QC Head

We are hiring a ”QC Head" for a leading Manufacturing Chemicals Company. Position is based at Ankleshwar, Gujarat. Find below more details about this job opportunity:

About The Company:

The Company is  Manufacturing Chemicals for Oil and Gas Exploration, Hydraulic Fracturing (Fracking) and coiled tube Chemicals.

Job title: QC Head

Industry: Manufacturer

Job location: Ankleshwar, Gujarat

Experience : 12 years to 15 Years  only pharma line (API)

Education : M.Sc.(Chemistry) , Bpharm , Mpharm.

Job Description:

• Sampling, inspection & testing as per specifications of Raw material for release or rejection & its documentation.
• Sampling, inspection & testing as per specifications of packaging material for release or rejection & its documentation.
• Sampling, inspection & testing as per specifications of in- process product for release or rejection for further processing or re processing & its documentation.
• Sampling, inspection & testing as per specifications of finished products for release or rejection for further processing or re-processing & its documentation.
• Release or rejection of every batch of Drug Products for distribution and sale.
• Stability chamber handling, Stability testing and evaluation of shelf-life of products as per he stability interval planner.
• To prepare or review of stability testing protocol and report and summary report.
• Microbiological analysis of raw material, finished products, water and environmental bio-burden monitoring.
• To review of monthly trend prepared for physicochemical and microbiological trend data and it’s complying with the predefined specifications.
• Analytical investigation for complaints and product recalls.
• Analytical support for evaluating the Change Control proposals & Systems.
• Out of specification investigations for laboratory results.
• Investigation of deviations in the analysis.
• Analysis of Returned products (salvage and disposal).
• Internal Quality System Audits and Quality Review.
• Analysis for Control of non-conforming products.
• Reference standards, working standards, solution preparations.
• To plan and manage all the activities of the Quality Control Department To assure the quality of all products manufactured by the Company.
• To co-ordinate with manufacturing department in controlling their process and products at every stage of manufacturing to meet the established specifications through testing, auditing and reporting.
• To co-ordinate for development of specifications, the analytical procedure in coordination with Quality Assurance Department and R&D.
• To review the adequacy and relevance of specifications & analytical procedures in coordination with the Quality Assurance Department and R&D.
• To be responsible for instruments qualification as per the guideline and prepare protocols and reports accordingly.
• To ensure that audit trail system are implemented including systems for data integrity and data security.
• To co-ordinate technical audits of the Quality Control Laboratory to determine the analytical Quality Systems are yielding the highest quality information and to ensure that the analytical instrumentation is functioning properly and calibration and servicing is as per schedule.
• To be responsible for glassware cleaning protocol and report, also establish of cleaning procedures.
• To be responsible for the Quality Control functions and records, which shall include:
• Maintenance of Quality Control records, Control samples of raw materials and drug products/excipient each batch manufactured.
• Records of release, quarantine or rejection of components and finished products, containers,
• closures and labels based on Quality Control test results.
• Routine “Good Laboratory Practices Auditing" of the control process, and related areas.
• To suggest and organize training programs for the development of technical and administrative skills of all the employees to meet with cGLP regulations on the continuous basis, which shall be done by co-ordination with Plant and Quality Heads.
• To establish guidelines and procedures on cGMP and Good Laboratory Practice — Standard Operating Procedures of overall Quality Control Activities.
• Protocols related to Method / Process/ Cleaning/ Analytical Method Validation etc.
• To evaluate the Change Control suggestions for overall reviews of non-conformances, failure investigations, analyzing the Quality trends, investigations of market complaints, batch failure investigations, deviations, verifications of change control procedures, updating the specifications, test procedures, manufacturing processes etc.
• Validation of analytical test procedures, specifications, standard operating procedures (both pharmacopeial and In-house).
• To follow the reporting system as per the company procedure.

Key skills require:

QMS , API Industry , QC head 

CTC: Rs. 12.0/lpa to 14.0/lpa