58 Quality Control Analyst jobs in Hyderabad

Role & responsibilities

• Candidates with relevant experience into the above speciality shall apply for this position
• Should be Quality oriented.
• Will be responsible for QA and coding of reports with 98 % to 100 % accuracy.
• Problem solving skills: Should have the ability to research and analyze data, draw conclusions, and resolve issues;
• Responsible production and delivery of quality services within the agreed turnaround time.
• Prepare and Maintain status reports.
• Preparing various process related documents & guidelines for better understanding for coding related issues.
• Providing trainings to new team members.

Desired Candidate Profile

Need Candidates for Quality Control Analyst in the below field:

• EMS /Ambulance (Emergency Medical Service / Ambulance)
• IPDRG (In-Patient Diagnosis-Related Groups)
• ED Profee (Emergency Department Professional)
• Anaesthesia
• E/M OP (Evaluation and Management Out Patient)
• Ancillary Coding

• Pathology (Surgical)

• Any Graduate can apply with relevant work experience can apply

• senior medical coder with the above speciality experience can apply
• Should have knowledge of PPT presentation
• Candidates should be interested other specialty
• Contributes to building positive team spirit.
• Good Communication: verbal and written
• Immediate joiners preferred

Responsibilities:

* Conduct wet analyses using HPLC equipment

* Ensure compliance with quality standards

* Collaborate with R&D team on product development

* Maintain accurate records and reports

Provident fund

• Perform routine and advanced analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods according to established protocols and regulatory guidelines.
• Analyze test results, interpret data, and prepare accurate and comprehensive reports.
• Investigate out-of-specification (OOS) results and deviations, documenting findings and recommending corrective and preventive actions (CAPA).
• Maintain laboratory equipment, ensuring calibration, qualification, and routine maintenance are performed.
• Ensure adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.
• Prepare and review standard operating procedures (SOPs) for analytical testing and laboratory operations.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues and support product development.
• Manage laboratory inventory, including chemicals, reagents, and consumables.
• Participate in internal and external audits as required.
• Stay updated with the latest advancements in pharmaceutical analysis and quality control techniques.
• Contribute to continuous improvement initiatives within the Quality Control department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Proficiency in wet chemistry techniques and compendial testing (USP/EP/BP/IP).
• Strong understanding of GMP, GLP, and ICH guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.
• Proficient in Microsoft Office Suite and LIMS (Laboratory Information Management System) software.
• Strong written and verbal communication skills.
• Experience with method validation and transfer is highly desirable.

• Perform a variety of chemical and physical tests on raw materials, in-process samples, and finished pharmaceutical products.
• Operate and maintain analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus.
• Analyze test results, interpret data, and prepare accurate and concise laboratory reports.
• Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
• Validate analytical methods and instruments according to established protocols.
• Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
• Maintain laboratory equipment and ensure calibration is up-to-date.
• Manage inventory of laboratory supplies and reagents.
• Collaborate with other departments, including R&D, production, and regulatory affairs, to resolve quality issues.
• Contribute 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.
• Minimum of 3-5 years of experience in a pharmaceutical quality control laboratory.
• Hands-on experience with analytical techniques and instrumentation commonly used in pharmaceutical QC.
• Thorough understanding of GMP, GLP, and regulatory requirements (e.g., FDA, EMA).
• Proficiency in data analysis and report writing.
• Excellent attention to detail and problem-solving skills.
• Strong organizational abilities and the capacity to manage multiple tasks.
• Ability to work effectively both independently and as part of a team.

• Perform routine analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy).
• Accurately record, review, and document all test results in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Analyze and interpret analytical data, identifying any deviations or out-of-specification (OOS) results.
• Investigate OOS results, conduct root cause analysis, and contribute to corrective and preventative action (CAPA) plans.
• Maintain laboratory equipment, ensure proper calibration, and troubleshoot any instrument issues.
• Prepare and review analytical methods and validation reports.
• Ensure compliance with all relevant regulatory guidelines (e.g., FDA, ICH) and internal quality standards.
• Collaborate with production, R&D, and regulatory affairs teams to resolve quality issues.
• Participate in internal and external audits as needed.

• Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 2-3 years of experience in pharmaceutical quality control or a related laboratory setting.
• Hands-on experience with common analytical instrumentation (HPLC, GC, dissolution testers) is essential.
• Thorough understanding of GMP, GLP, and relevant regulatory guidelines.
• Strong analytical and problem-solving skills, with a high degree of accuracy and attention to detail.
• Excellent written and verbal communication skills for documentation and reporting.
• Ability to work independently, manage time effectively, and maintain productivity in a remote environment.
• Proficiency in using laboratory information management systems (LIMS) and standard office software.
• This is a fully remote position, ideal for candidates based in or near Hyderabad, Telangana, IN .

ONLY FOR MALE CANDIDATES

Immediate requriment for QC AND EHS departments with 2 to 5 yrs

Roles and Responsibilities

• Conduct analytical method validation, stability analysis, and sample testing for bulk drugs and APIs.
• Ensure compliance with GLP guidelines and maintain accurate records of test results.
• Develop and execute experimental protocols for new product launches or changes in existing products.
• Provide technical support to production departments on quality-related matters.

Location: Hyderabad

Handling BET, XRD and XEM with a minimum of 4-10 years of experience.

Key Responsibilities:

Gravimetric / Instrumental analysis metals in samples, RND Support

2 Analysis using Instrumental Techniques like ICP, BET, Particle Size, Chemisorption, Hydrogen Uptake, XRF and HPLC

3 Record and Report Management

4 Following best practices in laboratory as per the directional support from Senior Staff.

5 Delivering and maintaining high quality and accurate results during handling and analyzing samples

6 Meet and/or exceed the Analytical Objectives and Goals

7 Execution of Calibration plan of Analytical Balances, Instruments and maintaining records

8 Implementing Health and Safety Guidelines

9 Working as Technical manager for NABL/ISO compliances

Key authorities:

1 Method Development & Validation

2 Working on ICP-OES, BET, Particle Size Analyzer, Chemisorption, Hydrogen Uptake, XRF and HPLC

3 Analytical Troubleshooting

4 Internal Calibration of Lab Instruments

5 Implementing testing Plan for daily samples

Documentation as per ISO 17025:2017

Roles and Responsibilities

• Conduct stability analysis, method validation, and OOS investigations to ensure product quality.
• Ensure compliance with regulatory requirements by maintaining accurate records and documentation.
• Collaborate with cross-functional teams to resolve quality issues and implement corrective actions.
• Perform HPLC, GC, FP, and OSD testing as per SOPs.

**Job title: Quality Control Manager

Location: Hyderabad, India (Onsite)**

The client is a robotics company creating intelligent, self-climbing robots for urban use, designed to clean skyscraper windows without human help. Their in-house solution combines custom hardware, advanced AI, and proprietary software, now moving into large-scale production.

We're looking for an experienced
Quality Control Manager
to lead our quality assurance processes as we scale from development to large-scale production. You'll work closely with hardware, software, and AI teams to ensure our products meet the highest standards for safety, reliability, and performance.

Key Responsibilities:

• Develop and lead quality strategies for hardware and software.
• Oversee testing, validation, inspection, and compliance processes.
• Collaborate across R&D, manufacturing, and supplier teams.
• Lead, train, and mentor the quality control team.
• Drive ISO certifications and regulatory compliance.

Requirements:

• 10+ years in quality control/assurance, ideally in robotics, automation, or aerospace.
• Strong expertise in both hardware and software quality management.
• Experience with Six Sigma, Lean Manufacturing, and AI-powered systems is a plus.
• Excellent leadership, problem-solving, and communication skills.
• Bachelor's or Master's in Mechanical Engineering, Robotics, Electronics, or related fields.

Be part of something groundbreaking. Let's build the future of urban robotics together. Apply now