Role
name:  QC (Analyst)

·        
Division                                  
–           Moraiya

·        
Department                          
–           Quality Control

·        
Category                                
–           Staff

·        
Qualification                         
–          
B.Sc./M.Sc./B.Pharma/M.Pharma

·        
Experience                             
–           3 – 5 Years

     Eligibility                      –         Minimum of 2 years in the same role at any formulation manufacturing site of Zydus in India. (minimum 2 performance rating in the current role)

Job Responsibilities:

·        
To perform the sampling of raw material and
re-test material.

·        
To perform Analysis of raw material/packaging
material/in-process samples/intermediate/bulk & finished products/ process
validation samples/ stability samples/ cleaning validation/method transfer
sample etc.

· Preferred to have a Hands-onexperience to perform analysis on HPLC/GC/UV-Visible Spectrophotometer / Dissolution Apparatus etc. 

·        
To make entries in SAP and LIMS as per requirement.

·        
To maintain the equipment/instrument in
operational, calibrated and qualified condition.

·        
To handle, store the testing samples as per
the respective material/ product requirement.

·        
To charge Stability samples as defined in SOP
and stability protocols.

·        
To handle and dispose the testing samples/rejections
after completion of analysis as per SOP.

·        
To ensure all primary standards/working
standards/certified standards/reference standards are stored as per the storage
conditions specified and documented.

·        
To ensure laboratory inventory management.

·        
To initiate incidence/ OOS/ OOT/ OOC/
Deviation /CAPA /Change control and investigate (if required) under
consultation with the department head/section head.

·        
To prepare the specification, standard
operating procedure, general test procedure and any other applicable document for
quality control department.  

·        
Responsible for maintaining a neat and systematic
work area at all times.

·        
Responsible for following Current Good
Laboratory Practices (cGLP).

·        
Identify and report quality issues.

·        
Report accidents and unsafe conditions or
unusual circumstances to section in-charge/ head.

·        
Other duties, which may be assigned from time
to time, by reporting manager.

·    Ensure/check proper cleaning of QC glass wares/tools/apparatus.

Essential job
requirements:

·        
Understands the purpose and function of analytical
process and equipment/instrument.

·        
Execute procedures for analysis in accordance
with standard test procedures (STP), general test
procedure (GTP), protocol and related SOPs. 

·        
Ability to document in log books, Test data
sheets while performing the job using good documentation practices.

·        
Attention to detail and ability to write and
record data as per ALCOA policy.

·        
Comply with the Privilege rights matrix (PRM)
of the Organization.