1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
8.00 LPA TO 10.00 LPA
Position: Manager - QA/QC
Location: Bhilad Near by Vapi
Experience: 8 - 10 Years
Industries: Cosmetic
Responsibilities:
Quality Assurance & Control:
Develop, implement, and maintain robust quality management systems (QMS) to ensure compliance with ISO, GMP, and other relevant standards.
Oversee the entire production process to ensure adherence to quality ...
1 Opening(s)
7.0 Year(s) To 15.0 Year(s)
25.00 LPA TO 30.00 LPA
Job Title: Quality Head – Pharma Plant (EU GMP & US FDA Compliant)Experience: Minimum 7 YearsLocation: [
We are looking for a highly skilled and motivated Quality Head to lead the Quality Assurance and Quality Control functions at our pharmaceutical manufacturing facility. The ideal candidate must have at least 7 years ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.50 LPA
Overall line responsibility from production to packaging• Start / Stop the machine and utility equipment.• Performs process setting & monitoring.• Monitor Material control (weight distribution, regrind levels, watch tail lengths, etc.)• Performs regular quality control throughout the shift and visual quality checks• Check & monitor process parameters like machine cycle ...
1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
2.00 LPA TO 2.40 LPA
PURULIA, MADHUKUNDA location
DRI- QC SR. S.I
Qualification:- B.sc in Chemistry
Exp. - 5 years
JOB DESCRIPTION OF QC SHIFT INCHARGE – DRI. Need to have 5 years exp. Supervising chemists: Overseeing shift chemists and casual labor Ensuring quality: Ensuring that quality standards are met Maintaining hygiene: Ensuring that the shop floor is clean and hygienic Handling ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
1.80 LPA TO 2.40 LPA
Description:
Provides data by operating a computer.
Determines sequence of operations by studying production schedule.
Performs defined tasks per documented instructions/processes.
Prepares equipment for operations by accessing software in computer.
Makes appropriate changes to the documentation, as needed.
Monitors and manipulates daily system jobs.
Starts operations by entering commands.
Maintains operations by monitoring error and stoppage messages, observing ...
1 Opening(s)
0 To 2.0 Year(s)
4.00 LPA TO 6.00 LPA
Position: R&D Officer
Location: Silvassa
Experience: 0 – 2 Years
Industries: Chemical
Responsibilities:
To develope new formulation on requirment basis from customer's side.
To take lab batches before standaridise on production floor for reconfirmation of formulation & specification.
Good knowledge of shade matching (solvent ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Inward Materials (Purchase & on surgery)
Prepare Surgery set ready & dispatch it.
To check physical inward materials with purchase invoice/delivery challan Quantity
Expiry Date, Batch number Rate
Checked inward material to be stored in proper manners ·
Proper usage and applicable stickers to be affixed on delivery challan.
Experience: 2 - 3 years
Education: Any graduate
Salary: 22K-25K ...
1 Opening(s)
15.0 Year(s) To 20.0 Year(s)
10.00 LPA TO 13.00 LPA
Position: Manager - QC
Location: Dabhel - Daman
Experience: 15 -20 Years
Industries: Pharma
Responsibilities:
Prepare quality plans in accordance with the specifications released by QA.
Overview of product evaluation and testing conducted at various stages and report on the conformity status against specified requirements.
Report any non-conforming to ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.60 LPA TO 5.40 LPA
Job Description:1. Responsible for Overall QA activities & to look after QMS compliance in accordance with ISO 13485/cGMP.2. Preparation & Up-gradation of SOP, Specifications3. Maintain the Records of BMR, BPR, Batch Inspection Documents4. Maintaining Document & Record Control5. Preparation & Up-gradation of Routine Validation Protocol & Reports.6. Handling CAPA, Non- ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 3.60 LPA
JD:
Responsible for documentation and implementation of all QA & QC activities
Verification and technical support for all technical documents master formula,standard operating procedure,raw material,finished product specifications.
Responsible for handling various quality management systems like deviation,change control and market complaints.
Responsible for providing quality assurance support to the manufacturing operations.
Internal auditing of QA/QC and other departments .
Review of ...