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...
...local as well as foreign and can good command on English speaking preference.
Quality Assurance,GMP Comliance ,Audit,Audit travelling
Designation: QA Manager -Pharmaceutical Intermediates & specialty chemicals
QMS: Maintain detailed documentation of QMS(change control, deviation, incident, market complaints, product recall)
VMP: maintain and execution of Validation plan as per schedule
Master index: Prepare and maintain of Master index for SOP, STP, ...
A quality assurance specialist ensures that the final product observes the company's quality standards. In general, these detail-oriented professionals are responsible for the development and implementation of inspection activities, the detection a...
Description:
# Quality Assurance Executive / Sr. Officer/ Sr. Executive
Total Experience- 05 -07 Year (Possession – 3 )
Function – Should be from formulation background
Area Responsibility – 1. Preparation and review of QMS Document, ...
# 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 ...
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...
· To supervise and control sampling of raw materials finished products and packaging material as per defined procedures.
· To analyze critical finished products and new products for Active content and impurity profile.
· Develop/Standardize/valid...
