and/or performance of GMP type training supporting plant performance and Quality Departmental training and hands on qualification.
• Responsible for Review/approval of the Validation Master Plan and all documentation associated with the validation or qualification of a process, system, equipment, facility, and/or the utilities associated with the site.

• B.sc/Msc in chemistry
• 4 to 10 years of experience
  

Manager Quality Systems

• Carrying out dispensing activities as per applicable procedure & responsible for recording the observation of reaction parameters on the batch card as per approve procedure

• Filling of all the batch card (production cleaning) as per approved instruction

• 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 equipment, update the equipment

• Report accident and irregularities at the work station to the Shift Officer. To prepare the production batch card, protocol and other relative document of production

• ERP operation related to Production activities

• Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production

• Coordinating with QA for Online compliance of GMP at shop floor

• All other Production related activities advised by the Superiors from time to time

• B.Sc./M.Sc. (Chemistry)/Diploma (Chemical Engineering)
• 2+ years of experience required

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. Overall responsible for New Project, Modification jobs activity in the plant as per requirement of site.
2. Project management and execution of new and expansion project from Design to till handing over to plant. Also closing of project with capitalization.
3. Responsible for execution of project with given time line.
4. Compliance of all statutory & GMP requirement in new project.
5. Design & compliance of safety practices at site and to ensure zero reportable incidents.
6. Coordination with consultant for technical aspect.
7. Evaluation of Design, drawing, technical specification as per Teva Standards.
8. Procurement assistance to SCM for project.
9. Installation and commissioning of project as per standard/ Teva guidelines. Indenting of material and technical evaluation of vendors.
10. Coordination with all vendor/ consultant for deliverables.
11. Responsible for project result, forecasting and controlling-project schedule & cost.
12. Preparations of budget estimate for proposed/ new project.
13. Manpower & Contract Management
14. Responsible for attending/rectification of mechanical breakdowns in the plant through job orders/permits.
15. Responsible for preventive maintenance of equipment’s as per schedule& closer in ERP system.
16. Co-ordinate with other service team for problem rectification in plant.
17. Responsible to overall maintenance of production block.
18. Responsible to carry out the preventive maintenance/overhauling of cGMP Equipment, critical equipment and its subparts etc. as per schedule.
19. Responsible for spare part main
20. Preparation of Equipment Layout, Plant Layout, P & ID (Piping & Instrumentation Diagram), PFD (Process Flow Diagram).
21. Responsible for Permit issuance & safety compliance of assigned plant.
22. Responsible for GMP& EHS CAPA and deviation closure and updation.

• B.E. / B.Tech(Mechanical)
• 8+ Years of 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.

• Carrying out dispensing activities as per applicable procedure
• Responsible for recording the observation of reaction parameters on the batch card as per approve procedure
• Filling of all the batch card (production cleaning) as per approved instruction
• 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 equipment, update the equipment
• Report accident and irregularities at the workstation to the Shift Officer. To prepare the production batch card, protocol and other relative document of production
• ERP operation related to Production activities
• Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production
• Coordinating with QA for Online compliance of GMP at shop floor
• All other Production related activities advised by the Superiors from time to time

• B.Sc./M.Sc. (Chemistry)/Diploma (Chemical Engineering)

• Minimum 3+ years of experience required

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 & responsible for recording the observation of reaction parameters on the batch card as per approve procedure

• Filling of all the batch card (production cleaning) as per approved instruction

• 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 equipment, update the equipment

• Report accident and irregularities at the work station to the Shift Officer. To prepare the production batch card, protocol and other relative document of production

• ERP operation related to Production activities

• Carrying out batch processing including raw material charging, unloading of material and sampling activities during intermediate production

• Coordinating with QA for Online compliance of GMP at shop floor

• All other Production related activities advised by the Superiors from time to time

• B.Sc./M.Sc. (Chemistry)/Diploma (Chemical Engineering)

• 5+ years of experience required

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.