3433 Hplc Jobs - Page 29

QC Head 1 Pos based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. 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 improvement (5S/Lean/Kaizen). Mana...

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...

Executive for Micro R&D 1 Post based in Amritsar. The ideal candidate brings 6 - 8 yrs exp. 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 improvement (5S/Lean/Kaizen). Lead...

Chief Manager Township Administration (MP 25/13) based in Narmada, Gujarat. The ideal candidate brings 15-20 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 improvement...

Sterile Manufacturing based in Waghodia, Vadodara. The ideal candidate brings 1- 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 improvement (5S/Lean/Kaizen). Additio...

The ideal candidate brings 1-6 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 improvement (5S/Lean/Kaizen) Lead microbiology practices including EM, MLT, sterility assur...

Analysis of raw materials, in-process, finished products using HPLC, GC, UV-Vis,& titration. Maintain instruments, ensure doc as per SOPs & cGMP. Support method transfer, prepare reports,coordinate with QA and Production while ensuring lab safety.

Role & responsibilities Perform isolation, culturing, and preservation of microbial strains, including bacteria (especially Bacillus) and fungi (Trichoderma spp.) Conduct molecular biology experiments, including DNA extraction and PCR analysis. Maintain microbial culture collections and ensure proper documentation of lab records. Support research and product development activities related to microbial formulations. Assist in analytical procedures such as TLC or HPLC, as required. Work collaboratively with cross-functional teams to ensure timely completion of research goals. Adhere to laboratory safety and quality standards. Preferred candidate profile B.Tech in Biotechnology or M.Sc in Micro...

In this role, you will be responsible for: - Strong capabilities of literature search, understanding, and selecting the most appropriate and scalable process for phyto-actives. - Executing lab experiments to convert herbal extracts into enriched cosmeceutical/nutraceutical actives. - Creating and overseeing the extraction strategy, including sourcing equipment and materials. - Mentoring and training the Extraction team on standard processes and operating procedures. - Conducting scale-up studies. - Standardizing extracts with HPLC, HPTLC, and other methods. - Conducting analytical and stability studies to strengthen the product portfolio. - Developing cost-effective extracts according to mar...

As an Executive - QC (Stability), your role involves conducting stability studies, analyzing samples, preparing reports, and ensuring compliance with regulatory guidelines to maintain product quality throughout its shelf life. You will work closely with stakeholders such as Operations, R & D, QA, and Regulatory affairs. Reporting to the QC Supervisor, you should have at least 3 years of experience in the stability section. Key Responsibilities: - Work in the stability section - Handle instruments like HPLC, UV, Culometer, KF-titrator, LCMS, etc. - Conduct stability sample analysis - Charge stability samples - Manage Stability Chamber - Have knowledge of instrument software such as Lab soluti...

Role Overview: As a Senior Technician Quality Control at Beckman Coulter Bangalore Development Centre, you will be responsible for conducting routine analysis of raw materials, in-process, and finished goods under supervision. Your main task will be to ensure compliance with Quality control procedures and activities according to 21 CFR 820, ISO 13485, ISO 9001, MDSAP, and Beckman Coulter corporate Quality system requirements. Your duties will include: Key Responsibilities: - Conduct routine analysis of raw materials, in-process and finished goods under supervision and in accordance with Standard Operating Procedures (SOPs). Compile data for documentation of test procedures and prepare report...

Job Title: Executive / Sr. Executive - Quality Management System (Analytical Assurance) Department: Quality Management System Reports to: Manager Location: Ankleshwar Position Type: Full-time Qualifications And Experience Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 68 years of experience in Analytical Assurance within the pharmaceutical industry Job Responsibilities & Accountabilities We are looking for an experienced Analytical Assurance professional to join our team and lead the Out of specification investigation, along with core QMS activities pertaining to QC. Key Responsibilities Trigger out of specification investigations upon ...

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

As a Scientist B in the Ayush/Pharma Department at Farelabs Pvt. Ltd., your role will involve conducting analytical procedures in alignment with Ayurveda, Yoga, Siddha, Unani, and Homeopathic pharmacopeia of medicine for the Ayush section. For the Pharma section, you will be responsible for having complete knowledge of different pharmacopeia such as IP, USP, BP, and utilizing analytical procedures accordingly. Additionally, you will need to be knowledgeable about regulatory authorities like NABL, USFDA, TGA, MHRA, WHO, and DCA (drugs and cosmetic act 1940). Key Responsibilities: - Well-versed with analytical procedures for Ayurveda, Yoga, Siddha, Unani, and Homeopathic pharmacopeia - Knowled...

Company Overview : Foundation for Neglected Disease Research (FNDR) is a not-for-profit biotech R&D organization dedicated to discovering and developing novel therapeutics, diagnostics, and devices for diseases with a high socio-economic impact. Since its inception in 2014, FNDR has generated a portfolio of therapeutics in tuberculosis, nontuberculous mycobacteria, malaria, dengue, leishmania, serious bacterial infections, fungal infections, COVID-19 and RSV, spanning over early-stage discovery to late-stage clinical trials. FNDR's R&D Centre, which includes state-of-the-art BSL2 and BSL3 laboratories for both in vitro and in vivo research, is in Bengaluru, India. For more information, pleas...

Job Summary: The purpose of this role is to handle technical trials, trouble shooting, new product introduction trials as part of after sales support in the assigned territory, key customers & category of Beverage Alcohol / Distilling unit of Brenntag India. This would be a client facing & an individual contributor role. Job Responsibilities: Work closely within the account team network to generate revenue from the existing customers and maintain good business relations with them. Support all the existing customers and prospective customers for product shift trials, new product introduction trials, conduct all trouble shooting activities. Handle Up Selling and cross selling technical activit...

Roles and Responsibilities Conduct quality control analysis using HPLC, GC, LCMS, Microbiology techniques for APIs and intermediates. Ensure compliance with cGMP guidelines during stability studies and batch release processes. Collaborate with cross-functional teams to resolve issues related to product quality and regulatory affairs. Develop and maintain documentation for laboratory procedures, protocols, and reports in accordance with company standards. Participate in training programs to enhance knowledge on new technologies and methodologies.

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...

Role Purpose The purpose of the role is to source and hire the right talent against the requirements shared by the business and ensuring a positive employer brand experience for the candidate throughout the hiring process. Do 1. Hire the required talent from the different sourcing channels Understand business projections and urgency of talent requirements across order and cadre demands, skill type (type A/B/C), volume vs. niche etc. As per the talent requirements shared by the business, Create sourcing plan as per hiring channel mix and cost considerations Utilize job portals, consultants, employee referral to find the right fit from the industry/ within Wipro For the shortlisted candidates,...

Hi Jobseeker, Greetings from Laurus Labs Ltd! Please find the below current openings at Laurus Labs Ltd- Visakhapatnam (Atchutapuram OSD Formulation Unit-2) Department : Quality Control-OSD Formulations Designation : Asst.Manager Section : HPLC Interested candidates can send their resume to seetaram.y@lauruslabs.com and please send the below details for further process. Total Exp : Current CTC : Expected CTC : Notice Period :

1.Monitoring of cGMP and GLP compliance and compliance to applicable regulatory requirement and filing commitments. 2.Resopnsible for investigation of LIR (Incident / OOS/ OOE). 3.Analysed data review. 4.Analysis of Finished, In process, Process validation, Cleaning Validation samples.

1.Preparation and standardize of volumetric solutions and maintaining its record. 2.Preparation of standard solutions and reagents and maintaining its record. 3.Water Analysis and data punching in SAP. 4.Analysis of Raw Material and Miscellaneous samples as per GTPs/ SOPs/ Spec & MOAs. 5.Raw materials Control sample management.

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey. Support departmental operations by managing documentation, reporting, and internal coordination. Execute standard operating procedures in compliance with organizational policies and regulatory norms. Monitor workflow, assist senior officials in audits or reviews, and maintain accurate data records. Participate in cross - functional initiatives, ensuring timely completion of administrative and operational tasks. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify al...

Roles & Responsibilities for Analyst 1. Understanding and maintenance of Quality Management System. 2. Performing the analysis as per the guidelines under supervision of Senior Analyst/ Lab manager. 3. Instrument operation and calibration on regular interval for Analytical balance, pH meter, HPLC, LCMS, etc. 4. Maintenance of the technical records, certificate of analysis as per requirement. 5. Recording Initial observations, necessary data, and calculations. 6. Inform the lab manager for any kind of equipment breakdown, fault or any kind of irrelevant test results (Preventive maintenance). 7. Perform method development, method validation and project related activities as per SOP/ Protocol. ...

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,