1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.40 LPA TO 3.00 LPA
Position: Production Officer
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)
10.0 Year(s) To 15.0 Year(s)
12.00 LPA TO 14.00 LPA
Position: Area Incharge - Production (Liquid Oral)
Location: Ahmedabad
Experience: 10 - 15 Years
Industries: Pharma
Responsibilities:
Production Planning & Batch Execution
Plan and schedule daily and weekly production based on Production Plan.
Ensure availability of dispensed raw materials, purified water, utilities, and manpower.
Supervise preparation of ...
1 Opening(s)
6.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 7.50 LPA
Position: Sr. Executive - QA
Location: Sarigam near by Vapi
Experience: 6 - 8 Years
Industries: Chemical
Responsibilities:
Oversee the generation, review, and archival of documents used to support Good Manufacturing Practice manufacture of Final Product.
Review of raw material related documentation and release of raw materials
Provide quality support for the development ...
1 Opening(s)
0 To 1.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: Asst. Manager - Quality (GET)
Location: Silvassa
Experience: Fresher
Industries: Engineering
Responsibilities:
Able to manage Quality Lab & Quality Team independently.
Able to manage quality department work as per defined quality plan.
Detailed knowledge of material testing specifically Physical Testing, Thermal Testing & mechanical testing.
Hand-on experience ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QA Officer
Location: Panoli - Ankleshwar
Experience: 3 - 5 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 ...
1 Opening(s)
1.0 Year(s) To 2.0 Year(s)
2.00 LPA TO 2.40 LPA
Position: QC Officer
Location: Valsad
Experience: 1 - 2 Years
Industries: Packaging
Responsibilities:
To conduct material analysis (in-process, raw material, samples, finished goods, etc.) and maintain records of the same
To maintain lab equipment’s functioning.
To maintain documentation for all lab procedures
Thorough knowledge of chemistry, analytical ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
4.00 LPA TO 5.00 LPA
Position: QC Officer
Location: Vapi
Experience: 3 - 5 Years
Industries: Pharma
Responsibilities:
Responsible for Documentation work in QC Department
Candidate must have knowledge of HPLC
Responsible for manufacturing the batch as per MOM or BMR.
Shall maintained all records related to manufacturing
Overall looking after the complete filling, packing activities and ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
9.00 LPA TO 10.00 LPA
Position: Dy. Manager - QA
Location: Mundra
Experience: 7 - 8 Years
Industries: Chemical
Responsibilities
To strengthen IMS systems
Ensure timely Internal audit process of Mundra
Support QC Documentation
Quality Plan In process & Finished Goods Inspection
PDI Checks
Audit findings to be closed by appropriate Corrective / Preventive Actions.
Required Skills
Know ...
1 Opening(s)
5.0 Year(s) To 6.0 Year(s)
5.00 LPA TO 6.00 LPA
Position: QA Officer
Location: Mundra
Experience: 5 - 6 Years
Industries: Chemical
Responsibilities
Process and Product audit
Inspection and audit to identify gaps
Ensure good quality Product
Rework / Repack activity reduction
Reduction in the customer complaints
PDI Checks
Required Skills
Good communication skills
Effective time
management
Ability to perform trend analysis
Understanding of statistical methods
Knowledge of ISO ...
2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Saykha near by Bharuch
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of ...