Actide International
Location
Ahmedabad | India
Job description
To establish quality management system across all functions of plant related to quality
To execute & control QMS on a routine basis.
To prepare & approve all GMP related documents and control issuance, review, retrieval & storage securely.
To approve vendors for RM\PM.
To prepare specification, MOA, BMR, BPR, and control as per SOP of SOP.
Responsible for protocol & report approval of validation activities
To effectively train staff for GMP.
To plan & carry out Holding time studies and decided on final packing and retest dates based on study.
To prepare & approve APQR.
To Handle , Deviations , Change controls & market Complaints as per SOP in a timely manner & investigate take CAPA and follow through on compliance & final approval.
To Maintain GMP in production, warehouse & QC area.
To approve finished products for sale.
To carry out internal/external audits.
To monitor audit agreement done with customers.
To monitor equipment cleaning procedures for product change over & contamination control.
Any other specific task assigned by management from time to time.
Quality Assurance,QA Testing,QMS,MOA ,BMR,BPR,APQR
Designation: Quality Assurance - Medical Equipment
Vacancies: 1
Experience: 4.0 Year(s) - 5.0 Year(s)
Job tags
Salary
Rs 3 - 6 lakhs p.a.
