802 Hplc Jobs - Page 31

To perform analysis on HPLC and Gas Chromatography Responsible for preparing SOPs Responsible for calibration of HPLC and Gas Chromatography as per schedule calibration of QC instrument To assist the Head QC in investigation of OOS results.

Looking for a Service Engineer who can capable to handle service-related activities for Core as we'll as Chromatography systems. The Services Technician will be responsible for delivering the desired customer service experience. The goal is to drive service success that improves customer satisfaction, maximizes customer retention and increases profitability. Main Responsibilities & Tasks: Engineer should have experience on LPLC and HPLC product segments. Overall chromatography experience will get priority. Provide service and customer support during field and inhouse visits or dispatches. Manage all on site installation, repair, maintenance and test tasks. Diagnose errors or technical problems and determine proper solutions. Produce timely and detailed service reports. Ensure the timely and correct documentation of processes. Operate vehicle in a safely manner and use field automation systems Follow all companys filed procedures and protocols Cooperate with technical team and share information across the organization Comprehend customer requirements and make appropriate recommendations / briefings Contact customers concerning processes of the customer file Build positive relationships with customers Qualification & Skills: Engineering degree in chemistry, Electronics, Electrical and Instrumentation or similar 5-10 years of proven field service experience Ability to troubleshoot, test, repair and service technical equipment Ability to work flexible shifts and to adapt to changing work schedules High customer orientation Team spirit Familiarity with mobile tools and applications Good command of spoken and written English

Role & responsibilities Should able to handle HPLC & GC,PH Meter, Knowledge on GMP&GLP Preferred candidate profile Familiarity with analytical testing techniques using HPLC/GC/FTIR/Dissolution/UV. Performing calibration of instrumentations Testing of finished product, raw materials, packaging and stability Perform analytical testing - HPLC, FTIR, UV

Quality Control (Immediate Joiners only) Role & responsibilities Sampling and Analysis of water, Raw materials, Packing materials. Sampling of swab samples. Analysis of In process, Finished product, Swab and Stability samples. Responsible for calibration of Balance, conductivity meter and pH meter. Responsible for preparation and pasting of approved labels. Responsible for In process and Finished product sample receipt and analysis. Responsible to perform the analysis by UV-Visible spectrophotometer, KF Autotitrator, Polari meter, HPLC, GC, FTIR, Dissolution, Disintegration, Friability and Hardness tester, Tap density, Melting point apparatus. Responsible for the preparation of Specifications, STP, Analytical Raw data sheets for Raw Materials, Packaging Materials. To ensure that the proper maintenance of department, premises and equipment. Preferred candidate profile B. Pharm / M. Sc in Chemistry or Organic Chemistry or General Chemistry or Pharmaceutical Chemistry or Industrial Chemistry Experience: 3 to 8 years

Dear Candidate, WE ARE HIRING Department: - Production- DS Designation: - Dy Manager / Manager Qualification: - Preferably Post Graduation in Science Experience: - 15+ Years Age: - Between 35- 40Years Mandatory: - Should come in all shifts, including Night shifts Role: Shift-in-charge for entire DS floor Job Description: > Strong Functional knowledge of DS Biologics (Chromatography and related purification experience protein/ Insulin handling experience preferable). Capable of handling large teams as we have around 45 members in each shift, around 50% of contractual staff. Strong administration / team management capabilities to streamline GMP across the floor. Monitoring the efficiency of employee performance on the job. > Coordinating with other departments to ensure that production runs smoothly Ensuring that all safety regulations are followed in the production area. Managing all aspects of production, including hiring workers, ordering supplies, maintaining production schedules, and overseeing equipment maintenance. Reviewing production schedules and work orders to ensure that production goals are being met in handling QMS activities. for more details please reach out Venkat -9381915043 or please share your CV to venkateswara.k@talent21.in

Handling of instruments like HPLC, GC, LC-MS, GC-MS, FTIR Interpretation for Analytical results and characterization data for LC-MS, GC-MS, FTIR and NMR Knowledge of Method development and validation Knowledge of OECD & GLP preferable Required Candidate profile M.Sc (Chemical) GLP Lab

Handling of instruments like HPLC, GC, LC-MS, GC-MS, FTIR Interpretation for Analytical results and characterization data for LC-MS, GC-MS, FTIR and NMR Knowledge of Method development and validation Knowledge of OECD & GLP preferable Required Candidate profile M.Sc (Chemical) having 10-12 years of experience

Preferred Qualification: M.Sc Organic Chemistry with more than 70% aggregate Looking for freshers who can join immediately Roles & Responsibilities: Synthesize, and characterize novel bioactive molecules under supervision of scientist/senior scientist Knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, multi-step synthesis. Knowledge of techniques in synthesis, purification, and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, etc.). Maintain Lab note book. Understanding of systems and process pertaining to safety, health and environment. LAST DATE for application: 14th May 2025. Selection Process: Candidates who have applied shall be shortlisted based on their academic marks. Technical test and aptitude test will be conducted online on 15th May 2025. Interviews will be scheduled on 17th May 2025 for the shortlisted candidates at Aurigene Oncology Ltd, Bangalore.

Ensure that the manufactured products consistently meet established standards, customer specifications, and industry regulations Optimize processes and drive continuous improvement initiatives Product Modification/ Development as per customer need Required Candidate profile B. Sc Chemistry with M. Sc Polymer Science mandatory 12+ years' experience in Quality Assurance & Control in a chemical/ polymer manufacturing company (preferably in polystyrene manufacturing)

Company Overview: We are a reputed pharmaceutical company specializing in the manufacturing of Oral Solid Dosage (OSD) formulations. Committed to high-quality standards and regulatory compliance, we are looking for a dynamic and experienced professional to join our Quality Control team. Job Purpose: The Assistant Manager Quality Control will oversee and manage day-to-day QC operations to ensure compliance with cGMP, GLP, and regulatory requirements for OSD manufacturing. This role is critical for maintaining product quality and supporting internal and external audits. Key Responsibilities: Supervise and lead a team of QC analysts and chemists in routine testing of raw materials, in-process samples, finished products, and stability samples. Review and approve analytical data, reports, and documentation in compliance with regulatory standards (USFDA, MHRA, EU, etc.). Ensure adherence to SOPs and perform periodic reviews and updates of QC procedures. Investigate out-of-specification (OOS), out-of-trend (OOT), and laboratory incidents, and implement CAPA. Coordinate and support analytical method validation, method transfer, and instrumentation qualification. Maintain and calibrate laboratory instruments such as HPLC, GC, UV, IR, and Dissolution testers. Assist in audit readiness and participate in regulatory and customer audits. Maintain LIMS or other data management systems effectively. Prepare and deliver periodic training sessions for QC staff. Desired Candidate Profile: Education: M.Sc. (Chemistry), B.Pharm, or M.Pharm Experience: 6–10 years in Quality Control within a regulated OSD manufacturing environment Skills: Hands-on experience with HPLC, GC, and other analytical instruments Sound understanding of cGMP, GLP, ICH guidelines Good documentation and review skills Proficiency in handling OOS/OOT and deviations Strong communication, leadership, and team management abilities Why Join Us? Opportunity to work in a growing, globally compliant pharma facility Competitive salary and performance-based incentives Strong focus on career development and technical training

QC Testing,HPLC,RP, Stability,GLP

Supervision of Sampling, Sample preparation, Sample Analysis, Instrument Calibration, Documentation etc.

We are hiring for a Public listed BSE / NSE - Pharma - API / Crop Protection / Animal Health Intermediates Mfg CDMO / CRAM Company. Role : Team Leader - ADL Title : Sr. Scientist R&D Centre Level : Deputy Manager CTC : Ceiling Rs 15 Lpa Experience: Minimum 14 years to Max 18 years Those working at R&D Centres of Crop Sciences / API / Specialty Chemicals are only eligible. Formulations / Vaccines / Bio labs are not eligible. Formulations Qualification : Full Time M.Sc in Organic Chemistry / Analytical Chemistry only. Those in other specialisation of Chemistry are not eligible. Those with Correspondence Masters degree won't qualify. Location: Pune Saturdays: 2nd / 4th Not working Local Company Transport on the major Trunk Road available. Those working in QC Labs not eligible. Those working in Foods Lab not eligible. Those working in Testing Laboratories should not apply. Role: To follow Good laboratory Practices. To follow the procedures mentioned in SOP's and General test Procedures To ensure availability of respective working standards/samples for method validation and method transfer activity To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working To fulfil the requirement of RA department for different filings To review method validation data & preparation of respective protocol reports To ensure documentation of analytical activities as per Co. policy To provide complete support for internal & external Audits at Pune location To develop suitable analytical methods to support cross functional teams To prepare and review method validation protocols, data and reports

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Prepares medications by reviewing and interpreting physician orders; detecting therapeutic incompatibilities. work flow; verifying their preparation and labeling of pharmaceuticals; verifying order entries, charges, and inspections.

Job Summary: We are looking for a passionate and detail-oriented QC Chemist (Fresher) to join our Quality Control team. The ideal candidate will assist in ensuring the quality and compliance of raw materials, intermediates, and finished products through rigorous testing and documentation. This is an excellent opportunity for recent postgraduates to begin a rewarding career in the pharmaceutical or chemical industry. Key Responsibilities: Perform routine and non-routine chemical analyses of raw materials, in-process samples, and finished products. Conduct analytical tests using instruments such as HPLC, GC, UV-Vis Spectrophotometer, IR, and titration methods under supervision. Maintain proper documentation of test results, calibration data, and standard operating procedures (SOPs) in compliance with cGMP and regulatory requirements. Assist in the preparation and standardization of reagents, solutions, and reference standards. Follow safety procedures and maintain cleanliness and orderliness in the laboratory. Participate in internal audits, investigations, and training programs as required. Report any non-conformances or deviations to the QC Supervisor or Manager promptly. Key Skills: Basic knowledge of analytical techniques and instrumentation Good understanding of laboratory practices and chemical safety Strong attention to detail and willingness to learn Excellent documentation and communication skills Ability to work collaboratively in a team environment Preferred Attributes: M.Sc. in Organic or Analytical Chemistry (2024 or 2023 pass-out) Internship or project experience in a pharmaceutical, chemical, or academic lab (if any) Willingness to work in shifts, if required

Responsibilities: Conduct wet analyses and method validations Ensure compliance with industry standards and regulatory requirements Maintain cleanliness and safety protocols in the lab environment Share cvs to ramya_n@hikal.com

Role & responsibilities We are seeking a diligent and experienced QA & QC & production. The successful candidate will Ensure that our products meet specified quality standards. This role involves managing both Quality Assurance ( QA ) and Quality Control (QC) processes, conducting inspections, and implementing improvements to maintain and enhance product quality. Expanding role in building a team of QA/QC executives. Salary Range: 15,000 to 25,000 (negotiable based on experience & skills) Experience: Minimum 2 years in QA/QC department of Tablet & Capsule or pharma manufacturing unit Preferred candidate profile Quality control analyst Responsible for testing and analyzing pharmaceutical products to ensure they meet established quality standards. They work in laboratories, using analytical Techniques to test raw materials, in-process samples, and finished products. Quality assurance analyst Responsible for ensuring compliance with regulatory requirements by conducting audits, inspections, and assessments Preferred candidate profile Qualification B.Pharma , B.Sc or B.Tech Biotech D.Pharma DIKSHA ( 8628944666 ) (9:30 AM to 7:30 PM ) Preferred candidate profile Company - Top Pharmaceuticals Companies based at Baddi HP. Fresher & Experience. Job Location- Chanigarh,Panchkula, Paonta Sahib ,BADDI ( Himachal Pradesh ) Functional : QC,QA & Production.Industry: Pharma manufacturing unit/ Food Technology The Saksham Success Enterprises Near Sunder Ayan by pass solan 173212 Himachal Pradesh Contact us DIKSHA ( 8628944666 ) (9:30 AM to 7:30 PM )

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).

VACANCY FOR TEAM LEADER - ANALYTICAL METHOD DEVELOPMENT (FORMULATIONS) - REGULATED MARKET Experience: 10 to 15 years Designation : Asst. Manager/ManagerEducational qualification : M.Sc Job profile : Need to work independently and should have handled a team of 6 to 8 members for method development and routine testing To guide and mentor analysts with practical training for developing analytical methods. SOP training and Analyst certification for new joinees within the team. Work allocation and planning of daily activities for the team subordinates Monitoring of routine analysis and trouble shooting To support site for critical trouble shooting and investigation Review of raw data , LNB and filing of routine analysis SOP preparation and training Pharmacopoeia & DMF Review Interaction with cross functional teams Review of calibration data of analytical instruments Review and check file note/deviation with investigation and CAPA for the same.

Role & responsibilities HPLC(Waters Alliance and arc Empower3 software) DISSOLUTION (DISTEK,LAB INDIA Auto and manual sampler) UV (LAB SOLUTION) IR (PERKIN ELMER) KF AUTO TITRATOR

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.

Preferred Qualification: M.Sc Organic Chemistry with more than 70% aggregate Looking for freshers who can join immediately Roles & Responsibilities: Synthesize, and characterize novel bioactive molecules under supervision of scientist/senior scientist Knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, multi-step synthesis. Knowledge of techniques in synthesis, purification, and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, etc.). Maintain Lab note book. Understanding of systems and process pertaining to safety, health and environment.

Role & responsibilities Literature search using various search engines. Analytical Method Development of raw materials, active substances and Finished product. Analysis of raw materials, active substances and finished products. Preparation of test protocol. Experience in handling instruments like spectrophotometer, HPLC, and GC. Knowledge of analytical method validation. Knowledge of natural chemistry background and its analysis.

At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Performing analytical method validations and related documentation, as well as analysis of RM, PM, Intermediates, API, and Finished products. Key Responsibilities: Performing Chromatographic and Non-chromatographic analysis for Drug substances, Drug products, Intermediates, Excipients, etc ). Conduct the analysis on qualified techniques per the approved specification / protocol / procedures , interpret the data from analytical instruments, report the results, and promptly submit the completed documents for review within the established window. Recording of analytical observations/findings, reporting of data and results in observation data sheets, forms, logbooks, LIMS, and ELN application software, and support in preparing stability summary reports and review of final documents. Responsible for timely intimation/investigation of any events or deviations to the Department Head, QA function, supporting the related investigations to the clients, and timely closure. Instrument calibration as per schedule, hot water flushing of HPLC, and general preventive checks for laboratory instruments. Perform validation activities and method transfers for multiple client projects. Actively participate in client and regulatory audits. Ensure to follow cGMP and GDP. Preparing the certificate of analysis for standards and impurities and Reports for Analytical Method Validation and Analytical Method Transfer. Support in performing Qualification and Calibration of assigned Instruments and Equipment. Create/prepare documents, master data, and static data in LIMS, ELN, and LMS software as applicable. Outsourcing of sample testing is based on requirements and updating in respective logbooks. Coordination with engineering & maintenance and external vendors for preventive maintenance and calibration activity. Support in preparation of instruments URS, DQ, and IOP. Supported preparing standard operating procedures and uploading data in LIMS and other relevant activities per departmental requirements. Use of required safety PPE while sampling, analyzing, and working in the Laboratory. Individuals working in the GMP environment are responsible for documenting/recording the activities contemporaneously and accurately as per good documentation practices. Ensure safety compliance as per Syngene policy and EHSS requirements. Taking any other jobs by the Head QC/Group Leader/Designee. To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc / M Pharma (Analytical/General chemistry) Technical/Functional Skills: Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous. Experience: 3- 6 years