2096 Hplc Jobs - Page 26

Will be responsible for setting up and managing theend-to-end plant stores operations, including receipt, storage, issuance, andtracking of raw materials (SS plates, beams, fasteners), bought-out items,consumables, welding materials, and project-specific materials. This role iscritical to ensure real-time inventory accuracy, prevent stockouts, and supporttimely production with efficient inward and outward material flow. Key Responsibilities A. Stores Operations Material Handling Set up and maintain a 5S-compliant store layoutwith clear zones for raw materials, consumables, scrap, and rejected items. Define and implement material identificationsystems (bin cards, tagging, heat numbers, and location marking). Supervise the inward and outward movement of SSplates, fasteners, consumables, and BOPs in coordination with QA and PPC. Ensure shelf-life-sensitive items (e.g., flux,gases, paint) are tracked and consumed within validity. Plan shift-wisemanpower deployment and cross-training across store assistantsand handlers. Support ProductionCoordinators in issuing tagged materials as per released jobs and the shiftplan. Coordinate with material handling teams for safeEOT/forklift movement and stacking of large items. B. Inventory Accuracy Traceability Maintain updated,traceable stock records in ERP (SAP/MM or equivalent) covering GRNs, issues, returns, and job-wise tagging. Align with PPC, Central PPC, and Nesting teamsto ensure material availability as per job release sequence. Conduct daily cycle counts and monthly physicalstock audits; reconcile system vs. physical stock and flag deviations. Track BOM vs. actualmaterial issuance and flag excess consumptionor loss trends to the Plant Head and Finance. Monitor stock health avoid overstocking ormaterial gaps that impact flow. C. Escalation Coordination Escalate materialmismatches, excess withdrawals, unidentified stock, or tagging gaps to the Plant Head and Quality team. Liaise daily with QA, PPC, Purchase, andProduction for flow-aligned inventory operations. Maintain documentation readiness for ISO,internal, or client/TPI inspections. ResponsibilitiesOutside the Scope of This Role Does not decide what job to release or sequence supports PPC-released jobs only . Does not fabricate or inspect material ensurestraceability, escalation, and clear flow. QualificationsExperience Diploma or Graduate in Inventory Management,Commerce, Logistics, or Industrial/Production Engineering Preferred: Certification in Stores or Materials Management (e.g., NIIT, IIMM) 610 years of experience in fabrication,engineering, or EPC stores; at least 2 years managing a team Experience handling stainless steel (SS) plates,consumables, and job-wise traceability Proficient in using ERP systems (SAP-MM, Oracle,or equivalent) and MS Excel Familiar with shelf-life tracking of consumablesand documentation for audits Strong understanding of material tagging,physical stock control, and inventory reporting KeySkills Traceable material handling and job tagging BOM vs. issuance tracking and variance reporting Forklift/EOT coordination for heavy materialmovement Team supervision, shift coordination, andtraining Inventory layout planning, 5S practices, and bincard management Loss prevention, non-moving stockidentification, and cost awareness ERP usage, GRN documentation, and Excel-basedstock analysis

Vipul Organics Limited (VOL) is a leading manufacturer of specialty chemicals and colorants, committed to innovation, quality, and environmental safety. With a strong legacy and global presence, we are now looking to strengthen our team with a dedicated Instrumentation Chemist at our Palghar unit. Key Responsibilities: Conduct precise chemical analysis using Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC) . Ensure regular calibration, maintenance, and troubleshooting of GC and HPLC instruments. Record, analyze, and report test results in a timely and accurate manner. Maintain laboratory standards as per safety, regulatory, and quality protocols. Support the QC and R&D teams in routine and special analysis projects. Candidate Profile: Education: B.Sc. in Chemistry (mandatory) Experience: 1- 2 years in instrumental analysis (GC and HPLC expertise required) Skills: Strong analytical ability, attention to detail, and familiarity with laboratory documentation Availability: Immediate joiners preferred Job Location: Palghar, Maharashtra

Job Description Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. Having analytical knowledge of Nasal/Derma products. 3. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 4. Ensuring data integrity policy, GDP and its effectiveness up to compliance 5. To maintain the stability chamber and tracker. 6. To maintain the stability chamber and tracker. 7. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Role & responsibilities Ensuring the cleanliness and housekeeping activities in the laboratory. Ensuring the laboratory safety. Calibration of analytical instruments like High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). Analysis of raw material, in-process, finished product and stability samples using HPLC & GC. Analysis of vendor samples as part of vendor qualification. Analysis of cleaning samples using UV & HPLC. Analytical method validation, method transfer and verification analysis as per protocol. Analytical column performance and maintenance. Temperature and humidity daily check in HPLC room. Preferred candidate profile Analytical Chemistry Documentation skills GMP, cGMP/ GLP Skills Interpersonal skills 5S skills( Sort, Straighten, Shine, Standardize& Sustain)

New campaign and new plant products,Execution of analytical requirements for products,Analysis reporting,Maintain & follow IMS & NABL Procedures for products,Timely Approval of Raw material and finished products,5S, TQM, eAM and IMS.

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control Experience: (01 12Years) HPLC/ Stability/ GC/ IP/ FP/ RM/ Validation/ Reviewer QUALIFICATION : B.Sc, M.Sc, B. Pharm and M.Pharm with relevant experience DESIGNATIONS: Officer, Jr.Executive, Executive, Sr.Executive & Asst. Manager INTERVIEW VENUE: Hotel: RAUNAK Restaurant Ground Floor, Opp. Axis Bank, Bitna Road, Kalka Shimla National Highway, Pinjore, Haryana 134102 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates Experience in HPLC - Formulation is Mandate Preferred for Male Candidates Share with your friends, collegues and in known groups for better reach CONTACT INFO: E-mail: Harishwar.M@hetero.com & Contact: 8121005416, 9218677050 for further info

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 02-08-2025. 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 : 02-08-2025 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

As an In vitro Bioanalytical Scientist at Syngene, based in Hyderabad, you will be responsible for participating in sample processing for PK and ADME assays, as well as handling LCMS/MS. Your role will involve adapting to a dynamic team environment, processing various matrices samples for PK studies, optimizing test compounds manually and automated on LCMS/MS, and independently handling HPLC for UV-based sample analysis. Additionally, you will be expected to develop methods with the team lead, document lab notebooks online, and manage compounds effectively. You will need to demonstrate expertise in column selection, mobile phase selection, solvent preparations, and sample processing techniques such as protein precipitation, liquid-liquid extraction, and solid-phase extraction. It is essential to have experience in handling ADME assays and HPLC and LCMS/MS, with a minimum of 3-5 years of relevant experience. Moreover, you should be capable of developing and validating LC-MS based qualitative/quantitative methods, conducting internet-based literature searches, and interpreting Mass/UV Spectra. As a part of the Syngene team, it is mandatory to adhere to safety guidelines, procedures, and SOPs, ensuring the safety of yourself, teams, and the lab/plant at all times. You must also complete all assigned mandatory trainings related to data integrity, health, and safety measures promptly. Furthermore, you will be expected to comply with Syngene's quality standards, hold yourself and your teams accountable for safety goals, and review safety metrics periodically. Syngene values excellence, integrity, and professionalism, and expects all employees to consistently demonstrate alignment with these core values. As a leader at Syngene, you will champion effective Environment, Occupational Health, Safety, and Sustainability (EHSS) practices, foster a corporate culture promoting an EHSS mindset, and uphold the highest standards of quality, integrity, and compliance. The ideal candidate for this role should possess a M. Pharm in Pharmaceutical Sciences or Pharmaceutical Analysis with a passion for LC/MS related bioanalysis. You should have a general understanding of drug metabolism and pharmacokinetics, be able to deliver scientific presentations, and write official project reports. Additionally, you should ensure preventative maintenance and calibration schedules of HPLC and mass spec by coordinating with vendors and support staff. Syngene is an equal opportunity employer, committed to providing integrated scientific services from early discovery to commercial supply, with safety as a top priority in all aspects of operations.,

As a member of the team, you will be responsible for carrying out technical tasks related to experiments and maintaining laboratory equipment with accuracy. This includes setting up reactor assemblies and experimental setups for tests and experiments, as well as preparing and synthesizing samples at a lab scale. Additionally, you will be conducting structural, textural, and mechanical testing using various equipment such as XRD, Physisorption/chemisorption unit, TPD, microscopy, Thermal analyzer, IR/UV-Visible spectrometer, GC, HPLC, etc. It is essential to ensure the proper upkeep of reactors, analytical instruments, and maintain usage logs in the laboratory and pilot plant. Keeping records of spares and consumables in the lab and initiating procedures for replenishment is also part of your responsibilities. The ideal candidate for this position should hold an MSc degree in chemistry or biology. Previous experience ranging from fresh graduates to individuals with up to 3 years of experience in an Industrial Chemical laboratory or QA/QC laboratory is preferred. Skills and competencies required for this role include the ability to follow applicable HSE procedures and practices during experiments and ensuring team members" compliance. You should demonstrate a high level of awareness regarding environmental, site, statutory, and IP regulations and adhere to them diligently. Handling chemicals and tools according to safety norms, understanding the Material Safety Data Sheets (MSDS) of chemicals used in experiments, and taking necessary precautions to mitigate hazards are crucial aspects of this role. Maintaining safe working conditions in the laboratory and pilot plant, as well as ensuring good housekeeping practices in the workplace, are also key responsibilities.,

Sampling and Inspection of received goods in stores, observation to be maintain. Operation, calibration and record maintained of Q.C Instruments Handling of sophisticated instruments (like GC, HPLC, UV.etc)

Job Description To review/approval/closure, rejection/drop (if required) of Quality system documents such as Deviation, change control, CAPA, OOS, OOT, Re-process & Re-work, market complaint, market returns & LIR. To ensure & handle the investigation for Out of Specification Results, OOT, Deviations, Product failures and Market Complaints are adequately performed and documented with appropriate Quality Risk Assessment activity, Corrective and Preventive Actions based on the results of the investigations are identified and implemented. To preparation review & Approval of Quality system trend. To verify In-process Quality Assurance during production activity and sampling at different stages of processing/packing as per requirement. To review & approval of API Analytical Method Transfer Protocol/Report and method validation documents. Preparation & review of Annual Product Quality Review. Preparation, Review & Approval of Hold Time Study Protocol/Reports, and other study protocols/reports Work Experience 7-9 year Education Masters in Science or Pharmaceutical Chemistry Post Graduation in Pharmacy Competencies

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Auto titrator e.t.c. Responsible for sampling, testing and release of Raw material, packing material and miscellaneous material samples and maintain reserve sample as per SOP. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Analysis related to qualification of Instrument/Equipment and Standards Qualification of Standards and Instruments Knowledge and Skill on Sophisticated instruments like UV, HPLC, GC, UPLC, FTIR, Polarimeter and KFtitrator. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Knowledge of current pharmaceuticals guidelines (eg. ICH, cGMP etc.) Troubleshooting and decision skills for analytical problems. Responsible to perform activities with respective TNI . To ensure the timeline for initiation and completion of testing. Responsible to maintain quality standards that apply to product Analysis, ensuring proper implementation. To maintain the cleaning in quality control department Skills and Proficiency: Analytical Instrumentation Handling Expert Particulate Matter Testing Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner Analytical testing expertise and evaluation skills Expert Handling of Analytical Instruments and Interpretation of Resulting Data Practitioner Laboratory Instrument qualification, Calibration & Maintenance Practitioner Quality Control & Compliance Practitioner LIMS Operation & Data Management Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Autotitratior e.t.c. Responsible for sampling, testing and release of Raw material, packing material and miscellaneous material samples and maintain reserve sample as per SOP. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Skills and Proficiency: Analytical Instrumentation Handling Expert Particulate Matter Testing Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner Analytical testing expertise and evaluation skills Expert Handling of Analytical Instruments and Interpretation of Resulting Data Practitioner Laboratory Instrument qualification, Calibration & Maintenance Practitioner Quality Control & Compliance Practitioner LIMS Operation & Data Management Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC, Polarimeter , KF, Auto titrator e.t.c. Responsible for QCC-QMS Section regarding the test procedure, OOS, OOAL, Deviation, Change Control Note, Incident, Investigation Report Preparation e.t.c. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Responsible for QCC-QMS Section regarding the test procedure, OOS, OOAL, Deviation, Change Control Note, Incident , Investigation Report Preparation e.t.c. Skills and Proficiency: Analytical Instrumentation Handling Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy Practitioner Data Integrity & Documentation Practitioner Regulatory Compliance Practitioner SOP Preparation & Revision Practitioner Handling of Analytical Instruments and Interpretation of Resulting Data Practitioner Quality Control & Compliance Practitioner LIMS Operation & Data Management Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) Beginner CAPA, Deviation, and Change Control Management Beginner

Rejection Material Inward Analysis Faulty material Replacement or Repair RMS Visit of Principal Specifically Siemens Repair Material to be transferred to EX within 7 days

Job Purpose and Impact The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up. Perform method validation and verification to roll out new testing method in the lab. Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system. Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports. Maintain systems and techniques for reporting data across functional areas. Organize and participate ring tests with the goal to check and control methods and equipment. Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff. Other duties as assigned Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience Preferred Qualifications "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively" Necessary English reading capacity Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc. Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing Minimum of Three years of working experience in the Food industry Lab.

The Analytical Development Scientist-I with some supervision from the Analytical Development Lead focuses on the analysis of route scouting and Chemical Process Development of Bayers' existing and pipeline crop protective agents Collaborates with all internal and external functional teams, The job holders ensure all the analytical work is done following the highest safety standards with GLP and document the generated data The applicant will have an excellent practical and theoretical understanding of analytical chemistry or a relevant technology and can design and execute high-quality, thoughtful outcomes by analyzing different experiments while making significant contributions both independently and as a member of a team The candidate will work within an interdisciplinary and cross-divisional team in the Crop Protection Innovation organization, TASKS AND RESPONSIBILITIES: Method development for new entities and in-process on GC, GC-MS, HPLC, and various analytical techniques, Analyze and solve complex analytical problems and challenges daily using different instruments and wet chemistry, Document analytical data to support product development and registration, Write analytical laboratory-related Standard Operating Procedures (SOPs)/test methods, To calibrate and maintain instruments and analytical development laboratory with all aspects, Participation in internal/external inspection/audit preparations and documentation, Ability to prioritize and manage numerous activities simultaneously, to ensure timely delivery of analytical objectives, KEY WORKING RELATIONS: Internal Coordinate with ADL team members as well as synthesis chemistry lab for analytical development-related activities, Co-ordinate with site QC and GMP team for analytical development-related activities, External Coordinate with various vendors and engineers for instrument installation/maintenance activities WHO YOU ARE: Sc/ Mpharm in Analytical/Organic Chemistry with more than 5 yearsexperience Deep understanding of analytical tools and supporting software like Empower, OpenLab CDS, and LabSolutions And Chromeleon Strong problem-solving skills with the ability to do structure elucidation, Demonstrated ability to work within a dynamic and interdisciplinary environment to achieve results High assertiveness enjoys working as an individual contributor in a team, Excellent written and verbal communication skills, ability to multitask, effectively plan and follow through on complex projects in a multi-disciplinary international team Embraces ambitious goals and drives progress with urgency, Consistently seeking opportunities to acquire knowledge, develop skills, and share insights, Possesses a strong willingness to learn and grow through challenging experiences, actively engaging in giving and receiving constructive feedback to foster continuous improvement, Effectively interacts with diverse teams across functions, cultivating strong working relationships with both internal and external collaborators to enhance overall performance Ability to work in the shifts

Role Name In Community Title Senior Executive Department Sales Hiring Manager Deepak Subramanian Brief Role Description Narayana One Health is in the process of setting up a strategic team tasked with bringing health and insurance closer to patients. The initiative involves setting up primary and secondary care services that are easily accessible to patients and are supported by hyper-responsive processes built to keep patient needs and satisfaction at the center of focus. The initiative aims to bridge the gap between Narayana One Health’s in-hospital offering and patient’s everyday healthcare needs and provide patients access to a continuum of care tailored to their specific healthcare needs. Narayana One Health is looking for Senior Executives for Bangalore, India. This is an individual contributor role in an employee-oriented, high-performance environment that emphasizes spreading Nayana One Health Care Benefits in Bangalore (Karnataka). Your role will entail, Qualification of Leads (via various channels), by calling them, meeting face to face and selling Narayana Arya insurance plans to customers and briefing them about the HealthCare benefits of Arya Insurance via individual reach and through a referral channel model known as One to Many. Responsibilities: 1. Identify Engage and build relationships with Key Community Leaders of Cultural Associations, RWAs etc. 2. Manage Engagement with Community by executing agreed formats of events and sponsorships 3. Generate Interest for Arya Insurance Plans 4. Carry out Right Execution Daily (RED) and adhere to P-100 Program Guidlines 5. Ensure correct Activation and closures at Individual and at channel level. 6. Deliver Monthly targets on Inputs and Outputs Requirements and skills 1. Graduate Degree with Minimum 3-4 years' experience in sales (B2C, B2B or both)- preferred experience in Insurance or financial products and services. 2. Keen Interest in Healthcare and Health Insurance. 3. Passion for new Business Initiatives. 4. A knack for sales and positioning an idea. 5. Highly creative with experience in identifying target audience. 6. Good Communication Skills. 7. Proficient in using CRM, Analytical Tools. Location – Bangalore

Role & responsibilities Analytical test including physical and wet analysis. Expertise in handling of HPLC, GC , UV and IR Knowledge on OOS and OOT Calibration of laboratory Instruments. Preparation and standardization of Reagents/Volumetric solutions. To ensure cGLP compliance and Data Integrity Note : Candidate who can Join Immediately are preferred and willingness to work in Shift basis. Candidate should have experience in Pharmaceutical Formulation - OSD - Tablets Manufacturing facility

We're Hiring! Assistant Manager Quality Control Location: Hosur | Company: Global Calcium Unit III Experience: 712 years | Full-time | On-site Global Calcium is looking for a passionate and experienced Assistant Manager – Quality Control to join our team at Unit III in Hosur. In this role, you'll be responsible for leading day-to-day QC operations — from testing and inspecting materials to ensuring regulatory compliance, analyzing trends, and driving quality improvement initiatives. You’ll collaborate with production teams to proactively address and resolve quality issues. What We’re Looking For: Strong background in Quality Control with leadership experience Knowledge of regulatory standards and QMS (Area Qualification, Analytical Method Validation, Instrument Qualification) Hands-on experience with instruments like ICP-MS and AAS Excellent analytical, documentation, and problem-solving skills Proficiency in team communication and management Master’s degree in Chemistry, Pharmaceuticals, or related field Prior experience in the pharmaceutical or manufacturing industry is a strong plus Interested candidates can share their profiles at: dhanushkumar@globalcalciumpharma.in Join us at Global Calcium and be a part of a company committed to quality, innovation, and growth.

Exp. in ARD/AMD of minimum -15 to 20 years Lead the development and validation of analytical methods Prepare and review technical documentation Drive analytical strategy in global or cross-functional project teams

Quality officer Male Instrument Analysis GC/HPLC Min 2-5 only API CO 2 to 35year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

The role offers you the opportunity to complete product quality checks under close supervision. You will be responsible for conducting routine testing and analysis of production work, ensuring accuracy in quality checks and documenting quality control issues as needed. Your essential functions will include timely analysis of samples under test, coordinating with production for quality-related issues, sampling and analyzing RM/Intermediate/Finished Goods, ensuring compliance of ATR, assisting in ISO implementation, and possessing knowledge of calibration, standard preparation, standardization, and relevant documentation. Furthermore, you will need to have expertise in handling HPLC, GC, and wet analysis. As part of your department-specific and ongoing functions, you will be required to provide timely reports to SAP for result recording, fill and update all relevant documents, maintain zero accidents in quality operations, achieve batch-wise timelines, quantity, and quality, train and supervise operators in your department, participate in the Emergency response team, and maintain ISO 9001:2008 and ISO/IEC 17025:2005, SAP, and other Quality systems. To qualify for this position, you must hold an M. Sc. in Chemistry and have 3-4 years of experience in Quality, including cGMP, ISO, and regulatory audits, as well as laboratory safety. Preferred skills and qualifications include knowledge of Quality Control in Fine Chemicals and pharmaceutical companies and experience of cGMP. Desired skills and competencies for this role include willingness to learn, being a team player, and possessing good communication skills. Please note that the above statements are a general description of the nature of work performed in this classification and are not exhaustive. Avantor is an equal opportunity employer committed to diversity and inclusion. Join our global team of 14,000+ associates at Avantor and make a difference in people's lives through life-changing science. Dare to go further in your career, contribute your talents, learn new skills, and grow with us. Apply today and be part of a culture that supports your career growth and success. If you require a reasonable accommodation during the employment process, please contact us at recruiting@avantorsciences.com to discuss your needs. Requests for accommodation will be considered on a case-by-case basis. By submitting candidates without a formal assignment or contract from Avantor, you forfeit any fee, as per our 3rd Party Non-solicitation Policy. Avantor engages with recruitment agencies based on its needs and does not accept unsolicited solicitations.,

As a Peptides Production Executive at Piramal Pharma Solutions (PPS), your primary responsibility will be to learn and assist in the production of peptides following established protocols and quality standards. This role is designed to provide hands-on training in peptide synthesis, purification, and related processes. Your key responsibilities will include understanding and adhering to standard operating procedures (SOPs) for peptide synthesis, assisting in the preparation of reagents, solutions, and equipment, executing peptide synthesis under the guidance of experienced personnel, and learning and performing purification techniques such as HPLC, chromatography, and filtration. You will also be expected to maintain accurate records of production and testing activities, follow Good Manufacturing Practices (GMP) and safety guidelines, operate and maintain peptide production equipment, and report any equipment malfunctions promptly. Additionally, you will be required to maintain detailed records of all production activities, compile data, assist in preparing production reports, communicate effectively with team members and supervisors, contribute to process improvements, provide feedback on procedures to enhance efficiency and quality, attend training sessions to enhance knowledge and skills, and actively participate in professional development opportunities. The preferred candidate profile for this role includes a basic understanding of peptide synthesis principles, strong attention to detail, commitment to quality, ability to work in a team-oriented environment, good communication and interpersonal skills, and willingness to learn and adapt to new processes. To be considered for this position, you should have a minimum of 2 years of experience in peptides production. Piramal Group values inclusive growth and ethical practices, and as an equal employment opportunity employer, bases its decisions on merit, considering qualifications, skills, performance, and achievements. The organization strives to ensure that all applicants and employees receive equal opportunities in personnel matters, including recruitment, selection, training, placement, promotion, compensation, and benefits, among others.,

We are looking for a Chemistry Research Intern who is eager to learn best laboratory practices, assist in ongoing research activities, and contribute to experimental workflows to drive innovation at altM. The candidate will get hands-on exposure to organic synthesis, characterization techniques, and cross-functional research environments, working closely with senior scientists and engineers. Responsibilities include supporting lab-scale synthesis and formulation activities, assisting in purification and characterization of compounds using instruments such as NMR, GC-MS, HPLC, and IR, helping prepare reagents, setting up reactions, and monitoring experimental progress. The role also involves maintaining accurate lab records, inventory, and data logs, staying curious and engaged, with support provided for literature review, method development, and data interpretation over time, as well as adhering to safety protocols and best practices in lab settings. Requirements for the role include being a student or recent graduate with a Bachelors or Masters in Chemistry (preferably Organic or Applied Chemistry), with prior lab and project experience and internships being a nice-to-have. Strong theoretical and practical knowledge of organic chemistry principles and techniques, proficiency in using lab equipment and analytical instruments, excellent problem-solving skills, attention to detail, strong communication and interpersonal skills, with the ability to collaborate effectively in a team, commitment to safety, compliance, and ethical conduct in scientific research, and the ability to work from our lab in Bangalore with a willingness to travel for fieldwork or partner projects. The compensation and benefits offered include competitive cash compensation, negotiable for the right talent and qualifications.,