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)
									 
									5.0 Year(s) To 7.0 Year(s)								
							
									 
									3.00 LPA TO 4.80 LPA								
							
									Position:          QC Executive
Location:          Daman
Experience:      5 - 7  Years
Industries:       Pharma
 
Responsibilities:
Analytical Testing:
Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, IR, etc.
Conduct assay, dissolution, impurity profiling, and related substance testing as per pharmacopeial standards (USP, BP, ... 
								
							1 Opening(s)
									 
									8.0 Year(s) To 12.0 Year(s)								
							
									 
									13.00 LPA TO 15.00 LPA								
							
									 Position:         Maintenance Manager
Location:         Ankleshwar
Experience:     8 - 12 Years
Industries:       Pharma
 
Responsibilities:   
Maintenance operations
Lead the planning, scheduling, and execution of all maintenance activities, including corrective, preventive (PM), and predictive (PdM) maintenance.
Develop and implement preventive maintenance schedules and standard operating procedures (SOPs) for all production ... 
								
							1 Opening(s)
									 
									12.0 Year(s) To 18.0 Year(s)								
							
									 
									20.00 LPA TO 25.00 LPA								
							
									Position:        Sr. Manager - QC 
Location:        Ahmedabad
Experience:    12 - 18 Years
Industries:     Pharma
 
Responsibilities:        
Lead and oversee the entire Quality Control department operations.
Ensure compliance with cGMP, regulatory guidelines, and company quality standards.
Review and approve analytical methods, specifications, and validation protocols.
Supervise raw material, in-process, and ... 
								
							1 Opening(s)
									 
									5.0 Year(s) To 6.0 Year(s)								
							
									 
									6.00 LPA TO 7.00 LPA								
							
									Position:         RA Executive (Khopoli)
Location:        Khopoli - Raigarh
Experience:     5 - 6 Years
Industries:      Pharma 
 
Responsibilities:
Dossier Preparation & Submission
Prepare, compile, and review CTD / ACTD / eCTD dossiers for product registration in global markets.
Coordinate for ANDA, DMF, CEP, COS, and other regulatory submissions for APIs and ... 
								
							2 Opening(s)
									 
									3.0 Year(s) To 8.0 Year(s)								
							
									 
									3.00 LPA TO 6.00 LPA								
							
									Key Responsibilities:
Handle QMS activities including CAPA, Change Control, Deviation, and OOS/OOT.
Prepare, review, and maintain QMS documentation as per cGMP and regulatory guidelines.
Support internal audits, external audits, and regulatory inspections.
Ensure timely closure of quality incidents and continuous improvement initiatives.
Coordinate with cross-functional teams for compliance and quality culture.
Requirements:
B.Pharm / M.Sc (Chemistry) with ... 
								
							1 Opening(s)
									 
									6.0 Year(s) To 10.0 Year(s)								
							
									 
									6.00 LPA TO 7.00 LPA								
							
									Position:          QC Executive
Location:          Silvassa 
Experience:      6 - 10  Years
Industries:       Pharma
 
Responsibilities:
Analytical Testing:
Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, IR, etc.
Conduct assay, dissolution, impurity profiling, and related substance testing as per pharmacopeial standards (USP, BP, IP, etc.).
Instrument Operation & ... 
								
							1 Opening(s)
									 
									15.0 Year(s) To 25.0 Year(s)								
							
									 
									15.00 LPA TO 20.00 LPA								
							
									
To review and implement a Quality Management System for cGMP compliance at the Production (Injectable) plant.
To prepare, Review and Approve BMR, BPR and related documents.
Handling of Caliber QAMS, DMS, Nichelon 5 CMS, Dynamic, Schedule and Track and trace Serialization & aggregation.
Giving the required training also Responsible for Media fill and ... 
								
							15 Opening(s)
									 
									2.0 Year(s) To 7.0 Year(s)								
							
									 
									2.00 LPA TO 6.00 LPA								
							
									 
Key Responsibilities
 
1. Sample Analysis and Testing:
Perform chemical and instrumental analysis of raw materials, intermediates, and finished API products according to approved specifications and Standard Testing Procedures (STPs).
Conduct testing using a range of laboratory instruments, including but not limited to:
High-Performance Liquid Chromatography (HPLC)
Gas Chromatography (GC)
Fourier-Transform Infrared (FT-IR) Spectroscopy
Ultraviolet-Visible (UV-Vis) Spectroscopy
Karl Fischer ... 
								
							1 Opening(s)
									 
									4.0 Year(s) To 5.0 Year(s)								
							
									 
									Not Disclosed by Recruiter								
							
									Job Description:
We are hiring an experienced QC professional to lead and manage quality control operations in our API manufacturing unit. The Assistant Manager will be responsible for supervising analytical activities, ensuring regulatory compliance, handling audits, and supporting continuous improvement initiatives.
Key Responsibilities:
Supervise routine analysis of raw materials, intermediates, and finished APIs
Review ...