Quality Control Supervisor

Location

India | India

Job description

• In-process Quality laboratory operation monitoring for SUGAR labs.
• Communication Co-ordination with production against Process Product Quality deviation in all product processes.
• Checking and verification of process logs for avoiding gaps in good documentation and testing frequency.
• Check verify laboratory equipment calibration logs against frequency and communicate and correct if any deviation observed.
• Checking and verification of GLP Hygiene in both process Labs and corrective action whereas required.
• Ensure to check gaps in following SOPs by Quality Control analysts in both lab and take corrective action against same if required.
• Ensure to check and verify the scheduled meetings are attended by QC-Analyst every process area on scheduled time without fail.
• Allocation of manpower as per capability of Quality Control analysts and plan by managing shift schedule and leave alteration by making sure that there may not any gap in process labs regarding operational and analytical knowledge. Ensure to manage product process release as per adhered specification for customer/company. Ensure to develop Quality Control analysts by making them available for training (External Internal) to drive company agenda for skill behavioural development.
• Co-ordinate with production for planning and requirement in process laboratory and communicate the same to process Quality Control analysts.
• Maintaining Chemicals Inventory through stock verification making its indent requisition and get issuing from Store as per requirement and availability. Maintaining Logs Stationary Inventory through stock by making its indent requisition, proof verification approval, get issuing from Store as per requirement and Availability.
• By maintaining instrument spares Inventory through stock verification making its indent requisition and get issuing from Store as per requirement and availability.
• Make new equipment/machine indent requisition as per process requirement and improvement by taking approval from HOD and co-ordination from purchase Store.
• Investigation for process and finished goods deviation for Root Cause, record and escalate the same to take corrective action by co-ordinating with concern departments and stake holders.
• Visit to customer site against product customer complaint in finished goods whenever asked, for check investigate the root cause against issue and report the same to stake holders management along with customer. Do continuous improvement in working conditions, equipments, methods and records by implementing ideas innovation to reduces documentation gap, wastage, storage and work load reduction by co-ordinating with management.
• Co-ordination with QA-Product for final release and deviations, if any issue/deviation then take corrective action on the basis of investigation against same and acknowledge/communicate the same to all Process Executive QA to prevent reoccurrence and awareness. Visit process (production) shop floor PLC on routine basis and check for any abnormality or changes in process, ask for corrective action or reason against same to production and communicate the same to stake holders.
• Ensure to do Sensory analysis and record of finished good MDP with plant sensory panel and escalate if any abnormality is observed.
• Initiate Change control for Document/Facility changes and do comply all requirements as per standards by taking authorization and follow-ups from concern department till work is not completed.
• Trials for quality issues in products by co-ordinating with production to identify the issues, record and communicate the same with management and concerns. Make process deviation report of finished goods and highlight the major deviated parameter to management for acknowledgement and improvement against same.
• Investigation for Root Cause against customer complaint of Finished Products and Share the same to take corrective action by co-ordinating with concern departments and stake holders.
• Co-ordinate with logistics department for quality concern and do visit in Godown and communicate the issues abnormality to management and concern for immediate action Escalation and Implementation of management requirements policies in both process laboratory Quality Control analysts. As - 5S implementation in Process Labs by guiding and training to executives for sustaining the same.
• Active participation in Quality Food Safety Week celebration in plant as a team. Active Participation in hygiene drive week in plant as a team.

Key Accountabilities AS HYGIENIST:

• Maintain Hygiene throughout the plant. Maintain strict micro norms in Infant based material and ensure that no deviation regarding food safety aspects and plant is free from the pest.
• To check working of CIP activities related with hygiene SOPs of Dryers.
• To ensure implementation of rules regulations of HACCP ISO 22000 system in all dryers by following SOPs Records checking.
• To ensure functioning of OPRP CCP in plants (DMH, MDP LG), ensure no violation.
• Responsible to update on CCP OPRP status to QA Central Lab which works for release the finished product.
• Responsible for Laundry activities.
• Responsible for up-dation of records like HIRA, SOPs, HACCP Logbooks.
• To update all the boards after cleaning of filters of all dryers.
• Responsible for identify elimination of Hazards.
• To provide training to employees contract workers on troubleshooting MR1 culture of hygiene.
• Ensure all packaging area and warehouse are free from pest activities.
• Ensure GMP GHP compliance on the shop floor and implementation of Hygiene maintenance jobs throughout the plant.

What we will love about you:

Good Interpersonal Skill and Positive attitude

Ability to deal with plant people good in teamwork

Act as a valuable team player

Drive for Quality and Excellence

Discipline and Compliance

Make decisions with speed and determination

Education: M.Sc. (Food Tech, Microbiology, Chemistry)/ B.Tech-Food tech/ Chemical/ Biotech (Female preferred)

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