1373 Hplc Jobs

You are looking for a QC Chemist with 4-5 years of experience or a Fresher in quality control lab. The ideal candidate should be familiar with operating sophisticated instruments such as HPLC, GC, and SPECTOPHOTOMETER. It is essential that the candidate has received training in cGMP. Salary is negotiable based on the candidate's experience. If you are interested in this position, please apply with your resume to the provided email address. This is a full-time, permanent role with benefits including Provident Fund. The preferred education level for this position is a Bachelor's degree. The preferred total work experience required is 2 years. The work location for this position is in person.,

You should have a minimum of 10 to 15 years of experience in the QC department of Pharmaceutical formulation. Your responsibilities will include troubleshooting sophisticated instruments such as HPLC, IR, UV, etc. It is essential to have knowledge of calibration, validation of instruments, and system management. You will also be responsible for managing sample inventory, conducting analysis, and ensuring timely release of samples. A degree in M.Pharm, B.Pharm, or M.Sc. is required for this position at Surmount Laboratories Pvt. Ltd.,

As an Analytical Chemist at our company, you will be responsible for developing analytical methods using techniques such as HPLC, GC, LCMS, KF, and FTIR for routine analysis. You will also be in charge of maintaining analytical documentation including protocols, specifications, etc. Calibration of HPLC and GC instruments will be part of your regular tasks. It is essential that you are knowledgeable about data integrity and ALCOA guidelines. Additionally, you will be involved in chiral method development to support our analytical processes.,

As a Peptide/Peptidomimetic Purification and Analysis Specialist, your primary responsibility will be to purify complex peptides with a high level of purity using PREP HPLC techniques. You will also be involved in the purification of peptides for scale-up activities. Your productivity will be measured based on the number of purifications and analyses you perform. It will be essential to ensure the proper maintenance of instruments such as HPLC, MPLC, lyophilizer, peptide synthesizer, centrifuge, etc., and to adhere to SHE/regulatory guidelines. Collaboration with the peptide synthesis team will be crucial for successful project outcomes. Regular updates in the form of PowerPoint or Excel presentations will need to be prepared, and maintaining a detailed lab notebook is a key requirement. Key Competencies for this role include excellent communication and interpersonal skills, the ability to work effectively in cross-functional teams, a positive attitude, and strong problem-solving abilities. Additionally, having good analytical skills will be essential for carrying out peptide purification and analysis tasks efficiently.,

As a Chemist, you will be responsible for carrying out production and quality control activities in the pesticides industry. The role will be based in Raipur (Chhattisgarh) and Rawanbhata Industrial Area. Your primary duties will include operating laboratory equipment such as GLC, HPLC, UV spectrometer, and other related instruments. To excel in this role, you should have previous experience in handling production and quality control activities within the pesticides industry. If you have a strong background in chemistry and the capability to work with precision and attention to detail, we encourage you to apply for this position.,

Scientist med chem: 2 5 years To Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. To have broad knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. To work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports, powerpoint presentations and other scientific documents by using the chemdraw as needed. Should be able to scout new / alternate schemes & know the use of scifinder, reaxys etc. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Show more Show less

Job Description Synthesize and characterize novel NCEs as per client specifications, in an efficient and independent manner. Broad knowledge of modern organic chemistry and synthetic methods Heterocyclic chemistry, metal catalyzed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc. Work with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Up to date maintenance of Lab Note Books, as per client specifications and guidelines. Generation of final reports and other scientific documents, as needed. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Required Candidate Profile M.Sc. Organic Chemistry/Chemistry Experience:- 2 to 8 years in Synthetic Chemistry(Small Scale) Job Location: Bengaluru. Show more Show less

Aurigene Pharmaceutical Services Limited is seeking a talented and motivated Scientist - Medicinal Chemistry - to join our growing team. In this role, you will play a key role in the discovery and development of novel drug candidates by designing, synthesizing, and characterizing target molecules. Responsibilities Synthesize novel target molecules according to client specifications, working independently and efficiently. Utilize your broad knowledge of modern organic chemistry and synthetic methods, including: Heterocyclic chemistry Metal-catalyzed reactions Handling air/moisture sensitive reagents Hydrogenations Multi-step synthesis Apply a wide range of techniques in synthesis and purification: Chromatographic methods (including expertise in MPLCs) Spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR) Demonstrate problem-solving skills and the ability to think creatively to overcome synthetic challenges. Maintain laboratory notebooks and meticulously, adhering to client guidelines. Generate final reports and other scientific documents as required. Demonstrate a strong understanding of safety protocols and adhere to EHS guidelines as per our zero-tolerance policy. Key Skills And Competencies M.Sc. in Organic Chemistry with 2to 8 years of relevant experience. Strong knowledge of modern organic chemistry principles and synthetic methods. Expertise in various techniques for organic synthesis, purification, and characterization. Excellent problem-solving and critical thinking skills. Ability to work independently and as part of a team. Strong communication and interpersonal skills. Proficiency in scientific writing and record keeping. Show more Show less

Position Scientist Medicinal Chemistry (CRO) Location Hyderabad/Bangalore Desired Profile M.Sc. (Organic Chemistry/Chemistry) with 3-8 years Job Description, Key Skills And Competencies To synthesize, and characterize novel target molecules as per client specifications, in an efficient and independent manner. To have broad knowledge of modern organic chemistry and synthetic methods: heterocyclic chemistry, metal catalysed reactions, handling air/moisture sensitive reagents, hydrogenations, carrying out multi-step synthesis etc.. Hands-on experience with a wide range of techniques in synthesis and purification (Chromatographic methods including smooth knowledge of MPLCs), and spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR etc.). Ability to think outside the box and independently solve synthetic problems. Troubleshooting for the whole team and being able to take quick and decisive actions (for PhD candidates and/or lab leaders). Maximize the productivity of the group and provide intellectual input to the department. Ability to manage a small team of 3-4 chemists, in addition to his/her individual work (for lab leaders/PhDs). Interaction with the clients and smooth communication of project goals/results during the weekly TCs/VCs (for lab leaders/PhDs). Up to date maintenance of Lab Note Books, as per client guidelines. Generation of final reports and other scientific documents, as needed. Understanding of systems and process pertaining to safety, health and environment. Follow the EHS guidelines, as per zero tolerance policy. Competencies Good Communication Skills Interpersonal Skills Team Player Show more Show less

Trending Job Description To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation. Intimation & result reporting after completion of analysis & relevant documentation. Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state. Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, glassware, water preparation equipment, water bath, sonication baths, mobile phase bottle etc. Ensure the online documents pertaining to day-to-day analysis are efficiently completed in timely manner. Reporting the activities daily to immediate supervisor. Destruction of QC Samples like Retention samples, analyzed samples etc. To take out the quality reports, Data / Results entry in SAP system. To prepare and maintain the working standards & documentation. Ensure timely raising and closure of deviations, quality events, change controls, OOS/OOT. Preparation and maintenance of Analytical data sheets and Excel spread sheets. Adequate knowledge of all equipment/instruments & their functioning in the laboratory & assist in equipment/instrument qualification activities. Ensuring the quality and integrity of all GxP data and documentation generated. Ensuring effective execution requirements of food regulations (US)-21 CFR Part 111. Ensure fully Engagement and Involvement regarding awareness, clarity maintained related to data integrity. Ensure the 21 CFR Part 11 compliance in the Laboratory. Ensuring good housekeeping and accident-free working in the Laboratory. To perform safe Laboratory operations (as per MSDS) ensuring proper usage of PPEs, safe, secure storage of hazardous, toxic, explosive, corrosive, irritant materials. Ensure proper maintenance of HPLC and GC column and related logbooks in QC lab. To fulfill the analytical requirements of FSSAI regulation. To undergo assigned trainings on cGMP, HSE & departmental procedures / policies. To determine internal and external QEHS issues as well as needs and expectations of relevant interested parties and monitor the same.To implement QEHS policy & objectives. To ensure participation and consultation of worker. To identify & communicate incidents, QEHS non conformities, investigate and take corrective actions on the same. To ensure work permit system during maintenance activities. To ensure disposal of waste. Qualifications QC Analyst (Apprentice) Qualification: M.Sc. Chemistry About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limiteds investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 9087 Job Category Quality Control Posting Date 07/29/2025, 08:05 AM Job Schedule Full time Locations Piramal Enterprises Limited, Plot no. K-1, Mahad, Maharashtra, 402302, IN Show more Show less

You should have a Master's degree in Chemistry, Food Science, or Life Sciences with 0 to 5 years of experience in the FMCG/Cosmetics/Foods/Pharmaceutical industry. Your responsibilities will include operating, calibrating, performing intermediate checks, and maintaining various laboratory equipment such as UV-Vis spectrophotometer, K.F. Titrator, Conductivity meter, Viscometer, FT-IR, Tintometer, Analytical balance, pH meter, GC, and HPLC. Experience in handling Kjeldahl digestion and Distillation Unit, as well as preparing and maintaining Reference standards and volumetric standard solutions, is required. You will be involved in quality control and quality assurance activities, including testing retained samples, spiked samples, and participating in inter-laboratory comparisons and proficiency testing programs related to skincare, hair care, hair color, specialty products, foods, snacks, dairy products, beverages, and bakery products. Additionally, you will be responsible for preparing STPs, Validation documents, and Raw material/Product specifications. Proficiency in using Viscometer, Refractometer, and Tintometer is essential. Strong documentation skills and adherence to Good Laboratory Practices are necessary. You should possess excellent English written and oral communication skills to effectively communicate analytical results to both scientific and non-scientific team members. Immediate joining is required for this position located in Ekkathangal, Chennai. This job is with HEPL, a Group company of a 35-year-old FMCG Brand known for manufacturing popular products such as shampoos, hair colors, and food products like milk, milkshake, curd, and ghee. This is a full-time, permanent position with benefits including health insurance and Provident Fund. The work schedule is day shift from Monday to Friday, with a yearly bonus. To apply, you should have experience in Research, NABL, and Laboratory work for at least 1 year each. Immediate joiners who meet the educational and experience requirements are encouraged to apply for this role.,

As a Sales Executive at Anand Brothers, you will be an integral part of our team serving the diagnostic industry with a dedication to quality and reliability since 1978. Your role will involve working with various technology platforms such as ELISA, RIA, IFA, HPLC, and Molecular. With a diverse portfolio of over 1700 products from international companies, you will have the opportunity to engage with customers, provide technical support, explain products, handle inquiries, and manage customer relationships. Your responsibilities will also include maintaining records and contributing to sales strategies to drive revenue growth. To excel in this position, you should possess strong customer engagement, communication, and relationship management skills. Technical knowledge in diagnostic platforms and products will be essential, along with proficiency in sales strategies, record-keeping, and data management. Problem-solving and technical support capabilities are key attributes that will contribute to your success in this role. Prior experience in the diagnostic or healthcare industry is advantageous, and a bachelor's degree in a relevant field will be beneficial. Join us in our mission to deliver exceptional service to the diagnostic industry and be a part of a dynamic team that values innovation, excellence, and customer satisfaction. If you are passionate about sales, support, and driving growth in a challenging yet rewarding environment, we welcome you to apply for the Sales Executive position at Anand Brothers.,

You will be responsible for maintaining the Laboratory's Quality System and performing analytical tests in the laboratory. Additionally, you will assist with laboratory administrative duties to ensure smooth workflow. Your role will involve obtaining lab certifications, completing QA/QC assignments, and promoting good customer relations with all clients. To excel in this position, you must possess strong analytical and problem-solving abilities, as well as team-building skills. Effective verbal and written communication skills are essential, along with the ability to adapt to and drive change. Experience with ISO standards, ASTM, and/or DIN standards is required. The ideal candidate should have a strong knowledge of ISO 17025:2017 and must have implemented the same in any laboratory setting. Knowledge of GC and HPLC will be considered an added advantage. Familiarity with MoU and experience in calculations and document maintenance are also desired qualifications. Qualifications for this role include a Graduate degree with training in ISO 17025:2017 and a minimum of 5-7 years of relevant experience. The job is located in Bahadurgarh, Haryana with one vacancy available. Key Skills: - Medical LAB Executive - Laboratory Assistant - Sample collection - ISO 17025 - HPLC Experience Required: 5 - 11 Years Salary: INR 4,50,000 to 6,00,000 per annum Industry: Manufacturing / Production / Quality Education: Professional Degree Please note that only shortlisted candidates will be contacted for further evaluation.,

You are seeking a Senior Chemist with experience in handling GC-MS and HPLC instruments. As a Senior Chemist, you will be responsible for conducting analytical chemistry experiments, data analysis, and reporting results. This is a full-time position with benefits including paid sick time, paid time off, and a performance bonus. The work schedule is during the day shift. The ideal candidate should have a Bachelor's degree in Chemistry or a related field. A minimum of 1 year of experience in analytical chemistry is preferred. This position is located in Bangalore City, Karnataka. Candidates should be able to reliably commute to the work location or be willing to relocate before starting work.,

You will be joining our team as a Deputy Manager/Manager, Analytical method transfer, responsible for delivering developed analytical assays from R&D scale to GMP-compliant commercial quality control labs. Your role will involve overseeing projects related to analytical method transfer, collaborating with cross-functional teams, and ensuring technology transfer and assays qualification activities are conducted in compliance with GLP and GMP standards. The ideal candidate will possess expertise in cGMP, regulatory requirements, technical troubleshooting, method transfer, method validation, technology transfer, and laboratory techniques to support routine testing and release of research and cGMP grade materials. You will be directly involved in drafting technology transfer documents, risk assessments, process FMEA, method validation protocols, facility fit assessments, and other related activities necessary for the release and testing of microbial and mammalian fermentation-based products. You should have familiarity with analytical assays such as HPLC, GC, SDS-PAGE, agarose gel electrophoresis, densitometry, dd-PCR, RT-PCR, ELISA, UV-Visible spectrophotometry, western-Blot, as well as microbiological techniques like BET, BioBioburdend Sterility testing. Additionally, the position may entail assisting in cell bank testing and release under cGMP regulations and coordinating with third-party collaborators for external testing as needed. Your responsibilities will also include authoring and reviewing research studies, compiling experimental data, and contributing to protocols, study reports, and publications with minimal supervision. You will work as part of the method transfer and method validation team, ensuring timely and successful completion of process transfers while addressing any unexpected technical challenges. We are looking for individuals who are enthusiastic, highly motivated, and capable of multitasking. The role requires working collaboratively within a team environment and independently across various aspects of projects related to microbial-derived products.,

As a key member of the Quality Control team, your main responsibility will involve performing laboratory analysis and instrumentation tasks efficiently. This will include conducting analytical tests on raw materials, finished products, and various samples within specified timelines. You will also play a crucial role in maintaining control of the data generated from these analyses. To excel in this role, you should possess the following skills: - Proficiency in wet analysis techniques such as titrimetry and other relevant methods - Familiarity with a range of analytical procedures - Hands-on experience in operating instruments for analyzing color, moisture, etc. - Ability to carry out maintenance, calibration, and validation of laboratory equipment - Prior exposure to handling GC/HPLC instruments would be highly advantageous In terms of experience, we are looking for candidates with a minimum of 2-3 years of relevant experience in the food or food-related industry. This experience should cover a broad spectrum of activities related to quality control and laboratory analysis. For more information on our commitment to workplace diversity and inclusion, please visit IFF.com/careers/workplace-diversity-and-inclusion. We look forward to welcoming a dedicated professional like you to our team!,

As a Process Development Chemist, you will be responsible for designing and conducting experiments to create new chemical processes and enhance existing ones. You will scale up laboratory procedures to pilot and production levels, ensuring scalability and reproducibility. Analyzing current processes, identifying areas for enhancement, and implementing modifications to boost efficiency, yield, and safety will be a key aspect of your role. Utilizing statistical methods and tools to assess process performance will be crucial. You will collaborate closely with cross-functional teams, such as R&D, quality assurance, production, and regulatory affairs, to seamlessly integrate processes. Providing technical support and expertise to production teams will be essential. Additionally, you will prepare detailed documentation for processes, including protocols, reports, and standard operating procedures (SOPs), while ensuring compliance with safety, environmental, and quality standards. In the event of issues during production, you will investigate and resolve them promptly to minimize downtime. Conducting root cause analysis and implementing corrective actions will be part of your troubleshooting responsibilities. Staying updated on the latest advancements in chemical processes and technologies, and evaluating and recommending the use of new tools and technologies to enhance process performance will be vital for research and development. To qualify for this role, you should hold a Bachelors or Masters degree in Chemistry, Chemical Engineering, or a related field, along with years of experience in chemical process development or a related area. A strong understanding of chemical reactions, kinetics, thermodynamics, and safety regulations is required. Proficiency in analytical techniques such as HPLC, GC, NMR, and others relevant to process chemistry is essential. Excellent problem-solving skills, attention to detail, and strong communication and teamwork abilities are desired qualities. This is a full-time, permanent position with benefits such as provided food, paid sick time, and Provident Fund. The work schedule may involve day shifts or rotational shifts, with the work location being in person.,

You will be joining an independent private testing laboratory located in Panipat, Haryana, in the National Capital Region (NCR) near Delhi. Established in 2002, the organization is Accredited by NABL (National Accreditation Board for Testing and Calibration Laboratories) and recognized by the FSSAI, EIC, APEDA, BIS & FDA. We strictly adhere to ISO/IEC/17025-2005 standards in chemical and mechanical testing. As a Sr. Analyst in this full-time on-site role, your primary responsibility will be the testing of pharmaceutical products and raw materials using HPLC. Your daily tasks will involve data analysis, preparation of detailed reports, ensuring compliance with industry standards, and collaborating with team members to uphold the highest level of accuracy and reliability in test results. To excel in this role, you should possess the following qualifications: - Proficiency in Data Analysis and Report Preparation - Knowledge and experience in handling HPLC and Pharma testing equipment - Understanding of Quality Control and Compliance with Industry Standards - Excellent written and verbal communication skills - Capability to work both independently and collaboratively on-site - A Bachelor's or Master's degree in Pharmacy or Science - Previous experience in a NABL-accredited laboratory would be advantageous If you are passionate about pharmaceutical testing, possess strong analytical skills, and thrive in a collaborative work environment, we encourage you to apply for this exciting opportunity to contribute to our commitment to excellence in testing and calibration.,

Urgent Requirement in PHARMA Industry Experience persons wanted in QC (WET ANALYSIS / HPLC / GC) Department, candidate should have good working experience in pharma industry. Qualification: B.SC /M.SC (Chemistry) Experience: 2-5Years Location: Jeedimetla , Hyderabad. Note: Only Male Persons Required. Contact: 8977333658.

Let s build the future of medicine together. Join Enveda as an Research Associate / Senior Research Associate In Vitro ADME in Hyderabad, India, and help us transform natural compounds into life-changing medicines. We re a team driven by curiosity and innovation are you ready to make a difference On-Site | Hyderabad, India | Full-Time | What Makes Us Enveda Life is smart, and we can learn from it. We re reinventing drug discovery by harnessing nature s intelligence. Our platform identifies new medicines four times faster than the industry standard because patients can t wait. What sets Enveda apart isn t just what we do it s how we do it. Our culture is built on creativity, collaboration, and deep respect for each other. We believe People Create All Value, and our success is driven by the extraordinary team turning our mission into reality every day. We re proud of the momentum we ve built: - Jan 2024: Named a LinkedIn Top Startup to Watch - Mar 2024: Forbes America s Best Startup Employers - Oct 2024: First drug to Phase 1 Clinical Trials - -Dec 2024: Raised a $130M Series C These milestones reflect the impact of our team and we re just getting started, but they re only possible because of the diverse talent, perspectives, and relentless drive of our team, and people like you. Your Role in Our Mission At Enveda, every role drives impact. As a Research Associate / Senior Research Associate In Vitro ADME , you ll be at the forefront of delivering hope to patients everywhere. Your expertise in in vitro ADME studies will be critical in advancing our novel therapeutics from lab to clinic because every breakthrough starts with bold questions and brave actions. What You ll Do Design and execute in vitro ADME studies for novel compounds Optimize and validate protocols for reliable assay performance Analyze and interpret data to inform drug discovery strategy Collaborate with cross-functional teams to meet project milestones Mentor junior scientists and stay current with evolving methodologies We re Looking For: Master s degree in Pharmaceutical Sciences or related field 5 7 years of relevant industry experience in DMPK Hands-on experience with microsomal/hepatocyte assays and LC-MS/MS or HPLC Strong problem-solving mindset and excellent communication skills If you re passionate about innovation and impact, we encourage you to apply even if you don t meet every requirement. Our Values: Curiosity | Agency | Journey | Charity | Unity Benefits: Culture | Medical | Block Leaves | Work-Life Harmony At Enveda, we re building a place where everyone can do the best work of their life. We are an equal opportunity employer and value diversity in all its forms. Apply now and join a team committed to shaping the future of drug discovery.

The Roles Responsibilities are: To arrange laboratory as per Good Laboratory practice (GLP). To prepare Standard operating procedures. To prepare Standard testing procedures To prepare Instrument Operating procedures. To calibrate all the instruments at specified regular intervals. Method development. To prepare and maintain QA/QC documents and registers. To maintain standard records and documents as per FAMI-QS. Inspect, test, or measure materials or products being produced Report inspection and test data. To carry out any work given by QC/Lab Incharge. To carry out the analysis work and report any abnormality to Seniors To do the analysis of RM / In-process / FP by chemicals instrumental methods of analysis. To prepare SOP for QC Instruments, and STP for RM / FP. To do the calibration of Instruments as and when required. Mandatory Skills: B.Sc or M.Sc with Chemistry. Should have working experience of 3-5 yrs. Knowledge of Wet Chemical analysis. Knowledge of Instrumental Analysis. Knowledge of Documentation SOPs and STPs. Knowledge of preparation of COA. To carry out daily calibration of instruments Desired Skills Well Versed with Titrimetric analysis. Well Versed with the handling of UV, GC, and HPLC. Should be able to prepare SOPs, STPs of RM, and FP when required. Should be able to prepare COA of FP when needed. To do daily calibration of Instruments like balance, PH meter, periodic calibration of GC, HPLC, UV. Designation: QC Executive / QC Officer. Job Location: Bhiwandi. Experience: Candidate with 3 to 5 years of experience. Qualification: B.Sc. or M.Sc. in Chemistry Qualifications Experience can be relaxed in the case of exceptionally talented candidates with the approval of Management

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary Under the guidance of Manager-Instrumentation / R&D , responsible for installation, maintenance and calibration of all the instruments in Apotex Research Pvt Ltd as per GMP/GLP requirements. Also responsible to generate and maintain laboratory equipment documentation. Job Responsibilities Conducts duties following established Apotex Research Pvt. Ltd., Standard Operating Procedures and in a consistent manner consistent with current regulatory (GMP, DCGI- CDSCO,TPD, USFDA, TGA, ICH, GLP, EMEA) guidelines / established practices / expectations. Perform maintenance and calibration of analytical instruments like HPLCs, GCs, pipettes, balances, etc and maintain instruments in good working order. Monitor and support during instruments installations and qualifications. Prepare and revise instrument related SOPs. Assists and involve in preparation and execution of documents for software validations. Maintain/Oversee all the instrument related qualification files, software validation reports, routine calibration records their scheduled archiving. Arrange vendor engineers for maintenance/calibration and maintain necessary AMC contracts with vendors. Update and maintain the Master list of instruments and calibration schedules. Monitor freezer/environmental monitoring system and respond to the alarms. Documents all the work and results of all assignments as required. Investigates and corrects analytical, instrumental, and procedural problems, if necessary in consultation with supervisor or management. Ensures that all work is performed in compliance with all pertinent SOP, GLPs, GALP and Safe Work Practices. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Minimum BE / B.Tech / M.Sc. Instrumentation. 2 to 4 years of experience in Instrumentation of AR&D, Bioanlaytical lab, QC labs. Experience with analytical laboratory equipment like HPLC, LC/MS/MS, GCs etc. for trouble shooting, repairs, calibraitons, qualifications, etc. Fundamental understanding of concepts of GMP, GLP, GCP, 21 CFR Part 11guidelines. Computer skills in laboratory data acquisition software(s), spreadsheets and word processing. At Apotex, we are committed to fostering a welcoming and accessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

Responsibilities: Observing and complying with Good Laboratory Practice, Good Manufacturing Practice (GMP), and data integrity. Observing and complying with company. Writing/Reviewing Standard Operating Procedures (SOPs), Office cab/shuttle Food allowance

Amneal Pharmaceuticals is looking for Officer, Quality Control to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes

Department: ADL Experience: 5+ Years Qualification: M.Sc. (Analytical Chemistry) Location: Vadodara Job Description: We are looking for an experienced Executive in the Analytical Development Laboratory (ADL) to support R&D activities. The role involves method development, validation, analytical testing, and ensuring regulatory compliance of pharmaceutical products. Key Responsibilities: Develop and validate analytical methods for pharmaceutical substances and products. Conduct analytical testing using HPLC, GC, UV, Mass Spectrometry, etc . Troubleshoot analytical issues and ensure data accuracy and reliability. Adhere to quality control protocols and support audits (Customer/Regulatory). Maintain and calibrate lab instruments and stay updated with new analytical technologies. Follow QMS, SOPs, and safety standards. Skills Required: Strong knowledge of analytical chemistry techniques. Experience in pharmaceutical R&D. Good documentation and communication skills.