Quality Control Chemist

751001 Bhubaneswar, Orissa ₹55000 Monthly WhatJobs

Posted 2 days ago

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Job Description

full-time
Our client is seeking a meticulous and qualified Quality Control Chemist for their pharmaceutical manufacturing facility in Bhubaneswar, Odisha, IN . This role is critical in ensuring the quality and safety of our pharmaceutical products by conducting rigorous testing and analysis. You will be responsible for performing in-process and finished product testing, validating analytical methods, and maintaining detailed records of all quality control activities. The ideal candidate will have a strong understanding of analytical chemistry techniques, pharmacopeial standards, and regulatory requirements within the pharmaceutical industry. This position requires excellent laboratory skills, a keen eye for detail, and a commitment to upholding the highest standards of quality.

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.
Required Qualifications:
  • 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.
If you are a dedicated chemist passionate about ensuring pharmaceutical quality, apply today!
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Senior Quality Control Engineer

751001 Bhubaneswar, Orissa ₹85000 Annually WhatJobs

Posted 5 days ago

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full-time
Our client, a leader in advanced manufacturing solutions, is seeking a highly motivated and experienced Senior Quality Control Engineer to join their fully remote team. This is an exceptional opportunity for a proactive individual to contribute to the continuous improvement of our production processes and ensure the highest standards of product quality are met. You will be instrumental in developing and implementing robust quality assurance strategies, conducting rigorous inspections, and analyzing data to identify areas for enhancement. The role requires a deep understanding of manufacturing methodologies, statistical process control (SPC), and various quality management systems (QMS) like ISO 9001. You will collaborate closely with cross-functional teams, including R&D, production, and supply chain, to resolve quality issues, implement corrective and preventive actions (CAPA), and drive a culture of quality excellence across the organization. Your responsibilities will include managing quality documentation, performing root cause analysis for defects, and training junior team members on quality best practices. This position is based in Bhubaneswar, Odisha, IN , but operates entirely remotely, offering flexibility and work-life balance. We are looking for candidates who are meticulous, detail-oriented, and possess strong problem-solving and communication skills. If you are passionate about ensuring product integrity and have a proven track record in quality engineering within the manufacturing sector, we encourage you to apply.

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.
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Senior Pharmaceutical Quality Control Analyst

751001 Bhubaneswar, Orissa ₹55000 Monthly WhatJobs

Posted 3 days ago

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Job Description

full-time
Our client is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst to join our state-of-the-art facility in Bhubaneswar, Odisha, IN . This role is critical to ensuring the safety, efficacy, and quality of our pharmaceutical products. You will perform a wide range of analytical tests on raw materials, in-process samples, and finished products using various laboratory techniques and instrumentation. Responsibilities include operating and maintaining analytical equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers. You will be responsible for method validation, stability testing, and preparing detailed analytical reports and documentation in compliance with cGMP guidelines. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, regulatory requirements (e.g., ICH, FDA), and quality assurance principles. You will also be involved in troubleshooting analytical methods and equipment issues, as well as participating in internal and external audits. Contributing to continuous improvement initiatives within the QC department and mentoring junior analysts will be key aspects of this position. Excellent attention to detail, strong problem-solving skills, and the ability to work effectively both independently and as part of a team are essential. A Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science discipline, along with substantial experience in a pharmaceutical QC laboratory setting, is required. Join our dedicated team and contribute to delivering high-quality medicines to patients.
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Remote Pharmaceutical Quality Control Scientist

751001 Bhubaneswar, Orissa ₹80000 Annually WhatJobs

Posted 6 days ago

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full-time
Our client, a forward-thinking pharmaceutical research and development company, is looking for a highly analytical and meticulous Pharmaceutical Quality Control Scientist to join their innovative team. This fully remote position offers a unique opportunity for experienced scientists to contribute to the development and manufacturing of high-quality pharmaceuticals without the need for physical office presence. You will be responsible for ensuring that all products meet stringent quality standards through rigorous testing and analysis, adhering to global regulatory requirements.

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.
Qualifications:
  • 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.
This remote role provides a challenging and rewarding career path for scientists passionate about ensuring the safety and efficacy of pharmaceutical products. Join our client and contribute to critical advancements in healthcare.
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Remote Pharmaceutical Quality Control Manager

751001 Bhubaneswar, Orissa ₹1500000 Annually WhatJobs

Posted 16 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking an experienced and highly detail-oriented Remote Pharmaceutical Quality Control Manager. This position is critical in ensuring that all manufactured products meet stringent quality standards and regulatory requirements. As a remote manager, you will oversee and direct all quality control activities, including laboratory testing, data analysis, and documentation, from your own location. You will be responsible for developing, implementing, and maintaining robust quality control systems and procedures that comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines. Your role will involve managing a remote team of QC analysts, ensuring efficient workflow, accurate testing, and timely reporting of results. You will review and approve batch records, analytical data, and validation reports, identifying any deviations and initiating corrective and preventive actions (CAPA). A deep understanding of pharmaceutical analytical techniques, quality assurance principles, and regulatory affairs is essential. You will collaborate closely with R&D, production, and regulatory affairs departments to ensure seamless integration of quality processes. The ideal candidate will possess exceptional leadership skills, strong analytical and problem-solving capabilities, and the ability to work independently in a remote setting. This role requires a commitment to maintaining the highest standards of pharmaceutical quality and patient safety.

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.
Qualifications:
  • 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.
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Senior Quality Control (Microbiology + Chemistry) Trainer

Bhubaneswar, Orissa Tek Support

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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