Require Formulation Researcher at Teva Pharmaceutical @ Apply Now

Post : Formulation Researcher II

Job Description
• Formulation development of solid oral dosage form.
• Planning detailed activities related to formulations and execution of the same within targeted time limits.
• Optimization of formula, process optimization trials, feasibility batches, stability studies for smooth execution at scale up level.
• Co-ordination with various departments like ARD, regulatory, MS&T, vendors, purchase and other cross functional teams for smooth development and execution of project.
• Technology transfer of developed products to production/manufacturing site.
• Pharmaceutical dosgae form development experience.
• Should have exposure to regulatory erquirement of market like US, Europe etc.
• PC skills – familiarity with Microsift Office product including Word, excel, powerpoint TACT, SRS Standards.
• Good critical thinking capability and the ability to advance logical arguments.
• Good communication skills including the capability to lead from a technical perspective.
• Systematic troubleshooting skills
• Good organizing and coorinating skills.
• Ability to work independently and reliably deliver results.

Additional Information
Qualification : M.Pharm
Location : Mumbai
Industry Type : Pharma / Healthcare / Clinical research
Functional Area :  Formulation
End Date : 25th May, 2019

Require Clinical Research Scientist at Teva Pharmaceutical

Teva is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the world’s largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we’ve built a promising pipeline centered around our core therapeutic areas.

Post : Clinical Research Scientist

Job Description
• To be qualified by education, experience and training to assume responsibility for proper conduct of the study.
• Before study start:
• Comply with all applicable regulations, complete required forms
• Read and understand the IB or appropriate information on the drug prior to study start.
• Obtaining ethics committee approval and clarifying the issues / questions raised by the EC.
• Ensuring that all necessary trial related documents are generated and compliant with the protocol (for e.g vacutainer labels, dosing label study schedule stations).
• Responsible for all clinical or medical aspects of the study hence should personally conduct or supervise the study.
• Enrolling healthy volunteers as per the inclusion / exclusion requirements of the protocol.
• Supervision of activities like check-in, dosing, blood sampling and separation as applicable.
• Maintain accountability of the investigational products and clinical supplies from receipt till study completion.
• Ensure that queries (if any) related to the IP are resolved before dosing.
• Comply with randomization schedule during dispensing.

Additional Information
Qualification : B.Pharm, M.Sc, M.Pharm
Location : Bangalore
Industry Type : Pharma / Healthcare / Clinical research
Functional Area :  R&D
End Date : 10th May, 2019

Require Production Pharmacist at Teva Pharmaceutical @ Apply Now

Post : Production Pharmacist

Job Description

• To ensure compliance to standard operating procedures and CGMP aspects.
• To ensure compliance to the requirements of site procedures on Data integrity in GxP data handling.
• To check online production, schedule production, handle production staff mainly relating to coating and tablets inspection.
• To look after manufacturing activities related to coating and tablets inspection
• To ensure maintenance of production area in the state of cleanliness and ready for manufacturing activities, as per the regulatory requirements at all points of time.
• To check the maintenance of manufacturing facility, premises and equipment
• To exercise effective control over the environmental conditions in manufacturing and other related activities which may adversely affect the product quality.
• Oversee and manage the training records for the production personnel. To ensure that the required initial and continuing training of the department personnel is carried out and adapted according to the need.
• Preparation of the SOP’s, qualification documents and calibration schedules. 
• Preparation for the BMR & to develop, implement Validation protocols and maintain the production documentation.
• Carry out all SAP related activities in a timely manner
• Execution of batches as per daily/weekly/monthly manufacturing plan
• To check and ensure line clearance as per approved SOPs and completion of usage logs during activity
• To follow safe work practices by use of PPE’s required during material/product/equipment handling and to increase awareness with colleagues to eliminate the accident.
• To maintain the department with all the safety procedures and Health (Personal hygiene).
• To ensure all time readiness of department for system/facility/safety/documents.

Candidate Profile
B.Pharm / M.Pharm with 6 to 7 year experience

Additional Information
Qualification : M.Pharm, B.Pharm
Location : Goa
Industry Type : Pharma / Healthcare / Clinical research
Functional Area :  Production
End Date : 25th April, 2019

Quality Specialist at Teva Pharmaceutical @ Apply Now

Post : Quality Specialist III

Job Description 
1. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for Third party manufactured products marketed in various countries.
2. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites
3. Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/ PQRs.
4. Evaluate reviews, recommend actions and professionally communicate to sites/ Quality units so as to continually improve quality of products.
5. Coordinates with quality oversight units assigned for issues related to compilation of APRs/ PQRs
6. Supporting quality systems management within the PQR Centre and
7. Participate in continuous process improvement projects to improve efficiency of the unit

Additional Information
Qualification : M.Pharm, B.Pharm, M.Sc
Location : Mumbai
Industry Type : Pharma
Functional Area : Manufacturing Quality Assurance
End Date : 10th April, 2019

Apply for Regulatory Affairs Associate at Teva Pharmaceuticals @ Apply Now

Post : Regulatory Affairs Associate I - Publishing

Job Description
• Publish and dispatch major and complex routine/lifecycle management eCTD submission projects
• Perform document level publishing activities, troubleshoot document issues and perform quality control checks for submission ready documents
• Collaborate with scientific personnel for planning, preparation, publishing and quality control checks of submissions.
• Participate in Global Regulatory Affairs project teams
• Maintain working knowledge of internal and external publishing standards
• Working knowledge of industry legislation and best practices
• Knowledge of regulations/guidelines governing regulatory submissions (eCTD, NeeS, paper)
• Notices when data appear wrong or incomplete, or needs verification. Distinguishes information that is not pertinent to a decision or solution.
• Compares observations or finished work to what is expected to find inconsistencies. Remains aware and takes care of details that are easy to overlook or dismiss as insignificant.
• Sees opportunities for creative problem solving while staying within the parameters of good practice. Generates unique but workable and useful solutions to difficult problems.
• Delivers products and services when and where the customer needs them. Explores options when unable to deliver a requested product or service, and pursues solutions until the customer is satisfied.
• 1-2 years in Regulatory Operations or 4-6 years in Regulatory Affairs.

Additional Information
Qualification : B.Pharm /M.Pharm, Bachelor in life sciences
Location : Navi Mumbai
Industry Type : Pharma
Functional Area : Regulatory Affairs
End Date : 15th April, 2019

Require Research and Development Intern at Teva @ Apply Now

Post : R&D Intern

Job Description
• Perform sample processing as per bioanalytical method and documentation as per SOP.
• Calibration / performance check of testing equipments.
• To review raw data forms, log books for entries as per departmental SOPs.
• Literature search for molecules and active involvement during method development.
• To ensure that the instruments / equipments / pipettes used for sample processing are calibrated.
• To carry out any other responsibilities as and when assigned by management.
• To perform QC check for bio analytical activities whenever required.

Candidate Profile
• Must be a qualified Masters in Analytical Chemisty or relevant science with atleast 6 months's experience.
• Must be knowledgeable about method development, method validation, sample analysis

Additional Information: 
Qualification : M.Sc
Location :  Bangalore
Industry Type: Pharma / Healthcare / Clinical research
Functional Area: R&D
Last Date: 30th March, 2019

Require R&D Technician at Teva Pharmaceutical @ M Pharma can apply

Post : R&D Technician III (Officer - Analytical Formulation)

Job Description
1. Analysis of Solid oral dosage
2. To analyse the samples received from Formulation department (samples include in-process, finished products, pre-formulation study samples and stability samples etc.).
3. To carry out analytical method development, in-process samples and finished products, including the methods for cleaning studies.
4. To carry out analytical method transfer activity to Goa.
5. Calibration and maintenance of analytical instruments. Maintenance includes activities such as Qualification, keeping track of AMC, History, Spares, Usage records etc.
6. Trouble shooting of analytical instruments for difficulties faced during day-to-day operations.

Additional Information
Qualification : M.Pharm, M.Sc
Location : Navi Mumbai
Industry Type : Pharma
Functional Area : Analytical Formulation
End Date : 15th March, 2019

Apply for Clinical Research Associate at Teva Pharmaceutical @ Apply Now Online

Post : Clinical Research Associate

Job Description

• To monitor and do a Quality Check of all study activities such as check-in related procedures, dosing, sample collection, processing, segregation, transfer and check-out, as described in SOP

• Co-ordinating with Project Management Group (PMG) for compliance with the sponsor requirements and timelines.

• Periodic review on status of study files up to archival of files.

• Co-ordinating with PMG and lab technicians for the dispatch of biological samples to client and analytical department.

• Co-ordinating with Report Writing Group for the movement of files to the concerned department and ensuring to maintain timelines.

• Co-ordinating with PMG and Investigators in resolving the queries raised by the sponsors.

• Compilation of study data and review of clinical reports.

• To carry out other responsibilities as and when assigned by the management.

• Coordinating with the Ethics Committee for submission of protocol and other study related documents.

• Report to Principal Investigator on study related activities.

• To report to respective Centre Head on all activities.

• Must have strong communication and verbal skills in English

• Must possess strong influential skills and affirmative communication/interpersonal skills

Additional Information

Qualification : M.Pharm

Location : Bangalore

Industry Type : Pharma / Healthcare / Clinical research

Functional Area :  R&D

End Date : 05th March, 2019

Quality Specialist at Teva Pharmaceutical @ Click Here for more details

Post : Quality Specialist

Job Description 
1. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for Third party manufactured products marketed in various countries. 
2. Compilation of high quality Annual Product Reviews (APRs) / Product Quality Reviews (PQRs) for products manufactured at various manufacturing sites 
3. Liaising with third party contract manufacturers and QA personnel located globally for data collection required for compilation of APRs/ PQRs. 
4. Evaluate reviews, recommend actions and professionally communicate to sites/ Quality units so as to continually improve quality of products. 
5. Coordinates with quality oversight units assigned  for issues related to compilation of APRs/ PQRs 
6. Supporting quality systems

management within the PQR Centre and 
7. Participate in continuous process improvement projects to improve efficiency of the unit
Additional Information
Qualification : M.Pharm, B.Pharm
Location : Mumbai
Industry Type : Pharma
Functional Area : Quality Assurance
End Date : 28th February, 2019

Teva Pharmaceutical looking for Quality Analyst @ Apply Now

Post : Quality Analyst III

Job Description
• Preparation of Test Licence and Mfg. Licence, additional Bulk Pack or Blister pack application etc.
• Coordinate and follow up with local FDA for receipt of licence and addressing the queries initiated by Local FDA.
• Preparation of test license NOC for new drugs application.
• Complying any condition mentioned in the import licence and the NOC to DCGI
• Preparation of Import licence for stability and method transfer samples.
• Preparation of test license NOC for new drugs application.
• Complying any condition mentioned in the import licence
• Preparation of application for import & export licence for Narcotic & Psychotropic Substances.
•  Complying any condition mentioned in the Narcotic licence
• DATA INTEGRITY COMPLIANCE :
• Handling of training related activities as a TSA (Training system administrator) and Coordinating with other departments
• cGMP trainings to all employees.
• Maintenance of the training records of the employees.
• Responsible for imparting induction training, quality systems training, departmental training and maintenance of training records, Preparation of departmental training schedule.
• Responsible to monitor and to ensure the functioning of Trackwise Training manager at Site.

Candidate Profile
BSc/B Pharm with 9 to 12 years

Additional Information
Qualification : B.Pharm, B.Sc
Experience : 9 to 12 years
Location : Goa
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area :  Quality
End Date : 28th February, 2019

Apply for Quality Control Analyst at Teva Pharmaceutical @ Apply Now

Post : Quality Analyst

JOB SUMMARY
The primary responsibility of the, QAS In-Take Team Quality Analyst position is receiving, trending, logging and coordinating the return of the samples for product quality related complaints distributed and marketed in the United Sates. This includes product quality complaints received via phone, email, voicemail and social media and to ensure Customer Service concepts and metrics are maintained. Notifications to sites and management of critical/high profile complaint events.

Job Description
• Performs the functions associated with receiving, trending, logging and coordinating the return of the Samples for product quality related complaints.  This includes complaints received via phone, email, and internet.
• Utilize knowledge and experience to drive compliant resolution of complaint issue as well as ensure high level of customer service and customer satisfaction is maintained
• Participate in and contribute to Daily Team Huddle meetings to provide up-to-date information to QAS Team Members about products, manufacturing sites, revised Standard Operating Procedures (SOPs)/ Work Instructions (WIs), Trackwise capabilities and functions, difficult/unique customer related scenarios.
• Perform the weekly Pharmacovigilance (PV): QAS File Sharing reconciliation activity on a timely and accurate basis.
• Revise SOPs/WIs.
• Partner with other Teva Intake Centers to align on information flow and ensure customer satisfaction.
• Participate in the continuous improvement of the QAS Group to drive operational excellence by performing tasks and projects to increase compliance, efficiencies and effectiveness of actions within the Group.
• Tasks and Projects may include but are not limited to:
• Support  audits and inspections of QAS group
• Provide data related to product complaints, volumes, Deviation Reports
• Identify automation and defect proofing opportunities and highlight to QAS management via business cases, quantifiable data.
• Highlight gaps in SOP/WI procedures to management and provide suggestions for improved clarity and detail
• Other miscellaneous projects and duties as required/assigned

Candidate Profile
Bachelor’s degree of Pharmacy (B. Pharm) or Master’s Degree in Pharmacy (M. Pharm).

Additional Information
Qualification : B.Pharm, M.Pharm
Location : Mumbai
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area :  Quality
End Date : 20th February, 2019

Require Analytical Researcher at Teva

Post : Analytical Researcher I

Role Description Summary: To perform the analysis of ANDA and ANDA stability samples in the Laboratory.

Job Description:
• To maintain Good Laboratory Practices in the laboratory.
• To maintain the assigned Laboratory workplace, instruments and equipment’s.
• Maintenance and upkeep of Inspection Lot No. Register.
• Analysis and Reporting of In-process, validation, finished product, cleaning and ANDA samples of new project.
• To participate in Method transfer and method validation activities.
• Timely completion of Analytical reports of ANDA batches.
• To perform the gap analysis of new projects.
• Reporting of Events, chromatographic errors and OOS (If any).
• To maintain safety practice in laboratory.
• Any other responsibilities given by Section-Head.

Candidate Profile
• Good analytical skills, and knowledge on different instruments used in the laboratory for day today analysis.
• Good Job knowledge and hands-on experience on various laboratory instruments and analytical techniques.

Additional Information: 
Qualification : M.Sc
Location :  Goa
Industry Type: Pharma / Healthcare / Clinical research
Functional Area: R&D
Last Date: 30th January, 2019