• Responsible for the planning and supervision of all QC labs finished products and maintain online compliance in all activities.

• To assign the work for analysts and supervise the analysis of finished products and ensure on time completion of analysis.

• To coordinate with Production plants for planning of analysis.

• Handling and supervision of Technology transfer projects.

• To check and ensure proper usage of all the QC equipment.

• To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.

• Processing and approve for all HPLC &GC analytical data for all analysts, review and check all the Audit trial for all the instruments.

• To train the QC personnel on all the applicable procedures, specifications, testing methods and qualify analysts to perform various QC analysis.

• To prepare and revise the SOPs and work instructions.

• To ensure the analysis are performed correctly as per applicable procedures and the raw data is checked for correctness, accuracy and compliance.

• To perform investigation for the lab incidents, OOS, OOL results, deviations and take appropriate corrective and preventive actions.

• Follow up &Close all the EQMS actions ( CAPA , OOS , Deviations , CCF )

• To lock the results in SAP, to create notifications & reservations for maintaining enough stock of chemicals & consumables.

• To involve and support in external and internal audits and to close the audit observations on time.

• Review and approve protocols and reports such as method validation, method transfer, process validation and stability.

• To handle and close the Quality management system actions like Deviations, OOS, CAPAs, AMS and Change controls using Amplelogic system.

• To follow and ensure data integrity and good documentation practices are implemented in the QC labs.

• To ensure and follow GLP, GMP, safety procedures and maintain hygienic conditions in lab.

• Shall be authorized designee for responsibilities of QC Sr Manager.

• Apart from above, the works assigned by the Head of the department/designee.

• Bachelor\'s degree in Pharmacy / Science.

• Proficient with computer software application

• In terms of competency you are highly result oriented with strong sense of accountability & ownership.

• High on communication and collaboration, having an ability to manage multiple stakeholders at a time.

• Strong eye for details, having expertise to understand, review and implement the compliance inputs from Quality point of view.

• In-depth knowledge of the industry\'s standards and regulations guidelines excellent knowledge of reporting procedures and record keeping.

• Must be able to manage tasks and priorities and easily adapt to changing situations.

• Ability to create cross functional relations and manage conflicts.

• Problem Solving and high agility on taking right scientific decisions.

Julphar