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Sun Pharmaceuticals, Inc Executive - Analytical Development in India

Analysis and reporting of Analytical method validation, method verification and method transfer.

Calibration of instruments

Preparation of method transfer / co-validation intimation/ protocol/ report/ /waiver/certificate generated in laboratory.

Make availability of document package (Specification, STP and pre-validation reports and related follow-up as and when required.)

Make availability of Procurement of logistics for method validation / method transfer or batch analysis.

Timely query response with the help of section head and R & D Quality.

Oral / written communication with internal / external persons at the time of protocol & report etc. preparation.

Document submission for the product registration.

Training and development activities.

Maintain cleanliness and housekeeping of the working area.

Any other responsibilities assigned by Department head/Designee from time to time orally or in writing.

Preparation of Protocols/ Reports / Documents generated in Laboratory

Preparation of SOP

Online data, log books review on shop floor

Training and development to new analyst for analysis

Daily monitoring of laboratory activities for the compliance against GMP

Follow and maintaining GMP during analytical activities

In absence of XXXX designee with equivalent of higher experience in respective area or Subject matter expert can perform the task.

We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.

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