Quality Control Specialist - Mannitab Plant

ingredion; Nashik District; On-site; INR 900,000 - 1,300,000; Full time

Job summary

Ingredion is seeking a Quality Control Specialist for Mannitab Plant in Nashik. The role focuses on ensuring quality across raw materials, in-process and finished products with rigorous analytical testing and strict documentation.

The candidate will perform instrument calibration, stability studies, and maintain GLP/GDP records while supporting audits and training new staff. On-site work with potential cross-site flexibility.

Qualifications

• Education: B.Sc or M.Sc in Chemistry.
• 5+ years in a QC laboratory, preferably pharma/chemical.
• English fluency in written and spoken English.
• Knowledge of cGMP/GLP and regulatory guidelines.

Responsibilities

• Perform testing of in-process, finished product, raw material, packing material, and reference standards.
• Calibration and maintenance of laboratory instruments.
• Prepare and standardize volumetric solutions and glassware.
• Maintain GLP/GDP-compliant documentation and logbooks.
• Analyze samples for OOS, OOC and deviations.

Skills

English fluency

Strong communication

Attention to detail

Independent & teamwork

Education

B.Sc / M.Sc Chemistry

Tools

HPLC

GC

UV-Vis Spectroscopy

Job description

Quality Control Specialist - Mannitab Plant

LOCATION: Mannitab, Malegaon, Nashik

REPORTS TO: Senior Quality Specialist

DIRECT REPORTS: Quality Control Associates

SCOPE : Entire plant Quality responsibility.

WORKPLACE TYPE: On-site

Company Background:

Ingredion is a Fortune 500 provider of ingredient solutions that helps nourish, comfort, sustain, and delight people around the world. Ingredion's wide range of ingredient solutions is strategically designed to address changing consumer trends and preferences. Our specialty portfolio includes starch-based texturizers, clean and simple ingredients, plant-based proteins, sugar reduction and specialty sweeteners, and food systems. Our innovative ingredient solutions are used by consumers in everyday products, from foods and beverages to paper and pharmaceuticals. And we do it all in a planet-friendly sustainable manner.

Core Responsibilities:

• Procedures / Governance:
• Day to day assigned activities shall be performed and report to senior authority
• Any requirement related to QC shall be conveyed to reporting authority
• Testing of In process, Finished product, Raw material, Packing material, R&D sample, Reference standard, working standard & primary standard preparation, Toller samples, ETP samples, Water samples, out party samples and extra samples etc.
• Calibration activity of instruments.
• Perform Stability study analysis.
• Volumetric Solution Preparation & Standardization.
• General Cleaning of laboratory.
• Document Preparation related to laboratory.
• Stock solution preparation
• Perform Glassware Calibration
• Responsible for Instrument maintenance
• Maintain all Certificate Related to RM, Glassware
• Market complaint Sample analysis
• Sampling of RM/PM and other.
• Maintain records and logbooks of laboratory.
• Follow GLP and GDP.
• Testing sample for OOS, OOC, deviation and OOT.
• Maintain stock for chemicals and glass wares.
• Maintain control sample
• Responsible for discard expired and extra samples
• Any job activity assigned by HOD.
• Ensure to follow safety norms.
• Ensure to wear PPE during analysis.
• Training
• Impart training on Safety to new recruits, employees, contractors, contract employees.
• Periodically evaluate Training Effectiveness.
• Maintain updated records for all the Training activities.

Qualified candidates will have:

Mandatory requirements:

• Education requires, B.SC / M.SC Chemistry.
• Minimum of 5 years of experience in a quality control laboratory, preferably in the pharmaceutical industry / Chemical Industry.
• Relevant Experience in Quality Laboratory in Pharma / Chemical Industry
• English fluency, both written and spoken

Required behaviors and skills:

• Excellent problem-solving skills and attention to detail.
• Strong communication and documentation skills.
• Ability to work independently and as part of a team
• Proficiency in analytical techniques such as HPLC, GC, and UV-Vis Spectroscopy.
• Strong understanding of cGMP, GLP, and other regulatory guidelines
• Knowledge of MS Office / Quality Reports
• Preparing Quality reports & documents
• Fluence in working with different stakeholders within a manufacturing facility within a matrix organization
• Flexibility & Agility within the organization, working at different manufacturing sites within India.

Ingredion uses AI-enabled tools to support parts of the recruitment process, including resume screening and interview scheduling. These tools help match candidate skills to job requirements and streamline communication. All AI-assisted decisions are reviewed by our Talent Acquisition team to ensure fairness and compliance with applicable laws. By applying, you acknowledge that AI may be used to support your application journey.

Relocation Available:No