2096 Hplc Jobs - Page 11

0.6 - 4 years with In depth knowledge and skill set pertaining to Molecular Modelling, Docking, Molecular mechanics, Quantum Mechanism, Molecular Dynamics simulation and Quantum mechanics/Molecular mechanics simulations is must. Brief knowledge/ experience of protein structure, function, dynamics and engineering. Sound knowledge in programming and scripting languages like Fortran, C, C++, Perl and Python. Putting theory into practice Are you inquisitiveFinally looking for a place to put your expert skills in Molecular Dynamics, uantum mechanics, Molecular mechanics to solve real world problemsYou have arrived at the right place.

Develop and execute strategic business plans to drive growth in the pharmaceutical market. Identify, evaluate, and manage new business opportunities to expand market presence. Nurture and uphold strong relationships with key customers and team members. Collaborate with cross-functional teams to ensure alignment and successful implementation of business strategies. Analyse market trends and competitor activities to identify opportunities for growth. Represent the company at industry events and conferences to promote products and services. Prepare and deliver presentations, analysis, and data to senior management on business development activities and progress and to help in decision/ strategy making. Qualifications: Bachelors degree in Life Sciences, Business, or a related field (advanced degree preferred). Proven track record of success in business development within the pharmaceutical or biopharmaceutical industry. Strong understanding of various analytical instrument techniques, particularly HPLC and LC-MS/MS, and their application in the Pharma/Biopharma sector Excellent communication, negotiation, and interpersonal skills. Ability to work independently and as part of a team in a fast-paced, dynamic environment. Willingness to travel as needed to meet business objectives.

Dalmia Cement Bharat Ltd is looking for Shift Chemist to join our dynamic team and embark on a rewarding career journey Chemical Process Monitoring: Monitoring chemical processes, reactions, and operations to ensure they are running smoothly and in accordance with established procedures Quality Control: Conducting quality control tests and inspections on raw materials, intermediate products, and finished products to ensure they meet specified standards and regulations Sample Analysis: Collecting and analyzing samples of chemicals, compounds, or products using various analytical techniques and instruments, such as spectroscopy, chromatography, and titration Data Interpretation: Interpreting analytical data, test results, and laboratory reports to identify deviations or issues and take corrective actions Documentation: Maintaining detailed records of test results, procedures, and observations, as well as preparing reports for documentation and compliance purposes Instrument Maintenance: Calibrating and maintaining laboratory equipment and instruments to ensure accurate and reliable measurements Safety Compliance: Adhering to safety protocols, handling hazardous materials, and ensuring a safe working environment for oneself and others Compliance with Regulations: Ensuring compliance with regulatory standards, safety protocols, and industry-specific guidelines, such as Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) Troubleshooting: Identifying and addressing issues or deviations in chemical processes and recommending corrective actions or process adjustments

Dalmia Bharat Group is looking for Shift Chemist to join our dynamic team and embark on a rewarding career journey Chemical Process Monitoring: Monitoring chemical processes, reactions, and operations to ensure they are running smoothly and in accordance with established procedures Quality Control: Conducting quality control tests and inspections on raw materials, intermediate products, and finished products to ensure they meet specified standards and regulations Sample Analysis: Collecting and analyzing samples of chemicals, compounds, or products using various analytical techniques and instruments, such as spectroscopy, chromatography, and titration Data Interpretation: Interpreting analytical data, test results, and laboratory reports to identify deviations or issues and take corrective actions Documentation: Maintaining detailed records of test results, procedures, and observations, as well as preparing reports for documentation and compliance purposes Instrument Maintenance: Calibrating and maintaining laboratory equipment and instruments to ensure accurate and reliable measurements Safety Compliance: Adhering to safety protocols, handling hazardous materials, and ensuring a safe working environment for oneself and others Compliance with Regulations: Ensuring compliance with regulatory standards, safety protocols, and industry-specific guidelines, such as Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) Troubleshooting: Identifying and addressing issues or deviations in chemical processes and recommending corrective actions or process adjustments

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

Aquachem Industries Private Limited is looking for QC Chemist to join our dynamic team and embark on a rewarding career journey Chemical Analysis: Conduct chemical and physical testing on raw materials, in-process samples, and finished products to assess their quality and compliance with specifications Instrument Operation: Operate and maintain laboratory equipment and instruments, such as HPLC, GC, UV-Vis spectrophotometers, and other analytical instruments Data Analysis: Analyze and interpret test results, ensuring accuracy and consistency in data reporting Quality Control: Implement and maintain quality control standards and procedures to ensure that products meet regulatory and quality requirements Documentation: Prepare and maintain accurate and organized records, including test results, laboratory notebooks, and reports Sample Collection: Collect samples of raw materials and products for testing and analysis Method Validation: Develop and validate analytical methods for product testing, ensuring their accuracy and reliability Trend Analysis: Monitor and analyze quality trends, identifying deviations and recommending corrective actions Compliance: Ensure compliance with safety and regulatory guidelines, including Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) Problem Solving: Investigate and troubleshoot quality-related issues and provide recommendations for improvement Collaboration: Work closely with cross-functional teams, including production, quality assurance, and research and development teams

Role Purpose The purpose of the role is to source and hire the right talent against the requirements shared by the business and ensuring a positive employer brand experience for the candidate throughout the hiring process. Do 1. Hire the required talent from the different sourcing channels Understand business projections and urgency of talent requirements across order and cadre demands, skill type (type A/B/C), volume vs. niche etc. As per the talent requirements shared by the business, Create sourcing plan as per hiring channel mix and cost considerations Utilize job portals, consultants, employee referral to find the right fit from the industry/ within Wipro For the shortlisted candidates, facilitate the selection process with the technical panel As per the requirement by the business, facilitate different selection tests like technical programming language skills Conduct HR evaluation round and negotiate with the candidate(s) on the salary, position etc Take necessary approval from the tower lead/ head ensuring, hiring is strictly as per Wipros salary range, minimizing exceptions to meet average cost per candidate target Formally roll out the job offer to the selected candidate(s) and coordinate with him/ her for offer acceptance Motivate, engage and maintain relationship with the selected candidate(s) from time to time till their joining Coordinate with the HRSS team for background verification of the selected candidate Communicate with Business Teams and Managers to from time to time on the status of joining etc 2. Manage Candidate Experience throughout the recruitment process Conduct candidate connect and pre-hiring candidate engagement activities to ensure healthy joining ratio Adherence to Wipro guidelines, processes and protocols with respect to responsiveness, clarity, compensation structure, SLAs, quality and auditability in all candidate communication, and deliver Zero valid escalation on hiring process Resolve candidate concerns and manage candidate escalations, turnaround slightest negative experience Daily maintain the data on the recruitment tool (Synergy) and upload all the candidate documents from time to time Ensure the weekly/ monthly/quarterly dashboards are updated and readily available for the management review Conduct meetings with WMG teams to update on the progress, risk and issues involved in hiring for a position and seek help if necessary Follow checks and balances placed by the recruitment team and conduct regular reviews with the management to ensure reliability, quality and integrity of recruitment data in the system Applications from people with disabilities are explicitly welcome.

Conducting in-depth research on industry-related topics in order to develop original content. Developing content for blogs, articles, product descriptions, social media, and the company website. Assisting the marketing team in developing content for advertising campaigns. Proofreading content for errors and inconsistencies. Editing and polishing existing content to improve readability. Conducting keyword research and using SEO best practices to increase traffic to the company website. Creating compelling headlines and body copy that will capture the attention of the target audience. Identifying customers needs and recommending new content to address gaps in the company's current content. Developing educational content, blogs, articles, and promotional materials. Strong command of language and ability to create engaging content.

Network Development and sales growth. Service to Network. Focused on Product sales. Manage Brand positioning and DSO. Management of Internal and External relationship with stakeholders. Should have good communication and marketing knowledge. Candidates working in FMCG, Cement, Telecom and banking sectors are preferred MBA would be given preference.

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

Urgent Hiring for Qc Head for a leading pharmaceutical formulations company in Sion, Mumbai. Job Title: QC Head (Pharma OSD, Regulated Plant) Job Summary: We are looking for a QC Head to lead Quality Control operations in an Oral Solid Dosage (OSD) manufacturing facility catering to regulated markets (USFDA/EU). The role involves managing QC teams, ensuring compliance, handling audits, and driving lab excellence. Key Responsibilities: Lead QC operations: analytical testing, stability, method validation & documentation. Supervise microbiology lab: environmental monitoring, water testing, product analysis. Ensure compliance with USFDA/EU guidelines; handle inspections & client audits. Oversee testing of raw materials, in-process & finished products. Review QC documents as per GMP/GLP. Mentor & manage QC teams, driving efficiency & automation. Qualifications & Experience: 1218 years of QC experience in Pharma (OSD, regulated markets), with 5+ years in leadership roles. Masters in Pharmacy/Analytical Chemistry (PhD preferred). Strong expertise in analytical techniques (HPLC, GC, Dissolution, UV, IR). Proven track record in regulatory audits. Skills: Leadership, compliance, audit handling, documentation, problem-solving.

Job purpose Ecolab is a trusted partner at nearly three million customers locations, and it is the global leader in Water, hygiene and infection prevention solutions and services that protect people and vital resources. Around the world, customer in the food, healthcare, hospitality and industrial markets choose comprehensive Ecolabs solutions, data-driven insights and personalized service to advance food safety, maintain clean and safe environment, operate efficiently and achieve sustainability goals. To support the customers in IMEA market, Ecolab has established a state-of-the-art Research, Development and Engineering (RDE) center in Pune. The RDE center is focused on developing and deploying innovation technologies as well provide technical support in water treatment, customer process improvement and development of automation tools to improve the productivity and efficiency of operations. Also, the RDE center has world class analytical laboratory for supporting the water analysis and innovation projects as well conducting performance studies. We are seeking candidate who has strong collaboration and teamwork skills, is self-motivated, has good communication skills, is creative problem solvers, and possess strong observation and perception skills. Duties and responsibilities Following are some of the key duties and responsibilities for this position Follow all safety policies and guidelines during lab work and site visits Ensures compliance with Ecolab corporate safety standards, policies and procedures and manages the lab and other processes Ability to quickly learn processes, instruments, software’s as well as others like LIMS Fostering, collaborating and continuous improvement for digitalization and automation of QA Process Conduct water analysis/tests, performance studies of technologies, customer technical support and present the findings in meetings. Develop and maintain ISO17025 excellence and compliance of the lab Minimum Qualifications Master’s Degree in Analytical Chemistry/Biotech or related discipline 1+ years of industrial experience in handling analytical instruments like ICP, IC, HPLC, TOC, XRF, GC, etc Highly skilled in conducting water analysis like cations, anions, COD, BOD, Alkalinity, organic carbon, dissolved/suspended solids, etc Profound knowledge of ISO17025 certification Strong written and oral communication skills. self-motivated, open minded team player Focused and driven while at the same time agile and flexible with the approach and assignments Strong problem-solving skills

A Scientist 1 - ADL API with 1-3 years of experience in an analytical development lab is required. The position is ideal for a candidate with an M.Sc. in Analytical Chemistry . The role involves working in a development lab, so a basic understanding of analytical instruments like HPLC, GC , and Wet Lab instruments is essential. You should be ready to work in shifts. This is a hands-on role where you will apply your knowledge to support the development and analysis of APIs (Active Pharmaceutical Ingredients).

To be well worsed with analtical instruments like HPLC,GC,FTIR,UV,POTENTIOMETER ,POLARIMETER and their application softwares To be have good knowledge in trouble shooting of instruments Should be familiar with LIMS Documentation system Should be having the experience in review of documents and other systems Should have the QMS handling knowledge like , Lab incidents , Deviation , OOS ,OOT etc,,

You are invited to join Zydus LifeSciences Ltd. at their Injectable manufacturing plant in Ahmedabad. We are currently looking to fill the following positions: 1. Production: - Staff positions ranging from Executive to Assistant Manager require candidates with a B. Pharm / M. Pharm/ B.E background and 4 to 10 years of experience in Supervising and Controlling Production areas such as Isolator, Aseptic Filling, Vial Washing, Autoclave, Lyophilizer, and Visual Inspection. Knowledge of QMS activities is a plus. - Plant Operator and Technical Assistant roles require candidates with a Diploma or ITI qualification and 3 to 6 years of relevant experience in operating production machines like Isolator, Filling, Vial Washing, Autoclave, Lyophilizer, and Batch Manufacturing. 2. Engineering: - Executive to Assistant Manager positions in the Engineering department require candidates with a BE/ B. Tech/ Diploma background and 4 to 10 years of experience in the Maintenance of Breakdown, Instrumentation, and Calibration of Process equipment for Injectable Manufacturing Plant. - Plant Operator and Technical Assistant roles require candidates with a Diploma or ITI qualification and 3 to 6 years of relevant experience in the maintenance & operations of HVAC, AHUs, Water System, handling of breakdowns, Process maintenance, Instrumentation, and calibration of Process equipment for Injectable Manufacturing Plant. 3. Quality Control (Chemical): - Executive to Assistant Manager positions in the Quality Control (Chemical) department require candidates with a M.Sc. background and 4 to 10 years of hands-on experience on HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. Knowledge of weight analysis, stability studies for Injectable dosage forms, Bio Assay QMS, and analytical data Review is essential. 4. Quality Control (Microbiology): - Executive to Assistant Manager positions in the Quality Control (Microbiology) department require candidates with a M.Sc. (Microbiology) qualification and 4 to 10 years of experience in Injectable doses form. Experience in Media & Culture management, Sterility test, BET, M.L.T., Growth Promotion test, Bio-burden test, Water monitoring, Environment monitoring in aseptic area & Identification of environment isolates is required. - Sound knowledge of cGMP documentation and cGMP requirements is essential for all positions. If you have relevant experience, we welcome you to attend the Walk-in-interview with your updated CV, Salary Slip, CTC, Photo, and relevant documents on: Date: 2nd March 2025, Sunday Timings: 9.00 a.m. - 4.30 p.m. Location: AB Road, Near Dr. Hardia Eye Clinic, Rau, Indore Madhya Pradesh-453331, India.,

Perform routine/non-routine analysis of raw, in-process & finished products using HPLC, GC & other techniques. Maintain accurate documentation as per GLP and ensure strong reporting skills through logs, test reports & records.

Instrument Analysis GC/HPLC for QC department Min 2-5 only API CO 1 to 3 year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

Hiring for Assistant Manager / Manager in Analytical Method Development (Formulations) - Solid orals for Regulated Market. Experience : 10 to 15 years into analytical method development Qualification : M.Sc . / M.Pharma Your responsibilities will include: - Supervising a team of 6 to 8 members for method development and routine testing. - Providing guidance and mentorship to analysts through practical training in analytical method development. - Conducting SOP training and certifying analysts for new team members. - Planning daily activities and allocating work for team members. - Monitoring routine analysis and troubleshooting issues. - Assisting in critical troubleshooting and on-site investigations. - Reviewing raw data, LNB, and filing routine analysis reports.

Field Service Engineer We are seeking a highly skilled and experienced Field Service Engineer to join our team on a contract basis. This role requires a minimum of 1 year and a maximum of 3 years of experience in the Pharma/Healthcare/Lifesciences industry, providing on-site technical support and maintenance in Chandigarh, India. Tasks Provide on-site technical support and maintenance for gas chromatography and liquid chromatography equipment. Troubleshoot and resolve equipment malfunctions. Perform preventative maintenance and calibration procedures. Maintain accurate records of service activities and equipment performance. Collaborate with internal teams to ensure timely resolution of customer issues. Comply with all relevant safety regulations and company policies. Skills Proven experience (1-3 years) in field service engineering within the Pharma/Healthcare/Lifesciences industry. Strong understanding of gas chromatography and liquid chromatography principles and techniques. Proficiency in troubleshooting and repairing laboratory equipment. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills. Diploma in a relevant engineering discipline.

TECHNICAL /FUNCTIONAL SKILLS: Knowledge in analytical method development using HPLC/LCMS/GC/GCMS/PREPARATIVE HPLC Expertise in peptide purification. Hands on experiences on analytical instruments such HPLC/LCMS/GC/GCMS/PREPARATIVE HPLC Theoretical knowledge in various analytical techniques and skills in analytical data interpretation Should be familiar with Analytical instruments and techniques. Knowledge in Data Interpretation Able to work follow instructions and perform the tasks under the supervision of the project leader Fair interpersonal skills Undertake relevant safety and quality trainings BEHAVIORAL/MANAGERIAL SKILLS: Able to work follow instructions and perform the tasks under the supervision of the project leader Fair interpersonal skills OTHER JOB REQUIREMENTS: Undertake relevant safety and quality trainings

Dear All, We are seeking a highly motivated and talented Analytical R&D Scientist( Topicals ) to join our innovative team. The ideal candidate will have a strong foundation in Analytical development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 4-7 Years Job Responsibilities: 1. To ensure scientifically strong justification for the analytical tasks taken up. 2. To follow the departmental SOPs. 3. To ensure the error free and online documentation. 4. To ensure only calibrated instrument /equipment's are used for analysis. 5. To coordinate with supervisor and lead development of methods for IVRT, IVPT, ex-vivo, assay by UV/HPLC and RS by HPLC. 6. To coordinate with supervisor in developing the methods for residual solvents and other volatile components by GC. 7. To perform analysis of development samples for IVRT, IVPT, ex-vivo, Assay by UV/HPLC and RS by HPLC as per test method. 8. Perform validation of test procedures like IVRT, IVPT, ex-vivo, Assay, Related substances, residual solvents, Residue and Chiral purity etc., 9. To ensure the instruments/equipment are cleaned after completing the analysis and columns are washed to ensure maximum life. 10. Receipt, storage and management of samples/standards. 11. Labeling of standards, chemicals and reagents. 12. Receipt of logbooks and SOPs from QA. 13. To ensure GLP compliance in laboratory. 14. Supporting the installation of instruments and equipment's. 15. To ensure the reference, working standards and impurities are maintained as per GLP. 16. To ensure timely archival of completed files and LNB. 17. Assist and/or perform analysis of development samples for in-process and finished product parameters as per Analytical Test Method/Standard Test Procedure. 18. Coordinate and assist with timely completion of Instrument calibration and preventive maintenance. 19. To participate in formulation development trails. Note: Interested candidates can share their resumes to raghuveera.vutla@aizant.com and Immediate joiners are more preferable

Responsible for Analysis of RM/ inprocess/ FP/PM Samples, Instrument Calibration, Instrument Qualification Protocols & perform Qualification activity(OQ/PQ), analytical record, analytical cleaning method validation of the API, Online SAP Activity etc Required Candidate profile M.Sc./B.Sc. with 4 to 8 yrs exp in QC of cGMP, USFDA, MHRA approved Bulk drug/API unit. Sound exp & knowledge of handling GC, HPLC, KF, pH meter, Spectrophotometer, Auto Titrator, MP/BP etc.is must. Perks and benefits Negotiable

We are hiring for Quality Control for Executive / Senior Executive role Applications are invited for the position of Executive QC and Sr. Executive QC Interested candidates can apply for this position. Required experience: 2 to 10 years Candidates with experience in handling of sophisticated instruments e.g. HPLC, GC, UV, IR, Dissolution apparatuses and other laboratory equipment are preferred. Analysis of RM, In-process, FP Samples. Experience in calibration of all the instruments. Experience in analysis of Process Validation and Cleaning Validation Samples. Well versed with Good Laboratory Practices ,Data integrity concepts, investigations, OOS, OOT and Laboratory Deviations. Exposure of Regulated/Semi-regulated markets. Should be familiar with quality systems followed in the analytical Laboratory Educational Qualification: M. Sc. Chemistry/Analytical, B. Pharm, M. Pharm Salary: No bar for appropriate and early joining candidates Please bring following documents (Mandatory) 1) Updated CV 2) A color passport size photograph 3) Original and photo copies of all educational certificates, 4) Aadhar card, 5) PAN card 6) Salary slips of last 3 months. Please call on us on 04344-277937, 276618, for any queries. I f you unable to attend Walk-in interview, Send your updated CV to manjula.m@microlabs.in

QC

Key Responsibilities: Ensure proper installation, calibration, and maintenance of analytical instruments and equipment. Handle and troubleshoot Chromatographic systems (HPLC, GC), Atomic Spectrophotometers, Analytical Balances, pH / Conductivity meters, and Autoclaves. Support validation and qualification of instruments as per regulatory guidelines (USFDA, EU, WHO). Coordinate preventive and corrective maintenance schedules with vendors. Maintain calibration records and ensure compliance with GMP and GLP requirements. Provide technical support to analytical teams for smooth lab operations. Key Skills: Strong technical knowledge of laboratory instrumentation. Familiarity with pharma quality and regulatory requirements. Good documentation practices and problem-solving skills. Qualification: B.E. / B.Tech in Instrumentation Experience: 25 years preferred (Freshers with strong fundamentals may also apply)