33 Hplc Analysis Jobs - Page 2

Role & responsibilities Preferred candidate profile Perks and benefits

a. Candidates should have hands on experience in qualification and calibration of instruments like HPLC/Dissolution/UV/GC/IR/KF. b. Candidate should be well conversant with GXP, QMS and SOPs preparation. c. Should able to work on software like Empower, LIMS, Nichelon, QAMS & DMS. d. Qualification : M.Sc ./M. Pharma/B. Pharma. e. 4-7 years of experience will be preferred

Role & responsibilities Should be knowledge in handling of HPLC and GC Analysis to be performed for API, Stability, intermediate and in-process samples. Preparation of HPLC and GC Method validation protocols and reports. Perform analytical method validations by HPLC and GC and Maintenance of GLP and safety precautions in working laboratory. Responsible for maintenance and calibrations of HPLC and GC Please ensure the following mandatory documents are submitted before the interview day: Updated CV (1 copy) Copy of all Educational Certificates (1 set) Passport-size Photograph (1 copy) Aadhar Card Copy (1 copy) Documents pertaining to your previous employment(s) (Originals along with a set of photocopies, if applicable): Last 3 Months' Pay Slips Present Organization Appointment Letter Latest Increment / Salary Revision Letter Last Six Months Bank Statement of your Salary Account

Role: Officer / Executive - Quality Control 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 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 2 to 6 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.

Candidate should have Pharma API company background Conduct routine and non-routine analysis of raw materials, intermediates, and finished products using analytical instruments (HPLC, GC, UV-Vis, FTIR, etc.). Perform method development, method validation, and stability studies as per ICH guidelines. Operate and maintain analytical instruments and ensure proper calibration and documentation. Prepare and review analytical documents such as protocols, reports, and SOPs. Ensure compliance with GMP/GLP and regulatory requirements. Investigate out-of-specification (OOS) and out-of-trend (OOT) results and support root cause analysis. Coordinate with cross-functional teams for timely project execution.

Key Responsibilities Quality Strategy & Planning Develop and implement quality control standards, procedures, and policies. Define inspection criteria and quality benchmarks. Team Management Lead and supervise a team of quality inspectors or analysts. Provide training and guidance to QC staff. Manage and supervise QC laboratory activities Use effective negotiation skills to drive alignment and resolve conflict Inspection & Testing Oversee routine inspections and testing of raw materials, in-process, and finished products. Ensure compliance with internal and external specifications and regulations. Documentation & Reporting Maintain detailed records of quality control activities. Analyze QC data and generate reports to identify trends and areas for improvement. Compliance & Audits Ensure compliance with ISO, GMP, or other industry-specific standards. Coordinate and support internal and external audits. Problem Solving Investigate product quality issues and customer complaints. Implement corrective and preventive actions (CAPA).

Qualification : M. Pharmacy (Analytical)/M.Sc.(Analytical) Experience : 2-3 yrs. (Formulation Experience) Location : Balnagar (Hyderabad) Skills Required: Sound knowledge of Dissolution, Analytical method development for tablets, capsules, oral solutions, ICH stability testing, Water HPLC, UV-Visible Spectrophotometer, KF Auto tiltrotor, Analytical method validations, transfer and verifications as per ICH guidelines and USP/BP guidelines, Analysis of in-process, stability & protocol driven samples. Reports, Protocols and STP, SOPs Preparation. GLP Activities. Chromatographic software like Empower. Prefer Male people & Immediate Joiners.

Experience - 2 Years + In Formulation QC * QC - Finish Product - GC/HPLC/ Dissolution/AAS/UV * QC- In process- HPLC/UV/Dissolution/GC * QC - Validation- HPLC/UV/GC/Dissolution * RM - HPLC * Stability HPLC GC UV Dissolution * RM Reviewer