22 Sample Analysis Jobs

Key Responsibilities: Develop and validate analytical methods using HPLC, UV, IR, and GC. Prepare protocols and reports for method development and validation. Perform stability studies and sample analysis for new products. Maintain instruments and lab notebooks as per SOPs and GMP guidelines. Coordinate with formulation development and QA teams. Requirements: M.Sc. / B.Pharm / M.Pharm in Chemistry/Pharmaceutical Sciences. Knowledge of ICH guidelines and regulatory documentation. Hands-on experience with chromatographic techniques and software. Analytical Method Development of Assay, Related Substances, Residual Solvents & Dissolution Test Methods with Literature Search & Report.

Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertical Job Responsibilities: 1) Lead overall raw materials, lab process for the prototype lab. 2) Perform the validation tests for the SOPs for the prototype lab, for both Sannap and Diaper. 3) Regularly evaluate new technologies which can be inculcated in the current prototype lab setup. 4) Responsible for the preventive maintenance, calibration and proper functioning of the prototype lab machines. 5) Responsible for the production of prototype samples for both sannap and diaper as and when required. 6) Maintain expertise in the prototype lab function and train the new resources on the same. 7) Responsible for the product lab performance evaluation for the prototype samples and the commercial products for comparison. This position belongs to HCD vertical. Number of positions : 1 Job Location- Kasna Industrial Area, Greater Noida Office Timings- 09:30 am to 06:00 pm 2nd & 4th Saturday are off. Education : B.Sc.- Chemistry (Mandatory) Full Time Contact HR: Ms. Nancy Goyal Email- nancy.goyal@rsplgroup.com

Role & responsibilities Company : RSPL Group is more than 6,000 Cr diversified conglomerate, which is committed to value for money propositions & credited with several innovations over last 3 decades. The sagacity to weave its business around consumer needs has conferred RSPL Group with a distinct value and identity. Efficient capital structure, cutting edge technology, operational discipline and a widespread distribution network, have together attributed to enhance RSPL Group and enabled the organization to deliver value to consumers. Diversified Group having product category in FMCG, Dairy Products, Hygiene Care, Foot wear, Real Estate, Renewable Energy. This position belongs to HCD Vertical Job Responsibilities: 1) Lead overall raw materials, product lab tests process and the present the results in a right format and time. 2) Perform the validation tests for new test methods. 3) Regularly evaluate market samples and maintain proper records for the same. 4) Responsible for the preventive maintenance, calibration and proper functioning of the lab equipment. 5) Document knowledge, make the clear report and maintain the security of the result as required by RSPL policy. 6) Maintain expertise in at least one area of the company's technology as a Researcher for Feminine Care products. 7) Skillful handling of critical lab test equipment especially for those of Sanitary Napkin testing and evaluation. 8) Experience into pulp, paper & Non- woven. Number of positions : 1 Job Location- Kasna Industrial Area, Greater Noida Office Timings- 09:30 am to 06:00 pm 2nd & 4th Saturday are off. Contact HR: Ms. Nancy Goyal Email- nancy.goyal@rsplgroup.com

Strong Online Testing & Analysis knowledge Strong Sampling & Methodology knowledge Instrument Calibration & Validation Documentation & Label Method Development & Validation Strong SOP & QMS Compliance Candidates from Herbal/Phyto industry is required

Job Role: QC Assistant Job Location: Jaipur Education: BSC / MSC Experience: 1-2 Years About Brand: Minimalist (https://www.beminimalist.co) is a science-backed Indian skincare brand built on the core values of efficacy, transparency, and comprehensiveness. Known for its ingredient-first approach, the brand formulates high-performance skincare products using proven activities and clean formulations. The company believes in creating high-quality products using best-in-class ingredients at its own manufacturing facility. Minimalist empowers consumers with knowledgeclearly stating what goes into each product and whyso they can make informed choices. With a commitment to 'Hide Nothing,' the brand champions authenticity and honesty in skincare, creating solutions that work, without the fluff. With a robust portfolio of 60+ SKUs spanning Skincare, Haircare, and Bodycare, the brand is rapidly expanding its footprint. Focused on enhancing product availability, it is strategically deepening its penetration while strengthening both Modern Trade (MT) and General Trade (GT) channels in India. The brands global presence now extends across 15+ countries, including key markets such as the UK, USA, UAE, Malaysia, Indonesia, Germany, France & Italy. Roles and Responsibilities: Assist in the collection, labeling, and preparation of samples for analysis. Ensure proper storage and documentation of samples to maintain traceability. Perform regular cleaning and sterilization of laboratory equipment and workspaces. Dispose of waste materials following established safety protocols. Prepare reagents and solutions as per standard operating procedures (SOPs). Monitor inventory levels and assist in ordering laboratory supplies. Calibrate and maintain laboratory instruments to ensure accurate results. Maintain accurate records of all QC activities, including test results and equipment maintenance logs. Adhere to all laboratory safety guidelines and regulatory requirements. Qualifications: Bachelors degree in Microbiology, Chemistry, Biotechnology, or a related field. Minimum of 1-2 years of experience in a laboratory setting, preferably in quality control. Familiarity with laboratory equipment and basic analytical techniques. Strong organizational skills and attention to detail. Proficiency in using laboratory information management systems (LIMS) is a plus. Excellent communication skills and the ability to work collaboratively in a team environment.

We are seeking a skilled and detail-oriented Technician - Laboratory to join our team in India. The ideal candidate will have 1-7 years of experience in a laboratory environment and will be responsible for conducting experiments, analyzing samples, and maintaining laboratory equipment. RESPONSIBILITIES Prepare and analyze samples using laboratory equipment and techniques. Maintain laboratory equipment and ensure it is calibrated and functioning properly. Perform routine quality control checks on laboratory tests and results. Document and report laboratory findings in accordance with standard operating procedures. Assist in the development and validation of laboratory methods and procedures. Ensure compliance with safety regulations and maintain a clean laboratory environment. Collaborate with team members and other departments to support research and development activities. Skills and Qualifications Bachelor's degree in Biology, Chemistry, or a related field. 1-7 years of experience in a laboratory setting, preferably in a clinical or research laboratory. Proficient in laboratory techniques such as pipetting, centrifugation, and spectrophotometry. Familiarity with laboratory safety protocols and good laboratory practices (GLP). Strong analytical and problem-solving skills. Excellent attention to detail and ability to work independently or as part of a team. Effective communication skills, both written and verbal.

Responsible to prepare analytical method development, development validation, method transfer protocol and reports. Perform F&D Trial sample analysis, Wet analysis and stability sample analysis with proper data complication. Operation of machine and instrument like HPLC(Make = Shimadzu,Thermo Software =Chromeleon, Lab solution,LC Solution), UV spectrometer (Make = Shimadzu, Software = Lab Solution), IR (Make = Shimadzu, Software = Lab Solution) Dissolution apparatuses, Liquid partical counter and Karl fischer for water content. Perform instrument calibration as per respective SOP daily pH meter calibration and balance verification.

Role & responsibilities- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Experience in analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Fair understanding of ISO/IEC 17025, ISO 9001, ISO14001, ISO 22000, ISO18001 Lab safety & GLP management

Roles and Responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

sampling coordinator required for Textile Company at Kundli , Sonipat Qualification- Any Textile designing course Exp - Fresher or experienced salary- upto 20k Wtsapp me resume at 8295842337- Mr. Bansal

Supervision of Sampling, Sample preparation, Sample Analysis, Instrument Calibration, Documentation etc.

Job Description :- Opportunity :- Lab Technician Sampling method. Basic knowledge of analysis methods. o Preparation of analysis results. o Maintenance of lab documentation. o Basic Knowledge of ISO9001 Soft Skills: o Teamwork o Agile o Resilience o Empathy Computer Skills: o Basic knowledge Good knowledge of MS Office (word, excel, PowerPoint etc.) Job Description Sample preparation o Sample grinding o Sieving o Calcination o Color measurement o Sieving analysis o Loss on drying o Documentation of required process as described in SOPs o Warehouse visit for sample collection. o Inventory for lab equipments spare parts

Role & responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Preferred candidate profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Job Title: Sampling Coordinator Department: Sampling/ Merchandising Location: FashionC Overseas Pvt. Ltd. Job Summary: The Sampling Coordinator is responsible for managing the development of samples in alignment with buyer requirements and ensuring adherence to quality standards. This role involves close coordination with the merchandising, production, and quality teams to ensure timely execution of high-quality samples that meet customer expectations. Key Responsibilities: Sampling Management: Plan and coordinate the entire sampling process from proto to pre-production samples. Ensure timely development and dispatch of samples as per buyer deadlines. Maintain a detailed record of sample development processes and approvals. Quality Assurance: Ensure all samples meet buyer quality standards, specifications, and compliance requirements. Conduct thorough inspections and evaluations of samples to identify defects or deviations. Work closely with the quality team to implement corrective actions where necessary. Fabric & Trim Coordination: Source and coordinate required fabrics, trims, and accessories for sample development. Collaborate with suppliers and in-house teams to ensure material quality and timely availability. Cross-functional Coordination: Liaise with design, merchandising, and production teams to ensure proper execution of sample development. Provide feedback on design feasibility and suggest improvements for production efficiency. Communicate sample comments and buyer feedback to relevant teams. Process Improvement: Identify areas for improvement in the sampling process to enhance efficiency and quality. Implement best practices to reduce sample lead time and minimize rework. Documentation & Reporting: Maintain records of sample development, approvals, and quality assessments. Prepare reports on sample status, rejections, and improvements for management review. Key Skills & Competencies: Strong knowledge of garment construction, fabric types, trims, and quality standards. Familiarity with buyer requirements, technical specifications, and compliance standards. Excellent coordination and communication skills to manage cross-functional teams. Ability to troubleshoot quality issues and implement corrective measures. Strong organizational skills with attention to detail and problem-solving ability. Proficiency in MS Office. Qualifications & Experience: Bachelor's degree/Diploma in Fashion Designing, Textile Technology, or related field. 7-8 years of experience in sampling coordination within the garment industry. Prior experience working with export houses and buyers is an advantage. Strong understanding of quality assurance and garment testing standards. Salary- 35000-40,000 Full time Day shift

Role & responsibilities 1. Analytical Testing and Analysis : a. Analyze samples from various sources (raw materials, intermediates, finished products, and stability samples) to determine compound composition and quantities. b. Perform routine and complex analyses using HPLC, Prep HPLC, LCMS, UPLC, and Flash chromatography. c. Interpret analytical data and provide comprehensive reports of scientific results, including trend analysis and data summaries. d. Conduct testing, release, and documentation of raw materials, intermediates, and finished products, adhering to established specifications. e. Perform stability studies and analyze degradation products. 2. Method Development and Validation: a. Develop and validate HPLC, LCMS, and other analytical methods for various drug products and chemical compounds, including forced degradation studies. b. Ensure methods are robust, reliable, and compliant with regulatory requirements (ICH guidelines, etc.). c. Write and review method validation protocols and reports. 3. Instrument Management and Documentation: a. Perform routine calibration, maintenance, and troubleshooting of HPLC, LCMS, GC, and other analytical instruments. b. Prepare and maintain Standard Operating Procedures (SOPs) and Instrument Operating Procedures (IOPs). c. Maintain accurate and detailed documentation of all analytical activities, including raw data, instrument logs, and reports, in accordance with GLP/GMP. d. Participate in instrument qualification. 4. Quality Control and Compliance: a. Ensure all analytical activities comply with established quality control procedures and regulatory guidelines. b. Maintain awareness of and adhere to health and safety regulations, including chemical handling and waste disposal. c. Validate methods and equipment to ensure accuracy and reliability, participating in audits as needed. d. (Optional) Ensure compliance with cGMP and GLP guidelines. e. Participate in investigations of out-of-specification (OOS) results. 5. Collaboration and Communication: a. Work collaboratively in cross-functional teams, including R&D, formulation, and regulatory affairs. b. Liaise with customers, staff, and suppliers as needed. c. Report scientific results effectively to stakeholders, including presentations and written reports. d. Participate in project meetings. Preferred candidate profile Technical Skills: a. Extensive hands-on experience with HPLC, Prep HPLC, LCMS, UPLC, and Flash chromatography. b. Proven experience in developing and validating HPLC and LCMS methods. c. Knowledge of instrument calibration, maintenance, and troubleshooting. d. Proficiency in data interpretation, statistical analysis, and documentation. e. Knowledge of stability testing. Knowledge: a. Strong understanding of analytical chemistry principles and techniques. b. Knowledge of raw materials, intermediates, finished product, and stability testing. c. Knowledge of preparing SOPs, IOPs, validation protocols, and reports. d. Knowledge of regulatory guidelines (ICH, etc.). e. (Optional) Knowledge of cGMP and GLP compliance. Soft Skills: a. Excellent analytical and problem-solving skills. b. Strong attention to detail and ability to maintain meticulous records. c. Excellent communication skills (both written and verbal). d. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). e. Ability to work independently and manage multiple tasks effectively. f. Strong team player Key Attributes: a. Accuracy and reliability in analytical work. b. Commitment to quality, compliance, and safety. c. Proactive and adaptable to new challenges and technologies. d. Strong organizational and time-management skills. e. Ability to learn and keep up to date with new analytical techniques and regulatory requirements. f. Ethical conduct. Perks and benefits

Role & responsibilities Sampling and analysis as per standard operating process Wear and ensure all helpers adhere to safety PPE s and follow safety standards. If discrepancy found in samples coordinate with Senior Chemist Take samples from inward vehicles and conduct Quick Check analysis Take in process sample for analysis and take corrective measures if not in coordination with Senior Chemist Check all instruments are in working condition and if not inform Senior Chemist Prepare all lab reagents and chemicals as per standards and discard if expired in coordination with Senior Chemist Implement Good House Keeping Practices and keep laboratory clean (5S) Instrument Handling COD- Digester, Oven, muffle, Auto titrator, flame photometer, Bomb calorimeter, PH meter, Conductivity meter, TDS meter, flash point tester Preferred candidate profile 0 to 3 years of experience in Laboratory / Quality control Skill: Instrument Handling COD- Digester, Oven, muffle, Auto titrator, flame photometer, Bomb calorimeter, PH meter, Conductivity meter, TDS meter, flash point tester Perks and benefits Mediclaim (spouse and up to 3 child)

Role & responsibilities sample analysis; routine maintenance and verification of the functioning of instruments and equipment in the laboratory; organization and planning of laboratory operations; data collection and report writing; tests for the quality control of raw materials and finished products; a basic knowledge of laboratory tests perform laboratory analyzes of the solutions used in the chrome plating baths; knows how to carry out dimensional checks on the material with a micrometer and feeler gauge for the chrome thickness; Preferred candidate profile Product expertise; Quality control expertise; Specific technical expertise in the production process and related environmental risks; Autonomy; Proactivity; Analytical skills; Problem Solving; Suitability for handling products Perks and benefits Transport Facility from Pune City Canteen + Meal Facility Mediclaim Facility Competitive Policies for employees Opportunity to work with Global leaders

Role & responsibilities 1. Routine analysis of incoming RM/PM/FG 2. Collection of RM/PM/FG control sample 3. Routine water testing CI/DM/Soft water 4. Weighing balance validation 5. Calibration of all lab instruments internally 6. Retain sample analysis 7. Rm standard sample 8. Reporting and documentation 9. Qc clearance in sap system Preferred candidate profile Fresher can apply Only Male candidate can apply Job location Howrah Jalan Salary Negotiable

Hello Candidate, Greetings of the day from Hungry Bird!! We are currently hiring for Lab Incharge for our client. Location : Hyderabad. Job Summary: The Lab Incharge is responsible for overseeing the daily operations of the laboratory, ensuring compliance with safety and quality standards, and maintaining accurate records. This role involves conducting tests, managing samples, calibrating equipment, and training lab personnel. Responsibilities: Should maintain the company policy of personal hygiene, GMP and safety Requirements along with safeguarding the company assets as their primary responsibility. Conducting the checks for Clients block incoming checks for SFG / PM, FG as per customer specification. Clients block sample collection, identification, analysis and documentation. Sending courier samples to external testing lab and submission of invoice to accounts department. Train the lab helper in case of any requirements and change in existing practices. Verify and ensure the compliance in day-to-day lab operations. Carry out internal calibration of lab equipment's. Operate the lab in line with the GLP requirements. Communicate to HOD in case of any abnormality, deviations observed. Maintain the overall housekeeping of Lab, Timely disposal of samples. Monitor the retention sample and timely disposal in consultation with HOD. Track the courier samples sent. Participate in Clients customer complaint investigation. Authorities: To communicate with vendor with respect to online rejection in incoming material. To hold the incoming material with deviation in consultation with HOD. To raise the indents for lab as per requirements and coordinate with accounts department for PO preparation To maintain only update version of specification, artwork, shade card. To remove the obsolete copies of documents and discard as per SOP. To share the in-house testing report and COA with customer Prepare the COA for in house testing samples. Interested candidates can share their CV to renu@hungrybird.in / 8885825360 priya@hungrybird.in / 8008832123 hr@hungrybird.in / 9701432176 Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards renu@hungrybird.in / 8885825360 priya@hungrybird.in / 8008832123 hr@hungrybird.in / 9701432176

Pharma API Experience - Follow up with QC/QA for sample analysis - Ensure GMP norms in manufacturing - Achieve targeted production - Handle reactors & equipment - Maintain documents & safe working conditions - Monitor PPE usage & report incidents"

A Quality Control (QC) job in the pharmaceutical industry involves rigorously testing and analyzing raw materials, in-process samples, and finished products at various stages of drug manufacturing to ensure they meet established quality standards.

Role & responsibilities Development and validation of bioanalytical methods using LCMS and other sophisticated instruments. Routine calibration of the instruments. Strong basic knowledge about Analytical instruments of LCMS, HPLC, HPTLC, GC-MS and other instruments. Good understanding of GLP and documents thereof. Knowledge of USFDA guidelines. Excellent communication skills & co-ordination among all the team members. Should possess good interpersonal and management skills Accountable for the whole group productivity in terms of number of samples, analysis, quality, quantity timelines better Turn Around Time (TAT) improvement Preferred candidate profile The candidate should have 1-4 years of experience in Bioanalytical Lab.