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Opportunity for M.Pharm, B.Pharm as Associate at Sanofi

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Clinical research courses

Opportunity for M.Pharm, B.Pharm as Associate at Sanofi

Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.

Post : Associate

Job Description
• Operation of CIP and SIP for SCADA blending vessels in auto /manual mode. To ensure the calibration of pH meter / weighing balance/ conductivity meter. To ensure/ carry out material movement as per the approved process flows and layout.
• To carry out aseptic connections and disconnections for blending process, autoclave, peristaltic pump, digital weighing balance and magnetic stirrer operations as per SOP.
• To supervise and perform the blending of Shanchol, IPV, ShanTT, Shan5 and Shan6.
• To ensure line clearance and formulation activities are done as per procedure described in SOP/BMR.
• Bulk cold management with respect to storage, cleaning, temperature record and related logbooks.
• Communication of production plan to the respective cross functional departments for the smooth functioning of the activity.
• To ensure indenting and posting of materials through ATHENA and procurement of materials from warehouse as per the batch requirement.
• To ensure the sample submission status to QC as per the formulation sampling plan.
• To ensure and coordinate with QA and production, for issues related to SOPs, BMRs and QMS for evaluation and closure.
• To ensure that the premises and equipment’s are maintained in validated state and as per GMP requirements.
• To monitor and ensure of component preparation & sterilization activities.
• To impart training to all the staff related to process.

• Responsible for ensuring & maintenance of aseptic area.
• To plan manpower according to production plan.
• To ensure concurrent documentation as per GMP.
• To ensure the availability of issued current controlled copies (SOP’s) and submission of the superseded versions to QA.
• To ensure the equipment preventive maintenance as per schedule.
• To attend safety PEP talk discussion with shop floor persons.
• To attend the committee meetings, contribute ideas and suggestions for improvements towards safety.
• Report unsafe conditions and incidents to HOD & HSE.
• To maintain best practices and LEX reports,
• HSE trainings and safety alerts and audits.
• To provide orientation to new employees on health and safety risks and procedures in their workplace.


Additional Information
Qualification : B.Sc / B.Pharm / M. Pharm
Location : Medchal Mandal
Industry Type : Pharma / Healthcare / Clinical research

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