218 Analytical Chemistry Jobs - Page 3

You should hold a Master's degree in Analytical Chemistry and have 6-9 years of experience in method development and validation. You must be willing to work in shifts.,

The Chemist cum Analyst will play a crucial role in ensuring the quality and purity of Rhodium Sulphate production and developing complementary products. Your responsibilities will include conducting chemical analysis, operating analytical instruments like ICP-OES and XRF, and collaborating with production staff to optimize processes. Additionally, you will analyze various chemicals for manufacturing, formulate appropriate formulas, and assist in achieving desired outcomes. Your key responsibilities will involve analytical testing, quality control checks, formula development, and optimization. You will operate and maintain analytical instruments, develop and validate analytical methods, and contribute to related product development. Quality control measures, documentation, and reporting will also be part of your duties. To excel in this role, you must demonstrate excellent proficiency in handling ICP-OES and XRF machines, possess strong knowledge of analytical chemistry and quality control, and be familiar with regulatory requirements in chemical production. A Master's degree in Chemistry or related field, along with 2-3 years of experience in analytical chemistry, instrumental analysis, and quality control, is required. Experience in Rhodium Sulphate production or related industries would be advantageous. Your performance will be measured based on the accuracy of analytical results, the quality of chemical production, development of related products, instrument maintenance, compliance with regulations, and formulation of new products and processes. This is a fresher job type with a day shift schedule and in-person work location.,

Long Description 1. Perform characterization of peptides , nucleic acids-based (oligonucleotides) or other injectable drug products using High Resolution Mass Spectrometry (LC-HRMS) . Experience with QToF/Orbitrap instruments and Ion Mobility will be preferred. Additional experience in Fluorescence, particle size analysis (DLS), and other relevant techniques (e.g. SEC-MALS) are desirable. 2. Analyze and interpret LC-MS and MS/MS data for impurity profiling and characterization. Solve problems and implement new research methods through literature search, coordinate with cross-functional teams (formulation, QA, QC, regulatory, etc.), application specialists, etc. to complete analytical tasks. 3. Prepare, review and share LC-MS data and documentation (SOP, STP, Test Reports, etc.) in a timely manner for regulatory submissions. Follow good laboratory practices (GLP) , manage samples (collection, storage, and disposal), deviations and incidences as per established procedures. 4. Undertake routine maintenance & calibration of the analytical instruments, troubleshoot equipment malfunction often in coordination with service engineers, etc. Assist in the maintenance of the laboratory, inventory of R&D consumables, & other lab management activities from time to time Competencies Education Masters in Pharmacy or Applied Chemistry Doctorate in Pharmaceutical Technology or Analytical Chemistry Work Experience 5 – 7 years (with MPharm) or NIL (with PhD)

A Pharma Industry Jhagadia, Bharuch Analytical Chemist (Formulation R&D)(AAD-20-N1C) Qualification: M.Sc. in Analytical Chemistry. 2 to 4Experience: 2-4 Years in Analytical Chemistry in R&D, preferrably in Agrochemical Industry. Salary: No bar for right Candidate. Candidate will be responsible to conduct analysis such as GC, HPLC, Wet Chemistry, GC-MS, LC-MS, FTIR, UV-Vis, DSC, Particle Size Analyzer, Viscosity, Density etc. Click to Apply

Analytical Chemistry

The Analytical Product Specialist role provides technical expertise and support to customers and internal teams, focusing on India and extending to the APAC region. You will be responsible for both pre-sales and post-sales support, utilizing in-depth knowledge of Biotage analytical product lines to ensure customer satisfaction, product adoption, and business growth. You will be based in Hyderabad, Bengaluru, Mumbai, or Ahmedabad, with key responsibilities including: Technical Support: - Deliver pre- and post-sales technical and applicational support on Biotage's analytical sample preparation to customers, distributors, and internal teams in India and APAC. Customer Relations: - Establish strong relationships with key customers by offering tailored solutions. - Conduct product demos, seminars, and workshops. - Provide support to sales during customer visits and presentations. Sales Support: - Assist the sales team with product positioning and competitive differentiation. - Support regional sales strategies, identify new business opportunities, and offer market insights. Market Research & Feedback: - Stay updated on industry trends and competitor products. - Gather customer feedback to drive product improvements and R&D efforts. Education Qualifications & Experience: - Possess a Masters or PhD in Analytical Chemistry (PhD preferred) with a strong understanding of sample preparation and LC-MS/MS techniques. Experience: - Demonstrate proven experience in analytical workflows, with at least 5 years in technical support or as a product specialist in the analytical chemistry industry, or equivalent hands-on technical experience. Skills: - Showcase a strong technical problem-solving ability. - Exhibit excellent communication and presentation skills. - Display willingness to travel frequently in India and APAC. Travel: - Expect frequent travel within India and occasionally across APAC. Languages: - Fluency in English is a must; proficiency in regional languages is considered a plus.,

The R&D Executive at PTC - MORAIYA will be responsible for performing analysis of Drug Product and Drug Substances for various test parameters according to product development requirements. This includes Method Development of Drug Product and Method verification of Raw Materials. The role also involves compiling analytical results and preparing Method Development Reports. Additionally, the R&D Executive will be responsible for ensuring Good Laboratory Practices (GLP) aspects in the analytical laboratory. The ideal candidate should have 0 - 3 years of experience in a similar role.,

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of general lab SOPs and instrument sops. Desired candidate profile: 1. Must have worked analytical lab. 2, Knowledge of HPLC,

We are looking for a talented Sensor Development Engineer who possesses expertise in electrochemical techniques and materials science. The ideal candidate will have a strong background in sensor calibration, microfabrication, and data analysis. Your responsibilities will include the development and optimization of sensors, troubleshooting performance issues, and ensuring compliance with laboratory safety protocols. Key Requirements: - Proficiency in electrochemical techniques such as cyclic voltammetry and EIS - Knowledge of nanomaterials and conductive polymers - Hands-on experience with microfabrication processes like screen printing and photolithography - Expertise in analytical chemistry - Ability to acquire and analyze data using tools like Origin, MATLAB, or LabVIEW - Strong skills in documentation and problem-solving If you meet these qualifications and are excited about the opportunity to work in sensor development, please send your resume to khushal.bansode32084@paruluniversity.ac.in within the next 7 days. We look forward to hearing from you.,

Analyse raw, in-process, and finished products using GC, HPLC, and other instruments. Role includes sampling, testing, equipment calibration, and ensuring compliance with SOPs in a pharma QC environment. Required Candidate profile (Minimum 2 years’ experience, preferably in ADL within the pharmaceutical industry)

Position : Sr. Manager Application Support / Head Applications Support Reports to : President Location : Mumbai Minimum Years of Experience : 13 Years (Total) - In any mid to large size Chemical Industry with at least 3 years as a Lab Manager handling a team of chemists and responsibility of QC / R&D / Testing Lab Maximum Years of Experience : 15 Years (Total) - In any mid to large size Chemical Industry with at least 5 years as a Lab Manager handling a team of chemists and responsibility of QC / R&D / Testing Lab Minimum Qualifications : M. Sc (Analytical Chemistry / Organic Chemistry / Inorganic Chemistry) Preferred Qualifications : PhD (Analytical Chemistry or relevant Chemistry Stream) Type of Work Experience Required (Mandatory) ** : Of the total 13 to 15 years of experience, 3 to 5 years of experience as Lab Manager or Group / Team Leader managing a team of minimum 5 analytical chemists and managing the complete operation of any analytical lab. Responsibilities handled would be to assign analysis work on analytical instruments like GC, GC-HS, GCMS, ICPMS, UV, FTIR etc.; Review the work; guide in resolving any analysis challenges faced by the team; plan their analytical skill development and directly or indirectly develop their analytical chemistry skills Above experience is mandatory but anyone having similar experience in a mid / large size Pharma Industry; Commercial Testing Labs also can be considered Responsibilities: To manage a team of 15 to 18 Field Application Specialists (FAS) across branches and 2 to 5 Lab Application Chemist (LAC) in the in-house Application Centre. FAS are responsible providing post sales application support to customers on TQ / SQ-GCMS; ICPMS; GC / GC-GS; Molecular Spectroscopy and Elemental Analysis To review the application support activity of the FAS with customers on day-to-day basis and monitor the satisfactory completion of the assigned tasks and projects To remotely guide and support the FAC and LAC on their field application support to customers To be aware and regularly be updated on global regulations and regulatory test methods of trending applications in core markets like Pharma, Food, Environment and train the FACs and LACs on these Monitor the development of FAC and LAC organise their trainings through Principals or internally Regular interactions with Principals applications team for exchanging information on global and local applications and coordinating on support required by Principals Key Success Behaviours (Key Competencies): The candidate should have strong analytical chemistry knowledge Hands-on industrial experience on handling core analytical technologies like GC; GC-HS; GCMS; GCMS-MS; ICPMS; AAS; FTIR; UV et Strong knowledge in Analytical Method Development; Validations; Analytical Troubleshooting; Data Analysis and Interpretation Effective team handling skills Reviewing assigned activity / performance and Team Development Effective presentations skills Conducting presentations; webinars and applications seminars

QC Chemist

Strong theoretical knowledge (HPLC/LCMS) Plan and conduct the analysis with required skills Record the observations meticulously and update to the TL/SME Share and discuss the observations with supervisor Independent in maintaining the instrument and setting up the instrument for analysis Expected to be aware of basics in analytical chemistry (basic analytical techniques Theory and application) as well as handling of laboratory equipment / instruments with basic understanding

Interested candidates can share resume to sanjay.behera@thyrocare.com or whatsapp to 8928285213 Key Responsibilities: Operate, calibrate, and maintain ICP-MS and LC-MS instruments according to established SOPs. Prepare samples for analysis, including digestion, dilution, filtration, and extraction techniques. Perform quantitative and qualitative analysis of environmental, biological, food, or pharmaceutical samples. Conduct method development and optimization under guidance of senior staff. Document all laboratory activities, observations, and results accurately in lab notebooks or LIMS. Ensure compliance with all safety, QA/QC, and regulatory standards (e.g., ISO 17025, GLP/GMP). Assist in troubleshooting instrument and method-related issues. Maintain inventory of reagents, standards, and consumables. Participate in equipment validation, method validation, and proficiency testing programs.

Job Title: Senior Specialist - GOE CAL Location: Mumbai, India Work Mode: On-site At dsm-firmenich we strive to achieve a world where you don t have to choose between taste, texture, or health - and can enjoy it all. Our innovative ingredients, expertise, and solutions bridge the gap between the delicious, the nutritious, and the sustainable. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your Key Responsibilities Execute and support analytical work with a focus on quality control, GC-MS and LC-MS analysis of flavors, aroma chemicals, perfumes, and natural products. Ensure smooth lab operations by maintaining instruments, updating SOPs, and managing documentation and inventory databases. Support technical development through method development and collaboration with scientific staff. Coordinate and collaborate with cross-functional teams including Creation, Application, Purchasing, Quality Assurance, and regional/global partners. Handle administrative tasks including SAP for sample tracking, vendor follow-ups, and SRM creation. Work in full compliance with ISO17025:2017 standards and contribute to continuous lab improvement. We bring A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You Bring BSc or MSc in Analytical Chemistry or related field. 3-5 years of relevant experience in a commercial or research laboratory. Solid hands-on experience in GC-MS and LC-MS, and an understanding of quality control processes. Working knowledge of ISO17025:2017 standards is an added advantage. Strong desire to achieve results with a proactive and accountable mindset. Familiarity with SAP and ability to handle both technical and administrative responsibilities. The application process: Interested in this position? Please apply on-line by uploading your resume in English via our career portal. For . We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate : theres a place for everyone at dsm-firmenich. Dsm-firmenich is an Equal Opportunity and Affirmative Action Employer. dsm-firmenich people are as diverse as our customers. For us that includes a commitment to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicants race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the worlds growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.

Job Title: Lead Specialist - GOE CAL (Experience in Metal & Pesticide Analysis) Location: Mumbai, India Work Type: On-site At dsm-firmenich we strive to achieve a world where you don t have to choose between taste, texture, or health - and can enjoy it all. Our innovative ingredients, expertise, and solutions bridge the gap between the delicious, the nutritious, and the sustainable. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your Key Responsibilities Perform GC-MS and LC-MS analysis of flavors, perfumes, aroma chemicals, and natural products. Manage and maintain lab instruments, SOPs, documentation, and inventories to ensure ISO17025:2017 compliance. Develop and validate analytical methods and contribute to team knowledge sharing. Collaborate with cross-functional teams including Creation, Application, QA, and regional/global counterparts. Prepare, review, and communicate analytical reports using internal tools and databases. Lead coordination of analytical support from global or external resources and provide subject-matter expertise. We bring A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You Bring MSc (+5 years) or PhD (+2 years) in Analytical Chemistry or related fields. Hands-on experience with GC-MS and LC-MS techniques in commercial/research labs. Strong skills in mass spectrometry and analytical method development. Familiarity with ISO17025:2017 and exposure to metal & pesticide analysis. High level of ownership and drive for results in a cross-functional environment. Strong communication skills with the ability to collaborate and influence across teams. The application process: Interested in this position? Please apply on-line by uploading your resume in English via our career portal. For . We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate : theres a place for everyone at dsm-firmenich. Dsm-firmenich is an Equal Opportunity and Affirmative Action Employer. dsm-firmenich people are as diverse as our customers. For us that includes a commitment to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicants race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the worlds growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss-Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people.

Job Description Summary This analyst role is responsible to perform analysis of stability samples, Raw materials, analytical method validation/verification and method transfer studies Job Description To perform Nitrosamine & extractable and leachable analysis of analytical method development / validation / verification and method transfer. Handling of LCMS, ICPMS instruments. Knowledge on nitrosamine method development / validation / verification. Experience: 7 to 9 years with M.Sc./ M. Pharm

JOB DESCRIPTION Designation: Research Scientist (7-I) Job Location: Bangalore Department: DAS 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&D productivity, speed up time to market and lower the cost of innovation . Job Purpose (1-2 Lines): Lead a team of scientists specializing in LCMS Key Responsibilities: (Maximum 5-8 Points) Proven ability to independently develop analytical methods for both reverse-phase (achiral) and polar organic (chiral) separations, with experience in scaling up methods to preparative scale. Hands-on experience with LC-MS and UPLC techniques is a strong advantage. Skilled in performing minor instrument troubleshooting, calibrations, and recovery analyses as required. Excellent written and verbal communication skills. Strong adherence to company health, safety, and compliance protocols. Flexibility to undertake additional responsibilities from the Line Manager in alignment with business needs. Educational Qualification: MSc in analytical chemistry or allied disciplines. Technical/functional Skills: (Maximum 4-6 Points) HPLC and LCMS. Experience: 10 to 15 years of hands-on experience on LCMS, UPLC and HPLC Behavioral Skills: Must have very good communication skills Equal Opportunity Employer: .

Your Key Responsibilities Perform GC-MS and LC-MS analysis of flavors, perfumes, aroma chemicals, and natural products. Manage and maintain lab instruments, SOPs, documentation, and inventories to ensure ISO17025:2017 compliance. Develop and validate analytical methods and contribute to team knowledge sharing. Collaborate with cross-functional teams including Creation, Application, QA, and regional/global counterparts. Prepare, review, and communicate analytical reports using internal tools and databases. Lead coordination of analytical support from global or external resources and provide subject-matter expertise. We bring A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You Bring MSc (+5 years) or PhD (+2 years) in Analytical Chemistry or related fields. Hands-on experience with GC-MS and LC-MS techniques in commercial/research labs. Strong skills in mass spectrometry and analytical method development. Familiarity with ISO17025:2017 and exposure to metal & pesticide analysis. High level of ownership and drive for results in a cross-functional environment. Strong communication skills with the ability to collaborate and influence across teams.

Job Summary We are seeking a highly skilled Analytical Scientist to join our Research and Development team. The successful candidate will be responsible for developing, validating, and implementing analytical methods for the quantification and identification of genotoxic impurities in pharmaceutical products. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, method development, and data analysis, with a keen eye for detail and a commitment to ensuring the highest quality standards. Roles & Responsibilities You will be responsible to review relevant Literature and stay updated with the latest research and scientific literature relevant to the field of genotoxic impurities and chromatography methods. You will be responsible to develop and optimize chromatography-based methods for accurately quantifying genotoxic impurities in various samples. You will be responsible to address regulatory deficiency queries concerning the analytical methods and data related to genotoxic impurities. You will be responsible to ensure the quality and accuracy of reference standards and working standards used in analytical testing and method development. You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department. You will be responsible to prepare comprehensive reports documenting method development, validation results, and any forced degradation studies performed. You will be responsible to conduct forced degradation studies to identify potential impurities and establish their chemical nature and behaviour. You will be responsible to perform real-time analysis of samples during product development stages to ensure product quality and consistency. You will be responsible for compilation of Stability Data to assess the stability profile of the products under various conditions. You will be responsible to evaluate the effectiveness of the product development strategy and identify any cross-functional issues affecting the process. You will be responsible to identify and plan for the developmental needs of the product, considering factors such as scale-up and potential process improvements. You will be responsible to source and manage the procurement of necessary chemicals, solvents, columns, and other laboratory equipment. You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results. You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy. You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions. You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. Qualification Educational qualification: Masters in Science/ Organic chemistry Minimum work experience: 5 years of experience in analytical method development Skills & attributes: Technical Skills Have work experience on Process scale up of Active Pharmaceutical Ingredients. Experience in Process Optimization (Manufacturing) Experience in the development and regular analysis in Wet analysis-IR, Ultra Violet, Moisture analysis, Chromatographic techniques Strong understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis. Proven experience in method validation and documentation in compliance with regulatory requirements. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Job Summary We are seeking an associate for the Quality Control team responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. Roles & Responsibilities • You will be responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. • You will ensure accuracy of the documentation before submitting it for the Group Leader’s review or uploading online. • You will adhere to safety precautions and procedures during analysis. • Lab safety, following JSA (Job Safety Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized. Qualification Educational qualification: A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field Minimum work experience : 5 to 7 years of experience in a laboratory setting, preferably in the pharmaceutical or related industry Skills & attributes: Technical Skills • Proficient in various analytical techniques, including sampling and analysis of packaging and raw material samples. • Experience with the operation and maintenance of analytical instruments, ensuring proper use and care as per SOPs. • Competent in SAP activities related to sample tracking, documentation, and data entry. • Knowledgeable about cGMP, SOPs, and STPs, ensuring accurate documentation and adherence to specifications. • Adheres to safety precautions and procedures during analysis, emphasizing the importance of lab safety, JSA (Job Safety Analysis), and proper use of PPE (Personal Protective Equipment). • Expertise in handling and upkeep of the chemical and solvent store, including the preparation and maintenance of volumetric solutions and reagents. Behavioural Skills • Keen attention to detail in analysis and documentation, ensuring accuracy in all tasks. • Effective communication and collaboration skills for communicating with the Group Leader, reporting discrepancies, incidents, and providing timely updates. • Takes initiative in ensuring the proper use and care of instruments, timely destruction of samples, and other assigned responsibilities. • Demonstrates problem-solving skills in addressing discrepancies, incidents, and ensuring smooth laboratory operations. • Upholds ethical standards, compliance with SOPs, and follows regulatory requirements in all activities. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Industrial Post-Doctoral Fellow-HPLC Method Development (Protein Biologics) About Mynvax Mynvax is a clinical-stage vaccine biotechnology company headquartered in Bangalore, India, developing novel, recombinant, and thermostable vaccines against respiratory viral infections, including influenza and RSV. With a pipeline of promising candidates and multiple ongoing collaborations, Mynvax offers a unique opportunity to work at the cutting edge of vaccine development. Role Design, develop, and optimize HPLC/UPLC methods (e.g., SEC, RP-HPLC, IEX, HIC) for protein characterization, including purity, aggregation, charge variants, and stability. Conduct protein analysis using HPLC and orthogonal techniques for in-process and final DS samples. Interpret results, troubleshooting analytical challenges, and ensure data quality and integrity. Prepare analytical protocols, reports, and SOPs, and contribute to method development and qualification. Collaborate with upstream, downstream, and formulation development teams. Support regulatory submissions with high-quality analytical documentation. Required Qualifications Ph.D. in Biophysics, Biochemistry, Analytical Chemistry, Biotechnology, or a related field. Hands-on experience in HPLC method development for proteins (during Ph.D. or postdoc). Basic understanding of protein structure, behavior, and physicochemical properties. Familiarity with HPLC data acquisition and analysis software (e.g., Openlab CDS, Empower, ChemStation). Desirable Skills Knowledge of ICH Q2/WHO guidelines for analytical method validation. Experience with protein biologics, vaccine antigens, or biosimilar analytics. Familiarity with other techniques such as CE, SDS-PAGE, Western blotting, or ELISA. What Mynvax offers: A stimulating industrial research environment with real-world impact. Exposure to state-of-the-art technologies and multidisciplinary collaboration. Mentorship and professional development support from experienced scientists. Full-time salary and benefits include health coverage, generous leave package, and statutory entitlements. Location: Bangalore, India Company: Mynvax Private Limited Position Type: Full-Time | Fixed Term (12-24 months, extendable) Start Date: Immediate Compensation: Competitive salary with full-time employee benefits How to apply: Email your CV and a brief cover letter to careers@mynvax.com Subject line: "Post-Doctoral Fellow-HPLC Application" Apply on LinkedIn: Post-Doctoral Fellow-HPLC Application

Job Description Planning /Analysis (Routine and stability and QBD analysis) of ongoing projects by performing analysis of various tests (e.g. Dissolution, assay, Related substances test, or as per requirement) within given Time. Analytical Method development as per current SOP/guideline wherever required. Regulatory query/Plant Query related analysis for different products. To follow Good Laboratories practice while working. Documentation and compliance and review of data generated on all analytical activities as per the GLP/GMP norms and to keep working place neat and clean. Method transfer at plant. Method equivalency, method verification, pharmaceutical equivalency analysis of Pharmacopeial method. Preparation/review of various documents like method transfer waiver, method equivalency report, cleaning validation report SOP, T-STP/FP STP etc. Coordination with team members, superiors and subordinates within the group and across all relevant groups (customers) to achieve target timelines. Procuring of columns, reagents and miscellaneous items for analytical product development/support. Whenever required give training to subordinates/colleagues to upgrade their knowledge and current requirements. Work Experience 3 to 5 years of experience Education Masters in Analytical Chemistry or Analytical Chemistry Post Graduation in Pharmacy or Analytical Chemistry Competencies

We are looking for an experienced and dedicated Senior R&D Chemist to join our dynamic team. The candidate will be responsible for developing and optimizing chemical formulations, conducting lab experiments, and collaborating with production Team. Required Candidate profile Lead R&D projects for new product development and process improvements Conduct experiments using equipment like UV Cabinet, Fume Hood. Work with cross-functional teams to scale up formulations

2-5 years work experience in a corporate environment in a technical role within the chemical industry, ideally in a multinational environment. Proficiency in Microsoft Office Suite Word, Excel, Outlook & ERP system. B.Sc Chemistry