Cipla Ltd Team Member Formulation Vacancy - Apply Online

Cipla Ltd Team Member Formulation Vacancy – Apply Online

M Pharma job opening 2020. Pharma job opening 2020. Cipla Ltd invites B Pharmacy candidates for the post of Team Member – Formulation Tech Transfer (Analytical) post vacancy at Cipla Ltd. Candidates looking for Pharma jobs can grab this opportunity of working with Cipla Ltd.

Job Title: Team Member – Formulation Tech Transfer (Analytical) (42289)

Division IPD

Department Formulations Technology Transfer

Employment Type Permanent

Eligibility

M. Pharm (Analytical/Pharmaceutical Chemistry)

Relevant Work Experience

2-5 years of experience in Analytical method development and transfer with sound practical knowledge of analytical Instruments such as (HPLC, UPLC, GC, GCMS, Autotitrator, Zetasizer, Mastersizer, Dissolution apparatus, IR, Coulter counter for particulate matter test, Viscometer etc.)

Job Purpose

Execute analytical technology transfer activities in the plant to ensure successful transfer to commercial plant in line with defined safety norms, cost, quality and delivery timelines for new product registrations driving on time commercial launch

Accountabilities

i. Perform effective transfer of knowledge about the analytical process to Quality Control team with required documentation for successful implementation of new molecule analytical process

ii. Review the Method validation, Method verification, Specification and method of analysis and relevant analytical transfer documents to identify and remove errors

See Also
CSIR IHBT Pharmaceutical Science Job - Applications Invited

iii. Review batch documents (analytical reports) and initiate/ensures procurement of prerequisites (Column, Impurity, working standards etc.) for batches execution to ensure alignment with 6M Planner and Target filling date

iv. Participate in batch analysis (feasibility, registration, assessment, validation, query response and first three commercial batches) to ensure smooth execution.

v. Compile batch analytical results and stability for RBDR (registration batches documents review) to perform comparisons and compilations

vi. Provide technical inputs for regulatory deficiencies to support RA to respond to queries efficiently

vii. Monitor the R&D and feasibility batches at Pilot plant to understand the process

Apply Online

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