1 Opening(s)
20.0 Year(s) To 25.0 Year(s)
45.00 LPA TO 55.00 LPA
Position: Operation Head (Corporate)
Location: Ahmedabad
Experience: 20 - 25 Years
Industries: Pharma – Formulation
Responsibilities:
Strategic Leadership:
Overall responsible for all manufacturing units operations
Develop and implement operational strategies aligned with the company’s goals and objectives.
Drive continuous improvement initiatives to enhance efficiency, quality, and profitability.
Collaborate with senior management to set performance ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 20.00 LPA
Position: QC Manager
Location: Ahmedabad
Experience: 10 - 12 Years
Industries: Pharma - Formulation Responsibilities:
Responsible for Overall management of Quality Control Laboratory and compliance to applicable standards.
To approve or reject, as he sees fit, raw materials, packing materials, semi-finished product and finished products ...
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
5.00 LPA TO 7.00 LPA
Position: Sr. Executive - PPIC
Location: Ahmedabad
Experience: 5 - 8 years
Industries: Pharma
Job Responsibilities:
Process Improvement: Identify areas for improvement in the manufacturing process and implement changes to increase efficiency, quality, and compliance.
Product Knowledge: Provide in-depth knowledge of products, including formulation, manufacturing, and quality control.
Regulatory Compliance: Ensure adherence to regulatory ...
1 Opening(s)
8.0 Year(s) To 10.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: Sr. Executive - Production & Project
Location: Ahmedabad
Experience: 8 - 10 years
Industries: Pharma
Job Responsibilities:
Operational Management
Preparation of URS, ensure equipment qualification, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
Oversee operations, ensuring efficient and compliant production.
Manage project & production schedules, production planning, ...
1 Opening(s)
20.0 Year(s) To 22.0 Year(s)
20.00 LPA TO 25.00 LPA
Position: Head Production (Project Specialist)
Location: Ahmedabad
Experience: 20 -22 years
Industries: Pharma
Job Responsibilities:
Project Planning: Develop and manage project plans, timelines, and budgets.
Team Leadership: Lead and coordinate cross-functional project teams, including R&D, Manufacturing, Quality, and Regulatory Affairs.
Objective Setting: Define and communicate project objectives, scope, and deliverables.
Risk Management: Identify, assess, and mitigate project ...
1 Opening(s)
10.0 Year(s) To 12.0 Year(s)
10.00 LPA TO 12.00 LPA
Position: Plant Head
Location: Silvassa
Experience: 10 - 12 Years
Industries: Pharma - Formulation
Responsibilities:
Direct and co-ordinate daily operation of the plant.
Oversee all levels of staff activity and performance. To maintain strict discipline in the plant
Develop process to increase productivity and performance.
To ensure maximum utilization of manpower & machinery
To ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: QA Officer
Location: Vapi
Experience: 2- 3 Years
Industries: Pharma API
Responsibilities:
Responsible for document and data control activities
To prepare and update all master document list as per requirement.
To initiate change control/document amendment for any change or improvement in the process.
Review of BMR/BPR, APQR and QMS Documents
Responsible ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
3.80 LPA TO 4.80 LPA
Position: Officer/Executive - Production
Location: Vapi
Experience: 1 - 5 Years
Industries: Pharma
Responsibilities:
Responsible for shift production quantity & quality
Responsible for plant's housekeeping
Monitor plant to ensure efficient production.
Responsible for handling distillation process.
Required Skills
Logical thinking.
Organizing.
Good in communication.
Required Qualification: - B.Sc/M.Sc - Chemistry/B.Pharm/M.Pharm
Salary :- ...
1 Opening(s)
7.0 Year(s) To 8.0 Year(s)
7.00 LPA TO 9.00 LPA
Position: Sr. Executive - RA
Location: Daman
Experience: 7 to 8 Years
Industries: Pharma
Responsibilities:
Maintaining compliance with Dossiers, ISO 13485, WHO/GMP requirements.
Preparing technical and Drug master files
Preparing and compiling documents for registration to various countries.
Reviewing and updating of documents w.r.t various regulatory requirements
Reviewing and updating of ...
1 Opening(s)
1.0 Year(s) To 3.0 Year(s)
2.50 LPA TO 3.00 LPA
Review and approval of artwork.
Validate, Checking, analysis and maintain data for samples before final dispatch of each product.
Vendor audit and online proof verification and personal visit if required.
Prepare document of Export Po, Product information sheet, finished product specification.
Follow up from Party for approval of finished goods sample before dispatch.
Sample approved ...