1 Opening(s)
2.0 Year(s) To 4.0 Year(s)
4.00 LPA TO 4.50 LPA
Job Description:1. Line clearance-Verify the Job order for correct resin, MB grade, Packing qty, Product code & Customer name etc.-Verify area line clearance effectiveness and decision making which includes the following :-Verify the machine & surrounding area and ensure that it should be free from dust/dirt, oil, grease, loose nut ...
5 Opening(s)
2.0 Year(s) To 4.0 Year(s)
1.80 LPA TO 2.40 LPA
At machine start up1) Ensure the Labels for the next job is perfectly matched and ready 2) Make sure material for next 2 jobs is ready 3) Set up machine as per the specification sheet a. For Polytype and Flexo use recipes (to be developed) b. For other machines use ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
8.00 LPA TO 10.00 LPA
• To achieve the secondary packing/NDT/BIJ targets as per schedule. Ensure that productmanufactured are free from defects and meet company quality standards.• To monitor the shift activities as per quality compliance.• Promote and foster good human relations within the department and plant-wide and work toensure that employees embrace the company Values.• To ...
1 Opening(s)
1.6 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.70 LPA
Hiring for MNC Pharma QA Officer ( IPQA)
POSITION : Officer
Education : B.Sc/M.Sc/D.Pharm/M.Pharm.
Experience : Min, 2+years from Pharma Industry.
Salary: 2,20,000/- to 2,60,000 LPA.
Location:- ( Aurangabad.)
Role & Responsibility
Checking and ensuring online completion of documents and line clearance activity.
To carry out line clearance activity at dispensing, manufacturing , & packaging
Performing Sampling activity like in process, ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 2.80 LPA
min experience 1 -2 yr on HPLC Machine
CTC - 2 LAC - 2.8 LAC.
Quality Control Team is responsible for sampling, analysis, Testing, line clearance, release, related documentation and other related Quality Control functions in respect of RM/PM/Finished goods/ in process /Validation and stability samples.
Job Responsibilities1. To sample the Incoming RM/Packaging material.2. ...
1 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 6.00 LPA
Position: IPQA Officer
Location: Sarigam near by Vapi
Experience: 2 -5 Years
Industries: Pharma
Responsibilities:
USFDA, MHRM AND WHO GENEVA Audits Handling.
Handling & Monitoring of all IPQA activity
Handling & Monitor of day to day dispatch related activity
Review & Monitor ongoing validation activity
Review of EIMR & Cleaning ...
10 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.20 LPA
Position: Quality Officer
Location: Daman
Experience: 1- 3 Years
Industries: Plastic
Responsibilities:
Line clearance during manufacturing and packing activities.
Testing of incoming material (RM & PM), Semi-Finished and Finished Goods as per specification.
IN process Inspection.
Redispatch Inspection.
Preparation of dimensional report.
Attending Customer place.
Preparation of COA
Knowledge about system & Documentation ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.40 LPA TO 4.00 LPA
Position: QC Executive
Location: Vapi
Experience: 1– 5 Years
Industries: Plastic
Responsibilities:
Line clearance during manufacturing and packing activities.
Testing of incoming material (RM & PM), Semi-Finished and Finished Goods as per specification.
IN process Inspection.
Redispatch Inspection.
Preparation of dimensional report.
Shift Handling.
Attending Customer place.
Preparation ...
2 Opening(s)
2.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 7.00 LPA
Generic
Implement Quality Assurance activities for Pharmaceutical at Ankleshwar adhering to standard operating procedures with optimum utilization of resources to ensure consistent good quality of products to meet with customers’ requirements, living Group’s Values and Code of Ethics.
Specific additions (if needed)
KEY ACCOUNTABILITIES
Quality Management/Continuous Improvement
Line Clearance and shop floor compliance
Assisting in Complaint ...
1 Opening(s)
2.0 Year(s) To 6.0 Year(s)
1.00 LPA TO 5.00 LPA
RESPONSIBILITIES:1. To issue the Batch Manufacturing Record, Equipment cleaning record, Logbooks, AnalyticalReport for raw material, finish product and packing material.2. Assistance in preparation of SOP of various departments/ preparation of draft SOPs.3. During plant round QA Executive to verify documents as per cGMP and GLP norms.4. Line Clearance activities for ...