REQUIREMENTS
Education / Experience
Education:
Graduate / Post Graduate in Pharmacy or Chemistry
Experience:
2-3 years in Pharma industry with awareness of Quality management systems, manufacturing activities, process validation, Quali...
# Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
# To approve or reject, as he sees fit, raw materials, packing materials, semi finished product and finished products as per agreed/approved ...
...performance in terms of cost, quality, production, service and safety.
Support in compliance of regulatory standards (GPCB, Factory Inspectorate, ISO etc.) internal auditing.
Support in whatever way possible M...
...statutory requirements and company policy. By preparing proper Additions Schedule and maintaining Fixed Assets Register.
Knowledge
Accounts and Finance – Accounting standards and Indian GAAP
Statutory compl...
Required Pharmaceutical Production Formulation Specialist
Location: Ankleshwar Gujarat India
Industry Pharma Formulation
Must have 35 Years of Experience (Must be from Formulation Industry)
Job Description:
As a Pharmaceutical Producti...
Designation : QA
Qualification : M.sc/ B.sc/ M.pharm/B.pharm
Total experience : 2 - 5 years
Total Position : 2
Gender : Male
Location : Valia
Salary Range : Upto 4 LPA
1. To perform all the activities of Quality assurance departme...
~ Role & Responsibilities: 1. Organize & Execute logistics & store department in order to achieve business targets and improve profitability. 2. Ensure quality related compliance during Material Management & timely completion of corrective and prev...
The candidate should be a graduate or Post grauduates Engineer with 20 years of experience on all shop floor activities in an engineering Extrusion industry And Export unit. Knowledge of Export Import Documentation and Preparation for at least 10...
Internal Job Description
~ Contribution in management and control of both site project/transfer as well as donor Documentation, such as Product transfer protocols, product transfer checklist, associated BMRs, Master Documents, etc. • Preparing & r...
