156 Hplc Analysis Jobs - Page 5

Key Skills: Hands-on experience in HPLC handling . Proficiency in Empower3 software . Strong knowledge and practical exposure to instrument analysis . This is a walk-in post. Even then candidates are encouraged to share their resumes in advance at talenthire-unit4@metroapi.com with the subject line Profile for Quality Control . This will help our team connect with you beforehand and guide you about the position. We warmly welcome candidates who are currently working in Visakhapatnam and nearby areas. Note: Candidates with relevant skills in the Quality Control department are requested to apply for this position. .

B.Sc./M.Sc. with 1–4 years in QC (API). Hands-on with HPLC, GC, UV, and wet analysis. Experienced in raw material, in-process, and finished product testing. Strong in GMP, documentation, and analytical techniques. Required Candidate profile B.Sc./M.Sc. with 1–4 years’ QC experience in API. Proficient in HPLC, GC, wet lab testing, and GMP documentation. Detail-oriented, accurate, and skilled in analytical methods. Perks and benefits GMP GLP plant| Growth| Safety| Compliance| Perks

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control Experience: (01 12Years) HPLC/ Stability/ GC/ IP/ FP/ RM/ Validation/ Reviewer QUALIFICATION : B.Sc, M.Sc, B. Pharm and M.Pharm with relevant experience DESIGNATIONS: Officer, Jr.Executive, Executive, Sr.Executive & Asst. Manager INTERVIEW VENUE: Hotel: RAUNAK Restaurant Ground Floor, Opp. Axis Bank, Bitna Road, Kalka Shimla National Highway, Pinjore, Haryana 134102 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates Experience in HPLC - Formulation is Man...

Sampling and Inspection of received goods in stores, observation to be maintain. Operation, calibration and record maintained of Q.C Instruments Handling of sophisticated instruments (like GC, HPLC, UV.etc)

Location: Ankleshwar Department: Quality Control Experience: 4 to 7 years Position : Executive Job Description: We are looking for a skilled HPLC Analyst (Executive QC) who will be responsible for ensuring quality compliance in laboratory testing of pharmaceutical raw materials, intermediates, finished goods, and stability samples. Key Responsibilities: Adhere to GLP (Good Laboratory Practices) and laboratory safety protocols . Perform routine and stability analysis of raw materials, intermediates, finished products, in-process samples , returned goods, hold time studies using HPLC . Maintain online documentation and ensure CFR 21 Part 11 compliance. Record and maintain analytical results in...

Role & responsibilities Team: Excipients Team , Analytical Sciences Qualification : Masters with 5+ years or Ph.D. with 0-2 years of industrial experience. For candidate with PhD, expected to have PhD degree in field of Excipients or Biopharmaceutical drug analysis related topic. Key Words : HPLC Analysis, ELSD, CAD and RI detector, Excipient analysis, Analytical method development, qualification and method transfer, mABs/Large molecules Key Job Responsibilities : Candidate should have hands on experience on analytical methods like Spectrophotometry, HPLC based methods (ProA, SEC, CEX, RP) with knowledge of HPLC softwares like Empower/Chromeleon. Candidate should have experience in biologica...

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

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 thi...

You should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of experience. Immediate joiners are preferred for this role. As a part of your role, you will be responsible for conducting HPLC analysis of solid orals/nasal products, handling QC activities related to Raw Materials, Packing, In Process, and Finished Products, and ensuring compliance with GMP/GLP Practices. The ideal candidate should have 2-8 years of experience and should have prior experience working in regulated plants approved by USFDA/MHRA. Working in this position will provide you with the opportunity to work in a fully automated world-class manufacturing facility, handle diverse dosage forms in ...

The ideal candidate for this role should possess a Bachelor's or Master's degree in Pharmacy or Science with 3-8 years of relevant experience. Immediate joiners are preferred for this position. As a member of our team, your responsibilities will include conducting HPLC analysis of Solid Orals and Nasal products, hands-on experience in Quality Control activities related to Raw Materials, Packing, In Process, and Finished Products, as well as ensuring compliance with GMP/GLP practices. The preferred candidate will have 2-8 years of experience and prior exposure to working in regulated plants, specifically those approved by USFDA/MHRA. In return, you will have the opportunity to work in a fully...

Role & responsibilities :- 1) Knowing HPLC/ GC, Dissolution, UV, FT-IR, Potentiometer Troubleshooting, Calibration, Method Validation and Method Development. 2) Perform the analysis individually for In process and stability samples as per plan. 3) Follow Good manufacturing practices, Good laboratory practices and Good documentation practices in ADL. 4) Method Development of new products for test like Cleaning, Assay, Residual solvent, Dissolution & organic impurities. 5) Preparation, storage and usage of Volumetric / Reagent / Standard / Indicator solution. 6) Perform the calibration and verification of all instrument / equipment as per calibration scheduled. Preferred candidate profile :- P...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (01-10 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC ARD - OSD Experience: (02-05 Years) •HPLC/ FG/Analytical Method validation/ Stability/liquid chromatographic PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, PACKING Experience: (02-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer, Jr.Executive, Executive & Sr.Executive INTERVIEW VENUE: Hetero Labs Limited (Formulation Unit). Chakkan Road, Kaly...

Role & responsibilities Familiar/experienced of HPLC/Dissolution apparatus breakdown/services Preferred candidate profile Male

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Role & responsibilities Quality Control: Min 2-5 years relevant experience in Quality Control Lab. Hands on experience in handling various instruments like (HPLC is must),GC,KF. Knowledge of GLP, GDP and lab safety. Awareness of Quality-QAMS, LIMS software. Qualification: M.SC / B.SC (Chemistry) with min. 02 to 05 Years Quality Assurance: Min 2-5 years relevant experience in Quality Assurance. Sampling activity, IPQA, QAMS, Documentation, Review of BPR. Awareness of Quality-QAMS software etc. Qualification: M.SC / B.SC / B. Pharma with min. 02 to 05 Years Note: Highest degree must have 1st Class/60 % marks and if 2nd class then 05 years of experience is must

Role & responsibilities Quality Control: Min 2-5 years relevant experience in Quality Control Lab. Hands on experience in handling various instruments like (HPLC is must), GC,KF. Knowledge of GLP, GDP and lab safety. Awareness of Quality-QAMS, LIMS software. Quality Assurance: Min 2-5 years relevant experience in Quality Assurance. Sampling activity, IPQA, QAMS, Documentation, Review of BPR. Awareness of Quality-QAMS software etc. Note: Highest degree must have 1st Class/60 % marks and if 2nd class then 05 years of experience is must.

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control (GMP / GC / LCMS / HPLC) Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits Common Requiremen...

Instrument Analysis GC/HPLC for QC department Min 2-5 only API CO 1 to 3 year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

1. To maintain and ensure cGMP/cGLP in the Quality Control Department. 2. To maintain documents as per GLP requirements. 3. To perform the activity as per work allotment. 4. To follow the SOP/ATP/STP and protocols. 5. To maintain the laboratory neat and clean. 6. To perform sampling and analysis of Packing material sample and maintain online documentation. 7. To maintain the data integrity and to plan the work such as to give maximum productivity within stipulated time. 8. To perform daily monitoring of temperature. 9. To participate with supervisor to close the investigation for deviation, Incidents, OOT and OOS. 10. To follow safety procedure in the laboratory. 11. To report the result of ...

Roles and Responsibilities Conduct quality control tests on finished products, packing materials, and raw materials using HPLC analysis. Ensure compliance with GMP guidelines and company standards for product testing. Validate stability studies, batch records, and release finished products to the market after successful testing. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of test results, reports, and documentation.

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with...

QC Daily Analysis Conducted tests Assay and Dissolution KF ,PH Preparation of solutions for HPLC Analysis Documentation preparation like SOP,MOA,MSDS,STP

3 to 6 years Food testing experience NABL accreditation (ISO-17025:2017) compliance Aware of FSSAI / APEDA / EIC / IOPEPC regulatory requirement Strong analytical analysis of Fatty acid profile, Vitamin & Aflatoxins analysis using HPLC & GC equipment

Hands on experience in HPLC/GC including method development, routine analysis and method validations along with good documentation practices. Responsible to perform the Analytical method validation, method verification and method transfer activities.

Roles and Responsibilities Conduct quality control analysis of bulk drugs, APIs, and finished products using GC, HPLC, and other relevant techniques. Develop and maintain SOPs for laboratory operations, sampling procedures, and testing protocols. Ensure timely reporting of test results and maintain accurate records.