523 Method Development Jobs - Page 4

Job Description: Knowledge of calibration and operation of LCMS/GC systems with Empower software. Sound knowledge of analytical method development and validation. Handling final compilation of raw data and chromatographic data complying with GLP requirements. Preparing general lab SOPs and instrument SOPs.

We are looking for a skilled HR professional with strong expertise in Payroll Management, HR Analytics, and Dashboard Reporting, coupled with hands-on experience in Darwinbox HR Core Modules. The ideal candidate will drive operational excellence across payroll processes, ensure compliance, and enable data-driven decision-making through analytics and reporting.

JD: 1) Working as per company / management policy & reporting to Quality Control Head. 2) To conduct analysis and testing of Raw Material, Packing Material, In-Process sample, Finished goods, Stability samples etc. with the help of analytical instruments and techniques. 3) To calibrate / verifies analytical instruments i.e. ICP-OES, Ion Chromatography etc..and balances. 4) To trouble shoot analytical instruments. 5) Preparation and standardization of Volumetric Solution. 6) Preparation and maintenance of records for stock / reagents. 7) Analysis of samples for qualitative and quantitative test parameters as per specification. 8) To maintain record of analysis and supporting logbooks as per G...

Walk In drive for Formulation Analytical Research & Development - department (FAR&D) - Quality Inn Ramachandra, Ward No- 58, 31-41/10/1, Duvvada, Revenue, Visakhapatnam, Andhra Pradesh on 25.10.2025 (Saturday ) Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Roles & Responsibilities : Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal,...

Dear All, We are looking for an experienced professional to lead Analytical Method Validation activities for Finished Dosage Formulations (OSD) . The ideal candidate should have extensive experience in analytical development, method validation, and regulatory compliance for both domestic and international markets. Experience: 11-13 Years Location: Hyderabad(Dulapally) Key Responsibilities: Plan, design, and execute Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) activities for formulations as per regulatory guidelines (ICH, USP, EP, WHO, etc.). Review and approve Validation Protocols, Reports, Method Development Reports, and Specifications. Ensure method robustness, a...

Responsibilities: Analytical Operations: Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG). Operate and maintain analytical instruments :- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus Ensure compliance with GLP, 21 CFR Part 11, and data integrity standards. Review and approve analytical reports and LIMS entries , Quality Systems & Compliance Implement and monitor Quality Management Systems (QMS). Lead investigations for OOS, OOT, Deviations, and Laboratory Incidents. Prepare and review SOPs, STPs, and validation protocols. Ensure audit readiness and support regulatory inspections (USFDA, WHO-GMP, etc.) Documentation & Reporting Maintain ac...

Responsibilities: Synthetic Chemistry / Lab Work Perform multi-step organic synthesis of target molecules as per project requirements. Conduct reaction monitoring, work-up, purification, and isolation of intermediates and final products. Maintain accurate lab records and notebooks (ELN or manual) as per GLP standards. Process Development Assist in the optimization of reaction conditions to improve yield, purity, and scalability. Conduct literature searches and suggest alternative synthetic routes under supervision. Evaluate critical process parameters through small-scale experiments. Analytical Coordination Coordinate with the analytical team for sample submissions, impurity profiling, and m...

JOB DESCRIPTION We are seeking a detail-oriented and proactive Regulatory Affairs Associate to join our Global Regulatory team. In this role, you will be responsible for development and execution of CMC regulatory strategies, marketing applications and Life Cycle Management for biosimilar products. RESPONSIBILITIES: • Plan and manage development of high quality regulatory documents, including briefing documents, CTAs, IND / IMPD, MAA / BLA, and responses to questions for products in compliance with approved filing plans, timelines, and regulatory requirements • Provide regulatory direction on global regulatory requirements to support product development • Ensure all filings are maintained pe...

Responsibilities: Lead formulation development for OSD, external preparations, oral liquids, and injectables. Oversee pre-formulation studies, prototype development, and scale - up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (QA, QC, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation. Required skills: Strong knowledge of formulation science and process optimization. Experience in QbD, DoE, and stability studies. Excellent leadership and communication skills. Required Qualification: - B.Pharm/M.Pharm

Job Description Job Title: Assistant Manager - Research & Development About The Function Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageo's 30,000+ people work in Supply Chain and Manufacturing. It's an intricate and sophisticated operation that's the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. We're committed to realising our Society 2030: Spirit of Progress goals, to protect the environment an...

In this role, your main responsibility will be XRD analysis, method development, and polymorph quantification. You will also be supporting routine analysis tasks such as PSD, DSC, TGA, etc. Key Responsibilities: - Conduct XRD analysis - Develop methods for analysis - Quantify polymorphs - Support routine analysis such as PSD, DSC, TGA, etc. Qualifications Required: - Bachelor's degree in Chemistry or related field - Experience with XRD analysis techniques - Strong understanding of polymorph quantification - Proficiency in PSD, DSC, and TGA analysis,

As a member of the o2h discovery team, your role involves: - Strong knowledge and hands-on experience in LC-MS/SFC/HPLC/Prep. method development for all types of chemistry molecules. - Strong understanding of various column chemistry. - Skilled in troubleshooting, instrument maintenance, and calibration. - Leading, training, coaching, and mentoring a team of motivated young scientists. To qualify for this role, you should: - Have a passion for HPLC/Prep./LCMS/SFC analysis and characterization techniques, along with a willingness for continuous learning and education. - Demonstrate creative thinking to identify new techniques and growth opportunities. - Be highly organized with the capability...

Job Objective Searching for highly motivated candidate having technical expertise in Biosimilar product analysis. Key Responsibilities The candidate is expected to develop HPLC based methods for protein and peptide products. The candidate is expected to design and implement integrated strategies, linking appropriate analytical tools, to perform a qualitative and quantitative assessment of product related variants and impurities. Develop and apply novel sample preparation with emphasis on RP-HPLC, SEC-HPLC, CEX-HPLC..etc Responsible for designing advance workflows to measure & characterize process related impurities at different stages of product development such as Host cell protein (HCPs), ...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

oversee l operations and quality systems in a regulated CRO environment. ensuring microbiological data integrity, method development/validation, audit , and compliance (e.g., GLP, GMP, GCLP, ISO). Lead a team of microbiologists and QA personnel,

To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to align with organization goal and other responsibilities assigned by reporting authority. Responsible to perform the calibration of instrument and to maintain instrument/equipment as per SOPs. Responsible to follow safety precaution as per laboratory procedure. Responsible for method development studies of Drug Substance, Drug Product & In process Materials related to Peptides. Responsible for method Validation studies of Drug Substance, Drug Product & In process Materials related to Peptides. Responsible for analysis of routine samples and stability studies of Drug Product & In process Material Dr...

Walk-In Drive For API Analytical Research & Development(AR&D)- MSN Laboratories, Pashamylaram, R&D center on Wednesday 08-10-2025. Requirement for Executive / Senior Executive - API AR&D - API Analytical Research & Development(AR&D) HPLC,LCMS,GC,GCMS,PXRD High performance liquid chromatography HPLC,LCMS,GCMS,PXRD HPLC with Software lab solu. UV-VIS Spectrometer GC with Software lab solution PH-Meter Moisture Analyser Karl Fischer titrator Micro- Weighter Balance Responsible for an Analytical team involved in Method development, Method Transfer and Validation for various stages of drug development. Method Validation of analytical methods as per internal and country specific regulatory guideli...

Walk-in drive: Senior Chemist / Junior Research Associate - HPLC Analytical Method Validations Work Location: Hyderabad Eligibility: Must have 1 to 3 Years of experience in Analytical Method Validations by using HPLC for Formulation products. M.Sc. / M-Pharmacy or Equivalent Qualification. Job Description : Analytical method validations and method transfer as per cGMP requirements for drug products. Strong experience in handling various analytical instruments like HPLC, UPLC, UV and Dissolution USP type-I and II and type-IV. Dissolution, Assay and Related Substances method validationand method development of finished products like Tablets, Capsules, Pellets, oral suspensions and Injectables ...

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. Experience : 2 - 6 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of Tentative me...

To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to take training before execution of allotted work & maintaining the training file. Responsible to follow safety precaution as per laboratory procedure. Responsible to escalate any issue / incident to reporting manager for prompt corrective action. Responsible for method development studies of API, Drug Product & In process Material preferably Peptide molecules Responsible for method Validation studies of API, Drug Product & In process Material preferably Peptide molecules Responsible for routine and stability studies of API, Drug Product & In process Material preferably Peptide molecules Responsible...

To work as per cGMP and ensure its compliance as per current guideline and SOPs. Responsible to take training before execution of allotted work & maintaining the training file. Responsible to follow safety precaution as per laboratory procedure. Responsible to escalate any issue / incident to reporting manager for prompt corrective action. Responsible for method development studies of API, Drug Product & In process Material preferably Peptide molecules Responsible for method Validation studies of API, Drug Product & In process Material preferably Peptide molecules Responsible for routine and stability studies of API, Drug Product & In process Material preferably Peptide molecules Responsible...

Product development Process improvement Regulatory compliance & innovation Must have strong knowledge of food science, formulations & industry standards Experience in R&D leadership required. Required Candidate profile Must have experience of PVC Stabilizers, Metallic Stearates & Paint Additives manufacturing industry.

We are hiring Senior Executive - Analytical Quality Assurance from API - Pharma background with 5- 8 years experience. Job Description Preparation and review of SOPs. Review of specification and testing procedures as per method development and guidelines requirement. Review of method validation protocol and reports. Review of calibration reports of analytical instruments. Review of method transfer protocols and reports. Review of lab note books. Ensuring of lab compliance. Handling of documentation.

Job Description: Will work in Analytical development Lab of BRL. Responsible for analytical deliverables of Biologics Projects for regulated markets. Deliverables involves but not limited to Method Development, Qualification, Technology transfer, Biosimilarity assessment, Forced degradation and Characterization activities. Responsible for Independent planning and execution of experiments. Techniques include but not limited to Chromatography, Electrophoresis, Spectrophotometry and Colorimetric assays for Biotherapeutics. Major responsibility will be planning and execution of HPLC, UPLC and CE based analysis Skill sets: Knowledge and hands-on experience of different chromatography modes like R...

About the role: This role is responsible for executing and managing analytical R&D projects related to alcoholic beverages. It includes conducting precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods, Good Laboratory Practices (GLP), and ISO 17025 requirements. The position also supports senior analysts in innovation and research initiatives and contributes to technical capability building across stakeholders through training and knowledge sharing. Role Responsibilities: Key Technical Responsibilities: Conduct and support analytical R&D projects for product and process development Perform chemical analysis on ...