Executive
To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline. To ensure Renewal of registered product prior to validity expiration of Africa
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To ensure Registration dossier submission of products in different Africa countries (Region I) as per agreed timeline. To ensure Renewal of registered product prior to validity expiration of Africa
Major purpose of the job: Preparation of DMF, annual update and its submission to various regulatory authorities. Preparation of Applicant's part CEP/DMF/ASMF and responses of various Applicant's pa
• To follow cGMP as per training guidelines from the premises to their section. • To follow the respective equipment SOP’s and written procedure from BMR • To ensure environmental condition of Gran
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi
"JOB RESPONSIBILITIES • Review of Literature summary report, patent summary report and development protocols. • New product development, Planning and Resource allocation for Domestic, ROW, US, EU, C
JOB RESPONSIBILITIES "Purification of recombinant vaccine candidates. • pH and conductivity meter calibration and operation • Stock buffers and working buffer preparation • Column packing for puri
Principal task and responsibilities : • Submission of product dossiers for registration, in various countries including India as per the agreement with customers or as per the internal plan • Submis
Major Purpose Of The Job:- • To follow cGMP as per training guidelines from the premises to their section. • To follow the respective equipment SOP’s and written procedure from BPR • To ensure env
JOB RESPONSIBILITIES •To prepare, review and submit dossiers for Life cycle management, and other submissions as required for UK, EU regions. •Preparation, review and submission of eCTD Renewal, var
Major Purpose Of The Job:- • To follow cGMP as per training guidelines from the premises to their section. • To follow the respective equipment SOP’s and written procedure from BMR • To ensure en
• To operate Effluent Treatment Plant at Dholka. • To carry out preventive maintenance of ETP equipment’s. • Treatment of inlet effluent to be done in ETP plant as per SOP. • Records to be update a
Principal Tasks: • To analyse finished goods, semi-finish and In-process samples. • Analytical result recording in LIMS and SAP. • Specification, Master, Record of Analysis preparation/correction i
Major Purpose of the Job: - • To ensure that cGMP practices shall be followed from the premises to their section. • To follow the all respective SOPs & BMR procedure in the department during operati
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
Production : • To check the labels of raw material, packing materials and solvents before usage. • To maintain storage conditions of raw material/intermediates in plant. • To maintain process condi
• To plan daily Dry syrup filling activity per norms of cGMP. • To supervise Cleaning & dry syrup activity as per requirement in Cephalosporin block. • To carry out in process checks during dry sy
Production : • Cleanliness of the equipments and area under his charge. • Operations of Reactors, Centrifuge and other equipments like vacuum pumps, Filter units, scrubbers, dryer, blender, shifte
New Product evaluation and regulatory assessment as per WHO PQ and Russia - CIS. To review Registration and Requalification Dossiers before submission in WHO PQ and also its expansion in other eme
• To maintain and adherence of the GLP and safety procedures in laboratory. • To perform the analysis as per work allocation and records the results in work sheet (Protocols) for raw material / packi
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