Executive - Quality Control

KEY ACCOUNTABILITIES 

Analysis and approval 

Sampling, analysis and ascertaining quality of raw materials, packaging material, intermediates, In-process samples and API for Chemistry Ankleshwar. 

Testing of the method validation samples and process validation samples and cleaning validation. 

Perform analysis and documentation of API finished product stability study as per stability study protocol. 

Coordinating with Production, Stores and QA for Approval / Rejection of raw materials/finished product. 

Validation and verification of analytical procedures as per requirement. 

Reporting OOS / OOT results and deviations. 

Maintaining retained samples as per standard procedure. 

 Assisting in investigation of customer complaint. 

 Testing of new samples (Vendor approval) 

 Training of subordinates 

Give required suggestion for corrective actions and to plan effective preventive actions for the up gradation of the quality system. 

To ensure proper maintenance of the stability samples and their management. 

Disposal of waste according to the approved procedures. 

Continual reduction in the waste generation and effluent management. 

Co-ordination with microbiology lab (Pharmaceuticals) for microbial analysis of products and utilities. 

Documentation 

Generation, managing and archiving Documents including raw data, reports, COA etc as per requirements. 

Preparation and implementation of the SOPS in the laboratories system. 

Specification preparation and implementing for API raw material and API finished product according to requirement. 

Providing technical support in compiling Annual Product Review. 

Analytical method development when required. 

     2.6.Executing on line documentation 

Laboratory Management 

Qualification and Validation of instruments/equipments 

Appropriate training and guidance to the subordinates. 

Safety in the laboratory. 

Regular housekeeping and upkeep of the work area.  

Maintaining adequate inventory of chemicals and reference standards. 

Adapting relevant technologies and systems in Analytics. 

Laboratory equipment calibration and their maintenance. 

Developing training modules for improvement / training for HSE and Quality      systems 

Generate up gradation plans as need basis. 

Any other activity assigned by the In charge, Analytics 

Regulatory and other Compliance 

Compliance to current GMP guidelines. 

Compliance to local and international HSE norms. 

Regulatory compliance 

ISO 14000 related activities. 

Regular Pharmacopoeia and regulatory requirement review for compliance. 

To participate in any regulatory inspection that takes place at the site. 

Training of self and subordinates on quality and HSE systems 

Team member 

Member of validation team. 

Member of Analytical transfer team. 

Participating in discussions and giving feedback to Manager, Analytics regarding on-going activities. 

Other projects 

Trouble shooting activities. 

Participation in Industrial Excellence projects. 

Identifying and correcting unsafe conditions or behaviors and promptly reporting other potentially hazardous situations 

Plant round 

Plant round in absence of QA and during IInd and IIIrd shift. 

Online checking of critical process parameters during round.