Qc Manager

About Us :

Sydler Group of Companies is a leading manufacturer and exporter of excellent quality and reliable Pharmaceutical Formulations, Herbal formulations, Nutraceuticals & Dietary Supplements, and Nutritional food products, catering to discerning market needs globally. Ever since its inception in 2004, we have set new benchmarks in the arena of herbal products manufacturing, leveraging state-of-the-art infrastructure, skilled professionals, and uncompromised commitment towards quality and innovation.

Role : QC Manager

To be overall responsible for all quality control functions in the factory.

To review and check all sops related with QC and quality systems.

To review and check all specifications, test method, protocol of Finished goods, raw material, packing material, intermediates etc.

To ensure that all necessary testing is carried out and the associated records evaluated.

To approve and analytical validations of procedures.

To preparation of working standard & related document for working standard certificate & consumption record.

To Approved the finished product& Bulk sample Analysis certificate and documents.

To impart training to all personnel and To Prepare Training Need Identification of QC department.

To check and ensure the GMP and GLP compliances.

Responsible to work allocations for finished product & planning working standard preparation.

To ensure the calibration, qualification and maintenance of quality control department and equipment.

To check for the sanitation of premises and equipments, hygiene & housekeeping of factory.

To participate in self-inspection, risk assessment, external audit, CAPA meeting, complaint, OOT, OOS, deviation investigation.

To review complaint, recall, deviation, change control, OOS, process and hold time validation, equipment / system qualification, calibration, risk assessment, new or additional vendor, Query, APR, non-conformity, reprocess, returned good etc. if any in impact in process, report and practices.

Review regularly the validation master plan for the effectiveness of the implementation for QC equipment / Method Validation.

Instrument procurement, Purchase order Initiation and Approval for requirements of QC.

Party testing laboratories Invoice checking and submission.

Preparation of Artwork and approval of shade card.

To monitor compliances for systems and documents.

To comply with global regulatory guidelines.

To participate in management reviews of process performance, product quality and quality management system.

To understand the method study & motion study of all the operation procedures for identifying areas of quality improvements.

To attend Regulatory Affair (IRA) departments queries and work accordingly and To organize all needed the documents for regulatory submissions.

To do budgeting of his department and ensure resource availability.

Assist subordinate to carry out job responsibility smoothly.

To ensure the weekly and monthly report against activity.

Time to time communicates any failure or abnormal notification/critical observations / non-compliance/extraordinary observation to Quality Head for their attention and progress report.

To communicate system enhancement or a improvement in exiting system to the management.

To Monitor all analytical validation related and technology transfer activities.

Set quality goals and objectives for the company and develop plans to meet those goals and objectives.

To coordinating with QA, production, engineering and warehouse team, Purchase, business, regulatory so as to manufacture product with quality attributes and in given timelines.

Activities related to ERP.