1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 5.00 LPA
Job title : Supervisor - GMP DocumentationDesired Qualifications : BSc./MSc./Diploma (Chemical)Experience Required : 1.0 Years+Industry : Pharmaceutical/ Fine/Speciality ChemicalsJob Function Dept- : Production (GMP)Location : DahejTechnical:? Having Batch processing experience on shop floor and familiar with equipment like reactor,centrifuge, dryer etc.? Having basic awareness about unit operation and unit process.? ...
2 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 5.00 LPA
Exp in Soft gelatine capsules manufacturing
Knowledge of Gelatin
Medicine Preparation
Encapsulation Machine
knowledge of documentation Of BMR and Log Book, SOP
Exp in Soft gelatine capsules manufacturing
Knowledge of Gelatin
Medicine Preparation
Encapsulation Machine
knowledge of documentation Of BMR and Log Book, SOP
Exp in Soft gelatine capsules manufacturing
Knowledge of Gelatin
Medicine Preparation
Encapsulation Machine
knowledge of documentation Of BMR and Log ...
3 Opening(s)
4.0 Year(s) To 7.0 Year(s)
Not Disclosed by Recruiter
Job Responsibilities:
Review & Control all QMS related document like change control, Deviation, out of Specification, CAPA and incident.
Review of master BMR/BPR, SOP and specification.
Preparation & review of departmental SOP.
Participate in internal audit and coordinate for complies and closure.
To coordinate in root cause and risk assessment.
Review and maintain the executed documents ...
1 Opening(s)
2.0 Year(s) To 10.0 Year(s)
2.00 LPA TO 8.00 LPA
ProductionReports To: Production Manager / Plant HeadLocation: Manufacturing PlantPurpose of the RoleTo schedule, operate, and monitor the production process of aroma chemicals(fragrance & flavour intermediates) in the plant, ensuring timely production in line withquality, safety, and output targets.Key Responsibilities1. Production Planning & Execution• Prepare and implement daily/ shift wise production ...
50 Opening(s)
3.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 5.00 LPA
Department: Production Location: Manufacturing Plant Experience: 2–6 Years
Qualification: B.Sc/M.Sc Chemistry or Diploma/B.E./B.Tech Chemical Engineering
Key Responsibilities:
Execute daily/shift-wise production plans and batch scheduling.
Handle batch reactor, reaction, distillation, filtration, extraction & drying operations.
Monitor process parameters such as temperature, pressure, pH and reaction time.
Ensure compliance with SOPs, BMR, GMP/ISO and safety procedures.
Coordinate with QC/QA, ...
1 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.50 LPA TO 4.50 LPA
Requirement :
Position : Production Officer
Location : Panoli
Experience : 3 – 5 yrs
Salary Budget : 2.50 to 4.50 LPA
Qualification : Bsc Chemistry / Dip Chemical
Gender : Male
Responsibilities Includes:
Monitor & oversee all the production operations & ensure they are being performed as per SOP
Ensure safety of manpower at production ...
2 Opening(s)
3.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 6.00 LPA
Key Responsibilities:
Perform in-process checks during manufacturing and packaging (weight variation, hardness, friability, disintegration, pH, viscosity, leak test, etc.).
Ensure batch manufacturing records (BMR/BPR) are correctly filled and compliant.
Monitor line clearance, environmental conditions, and GMP practices on shop floor.
Review and verify critical process parameters (CPP) and ensure adherence to SOPs.
Check and approve ...
1 Opening(s)
0 To 2.0 Year(s)
0.00 LPA TO 2.40 LPA
Executing production activities as per approved Batch Manufacturing Records (BMR) and Standard Operating Procedures (SOP).
Monitoring production parameters such as temperature, humidity, and pressure during manufacturing.
Maintaining accurate records, including logbooks, BMR, and cleaning checklists.
Conducting in-process checks to ensure quality standards are met at each stage of production.
Coordinating with Quality Assurance (QA), ...
1 Opening(s)
3.0 Year(s) To 4.0 Year(s)
3.00 LPA TO 4.50 LPA
Duties & Responsibility :· Quality Management System Implementation and Modification control.· Document Control.· Approval for batch release.· Review and approval of Qualification Document.· Review and approval of Calibration and Validation document.· Planning, execution and compliance of both internal and external audits.· Preparation of audit compliance report· Review and approval ofSMF, VMP and Quality manual.· Review and approval of BMR, ...
1 Opening(s)
6.0 Year(s) To 9.0 Year(s)
3.00 LPA TO 6.90 LPA
Major Responsibilities:
Ø Quality Management System Implementation and Modification control.
Ø Document Control.
Ø Approval for batch release.
Ø Review and approval of Qualification Document.
Ø Review and approval of Calibration and Validation document.
Ø Planning, execution and compliance of both internal and external audits.
Ø Preparation of audit compliance report.
Job description
Minor Responsibilities:
Ø Review and approval of SMF, VMP and Quality manual.
Ø Review and approval of ...