163 Ftir Jobs

As an Analyst, you will be required to possess knowledge of various analytical instruments such as HPLC, UV, FTIR, GC, Polarimeter, KF, Auto titrator, and more. You will be responsible for the QCC-QMS Section, overseeing test procedures, handling OOS, OOAL, Deviation, Change Control Note, Incident, and preparing Investigation Reports. Additionally, you will review instrument logbooks, raw data of materials, in-process, finished products, and water analysis. Your skills and proficiency should include expertise in Analytical Instrumentation Handling, Good Laboratory Practices (GLP) & Documentation Accuracy, Data Integrity & Documentation, Regulatory Compliance, SOP Preparation & Revision, Interpretation of Resulting Data from Analytical Instruments, Quality Control & Compliance, LIMS Operation & Data Management. You should also have a basic understanding of QMS Documentation (OOS, OOT, Deviation & Incident) and CAPA, Deviation, and Change Control Management. To qualify for this position, you should have a minimum of 1 to 4 years of relevant experience in the QCC Department. Candidates applying for internal job postings must have completed at least 2 years in their current job role.,

As an Analytical Chemist at our company, you will be responsible for developing analytical methods using techniques such as HPLC, GC, LCMS, KF, and FTIR for routine analysis. You will also be in charge of maintaining analytical documentation including protocols, specifications, etc. Calibration of HPLC and GC instruments will be part of your regular tasks. It is essential that you are knowledgeable about data integrity and ALCOA guidelines. Additionally, you will be involved in chiral method development to support our analytical processes.,

Analytical method development Routine Analysis by HPLC, GC, LCMS, KF and FTIR Analytical documentation as like Protocols, specifications etc. Calibration of HPLC, GC instruments Aware about data integrity and ALCOA Chiral method development Show more Show less

You should have a Master's degree in Chemistry, Food Science, or Life Sciences with 0 to 5 years of experience in the FMCG/Cosmetics/Foods/Pharmaceutical industry. Your responsibilities will include operating, calibrating, performing intermediate checks, and maintaining various laboratory equipment such as UV-Vis spectrophotometer, K.F. Titrator, Conductivity meter, Viscometer, FT-IR, Tintometer, Analytical balance, pH meter, GC, and HPLC. Experience in handling Kjeldahl digestion and Distillation Unit, as well as preparing and maintaining Reference standards and volumetric standard solutions, is required. You will be involved in quality control and quality assurance activities, including testing retained samples, spiked samples, and participating in inter-laboratory comparisons and proficiency testing programs related to skincare, hair care, hair color, specialty products, foods, snacks, dairy products, beverages, and bakery products. Additionally, you will be responsible for preparing STPs, Validation documents, and Raw material/Product specifications. Proficiency in using Viscometer, Refractometer, and Tintometer is essential. Strong documentation skills and adherence to Good Laboratory Practices are necessary. You should possess excellent English written and oral communication skills to effectively communicate analytical results to both scientific and non-scientific team members. Immediate joining is required for this position located in Ekkathangal, Chennai. This job is with HEPL, a Group company of a 35-year-old FMCG Brand known for manufacturing popular products such as shampoos, hair colors, and food products like milk, milkshake, curd, and ghee. This is a full-time, permanent position with benefits including health insurance and Provident Fund. The work schedule is day shift from Monday to Friday, with a yearly bonus. To apply, you should have experience in Research, NABL, and Laboratory work for at least 1 year each. Immediate joiners who meet the educational and experience requirements are encouraged to apply for this role.,

Amneal Pharmaceuticals is looking for Officer, Quality Control to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes

Job Description Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. Having analytical knowledge of Nasal/Derma products. 3. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 4. Ensuring data integrity policy, GDP and its effectiveness up to compliance 5. To maintain the stability chamber and tracker. 6. To maintain the stability chamber and tracker. 7. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Auto titrator e.t.c. Responsible for sampling, testing and release of Raw material, packing material and miscellaneous material samples and maintain reserve sample as per SOP. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Analysis related to qualification of Instrument/Equipment and Standards Qualification of Standards and Instruments Knowledge and Skill on Sophisticated instruments like UV, HPLC, GC, UPLC, FTIR, Polarimeter and KFtitrator. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Knowledge of current pharmaceuticals guidelines (eg. ICH, cGMP etc.) Troubleshooting and decision skills for analytical problems. Responsible to perform activities with respective TNI . To ensure the timeline for initiation and completion of testing. Responsible to maintain quality standards that apply to product Analysis, ensuring proper implementation. To maintain the cleaning in quality control department Skills and Proficiency: Analytical Instrumentation Handling Expert Particulate Matter Testing Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner Analytical testing expertise and evaluation skills Expert Handling of Analytical Instruments and Interpretation of Resulting Data Practitioner Laboratory Instrument qualification, Calibration & Maintenance Practitioner Quality Control & Compliance Practitioner LIMS Operation & Data Management Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Autotitratior e.t.c. Responsible for sampling, testing and release of Raw material, packing material and miscellaneous material samples and maintain reserve sample as per SOP. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Skills and Proficiency: Analytical Instrumentation Handling Expert Particulate Matter Testing Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner Analytical testing expertise and evaluation skills Expert Handling of Analytical Instruments and Interpretation of Resulting Data Practitioner Laboratory Instrument qualification, Calibration & Maintenance Practitioner Quality Control & Compliance Practitioner LIMS Operation & Data Management Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC, Polarimeter , KF, Auto titrator e.t.c. Responsible for QCC-QMS Section regarding the test procedure, OOS, OOAL, Deviation, Change Control Note, Incident, Investigation Report Preparation e.t.c. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Responsible for QCC-QMS Section regarding the test procedure, OOS, OOAL, Deviation, Change Control Note, Incident , Investigation Report Preparation e.t.c. Skills and Proficiency: Analytical Instrumentation Handling Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner Handling of Analytical Instruments and Interpretation of Resulting Data Practitioner Quality Control & Compliance Practitioner LIMS Operation & Data Management Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Role Name In Community Title Senior Executive Department Sales Hiring Manager Deepak Subramanian Brief Role Description Narayana One Health is in the process of setting up a strategic team tasked with bringing health and insurance closer to patients. The initiative involves setting up primary and secondary care services that are easily accessible to patients and are supported by hyper-responsive processes built to keep patient needs and satisfaction at the center of focus. The initiative aims to bridge the gap between Narayana One Health’s in-hospital offering and patient’s everyday healthcare needs and provide patients access to a continuum of care tailored to their specific healthcare needs. Narayana One Health is looking for Senior Executives for Bangalore, India. This is an individual contributor role in an employee-oriented, high-performance environment that emphasizes spreading Nayana One Health Care Benefits in Bangalore (Karnataka). Your role will entail, Qualification of Leads (via various channels), by calling them, meeting face to face and selling Narayana Arya insurance plans to customers and briefing them about the HealthCare benefits of Arya Insurance via individual reach and through a referral channel model known as One to Many. Responsibilities: 1. Identify Engage and build relationships with Key Community Leaders of Cultural Associations, RWAs etc. 2. Manage Engagement with Community by executing agreed formats of events and sponsorships 3. Generate Interest for Arya Insurance Plans 4. Carry out Right Execution Daily (RED) and adhere to P-100 Program Guidlines 5. Ensure correct Activation and closures at Individual and at channel level. 6. Deliver Monthly targets on Inputs and Outputs Requirements and skills 1. Graduate Degree with Minimum 3-4 years' experience in sales (B2C, B2B or both)- preferred experience in Insurance or financial products and services. 2. Keen Interest in Healthcare and Health Insurance. 3. Passion for new Business Initiatives. 4. A knack for sales and positioning an idea. 5. Highly creative with experience in identifying target audience. 6. Good Communication Skills. 7. Proficient in using CRM, Analytical Tools. Location – Bangalore

We are Reckitt Home to the worlds best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose.Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. About the role Reckitt Research and Development (Gurugram, Haryana, India) is seeking a self-motivated, experienced analytical chemist to join our team in the role of Senior Associate in the Germ Protection Analytical Research & Development team. The successful candidate will be active scientist in the lab and a people leader of other analytical chemists. The role plays a key role in product development of Germ Protection brands including Dettol, Harpic, and Lizol brands. Your responsibilities Contribute to the development of new products and technologies, conducting studies to understand product functionality and efficacy. Lead the development and validation of new methods for product launch and claim support. Utilize a wide range of Analytical techniques, including chromatography (LC and GC), mass spectrometry, and spectroscopy to provide efficient and robust analysis. Support the advancement of analytical capabilities through identification of new technologies and methodologies. Conduct studies in a timely manner and concisely communicate results to a variety of audiences. Prepare scientific reports, technical documents, SOPs, and protocols for internal or external publication/presentation. Serve as manager for chemists within the Analytical team Manage multiple projects within established timelines and concisely communicate results to a variety of audiences. Prepare scientific reports, technical documents, standard operating procedures, and test protocols. The experience were looking for PhD plus 5 years, MS plus 8 years, or BS in chemistry or related field plus 10 years of relevant work experience in an R&D analytical laboratory setting Knowledge of a wide range of analytical techniques such as LC, GC, FTIR, and wet chemistry techniques Advanced knowledge in liquid chromatography is preferred. Strong communication skills (both written and verbal). Results-oriented and self-motivating, seeking information from others to accomplish objectives. Intellectual curiosity and proven problem-solving skills. Ability to work well independently and in a cross-functional team environment while remaining flexible to changing project priorities. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way.We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitts potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitts pay for performance philosophy. We recognise that in real life, great people dont always tick all the boxes. Thats why we hire for potential as well as experience. Even if you dont meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you.All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.

Analytical Development Laboratory Associate Male Min 2-5 Exp only API Co Salary: 2-3 LPA Location: Vadodara( Nandesari ), Gujrat

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the Department of Physics, School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “Development of cost-efficient and scalable perovskite based colloidal nanoparticles for high performance plastic scintillators” Qualification : M.Sc./ M.Tech. in Physics/ Materials Science or related fields from recognized universities/institutes with a minimum of first class and with GATE / CSIR-UGC JRF / NET-LS qualification. Mandatory Skills : Candidates should have a strong research background in synthesis and characterization of nanomaterials. Experience with colloidal semiconductor nanomaterials and related photo physics is desirable. Stipend : Rs. 37,000 p.m. + 8% HRA for the first two years (JRF); Rs. 42,000 p.m.+ 8% HRA for the third year (SRF) will be as per Institute norms. No. of Vacancies : 01 Post (ONE) Age Limit (if any) : Not exceeding 30 years i.e. Age must be from 18 to 30 years Sponsoring Agency : ANRF, PMECRG program, New Delhi, India Duration : 36 Months Principal Investigator : Dr. Abhinav Anand, Assi stant Professor, Department of Physics School of Advanced Sciences, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Interested candidates with the above-mentioned qualifications can send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 18/08/2025) through the website: http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

As an ADL Officer/Executive at our Analytical Development Laboratory (ADL) located in Changodar, Ahmedabad, Gujarat, India, you will be an integral part of our team dedicated to developing, validating, and executing analytical methods to ensure the quality and compliance of our pharmaceutical products. Your key responsibilities will include developing, optimizing, and validating analytical methods for raw materials, intermediates, and finished products using techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy while adhering to ICH guidelines. You will also be responsible for conducting routine quality control tests on pharmaceutical products, analyzing raw materials, in-process samples, and finished products for various physical and chemical parameters. In addition, you will play a crucial role in maintaining accurate and detailed laboratory records, preparing and reviewing standard operating procedures (SOPs) and analytical method documents, and ensuring regulatory compliance with GMP and GLP regulations. You will also be involved in the calibration, maintenance, and troubleshooting of laboratory equipment and collaborate closely with formulation, R&D, and production teams to support product development and troubleshooting. To be successful in this role, you should possess a Bachelor's or Master's degree in Science (Chemistry, Biochemistry) or Pharmacy, proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy, familiarity with regulatory guidelines (e.g., ICH, FDA, EMEA), strong attention to detail, excellent organizational skills, effective communication, and teamwork abilities. Both freshers and experienced candidates are encouraged to apply. Joining our team will offer you the opportunity to be part of a dynamic environment committed to excellence in the pharmaceutical industry. We provide opportunities for professional growth, continuous learning, and the chance to make a meaningful impact on healthcare. This is a full-time, permanent position with benefits including commuter assistance, life insurance, and provident fund. The work location is in person. If you have 2 years of experience in pharmaceuticals and 1 year of experience in analytical chemistry, we welcome your application to join our team and contribute to our mission of ensuring quality and compliance in pharmaceutical product development.,

Perform Calibration and Instrumental analysis of Raw Material, In process samples and finished product. Hands on experience on HPLC, GC, FTIR, Polarity meter & UV spectrophotometer. Good knowledge of software specially Empower. Able to do trouble shooting on instrumentation & able to resolve problem on line. Sound Knowledge of investigation and handling OOS/OOT/Deviation & Lab incident. Perform qualification of working standard and its management.

1. Educational Qualification & Work Experience Preferred Qualification M.Sc. Chemistry / M. Pharm Preferred Years of Experience 3 - 7 yrs. Experience profile required We are seeking a highly skilled Analytical Scientist to join our Analytical development team. The ideal candidate will possess advanced expertise in analytical chemistry, with demonstrated proficiency in HPLC/UPLC, GC, IC, UV, FTIR, and related techniques. The candidate should have a deep understanding of cGMP, GDP, and regulatory standards, along with strong analytical thinking, problem-solving, and decision-making skills. This role requires the ability to manage multiple projects, prioritize tasks, and lead scientific initiatives. The Senior Analytical Scientist will play a pivotal role in advancing scientific excellence and operational effectiveness, contributing directly to the organization s scientific goals. 2. Job Role (Describe the primary purpose, objective and/or function of this job) Key Responsibilities: Design and execute experiments. Operate various analytical instruments (HPLC/UPLC, GC, IC, UV, FTIR etc.). Contributes to scientific problem-solving, analytical thinking, and decision-making. Drives innovation and scientific excellence in laboratory operations and projects. Leads scientific initiatives, manages projects, and prioritizes tasks for project teams. Acts as a pivotal influence in strategic decisions impacting the direction and success of project teams. 3. Job Description - Responsibilities & Duties (The personnel must be able to perform all of the following duties and responsibilities)) Manage laboratory activities with in-depth knowledge of daily operations and verify assigned tasks for accuracy and compliance. Demonstrate significant hands-on experience with analytical equipment such as HPLC/UPLC, GC, IC, UV, FTIR, and other advanced instruments. Possess a strong background in analytical method development, validation and transfer. Carry out peer reviews of colleagues work, ensuring scientific rigor and data integrity. Act as a technical resource and provide expert consultation within the work group or project team. Develop and implement novel processes or hypotheses, frequently using new ideas and knowledge to solve complex problems. Manage projects, prioritizing activities, evaluating resource use, and making insightful, timely decisions that may impact the entire work group or project team. Propose mitigation and contingency plans in anticipation of potential changes or risks within projects. Receive instructions primarily for unusual or complex problems; otherwise, perform activities under limited supervision with periodic review. Identify and devise initiatives, align action plans, and drive scientific activities/projects to support group or project team goals. Understand and apply industry-specific standards and regulations, including cGMP, Environmental, Health, and Safety guidelines. Work Location Assignment: On Premise Research and Development #LI-PFE

1. Educational Qualification & Work Experience Preferred Qualification M. Pharm / M. Sc. Preferred Years of Experience 0 to 2 years Experience profile required We are seeking a highly motivated scientist to join our dynamic research team. The ideal candidate will hold M. Pharm / M. Sc (Chemistry) and possess extensive basic knowledge on modern analytical techniques. The incumbent preferred to have proficiency in handling of analytical techniques such as Spectroscopy (UV-Vis, FT-IR), Chromatography (HPLC) and other instruments (Potentiometric titrator, KF), etc. and have adequate interpretation skills. 2. Job Role Key Responsibilities: Analysis of raw material, In-Process and finished products. Generation of analytical data with respect to accuracy and adequacy. Preparation of reference, working and Impurity standards. To ensure timely completion of assigned Training Modules and Skill Evaluation. Ensure the availability of all the consumables like chemicals, columns, Standards etc. before and during experimental activities. Maintain and adhere to safety and quality culture. Participate in Lab activities necessary to maintain compliance in the lab. 3. Job Description - Responsibilities & Duties Knowledge on Method development /Stability analysis Expertise in Handling Spectroscopy (UV-Vis, FT-IR), Chromatography (HPLC) and other instruments (Potentiometric titrator, KF) Basic knowledge of cGMP, GLP and GDP procedures etc. Understanding of development activities and processes in pharmaceutical industry. Actively listens, shares information in a clear, concise and impartial manner. Actively contributes to achieving team Goals Maintain accurate records of research activities and results. Safety: To follow appropriate safety practices in the workplace. Participate in routine safety training and maintain current knowledge on safety related corporate and site policies. Enforce safety requirements as they relate to job function. Work Location Assignment: On Premise Research and Development #LI-PFE

Approving all Specifications, Test Methods, and Batch Process and Control Records (BMRs). approving validation protocols and reports, and conducting the General Good Manufacturing Practices (GMP) training.

Associate / Senior Associate- Analytical Services Location: Pune Date posted: 23 Jul 2025 Apply until: 30 Aug 2025 Position: Regular Experience: 2-7 years Job function: Analytical Services Role: Full time Job Description We are seeking a skilled and motivated Senior Associate, Analytical Services to join our team. This role requires a robust theoretical understanding in instrumental analysis, coupled with extensive practical experience in operating and troubleshooting equipments such as HPLC, GC, FTIR, Elemental, and Thermal Analyzers. Independently executing complex analytical workflows. Actively undertake method development on various analytical equipments for a diverse range of molecules. Prepare and participate in laboratory expansion strategies through new service delivery. Participate in writing project proposals to seek various types of funding. Performing routine maintenance and calibration of laboratory instruments. Actively participating in laboratory inventory management and procurement of essential consumables and equipment. Designing and delivering impactful workshops on various analytical chemistry topics. Candidate Profile MSc in Analytical /Organic/Inorganic /Pharmaceutical Chemistry. The candidate should demonstrate good written and verbal communication skills, a proactive and enthusiastic approach to their work, and a strong desire to learn and a proactive attitude. Experience of 2-5 years in similar roles. General requirements and expectations from Venture Center employees: Venture Center is a non profit organization with aim to benefit society by promoting entrepreneurs and start ups. Thus, Venture Center seeks employees and consultants with a strong interest and passion in seeing technology innovators, entrepreneurs, and start ups succeed, and a strong "service" ethos. A strong feature of Venture Center jobs is the rich learning environment and opportunity provided to employees to experiment, take initiative and be creative. The work of most employees has visible impact which can be satisfying. All employees benefit from access to high quality facilities and work environments. Compensation packages can be flexible but are often conservative due to Venture Center s non profit status. General requirements include: a) strong ethical standards and work ethics, b) comfort with computers, computer applications and internet, c) strong communication skills spoken and written. Venture Center s working hours are 9 AM 6.00 PM (Monday to Saturday) and are designed to keep operations of Venture Center convenient for the start ups, entrepreneurs, inventors and others that the organization serves. Managers in certain functions are provided the opportunity to avail of flexible hours. All jobs are located at Pune, Maharashtra, India. Our Company is an equal-opportunity employer and does not discriminate against any employee or applicant based on age, color, disability, gender, national origin, race, religion, sexual orientation or parental status.

Must Abide by the rules & regulations of the laboratory. Responsible for Performing tests as per authorization and ensuring the TAT Compliance. Ensure Safe Handling of Equipment’s. Filling all logbooks for the equipment’s as per usage Ensure to wear all the PPE’s and lap aprons before performing the tests without fail. Ensure to follow safety rules & Maintain 5S. Pesticides & Mycotoxins analysis in food & agriculture as per authorization. Follow ISO 17025 requirements in lab with respect to Quality compliance and other regulatory requirements. Internal calibration of equipment’s Maintenance. Handling, Operating & Calibration, Maintenance of LC MSMS. Handling, Operating & Calibration, Maintenance of GC MSMS. CRM Management, Preparation, Storage, Disposal and Record maintenance. Roles and Responsibilities • Must Abide by the rules & regulations of the laboratory. • Responsible for Performing tests as per authorization and ensuring the TAT Compliance. • Ensure Safe Handling of Equipment’s. • Filling all logbooks for the equipment’s as per usage • Ensure to wear all the PPE’s and lap aprons before performing the tests without fail. • Ensure to follow safety rules & Maintain 5S. • Pesticides & Mycotoxins analysis in food & agriculture as per authorization. • Follow ISO 17025 requirements in lab with respect to Quality compliance and other regulatory requirements. • Internal calibration of equipment’s Maintenance. • Handling, Operating & Calibration, Maintenance of LC MSMS. • Handling, Operating & Calibration, Maintenance of GC MSMS. • CRM Management, Preparation, Storage, Disposal and Record maintenance.

Should be capable of handling instrument like HPLC, GC , UV, IR and potentiometry Should have the GMP knowledge and compliance requirement of QC Should have the knowledge on Good laboratory practices .

Qualification : M.Sc Chemistry Experience : 0-2 Yrs Job Responsibility Basic knowledge on chemistry (Organic and Inorganic Reactions) Analytical skills (eg. Titration, pH meter, FTIR, distillation, etc) Knowledge on research and literature survey

Looking for a skilled Quality Control Analyst to join our team in Chennai. The ideal candidate will have 3-5 years of experience in quality control, preferably in coding. Roles and Responsibility Monitor and evaluate the quality of coding services to ensure high standards. Develop and implement quality control processes to identify areas for improvement. Collaborate with cross-functional teams to resolve quality-related issues. Analyze data to identify trends and patterns in quality performance. Develop reports to track quality metrics and provide insights for process improvements. Ensure compliance with industry regulations and standards. Job Strong understanding of quality control principles and practices. Experience in coding and healthcare management services. Excellent analytical and problem-solving skills. Ability to work effectively in a team environment. Strong communication and interpersonal skills. Familiarity with CRM/IT enabled services/BPO industry is an added advantage.

Key Responsibilities Operational Oversight : Manage daily operations, schedule workflows, and oversee process improvements Strategic Planning : Develop and implement short-term and long-term plans; forecast resource and budget needs

Lab chemist required at pio manihari, sonipat for a spices company Qualification- Any graduate Exp- min 2 yrs Salary- upto 25k Timing - 9.30 to 7 pm