Assistant Manages quality operations or initiatives in the laboratory or the manufacturing environment in a smaller or less complex plant. Responsibilities may include reviewing and updating lab quality control processes, reviewing the results of product tests and audits, and working with internal and external customers to resolve problems. This role is distinguished from the Quality Managerial by working within a smaller or less complex plant. This Position also will be responsible for Implementing the ISO system Documentation.
EXPERIENCE REQUIREMENTS:
08-10 years of quality control or production experience within the manufacturing industry as a production supervisor, chemist, or equivalent.
EDUCATIONAL REQUIREMENTS:
Must have a bachelor s degree, Chemistry, Engineering, or Science.
KNOWLEDGE EXPERIENCE:
Must have at least 08 years of experience in Operations, Quality, or Technical with ISO /TS Knowledge.
Strong written and verbal communication skills.
Demonstrated ability to lead a cross-functional team to a successful outcome.
Strong Presentations skills Facilitator.
Results oriented.
Program knowledge of Microsoft Excel, Word, Access, Minitab.
Demonstrated success in leading Root Cause investigations and analysis tools.
Prefer Six Sigma Green Belt.
Able to work with an international team to drive improvement.
TECHNICAL/SKILL REQUIREMENTS:
Business Knowledge - Understanding of SW s BU s, products, Operations, and processes.
System Knowledge - Working knowledge of the basic functions and benefits of the SW systems.
Continuous Improvement Knowledge - Working knowledge of stats, ARC, and Lean.
WORK ENVIRONMENT:
Incumbents may be subjected to moving mechanical parts, electrical currents, vibrations, fumes, odors, dusts, gases, chemicals, oils, and other conditions found in manufacturing and laboratory environments.
ESSENTIAL JOB FUNCTIONS:
The Asst Manager - Quality Systems is accountable for all FG System Implementation.
Cycle time, FRC process improvement based on history.
Follow up for internal rejection/shop floor QC issues -coordinate with Production support in RCA process.
Follow up with technical -to resolve internal issues of Regular/ technical batches.
Support External /internal audits for QMS compliance maintain proper documentation.
QC document review - against QMS requirements.
Rework- Planning support to reduce the inventory.
Revalidation support.
Shift Management-Plan support of team s responsibility.
Color matching skill Supporting QC activities in the absence of QC team members.
QC Monthly report Overall - responsibility of safety compliance in QC.
Purchase-order and follow up (consumables, instruments, chemicals, Glasswares -Have tracking of receipt monthly requirements.
Support train team with respect to MOC/Risk assessments/gap assessments/sustainability ergo.
Tasks :
Responsible for Process Improvement activities leading to improvement in Quality, Productivity, Cost, Service Safety in Quality Function
Prepare and upgrade Work instructions and Work standards in all areas of Production to improve awareness of Operating personnel.
Responsible for the preparation, implementation, monitoring, and continuous up gradation of quality documents such as Control Plan, FMEA, etc
Conducting gauze R R
Preparation of Quality control documents that relate to QMS.