Role & responsibilities Preferred candidate profile Perks and benefits
Role & responsibilities We are seeking a qualified individual with strong expertise in organic chemistry, including in-depth knowledge of chemical reactions and mechanisms. The role involves: Distillation of organic solvents and purification of organic compounds using column chromatography, vacuum distillation, and crystallization. Scaling up chemical reactions from gram to kilogram scale. Conducting experiments for assigned projects and maintaining accurate records of observations in the lab notebook. Proficiency in using online resources, including chemistry-related searches, to support research and project work. Operation and maintenance of laboratory equipment such as round-bottom flasks (RBF), TLC chambers, pH meters (calibration and use), rotary evaporators, Buchner filters, microfilters, vacuum systems, and tray dryers. Candidates should demonstrate hands-on experience and attention to detail in laboratory practices. Preferred candidate profile:- API/CRO- R&D Qualifications:- M.sc Organic Chemistry/Industrial Chemistry / M. Pharma (Medicinal Chemistry)
Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications. Perks and benefits: Mention available facilities and benefits the company is offering with this job.
Role & responsibilities 1. He shall be responsible to undertake training from the Section in Charge and the senior Analyst to make independent to carry out analysis. 2. He shall report to the senior analyst or analyst if any chemical, reagents or reference material is not available as per the requirement to carry out the analysis. 3. He shall be responsible to analyse samples received as per the specifications and for reporting of the results under the supervision of the senior analyst. 4. He shall be responsible to follow the quality system as per the policies laid down in the quality manual. 5. He shall be responsible for the preparation and standardization of the chemicals under the guidance of the senior analyst or analyst. 6. He shall be responsible to ensure proper documentation of all the data and its maintenance under the guidance of senior analyst or analyst. 7. He shall be responsible to follow the quality policies as per ISO/IEC17025, cGMP, GLP under the supervision of section In-charge or senior analyst. 8. He shall be responsible to perform all the chemical analysis. 9. He shall be responsible for operation, maintenance, timely calibrations of the following instruments: Weighing Balances pH and Conductivity Meter Melting Point Apparatus FTIR Instrument TOC Analyser Hot air ovens and Vacuum Oven Muffle furnace Disintegration Tester Dissolution Tester UV spectrophotometer Polarimeter Refractometer KF Auto titrator Melting point apparatus Tap density apparatus Friabilator
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,
Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.
Role & responsibilities: Perform routine and non-routine analysis using GC and GC-MS as per SOPs and approved test methods. Prepare samples, reagents, and calibration standards accurately. Conduct method validation, system suitability, and performance checks for GC instruments. Maintain proper documentation of all analytical results in accordance with GMP/GLP requirements. Troubleshoot analytical issues and assist in resolving deviations and OOS (Out of Specification) results. Ensure proper calibration, maintenance, and operation of GC instruments. Support development and validation of new methods as required by R&D or Quality Assurance teams. Maintain a clean, organized, and safe laboratory environment.
Role & responsibilities Internal Sales: Actively engage with all our laboratories across locations to capture their requirements, take regular orders, and ensure timely supply of reference standards and impurities. External Sales & Business Development: Maintain updated stock lists and price lists , share them with existing and potential customers via WhatsApp, email, and social media . Build strong relationships with customers to secure repeat and new orders. Identify new sourcing opportunities arrange supply if items can be sourced or coordinate synthesis if custom-made. Coordination: Work closely with the Technical Head of the Synthesis Division to support government tenders, manage documentation, and ensure smooth execution. Regulatory Outreach: Liaise with pharmacopoeia commissions such as USP, BP, EP, IP , etc., to explore collaboration and supply opportunities. Stock & Operations Management: Maintain real-time stock records, pricing, and availability to ensure prompt response to customer and lab needs. Preferred candidate profile Bachelors degree in Science / Pharmacy / Chemistry preferred. 1–3 years of sales, business development, or coordination experience (life sciences, chemicals, pharma, or lab supplies preferred). Strong communication skills (written & verbal) and ability to manage customer relationships over calls, WhatsApp, and email. Organized, detail-oriented, and comfortable managing stock and documentation . Self-motivated, proactive, and willing to work closely with technical teams.
Role & responsibilities 1. Managing the quality documents and conducting internal Audit & data review etc. 2. Maintaining all records and documentation as per 17025:20053. 3. Maintaining regularly and tracked calibration and standard log books, 4. Directing all quality activities for the laboratory such as ILC, IQC, Training, etc. 5. Preparing compliance report for the audit or for the closure of various shortcomings or NCs. 6. Having sound knowledge of QMS and LIMS. 7. Knowledge of 21cfr, OOS, Market complaints, APQR.
Role & responsibilities Perform chemical analysis using ICP-MS and AAS for a diversity of applications. Familiarity with GLP and ISO 17025 quality system standards. Expert in sample Preparation for metal analysis.. Having Good Experience in metal analysis in food and water. Develop and validate ICP-MS methods in support of API and/or drug product manufacture as well as stand-alone analytical projects. Write protocols, methods and reports; as well as be involved in client project meetings; whilst being a point of contact for technical issues relating to ICP-MS analysis. Responsible for equipment maintenance and qualification, and interaction with vendor services and application support.
Role & responsibilities Preferred candidate profile
Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.
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 in method validation, ADL, analytical lab. 2, Knowledge of HPLC,
Role & responsibilities Preferred candidate profile
Role & responsibilities We are seeking a qualified individual with strong expertise in organic chemistry, including in-depth knowledge of chemical reactions and mechanisms. The role involves: Distillation of organic solvents and purification of organic compounds using column chromatography, vacuum distillation, and crystallization. Scaling up chemical reactions from gram to kilogram scale. Conducting experiments for assigned projects and maintaining accurate records of observations in the lab notebook. Proficiency in using online resources, including chemistry-related searches, to support research and project work. Operation and maintenance of laboratory equipment such as round-bottom flasks (RBF), TLC chambers, pH meters (calibration and use), rotary evaporators, Buchner filters, microfilters, vacuum systems, and tray dryers. Candidates should demonstrate hands-on experience and attention to detail in laboratory practices. Preferred candidate profile:- API/CRO- R&D Qualifications:- M.sc Organic Chemistry/Industrial Chemistry / M. Pharma (Medicinal Chemistry)
Role & responsibilities Manager technical is the In-charge of Analytical Division. He/She shall report to the SBU-head about all the activities in the Analytical Division. He/She shall look after all the operations of the Division under the guidance/ supervision of SBU-Head. He/She shall be responsible for the standardization and validation of the test methods. He/She shall be responsible for ensuring the availability of the reference material / working reference standard. He/She shall be responsible for assigning the jobs to the analyst as per their calibre. He/She shall be responsible for checking the calculation part and reporting of the results before sending for authorized signatory. He/She shall be responsible for the smooth operations of the equipments/Instruments. He/ She shall be responsible for signing the test certificate / test reports. He/ She shall be responsible for verifying the outside calibration certificates. He/She shall be responsible for the supervision of technical staff working under him/ her. He/She shall be responsible for filling the change control, deviation control, OOS, CAPA raised by technical department. He/She shall be responsible for the preparing / reviewing the scope as per requirements. He/She shall ensure that the glassware used in his / her section should be duly calibrated or verified as required. He/She shall be responsible for the qualification and calibration of new instruments/ equipment. He/She shall be responsible for the maintaining overall quality as per ISO/IEC 17025. He/She shall be responsible for all the relevant works of VP- Technical/GM Operation in his absence.
1. Managing the quality documents and conducting internal Audit & data review etc. 2. Maintaining all records and documentation as per 17025:20053. 3. Maintaining regularly and tracked calibration and standard log books, 4. Directing all quality activities for the laboratory such as ILC, IQC, Training, etc. 5. Preparing compliance report for the audit or for the closure of various shortcomings or NCs.
Role & responsibilities Market Development & Client Acquisition Identify, target, and onboard new clients in the pharma, cosmetics, nutraceuticals, and clinical research industries. Develop opportunities across services: analytical testing, stability studies, clinical research, claims substantiation, regulatory compliance, CDMO (formulation & manufacturing). Generate leads via digital outreach, networking, and partnerships. Build a strong pipeline of opportunities across domestic and export markets. Client Relationship Management Maintain strong client relationships to increase wallet share through cross- selling and upselling services. Serve as a trusted partner by understanding client challenges and aligning solutions to their needs. Manage regular follow-ups, virtual calls, physical meetings and client engagement across USA, India, EU, and MEA time zones. Proposal, Negotiation & Closures Draft tailored proposals, quotations, and agreements in compliance with regulatory and commercial requirements. Collaborate with technical, regulatory, and R&D teams to ensure feasibility and accuracy. Lead contract negotiations and ensure deal closure to meet revenue targets. Coordination and Delivery of time projects with the coordination of execution team Market Intelligence & Strategy Monitor regulatory and industry trends: USFDA, EMA, CDSCO, MoCRA (cosmetics), FSSAI (nutraceuticals/food), AYUSH, WHO-GMP. Conduct competitor mapping, pricing analysis, and business intelligence for international and domestic markets. Share insights with management to support strategic decision-making and market-entry initiatives. Collaboration & Reporting Work closely with regulatory, R&D, analytical, and clinical research teams to deliver client projects seamlessly. Work closely with International partners for business development. Prepare pipeline reports, sales forecasts, and weekly and monthly reviews. Support branding, webinars, client visits, and participation in trade shows. Preferred candidate profile Strong knowledge of pharmaceuticals, cosmetics, nutraceuticals, and CRO/CDMO services. • Familiarity with international and Indian regulatory frameworks (USFDA, EMA, CDSCO, MoCRA, FSSAI, AYUSH). • Excellent client engagement, presentation, and negotiation skills. • Ability to work across different time zones (USA, EU, MEA) with flexible hours. • Strong networking abilities and experience in B2B sales for regulated industries. • Proficiency in CRM tools, MS Office, and virtual communication platforms.
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 in method validation, ADL, analytical lab. 2, Knowledge of HPLC,
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