3,933 Chemical Production jobs in India

We are looking for a Production Chemist to join our team for the preparation and manufacturing of laboratory reagents, buffers, and chemical solutions. Responsible for accurate preparation, documentation, and quality control of Reagents.

Required Candidate profile

Strong understanding of chemistry concepts (molarity, normality, titration, solution preparation)

Knowledge of laboratory reagent preparation handle laboratory equipment and glassware.

Perks and benefits

Bonus, over time

Will be handling the Production Process,

Planning Process.

Handling of DCS Systems & SCADA System

knowledge of Handling of the Flammable Chemical process.

Proper utilisation of Man, Machine Materials

Planning and deliverances on time.

Job Description

1. QC Manager

Responsibilities:

• Lead the QC department, ensuring testing of raw materials, intermediates, and finished products as per cGMP standards.
• Review and approve analytical reports, stability studies, and method validations.
• Ensure compliance with regulatory guidelines (USFDA, EU, WHO, ISO).
• Handle laboratory audits, OOS/OOT investigations, CAPA, and data integrity compliance.
• Manage team performance, training, and lab resource planning.

Requirements:

• M.Sc./B.Pharm/M.Pharm with 1012 years of QC experience in pharma.
• Strong knowledge of regulatory audits, HPLC/GC, and QC systems.
• Leadership and team management skills.

2. QC QMS Manager

Responsibilities:

• Manage QC-related Quality Management Systems (QMS).
• Ensure implementation of SOPs, change controls, deviations, CAPA, and risk management.
• Drive data integrity compliance and electronic documentation practices.
• Support regulatory inspections and customer audits.

Requirements:

• M.Sc./M.Pharm with 810 years in QC/QMS functions.
• Strong understanding of QMS, audit handling, and regulatory expectations.

3. QC Sr. Executive (Reviewer)

Responsibilities:

• Review analytical data generated by QC analysts.
• Ensure compliance with SOPs, specifications, and regulatory guidelines.
• Support OOS/OOT investigations and CAPA implementation.
• Coordinate with QA for document control and release processes.

Requirements:

M.Sc./B.Pharm with 58 years in QC reviewing role.

• Strong knowledge of chromatography (HPLC, GC), dissolution, and wet chemistry.

4. Microbiology Executive

Responsibilities:

• Perform microbiological analysis of raw materials, finished products, and water systems.
• Conduct environmental monitoring, sterility testing, and microbial limit testing.
• Maintain laboratory cultures, reference standards, and GLP compliance.
• Support regulatory audits and documentation.

Requirements:

• M.Sc. Microbiology with 3–6 years in pharmaceutical microbiology.
• Knowledge of clean room practices and sterile area monitoring.

5. QA Manager

Responsibilities:

• Lead QA operations including batch release, documentation review, and QMS compliance.
• Oversee change controls, deviations, CAPA, and training programs.
• Ensure adherence to cGMP, GDP, and data integrity standards.
• Prepare and coordinate regulatory and customer audits.

Requirements:

• M.Pharm/B.Pharm with 10+ years in QA roles.
• Strong expertise in QMS, audit handling, and regulatory guidelines.

6. QA Executive

Responsibilities:

• Execute batch record review, in-process quality checks, and document control.
• Monitor shop floor activities for cGMP compliance.
• Assist in handling deviations, change controls, and CAPA.
• Support internal audits and training sessions.

Requirements:

• B.Pharm/M.Sc. with 2–5 years in QA operations.
• Good knowledge of documentation practices and regulatory compliance.

Company Description

FDC Limited is a leading pharmaceutical company with accreditations from the US-FDA, UK-MHRA, MCC-RSA, and the UAE. Known for its innovation in manufacturing ORS and Ophthalmics, FDC operates globally approved facilities in Maharashtra, Goa, and Himachal Pradesh. Since 1936, FDC has been dedicated to innovating, manufacturing, and marketing high-quality healthcare products, exporting over 300 products to more than 50 countries. Our committed employees and partners ensure the delivery of world-class quality products and services.

Role Description

This is a full-time on-site role for a Quality Control - Officer to Sr. Executive located in Aurangabad. The role involves conducting quality control tests, performing laboratory analyses, and ensuring products meet regulatory standards and quality assurance protocols. The candidate will work closely with the quality assurance team to maintain high standards of product quality and contribute to continuous improvement efforts.

Qualifications

• Proficiency in Quality Control and Quality Assurance
• Strong Analytical Skills and Laboratory Skills, HPLC, GC, LIMS
• Effective Communication skills
• Attention to detail and problem-solving abilities
• Bachelor's or Master's degree in Pharmacy, Chemistry, or relevant field
• Experience in the pharmaceutical industry is preferred
• Familiarity with regulatory requirements and quality standards

Job Purpose:

To ensure that all products manufactured meet the quality standards and specifications of METAIL Industries. The Quality Employee is responsible for inspecting, testing, and evaluating raw materials, in-process production, and finished goods to maintain consistent quality and minimize defects.

Key Responsibilities:

Perform regular inspections and tests on incoming materials, in-process items, and finished goods.

Monitor production processes to ensure compliance with quality standards.

Identify non-conforming products or processes and recommend corrective actions.

Maintain detailed reports on inspections, tests, and quality checks.

Work closely with production and engineering teams to resolve quality issues.

Assist in the development and implementation of quality control procedures and standards.

Support internal audits and prepare documentation for external quality certifications (e.g., ISO).

Ensure that measuring instruments and inspection tools are calibrated and maintained.

Train and support production staff on quality requirements and best practices.

Participate in continuous improvement initiatives (e.g., 5S, Kaizen, Six Sigma).

Qualifications & Skills:

Diploma or Bachelor's degree in Mechanical Engineering / Industrial Engineering / Quality Management or related field.

1–3 years of experience in Quality Assurance / Quality Control in a manufacturing setup (preferably textile, automotive, or consumer goods).

Strong knowledge of quality inspection tools (e.g., Vernier caliper, micrometer, etc.).

Familiarity with ISO 9001, Six Sigma, or other quality standards is a plus.

Good documentation and report-writing skills.

Strong attention to detail, problem-solving ability, and a proactive mindset.

Basic computer skills (MS Office, Excel, etc.).

Job Type: Full-time

Pay: ₹15, ₹20,000.00 per month

Work Location: In person

Job Title: Quality Control Assisstant

Job Description:

• Ensure the Product outcomes as per drawing
• Updating and maintaining the report
• Need to check the product on cycle count
• Basic knowledge in measuring tools

Freshers can also apply

Immediate joining is required

Job timing : 9:00AM to 6:00PM

Working days: Monday to Saturday

For Contact:

Job Types: Full-time, Permanent

Pay: From ₹9,000.00 per month

Benefits:

• Leave encashment
• Paid time off

Work Location: In person

Company Overview

Founded in 1987, Miraj Group has established itself as a leading player in various industries, including printing, packaging, and FMCG. Serving millions of customers in India, the company is known for its valuable products and services. Headquartered in Nathdwara, Miraj Group continues to grow with a workforce of employees in the manufacturing sector.

Job Overview

We are seeking a dedicated Quality Control professional to join our team in a full-time, mid-level position located in Korba. The candidate should have 4 to 6 years of relevant work experience, focusing on maintaining the highest quality standards in our manufacturing processes. The ideal candidate will be adept at ensuring product consistency and reliability in commercial projects.

Qualifications and Skills

• Minimum of 4 years and a maximum of 6 years of experience in quality control operations within the manufacturing sector.
• Must have hands-on experience in quality inspection and the use of inspection techniques for ensuring product excellence (Mandatory skill).
• Expertise in overseeing commercial projects and ensuring adherence to quality parameters (Mandatory skill).
• Proficient in site quality supervision, capable of managing on-site quality checks and ensuring compliance.
• Experience as a quality control engineer, with a focus on implementing quality assurance practices.
• Skilled in material testing, with the ability to perform and interpret various test results to ensure integrity and performance.
• Understanding of concrete testing processes and methodologies to ensure structural quality.
• Ability to collaborate effectively with various departments to enhance quality standards and processes.

Roles and Responsibilities

• Conduct thorough inspections and evaluations of manufacturing processes to ensure quality standards are met.
• Implement inspection techniques and perform regular quality checks on products and materials used.
• Oversee commercial projects to maintain the highest quality standards and ensure compliance with regulatory requirements.
• Collaborate with engineering teams to address quality issues and develop improvement strategies.
• Prepare and maintain detailed reports on inspection findings, quality issues, and corrective actions.
• Organize and execute material testing and verification processes, ensuring test results meet requisite standards.
• Manage site quality supervision, providing guidance to ensure operational quality remains uncompromised.
• Stay updated with industry trends and advancements in quality control technologies and methodologies.

Role & responsibilities :-

Proficiency in using laboratory instruments like HPLC, UV-Vis spectroscopy, KF apparatus and other analytical tools for testing of finished products and stability samples.

Analytical Testing: Proficiency in using laboratory instruments like HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), UV-Vis spectroscopy, and other analytical tools for testing Stability sample and finished products.

Troubleshooting Analytical Instruments: Skill in identifying and addressing technical issues with laboratory equipment.

Must have knowledge of ALCOA+ principals.

Good Laboratory Practices (GLP): Familiarity with GLP guidelines for maintaining the quality and integrity of lab tests and results.

Communication Skills: Ability to communicate effectively with cross-functional teams, including R&D, production, and regulatory affairs.

Familiarity with GLP guidelines for maintaining the quality and integrity of lab tests and results.

Familiarity with global regulatory guidelines for pharmaceutical testing and quality control.

Preferred candidate profile

Perks and benefits