HPLC Jobs

Perform testing of Raw Materials, Finished Goods, and In-Process Materials and report analytical results accurately.2 Handle and operate analytical instruments such as HPLC, UPLC, GC, ICP, DSC, XRD, and PSA.3 Carry out calibration of analytical instruments as per the master calibration schedule.4 Investigate analytical errors/deviations, identify root causes, and implement corrective and preventive actions (CAPA).5 Prepare laboratory SOPs, analytical study reports, and related technical documentation.6 Execute method validation activities and prepare validation protocols and reports.7 Review analytical chemistry testing records for raw materials, stability samples, and finished products for compliance and accuracy.8 Prepare and review specifications, methods of analysis, and analytical development reports.9 Ensure compliance with quality systems, laboratory procedures, and regulatory guidelines.10 Discuss daily work plans with supervisors/managers and mentor junior laboratory personnel.11 Participate in project meetings and prepare weekly and monthly progress reports for management review.12 Perform routine laboratory activities including equipment maintenance, chemical inventory management, and laboratory housekeeping.13 Maintain strict IP confidentiality and comply with all related data privacy and company policies.If You are interested then send me cvcapitalplacement21@gmail.com931559078`17

We are seeking a dedicated Quality Control Analyst to join our team in Nalagarh. The ideal candidate will have 2 to 4 years of experience and possess a degree in B.Pharma or B.Sc. This role requires a strong focus on ensuring product quality and compliance with regulatory standards.**Key Responsibilities:**- **Conduct Testing**: Perform various tests on raw materials and finished products to ensure they meet quality specifications. This includes physical, chemical, and microbiological analysis.- **Documentation and Reporting**: Maintain accurate records of test results and document deviations or issues. Timely reporting helps in identifying trends and implementing improvements.- **Quality Assurance Compliance**: Assist in maintaining compliance with quality standards and regulations set by industry and government bodies. This includes understanding and following standard operating procedures (SOPs).- **Collaboration with Teams**: Work closely with production and R&D teams to address quality-related concerns. Effective communication is essential for improving processes and products.- **Problem-Solving**: Identify root causes of quality issues and propose corrective actions. This analytical approach aims to prevent reoccurrence of defects.**Required Skills and Expectations:**Candidates must have strong analytical and critical thinking skills to assess complex quality issues effectively. Attention to detail is essential to ensure accurate testing and documentation. Knowledge of quality control regulations and practices is required. Proficiency in software applications for data analysis and reporting is preferred. A collaborative mindset is crucial for working well within a team. Candidates should also demonstrate a commitment to continuous learning and improvement in quality processes.

We are looking for a QC Chemist to join our team in Dahej. This is a full-time position suitable for fresh graduates with a B.Sc degree. The ideal candidate must be male and will work from the office.**Key Responsibilities:**- **Conduct Quality Control Tests:** Perform various tests on raw materials and finished products to ensure they meet required standards and specifications.- **Record Data Accurately:** Document all findings and results from testing processes accurately to maintain a clear record of quality assessments.- **Assist in Troubleshooting:** Identify any quality-related issues during testing and collaborate with the team to develop effective solutions.- **Maintain Lab Equipment:** Regularly check and maintain laboratory equipment to ensure they are in good working condition and ready for use.- **Follow Safety Protocols:** Adhere to safety guidelines and protocols in the laboratory to ensure a safe working environment.**Required Skills and Expectations:**- Candidates should have a B.Sc in Chemistry or a related field.- Strong attention to detail is essential, as accuracy is crucial in quality control processes.- Good communication skills are required to effectively share findings and collaborate with team members.- Basic knowledge of laboratory safety and testing procedures is expected.- Willingness to learn and adapt to new techniques and technologies in the field of quality control. If you are passionate about chemistry and quality assurance, we encourage you to apply.

About Company- We are a WHO-GMP Certified company , having 29+ yrs of experience in Pharma sector. Consern's portfolio comprises of over 400+ products and a nexus of prescribing Doctors from Neuro, Gynea, Cardio, Diabetics, Derma, Gastro, Ortho & General health care.Job role- - Review QC doc (Online or Offline)- Review audit trail- Knowledge of QC instruments - Documents for OOS/OOT incident

Designation :- Senior Officer/Officer/ExecutiveQualification:- MSc/B. Pharma Experience :- 4 Years To 8 YearsSalary:- As Per Interview Gender:- MaleJob Responsibilities:- i) Candidate should have good analytical techniques of chromatography (Operation of HPLC, GC etc.)ii) Sample analysis of FP and Stability samples (e.g. RS, Assay, Dissolution, Content uniformity, Blend Uniformity)iii) Candidate should have chromatographic processing skill on Empower software.iv) Knowledge of LIMS/ELIMS.v) Expertise in good laboratory practices (GLP), and the operation and maintenance of laboratory equipment.vi) Monitor and analyze test data trend identifying OOT, OOS and Lab incident.vii) Ensure compliance with safety, regulatory guideline including good workbench practices.viii) Preparation of analysis data record accurately in LIMS/ELIMS.ix) Stability Sample analysis and trending of stability dataJob Location:- Daman,DNDIndustry:- Reputed Manufacturing Industry

Industry :- Chemical / Api / Pharmaceuticals education :- Bsc / Mscexp:- Fresher to 8 Yearrequired :- Male / Female

We have vacancy for 6 Quality Control Analysts in Rudrapur, Uttarakhand, Freshers can also apply. Educational Qualification : B.Sc, B.Pharma, M.Pharma, M.Sc Skill Chemical analysis, Instrumental analysis, Sample preparation. Equipment maintenance. etc.HPLC: 2 analystsGC: 2 analystsIR: analystsCandidates with prior experience in pharmaceutical quality control environment will be preferred.Send Resume @7861999933Email At toscrecruitments@gmail.com

BSC or MSC with 2- 4years experience in chemical testing laboratory, uv , hoc , gc , was, ice does etc preferred

HPLC, GC, AMV

Job Summary:We are seeking a detail-oriented and dedicated Quality Control (QC) Chemist to perform routine analysis and testing of raw materials, in-process samples, and finished products. The ideal candidate should have sound knowledge of analytical instruments such as HPLC, UV, IR, and dissolution apparatus, along with good documentation and GMP compliance understanding.Key Responsibilities:Perform chemical and instrumental analysis of raw materials, in-process, and finished products.Operate and calibrate analytical instruments such as HPLC, UV-Visible Spectrophotometer, IR, and others as per SOPs.Maintain and review analytical documents, logbooks, and test reports.Ensure all activities are performed in compliance with GMP, GLP, and regulatory requirements.Conduct stability studies and prepare required documentation.Assist in method validation, equipment qualification, and troubleshooting.Ensure proper sampling, labeling, and storage of reference standards and samples.Participate in internal audits, inspections, and quality improvement initiatives.Timely reporting and escalation of any deviations or non-conformance.Skills & Competencies:Sound knowledge of analytical techniques and instrumental analysis.Proficient in handling HPLC and other laboratory instruments.Familiarity with Good Laboratory Practices (GLP) and documentation practices.Strong attention to detail and a quality-oriented mindset.Good communication and team coordination skills.Eligibility Criteria:Educational Qualification: B.Sc / M.Sc in Chemistry, B.Pharm / M.PharmExperience: 0 to 2 years of experience in QC (Freshers with relevant academic background are also welcome)Should have basic understanding of GMP, GLP, and ICH guidelines.

Location: On-site Nalagarh, Himachal PradeshExperience: 12 years (Mandatory)Qualification: B.Sc. in Chemistry / Microbiology / Biotechnology / Life SciencesAbout the Role:We are looking for a dedicated Quality Control (QC) Officer to join our pharmaceutical manufacturing team at our Nalagarh facility. The ideal candidate will have hands-on experience with laboratory testing and strong documentation practices in a GMP-regulated environment.Key Responsibilities:Conduct testing of raw materials, in-process samples, and finished products.Operate and maintain analytical instruments like HPLC, UV, IR, pH meter, etc.Ensure accurate and timely documentation as per cGMP and GLP guidelines.Perform stability studies and environmental monitoring (if required).Participate in lab audits, calibration, and equipment qualification.Maintain safety and hygiene in the lab environment.Desired Profile:B.Sc. in Chemistry / Microbiology / Biotechnology or relevant field12 years of QC experience in a pharmaceutical formulation unit (mandatory)Sound knowledge of GMP practices and analytical techniquesAttention to detail, good documentation habits, and strong analytical skillsMandatory Proficiency in written and verbal EnglishJoin a team committed to delivering high-quality, affordable medicines.Apply now to become part of our quality-driven organization!#QualityControl #PharmaJobs #ChemistryJobs #QCOfficer #PharmaceuticalIndustry #HimachalJobs #BScJobs #NalagarhJobs #PharmaCareers #GMPCompliance

Performing HPLC Analysis: Running samples through HPLC instruments, interpreting results, and documenting findings. Maintaining Equipment: Ensuring HPLC systems are calibrated, maintained, and operating correctly. Method Development and Validation: Contributing to the development and validation of HPLC methods for various applications. Data Handling and Reporting: Managing raw data, compiling results, and generating reports as needed. Compliance with GLP/GMP: Adhering to Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) guidelines. Troubleshooting: Addressing any issues or problems that arise during HPLC analysis. Safety and Housekeeping: Maintaining a safe and organized laboratory environment. Documentation: Keeping accurate records of all analytical activities and data.

* HPLC/GC analysis *Assay, RS* Chiral, Purity*Residual solvent analysis

Need Qc chemist who having knowledge of Hplc

QC Officer: (Daman)QC Officer is responsible to perform all functions related to quality of product of the company.He is responsible to test the product of the company.He has to develop strategies to develop the products of the company.He must be familiar with production process so that he can contribute in error reduction and process enhancement..He has to make sure that all the products pass through auditing and testing.He also has to make sure that all the legal standards are met.He has to review the organization process and have to suggest continuous improvement.He must have very good communication skills.He must have a problem solving skills and should be able to provide effective solution.He must have a deep knowledge of HPLC.B.Sc or M.Sc (Chemistry) with 2 to 3 years experience in pharmaceutical company If Experience in Inject able plant than it will be more preferable.Send me resume on career.talenthunt.th@gmail.com/cv.talenthunt1@gmail.com Whatsapp me on 9998137070/7016504771

Job Openings for 3 Pharmaceutical Quality Assurance Executive Jobs with minimum 2 Years Experience in Siltara, Raipur, having Educational qualification of : B.Pharma, M.Pharma with Good knowledge in Quality Check, Hplc, Uv-visible Spectrophotometer, LAB Testing, Pharmaceutical Quality Control, Quality Analysis, Testing etc.

Formulation Company Shaimil laboratoriesTime : 9 to 5: 30BonusPF also Available

Responsibilities:* Collaborate with production team on quality improvement initiatives* Ensure compliance with regulatory standards through documentation and training* Conduct regular quality checks using HPLC methods

Job Openings for 2 Quality Control Chemist Jobs with minimum 2 Years Experience in Siltara, Raipur, having Educational qualification of : B.Pharma, M.Pharma with Good knowledge in Hplc, Uv-visible Spectrophotometer, Product Quality, Quality Check etc.

We are seeking BSC or MSC chemist with experience in GC MS( Gas Chromatography- Mass spectrometry ).at NaviMumbai laboratory.

Preparing test solutions, compounds,and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials.Experience in making lab SOPs and study reports6+ yrs of Agrochemicals/chemicals in Green field/brown field ProjectsExp in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD & DSC

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automationPreparation and review of Specifications, Method of analysis procedures and Analytical development reportsExperience in making lab SOPs & study reports

1.Understand the project requirements & deliverables from supervisor/manager2.Carry out literature search by using SciFinder, Reaxys and other search engines3.Comprehend and discuss the MSDS with supervisor/ team members.4.Identify and mitigate any potential safety risk with the help of Manager5.Plan, setup, monitor, and workup chemical reactions independently6.Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc)7.Isolate product and Optimize reaction conditions for improved yields and output8.Purify compounds by different methods using chromatography, distillation and crystallization etc.9. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc10.Ensure parallel execution of multiple reactions conducted both by self and the team11.Scale up of R&D developed products to kg scale and then technology transfer to pilot plant12.Troubleshoot as appropriate for successful execution with intimation to supervisor13.Discuss research findings and work plan on daily basis with supervisor/ manager and Mentor junior lab personnel14.Document reactions, research findings/ observations accurately in lab note books to ensure data integrity15.Participate in project meetings and prepare daily, weekly and monthly reports and submit to Manager16.Writing regular updates, final reports, PDR preparations and inter departmental communications17.Regular lab duties including equipment maintenance, chemical inventory and lab clean-up18.Maintain strict IP Confidentiality and adhere to all related data privacy policies