5 Opening(s)
8.0 Year(s) To 12.0 Year(s)
4.20 LPA TO 5.00 LPA
Quality Control Chemist Job Description Template
Our company is looking for a Quality Control Chemist to join our team.
Responsibilities:
Perform analysis with a practical understanding of the test procedure and instrument operation;
Work under direction provided by supervisor and Other duties as assigned;
Maintain required level of training needed to perform a GMP task;
Organize ...
6 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 10.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...
2 Opening(s)
5.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 10.00 LPA
Following GMP during operation of the equipment and handling of products.
Responsible for Operation of moisture analyzer and ERH apparatus.
Responsible for the following SOPS and BMR’S in the area without any deviations.
Responsible for integrity of punches & dies and sieves, screens, finger bags.
Responsible for the Maintenance of change parts and punch ...
2 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 2.50 LPA
Receive & verify material as per SOP
Good warehouse practices
Dispensing & sampling as per SOP
Follow FIFO & FEFO
Material weighing
Inventory level
Adhere GMP norms
Well versed with documentations related to a pharma.
Receive & verify material as per SOP
Good warehouse practices
Dispensing & sampling as per SOP
Follow FIFO & FEFO
Material weighing
Inventory level
Adhere GMP norms
Well versed with ...
2 Opening(s)
0 To 2.0 Year(s)
1.00 LPA TO 3.00 LPA
Receive & verify material as per SOP
Good warehouse practices
Dispensing & sampling as per SOP
Follow FIFO & FEFO
Material weighing
Inventory level
Adhere GMP norms
Well versed with documentations related to a pharma.
Receive & verify material as per SOP
Good warehouse practices
Dispensing & sampling as per SOP
Follow FIFO & FEFO
Material weighing
Inventory level
Adhere GMP norms
Well versed with ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
Not Disclosed by Recruiter
Job description for the post of Production Assistant-
(a) one who is able to handle all pharma reactors. (b) Able to handle glass assembly 20L, 50L, 100L, 200L, 300L.(c) Knowledge of Centrifuge 24’’ & 36’’.(d) having exposure of handling CF, multi mill, Nutseh Filter, Blender, Shifter.(e) Equipment handling(f) Knowledge of GMP ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
6.00 LPA TO 12.00 LPA
Responsible for supervise of production planning for in-house manufacturing.Ensuring proper Planning & execution of complete sampling activity.Optimum utilization of man & machine , material etc.Develop and maintain effective relationships with internal suppliers and customers for ensuring that required inputs are available on time.Provide forecasts and demand profiles to major suppliers
Knowledge of current ...
6 Opening(s)
3.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 5.00 LPA
Provide analytical support for maintaining in-process control and product quality.Analysis of In-process samples and Finished Product (Syrup).Analysis of Cleaning validation and verifications samples.Documenting the activities performed online for GMP & GLP.Performed all analytical technique in Tablets, Capsules manufacturing.Responsible for Preventive maintenance of HPLC.Testing of all finish dosage form SyrupDocumentation(R.M, F.P ...
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 ...