2096 Hplc Jobs - Page 18

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities.

"We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities."

"We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities."

"We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities."

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities.

We are looking to hire Research Ops Interns - Pharma & Biotech who will work closely with our US-based Business Development team to identify industry trends, conduct pipeline analysis, and benchmark companies in the Pharmaceuticals, Vaccines, and Medical Devices space. Roles & Responsibilities include the following : Conduct clinical pipeline analysis, clinical trial analysis, medical conference tracking, and draw appropriate insights Create insights on the company's performance and benchmarking with competition to identify areas of competitive advantage, differentiation, and growth, areas that need improvement Understand competing platforms, technologies, capabilities and contextualize them for the company Identify industry trends, shifts, and disruptions and put them into perspective with the company's strengths and capabilities.

Dear All, We are conducting Walk-In Interview on 29th August 2025(Friday) for Quality Assurance and Quality Control( Formulations ) departments. Quality Assurance: Validations - 4-5 Years of experience in Process and Cleaning validations and equipment qualifications Quality Control: IPFP - 4-5 Years of experience in HPLC, GC, UV, Dissolution and RS. Stability - 4-6 Years of experience in Dissolution, GC, UV and Sample management Raw Materials - 2-3 Years of experience in sampling of Raw and Packing materials Analytical Method Validations - 3-5 Years of experience in Method validations, GC and Dissolution instruments GLP - 2-4 Years of experience in management of working and reference standards, HPLC, GC and RS. Material Science Lab - 3-5 Years of experience in XRD, TGA, DSC and ICPMS 2-5 Years of experience in Nitrosamines and NDSRI's and LC-MS Note: Candidates who are unable to attend the interview, can share their resumes to raghuveera.vutla@aizant.com Venue Aizant Drug Research Solutions Pvt Ltd, Sy.No. 172 & 173, Apparel Park Road, Dulapally, Dundigal-Gandimaisamma Mandal, Medchal-Malkajgiri District-500100

The Opportunity: Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. Education: B. Sc. M. Sc. (Chemistry) Experience: 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Preferred Skills/Qualifications: Knowledge of Quality Control in Fine Chemicals and pharmaceutical company. Experience of cGMP Skills/Competencies: Willingness to learn Team Player Good communication skills How you will thrive and create an impact :- Give timely reports to SAP for result recording. Fill and update all documents. Zero accidents in the Quality operations. Achieving batch wise timelines, quantity and quality. Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation. Will be member of the Emergency response team and will guide & train other team members in case of Emergency. Maintain ISO 9001:2015, SAP, and other Quality system into department. Will maintain the analytical records log sheets as per GMP & ISO guidelines.

The Opportunity: To Sell entire Biopharma product portfolio, with emphasis on Small Molecule Market. Close sales on more technical products, working in conjunction with internal functions, Identify and ensuring the process of converting sales opportunities for relevant products from Avantor Biopharma offerings. What we are looking for : Experience: 7-8 years of Biopharma Pharma Life science - Sales industry experience required. Education: BS degree in a life science area, or equivalent work experience required. Identify and close new biopharma business. Meeting the budgets for both top and bottom line, ensuring growth in sales figures along with market share by virtue of careful product positioning and developing relationship with people that ultimately delivered for customers and business. Assume overall territory ownership, by attending regional meetings, strategy sessions, key account blitzes and on-site technical seminar. Perform other duties as assigned. How you'll thrive and create an impact: Must have a firm understanding of and experience within the Biopharma life science marketplace Be a proactive individual, as well as have solid communication, organizational, time-management, and PC skills Be a self-starter that is quickly motivated, effectively implements programs, recognizes opportunities, communicates ideas, and acts with little direction in a fluid and matrixed environment Overnight travel is required Environmental working conditions & Physical effort (Under Typical Positions) Typically works in a home office environment with extensive regional travel to customer locations. Work assignments are diversified. Examples of past precedent are used to resolve work problems. New alternatives may be developed to resolve problems. A frequent volume of work and deadlines impose strain on routine basis.

!! Greetings from Natco Pharma Limited..!! We are conducting Walk-in Interview for Formulation Analytical Research & Development Department for our Pharma Division located at Kothur (Near to Shamshabad) Roles: Trainee /Officer / Executive / Sr. Executive / Asst. Manager Qualification: B. Pharmacy / M. Pharmacy (Pharmaceutical Analysis) / M. Sc (Analytical Chemistry) / B.Sc (Chemistry) Experience: 0 to 15 Years (Only freshers who graduated in 2024 or 2025 are eligible to attend) Skills Required: Analytical method development & validation Complex Injectable, Peptide chemistry knowledge preferred Analysis of raw materials, finished products, stability samples, Discriminatory dissolution studies, pre formulation studies, solubility studies etc Experience with instruments: LCMS, HRMS, CD, NMR, FTIR, HPLC, UPLC, GC, etc. Gender: Male only (due to shifts and oncology plant requirements) Important Notes: Only candidates with formulation experience and regulatory exposure will be considered. Candidates Interested to work in Kothur location are only requested to attend interview. Interview Date & Venue : Date: 30th August 2025 (Saturday) Time: 09:00 AM to 02:00 PM Venue: Natco House, Road No.-2, Banjara Hills, Hyderabad - 500034. (Opposite A.P. Productivity Council)

Job Summary: We are looking for a skilled QC Chemist to join our QC team. The candidate will be responsible for conducting routine analysis of raw materials,intermediates and finished products,ensuring compliance with internal specifications. Provident fund

Manage QMS activities: Change Control, Deviation, CAPA, OOS, OOT, Lab Events. Conduct Risk Assessments, SOP reviews, and assist in grievance handling. Document & review: Specifications, SOPs, Test Data Sheets, Analytical Test Reports, and Master documents. Review Method Validation Protocols & Reports. Monitor calibration and preventive maintenance schedules. Initiate procurement of impurity/reference standards, chemicals, reagents, columns, and laboratory glassware. Develop and implement site policies and procedures ensuring regulatory compliance. Supervise deviation and CAPA review, approval, and implementation. Create QC goals, objectives, and metrics to drive continuous improvement. Ensure data integrity systems are in place with frequent checks and challenge tests. Lead root cause investigations. Prepare experimental plans during investigations. Implement CAPA parameters post-investigation. Verify CAPA effectiveness.

Walk In Drive For Quality Control In Formulation Division @ MSN Formulation Unit -II , Kothur . Department :- Quality Control Formulations Experience:- 2 to 8 Years Skills :- Formulation QC - HPLC | GC | GC MS | LIMS | LCMS | ICPMS | Dissolution | IP/FP | Stability | Method Validation | Method Development | Method Transfer | E&L | | Proficiency with Equipment | Method Development & Optimization | Understanding of Regulations | Data Analysis | Testing and Inspection | Process Improvement | Regulatory Compliance | Equipment Maintenance | Training and Support | Root-cause analysis | Method development and validation | (OSD & Injectables) | USFDA | Regulatory Approvals Division :- Formulation Interview Date:-30-08-2025 - Saturday Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur, MSN Unit -V R K Puram. Venue Location :- MSN Laboratories Pvt Ltd| Formulation Unit -2 | Kothur | Sy. No 1277&1319 -1324| Nandigama|Rangareddy| Telangana - 509216 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

As a skilled Analytical Chemist, you will be responsible for various tasks related to method development, validation, and query response for finished products. Your duties will include preparing analytical method development reports, Certificates of Analysis (COA), and performing analysis of in-process samples, finished goods, and stability samples in accordance with cGMP requirements. It will be your responsibility to monitor the general laboratory and ensure its maintenance as needed. Your role will involve routine analysis and stability testing of finished products for parameters such as assay, related substances, dissolution, residual solvent, etc. Additionally, you will be required to review analytical data, calibration data, and qualification data. Troubleshooting and maintenance of analytical instruments like HPLC, GC, UV/Visible, and spectrophotometer will also be part of your tasks. Calibrating analytical instruments such as Analytical Balance, pH meter, UV spectrophotometer, and Karl Fischer Potentiometer according to the schedule will be essential. Compliance with in-house systems and procedures to uphold cGMP practices and regulatory requirements is crucial. You will also be responsible for maintaining reference standards, working standards, and coordinating activities in Chemical and Instrumentation departments. Handling troubleshooting and updating instrument log book entries will be part of your routine activities. Desired Skills: - Previous experience in formulation testing within reputable pharmaceutical organizations. - Proficiency in handling instruments like HPLC, GC, UV, UPLC, Dissolution tester, KF, and FTIR. - Strong knowledge of Microsoft Word, Excel, and PowerPoint. - Excellent communication and problem-solving abilities. - Assertive, proactive, and self-driven attitude. - Willingness to work in a dynamic work environment. Pedigree: - Bachelor of Science (B.Sc) in Chemistry, Master of Science (M.Sc) in Chemistry. - 1-3 years of relevant work experience.,

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of how best teams integrate and work together to achieve company goals. Impact Responsible for the accuracy of own work. Receives close supervision and duties are clearly defined. Methods and tasks are described in detail. Leadership Has no supervisory responsibilities. Problem Solving Uses existing procedures to solve standard problems. Has limited opportunity to exercise discretion. Interpersonal Skills Exchanges information and ideas effectively. Responsibility Statements Maintains employee records through data entry. Performs calculations for outstanding payments due on termination or leave of absence. Coordinates termination details to ensure assets are returned/access is revoked on the employee 2019s last day. Compiles data for review and reporting. May perform routine analysis for internal review. Performs other duties as assigned. Complies with all policies and standards.

The Role The Research Associate/ Executive/ Analyst for the Small Molecule Bioanalytical Laboratory is a technical role responsible for conducting BA/BE studies in the laboratory. Job responsibilities include performing critical method development and validation programs, technical and regulatory compliance of all studies. This role requires an individual with a robust background in pharmaceutics, or other related life sciences, coupled with extensive experience in the bioanalytical field, particularly within small molecule bioanalysis. This role demands an individual with a strong commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecule analysis. The role reports into the Project Leader / Group Leader, Small Molecule Bioanalytical Laboratory and is a full-time position based out of Bangalore, India. Key Responsibilities of the Role: Perform the bioanalytical work including sample processing for method development, method validation and study sample analysis as per the protocol in compliance with SOPs, STPs. Prepare STP, MV protocol and study sample analysis protocol. Coordinate with maintenance department for any problems related to utilities and equipment / instrument (e.g. LC-MS/MS, HPLC, etc) failures. Document data generated, entries in official documents. Ensure all studies adhere to regulatory guidelines and expectations set by GCP/ GLP. Participate in all discussions on project-specific scientific details. Education and Experience Education Masters in Pharmaceutics or other related life sciences from a reputed university. Industry Experience Minimum of 3 years of experience in regulated small molecule bioanalysis Hands-on experience in small molecule regulated bioanalytical experiments People leadership experience NA Exposure and experience Experience with working for a Bioanalytical CRO lab will be an added advantage. Core competencies required for the role Scientific: Brings a creative and an innovative advantage to projects Is curious, eager to learn and make a difference Thinks scientifically and understands the problem statement in assigned programs/assays Publishes posters, papers and articles regularly Technical Conducts/plans experiments without errors and gaps Reports/analyzes data punctually and communicates effectively Troubleshoots and investigates logically (is able to defend the logic behind experimental results) Is able to forecast risks and make mitigation plans ahead of time Has good organizational, project management skills Documentation Records data as per ALCOA++ policy Pays attention to detail Is punctual in responding to QC and QA reports Displays minimal audit finding index Writes clearly and concisely with English skills at >B+

Qualifications: - Essential- MD / DNB / or Equivalent in the relevant Specialty (Pathology ) Essential Experience: Minimum 3 years Post MD / DNB experience in Laboratory Haematology & Molecular Pathology Desirable Qualification / Experience- Post Doctoral Fellowship in Laboratory Hematology / Fellowship in Molecular Pathology / DM HematoPathology DM HaematoPathology candidates should have atleast one year Fellowship in Molecular Pathology Job Description: Laboratory Responsibilities: ( expected but not limited to ) The Consultant is expected to: Do option appraisal of different diagnostic strategies and systems and make recommendations about the inclusion or exclusion of a system in a clinical context, Provide guidance or participate in the writing of standard operating procedures as per CLIA / NABL standards, Develop evidence based diagnostic algorithms for different clinical situations To analyse, interprete and authorize all laboratory reports related to laboratory haematology Perform a cost benefit analysis of different diagnostic options and make suitable recommendations, Help laboratory technical and scientific staff in the routine diagnosis through supervision, guidance and technical support as and when required, Ensure participation and satisfactory performance of the laboratory in relevant internal quality control and external quality assurance activities, Ensure processing and transport of clinical samples / genetic material in accordance with standard operating procedures and legal requirements Provide clinical interpretation of laboratory reports either through interpretative comments or during verbal communications Provide strategic guidance to users (other clinical colleagues) with regards to diagnostic dilemmas related to haematology Ensure the implementation of appropriate measures for the accreditation of the laboratory with national or international bodies (National Accreditation Board for Testing and Calibration Laboratories (NABL) and Joint Commission International (JCI) Analysing, reporting and authorizing the peripheral blood smears, bone marrow aspirates, bone marrow biopsies, flowcytometry, various body fluid examinations The Consultant will be responsible for clinical diagnostic services in molecular pathology This would involve as per rotation working in various diagnostic areas such as molecular haematology (RT-PCR, Chimerism, MPN, AML, ALL etc), solid tumour molecular pathology (lung, colon, lymphoma etc) and HLA typing He / She will perform real-time review of clinical case histories involving peripheral blood smears, histopathology slides for tumour adequacy, bone marrow aspirate smears and bone marrow biopsies and correlate with molecular diagnostic reports He / She will be signing out of molecular pathology reports as per departmental rotations He / She will be involved in the validation / verification process including internal QC, external QA processes The Consultant will independently review all the data with the Fellow (Molecular Genetics) for clinical correlation and offer molecular diagnoses He / She will be supervising all aspects of the bench work in the laboratory including performing, demonstrating, supervising and troubleshooting Administrative Responsibilities Supervising and overseeing the duties, leaves, appraisals of the technologists and scientific officers Supervising procuring of various reagents and stock maintenance of the same Overseeing strategic planning for the laboratorys technologies, instrumentation, staffing, budgeting and regulatory issues Continous monitoring of quality control and all other aspects required for the accreditation of the laboratory Scientific / Technical Responsibilities Formulating and updating the Standard operating procedure documents (SOPs) of the various techniques and tests done in the laboratory Involved in all aspects of the bench work in the laboratory including performing, demonstrating, supervising and troubleshooting Academic Responsibilities Running Fellowship programmes in Laboratory Haematology and Molecular Pathology Screening applications, organizing entrance examinations and selection of Fellows in various subspecialities of the laboratory The consultant is expected to develop, implement, maintain and monitor a teaching / training program for the laboratory staff, junior doctors and for others in relevant areas He / She will actively participate in monthly / fortnightly / weekly intra & inter-departmental conferences / meetings (Clinical Grand Rounds / MDTs / DMGs ) The Consultant will supervise Fellows to prepare, present, and discuss cases at inter-departmental conferences / meetings attended by the faculty and fellows of the Departments of Clinical Hematology / Medical Oncology / Surgical Oncology / Radiation Oncology He / She will actively participate in Journal Clubs / Lab Meetings / Seminars / Symposia as scheduled from time to time He / She will be expected to assist in ongoing research projects and to develop his / her own research areas and apply for grants Consultant will also present papers at national conferences and international conferences as per institutional rules He / She will teach / guide students enrolled for DrNB, DNB, PhD, MSc, DMLT and other courses He / She will train and supervise the Observers / Interns coming in from different institutions Audit responsibilities Identify potential areas of laboratory and clinical audit Help formulate the methodology and identify resources to conduct the audit & get requisite approval Monitor the conduct and evaluate the data, Ensure appropriate communication and follow up The Consultant would be involved in laboratory and clinical audit He / She is expected to participate in research programmes which would involve functioning as Co-PI Research Responsibilities plan, conduct and guide research programs, contribute to the development of research grant applications present papers in scientific conferences in India & abroad publish articles in Pubmed indexed journals He / She will be encouraged to write research grant applications, write original articles in peer reviewed journals, guide Fellows in write papers and analysing clinical & laboratory data Management Responsibilities This would include: business case development for new laboratory / clinical initiatives ensure the laboratories overall clinical relevance and financial viability give strategic direction for future development identify risks and manage risks ensure health and safety of staffs / visitors working / visiting the laboratory, ensure the safety and security of laboratory assets, deal with staffing, organization and disciplinary issues Provide leadership to the laboratory The Consultant would be expected to help other laboratory staff in writing standard operating procedures, drafting policy documents, carrying out health and safety audits, participate in equipment maintenance and quality control activities He / She will actively participate in NABL / CAP accreditation processes for the molecular laboratory The Consultant is expected to integrate high end molecular diagnostic platforms (like NGS, ONT , PacBio, Nanostring etc) into clinical and research use

Our Responsibility Careers Senior Scientific Manager Hyderabad, India DEPARTMENT Chemistry Solutions Scope This role is responsible for supporting chemistry services team in delivery of final compounds to clients in a time bound manner by testing enhancing purity levels as per requirements through a team of analysts. Responsibilities Build lasting internal client relationship: Conduct technical discussion with clients (synthesis team) to understand project requirement(s) Support team members in closing identified gaps to improve client satisfaction score Ensure seamless execution of project through effective lab support and planning: Estimate lab related requirements Review status of calibration of all instruments Review Standard Operating Procedures (SOP) for instruments to be used for tests Review monthly shift schedules for team members and allocate instruments and manpower based on daily work plan Improve delivery efficiency and quality through delivery management: Evaluate solvent/ sample based on its analytical test suitability Review and approve the analytical method developed to test for purity and support optimization of compound purification Ensure release of final report to client in a timely manner Resolve method development and ionization issues Coordinate with RD scientist and resolve any analytical queries related to sample analysis Review/ approve the certificate of analysis prepared by analysts for the intermediates/ final compounds Interact with external client for resolving issues on need basis Ensure safety at work through enforcement of best lab management practices: Ensure that adequate infrastructure and processes are in place to enforce safety requirements Handle all chemicals and instruments in a safe manner In case of new analytical techniques being introduced, ensure its successful implementation in lab Maintain data integrity and IP confidentiality: Maintain strict IP Confidentiality and adhere to all related policies Ensure adherence by team members Ensure high morale and skill development of self and team: Select retain right talent Enhance knowledge related to NMR, HPLC, GCMS, LCMS, ATR generation and wet analysis etc. Mentor and coach subordinates to develop their technical capabilities Improve on the employee satisfaction score Functional/ Technical Skills Knowledge of various analytical tools techniques Operational knowledge of analytical instruments Knowledge of documentation process Knowledge of safety protocols Knowledge of IP Confidentiality and Data Integrity Ability to conduct cost benefit analysis optimum usage of solvents Required Educational Qualification Relevant experience Post Graduate (Analytical Chemistry/Organic Chemistry) with 9 12 years of relevant experience Ph. D (Analytical Chemistry/ Organic Chemistry) or M. Pharm (Pharmaceutical Analysis)with 7 - 10 years of relevant experience Additional Requirements Advanced knowledge of MS Office Basic knowledge of ChemDraw is preferred Additional Responsibilities: Reporting Team Reporting Designation: Reporting Department: Educational qualifications preferred Category: Field specialization: Degree: Academic score: Institution tier: Required Certification/s: Required Training/s: Required work experience Industry: Role: Years of experience: Key Performance Indicators: Required Competencies: Required Knowledge: Required Skills: Required abilities Physical: Other: Work Environment Details: Specific requirements Travel: Vehicle: Work Permit: Other details Pay Rate: Contract Types: Time Constraints: Compliance Related: Union Affiliation: Learn more about our end-to-end capabilities Manage consent

Job Title: Quality Control ???? Location: Ahmedabad ???Company: Dermatouch Indias Fast-Growing Dermo-Cosmetic Brand About Dermatouch: Dermatouch is a fast-growing dermo-cosmetic skincare brand trusted by thousands of dermatologists and over 2 million customers across India Our clinically tested formulations solve real skin concerns, and we are committed to delivering safe, high-efficacy skincare solutions Location: Onsite: In-house QC Lab / HO / Warehouse Offsite: Third-party Manufacturing / RM Suppliers Employment Type: Full-Time Website: dermatouch About Dermatouch Dermatouch creates safe, effective, and clinically backed skincare products trusted by dermatologists and loved by customers across India We ensure top-tier quality in every batch we release Key Responsibilities: Conduct physical, chemical, and microbiological testing of raw materials, packaging materials, bulk, and finished skincare products Prepare and maintain COAs, test reports, and sample records Ensure quality standards across product appearance, pH, viscosity, stability, and fragrance Handle third-party lab coordination for additional compliance testing (like dermatological tests, preservative efficacy, etc,) Perform stability studies and assist in shelf-life determination Visit offsite vendors to inspect RM/PM and finished product QC processes Requirements Requirements Education: B Sc / M Sc in Chemistry, Cosmetic Science, Microbiology, or B Pharm Experience: 25 years in QC for skincare / personal care / cosmetics Familiar with instrumentation testing (e-g , pH meter, viscometer, UV, HPLC) and cosmetic testing parameters Understanding of cosmetic BIS/ISO standards Strong documentation, coordination, and observation skills Open to travel for offsite checks

This position deals with the development, validation and transfer of analytical methods, preparation of analytical gap assessments as well as support of analytical/stability testing/design experiments with Vantive external partners. The successful candidate would apply sound chemistry to engage in cross-functional analytical leadership activities and problem solving and would apply appropriate analytical methodologies to the development of new products and the support of existing products. Essential Duties and Responsibilities: Represent Global R&D Analytical on project teams as a key part of the project teams goals and success. Develop and execute analytical plans for new product development (NPD) and sustaining product projects (SPO) Execute lab activities related to analytical method development, validation, and transfer of methods to within/other R&D/manufacturing sites to support business needs. Ensure laboratory compliance and follow best practices. Represent R&D Analytical as member of project teams. Actively participate in success of project team goals Identifies and plans for all analytical resources needs capabilities and capacity required for the execution of the analytical strategy plan. Support and lead the analytical transfer plan globally to manufacturing plants, CRO and other RD centers. Without assistance, make sound technical recommendations regarding analytical method validation, transfer and testing that are more routine than not. Provide some analysis/redesign of key experimental procedures. Independently select techniques and procedures to solve problems within area of responsibility. Employ appropriate techniques/methods to execute routine analytical activities successfully and independently within negotiated deadlines. Identify alternative methods and technologies for improving existing or new products/processes. Act as a study director for these designs and execute method validation and transfer studies. Perform analytical gap assessment of in-use analytical methods and provide strategic action plan to remediate. Contribute to technical feasibility analysis of complex research and design concepts, execute studies such as development, validation, and transfer of analytical methods as on when required. Support analytical problem-solving efforts to meet urgent business needs. Prepare and review analytical documents (Validation / Transfer / Development protocols/reports, special reports) in compliance with analytical methods, global and local procedures. Contribute to Analytical sections intended for submission to regulatory authorities and responses to authorities. Demonstrate the ability to identify risks, issues, and opportunities. Support the analytical problem-solving efforts to meet urgent business needs and contribute to efforts beyond own scope of responsibilities to ensure project milestones are met. Support and prepare investigation plan for validation/transfer failure, OOS, deviations, and Incidents. Leverage critical thinking skills to drive the investigation to conclusions based on sound scientific principles. Demonstrate the ability to identify risks, issues, and opportunities. Collaborate with other global functions, such as project management, regulatory, formulation, manufacturing, external supplier, external partners, and quality control in project teams to ensure successful execution of analytical testing and study designs. Maintain knowledge of relevant QSR and safety requirements while building knowledge of other regulatory requirements related to R&D (product development, design, and safety) to ensure compliance in all research, data collection and reporting activities. Demonstrate ability to contribute and apply technical theories and principles to projects within area of expertise beyond own scope of responsibilities to ensure project milestones are met. Analyze and determine best solutions to non-routine experimental design or research problems with minimal assistance. Accurately assess results for validity and conformance to specifications. In addition to having an in-depth knowledge and understanding of current regulatory guidelines, cGxP and related regulations and guidance, can provide expert advice and/or is an active participant in the generation, review, adoption and interpretation of such regulations. Contribute to efforts beyond own scope of responsibilities to ensure project milestones are met. Coach and mentor junior members working in analytical activities not limited to methods development, validation, transfer, and gap assessment. Co-ordinate with technical lead/study director to execute a series of study designs and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines. Ownership of analytical methods, testing procedures, standard operating procedures and laboratory analytical instruments as applicable. Develop budgets and activity schedules of limited scope. Provide expert support within and across team as on when required. Qualifications: Experience with analytical method development, validation, and transfer. A good understanding of ICH, Ph. Eur, USP guidelines and cGxP practice. Familiarity and hands-on experience with HPLC, GC, Potentiometer, UV, AAS, FES, Empower and other analytical instruments and software. Ability to learn quickly and to solve problems in a timely manner using analytical chemistry skills. Ability to organize, assess and communicate complex information that engages the audience. Ability to make decisions when provided with limited information and to make routine decisions independently. Ability to design experiments and draw meaningful conclusions from lab data. Experience in working in global cross-functional teams across multiple time zones. Ability to adapt to changes and to work in a team environment. Ability to identify and solve technical issues. Good communication skills and having multi-tasking ability. Must possess strong verbal and technical writing skills. Having critical mind and scientific curiosity. Ability to manage different priorities, deadlines, and conflicts. Education: Master s in chemistry or Pharmaceuticals, with 7 to 10 years of experience

Testing & Analysis: Perform testing using HPLC, GC, UV, IR, and Dissolution techniques to ensure accuracy and reliability of test results. Maintain consistency in analytical procedures to meet quality standards. Quality Monitoring: Ensure quality is maintained across warehouse, dispatch, and packaging activities. Collaborate with operations teams to identify and resolve quality issues in real-time, preventing defects and ensuring compliance. Compliance & Documentation: Adhere to cGMP and regulatory guidelines while maintaining accurate documentation of all quality-related activities. Ensure records are up to date and comply with industry standards. Deviation & CAPA Management: Investigate deviations and non-conformances, conduct root cause analysis (RCA), and implement corrective and preventive actions (CAPA) to mitigate risks and enhance process efficiency. Audits & Inspections: Participate in internal and external audits, ensuring compliance with regulatory requirements. Assist in preparing responses to audit observations and contribute to continuous improvement initiatives. Training & Process Improvement: Provide training to teams on quality standards, best practices, and regulatory updates. Support the development and review of quality procedures to enhance operational efficiency and ensure adherence to the latest industry trends. Experience: Relevant years in Quality Control for speciality industrial chemicals. Knowledge of cGMP & regulatory standards. Strong skills in deviation investigation, RCA & CAPA. Experience in audits & documentation. Good analytical, problem-solving, and communication skills

INDIANOIL PETRONAS PRIVATE LIMITED is looking for Junior Executive - I ( QC Lab ) to join our dynamic team and embark on a rewarding career journey They work under the guidance of senior executives and managers to support the organizations goals and objectives Must have excellent written and verbal communication skillsMust be able to analyze complex problems and develop effective solutions Managing internal and external communication, including preparing reports, presentations, and other materials

Earth Medisys is looking for QA / QC Executive to join our dynamic team and embark on a rewarding career journey Assisting with the preparation of operating budgets, financial statements, and reports. Processing requisition and other business forms, checking account balances, and approving purchases. Advising other departments on best practices related to fiscal procedures. Managing account records, issuing invoices, and handling payments. Collaborating with internal departments to reconcile any accounting discrepancies. Analyzing financial data and assisting with audits, reviews, and tax preparations. Updating financial spreadsheets and reports with the latest available data. Reviewing existing financial policies and procedures to ensure regulatory compliance. Providing assistance with payroll administration. Keeping records and documenting financial processes.

About Info Edge Info Edge is the parent company of established brands like naukri.com, 99acres.com, shiksha.com, jeevansathi.com, and many others. At Info Edge, our mission is to create world-class platforms that transform lives by continuously innovating. Our products and services are built keeping our customers in mind. We always delight our customers by delivering superior value through enhanced offerings on the internet and other platforms. At Info Edge, people are our core competitive advantage and we will continue doing all that is needed to attract and retain the best available talent. About BU: 99acres.com 99acres is a gateway to one of the fastest-growing property markets of the world for buying, renting and selling of all types of properties in India. With over 9 million visitors visiting the website every month looking for real estate solutions, 99acres.com has over 10 lakh residential and commercial property listings and over 1.5 lakh new projects. Title: Associate Senior Executive / Senior Executive Required Educational Qualification: Any Graduate or Postgraduate Desired Experience: 1-2 years Job Objective: The objective of this role is to sell 99acres customized subscription packages to the already registered members (Property Owners) of the platform. Job Description: • Speak with pre-generated leads via calls and sell Paid Plans • Understand customer needs and handle their queries about paid plans • Close sales and achieve monthly sales targets • Ability to influence & negotiate with the customers • Fast learner who has a passion for sales • Proven track record of achieving sales target Required Skills: • Good communication and interpersonalskills • Active listening skills & strong convincing skills Other Details : • 5.5 Days working (rotational week offs) • Upto 150 calls / day and daily Talk time of 3 hours Functional Attributes / Competencies: Sales Acumen Target Orientation Influencing & Negotiation Client Handling & Engagement Product Knowledge Behavioral Attributes / Competencies: Customer Focus Focus on Results Execution Excellence Communication Intrapreneurial Orientation Leadership Attributes / Competencies: NA

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in No walk-in interviews on 27-Aug-25