The QA/QC engineer's duties and responsibilities and functions of the QA/QC department. or Duties and responsibilities of QA QC inspector
Testing
& Confirmation of all Raw Materials & Packing materials.
Testings
& Confirmation of all Finished Goods, Intermediates & Sale returns.
Testing
& Decision on approving for new RM supplier selection.
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Reports,
Records, counter & Control samples as per IMS.
Redressal of
complaints after analysis of counter sample & all possible causes with concerned
departments.
Training for
improving the testing capabilities & versatilities and Capex for modification
& improving the testing facilities, daily calibration of QC equipment.
Coordinating
with R&D for any deviated production batches & their liquidation.
Coordinating
with Purchase department for any deviated raw material supplies & on
supplier substitution.
Coordinating
& communicating with all production departments & application facilities
for respective results & adjustments in production batches.
 Evolving new testing procedures for
strengthening & upgrading the testing facility.
Internal / External
audits with respect of IMS & MIS to all concerns.
 Monitoring of day-to-day base customer
requirements related to REACH, RSL, Â VOC,
OKOTEX, MSDS, TDS, SGS, COA & Other External Laboratory  Reports.
Involvement
in CACA of Internal Deviations with all concerns.
Correction,
Collection & monitoring of production BMRs, SOP’s & Methods.
Testing of
Raw Materials as per the defined standards & confirmation to Purchase &
Store departments.
Replacement of
R.M. counters & Control samples as per the defined schedule.
Standard
reagents preparation for testing.
A sampling of
raw material as per IMS norms.
Testing of
Sale- return material & confirmation to all concerns.
Documentation
work related to Raw-Materials and Sale Return as per IMS.
Operating of
S.T.P. plant on regular basis.
Testing of
E.T.P. & S.T.P. samples as per schedule.
Internal
communication with store & Purchase departments for respective Results
& Test Reports.
Testing of
New Supplier Selection samples for Substitution of RM & Confirmation to
Purchase.
Involving in
New testing implementation with Manager QC & Manager R&D.
Co-relate
the Existing Testing method with ASTM Method.
Maintaining
5S and Housekeeping on Daily Basis.
Monitoring
of Sale Return liquidation & proper storage with respect to quality.
Involving in new testing’s implementation with Manager QC / Manager R&D.
Preparation and correction of Standards of RM and FG, Method of Testing of RM and FG, and application also.
Testing of both R.M. and F.G. products in the absence of both the Executive.
Involvement in Liquidation of Deviated FG batches and Sale Return.
ADDITIONAL
RESPONSIBILITIES:-
 MR (ISO’s / IMS)
Coordination
& Communication with the Certification body regarding Audit Schedule, Audit
Plan, and Quotation & Certification.
Conducting Internal & External Audits & Closer of
Non-Conformists (NC).
IMS manual, Risk Assessment, Management Program, Management Review
Meeting, Organization Knowledge, On-site emergency Plan, Rule & Regulation
Register, Work Instruction, Master list, Int. & Ext. Communication.
To get the
external calibration of equipment as per their respective time schedule.
PCB, EHS, NARCOTICS
PCB Data
preparation & submission (Hard & Soft both) to the office-&
Head-office as per the schedule.
Environmental
testing on various points like Nose-Level, Lux-Level, Drinking Water, Ambient
Air Quality, Stack Emission, Work-zone area, etc as per schedule.
Communication,
coordination & follow-up regarding PCB Consent & Authorization.
Quarterly
return & Record maintenance for the Narcotics department regarding some specific
reagents.
HWM & TREATMENT PLANT
Identification
of Key focus area to reducing the Process- Waste, Monitoring & Maintaining
of “Hazardous Waste Data “& Hazardous waste disposal to SSWML as per the
PCB norms.
Monitoring
Performance and results of ETP & STP plants and related Compliances.
Coordination
& communication with external Bodies like SSWML, CETP etc.
