1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
10.00 LPA TO 11.00 LPA
Position: QA Manager
Location: Panoli - Ankleshwar
Experience: 8 - 10 Years
Industries: Pharma
Responsibilities:
All responsibility of quality assurance & quality control.
Preparation of system SOPs and authorization of SOPs of operating departments.
To monitoring of all the Q.C. testing & its complete follow up.
To approve all the Raw materials, ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Executive
Location: Silvassa
Experience: 4- 5 Years
Industries: Chemical
Responsibilities:
Ensuring Compliances: Quality Assurance professionals play an important role in ensuring that all processes & product comply with QMS/IMS and other relevant regulations.
Quality Control: Quality Assurance professionals involved in the development, maintenance & implementation of procedures ...
10 Opening(s)
3.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 3.50 LPA
Position: Plant Operator
Location: Silvassa
Experience: 3 - 5 Years
Industries: Chemical
Responsibilities:
To run plant equipment and make sure it is operating safely and efficiently.
You may transport materials , check equipment, monitor production and keep operating record.
To work with shift chemist to fix problems or troubleshoot issues ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 4.80 LPA
Position: QA Executive
Location: Ankleshwar
Experience: 4- 5 Years
Industries: Chemical
Responsibilities:
Ensuring Compliances: Quality Assurance professionals play an important role in ensuring that all processes & product comply with QMS/IMS and other relevant regulations.
Quality Control: Quality Assurance professionals involved in the development, maintenance & ...
1 Opening(s)
1.0 Year(s) To 4.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: QA Executive
Location: Ankleshwar
Experience: 1 - 4 Years
Industries: Pharma
Responsibilities:
Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies.
LNB's and Logbooks Issuance and Checking for daily entries in Logbooks.
To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: Production Officer(Documentation)
Location: Daman
Experience: 1 - 2 Years
Industries: Pharma
Responsibilities:
Maintaining product recipe and standard operating procedure (SOP).
Planning and supervision of man power during shift Making sure that production facilities are clean and when appropriate and disinfected.
Feeling and reviewing daily log sheets and daily ...
1 Opening(s)
4.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Jr. Lab Technician
Location: Silvassa
Experience: 4 - 5 Years
Industries: Chemical
Responsibilities:
To set-up the reactions , Charge the batch & carry out the process.
To carry analysis of the lab batches.
To maintain & record the observations of the lab experiments.
handling of lab chemicals & setting up a chemical reaction experiment
Recording ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Position: Production Associate
Location: Vapi
Experience: 1 - 3 Years
Industries: Pharma
Responsibilities:
Maintaining product recipe and standard operating procedure (SOP).
Planning and supervision of man power during shift Making sure that production facilities are clean and when appropriate and disinfected.
Feeling and reviewing daily log sheets and daily verification ...
1 Opening(s)
10.0 Year(s) To 15.0 Year(s)
10.00 LPA TO 15.00 LPA
Position: EHS Manager
Location: Sarigam near by Vapi
Experience: 10 - 15 Years
Industries: Chemical
Responsibilities:
Implement EHS Policies: Implement Environmental, Health, and Safety (EHS) policies and procedures in alignment with the plan.
Compliance Monitoring: Oversee and ensure adherence to statutory compliances for all facilities.
Risk Identification: Inspect facilities ...
1 Opening(s)
12.0 Year(s) To 15.0 Year(s)
25.00 LPA TO 30.00 LPA
Position: QA Manager
Location: Ahmedabad
Experience: 12 - 15 Years
Industries: Pharma
Responsibilities:
Ensure compliance with GMP, regulatory guidelines, and quality standards in pharmaceutical formulation manufacturing.
Manage quality systems, audits, documentation, validations, and batch release while leading the QA team.
Implement and maintain Quality Management Systems (QMS) as per USFDA, WHO-GMP, ...