6

UV Spectrometer Jobs

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  • 5 - 10 yrs
  • 8.5 Lac/Yr
  • Siltara Raipur
Quality Control Analysis Quality Check Testing Gas Chromatography Laboratory Chemist Hplc Chromatography Analyst UV Spectrometer
We are seeking a QC Manager with 5 to 10 years of experience to oversee quality control processes at our facility in Siltara, Raipur. This full-time position requires a dedicated professional to ensure product quality and adhere to industry standards.nnKey Responsibilities:nn1. Oversee Quality Assurance: Ensure that all products meet quality standards and comply with regulatory requirements through systematic inspections and testing processes.n n2. Develop Quality Control Plans: Create and implement effective quality control procedures to enhance product reliability and consistency.nn3. Lead the QC Team: Manage and mentor a team of quality control staff, providing training and support to foster a culture of quality awareness.nn4. Analyze Data: Review quality control data and generate reports to identify patterns or areas for improvement, making recommendations based on findings.nn5. Coordinate with Departments: Collaborate with production, engineering, and supply chain teams to address quality-related issues and drive continuous improvements.nnRequired Skills and Expectations:nnThe ideal candidate should possess a strong educational background with a degree and relevant experience in quality control. Strong analytical and problem-solving skills are essential for identifying issues and developing solutions. Effective leadership and communication skills are important for managing teams and coordinating with various departments. A keen attention to detail and organizational abilities will aid in maintaining high-quality standards in all operations.
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  • 5 - 10 yrs
  • 8.5 Lac/Yr
  • Siltara Raipur
Quality Control Hplc UV Spectrometer Instrument Testing Documents
We are seeking a Quality Control Manager with 5 to 10 years of experience to ensure the highest quality standards in our products. This role, based in Siltara, Raipur, requires a graduate with a keen eye for detail and a deep understanding of quality management processes.nnKey Responsibilities:nn- Develop and implement quality control processes: Create procedures to ensure that products meet quality standards at every stage of production.n n- Conduct regular inspections and audits: Assess product quality through periodic checks and ensure compliance with industry regulations.n n- Lead quality control teams: Manage a team of quality control inspectors, providing guidance and training to maintain high performance.n n- Analyze quality data: Review testing results and quality reports to identify trends, areas for improvement, and ensure corrective actions are taken.n n- Collaborate with other departments: Work closely with production, engineering, and supply chain teams to achieve overall operational excellence.nnRequired Skills and Expectations:nnThe ideal candidate will possess strong analytical skills and attention to detail, allowing them to identify quality issues swiftly. Excellent communication skills are essential for interfacing with other departments and leading a team. A deep understanding of quality management systems and regulatory requirements is necessary to ensure compliance. The candidate should demonstrate strong problem-solving abilities, enabling them to address quality concerns effectively. A proactive approach and the ability to work in a fast-paced environment are also expected.
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Quality Control Analyst (2-4 Years)

Theon Pharmaceuticals Ltd

  • 2 - 4 yrs
  • 3.5 Lac/Yr
  • Nalagarh Solan
Quality Check Quality Standards Quality Metrics Hplc GLP UV Spectrometer
We are seeking a dedicated Quality Control Analyst to join our team in Nalagarh. The ideal candidate will have 2 to 4 years of experience and possess a degree in B.Pharma or B.Sc. This role requires a strong focus on ensuring product quality and compliance with regulatory standards.Key Responsibilities:- Conduct Testing: Perform various tests on raw materials and finished products to ensure they meet quality specifications. This includes physical, chemical, and microbiological analysis.- Documentation and Reporting: Maintain accurate records of test results and document deviations or issues. Timely reporting helps in identifying trends and implementing improvements.- Quality Assurance Compliance: Assist in maintaining compliance with quality standards and regulations set by industry and government bodies. This includes understanding and following standard operating procedures (SOPs).- Collaboration with Teams: Work closely with production and R&D teams to address quality-related concerns. Effective communication is essential for improving processes and products.- Problem-Solving: Identify root causes of quality issues and propose corrective actions. This analytical approach aims to prevent reoccurrence of defects.Required Skills and Expectations:Candidates must have strong analytical and critical thinking skills to assess complex quality issues effectively. Attention to detail is essential to ensure accurate testing and documentation. Knowledge of quality control regulations and practices is required. Proficiency in software applications for data analysis and reporting is preferred. A collaborative mindset is crucial for working well within a team. Candidates should also demonstrate a commitment to continuous learning and improvement in quality processes.
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  • 2 - 4 yrs
  • 3.0 Lac/Yr
  • Makarpura Vadodara
Hplc UV Spectrometer Quality Control Quality Analysis
Formulation Company Shaimil laboratoriesTime : 9 to 5: 30BonusPF also Available
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Quality Control Manager

Vowcare Products

  • 5 - 10 yrs
  • 9.0 Lac/Yr
  • Srinagar
UV Spectrometer UV-visible Spectrophotometer Hplc GC Analysis Quality Control Inspections
Vowcare Products is seeking a Quality Control (QC) Manager to oversee and ensure the highest standards of pharmaceutical product quality at our manufacturing plant. The QC Manager will be responsible for managing the quality control team, implementing stringent testing procedures, ensuring regulatory compliance, and driving continuous improvement in product quality.
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  • 10 - 12 yrs
  • 6.0 Lac/Yr
  • Rudrapur
HPLC GC Analysis UV Spectrometer CGMP GLP Formulations
The QC manager must have a minimum of 12 years of experience in a pharma QC lab.He/she must have hands-on experience in operation of HPLC, GC, IR, UV and other instruments used in pharmaceutical analysisResponsible for managing the QC laboratory in accordance with cGMPand GLP requirements. The Manager must be able to manage and lead a team of QC analysts in order to maintain smooth running of the laboratory. He will have to supervise regular testing on the incoming raw material, bulk and semi-finished product and finished product.Maintain regularity of testing and timely release of test reports.
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