1,541 Quality Control Analyst jobs in India

Job Title: QC Analyst – HPLC Specialist

Location: Dabaspet , Bangalore – , India

Department: Quality Control

Industry: Pharmaceuticals (Formulations)

Experience: 2–5 years

Employment Type: Full-time

Company Overview:

We are a reputed pharmaceutical formulation company based out of Bangalore committed to delivering high-quality products to domestic  and export markets. We are currently seeking a skilled and detail-oriented QC Analyst with hands-on experience in HPLC to join our Quality Control team.

Position Summary:

The QC Analyst will be responsible for conducting analytical testing of raw materials, in-process samples, and finished products with a primary focus on HPLC. The ideal candidate should be well-versed in regulatory standards and capable of working in a fast-paced, cGMP-compliant laboratory environment.

Key Responsibilities:

• Perform routine and non-routine analysis using HPLC for assay, dissolution, related substances, and stability studies
• Preparation, review, and maintenance of test data, analytical records, and reports in compliance with GMP and GLP
• Calibrate, operate, and troubleshoot HPLC and other analytical instruments (e.g., UV, FTIR, pH meter)
• Conduct testing of raw materials, intermediates, and finished formulations as per pharmacopeial and internal specifications
• Assist in method validation and

Job Title: Quality Control

Department: Newspaper Ad Design

Employment Type: Full-time, On-site (Work from Office)

Salary Range: ₹15,000 – ₹45,000 per month

Working Days: 5 Days a Week

Shift Timing: Night Shift (Rotational)

Willingness to work on weekends may be required during system upgrades or emergency situations.

Job Summary:

We are seeking a meticulous and detail-oriented Quality Control (QC) professional to ensure the accuracy, consistency, and overall quality of advertising and editorial content across print and digital platforms. This role is crucial to maintaining the brand reputation and production standards of our publications and client advertising. The ideal candidate should have a keen eye for detail, strong editorial sensibility, and a solid understanding of print and media production workflows.

Key Responsibilities:

1. Advertisement Quality Assurance

• Review ad content for accuracy, grammar, legal compliance, and adherence to client or brand guidelines.
• Validate ad placement, sizing, layout alignment, and image resolution across print and digital formats.
• Coordinate with the ad sales, creative, and design teams to resolve quality issues pre-publication.

2. Editorial & Content Verification

• Proofread headlines, articles, and captions to ensure correct language usage, consistency, and factual accuracy.
• Conduct final checks for typographical, grammatical, and formatting errors before publishing.
• Ensure content aligns with editorial standards and journalistic integrity.

3. Print Production QC

• Inspect pre-press files and printed materials for alignment, color fidelity, trimming, and finish quality.
• Collaborate with the printing and production team to approve print runs and minimize reprints or errors.
• Monitor output consistency between print proofs and final copies.

4. Digital Publishing QA

• Validate the accuracy and visual integrity of ads and content across websites, e-papers, mobile apps, and social platforms.

This is an on-site role. Please apply only if you are able to work from our Pune office.

Job Title: QC Analyst – HPLC Specialist

Location: Dabaspet , Bangalore – , India

Department: Quality Control

Industry: Pharmaceuticals (Formulations)

Experience: 2–5 years

Employment Type: Full-time

Company Overview:

We are a reputed pharmaceutical formulation company based out of Bangalore committed to delivering high-quality products to domestic and export markets. We are currently seeking a skilled and detail-oriented QC Analyst with hands-on experience in HPLC to join our Quality Control team.

Position Summary:

The QC Analyst will be responsible for conducting analytical testing of raw materials, in-process samples, and finished products with a primary focus on HPLC. The ideal candidate should be well-versed in regulatory standards and capable of working in a fast-paced, cGMP-compliant laboratory environment.

Key Responsibilities:

• Perform routine and non-routine analysis using HPLC for assay, dissolution, related substances, and stability studies
• Preparation, review, and maintenance of test data, analytical records, and reports in compliance with GMP and GLP
• Calibrate, operate, and troubleshoot HPLC and other analytical instruments (e.g., UV, FTIR, pH meter)
• Conduct testing of raw materials, intermediates, and finished formulations as per pharmacopeial and internal specifications
• Assist in method validation and

• Performing a variety of analytical tests on raw materials, in-process samples, and finished products using established laboratory procedures and instrumentation.
• Operating and maintaining laboratory equipment, including HPLC, GC, UV-Vis spectrophotometers, and other analytical instruments.
• Preparing reagents and solutions according to established protocols.
• Documenting all testing procedures, results, and observations accurately and comprehensively in laboratory notebooks and electronic systems.
• Reviewing and interpreting analytical data to determine product conformity to specifications.
• Identifying and reporting any deviations or out-of-specification results to the Quality Assurance department.
• Participating in method validation and equipment qualification activities.
• Ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Maintaining a safe and organized laboratory environment, adhering to all safety protocols.
• Collaborating with other departments, such as Production and Research & Development, to resolve quality-related issues.
• Assisting in the investigation of product complaints and non-conformances.
• Contributing to the continuous improvement of quality control processes and procedures.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• 1-3 years of experience in a Quality Control laboratory setting, preferably within the pharmaceutical industry.
• Hands-on experience with analytical techniques such as HPLC, GC, titration, and spectroscopy.
• Knowledge of cGMP, GLP, and relevant pharmaceutical regulations.
• Strong analytical and problem-solving skills with a keen attention to detail.
• Excellent documentation and record-keeping abilities.
• Proficiency in using laboratory software and data analysis tools.
• Good communication and teamwork skills.
• Ability to work independently and manage time effectively.

Job Title: QC Analyst – HPLC Specialist

Location: Dabaspet , Bangalore – , India

Department: Quality Control

Industry: Pharmaceuticals (Formulations)

Experience: 2–5 years

Employment Type: Full-time

Company Overview:

We are a reputed pharmaceutical formulation company based out of Bangalore committed to delivering high-quality products to domestic  and export markets. We are currently seeking a skilled and detail-oriented QC Analyst with hands-on experience in HPLC to join our Quality Control team.

Position Summary:

The QC Analyst will be responsible for conducting analytical testing of raw materials, in-process samples, and finished products with a primary focus on HPLC. The ideal candidate should be well-versed in regulatory standards and capable of working in a fast-paced, cGMP-compliant laboratory environment.

Key Responsibilities:

• Perform routine and non-routine analysis using HPLC for assay, dissolution, related substances, and stability studies
• Preparation, review, and maintenance of test data, analytical records, and reports in compliance with GMP and GLP
• Calibrate, operate, and troubleshoot HPLC and other analytical instruments (e.g., UV, FTIR, pH meter)
• Conduct testing of raw materials, intermediates, and finished formulations as per pharmacopeial and internal specifications
• Assist in method validation and

This role is for one of Weekday’s clients
Salary range: Rs - Rs (ie INR 2-7 LPA)
Min Experience: 2 years
Location: Hyderabad
JobType: full-time

Requirements

We are seeking a motivated Quality Control Analyst with 2-7 years of experience specializing in HPLC, GC, and wet chemical analysis to join our botanical healthcare manufacturing operations. The ideal candidate will ensure that raw materials, in-process samples, and finished products meet quality standards as per regulatory and company guidelines. The role involves hands-on testing, data interpretation, and reporting for botanical and herbal healthcare products.

• Perform routine and non-routine analysis of raw materials, intermediates, and finished products using HPLC, GC, and wet chemical methods.
• Ensure compliance with standard operating procedures (SOPs), Good Manufacturing Practices (GMP), and regulatory requirements.
• Prepare and maintain accurate analytical records, test results, and reports.
• Conduct method validation and troubleshooting of analytical instruments as needed.
• Collaborate with R&D and production teams to ensure quality standards during product development and manufacturing.
• Monitor and maintain laboratory equipment, ensuring calibration and maintenance schedules are followed.
• Participate in internal and external audits and assist in implementing corrective actions.
• Maintain cleanliness and safety standards in the QC laboratory.
• Support stability studies and other quality-related projects.

• Bachelor’s degree in Chemistry, Pharmacy, Life Sciences, or a related field.
• 2-7 years of experience in quality control, preferably in the botanical or herbal healthcare industry.
• Hands-on experience with HPLC, GC, and wet chemical analysis.
• Good understanding of GMP and quality standards.
• Ability to interpret chromatograms and analytical data accurately.
• Strong attention to detail and problem-solving skills.
• Good communication and teamwork abilities.

• Experience working in manufacturing or factory environments.
• Knowledge of regulatory requirements applicable to botanical healthcare products.
• Experience with documentation and data management software

Job Title: QC Analyst – HPLC Specialist

Location: Dabaspet , Bangalore – , India

Department: Quality Control

Industry: Pharmaceuticals (Formulations)

Experience: 2–5 years

Employment Type: Full-time

Company Overview:

We are a reputed pharmaceutical formulation company based out of Bangalore committed to delivering high-quality products to domestic  and export markets. We are currently seeking a skilled and detail-oriented QC Analyst with hands-on experience in HPLC to join our Quality Control team.

Position Summary:

The QC Analyst will be responsible for conducting analytical testing of raw materials, in-process samples, and finished products with a primary focus on HPLC. The ideal candidate should be well-versed in regulatory standards and capable of working in a fast-paced, cGMP-compliant laboratory environment.

Key Responsibilities:

• Perform routine and non-routine analysis using HPLC for assay, dissolution, related substances, and stability studies
• Preparation, review, and maintenance of test data, analytical records, and reports in compliance with GMP and GLP
• Calibrate, operate, and troubleshoot HPLC and other analytical instruments (e.g., UV, FTIR, pH meter)
• Conduct testing of raw materials, intermediates, and finished formulations as per pharmacopeial and internal specifications
• Assist in method validation and