1 Opening(s)
10.0 Year(s) To 20.0 Year(s)
10.00 LPA TO 25.00 LPA
A. Organization Context
PositionTitle: Plant Quality HeadEmployeeName: Grade :Department: Location:
Reports to: Unit Head Reported by:
Mgr. QualityChemists(Physical/Chemical/Microbiologist)
B. Job Objective• Develop and ensure Quality Management systems as per regulatory guidelines andquality standards within plant in order to ensure customer satisfaction and businesssustainability.• Develop and sustain Quality culture across the plant• Review product quality ...
3 Opening(s)
3.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
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, Protocols, MFR, BMR/BPR
Document control: Issue and retrieval of documents like BMR/BPR, SOP, Formats, and log books
APQR: Prepare the ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
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 ...
1 Opening(s)
7.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 6.00 LPA
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 ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
20.00 LPA TO 21.00 LPA
Position: Sr. Manager - QA
Location: Ahmedabad
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
ISO/GMP Systems: Maintenance and continuous improvements in procedures and documentation, certification and compliance.
Customer registrations, Handling customer audits and complaints, CAPAs and closures.
FG/RM/PM specifications, Test plans and Customer order review
Vendor qualifications, audits and ratings.
Internal and external audits and ...
1 Opening(s)
5.0 Year(s) To 5.0 Year(s)
2.40 LPA TO 3.00 LPA
JOB DESCRIPTION :
19.09.24
HPS/2024/590
QA Sr Executive
Male
1
5 to 6
B.Sc/MSc/B-Pharma/M-Pharma
Handling all the documentation process, perform the duties of IPQA, QMS SYSTEM9CHAIN CONTROL, DEVIATION,CAPA,APQR, BMR,BPR, INTERNAL AUDIT, ETC
A Senior Quality Assurance (QA) Executive's responsibilities may include:
Quality assessments: Performing QA engagements, including preparing for onsite visits, conducting onsite visits, and preparing draft reports
QA training workshops: Assisting with ...
3 Opening(s)
4.0 Year(s) To 7.0 Year(s)
Not Disclosed by Recruiter
Job Responsibilities:
Review & Control all QMS related document like change control, Deviation, out of Specification, CAPA and incident.
Review of master BMR/BPR, SOP and specification.
Preparation & review of departmental SOP.
Participate in internal audit and coordinate for complies and closure.
To coordinate in root cause and risk assessment.
Review and maintain the executed documents ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Vapi
Experience: 2- 3 Years
Industries: Pharma API
Responsibilities:
Responsible for document and data control activities
To prepare and update all master document list as per requirement.
To initiate change control/document amendment for any change or improvement in the process.
Review of BMR/BPR, APQR and QMS Documents
Responsible ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
5.00 LPA TO 10.00 LPA
Position: QA Manager
Location: Vapi
Experience: 8- 10 Years
Industries: Pharma
Responsibilities:
ISO/GMP Systems: Maintenance and continuous improvements in procedures and documentation, certification and compliance.
Customer registrations, Handling customer audits and complaints, CAPAs and closures.
FG/RM/PM specifications, Test plans and Customer order review
Vendor qualifications, audits and ratings.
USFDA, ...
1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: IPQA Officer
Location: Vapi
Experience: 2 -4 Years
Industries: Pharma Formulations
Responsibilities:
To perform IPQA activities at shop floor in each and every stage of manufacturing and packing.
QA overview for clean room behavior and personnel hygiene .
Review of batch processing records.
Review of all documents relating to the manufacturing, ...