218 Analytical Chemistry Jobs - Page 9

Roles and Responsibilities Routine and stability batches of assay, Dissolution, RS, CU, BU, PC on HPLC instrument. Qualification and calibration of HPLC, UV, Dissolution apparatus. Develop, validate, and implement analytical methods for pharmaceutical products. Operate and maintain analytical instruments (e.g., HPLC, UV, Dissolution apparatus) Communication with cross-functional teams. Ensure compliance with cGMP, GLP, and other regulatory guidelines. Knowledge on ICH guideline, forced degradation studies, impurity profiling Performing BCS, filtration, saturation solubility, API qualification test studies

Job Description Job Role: Research Officer Location: Zone-IV Pilot Plant (Analytical), Jhagadia, Gujarat Job Responsibilities: 1) Responsible for Laboratory execution of analytical activities on daily basis and ensuring compliance to the Safety and quality system as per cGMP. 2) Responsible for Laboratory execution of instrument calibration, stability analysis, WRS preparation/Qualification and for procurement of reference standard etc. 3) Responsible for maintaining stock of working reference standards and chemicals required routinely for raw material analysis. 4) Review and release of finished product, inprocess, intermediates, raw material, reaction monitoring results. 5) Responsible for Laboratory execution of analytical method validation/Verification and Method Transfer activites. 6) Coordination for reagents and volumetric solutions preparation, standardization and maintenance. 7) Coordination for maintaining analytical columns of HPLC, GC, IC and spare parts of instruments and Equipments. 8) Coordination of AMC / CMC of analytical laboratory instruments and its calibration. 9) Coordination for disposal of retained analytical samples of raw material, packing material, inprocess and stability samples. 10) Preparation, revision, review and checking of Raw material, inprocess, intermediates, reaction monitoring and finished products specifications and test procedure and departmental SOPs. 11) Planning and execution to review, checking of IQ, OQ and PQ documents of instruments and equipment. 12) Prepare and Review of certificate of analysis (COA) for finished products. 13) Responsible for investigation of incidents and Deviations in coordination with internal and cross functional team 14) Complying EHS promotional activities and complying EHS statutory requirements of the analytical department. 15) Handling of the ICP-MS/ ICP-OES, Ion Chromatography, GC-MS, UPLC,ION Meter and commissioning experience of the product and new Laboratory setup. Job specification Experience: 6-10 Years Qualification: M.Sc Analytical Chemistry or M.Sc (Chemistry with large industrial experience in analytical method development and structure elucidation.)

Job Summary We are seeking an associate for the Quality team responsible for conducting sampling and analysis of packaging and raw material samples. The role involves ensuring accuracy in documentation, adherence to safety procedures, reporting discrepancies, and maintaining lab safety. Roles & Responsibilities • You will be responsible for conducting sampling and analysis of raw material samples as allotted by the group leader. • You will also be responsible for the proper use and care of instruments or equipment as instructed in relevant SOPs (Standard Operating Procedure), including cleaning before and after analysis. • You will adhere to safety precautions and procedures during analysis. • Your responsibilities include placing SOP/STP/reference standards at their designated locations after analysis, and reporting discrepancies or incidents promptly to the Group Leader. • Lab safety, following JSA (Job Safety Analysis), and using proper PPE (Personal Protection Equipment) at the workplace are emphasized. • You will oversee the handling and upkeep of the chemical and solvent store, preparation of Spec-check, catalog, and result entries, as well as maintaining volumetric solutions and reagents. • Your role also includes preparation of out lab testing samples (as required), timely destruction of samples as per SOP and any additional responsibilities assigned by the Group Leader. Qualification Educational qualification: A Bachelor’s degree in Chemistry, Analytical Chemistry, or a related field Minimum work experience : 2 to 5 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 raw material samples. • Experience with the operation and maintenance of analytical instruments like HPLC, GC, Potentiometer, Particle Size Analyzer, XRD, ensuring proper use and care as per SOPs. • Competent in LIMS 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/#!/

Role & responsibilities Preferred candidate profile Perks and benefits

Product Development/Product performance/Process Parameter Knowledge on modification of activated carbon structure Develop specialty carbons for gas phase potable waters Testing as per international testing procedures Establishment of Quality system Required Candidate profile Contact: 8939813208 Mail ID: finadsorbent@carbons.in

Job Overview To lead and execute analytical method validation, transfer, and verification activities in compliance with regulatory and cGMP standards, ensuring robust analytical support for product development, regulatory submissions, and commercial manufacturing. Competencies Plan, perform, and document Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) for raw materials, intermediates, and finished drug products. Prepare and review protocols and reports related to method validation / verification / transfer in alignment with ICH Q2(R1) guidelines. Coordinate with R&D, AR&D, QA, RA, and manufacturing units for method transfer and troubleshooting activities. Perform routine and non-routine analysis using HPLC, UPLC, GC, UV, IR, dissolution apparatus, and other analytical instruments. Ensure timely qualification/calibration of instruments used in AMV lab. Review analytical documents like raw data, chromatograms, validation reports, SOPs, etc. Support regulatory inspections (USFDA, EU, ANVISA, WHO, etc.) and respond to queries related to AMV/AMT. Investigate OOS/OOT/Deviation/Incident related to AMV activities and provide effective CAPA. Maintain GLP and cGMP compliance across AMV operations. Experience: 4 -5 years in QC-AMV in a regulated pharmaceutical environment M.Sc. (Chemistry/Analytical Chemistry) / M.Pharm

Job Overview To lead and execute analytical method validation, transfer, and verification activities in compliance with regulatory and cGMP standards, ensuring robust analytical support for product development, regulatory submissions, and commercial manufacturing. Competencies Plan, perform, and document Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) for raw materials, intermediates, and finished drug products. Prepare and review protocols and reports related to method validation/verification/transfer in alignment with ICH Q2(R1) guidelines. Coordinate with R&D, AR&D, QA, RA, and manufacturing units for method transfer and troubleshooting activities. Perform routine and non-routine analysis using HPLC, UPLC, GC, UV, IR, dissolution apparatus, and other analytical instruments. Ensure timely qualification/calibration of instruments used in AMV lab. Review analytical documents like raw data, chromatograms, validation reports, SOPs, etc. Support regulatory inspections (USFDA, EU, ANVISA, WHO, etc. ) and respond to queries related to AMV/AMT. Investigate OOS/OOT/Deviation/Incident related to AMV activities and provide effective CAPA. Maintain GLP and cGMP compliance across AMV operations. Experience: 4 -5 years in QC-AMV in a regulated pharmaceutical environment M. Sc. (Chemistry/Analytical Chemistry) / M. Pharm

Lake Chemicals Pvt.Ltd., (Sterling Lab), is looking for Quality Control- Assistant/Deputy Manager to join our dynamic team and embark on a rewarding career journey Planning and designing test cases and test scenarios to validate the functionality and performance of software and systems Executing manual and automated tests to identify and document defects Debugging and troubleshooting software and systems to resolve any issues and improve their reliability Collaborating with cross-functional teams, such as software developers and project managers, to ensure that the software and systems are of high quality and meet the needs of the business Creating and maintaining documentation to ensure that the testing process, results, and defects are well understood by others Should be detail-oriented, have excellent problem-solving and communication skills Qualification: M.Sc in Organic/ Analytical Chemistry Skills: Experience in API Quality Control with expertise in Instrumentation (HPLC / GC) revie

Position : Sr. Selling Service Executive / Asst. Selling Service Manager Reports to : RM / SM / GL Location : Mumbai (Navi Mumbai), Vapi, Hyderabad, Kolkata Years of Experience : 4 to 6 years (E2 to M1 Grade) Minimum Qualifications : BSc Physics Or Electronics OR Diploma in Electronics / Instrumentation Or Diploma in Analytical Chemistry / BSc Chemistry (Flare for selling). Sales experience of about 2 years in selling (Field job Not telemarketing) Basic Knowledge of Excel, Word and Power Point required Preferred Qualifications : Diploma Electronics / Instrumentation OR Diploma in Analytical Chemistry with Post graduate Diploma OR Degree in Marketing Management. Sales experience of about 3 years in selling columns and consumables (Field job Not telemarketing) Basic knowledge of Chromatography Knowledge on Word, Excel and power point with little background on IT Responsibilities: To promote and sell maintenance services To convert AMC (Annual Maintenance Contracts) to CMC (Comprehensive Annual Maintenance Contracts) Convert non-AMC, CR (Chargeable Repairs), Out of warranty instruments in AMC / CMC To promote PM kits (Preventive Maintenance Kits) to CR and AMC customers To promote and sell Validation services To sell USP (United States Pharmacopeia) / EP (European Pharmacopeia) validations to regulatory customers (Shimadzu and Non-Shimadzu) for UV-Vis spectrophotometers To sell validation services (OQ Operational Qualification) for Shimadzu GC and GCMS customers To promote and sell Spectroscopy and chromatography consumables to existing Shimadzu and non-Shimadzu customers To promote rate contracts for Restek GC (Gas Chromatography) capillary columns and Shimadzu GC columns To promote and sell Spectroscopy and chromatography consumables to existing Shimadzu and non-Shimadzu customers To promote and sell spectroscopy accessories to Shimadzu and Non-Shimadzu customers To promote and sell Gas generators of Peak Scientific To arrange webinars / presentations / seminars at select customers place in regions Preferred Competencies : Have good selling skills / Flair for selling Have good negotiation skills H Good communication (Written and verbal) Good presentation skills High initiative, Self-starter & Energetic Evaluation Criteria: VAS SE will carry Service and SCA target as per mentioned below: Service Target: Overall target for Service as his reporting manager SCA Target: SCA target for Consumables and Accessories

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

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Role & responsibilities Job Title: Trainee Blending Department Department: Production / Blending Reporting To: Blending Supervisor / Manager – Production CTC: 2.47 LPA Experience Required: Fresher or 0–1 year (preferably in chemical or fragrance industry) Job Purpose: To assist the blending team in the preparation of aroma chemical formulations as per defined recipes, ensuring accuracy, cleanliness, and quality compliance during the production process. Key Responsibilities: Blending Operations Support: Assist in weighing and mixing raw materials as per batch instructions. Help operate blending equipment under supervision. Documentation: Maintain batch records, log sheets, and blending data accurately. Ensure proper labeling and storage of in-process and blended materials. Sample Preparation: Support in preparing samples for internal testing and customer evaluation. Ensure consistency and correctness in sample handling. Process Monitoring: Observe critical process parameters like mixing time, temperature, and viscosity. Report deviations or abnormalities to the supervisor. Housekeeping & Safety: Maintain cleanliness and hygiene in the blending area. Follow all safety guidelines and use PPE (Personal Protective Equipment) properly. Learning & Development: Learn standard blending procedures, raw material characteristics, and handling techniques. Participate in training sessions on aroma chemicals, quality standards, and production protocols. Key Requirements: Education: Diploma/B.Sc. in Chemistry / Industrial Chemistry / Chemical Engineering or equivalent Experience: Fresher or up to 1 year in chemical, fragrance, or FMCG manufacturing preferred Skills: Basic understanding of chemicals, measurements, and safety Willingness to learn and work in a production environment Attention to detail and discipline in following SOPs Physically fit and capable of manual work when required Career Path: Opportunity to be promoted to Blending Operator / Blending Chemist based on performance and skill development.

Prepares medications by reviewing and interpreting physician orders; detecting therapeutic incompatibilities. work flow; verifying their preparation and labeling of pharmaceuticals; verifying order entries, charges, and inspections.

Job Summary: We are looking for a passionate and detail-oriented QC Chemist (Fresher) to join our Quality Control team. The ideal candidate will assist in ensuring the quality and compliance of raw materials, intermediates, and finished products through rigorous testing and documentation. This is an excellent opportunity for recent postgraduates to begin a rewarding career in the pharmaceutical or chemical industry. Key Responsibilities: Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished products. Conduct analytical tests using instruments such as HPLC, GC, UV-Vis Spectrophotometer, IR, and titration methods under supervision. Maintain proper documentation of test results, calibration data, and standard operating procedures (SOPs) in compliance with cGMP and regulatory requirements. Assist in the preparation and standardization of reagents, solutions, and reference standards. Follow safety procedures and maintain cleanliness and orderliness in the laboratory. Participate in internal audits, investigations, and training programs as required. Report any non-conformances or deviations to the QC Supervisor or Manager promptly. Key Skills: Basic knowledge of analytical techniques and instrumentation Good understanding of laboratory practices and chemical safety Strong attention to detail and willingness to learn Excellent documentation and communication skills Ability to work collaboratively in a team environment Preferred Attributes: M.Sc. in Organic or Analytical Chemistry (2024 or 2023 pass-out) Internship or project experience in a pharmaceutical, chemical, or academic lab (if any) Willingness to work in shifts, if required

We are seeking a highly motivated and experienced Study Director to oversee chemical characterization studies within our research and development team. The ideal candidate will have a strong background in analytical chemistry, extensive knowledge of chemical characterization techniques, and a proven track record in managing complex projects. Key Responsibilities: - Lead and manage chemical characterization studies, including planning, execution, and reporting of results. - Develop study protocols and ensure compliance with regulatory guidelines and internal standards. - Coordinate and communicate with cross-functional teams. - Analyze and interpret data, preparing comprehensive reports and presentations for internal and external stakeholders. - Mentor and train junior staff in scientific techniques and best practices. - Ensure that laboratory safety protocols are followed and maintain a clean and organized work environment. - Stay current with industry trends and advancements in chemical characterization methodologies. Qualifications: - Ph.D. or equivalent degree in Chemistry, or a related field. - A minimum of 10 years of experience in chemical characterization or a similar role within a laboratory setting. - Expertise in techniques such as LCMS - QTOF, GCMS, NVR, ICPMS, IC and other relevant analytical methods. - Strong project management skills with the ability to lead multiple projects simultaneously. - Excellent communication, organizational, and problem-solving abilities. - Familiarity with regulatory requirements and guidelines in the pharmaceutical or biotechnology industry. This position offers a competitive salary and benefits package, along with opportunities for professional growth and development. If you are passionate about advancing scientific research and thrive in a collaborative environment, we encourage you to apply. Roles and Responsibilities 1. Oversee and manage chemical characterization studies from initiation to completion, ensuring adherence to regulatory standards and internal protocols. 2. Design study plans and methodologies that are scientifically sound and aligned with project objectives, including the selection of appropriate analytical techniques and equipment. 3. Coordinate with cross-functional teams, including project managers, chemists, and quality assurance personnel, to ensure effective study execution and communication. 4. Review and approve study protocols, analytical methods, and reports to ensure accuracy, compliance, and scientific integrity. 5. Provide technical expertise and guidance related to chemical characterization, including the interpretation of analytical data and results. 6. Ensure that all studies are conducted in compliance with Good Laboratory Practice (GLP) and other relevant regulations. 7. Manage study budgets and timelines, identifying potential risks and implementing mitigation strategies to ensure successful project delivery. 8. Train and mentor staff on appropriate methodologies and regulatory requirements related to chemical characterization studies. 9. Participate in project meetings, presenting study findings and progress updates to stakeholders, and incorporating feedback into study design and implementation. 10. Maintain up-to-date knowledge of industry trends, emerging technologies, and regulatory changes affecting chemical characterization and related fields. 11. Facilitate communication with regulatory agencies as needed, providing data and documentation to support submissions and inquiries. 12. Contribute to the continuous improvement of departmental processes and methodologies, ensuring best practices are followed in study design and execution.

Handling of ISO, IATF and other required certifications and all QMS systems. Handling customer audits and QMS queries. Responsible for heading a team of chemists Required Candidate profile Proper knowledge of QC SOP, MOA, Specification, BIS, ASTM, physicochemical Analysis and ISO documentation. Operating equipments like AAS, Surface Area Analyser, pH Meter etc.

Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA