6 Tata Steel jobs in Bhubaneswar
Quality Control Chemist
Posted 2 days ago
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Job Description
Key Responsibilities:
- Perform qualitative and quantitative analyses on raw materials, in-process samples, and finished products using various analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titrations).
- Ensure all testing is conducted in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Validate analytical methods and instrumentation according to regulatory guidelines.
- Maintain accurate and detailed records of all laboratory tests, results, and observations.
- Prepare certificates of analysis (CoA) for raw materials and finished products.
- Calibrate and maintain laboratory equipment, ensuring optimal performance and accuracy.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective actions.
- Participate in internal and external audits of the quality control laboratory.
- Stay updated with the latest pharmacopeial standards (e.g., USP, BP, IP) and regulatory requirements.
- Assist in the development and improvement of quality control procedures and protocols.
- Collaborate with production, R&D, and regulatory affairs departments to address quality issues.
- Ensure proper handling and disposal of chemicals and hazardous materials.
- Contribute to a culture of continuous improvement within the quality department.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Chemistry, or a related field.
- Minimum of 3-5 years of experience in pharmaceutical quality control or analytical testing.
- Proficiency in using analytical instruments such as HPLC, GC, UV-Vis, FTIR, etc.
- Strong knowledge of pharmacopeial standards and regulatory guidelines (e.g., ICH, FDA, GMP).
- Excellent understanding of analytical chemistry principles.
- Meticulous attention to detail and accuracy in testing and record-keeping.
- Ability to work independently and as part of a team in a laboratory setting.
- Good problem-solving and critical-thinking skills.
- Strong written and verbal communication skills.
- Experience with laboratory information management systems (LIMS) is a plus.
Senior Quality Control Engineer
Posted 5 days ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain quality control procedures and standards.
- Conduct comprehensive inspections and testing of raw materials, in-process products, and finished goods.
- Analyze quality data, identify trends, and prepare detailed reports for management.
- Lead root cause analysis for quality deviations and implement effective corrective and preventive actions.
- Ensure compliance with relevant industry standards and certifications.
- Collaborate with engineering and production teams to resolve quality-related issues.
- Manage and update quality documentation, including SOPs and work instructions.
- Oversee calibration and maintenance of quality control equipment.
- Mentor and guide junior quality control personnel.
- Contribute to the continuous improvement of manufacturing processes and product quality.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Industrial, or related field).
- Minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment.
- Strong knowledge of quality management systems (ISO 9001) and statistical process control (SPC).
- Proficiency in data analysis and problem-solving techniques.
- Excellent communication, interpersonal, and teamwork skills.
- Experience with lean manufacturing principles is a plus.
Senior Pharmaceutical Quality Control Analyst
Posted 3 days ago
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Job Description
Remote Pharmaceutical Quality Control Scientist
Posted 6 days ago
Job Viewed
Job Description
Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, IR spectroscopy, dissolution testing).
- Develop, validate, and implement analytical methods according to regulatory guidelines and internal procedures.
- Analyze and interpret test results, ensuring accuracy and completeness.
- Prepare detailed reports on testing activities, results, and deviations.
- Troubleshoot and resolve analytical method issues and laboratory instrument problems.
- Maintain laboratory equipment and ensure proper calibration and qualification.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory standards.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to support product development and issue resolution.
- Participate in internal and external audits as required.
- Maintain accurate and up-to-date laboratory records and documentation.
- Stay current with scientific literature, industry trends, and advancements in pharmaceutical quality control.
- Master's or Ph.D. in Chemistry, Pharmaceutical Sciences, Analytical Chemistry, or a related field.
- Minimum of 5 years of experience in pharmaceutical quality control or analytical development.
- Extensive hands-on experience with analytical instrumentation (e.g., HPLC, GC-MS, LC-MS).
- Proficiency in method development, validation, and transfer.
- Thorough understanding of GMP/GLP guidelines and regulatory requirements (e.g., FDA, EMA).
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong report writing and data interpretation abilities.
- Ability to work independently with minimal supervision and manage time effectively in a remote setting.
- Excellent organizational skills and attention to detail.
- Proficiency in laboratory information management systems (LIMS) and relevant software.
Remote Pharmaceutical Quality Control Manager
Posted 16 days ago
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Job Description
Responsibilities:
- Develop, implement, and manage comprehensive quality control strategies and procedures.
- Oversee all laboratory testing and analytical activities to ensure product quality and compliance.
- Ensure adherence to GMP, GLP, and other relevant pharmaceutical regulations.
- Manage and lead a remote team of Quality Control analysts, providing guidance and training.
- Review and approve batch records, analytical data, method validation reports, and stability studies.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing CAPA.
- Conduct risk assessments and implement quality improvement initiatives.
- Collaborate with R&D, Manufacturing, and Regulatory Affairs to ensure quality standards are met throughout the product lifecycle.
- Stay updated on current regulatory guidelines and industry best practices.
- Prepare for and participate in internal and external audits.
- Manage QC budget and resources effectively.
- Master's or Ph.D. in Pharmaceutical Sciences, Chemistry, Biology, or a related field.
- Minimum of 8-10 years of progressive experience in pharmaceutical quality control and assurance.
- Extensive knowledge of GMP, GLP, ICH guidelines, and other relevant regulatory requirements.
- Proven experience in managing QC laboratories and teams.
- Proficiency in analytical techniques (e.g., HPLC, GC, spectroscopy, dissolution testing).
- Strong understanding of data integrity principles and documentation practices.
- Excellent leadership, problem-solving, and decision-making skills.
- Ability to manage multiple projects and priorities in a remote environment.
- Strong communication and interpersonal skills for effective collaboration.
Senior Quality Control (Microbiology + Chemistry) Trainer
Posted 3 days ago
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Job Description
Job Title: Quality Control (Microbiology + Chemistry) Trainer
Location: Remote
Job Type: Part-time
Job Summary:
We are seeking an experienced QC (Microbiology and Chemistry) Trainer to design and deliver technical training programs , mentor professionals , and support their career success in the pharmaceutical and healthcare industries. This role involves hands-on guidance , GMP/GLP compliance training , documentation mentoring , and interview preparation .
Key Responsibilities:
- Deliver training on QC techniques:
- Microbiology: Environmental Monitoring (EM), Sterility Testing, Bioburden
- Chemistry: HPLC, GC, UV-Vis Spectroscopy, FTIR
- Mentor and coach on GMP, GLP, Data Integrity & Regulatory Compliance
- Guide candidates on laboratory practices, documentation & audit readiness
- Prepare real-world case studies on OOS, OOT investigations & CAPA handling
- Train on SOP creation, deviation management & lab report preparation
- Conduct mock interviews (Technical + HR) with actionable feedback
- Support career enablement: Resume building, project story development, certification guidance (ASQ, Microbiology, Analytical Chemistry)
Requirements:
- 10+ years of experience in QC (Microbiology + Chemistry) in a regulated Pharma / Healthcare environment
- Hands-on expertise with laboratory equipment & analytical techniques (HPLC, GC, UV, FTIR)
- Strong knowledge of regulatory standards: FDA, WHO, ICH, MHRA
- Experience with GMP, GLP, Data Integrity, CAPA investigations, OOS/OOT analysis
- Training/mentoring experience with excellent presentation skills
- Strong documentation skills and ability to prepare audit-ready records
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