2096 Hplc Jobs

Role & responsibilities Quality Control: Perform High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and various wet chemical analyses to ensure product quality. Analyze raw materials, intermediates, and finished products as per established quality standards. Prepare SOPs in line with regulatory requirements, including stability studies and market sample analysis. Ensure GLP-oriented documentation and maintain accurate records for audits and compliance. Work proficiently on multiple laboratory software platforms to support analytical testing and reporting. Quality Assurance: Ensure cGMP and regulatory compliance across all QA operations. Manage AQA, IPQA, batch release, deviations, CAPA, change control, and audits in line with quality standards. Oversee analytical data review and ensure strict adherence to data integrity principles (ALCOA+). Monitor on-floor QA activities, in-process checks, and documentation for accuracy and compliance. Maintain strong control over qualifications, preventive maintenance, and calibration reviews. Prepare quality documents independently as per regulatory and organizational requirements. Drive automation, digitalization, and continuous improvement initiatives.

Analytical Method Development of various pharmaceutical dosage forms like oral solid, oral liquid, Injectables, Nasal Spray JOB SPECIFICATION Analytical method development and validation for pharmaceutical dosage forms. Literature search related to the drug substance, create analytical profiles. Execution of analytical method transfer for pharmaceutical dosage forms. Analysis of routine samples (product development batches, stability study samples, raw materials etc). Operation and Calibration of analytical instruments/equipment s. Qualification of working standards. Data Review and Release (as assigned). Documentation of analytical activities as per Good documentation practices. Work in laboratory as per Good laboratory practices. To use PPEs and follow safe practices in lab. Preparation of SOPs, STPs, Specifications, COAs and stability reports Preparation of RM Specification and STPs Trouble shooting of analytical issues/problems/queries. Review of Analytical development & stability data. Analytical Activities related to Quality Control Department. Any other task assigned by management. Competencies Required: Good Knowledge about Analytical Method development, Validation and method transfer Knowledge about the Regulatory requirement and Quality requirement Must be able to perform the analysis as per the Good Laboratory Practices Functional Skills/ Know-how: Hands on experience on HPLC, GC, UV spectrophotometer, IR spectroscopy, Dissolution Test Apparatus, Disintegration Test Apparatus, Viscometer, Differential Scanning Calorimetry (DSC), Malvern Particle sizer.

Calibration of instruments2 Analysis of lab samples and pilot plant samples Documentation of all project of synthesis and pilot plant To maintain the all data of R&D lab and pilot plant projects the calibration of IC5 Maintain the system of housekeeping and 5-s 6 Preparation of Standards Volumetric solutions and standard of volumetric7 To maintain the monthly data of GC, LC and WET AnalysisDaily maintain the gas cylinder records To preparation the Standard for GC, LCand WET lab 10 Method development of R&D project

1) Responsible for managing and organizing laboratory operations of respective section i.e all aspect of analytical related activities including TAT and budget preparation. 2) Executing the first line supervision of laboratory personnel to ensure the analytical works are professionally carried out, to ensure accuracy & reliability of analytical results. Responsible for cross checking and validating the analytical results for release to customer. 3) Developing and maintaining an effective laboratory workforce by constantly improving the work methods and analytical competence of subordinates. 4) Implement and maintain quality system according to the ISO /IEC17025 requirements and the Nestl Quality System within NQAC Moga. Roles and Responsibilities Laboratory Management: -Team Management, cascading of KPIs & goals - Implement Safety regulations in the team to ensure a safe working environment for all. Awareness of team on safety zooms. - Manage the activities of the team, report analytical results to factories/divisions in defined waiting time, ensure correct prioritisation and allocation of work. -Hands on Experience on analytical methods of respective area -Instrument troubleshooting, ensure the on time maintenance of equipments as per CMC/AMC plan. -Manage Inventory and ensure chemical/consumable/Gas cylinders ordering on time. Ontime SES for timely payment. - To assist Lab Manager to plan and liaise with factories/divisions concerning current and future work. Ensures appropriate and efficient use of NQAC resources (personnel, equipment,Capex and Sundry budget). - In conjunction with Nestec,assist Lab Manager to identify and evaluate new techniques/methodologies to improve quality/performance of chemistry testing, taking full account of financial impact on the business. -Technical knoweldge on different techniques (HPLC, LCMSMS,UPLC,Spectrophotometer), methods (specifically for Vitmians & Aflatoxins) and impact on results. -Drive continous Improvement through implementation of NCE methdology. -Investigation, root cause analysis and ensure corrective actions for complaints, non conformances, Questionable & Unsatisfactory results through GSTD and other NCE tools. - Ensure timely and satisfactory response to all customer technical queries received. Manage analytical queries from stakeholders (e.g. Factories, comanufating units, CQA, regulatory etc) -Ensure timely response to method relaled queries or requirement of comments on various analytical methods i.e. Nestle, official, draft methods by official bodies etc. Quality system: - Establish validation files, MU calculation for new and exisiting methods according to Nestle validation standards and ensure accreditation to ISO17025 in accordance with business needs. Keep record of validation data. -Ensure accreditation of new anlalytes and new matrices. Ensure documentation as per requirement of Management system. -Ensure updation of relavant Managment procedures and formats - Appropriate corrective action in the event of adverse analytical results. - Ensure compliance to Good Laboratory Practice (GLP) policies in NQAC through regular internal/external auditing. 1) Responsible for managing and organizing laboratory operations of respective section i.e all aspect of analytical related activities including TAT and budget preparation. 2) Executing the first line supervision of laboratory personnel to ensure the analytical works are professionally carried out, to ensure accuracy & reliability of analytical results. Responsible for cross checking and validating the analytical results for release to customer. 3) Developing and maintaining an effective laboratory workforce by constantly improving the work methods and analytical competence of subordinates. 4) Implement and maintain quality system according to the ISO /IEC17025 requirements and the Nestl Quality System within NQAC Moga. Roles and Responsibilities Laboratory Management: -Team Management, cascading of KPIs & goals - Implement Safety regulations in the team to ensure a safe working environment for all. Awareness of team on safety zooms. - Manage the activities of the team, report analytical results to factories/divisions in defined waiting time, ensure correct prioritisation and allocation of work. -Hands on Experience on analytical methods of respective area -Instrument troubleshooting, ensure the on time maintenance of equipments as per CMC/AMC plan. -Manage Inventory and ensure chemical/consumable/Gas cylinders ordering on time. Ontime SES for timely payment. - To assist Lab Manager to plan and liaise with factories/divisions concerning current and future work. Ensures appropriate and efficient use of NQAC resources (personnel, equipment,Capex and Sundry budget). - In conjunction with Nestec,assist Lab Manager to identify and evaluate new techniques/methodologies to improve quality/performance of chemistry testing, taking full account of financial impact on the business. -Technical knoweldge on different techniques (HPLC, LCMSMS,UPLC,Spectrophotometer), methods (specifically for Vitmians & Aflatoxins) and impact on results. -Drive continous Improvement through implementation of NCE methdology. -Investigation, root cause analysis and ensure corrective actions for complaints, non conformances, Questionable & Unsatisfactory results through GSTD and other NCE tools. - Ensure timely and satisfactory response to all customer technical queries received. Manage analytical queries from stakeholders (e.g. Factories, comanufating units, CQA, regulatory etc) -Ensure timely response to method relaled queries or requirement of comments on various analytical methods i.e. Nestle, official, draft methods by official bodies etc.

Job Description Responsible for planning and execution of disinfectant preparation, equipment cleaning and laboratory cleaning activity. Responsible for Planning and execution of Microbial analysis of raw material, packing material, intermediate / in-process samples, Particulate matter testing, Bacterial Endotoxin testing, Antimicrobial effectiveness testing, Bio burden testing and swab testing. Responsible to perform the fogging activity in Microbiology area. Responsible to preparation, sterilization and maintenance of in-house / Ready to use culture media. Responsible to Dry heat sterilization of glassware’s. Responsible to maintain the equipment and instruments. Responsible for transfer, release and observation of microbiological analysis plates & tubes within timeline. Work Experience Education :-M.sc- Microbiology/Biotechnology Experience :- 2 to 6 yrs. Education Others Competencies

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitization and sterilization of the items to be sent into Grade-B area Destruction of the rejected & unwanted materials and recording of the same Release of vaccine from blending to filling area To follow the usage of personnel protective equipment (PPE) during handing of corrosive liquids, WFI and steam Solution preparation Operation of Filter integrity machine Perform aseptic operations in Grade B area Any other tasks assigned by the supervisor.

Job Description :- Quality Control Officer / Sr. Officer Scicore Nutra Private Limited is a state-of-the-art facility, located in Sanand Gujarat, is dedicated to producing high-quality nutrition products that are safe, effective, and meet the highest standards of quality. Our team of experts is committed to ensuring that every product we manufacture is produced with the utmost care and attention to detail. At our manufacturing unit, we use only the best raw materials and employ advanced manufacturing processes to ensure that our products are of the highest quality. We also adhere to strict quality control measures to ensure that every product meets our rigorous standards. This starts with doing a rigorous vendor qualification as well as testing of all raw materials supplied by these vendors for every batch. We do in-house stability studies to make sure our products last the full shelf life and give the best results to our customers. Our goal is to provide our customers with nutraceutical products that promote health and wellness, and we are committed to using science-backed ingredients and formulations to achieve this goal. We are also committed to continuous innovation and improvement and are always looking for new ways to enhance our products and processes. Benefits Provided: 1 Free Air-Conditioned Transportation to the Factory 2 Paid Leave 3 Tea/Coffee & Canteen Facility 4 Accident Insurance 5 Provision for Bonus & Gratuity 6 Training programs for professional advancement 7 Progressive work environment conducive to personal and professional growth Job Title :- Quality Control Officer / Sr. Officer Role & Responsibility: - To follow and ensure Good Laboratory Practices. To perform the work according to work allotment. To follow good documentation practices while making entries in Documents and records. To support the investigation and learn from the senior. To perform the Calibration of Laboratory instruments as per PM scheduled. To enter the details in respective equipment logbook. To enter the details of intimation in respective register. To performed the Inventory control of chemicals and Glassware. To prepare the volumetric solutions, reagents and indicator. To perform the Standardization of volumetric solutions. To perform the analysis of raw material, packing material, semi-finished goods and finished goods. Handling of Reference standard and Working standard and qualification of working standard. To performed testing and release of incoming, in-process, finished and stability product as per the laid down specifications and method of analysis/STP. To perform the preparation of CoA of raw material, packing material, stability and finished product. To performed the rejection of raw material / Packing Material/Finished/ Stability Product. Make sure that materials are appropriately tested and results are reported. To perform the Initiation and review of any change related to the department. To perform the Preparation and review of all SOPs related to department, Specification and test procedures. Testing of raw material, packing material and water sample as per respective method of analysis/STP. To performed testing and release of incoming, in process, finished and stability product as per the laid down specifications and method of analysis/STP. To prepare SPEC,STP and TDS. Any additional job responsibilities as assigned by HOD. Department :- Quality Control Number Of Positions:- 01 Experience : 2 to 4yrs Employment Type: Full Time, Permanent Education UG: B.SC in Any Specialization PG: M.SC in Any Specialization Compensation :- As per Industry norms & experience Key Skills QC, UV, HPLC, ADL, Analytical, Method Development

QC Chemist (Formulation OSD) Role & responsibilities Job Role: - Analysis of Raw Materials & Packing Materials - Sampling & analysis of Water, In-process, Finished products, Stability, and Swab Analysis Experience: 1 to 5 years Education: B. Pharm / M. Sc in Chemistry, Organic Chemistry, General Chemistry, Pharmaceutical Chemistry, or Industrial Chemistry Work Location: Bangalore Preferred candidate profile

Our plant is in Sihor, Bhavnagar and we have a requirement of QC Chemist. If you are comfortable to shift to Sihor, Bhavnagar, do share your CV on khushbushah@jenburkt.com We are looking for candidates who have completed MSC. Overall: Fresher to 1 yr. of experience. CTC : Can be discussed on the call. Kind Regards, Khushbu

- M.Sc / B. Pharm / M.Pharm - 03-05 years experience in pharmaceutical manufacturing machine maintenance 1. Sampling and Testing of raw material 2. Testing of Finished product & semi finished products 3. Knowledge of HPLC/ GC Empower software 4. Knowledge of Operation of instruments like Dissolution/ FTIR / HPLC / GC / Polarimeter 5. Knowledge about basic QMS in QC like Incidence / OOS etc.

Job Title: In-vitro Bioanalytical Scientist Job Location: Hyderabad About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. 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 at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role : To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment Processing of different matrices samples of PK studies Optimization of test compounds manually as well as automated on LCMS/MS Develop methods with the team lead Independently handling of HPLC for UV based samples analysis. Documenting the lab note books online and compound management Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Experience Minimum 1-3 years of experience in handling ADME assays and HPLC and LCMS/MS Skills and Capabilities Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis Should be well versed with internet-based literature search and capable of implementing the Learnings as and when required Candidate is expected to have basic understanding in interpretation of Mass/UV Spectra Should ensure preventative maintenance and calibration schedules of HPLC & mass spec by coordinating with vendor and support staff General understanding of Drug metabolism and Pharmacokinetics Should be able to deliver scientific presentation in departmental journal club and write official Project reports Education M. Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis Equal Opportunity Employer: .

Job Position: Study Director Location: Pragnapur, Hyderabad Company: Vivo Bio Tech Ltd Job Role: The Bioanalytical Associate role focuses on supporting in-vitro ADME studies and plasma sample analysis in preclinical drug development. The successful candidate will be integral in analyzing and interpreting bioanalytical data to support early-stage drug discovery efforts. Responsibilities Conduct routine ADME assays, such as protein binding and metabolic stability, to generate key data supporting drug development decisions. Prepare and analyze plasma samples for pharmacokinetic studies, including the measurement of drug concentration, metabolite profiling, and related biomarkers. Analyze data sets, provide scientific interpretation, and communicate results to cross-functional teams in a clear and concise manner. Maintain concise and accurate records of all study activities in accordance with industry guidelines and company policies. Troubleshoot assay issues, propose corrective actions, and implement process improvements to enhance the efficiency and reliability of bioanalytical data. Assist in the coordination of outsourced research studies or other tasks assigned by management. Requirements Bachelors degree in Analytical Chemistry, Biochemistry, or a related field. 5+ years of hands-on lab experience in bioanalysis, with a focus on ADME/PK studies and plasma sample analysis. Hands-on lab experience with ADME screening assays, such as protein binding and microsomal stability. Experience with plasma sample bioanalysis in support of non-clinical pharmacokinetic studies. Experience with LC-MS/MS, HPLC, UPLC, and related analytical techniques for the quantification and characterization of drug candidates in biological samples. Strong analytical and troubleshooting skills with the ability to interpret complex datasets. Nice-to-haves Familiarity with drug discovery and development, especially within preclinical research. Experience with quantitative LC-MS/MS bioanalytical techniques and ABSciex mass spectrometers. Knowledge of relevant bioanalytical software (e.g., Analyst, Prism). Thanks & Regards G NagaSravani|HRD nagasravani.g@virinchi.com

We are seeking a highly skilled Executive / Sr. Executive Quality Assurance with 8 to 10 years of experience in API / Bulk Drug Manufacturing . The role involves overseeing laboratory incidents, OOS/OOT investigations, analytical method validations, data integrity compliance , and ensuring adherence to GMP and regulatory standards . Key Responsibilities: Handle and review laboratory incidents, OOS (Out of Specification), OOT (Out of Trend), deviations, and root cause investigations . Review and monitor calibration schedules and records for critical analytical instruments (HPLC, GC, UV, IR, AAS, ICP-MS). Oversee analytical method validation, method transfers, and specification reviews in alignment with regulatory requirements. Provide training to QC teams on laboratory procedures, data integrity , and documentation practices . Conduct surprise lab audits/visits and proactively identify compliance gaps to ensure readiness for inspections. Ensure compliance with cGMP, ICH, and regulatory guidelines throughout QA operations. Eligibility Criteria: Education: B.Sc / M.Sc in Chemistry or related field. Experience: Minimum 8 to 10 years in pharmaceutical Quality Assurance (API / Bulk Drug). Preferred Candidates: Male candidates available for immediate joining .

Responsibilities: (1) To conduct analysis such as GC, HPLC, Wet Chemistry, GC-MS, LC-MS, FTIR, UV-Vis, DSC, Particle Size Analyzer, Viscosity, Density etc.(2) To maintain Analytical Lab note books, procedures, documents and records(3) To maintain laboratory and work place as per norms(4) To maintain ISO 17025 and ISO 9001 management systems(5) To work safely and maintain housekeeping of the lab(6) To work in shifts as per requirement of the job(7) Implement SOP for the storage of analytical standards and reference samples at Thane under required conditions and maintain a database

Monitor progress of the reactions by using standard methods & analytical techniques (TLC,GC,HPLC, LCMS etc).Plan, setup, monitor, and workup chemical reactions independently.Isolate product & Optimize.

Product Development: Assist in the design, formulation, and testing of new products or services, ensuring they meet quality and performance standards.

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 automation

Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA

Candidate must have strong knowledge in Core PHP, Laravel, MYSQL, jQuery, AJAX, HTML and CSS. Must have a work experience of 1-2 years on PHP & Laravel Framework. Web-based software application development and maintenance on PHP

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

1. Coordinate with Sales team and Plant from Order punching to despatch details 2. Regular Follow up for the Payments from clients 3. Support sales team for Quotes, Ledgers, PI, Debtor reports, monthly and weekly sales reports

Planned purchase to maintain stock. Having knowledge in IT Hardware & Software Procurement. Creating PO & Buying Activities. Having a good Knowledge in material Follow-up with Vendor & Supplier.

Key Responsibilities: Strategic Actively imbibing the values and philosophy of PI Industries. Efficient contribution to the overall success of product innovation (PRI) through scientific contribution to objectives and targets being set by the leadership team. Fullfilling requirements and achieveing goals set by the Team Leader and Group Leader Working as a team member, contributing to the team objective with special focus on achiving and exceeding the set target. Development of individual & team strengths by attending trainings based on the regular feedback as an individual and as a team Operational Monitoring reaction masses using LCMS/GCMS. Execution of purity assessment and assay determination of samples using GC/HPLC/UFLC. Able to carry method development for challenging compounds through GC/GCMS/HPLC/UFLC Developing methods on Prep HPLC for purification/isolation of impure compounds. Elucidating and confirming structures using NMR, FTIR and LCMS/MS Ensure the scheduled performance of calibrations, Preventive maintenance and troubleshooting of core analytical instrument. Following the set instrument maintenance practices like periodic solvent changes, system flushing, etc. Assist the other team members in day to day activities like sample preparation, method developments, report generation and data management. Following safety practices with out fail. Financial Planning the activities with existing resources and infra structure. Suggesting the cost-effective areas to the Team Leader / Group Leader Developing methods to improve the environment safety and to reduce the cost. People Collaborate with team members and cross functional teams to meet research objectives. Develop and foster positive relationships with other teams and support groups to maximize cooperation and consequent benefit to objective delivery Should be able to work in multitasking environment Ensure team harmony through collaboration and active participation in all team discussion Apart from the above responibilities, specific responsibilities of Research scientists Note : The Associate would in any of the areas listed below based on the requirement and should have sufficient knowledge and expertise in the area alloted as listed below 1. HPLC/UFLC Candidate should be well versed with normal and reverse phase chromatography techniques. Able to optimize chromatographic methods Keen knowledge on low level analyte-impurities quantification by HPLC. 2. LCMS SQD & TQD Well versed with operations of one or more makes of LCMS-SQD & TQD instruments. Aware of basic principles related to mass spectrometry, sources, analysers and detectors. Hands on experience in analysis of compounds using LCMS instrument and releasing the mass confirmation reports. Keen knowledge on ppb / ppm level quantification of analytes from AI, formulations, various matrices like microsomes, soil, plant extracts by LCMSMS. Perform possible structural elucidation/Identification of degradants/metabolites/impurities using LCMS/MS 3. NMR Perform suitable 1D/2D NMR experiments based on the requirement and confirm one among proposed structures or propose a new structure. Manage the NMR activities viz, perform routine NMR (1D&2D) analysis, QNMR, cryogen replenishing. Keen knowledge of NMR technology & instrument maintenance. 4. Physchem assays Have hands on knowledge of various in vitro ADME/ physchem assays like solubility, LogP, pKa and in vitro Metabolic stability assay. Able to develop methods, check method compatibility for accuracy, precision, matrix effect and apply it further for the quantification of formulations, plant extracts, various matrices like soil, microsomes etc. Perform the microsomal stability experiments to determine half-life and Clint. Awareness about Met ID using various scans, fragmentation tree & HRMS will be an added advantage. Knowledge about sample preparation and analysis of photo stability and hydrolytic stability. 5. Prep-HPLC Able to develop a robust chromatographic method both at analytical and preparative scale, by designing cost effective methods for chiral and achiral molecules. Knowledge of chiral chromatography and isolation of enantiomers using preparative HPLC. Please share updated resume on e-mail id Shubhi.chandnani@piind.com Mobile - 8875001305

analytical lifecycle: specs with RA, method validation, testing of RM/PM/IP/FP, water & environmental monitoring, stability programs.data integrity (ALCOA+), LIMS audit trails chromatography governance (integration, SST, system suitability).

ONLY FOR MALE CANDIDATES ROLES: Executives and chemists SALARY: 2 lpa to 6.5 lpa Please carry last 3 months pay slips,6 months bank statements,CTC details and updated CV. Desired Candidate Profile * Conduct quality control tests on bulk drugs using HPLC, GC, and other relevant methods. * Develop and implement quality assurance procedures for API manufacturing processes. * 2-7 years of experience in API production or related field. * Proficiency in HPLC, GC, and other analytical techniques for testing bulk drugs. * Experience with QA management systems and implementation of quality control procedures.