2105 Hplc Jobs - Page 36

Eligibility : M.Sc / M.tech (Life Sciences / Biotechnology) Probation Period : 3 Month (For junior post only) Technical Skills : Various Extraction Techniques Purification techniques General PCR RAPD RFLP Karyotyping SDS PAGE Blotting General Skills : Complete knowledge of MS Office Standardisation of SOP Sample flow management English (Reading and Writing) Candidate must have a personal Laptop

We are looking for a skilled MySQL DBA Professional with 5-10 years of experience to join our team in IDESLABS PRIVATE LIMITED. The ideal candidate will have a strong background in database administration and management. Roles and Responsibility Design, implement, and manage database architectures to support business requirements. Develop and maintain databases to ensure high performance, security, and availability. Collaborate with cross-functional teams to identify and prioritize database needs. Troubleshoot and resolve complex database issues efficiently. Ensure compliance with organizational standards and best practices. Optimize database queries for improved performance and efficiency. Job Requirements Strong knowledge of MySQL database administration and management. Experience with database design, development, and implementation. Excellent problem-solving skills and attention to detail. Ability to work collaboratively in a team environment. Strong communication and interpersonal skills. Familiarity with database security and access control measures. Proficiency in managing large-scale databases and ensuring data integrity.

3-5 yrs of experience as CRC JD: Preparation of SOP's for operation, establishment of work/trial conduct systems/ training to new joiners/ training to trainers internal trainings, QC Visit of current project remotes, Checking weekly logs, equipment management, market Research

o Handle collections for the assigned area and achieve collection targets on various parameters like resolution, flows, credit cost and roll rates (depending on the bucket)o Ensure that the NPA's are kept within assigned budget and active efforts are made to minimize it.o Increase the fee income / revenue and develop intiatives to control and reduce the amount of vendor payoutso Conduct asset verifications and possession as per SARFESI / Section 9 process through court receivers. o Track & control the delinquency of the area (Bucket & DPD wise) and focus on nonstarterso Ensure customer satisfaction by ensuring quick resolution of customer issues within specified TATo Build relationships with key clients to ensure timely collections are made and monitor defaulting customers by ensuring regular follow with critical/complex customers to identify reasons for defaultingo Represent the organization in front of legal/ statutory bodies as required by the legal team and ensure that the collection team adheres to the legal guidelines provided by the law in force o Allocate work to the field executives and ensure that all the agencies in the location perform as per defined SLA, ensuring payments and audit receipts get deposited within the defined SLA. o Ensure that there is adequate Feet on Street availability area-wise /bucket-wise/ segment-wise and o btain daily updates from all collection executives on delinquent portfolio & initiate detailed account level review of high ticket accountso Ensure compliance to all Audit / Regulatory bodies as well as policies and procedures of the company Qualification : Post Graduate/Graduate in any discipline

Job Title: Quality Control Head Industry: API / Pharma Manufacturing Job Location: Ankleshwar, Gujarat Experience Required: 15 to 20 years of relevant experience in Quality Control within the API pharma industry Salary: 12.0 LPA to ?15.0 LPA Education: M.Sc. / B.Sc. (Chemistry) or M.Pharm / B.Pharm or equivalent Key Skills Required: Strong knowledge of data integrity principles Hands-on experience with instruments like HPLC, GC, and UV Experience in cleaning validation and microbiological testing Familiarity with incident investigations and regulatory compliance About the Company: A leading API pharma manufacturing group known for its strong global presence and commitment to quality and innovation. Job Responsibilities: Lead and manage the Quality Control (QC) department to ensure quality at every stage of manufacturing and testing. Oversee sampling, inspection, and testing of raw materials, packaging materials, in-process, and finished products. Ensure timely release or rejection of batches based on quality data. Handle stability chamber management, testing, and shelf-life evaluations as per protocol. Conduct microbiological analysis for raw materials, finished goods, water, and environmental monitoring. Review trends in physicochemical and microbiological test data for compliance. Manage out-of-specification (OOS), deviation investigations, and analytical support for product recalls and complaints. Coordinate with QA and R&D on specifications, analytical procedures, and validations. Ensure equipment/instrument qualification, calibration, and preventive maintenance. Maintain and audit QC records, reference/working standards, and ensure data integrity systems are in place. Supervise glassware cleaning, protocol validation, and implementation of cleaning procedures. Plan and execute internal audits and ensure compliance with GLP and GMP standards. Review and validate SOPs, protocols, and test methods (pharmacopeial & in-house). Support employee training in alignment with cGLP and cGMP practices. Evaluate change control proposals, failure investigations, market complaints, and implement improvements in QC systems. Ensure all activities follow company reporting systems and regulatory expectations.

To own YBL Vision, Values and Mission. • The Candidate will contribute to product and process analytics, method developments and product characterization related activities. • To make sure timely coordination, data generation and data sharing of product development related analytical activities. • Planning and execution with minimum supervision. • To provide training and guidance to subordinates for execution and troubleshooting. • Product specific analytical method development, data interpretation, troubleshooting and Validation. • Data compilation, report writing and data presentation. • Coordinating with Internal and External stakeholders • Any other activity assigned by direct reporting authority and activities related to smooth functioning of YBL. Desired Expectation Working knowledge of Protein and Nucleic Acid related analytical techniques viz. various methods of protein quantification, SDS-PAGE, Western Blotting, ELISA based assays, DNA quantification; Agarose gel electrophoresis, PCR, RT-PCR, Enzymes unit defining assays etc. Working knowledge of HPLC, Capillary electrophoresis, DLS will be preferred. Strong experience with analytical development and ability to train scientists on new techniques. Proven supervisory experience. Good analytical skills in sorting information, formatting directions and problem solving. Smart Thinker and displays smart/ tactical moves & mental agility. Is open and flexible when faced with changing circumstances and finds ways and means of doing things and not get struck with the past. Comes up with ideas which are different and can be used commercially, profitably and growth.

1) Experience in preparing and reviewing of Method Development Report. 2) Knowledge of ICH Guidelines. 3) Strategic planning and performing Validation studies, Solubility Studies, Impurity and Standard Qualification. 4) Exposure of working on HPLC, LCMS, GC, UV and other equipment. 5) Ability to perform an analysis of related substances, assays and purity by using HPLC, IC. 6) Ability to perform analysis of residual solvents by using gas Chromatography. 7) Preparation and Review of development and validation/ method transfers/ protocols and reports based on R&D qualifications or monographs. 8) Ability to work in a team and contribute towards collective goals.

Manager/Sr. Manager (Injectable): Should have experience in following area; Having exposure of team leading in area of Analytical method development for various type of Injectable products (i.e. liquid, Lyophilized, Peptide & Complex injectable) Exposure of R&D analysis support for routine, development, in process and stability samples and data trending/interpretation etc. Having exposure of timely completion of calibration of various analytical instruments such as HPLC, GC, Dissolution app., IC, KF & Viscometer etc., Exposure in Dissolution method development for complex injectable on Type IV dissolution apparatus Pharmacopeia method updation & impact assessment on products Perform pre-validation of various analytical methods/technics Troubleshooting of Analytical methods & Plant queries Training to fresher s for proper handling of Instruments/activities

Manager/Sr. Manager (Injectable): Should have experience in following area; Having exposure of team leading in area of Analytical method development for various type of Injectable products (i.e. liquid, Lyophilized, Peptide & Complex injectable) Exposure of R&D analysis support for routine, development, in process and stability samples and data trending/interpretation etc. Having exposure of timely completion of calibration of various analytical instruments such as HPLC, GC, Dissolution app., IC, KF & Viscometer etc., Exposure in Dissolution method development for complex injectable on Type IV dissolution apparatus Pharmacopeia method updation & impact assessment on products Perform pre-validation of various analytical methods/technics Troubleshooting of Analytical methods & Plant queries Training to fresher s for proper handling of Instruments/activities

Scientist (Topical): Should have experience in following area; Analytical method development for various type of Topical products (i.e. cream, gel & ointment) + Reverse Engineering development work R&D analysis support for routine, development, in process and stability samples Calibration of various analytical instruments such as HPLC, GC, Dissolution app., IC, KF & Viscometer etc., IVRT study Solubility studies & Excipient Compatibility Study Pharmacopeia method updation & impact assessment on products Perform pre-validation of various analytical methods/technics Troubleshooting of Analytical methods & Plant queries Training to fresher s for proper handling of Instruments/activities

Role & responsibilities : 1) Having from OSD background. 2) Responsible for analysis of RM/IP/FG/Stability on HPLC. 3) Responsible for Calibration of HPLC 4)Having the Knowledge of the Pharmacopeia.IP/BP/Ph.Eur/USP Skill Required: 1) Handling of the HPLC, 2) Calibration Management. 3)Knowledge of the GLP Environment 4) Handling of the HPLC, 5) Calibration Management. 6)Working Standard, Ref. Standard, Imp Standard, Primary Standard Management Additional Remark: Required candidates background should be in Regulatory environments

HPLC, GC, UV-Vis, FTIR, Karl Fischer Titration GMP, GLP, FDA compliance Quality Management Systems (QMS) Lab equipment calibration Analytical method development/validation Wet chemistry techniques Data analysis, LIMS Problem-solving, troubleshooting

AMRITA VISHWA VIDYAPEETHAM is looking for Lab Instructor to join our dynamic team and embark on a rewarding career journeyLab Preparation: Setting up and preparing laboratory equipment, materials, and experiments before the students arrive.Demonstrations: Conducting demonstrations to show students how to perform experiments correctly and safely.Instructions: Providing clear and concise instructions to students on the objectives of the experiment, procedures to follow, and safety precautions.Guidance: Assisting students during the experiment, answering questions, and guiding them through the process.Safety Oversight: Ensuring that students adhere to safety protocols and guidelines while working in the lab.Troubleshooting: Helping students troubleshoot and resolve issues or challenges they encounter during the experiment.Data Collection: Assisting students in collecting accurate and reliable data during the experiment.Data Analysis: Supporting students in analyzing and interpreting the results of their experiments.

Dear All, Greetings from Vivo Bio Tech Limited! Job Title: Analytical Scientist, Phy-Chem Studies (Agrochemical & Pharma) Experience: 3+ years Location: Hyderabad MOI: - F2F/Virtual 6-day week Job Description: We are seeking a detail-oriented and skilled Analytical Scientist with hands-on experience in conducting Phy-Chem and validation studies for agrochemicals and pharmaceutical compounds. The ideal candidate will have strong knowledge of global regulatory guidelines and be capable of preparing study-related documentation while maintaining audit readiness at all times. Key Responsibilities: Conduct Physico-Chemical studies for agrochemical compounds in accordance with regulatory requirements. Perform method validation studies for agrochemical products as per SANTEE/SANCO guidelines. Execute validation studies for pharmaceutical compounds as per ICH guidelines. Carry out dose formulation analysis to support toxicological and regulatory studies. Prepare and maintain Standard Operating Procedures (SOPs) for newly initiated studies. Develop study plans and compile final study reports as per relevant regulatory guidelines. Ensure all studies are conducted in compliance with GLP, OECD, OPPTS, CIPAC, SANCO, and SANTEE guidelines. Maintain effective communication with Quality Assurance (QA) personnel throughout the study lifecycle. Utilize Microsoft Excel for accurate calculations, data analysis, and result interpretation. Remain audit-ready at all times for sponsor audits, NGCMA inspections, or other regulatory reviews. Desired Candidate Profile: Strong understanding of regulatory frameworks applicable to agrochemical and pharmaceutical studies. Prior experience working in a GLP-compliant environment. Excellent documentation and report writing skills. Detail-oriented with good communication and coordination skills. Flexible and proactive approach, especially regarding audit preparedness. Vivo Bio Tech Ltd Survey # 349/A, Pregnapur Village, Gajwel Mandal. Siddipet District, PIN 502311,Telangana, India. Regards, Chandra Kanth | HRD chandrakanth.k@virinchi.com

Food Tech -calibration ,maintenance and inter of LC-MS,GC-MS method validations and method verification for food and water samples, testing peptides, residue, antibiotics, water samples and water samples using GC-MSMS &LC-MSMS

Role Finance and Administration CSR: 360 degree CFO Like responsibility in running functions and entities Will be responsible for managing accounts, compliances and Tax for ~ 3 not for profit entities Will support financial reporting for CSR Hybrid work structure for work life balance Requirement CA with 5-7 years of experience Deep understanding of financial, legal, tax and compliances matter .

Role: Officer - Quality Control / Quality Assurance Job Location: Nashik At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life. We do so via: Access Providing high quality trusted medicines regardless of geography or circumstance; Leadership Advancing sustainable operations and innovative solutions to improve patient health; and Partnership Leveraging our collective expertise to connect people to products and services. Every day, we rise to the challenge to make a difference and here's how this role, will make an impact: Role Purpose We have Openings in Both QC and QA(IPQA / Documentation / QMS / AQA) . Seeking for candidates (Male/Female) with sound qualification background to ensure the testing of drug product in Quality control lab and to ensure every product is of the highest quality. They shall be concerned with sampling, specifications, testing, documentation, release procedures which ensure that the necessary and relevant tests are carried out under the norms of cGMP. Role & responsibilities Candidate must have relevant experience in Quality control OSD and QMS and able to operate & maintain laboratory equipment/instruments (HPLC, GC, Malvern Particle sizer, dissolution apparatus etc.) as per procedure. To maintain documents as per GLP requirements. To ensure the calibration status of laboratory equipment & instruments. To report and involve in incidence/Deviation/OOS/OOT investigations. Candidate must have sound exposure in the Quality Control Laboratory to supervise and maintain documents and retention of records as per GMP requirements. To ensure the review of QC documents like analytical reports SOPS, Qualification, Logbooks, Raw data sheet, analytical records, calibration and ensuring compliance to observations with proper root cause and justifications. Candidates participate in initiation, review, and closure of OOS/OOT and monitor the CAPA with implementation in Track wise. To ensure the compliance of the Corrective and Preventive Actions (CAPA) necessitated through various activities such as Regulatory Audits, Market Complaints, and Product Recall & Annual Product Review in the QC if applicable. To support Quality Assurance / Compliance /Regulatory Systems, Processes and ensure Monitoring, Execution, Initiation of the Quality Management Systems in Quality Control laboratory. Qualification & Experience Candidate must be B. Pharm/ M. Pharma/ M. Sc In Chemistry Experience- Candidate must have 1 to 4 years experience in a reputed pharma industry. Candidates must be willing to work in shifts Candidate who have faced regulatory Audits like FDA & MHRA Audit will be preferred.

The job requires a candidate with 2 to 7 years of experience in Analytical Chemistry for a position at a Chemical Manufacturing Company's Pharma Division in Ahmedabad. The salary ranges from Rs. 35,000 to Rs. 40,000 per month based on the candidate's knowledge. The responsibilities include handling analytical instruments such as HPLC, GC, UV, IR, performing instrument calibration, analyzing finished products and raw materials, and conducting wet lab analysis. The job type is full-time and requires in-person work at the specified location. Contact person for the position is Gopi (HR) reachable at 7777981971.,

You will be responsible for reviewing and conducting chemical testing of raw materials, finished products, cosmetics, Ayurveda, Sidha & Unani products. You will need to accurately enter the test results into the LIMS software. Additionally, you will be required to handle instruments like HPLC, GC, FTIR, Dissolution, etc. Technical documentation in compliance with FDA, CDSCO & Ayush standards for audits will also be part of your responsibilities. The position is based in Gurugram and requires a minimum qualification of B.Pharma, M.Pharma, MSc. Chemistry or a related field. The ideal candidate should have 2 to 15 years of relevant experience.,

Greetings from Avani Consulting. We are hiring QC Officer / Trainee and QC Associates for a leading Pharma API Company in Mysore. Positions: 1. QC Officer / Trainee : EXP: 2 to 3 year exp in Pharma Company. Salary : Up to 4LPA ( Take way home only . NO Parks & Benefits ) 2. Quality Control Associates - API : EXP: 5 to 9 year exp in Pharma API Industry. Salary : Up to 7.5LPA ( Including Parks & Benefits ) Preferred candidate profile Qualification : M.Sc. Chemistry Experience : Pharma -API Quality Control Role & responsibilities : Handling and troubleshooting of Analytical Equipment's like HPLC, GC-HS, FT-IR, UV, Potentiometry, Polarimeter, ICP and KF. Handling of Analytical Method development and Method Validations. Qualification of Equipments as per GLP requirements. Analysis of Inprocess, Stability and FG Samples as per the Specification. Operation, Maintenance and Calibration of HPLC and GC as per the schedule. Review of results and release of Analytical test report or Certificate of Analysis. Maintenance of minimum consumables in the Laboratory. Planning and coordination to release on time results delivery. Investigation of OOT/OOS in the laboratory. Sampling of Raw Material, Inprocess and Finished product samples. Basic knowledge on LIMS/SAP. Handling 21 CFR compliance. ***NOTE :: NO CHARGES Looking forward to know about your interest. Thanks & Regards Priyanka Palit [9518220852 | priyanka@avaniconsulting.com]

Experience in routine Analysis, Calibration, Analytical Method Development & Validation, Hands on experience over various analytical instruments like HPLC & GC, Documentation as per regulatory requirement.

Perform analysis of raw materials, in-process samples, and finished products using HPLC and GC as per approved specifications and methods. Operate, calibrate, and maintain analytical instruments like HPLC, GC, UV-Vis Spectrophotometer, FTIR, and Dissolution apparatus. Troubleshoot analytical instruments and coordinate with engineering or vendors for timely servicing when needed. Prepare and review analytical reports, SOPs, calibration records, and logbooks. Ensure all testing activities comply with cGMP, GLP Participate in internal audits, regulatory inspections, and support CAPA implementation where applicable. Manage sample receipt, labeling, storage, and disposal as per SOP. Ensure timely testing and release of materials and products. Participate in on-the-job training programs and ensure adherence to updated testing techniques and quality practices. Mentor junior analysts on analytical techniques and compliance requirements.

Job Purpose: To be courteous to patients and customers. Job Responsibilities: Be well informed of hospital hierarchy and key contact staff in every department. Departmental locations and its respective functions. Give complete and correct information to all (staff/visitors/patients/ attendants). Keep the list of doctors / staff/ functions of every department Proper grooming as per hospital uniform policy. Greeting the staff, seniors, patient attendants and visitors. Maintain Hospital premises and property. Deal with everyone with respect and integrity. Checking the nominal register daily to capture data required for funnel. Doing follow up call with the patient on daily basis. Guiding the patients who want to avail hospital services. Preparing statistical data as and when required by the management. Candidate Requirements: Able to work accurately and with minimal supervision. Ability to comprehend written instructions given by the related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team. Enthusiasm. Open-mindedness.

Job Title Executive Food Box Job Description Summary Food Executive responsibility to oversee operation of outlet, audit both internal & external, ensuring the house keeping manpower in terms of day-to-day activities, FSSAI audit coordination, making checklist and shift schedule. Job Description Food Executive responsibility to oversee operation of outlet, audit both internal & external, ensuring the house keeping manpower in terms of day-to-day activities, FSSAI audit coordination, making checklist and shift schedule.

Role & responsibilities Basic Biological Laboratory techniques. ELISA, Mammalian cell culture, HPLC, Flow cytometry. Molecular Biology Techniques. Documentation as per GLP. You can also share your CVs at pradnya.raut@accutestglobal.com for early call backs.