2105 Hplc Jobs - Page 44

Posted On 04th Jun, 2025 : The candidate will be primarily responsible for laboratory testing and R&D activities both in the lab and on the plant floor. The role involves developing and implementing testing procedures for new products, ensuring compliance with ISO 9000 standards, and maintaining accurate records and documentation. Key Responsibilities: Conduct lab-based testing and support R&D activities within the lab and plant environment. Develop and implement testing protocols for new and existing products. Maintain and update all ISO 9000 documentation and records related to lab activities. Coordinate with the designated ISO representative (e.g., Mr. X) for documentation control and compliance. Perform product testing with high precision (required accuracy0.2%). Carry out regular titration tests (approx. 80% of lab work) , and tests using instruments such as pH meters, TDS meters, NTU meters, etc. Ensure timely calibration and maintenance of lab instruments. Support the R&D function through effective internet-based research. Required Skills & Qualifications: Strong foundation in inorganic chemistry , particularly in wet lab testing. Hands-on experience with titration methods and chemical testing procedures. Familiarity with lab instruments such as pH meters, TDS meters, NTU meters, etc. Accuracy-oriented approach with an emphasis on result precision and compliance. Knowledge of calibration procedures for lab instruments. Proficiency in basic computer applications MS Word, Excel, Outlook, and PowerPoint. Ability to browse and research effectively for R&D purposes. Should possess an Android smartphone for operational support and communication. Basic proficiency in reading, writing, and understanding English; fluent spoken English is not mandatory. Location of Job At our factory, Changodar Bavla road, Dist-Ahmedabad Key Skills : Company Profile One of the leading companies in the chemical industry in Gujarat. With over six decades in the industry, they have not only established a strong presence in the domestic market but also built a long list of satisfied clients in more than 18 countries. Their products cater to various industries, including the oilfield industry, photographic ---, pharmaceutical raw materials, textiles, food processing, leather, industrial detergents, and metal finishing Company isregistered with The Gujarat Chamber of Commerce & Industry (GCCI), FIEO, CHEMEXCIL, FSSAI, SSI, NSIC, and GPCB. Above all, They are an ISO 9001-2015 certified company.

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

ADL hands on experience Exposure / Knowledge of HPLC and GC

Job Description Hands on industrial experience in Biotech/ Biologics industry on Raw/ Packaging Material Testing. Basic Knowledge/ Hands on experience in handling of equipment s pertaining to RM/PM testing including but not limited to HPLC/GC/UV-visible Spectrophotometry, FTIR, Polarimeter, Refractometer, Autotitrator, TOC analyzer, Weighing balance, pH/ conductivity meter, Melting range apparatus, Viscometer. Familiar with the basic cGMP systems including but not limited to sample management, OOS/OOT, Documentation control, Change Control, Audits, Deviation & CAPA Management. Timely sampling & testing of Raw/Packaging/ Consumable materials as per Pharmacopoeial/In-house procedures. Perform Daily sampling & testing of Utility samples with online documentation & trending. Preparation of SOP s/ STP s/ equipment URS/ Qualification/ Study protocols/ reports pertaining to RM/PM section Perform daily calibration/ verification/ requalification of analytical equipment s as per the approved procedures & calibration/ verification frequency with online documentation. The candidate should be conversant with Quality module of SAP and LIMS system. Timely Updation of RM/PM/CM and water analysis results in SAP and LIMS system. The candidate should be conversant procedure for procurement of chemicals/ Reagents/ consumables and maintain their inventory records. To Ensure cGMP compliance in laboratory and ensure that the laboratory is always maintained in audit ready status. Work Experience 2 to 4 years Education Masters in Chemistry or Analytical Chemistry Competencies

- Should be aware with GMP. - Should have worked experience of API. - Knowledge of Wet chemistry as well as Instrument like GC,HPLC,IR,UV etc. - Communication should be good. - Knowledge of QMS.

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of general lab SOPs and instrument sops. Desired candidate profile: 1. Must have worked in method validation, ADL, analytical lab. 2, Knowledge of HPLC,

JOB DESCRIPTION Job Title: Junior Analytical Development Scientist Oral Solids Job Location: Bangalore Department : Analytical Development Drug Product 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. 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 always. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always 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. Core Purpose of the Role: Analytical development supporting Formulation development Routine analysis of samples Method development Instrument calibrations Documentation Report preparation Miscellaneous lab responsibilities Role Accountabilities: Candidate should have very good educational and theoretical background. Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC Knowledge of any other instruments than the above will be added advantage. Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience: 1 to 3 years) Skills and Capabilities: Technical/functional Skills: Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line Behavioral Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Education: M.Pharm / M.Sc Equal Opportunity Employer . #LI-JK1

Overview 170+ Years Strong. Industry Leader. Global Impact. At Pinkerton, the mission is to protect our clients. To do this, we provide enterprise risk management services and programs specifically designed for each client. Pinkerton employees are one of our most important assets and critical to the delivery of world-class solutions. Bonded together, we share a commitment to integrity, vigilance, and excellence. Pinkerton is an inclusive employer who seeks candidates with diverse backgrounds, experiences, and perspectives to join our family of industry subject matter experts. The Global Security Operations Center (GSOC) Operator- Customer Service, assigned to one of Pinkerton’s largest global clients, will be responsible for utilizing best practices to identify, analyze, and support all incidents that are either impactful or potentially impactful to the people, assets, and reputation of the client. The Operator monitors multiple streams of security information, including emails, phone calls, alarms, camera systems, and other access control technologies. This role assists corporate employees, vendors, and visitors, by way of written correspondence, with concerns that pertain to safety and security around the globe. Responsibilities Represent Pinkerton’s core values of integrity, vigilance, and excellence. Provide first line assistance to the client’s employee, vendors, and visitors regarding all concerns relating to safety and security. Utilize effective writing capabilities to provide consistent and quality customer support. Communicate, detect, assess, and alert others of incidents which may impact the safety of people, products, property, and brand image. Follow procedures for managing a variety of incidents, from minor to major situations. Provide back-up support and on-call functions, as needed. All other duties, as assigned. Qualifications Associate degree (Bachelor’s preferred) in international affairs/relations, business, emergency management, political science, criminal justice, or related discipline or at least two years of equivalent work experience in customer service, contact centers, or corporate security. Experience within GSOC, SOC, TOC, or similar, preferred. Proficient English written and verbal communication skills. Able to maintain a high level of professionalism and approachability. Customer service skills. Able to multitask in a fast-paced, and at times, stressful work environment. Effective team player. Comfortable with a high-tech working environment, and willing to learn new tools and innovations. Computer skills; Microsoft Windows and Office. Working Conditions: With or without reasonable accommodation, requires the physical and mental capacity to effectively perform all essential functions; Regular computer usage. Occasional reaching and lifting of small objects and operating office equipment. Frequent sitting. Flexibility to work a variety of different shifts, and willingness to assist the team with overtime when needed. Travel, as required. Pinkerton is an equal opportunity employer to all applicants and positions without regard to race/ethnicity, color, national origin, ancestry, sex/gender, gender identity/expression, sexual orientation, marital/prenatal status, pregnancy/childbirth or related conditions, religion, creed, age, disability, genetic information, veteran status, or any protected status by local, state, federal or country-specific law.

Knowledge of analytical method development, Validation and stability analysis of Oral and Injectable dosage forms. Handling of Tablets, Capsules, Oral Liquids and Oral Suspensions. Handling of dissolution apparatus for Tablets, Capsules, Oral Liquids and Oral Suspensions.USP Type-I, USP Type-II & USP Type-IV. Knowledge about the handling of analytical instruments like HPLC,GC, UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc. Knowledge about the calibration of HPLC,GC,UV,SOR,IR,Particle size analyser,Osmometer,viscometer etc. Knowledge about regulatory guidelines and requirements. Knowledge about method transfer activities. Knowledge about the safety aspects. Knowledge about GLP and GMP. Knowledge about the qualification of equipment and instruments Location Hyderabad Apply to Job Send your resume to

NAB is looking for Analyst to join our dynamic team and embark on a rewarding career journeyGather, analyze, and interpret complex datasets to identify trends, patterns, and insights that support strategic decision-making within the organization.Develop, maintain, and update detailed reports, dashboards, and visualizations to communicate key metrics and findings to stakeholders.Collaborate with cross-functional teams to understand business needs, translating them into data requirements and actionable insights.Conduct market research, competitor analysis, and customer behavior studies to inform business strategies and improve performance.Monitor data integrity and accuracy, implementing quality control measures to ensure reliable, consistent reporting.

Lucknow Institute of Technology is looking for Lab Instructor to join our dynamic team and embark on a rewarding career journey Lab Preparation: Setting up and preparing laboratory equipment, materials, and experiments before the students arrive Demonstrations: Conducting demonstrations to show students how to perform experiments correctly and safely Instructions: Providing clear and concise instructions to students on the objectives of the experiment, procedures to follow, and safety precautions Guidance: Assisting students during the experiment, answering questions, and guiding them through the process Safety Oversight: Ensuring that students adhere to safety protocols and guidelines while working in the lab Troubleshooting: Helping students troubleshoot and resolve issues or challenges they encounter during the experiment Data Collection: Assisting students in collecting accurate and reliable data during the experiment Data Analysis: Supporting students in analyzing and interpreting the results of their experiments

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 05-07-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 05-07-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Overall responsibility of Quality Control department (Finished product, in-process, Raw Material, Packaging Material, stability etc. )and Microbiology department. Daily review /Monitoring of Quality Control activities Handling of all Quality Control related matters. In Process Control during batch manufacturing. Overall QC Data management and coordination with corporate team. Handling of Change Control Proposal, Out of Specification, Incidents and Planned Deviations etc. through CAPA track wise software. Well versed with Handling of HPLC, UV and Dissolution Apparatus etc. Preparation & Review of Analytical Method Validation/verification/CMV Protocols & Reports. In depth knowledge of ICH, PIC/S guidelines on AMV. Monitoring implementation of Good Laboratory Practices and ensuring laboratory compliance as per requirements of regulatory guidelines. Coordinate with Manufacturing/Ware house PPIC for planning of testing of required materials. Exposure of Regulatory Audits Review of QC and Microbiology Specifications, Standard testing Procure(STP) and Standard Operating Procedure Investigation of Laboratory events/OOS/OOT/Deviation. Monitoring of Stability studies for the products manufactured at the site as per respective protocols/procedure Review and approval of analytical testing/Microbiology testing reports

Job Profile : A Quality Control Officer is a professional who is Responsible for the Raw materials. in process and finished product and also stablility samples analysis and had knowledge of handling instruments like HPLC , UV-visible spectrophotometer , Dissolution Apparatus, pH meter , viscometer , KF, Polarimeter , Refractometer, Friabilator, D.T. Apparatus etc. Roles & Responsibilities: Responsible for inprocess and finished product analysis and also analysis of stability samples. Handling instrument like HPLC, UV-visible spectrophotometer, Dissolution Apparatus, pH meter, KF, Polarimeter, Refractometer, Friabilator, D.T. Apparatus etc. Analysis of finished product, stability product and raw material. Preparation of SOP for related to instrument and system. Preparation of protocol, worksheet for raw material and finish product. Documentation Validation protocol, Validation report, STP preparation. Performing sample based check, monitor transactions & provide feedback on quality. Sampling of Raw material, entry, packaging and labeling. Supporting completion of audit checklist in advance for all internal/ external audits. Assisting company's external auditors for preparation of documentation for control weakness/ error remediation. Standardization and Calibration of Instruments. Water analysis. Perform other duties as assigned. Candidate Profile / Skill required : Knowledge of GMP & GLP,ICH guidelines. Working knowledge of Analytical Method development and validation. Handling of instruments like HPLC/Spectrophotometer etc. In-depth understanding of company standards Up-to-date knowledge of federal and industry standards and best practices Basic computer and math skills to calibrate and measure specifications A keen eye for detail Good verbal and written Communication skills Proficiency in Microsoft Office Knowledge of pharmasuite/pharmacloud software. Required Qualifications : M.SC.,B.Pharm,M.Pharm A minimum of 1-2 years related experience in QC pharmaceutical manufacturing company.

QC Testing,HPLC,RP, Stability,GLP

Job Summary We are looking for an individual for the SIT Team to oversee the investigation of major and critical deviations, working closely with Cross-Functional Team (CFT) members to identify root causes and implement corrective and preventive actions. The role involves active participation in investigating Out of Specification (OOS) cases, ensuring accurate classification in the DCMS deviations log, and providing support during regulatory inspections. Roles & Responsibilities • You will be responsible for overseeing the investigation of major and critical deviations from the outset, collaborating closely with Cross-Functional Team (CFT) members to identify root causes, corrective actions (CA), preventive actions (PA), and preparing comprehensive reports. Your will also be working on the trending of the deviations and identification of adequate action items for reduction of the same. • Your role involves active participation in investigating OOS (Out of Specification) and other relevant cases, working closely with CFT members to determine root causes, CA, PA, and report writing. • You will review minor and critical , providing constructive feedback for improvement. • Your responsibilities include periodically assessing the trending of minor deviations, highlighting or escalating key observations, regularly reviewing the deviations log to ensure accurate classification, and utilizing the Rubrics template for crafting investigation reports. • You will offer necessary support to the site in readiness for or during regulatory inspections related to investigations. Qualification Educational qualification: A Bachelor's or Master's degree in a relevant scientific field, such as Chemistry, Biochemistry, Pharmacy, or related discipline Minimum work experience : 7 to 10 years of experience in a pharmaceutical or related industry with a focus on investigations and quality assurance Skills & attributes: Technical Skills • In-depth knowledge and experience in overseeing investigations, and familiarity with root cause analysis, corrective actions (CA), and preventive actions (PA). • Expertise in investigating valid OOS and other relevant cases. • Familiarity with reviewing deviations / OOS log and ability to perform classification of data. • Ability to craft comprehensive investigation reports. • Experience in providing necessary support for regulatory inspections related to investigations. • Knowledge of regulatory requirements pertaining to deviations investigations. Behavioural Skills • Ability to collaborate closely with CFT members. • Analytical mind set for identifying root causes and developing effective solutions. • Strong problem-solving skills and attention to detail in reviewing deviations, reports, and trending data and implementing corrective actions. • Effective communication skills for report writing and escalation of key observations. • Commitment to ensuring compliance with regulatory requirements in investigations. • Ability to offer necessary support to the site in readiness for or during regulatory inspections. Additional Information looking someone with strong QC Microbiological investigation background. Should have exp in Microbiological compliance. Education :M.Sc. Microbiology Exp : 8-10 Years Industry : Injectable preferred/ OSD will be second preference Person will be responsible to manage 3 sites Microbiological compliance at Baddi

ib vogt GmbH is looking for Civil & Structural Design - Engineer to join our dynamic team and embark on a rewarding career journey. Civil Structural Design Engineers With Experience Of Designing In Water Retaining Structures is responsible for various tasks including planning, execution, and management of related duties. They should possess relevant skills and experience to excel in this role. Duties include teamwork, problem-solving, and achieving organizational goals. Candidates must have strong communication and technical abilities. Responsibilities include project management, strategy execution, and performance optimization. (More details as per role requirements. )

myG is looking for EXECUTIVE-PEOPLE EXCELLENCE (S) to join our dynamic team and embark on a rewarding career journey Handles operational and administrative tasks effectively Coordinates with different teams for smooth workflow Manages reports and documentation Supports senior executives in business functions

Job Description Timely testing with online documentation of various sample stages including in-process, intermediate, drug substance/ drug product, stability samples of Biotherapeutics proteins for test parameters including but not limited to HPLC methods, Host cell DNA contaminants quantification by RT PCR, Host cell protein contaminants quantification by ELISA, Electrophoresis, ELISA based assays and general procedures including but not limited to extractable volume, sub-visible particle testing, pH, conductivity. Should work in shifts. Preparation of reagents/ solutions required for routine testing and maintenance of their records. Preparation and periodic updation of SOPs, STPs and Specifications pertaining to testing of Biotherapeutics. Perform In-house calibration/ verification of Analytical equipment as per the approved procedures and calibration/ verification frequency. Online monitoring and maintenance of equipment records. To ensure cGMP compliance and maintain the laboratory in audit ready condition. To report any Deviations/ Out of Specifications results and Safety risks to the supervisor as and when observed. Participation in transfer of analytical methods from R&D to QC. To attend all GMP/ On-job/ additional trainings as per the approved training matrix and update the training records. Work Experience Experience: 5 - 8 years in Quality Control Education Post Graduation in Biotechnology or Biochemistry Competencies

Department – Sales, New Generation Insulin BU Novo Nordisk India Pvt Ltd

Department – Sales, New Generation Insulin BU Novo Nordisk India Pvt Ltd

Department – Sales, New Generation Insulin BU Novo Nordisk India Pvt Ltd

Department – Sales, New Generation Insulin BU Novo Nordisk India Pvt Ltd

Business Unit Obesity BU Locations Mangalore Novo Nordisk India Pvt Ltd

Business Unit Obesity BU Locations Hyderabad Novo Nordisk India Pvt Ltd