54 Sample Analysis Jobs

Location: Hyderabad (Medchal) WorkDay: Monday to Saturday Key Responsibilities Plan and prioritize sampling activities. Operate instrumental techniques such as Vibratory Shifter, Splitters, Disc Mill/Ball Mill, and Representative Sampling. Monitor performance calibration of weighing balances and sampling equipment, while maintaining accurate records. Plan and follow preventive maintenance schedules for equipment. Achieve or exceed departmental objectives and goals. Troubleshoot sampling issues as per departmental requirements. Coordinate with Stores and Warehouse teams to ensure smooth entry/exit of material. Conduct sampling training sessions for new staff. Act as Quality Manager to ensure compliance with ISO standards. Maintain data records and manage clearance in software processing systems. Key Authorities Planning, management, and control of sampling activities. Implementation and oversight of sampling procedures. Execution of Corner Quadrant and Weight Reduction Sampling techniques. Troubleshooting sampling-related issues. Performing internal calibration of laboratory instruments. Ensuring adherence to health and safety guidelines.

You will be responsible for bioanalytical sample preparation using different extraction techniques. Additionally, you will conduct method development, method validation, and sample analysis as per regulatory requirements. You are expected to operate laboratory equipment such as Pipettes, centrifuge, evaporator, and extractors. Moreover, handling data generation, compilation, and reporting of results will be part of your detailed responsibilities. Qualifications required for this role include: - B.Pharm / M.Sc. / M.Pharm Preferred skills for this position are: - Good communication and analytical skills - Ability to work as a team player for the timely completion of tasks,

Officer Quality Control - API & Intermediates Education - M.SC - Analytical / Organic Experience 1 to 3 years experience in Quality Control from pharmaceutical industry. (This is a Fixed Term Contract role - On Company's Contract) Job Description - Sampling of raw, packing material, intermediate & finished product. Analysis of raw, packing material, intermediate, stability samples & finished product. Analysis of process & cleaning validation samples. Preparation of standard volumetric solution, reagent & standardization of volumetric solution and check for stability. Inventory of Instruments Spares, Chemicals & Glassware. To maintain cleanliness, personal and environmental safety & follow Good Laboratory Practices during work. Ensure environment protection by controlling Air / Water / Soil pollution from analytical activities. Accountable for the safe operation of the facility, their own safety and safety of other co- workers. Technical & Behavioral Competencies - • Instrumentation & Analysis in Quality Control • Aware of GXP requirement in Quality Control Laboratory, Data Integrity & ALCOA+ • Knowledge of laboratory investigation • Good Communication Skills, team player, collaboration. • Knowledge of MS Office - MS Word, Excel

Roles & Responsibilities : Perform Analysis: Collect samples for analysis from Custodian. Processing of samples by using various sample extraction technique (to determine the concentration of analyte). Batch sequence preparation and verification in coordination with LIMS Operator. Perform analysis via LCMS/ ICP-OES/ ICP-MS. Follow GxP. Mass Spectrometry operation and ESI, APCI conceptual clarity. Chiral chromatography, polar columns conceptual clarity. Sample extraction process using LLE, SPE, and PPT. Documentation and compliance: Receive controlled forms for various activities. Perform online documentation of development trial in Method Book (Laboratory Record Book), validation experiment documentations, entry in log books in control forms as per SOP, evaluate experiment outcome with pre-defined validation/ study protocol. Document all linked activities and forms as per SOP. Investigation approach in case of abnormality. Regulatory response and investigation writing skills. To check the documentation done by Jr. Analyst/ fresher. Solve the finding/ observation raised by the QC and QA in timely manner. Research & Development: Literature review i.e., published pharmacopeia guidelines/ research documents received from GL and SGL. Validation: Perform experiments as per protocol. Method development skills. Troubleshooting of method. Excel and MS-Word. Equipment Calibration : To calibrate lab equipments like micro-pipettes, analytical balance, pH meter, evaporators, roto spin extractor, centrifuge, Solid Phase Extraction (SPE) assembly and their performance check as and when required, to coordinate with engineer for any breakdown pertaining to lab equipment. Training : To coordinate assist/ support in on-the-job trainings for fresher. Regulatory guidelines and thorough training on SOPs. Presentation skill. Regulatory updates and latest guidance awareness. To understand GCP and GLP requirement and its awareness. General biosafety procedures, emergency procedures awareness. Knowledge of organization policies/ values. Desired Candidate Profile: Education: B.Pharm, M.Pharm, M.Sc Experience: 1-5 Years' experience in CRO.

Date: 2 Sept 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Discovery Services Job Title : Study Director - Pharmacokinetics and Immunogenicity Assays Job Location: Bangalore Department: Translational and Clinical Research About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R& productivity, speed up time to market and lower the cost of innovation. Job Purpose: The position holder is responsible for performing bioanalysis which includes performing ligand binding assays related to Pharmacokinetics and Immunogenicity. Key Responsibilities: Ensure activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures. Regular interaction and participation with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival. Will be involved in strategic planning for project execution, documentation of data, data analysis, interpretation and presentation of the results Ensure to complete the assigned tasks in timely manner. Actively involved in preparation of SOPs, protocols, method and reports Prepare reagents, buffers and maintain log book for assigned assays Interpret results anticipate and understand the issues related to the assay. Participate in, and present data for discussions. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted companyEducational Qualification: Masters degree in Biological Sciences (Preferably Biochemistry background) or a related fieldTechnical/functional Skills: Should have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays with a good understanding as per regulatory guidance/ industry practices/internal Standard Operating Protocols. Should have hands-on experience in Ligand Binding Assay (LBA) development, validation and Sample analysis. Knowledge of ELISA and MSD assays are highly desirable. Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines. Manuscript writing ability is preferable Proficiency in software like Laboratory Information Management System (LIMS), GraphPad, Adobe etc. Experience 6-9 years of experience in immunoassay laboratory. (CRO experience is preferable).Behavioral Skills: Ability to work independently as well as with team members A strong proactive and independent thinker Excellent communication skills - written and oral in English Should have good interpersonal skills Large degree of flexibility and ability to work under strong time pressureEqual Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities. Show more Show less

Date: 2 Sept 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Discovery Services Job Title : Study Director - Pharmacokinetics and Immunogenicity Assays Job Location: Bangalore Department: Translational and Clinical Research About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R& productivity, speed up time to market and lower the cost of innovation. Job Purpose: The position holder is responsible for performing bioanalysis which includes performing ligand binding assays related to Pharmacokinetics and Immunogenicity. Key Responsibilities: Ensure activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures. Regular interaction and participation with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival. Will be involved in strategic planning for project execution, documentation of data, data analysis, interpretation and presentation of the results Ensure to complete the assigned tasks in timely manner. Actively involved in preparation of SOPs, protocols, method and reports Prepare reagents, buffers and maintain log book for assigned assays Interpret results anticipate and understand the issues related to the assay. Participate in, and present data for discussions. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted companyEducational Qualification: Masters degree in Biological Sciences (Preferably Biochemistry background) or a related fieldTechnical/functional Skills: Should have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays with a good understanding as per regulatory guidance/ industry practices/internal Standard Operating Protocols. Should have hands-on experience in Ligand Binding Assay (LBA) development, validation and Sample analysis. Knowledge of ELISA and MSD assays are highly desirable. Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines. Manuscript writing ability is preferable Proficiency in software like Laboratory Information Management System (LIMS), GraphPad, Adobe etc. Experience 6-10 years of experience in immunoassay laboratory. (CRO experience is preferable).Behavioral Skills: Ability to work independently as well as with team members A strong proactive and independent thinker Excellent communication skills - written and oral in English Should have good interpersonal skills Large degree of flexibility and ability to work under strong time pressureEqual Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities. Show more Show less

Date: 2 Sept 2025 Location: Bangalore, KA, IN, 560100 Custom Field 1: Discovery Services Job Title: Study Director - Pharmacokinetics and Immunogenicity Assays Job Location: Bangalore Department: Translational and Clinical Research About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R& productivity, speed up time to market and lower the cost of innovation. Job Purpose: The position holder is responsible for performing bioanalysis which includes performing ligand binding assays related to Pharmacokinetics and Immunogenicity. Key Responsibilities: Ensure activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures. Regular interaction and participation with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival. Will be involved in strategic planning for project execution, documentation of data, data analysis, interpretation and presentation of the results Ensure to complete the assigned tasks in timely manner. Actively involved in preparation of SOPs, protocols, method and reports Prepare reagents, buffers and maintain log book for assigned assays Interpret results anticipate and understand the issues related to the assay. Participate in, and present data for discussions. Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety. Attend training on environment, health, and safety (EHS) measures imparted companyEducational Qualification: Masters degree in Biological Sciences (Preferably Biochemistry background) or a related fieldTechnical/functional Skills: Should have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays with a good understanding as per regulatory guidance/ industry practices/internal Standard Operating Protocols. Should have hands-on experience in Ligand Binding Assay (LBA) development, validation and Sample analysis. Knowledge of ELISA and MSD assays are highly desirable. Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines. Manuscript writing ability is preferable Proficiency in software like Laboratory Information Management System (LIMS), GraphPad, Adobe etc. Experience 6-15 years of experience in immunoassay laboratory. (CRO experience is preferable).Behavioral Skills: Ability to work independently as well as with team members A strong proactive and independent thinker Excellent communication skills - written and oral in English Should have good interpersonal skills Large degree of flexibility and ability to work under strong time pressureEqual Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities. Show more Show less

Please walk in to the interview on SUNDAY 13th Sep 2025 b/w 10:00 AM to 3:00 PM at below mentioned venue. Venue: Unison Pharmaceuticals Pvt. Ltd. Block A, Office Number: 905,6,7,8 Safal Pegasus, 100 Feet Anand Nagar Rd, Chinar Bungalows, Prahlad Nagar, Ahmedabad, Gujarat 380015 Apply now to become a part of a growing team!! 1) Analyst: ADL - Routine Analysis Experience: 2 to 8 years Job Role: ADL - Sample Analyst Markets: Domestic & Regulatory Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) Designation: Officer / Sr. Officer No. of vacancies: 05 Roles and Responsibilities : Perform chemical, physicochemical and wet analysis as per product requirements. Routine In-process, Finished product (Initial & Stability samples) analysis. Data reporting with good documentation practice and presenting results in informative report format. 2 ) Analyst: - ADL - LCMS Experience: 2 to 8 years Job Role: ADL - LCMS Analyst Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) Designation: Officer / Sr. Officer No. of vacancies: 05 Roles and Responsibilities : Method development of nitrosamine impurities/NDSRI/genotoxic impurities on LCMS/MS with proper documentation and prepare Analytical test procedure & worksheet. Routine API & Finished product (Initial & Stability samples) analysis like Nitrosamine impurities, Genotoxic impurities, NDSRI, related substances Method validation for analytical method on LCMS/MS Responsible to Stability data compilation for finish product as per requirement. Follow GLP in the laboratory. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive Regards, Team HR Unison Pharmaceuticals Pvt Ltd

Role & responsibilities Collect, prepare, and analyze ferro alloy samples using standard laboratory methods. Perform physical and chemical testing of raw materials, in-process, and finished products. Operate and maintain laboratory equipment (e.g., spectrometer, chemical balances, furnaces, etc.). Ensure test results meet defined quality standards and customer specifications. Record, maintain, and report laboratory data in accurate formats. Support production and quality teams with technical inputs on material testing. Follow safety protocols and maintain cleanliness in the laboratory. Calibrate instruments periodically and ensure proper documentation. Assist in developing and implementing quality improvement measures. Preferred candidate profile Diploma / B.Sc. (Chemistry / Metallurgy) or equivalent. 24 years of relevant experience in Ferro Alloys / Metallurgical / Chemical industry laboratory. Hands-on knowledge of ferro alloy testing and quality standards. Familiarity with spectrometry, wet analysis, and related equipment. Strong attention to detail, accuracy, and analytical skills. Good knowledge of laboratory practices and safety standards. Ability to work independently and in a team. Strong record-keeping and reporting skills. Basic computer knowledge (MS Office, data entry).

Post- Lab Technician Location - Pune Urlikanchan Factory Contact - 9356395439 Education: A post-secondary education (degree and/or diploma) in a science-related field (e.g., Chemistry, Geology, Mining Engineering) is often preferred. 2 -aboratory Experience: Prior experience in a laboratory setting, sample preparation and analysis techniques, is highly desirable. 3 -Sample Handling and Preparation: Sampling, sorting, and labeling samples. Crushing, pulverizing, splitting, and sieving samples according to established procedures. Preparing samples for analysis using various techniques (Wet analysis).

The Quality Assurance role involves the inspection and evaluation of raw materials, in-process goods, finished products, and packaging materials in accordance with Grasims specifications and quality standards. Your responsibilities include: For Raw Materials: - Conducting thorough inspections of raw materials based on Grasims specifications, supported by analytical records. - Following calibration procedures at predefined frequencies. - Preparing and standardizing solutions for analysis. - Ensuring timely analysis of sample results and updating records. - Minimizing the need for re-analysis and strictly adhering to SOPs or testing protocols. - Preserving retain samples as per protocol. For In-process Goods: - Inspecting in-process goods according to Grasims quality plan. - Following calibration schedules as required. - Minimizing re-analysis efforts. - Adhering to SOPs or testing protocols, conducting timely analysis of sample results, and updating records. - Preserving retain samples in compliance with protocol. - Preparing and standardizing solutions used for analysis. For Finished Products: - Inspecting finished products per Grasims specifications, supported by analytical records. - Following calibration procedures at predefined intervals. - Conducting timely analysis of sample results and updating records. - Preparing and standardizing solutions for analysis. - Minimizing the need for re-analysis. - Preserving retain samples according to protocol. For Packaging Materials: - Inspecting packaging materials based on Grasims specifications. - Following calibration procedures at specified frequencies. - Ensuring timely analysis of sample results and record updating. Overall, the Quality Assurance role requires meticulous attention to detail, adherence to protocols, and a commitment to maintaining high-quality standards throughout the production process.,

Job Overview: We are seeking a Lab Attendant to support our Chemical R&D team. The ideal candidate should have average to above-average knowledge of chemistry, willingness to learn, and passable communication skills. Key Responsibilities: Assist in routine lab operations, sample preparation, and testing. Maintain cleanliness, safety, and order in the lab. Support researchers with experiments and basic chemical handling. Ensure proper storage, labeling, and disposal of chemicals. Record and update experimental data as directed. Requirements: B.Sc. / M.Sc. in Chemistry (preferred). 01 year of experience in a lab environment. Basic understanding of chemical processes and lab practices. Ability to follow safety protocols and instructions. Eagerness to learn and contribute in a research-driven environment.

Detailed Job Role Perform testing on raw materials and finished products, manage lab operations, and ensure compliance with testing protocols. KRA (Key Responsibility Areas) Sample analysis, report generation, lab maintenance, equipment calibration KPI (Key Performance Indicators) Test turnaround, accuracy, non-conformance incidents, corrective action timeliness Job Summary: We are seeking a meticulous Quality Control Executive to perform testing of raw materials and finished products, manage laboratory operations, and ensure compliance with established testing protocols. The ideal candidate will maintain high standards of accuracy, reliability, and regulatory compliance in the QC laboratory. Key Responsibilities: Perform chemical, biological, and physical testing on raw materials, in-process samples, and finished products. Generate accurate and timely laboratory reports. Maintain laboratory equipment and ensure calibration and validation as required. Monitor and enforce adherence to SOPs and testing protocols. Investigate non-conformance incidents and implement corrective actions. Support method development, validation, and continuous improvement initiatives. Key Performance Indicators (KPIs): Test turnaround time and report submission Accuracy and reliability of laboratory results Frequency and resolution of non-conformance incidents Timeliness of corrective action implementation Skills & Competencies: Strong knowledge of QC testing techniques and laboratory procedures Attention to detail and analytical thinking Familiarity with GMP, GLP, and quality standards Effective documentation and reporting skills Ability to manage multiple tasks and maintain lab efficiency Education - B.Sc/M.Sc (Chemistry/Life Sciences), B.Pharm

Detailed Job Role Perform testing on raw materials and finished products, manage lab operations, and ensure compliance with testing protocols. KRA (Key Responsibility Areas) Sample analysis, report generation, lab maintenance, equipment calibration KPI (Key Performance Indicators) Test turnaround, accuracy, non-conformance incidents, corrective action timeliness Job Summary: We are seeking a meticulous Quality Control Executive to perform testing of raw materials and finished products, manage laboratory operations, and ensure compliance with established testing protocols. The ideal candidate will maintain high standards of accuracy, reliability, and regulatory compliance in the QC laboratory. Key Responsibilities: Perform chemical, biological, and physical testing on raw materials, in-process samples, and finished products. Generate accurate and timely laboratory reports. Maintain laboratory equipment and ensure calibration and validation as required. Monitor and enforce adherence to SOPs and testing protocols. Investigate non-conformance incidents and implement corrective actions. Support method development, validation, and continuous improvement initiatives. Key Performance Indicators (KPIs): Test turnaround time and report submission Accuracy and reliability of laboratory results Frequency and resolution of non-conformance incidents Timeliness of corrective action implementation Skills & Competencies: Strong knowledge of QC testing techniques and laboratory procedures Attention to detail and analytical thinking Familiarity with GMP, GLP, and quality standards Effective documentation and reporting skills Ability to manage multiple tasks and maintain lab efficiency Education - B.Sc/M.Sc (Chemistry/Life Sciences), B.Pharm

Detailed Job Role Conduct biochemical tests and research to support drug development and quality control processes. KRA (Key Responsibility Areas) Experiment design, sample analysis, data recording, method development KPI (Key Performance Indicators) Experiment accuracy, validation rate, milestone achievement, innovation outputs Job description Department: Research & Development / Quality Control Reports To: Senior Scientist / R&D Manager Job Purpose / Summary: To conduct biochemical tests, research, and analysis to support drug development and quality control processes, ensuring accurate data generation, method validation, and compliance with scientific standards. Key Responsibilities & Duties (KRA): Experiment Design & Execution : Plan and perform biochemical experiments for drug discovery and quality testing. Sample Analysis : Conduct biochemical and molecular assays on samples using standard laboratory techniques. Data Recording & Documentation : Accurately record experimental results, maintain lab notebooks, and prepare reports. Method Development : Support in developing, validating, and optimizing biochemical test methods. Collaboration : Work closely with R&D, quality, and cross-functional teams to achieve project goals. Compliance : Adhere to laboratory safety protocols, GLP/GMP, and organizational quality standards. Key Performance Indicators (KPI): Accuracy of Experimental Results (%) Method Validation & Success Rate Milestone Achievement (Projects/Timelines met) Number of Innovation Outputs (e.g., new techniques, process improvements) Compliance with Safety & Documentation Standards Education Required B.Sc / M.Sc (Biochemistry/Life Sciences)

As a QC Officer based in Bhiwandi, Maharashtra, you will be responsible for performing a comprehensive analysis of raw materials, finished products, and vendor samples. Your duties will include executing titration and other chemical testing methods to detect impurities, ensuring compliance with internal SOPs and external regulatory standards, and maintaining accurate documentation of records, reports, and validation protocols. You will be expected to adhere to quality guidelines such as GMP, ISO, and ICH regulations, as well as develop new testing methods for efficient sample analysis. Additionally, you will play a key role in the maintenance and calibration of lab instruments such as GLC, Flame Photometer, and pH Meter, as well as the preparation and standardization of volumetric solutions, reagents, and chemicals. Conducting quality checks on vendor-supplied materials and chemicals, implementing safety protocols in the QC area, and continuously evaluating Standard Operating Procedures for accuracy will also be part of your responsibilities. Utilizing Microsoft Excel, Word, and PowerPoint for efficient documentation and reporting will be essential in this role. To excel in this position, you must possess a strong knowledge of chemistry with expertise in organic and inorganic identification, proficiency in volumetric and analytical techniques, and the ability to detect impurities to ensure product integrity. Knowledge of Gas Liquid Chromatography (GLC), Flame Photometer, and pH Meter, along with excellent documentation skills and analytical thinking, will be crucial for success in this role. If you are looking to work in a challenging environment that values your expertise in sample analysis, documentation, compliance, chemistry knowledge, impurity detection, instrument handling, and analytical thinking, this opportunity as a QC Officer may be the perfect fit for you.,

The job involves consulting geological maps and aerial photographs to provide advice on site selection. You will be assisting with the design of built structures using specialized computer software or calculations. In addition, you will be responsible for collating data, producing reports, and overseeing the progress of specific contracts. Your role will also include planning detailed field investigations by drilling and analyzing samples of deposits/bedrock, supervising site and ground investigations, and visiting new project sites. You will be advising on and testing a range of construction materials such as sand, gravel, bricks, and clay. Moreover, you will be making recommendations on the proposed use of a site, providing information, and advising on problems like subsidence. As part of your responsibilities, you will manage staff, including other engineering geologists, geotechnical engineers, consultants, and contractors. You will also attend professional conferences and represent the company or organization at various events. This is a full-time, fresher job opportunity with benefits including Provident Fund. The work schedule is in the day shift, and the work location is in person.,

Company Profile Canpac Trends, established in 2011, is one of India's leading paper packaging manufacturers, backed by over 14 years of industry expertise. With a state-of-the-art production infrastructure spanning 1.35 million sq. ft., we operate across key regions including Gujarat, Delhi-NCR, Tamil Nadu, Telangana, and West Bengal. Our dedicated team of over 1,200 professionals including more than 100 technical specialists ensures consistent quality and continuous innovation. We proudly serve a network of over 500 esteemed clients. At Canpac, we Care deeply, Create passionately, and Commit fully delivering world-class packaging and printing solutions driven by excellence and innovation. Key Responsibilities Marketing Coordination Coordinate with the Marketing team to gather product design information for initiating new jobs. Procurement Indents Prepare board procurement indents with complete details and forward them to the Purchase department. Job Card Review & Release Check Job Cards thoroughly before releasing them ssfor production. Job Card Closure Ensure timely closure of Job Cards with proper documentation and follow-up. Stock Verification Verify in-house board stock once the Job Card is finalized by the Development team. Die Requirement Management Review die requirements and prepare die orders as per job specifications. Inventory Management Check in-house paper for any job and utilize in best possible way before ordering new paper Key Requirements Behavioural Skills Proficient in MS Office (Excel, Word) and ERP systems Must have knowledge packaging board. Attention to Detail Ensures accuracy in order booking, invoicing, and documentation. Time Management – Manages tasks efficiently to meet timelines and avoid delays. Ownership & Accountability – Takes responsibility for order processing and closure with reliability. Team Player – Works collaboratively across departments to ensure smooth execution. Adaptability – Flexible to handle changing priorities and business requirements.

As a Food Lab Technician, you will be responsible for conducting lab testing, sample analysis, quality control, and ensuring hygiene and safety compliance in the food industry. Whether you are a fresher or an experienced professional with a B.Sc or M.Sc in Food Technology, Microbiology, or a related field, you are encouraged to apply for this position. Both male and female candidates are welcome to join our team. This is a full-time, permanent position that offers a salary range of 15k-25k. Your work location will be in person, where you will have the opportunity to contribute to the quality and safety standards of food products.,

We are seeking a skilled and detail-oriented Lab Technician to join our team. The successful candidate will be responsible for conducting tests, analyzing samples, and maintaining laboratory equipment. The ideal candidate will have a strong background in laboratory procedures and protocols, excellent analytical skills, and the ability to work accurately in a fast-paced environment. Conduct laboratory tests and analyses on samples - Maintain and calibrate laboratory equipment - Prepare and store samples for testing - Record and report test results accurately - Follow laboratory protocols and procedures - Maintain a clean and safe working environment - Collaborate with other lab staff to achieve goals.

Responsibilities : To operate various high end instruments. To keep record on instrument usage. To maintain the SOP of the instruments. Keeps equipment operating by following operating instructions; troubleshooting breakdowns; maintaining supplies; performing preventive maintenance; calling for repairs. Resolves problems by examining and evaluating data; selecting corrective steps. Enhances laboratory and organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. Key Skills Handling sophisticated analytical equipment like Atomic Absorption Spectrophotometer, FT-IR, Raman, and Gas chromatograph for 2-4 years in a private or public laboratory. Extensive sample analysis experience is preferred. Sample analysis; troubleshooting; regular maintenance, and calibration of sophisticated analytical equipment. Educational Qualification MSc in Analytical Chemistry/Analytical Instrumentation

As an Analyst or Senior Analyst in Bioanalytical Research at Veeda Lifesciences, you will play a crucial role in conducting bioanalytical research activities. This includes method development, validation, and sample analysis utilizing a variety of techniques such as HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Your responsibilities will also involve developing and validating methods for bioanalysis of biologics and biosimilars in compliance with regulatory requirements, such as those set by the USFDA. Collaboration with cross-functional teams will be essential to ensure the timely delivery of high-quality results. Additionally, you will be tasked with performing stability testing of biological products under different conditions. Troubleshooting issues related to instrument calibration, maintenance, and operation will also fall within your scope of duties. The ideal candidate for this role should hold a Bachelor's degree in Pharmacy (B.Pharm) or a Master's degree in Pharmacy (M.Pharm) from an accredited institution, or alternatively an M.Sc. degree. Previous experience ranging from 0 to 4 years is preferred. A strong understanding of analytical instruments like HPLC, UPLC, GC, MS, ICP-MS, and wet analysis is highly desirable for this position.,

As a Quality Control department member at Actylis in Ahmedabad, you will be responsible for ensuring laboratory compliance with internal standards and procedures. Your key tasks will include analyzing Raw Materials (RM), Finished Goods (FG), Packaging Materials (PM), Purified water, In-process samples, and stability samples. Additionally, you may be assigned other duties by your reporting manager as needed. Actylis, with a rich history of 70 years, is a global chemical supplier that specializes in providing specialty chemicals, nutritional ingredients, and various products used in the pharmaceutical industry. Our operations span across ten countries, and we excel in core competencies such as Research & Development, Production, Quality Assurance, Supply Chain, Global Sourcing, and Regulatory Compliance. This diverse set of competencies allows us to offer agile solutions to our customers for the swift development and commercialization of innovative products. Your responsibilities will include: - Filling up sampling checklists as per guidelines and submitting them to the Assistant Manager for review. - Preparation and standardization of volumetric standard solutions while maintaining consumption records. - Extracting samples from production areas based on defined guidelines in the Sampling Checklist. - Conducting sample testing according to the Sample Analysis Report. - Performing sampling tests as per the Test Intimation sheet, filling up necessary forms, and attaching supporting documents. - Preparation of working standards and carrying out sample analyses as per the Method of Analysis (MOA). - Operating and calibrating various laboratory instruments such as pH meter, Refractometer, KF, MP, Tap density meter, sieve shaker, Auto titrator, weighing balance, oven/muffle furnace, Halogen moisture analyzer, and Distillation apparatus. - Maintaining records including consumption, humidity, and instrument log books. - Preparing standard solutions, indicators, and reagent solutions. Education: - B.Sc. / M.Sc. in Chemistry Experience: - 0 to 3 years Competencies & Skillset: - Functional/Technical Skills: Sample Analysis within stipulated timelines, Volumetric Preparations and Standardization, Method of Analysis of the Products. - Behavioral Skills: Documentation, Audit readiness, Self Development, Customer Intimacy, Simplify & Act with Urgency, Global mindset, Act as Owner, Adapt to change. This role may involve supervisory responsibilities based on the specific requirements.,

Job Overview: As a Microbiologist at our organization, you will be responsible for conducting research, experiments, and analysis within the fields of microbiology, water technology, and environmental science. Your role will involve collaborating on R&D projects, devising innovative solutions, analyzing data, and working closely with internal teams and external partners. It is essential to ensure compliance with scientific standards while contributing to the advancement of the organization's research objectives. Job Description: In this role, you will be expected to: - Execute scientific research and experiments in the microbiology field. - Develop new processes and technologies related to water, wastewater, and environmental applications. - Analyze and interpret data, and prepare comprehensive reports and presentations. - Collaborate effectively with cross-functional teams and external stakeholders. - Ensure that the laboratory complies with quality and safety standards such as NABL and ISO 17025. - Act as an authorized signatory for NABL reports. - Stay abreast of advancements in the field and integrate new technologies for continuous improvement. Key Qualifications: - Hold a Master's degree in microbiology, Environmental Science, or a related field. - Possess at least 5 years of experience in scientific research within the microbiology domain. - Demonstrate strong analytical, problem-solving, and data interpretation skills. - Proficient in the use of microbial lab equipment, research tools, and data analysis software. - Exhibit excellent communication and teamwork abilities. - Have knowledge of Microbial Test methods of APHA/BIS/BAM/ISO. - Skilled and experienced in testing water and wastewater samples. - Must be an NABL approved Authorized signatory for microbiology scope. - Capable of method development, validation, and evaluation of measurement uncertainty following International Standards. - Conduct sample analysis of water, wastewater, and sludge samples and coordinate with R&D projects. - Perform method verification and measurement uncertainty assessment. - Conduct critical consumables evaluation, media quality checks, and culture handling. - Monitor environmental parameters and instruments for calibration, breakdowns, and maintenance. - Handle ILC/PT raw data and calculations efficiently. - Develop documentation and systems in line with the Quality Management System per ISO/IEC 17025:2017.,

As a part of this role, you will be responsible for sample preparation, daily calibration, and the maintenance of equipment, including keeping a detailed log of all activities. You will also be involved in method development, method validation, and conducting sample analysis in accordance with ICH M10 guidelines. Operating, maintaining, and calibrating LCMS equipment will be a crucial part of your responsibilities. In addition, you will be required to adhere to documentation procedures as outlined in Bio analytical SOPs and ICH M10 guidelines. This will involve thorough record-keeping and ensuring all documentation is accurate and up to date. Furthermore, you will be expected to review data and reports to ensure quality and compliance with relevant standards. Your attention to detail, ability to follow guidelines meticulously, and commitment to maintaining accurate records will be essential for success in this role. If you are looking for a position that offers diverse responsibilities in a dynamic environment, this opportunity may be the perfect fit for you.,