166 Gas Chromatography Jobs

Calibration of instruments2 Analysis of lab samples and pilot plant samples Documentation of all project of synthesis and pilot plant To maintain the all data of R&D lab and pilot plant projects the calibration of IC5 Maintain the system of housekeeping and 5-s 6 Preparation of Standards Volumetric solutions and standard of volumetric7 To maintain the monthly data of GC, LC and WET AnalysisDaily maintain the gas cylinder records To preparation the Standard for GC, LCand WET lab 10 Method development of R&D project

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials

As a Sr. Territory Manager / Dy. Regional Manager at Toshvin Analytical, your role involves selling the full range of analytical and laboratory instruments handled by the company. You will be responsible for generating prospects in the assigned territory through customer visits, managing the sales funnel through CRM, and conducting commercial negotiations. Achieving sales targets, establishing contacts with prospects, and ensuring customer satisfaction through internal coordination are key aspects of your responsibilities. Key Responsibilities: - Sell the full range of analytical and laboratory instruments on your own and through assigned team members - Generate prospects through customer visits in the assigned territory - Update and manage the sales funnel through CRM - Demonstrate technical knowledge of related products - Conduct commercial negotiations to finalize sales - Achieve sales targets set by the company - Develop and maintain relations with prospects to drive sales - Coordinate internally with service and other related departments to ensure customer satisfaction Qualifications Required: - Minimum 5 years of experience in analytical instrument sales - Fluent in written and verbal communication in English - Proficient in MS Office package (Outlook, Word, Excel, PowerPoint) - Sincere, hardworking, and target-oriented mindset - Willingness to travel extensively - At least 2-3 years of team handling experience - Preferable technical knowledge about Molecular Spectroscopy, Elemental Analysis, Gas Chromatography, and Thermal Analyzer instruments If you are a bright, motivated, and committed individual with a Diploma in Electronics/Chemical/Instrumentation or a BSc. or MSc. in Chemistry / Biology / Physics, or Graduates / Diploma holders in Electronics / Chemical / Instrumentation Engineering, Toshvin Analytical offers you the opportunity for a long-term career with one of the leading instrumentation companies in India. Join our team of experienced professionals and contribute to our mission of providing the best quality service to our clients and helping businesses grow. If you are interested in this exciting opportunity, please email your CV to careers@toshvin.com.,

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation.

Setting strategy for evaluating and implementing new technologies within the Analytical Development department. Required Candidate profile with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis

We are seeking a dynamic and experienced Quality Control (QC) Manager to lead and manage QC operations, ensuring that products and processes meet stringent quality and regulatory requirements. The ideal candidate will possess deep technical expertise, a strong leadership background, and a commitment to data integrity and continuous improvement within the life sciences industry. A detail-oriented professional with expertise in Nitrosamines/NDSRI method development and validation by LC-MS focused on detecting and quantifying nitrosamine impurities in APIs and Finished Dosage Forms. You will contribute to method development, validation, instrument calibration, and document preparation while ensuring compliance with safety, regulatory, and cGLP standards. Preferred Manager profile: Design and implement robust QC procedures aligned with current Good Manufacturing Practices (cGMP) and industry standards. Ensure processes are optimized for efficiency, accuracy, and compliance. Regularly assess QC operations and procedures. Identify opportunities for improvement and implement enhancements to streamline workflow and ensure regulatory readiness. Ensure QC operations comply with global regulatory authorities including USFDA, EDQM, ANVISA, PMDA, and WHO. Maintain audit readiness and lead/support regulatory inspections. Team Leadership and Development Manage and mentor a team of QC professionals, ensuring high performance and ongoing professional development. Assign responsibilities, monitor progress, and promote a culture of accountability and collaboration. Data Integrity and Documentation Ensure accuracy, reliability, and confidentiality of all laboratory records and data. Enforce adherence to ALCOA+ principles for data integrity. Troubleshooting and CAPA Management Investigate quality-related issues, perform root cause analysis, and lead implementation of effective corrective and preventive actions (CAPAs). Cross-functional Collaboration Collaborate with AR&D, QA, and other departments to align quality strategies. Communicate quality metrics, performance, and issues to leadership and stakeholders. Quality System Contributions Support development and implementation of quality management systems (QMS). Review and approve analytical methods, validation protocols, and reports. Audit and Complaint Management Lead or support internal and external audits. Manage customer complaints and conduct trending analysis to drive quality improvements. Technical Skills: Hands-on experience and data interpretation of analytical instruments like LCMS, HPLC, GC,UV, KF, etc. Thorough understanding of cGMP, GLP, and regulatory requirements. Good documentation and analytical skills. Job Description: QC Data Review Specialist Job Summary We are seeking a meticulous and highly organized QC Data Review Specialist to join our Quality Control team. The successful candidate will be responsible for the comprehensive GMP (Good Manufacturing Practices) review of laboratory raw data, analytical reports, and related documentation. This role is critical to ensuring that all laboratory work is performed in compliance with established methods and protocols, that results are analytically sound and accurate, and that all documentation adheres to stringent GMP standards and regulatory requirements. Key Responsibilities Data and Document Review: Conduct detailed reviews of analytical data packages, including but not limited to raw data (e.g., chromatograms, spectra), laboratory notebooks, and summary reports for accuracy, completeness, and compliance with GMP. Compliance Verification : Ensure all testing was performed according to approved SOPs, analytical methods, and protocols. Verify that calculations and data transcriptions are correct and that any deviations or out-of-specification (OOS) results are properly documented, investigated, and reported. Method Validation Review : Review method validation/verification/transfer protocols and reports to ensure they meet regulatory and company standards. Stability Program Suppor t: Review stability testing data and reports, ensuring that data integrity is maintained throughout the stability study lifecycle. Audit Trail Review : Perform audit trail reviews of electronic data systems to ensure data integrity and identify any potential compliance risks. Documentation Management : Assist in the revision and approval of controlled documents such as SOPs, test methods, and specifications. Communication: Collaborate closely with laboratory analysts to resolve documentation errors, clarify discrepancies, and provide constructive feedback to prevent future issues. Act as a liaison between the QC laboratory and the Quality Assurance (QA) department. Continuous Improvement : Identify gaps in procedures and opportunities for improvement within the laboratory data review process to enhance efficiency and compliance. Qualifications Education: Bachelor of Science (B.S.) degree in Chemistry, Biology, Biochemistry, or a related life sciences field is required. Experience: A minimum of 3-8 years of hands-on experience in a GMP-regulated pharmaceutical or biotechnology laboratory environment. Direct experience in reviewing analytical data (e.g., HPLC, GC, UV-Vis, FTIR, wet chemistry) is essential. Prior experience in a dedicated data review or QA role is highly preferred. Knowledge: In-depth knowledge of GMP, GDP (Good Documentation Practices), and data integrity principles. Strong understanding of FDA, ICH, and other relevant regulatory guidelines. Familiarity with common laboratory software and electronic data systems (e.g., LIMS, Chromeleon, Empower). Required Skills and Competencies Attention to Detail: Exceptional ability to spot errors, inconsistencies, and deviations in complex technical documents. Analytical and Critical Thinking: Strong ability to interpret scientific data and assess its validity and compliance. Organizational Skills: Excellent time management skills with the ability to manage multiple review assignments and meet deadlines. Communication Skills: Clear and effective written and verbal communication skills are necessary to articulate findings and collaborate with team members. Problem-Solving: Proactive in identifying issues and working with the team to find compliant solutions. Integrity: Must uphold the highest standards of quality and ethical behavior. Teamwork: Ability to work effectively both independently and as part of a collaborative team. Behavioral & Leadership Skills: Strong analytical and problem-solving skills. Excellent communication and interpersonal abilities. Demonstrated ability to lead cross-functional teams and drive a culture of quality. Why JanSat? Our values and expectations are at the heart of everything we do and form an important part of our culture. These include Patient focus, Transparency, Respect, Integrity along with Courage, Accountability, Development, and Teamwork. As JanSat focuses on our values and expectations and a culture of innovation, performance, and trust, the successful candidate will demonstrate the following capabilities: Operating at pace and agile decision-making using evidence and applying judgement to balance pace, rigour and risk. Committed to delivering high quality results, overcoming challenges, focusing on what matters, execution. Continuously looking for opportunities to learn, build skills and share learning. Sustaining energy and well-being. Building strong relationships and collaboration, honest and open conversations. Budgeting and cost-consciousness.

Conduct Gas chromatography analysis of Pharmaceutical Samples To perform Validation of analytical methods To maintain all records as per cGLP and ISO 17025. Perform periodic calibration of Instruments/Equipments in Lab Preparation and Maintenance of standards

As a Laboratory Technician in our company, your role involves performing routine lab tasks to gain experience and familiarity with various methods, practices, and programs. Your key responsibilities will include: - Preparing samples using standard techniques and following standard operating procedures. - Performing chemical solutions, standards, and dilutions according to established procedures. - Evaluating and reporting data, and uploading it into the data reporting system. - Reporting any unusual test occurrences to the department manager. - Adhering to laboratory QA/QC practices. - Maintaining general housekeeping in your work area or department. - Conducting instrument maintenance, including Gas Chromatography / Mass Spectrometry. - Troubleshooting instrument issues as needed. - Assisting other laboratory technicians in different departments based on workload requirements. - Ensuring instruments are running efficiently to meet clients" needs. - Uploading calibration curves and data, and reporting full data packages. - Collaborating with the department manager to identify efficiency gains, reduce downtime, and control costs. - Updating Standard Operating Procedures (SOPs) as required. - Working with the department manager to meet benchmarks and continuously improve methods, instruments, and protocols. Your qualifications should include an M.Sc in Chemistry with 3-4 years of relevant experience in a laboratory setting.,

Role & responsibilities 1.Responsible for work planning and review of documents related to In process, DS, DP, stability testing, AMV and AMT activities within quality control laboratory. 2. To effectively plan and monitor shift duties of the QC analytical staff members to support 24*7 business operations. 3. Responsible for compliance to internal, external & statutory compliances as per quality policy of Enzene, pharmacopoeia guidelines and other regulated guidelines. 4. Responsible for periodic training management related to quality, GMP, regulatory aspects to quality control laboratory personnels and evaluation of effectiveness. 5. Responsible for the periodic assessments/audits to identify gaps / improvement opportunities for strengthening the quality & regulatory compliance. Prepare remediation/mitigation plan (CAPA) and execute it in a timely manner by coordinating cross functionally to uplift the level of compliance’s. 6. Responsible for review and approval of documentation such as SOP’s, Specifications, STP’s, TDS, reports for IRS analyst qualification, protocols, Qualifications and reports etc. 7. Responsible for investigations and approval of OOS, OOT and deviations. To recommend and approve CAPA, change controls. 8. To release or reject the samples handled in quality control laboratory.

Responsibilities: * Collaborate with production team on quality control measures. * Conduct HPLC, GC, Gas Chromatography tests on products. * Ensure compliance with industry standards and regulations. Free meal Accidental insurance

Job Title : LEAD SPECIALIST GOE CAL Location : Mumbai At dsm-firmenich we strive to achieve a world where you don't have to choose between taste, texture, or health - and can enjoy it all. Our innovative ingredients, expertise, and solutions bridge the gap between the delicious, the nutritious, and the sustainable. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your key responsibilities: Analytical Support & Method Development Plan and conduct GC-MS, LC-MS, and other analytical techniques for flavors, perfumes, aroma chemicals, and natural products, while contributing to method development and technical growth of the team. Instrument & Lab Management Manage and maintain analytical instruments and lab operations, ensuring SOP compliance, accurate documentation, and inventory control. Cross-Functional Collaboration Work closely with Creation, Application, QA, and global/regional teams to ensure alignment and effective analytical support across functions. Volatile Compound Analysis Apply isolation and analytical techniques-particularly GC with various detectors and GC-MS-for in-depth volatile analysis. Reporting & Documentation Prepare, review, and manage analytical reports using in-house tools, and clearly communicate findings and recommendations to stakeholders. Scientific Expertise & External Coordination Serve as a subject matter expert in analytical/flavor chemistry, supporting global collaborations, literature research, and coordination with external resources. We bring: A team of diverse employees who aren't afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you're empowered to grow and share your ideas. You bring: MSc. (with 5+ years experience) or Ph.D. (with 2+ years experience) in analytical chemistry or a related field. Proven expertise in gas chromatography and method development in commercial or research lab settings. Extensive hands-on experience with mass spectrometry for complex analytical applications. Knowledge of ISO 17025:2017 standards is a strong advantage. A curious, problem-solving mindset with a drive to explore new approaches and deliver innovative solutions. A strong sense of ownership and accountability , with the ability to deliver meaningful results and work collaboratively within diverse teams. The application process: Interested in thispositionPleaseapply on-line byuploadingyourresumein Englishvia ourcareer portal. For further information, please contact Shradha Tiwari , Talent AcquisitionPartner ( [HIDDEN TEXT] ). Equal Opportunities Commitment dsm-firmenich is fully dedicated to inclusion becausewhenpeople feelengagedand empowered,their creativityandinnovation drives unprecedented progress.We aimto buildaworkplace whereopportunity really is equal,soeveryonecanthrive.Wedonotdiscriminate: there'sa place for everyone at dsm-firmenich. Dsm-firmenich isanEqual Opportunityand Affirmative ActionEmployer. dsm-firmenich peopleareasdiverseas ourcustomers. For us that includesa commitmenttoensuring equal employmentopportunitiesfor alljob applicantsand employees.Employment decisions are baseduponjob-related reasons regardless ofan applicant'srace, color, religion,sex,sexualorientation,gender identity,age,nationalorigin,disability, maritalstatus, geneticinformation, protectedveteranstatus, oranyotherstatusprotected by law.Wearecommittedto providingreasonable supportfordisabledapplicants in our recruiting process.Shouldyouneedassistance, andarecomfortabletosharethis, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the world's growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.

Role and Responsibility: Technical Support: Provide expert technical support to customers and field personnel on HPLC troubleshooting, and resolving application issues. Application Development: Develop and optimize analytical methods and applications using HPLC for various industries, including pharmaceuticals, industrial, environmental, food, and life sciences. Customer Training: Conduct customer training sessions, webinars, and workshops to enhance user proficiency and satisfaction. Collaboration : Work closely with the sales and marketing teams to identify customer needs and develop tailored solutions. Collaborate with R&D to provide feedback on product performance and enhancements. Documentation: Prepare and maintain application notes, technical documents, and reports to support customer applications and product development. Innovation: Stay updated with the latest advancements in HPLC and contribute to the development of new applications and methodologies. Aware of calibration and operation procedure for instruments ( balance, K.F, HPLC. UV, refractometer and viscometer etc,) Experience of QC software like Empower, LIMS, Tiamo 3.0, Lab solution, SCM etc. Preparation of documents ( SOP, protocol etc) related to Quality control.Role & responsibilities Preferred candidate profile Qualification : B.Sc (chemistry)./ B.Pharma candidates only. Experience: 4-10 years experience working with HPLC/wet finish/Sampling is compulsory. Interested candidates can sent their CV to jagpal.dewal @ipca.com

As a Research Assistant at PolyCycl, you will have the opportunity to contribute to groundbreaking advancements in chemical recycling at our R&D center in Chandigarh, India. PolyCycl is dedicated to transforming post-consumer plastic waste into reusable, high-purity resources, thus advancing the circular economy. We are seeking a skilled Research Assistant with a Bachelor's or Master's degree in Chemistry, Petroleum, Pharmaceuticals, or Environmental Sciences, along with 2-5 years of hands-on experience in laboratory experiments and analytical equipment operation. Your role will involve preparing and analyzing samples, using lab analytical instruments such as Gas Chromatography-Flame Ionization Detector and Titrations, executing experimental protocols, collecting and reporting data, managing lab equipment, and ensuring quality assurance. Joining PolyCycl means being a part of a mission to address challenges in waste management by recycling hard-to-recycle plastic waste. You will play a key role in transforming the future of recycling technologies and will have the opportunity to work in a collaborative, high-energy environment where innovation and initiative are encouraged. We value autonomy and proactive mindsets, and we welcome individuals who thrive in small, goal-oriented teams. If you are interested in working at PolyCycl, please email your resume and a cover note to hr@polycycl.com, addressing specific points related to your interest in the company, alignment of your experiences with the role's responsibilities, experience in autonomous teams, relocation timeline (if applicable), and current CTC. For further queries, you can reach out to hr@polycycl.com or vivek.patil@polycycl.com. Join us at PolyCycl in reshaping the future of recycling and advancing your career in a purpose-driven organization!,

We are looking for skilled Analysts with expertise in HPLC and GC techniques for immediate joining. The candidate will conduct analytical testing to ensure pharmaceutical product quality, develop and validate analytical methods, and contribute to continuous laboratory improvement initiatives. Key Responsibilities: Perform analytical testing using HPLC, GC, UV-Vis, ICP-MS, and LC-MS techniques to assess product quality and purity. Develop, validate, and optimize analytical methods in compliance with cGMP guidelines. Collaborate with cross-functional teams to troubleshoot and resolve method validation and analytical issues. Maintain detailed and accurate records of test results, instrument calibrations, and maintenance schedules. Participate in continuous improvement projects to enhance laboratory efficiency and accuracy. Required Qualifications: Bachelors degree in Pharmacy (B.Pharma) or equivalent. Postgraduate qualifications such as M.Pharma, MS/M.Sc in Pharmacology, Food Technology, Biotechnology, Biochemistry, Biology, or Microbiology are preferred. 2-7 years of relevant experience in pharmaceutical analytical laboratories. Strong knowledge and hands-on experience with HPLC, GC, UV-Vis, ICP-MS, and LC-MS instruments. Familiarity with cGMP guidelines and pharmaceutical quality standards. Excellent documentation and analytical skills. Preferred Skills: Experience in method development and validation. Good understanding of pharmaceutical regulatory requirements. Ability to work effectively in a team-oriented environment.

Should have 1-2 Years of experience in Quality Control department

Hand on exposure on Gas Chromatography, Combustion analyzer & XRF. Collect, organize, and interpret data from instruments & enter those results into LIMS. Interact with R&D and Pilot Plant staff to provide support, analyzing and characterizing materials for Honeywell UOP Ability to work in shifts as per the designed schedule. Maintain compliance with HSE policies and procedures and adopt HSE requirements for safelaboratory operations. Communicate well with co-associates in the group and with internal customers. Recommend and implement safety, quality, and productivity improvements. Occasional lifting and moving of bags, samples, and other objects up to 10 pounds may be required. Qualifications: BSc or MSc in Material Science/Chemistry 2-3 years working experience in an industrial or testing lab. Computer literate - including MS word and excel. Ability to work both independently, and in team environments. Key Success Factors/Profile Customer focus and result oriented individual. Basic knowledge on safety pertaining to laboratory operation.

Field Service Engineer We are seeking a highly skilled and experienced Field Service Engineer to join our team on a contract basis. This role requires a minimum of 1 year and a maximum of 3 years of experience in the Pharma/Healthcare/Lifesciences industry, providing on-site technical support and maintenance in Chandigarh, India. Tasks Provide on-site technical support and maintenance for gas chromatography and liquid chromatography equipment. Troubleshoot and resolve equipment malfunctions. Perform preventative maintenance and calibration procedures. Maintain accurate records of service activities and equipment performance. Collaborate with internal teams to ensure timely resolution of customer issues. Comply with all relevant safety regulations and company policies. Skills Proven experience (1-3 years) in field service engineering within the Pharma/Healthcare/Lifesciences industry. Strong understanding of gas chromatography and liquid chromatography principles and techniques. Proficiency in troubleshooting and repairing laboratory equipment. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Diploma in a relevant engineering discipline.

Role & responsibilities: Perform routine and non-routine analysis using GC and GC-MS as per SOPs and approved test methods. Prepare samples, reagents, and calibration standards accurately. Conduct method validation, system suitability, and performance checks for GC instruments. Maintain proper documentation of all analytical results in accordance with GMP/GLP requirements. Troubleshoot analytical issues and assist in resolving deviations and OOS (Out of Specification) results. Ensure proper calibration, maintenance, and operation of GC instruments. Support development and validation of new methods as required by R&D or Quality Assurance teams. Maintain a clean, organized, and safe laboratory environment.

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample inward register / LIMS as required for assigning analytical reference number and to store at recommended storage condition until completion of the analysis. To operate and maintain laboratory equipment/instrument as per analyst qualification program. To ensure that entries in log books are made where ever instruments are used in the analysis. To perform all associated activities (bench reagents, indicators, volumetric solution preparation, factor determination etc.) required for sample testing by following the approved procedures. To perform analysis (Chemical) to qualify working standards against reference standard /certified standard/ primary standards. To ensure all primary standards/working standards/certified standards/reference standards are stored as per the storage conditions specified and documented. To check the availability of analytical resources like chemicals/reagents / standards etc. before start of the analysis. To take online print and perform data punching in the LIMS. To monitor temperature of laboratory daily. To send those samples to outside laboratory for analysis for tests not able to be carried out in laboratory. To maintain and ensure controlled laboratory practice in the quality control department. To document the raw data as per current GDP. To follow the SOPs of Quality control department and related area. To follow Specification, STP, GTP and protocol during analysis. To use applicable PPEs (personal protective equipment) while performing testing in the laboratory / during handling hazardous solvents/chemicals. To keep himself updated with current regulatory requirements and train the subordinates and colleagues for day to day activities as well as regulatory. To keep the things and his work area clean and tidy and get involved for the routine trouble shooting (if any). To ensure up-keeping of the instrument/equipment. To ensure laboratory inventory management. To inform section head any incident/ OOS/ OOT/ OOC on its immediate occurrence and for day to day activities. To investigate incident/ OOS/ OOT/ OOC (if any) under consultation with the department head/section head. To perform the analysis of stability samples as per the analyst qualification, requirements and respective procedure. To perform the calibration of instrument as per the planner and / or as and when required. To manage all standards for issuance and its usage. To co-ordinate with in-house service engineers and / or external service engineers as and when required. To ensure the destruction of remnant samples after analysis as per applicable procedure. To perform analysis at CHL inter locations whenever required. Responsible for implementing company quality ethics policy for data integrity and inform management and responsible data integrity compliance head on any data integrity issues as per corporate data governance policy. To escalate any issues related to discipline, availability of manpower, hygiene, contamination, cross contamination, Incidents or deviations, malfunctioning of equipments, any unusual observations, any safety risk or quality risk to next level or in absence further up. To perform any other activities as assigned by HOD after completion of the necessary trainings as applicable.