8 Opening(s)
2.0 Year(s) To 7.0 Year(s)
2.00 LPA TO 6.00 LPA
Monitoring of manufacturing related activity performed in Mfg facility.To maintain proper planning, scheduling and achievement of production with optimum utilization of resources.To preparation, review and implementation of all necessary standard operating procedure(SOP).To preparation and review of batch manufacturing record and protocol.Training given to all concern persons in their respective areas.To ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 3.60 LPA
Position: QA Officer
Location: Silvassa
Experience: 2 - 3 Years
Industries: Pharma
Responsibilities:
Control sample verification
Bmr bpr issurance, logbook
Format issurance and sop preparation
Documentation etc.
Required Skills:
Have good communication skills.
Logical Thinking
Organizing
Required Qualification: - B.Sc/M.Sc - Chemistry
Salary :- Upto 3.60 LPA
If you are interested for this opening please send updated resume ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Monitoring all processes in process & FG quality results and trends
Reporting periodic status on quality function periodically and formats as defined to operations and top management
Maintaining all documents as defined for integrated QMS/ EMS/ TS
Undertaking RCA for recurring failure of processes / products followed by evolving CAPA in consultation with ...
1 Opening(s)
10.0 Year(s) To 13.0 Year(s)
8.00 LPA TO 14.00 LPA
Role & responsibilities
1. Handling Deviations / Change Control / CAPA / Incidence Reports / Training Records.
2. Handling MFR / BMR / BPR preparation and Review
3. Handling preparation of SOPs / Protocols / QMS.
4. Handling Documentation Control.
5.. Handling of SMF /VMP / Qualification
6. Should be able to handle audit compliance and ...
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)
4.0 Year(s) To 10.0 Year(s)
3.00 LPA TO 5.00 LPA
Designation
Shift Incharge
Vacant Position
2
Department
Production
Location
Ankleshwar
Education
B.tech / B.E - Chemical
Required Experience
3 - 7 Yrs in Pharma Industry
CTC Range
3.00 to 6.00 LPA
Job Description
production operations in intermediate/API utility operations, Equipment Handling, online BMR/BPR filling, Distillation process, having exposure of handling CF, multi mill, AGNFD, FBD equipment.
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 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 ...
1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
15.00 LPA TO 17.00 LPA
Sr. Manager- Quality Assurance (QA QC)
Job Responsibilities?:-
Planning and execution of daily QA, QC operation activities for production in Injectable section to smooth Functioning work culture.
To prepare and review the SOPs of QA QC departments. Ensure qualification/ validation status of equipment’s
QA, QC of Internal and external Manufacturing as per SOP.
Experience of handling ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Position
Junior Executive - IPQA
CTC Range
Up to 4 LPA
Educational Qualification
B.Sc., B.Pharm, D.Pharm, M.Sc.
Total Experience
1 to 2 Years
Preferred Industry
Pharmaceutical (Parenteral Manufacturing unit)
Job Description
Batch Manufacturing record review
Batch manufacturing record issuance.
Line clearance
Calibration activity
Operation of Viable / Non-Viable monitoring
Preparation of annual product quality review.
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 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 ...