1074 Glp Jobs - Page 11

Conduct laboratory experiments related to synthesis, purification, and characterization of agrochemical intermediates and actives. Support formulation development (herbicides, pesticides, fungicides, insecticides). Perform reaction monitoring, analysis, and documentation of experimental results. Assist in scaling up lab processes to pilot level under senior supervision. Work with analytical teams to characterize compounds using NMR, HPLC, GC, LC-MS, etc. Ensure compliance with lab safety protocols, GLP, and EHS guidelines . Maintain accurate records of experiments, observations, and reports. Collaborate with cross-functional R&D and manufacturing teams to transfer learnings. Key Skills Quali...

Lead and oversee process development, technology transfer, and scale-up projects for CDMO clients. Manage a team of chemists/engineers, mentoring and fostering collaboration and technical excellence. Drive optimization of chemical processes for yield, purity, cost-effectiveness, and scalability. Collaborate with QA/QC, regulatory, manufacturing, and client teams to ensure smooth project execution. Ensure strict compliance with GMP, GLP, EHS, and other regulatory standards . Engage in client interactions , technical discussions, project reporting, and presentations. Identify and implement process improvements, innovations, and new technologies. Support business development and feasibility ass...

We are looking for a motivated R&D Executive to support research, product development, and laboratory operations. The candidate will assist in experiments, media optimization, formulation development, scientific analysis, and regulatory compliance. Key Responsibilities: Conduct laboratory experiments following SOPs, ensuring accuracy and reproducibility. Assist in product development, formulation optimization , and small-scale trials. Prepare and optimize microbial growth and fermentation media . Collect, analyze, and interpret experimental data. Review scientific literature , write research reports, and prepare technical documentation. Draft and maintain SOPs, research article reports, and ...

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control/Quality Assurance Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control and Quality Assurance Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: QC Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits...

Role & responsibilities Use of HPLC/GC/UV/Dissolution apparatus. Integration for Assay and RS. Method development and force degradation study for FP and API. Preparation of method development protocol. Dissolution development and impurity profiling. Force degradation study for FP and API. Pharmacopeia method interpretation, Literature/references search. Listing the requirements for method development. Review and interpretation of development trial data. Preparation and review of method development protocol and report. Descriptive method right up.

Vibonum Technologies Private Limited, Mysore, (Althera Group), is conducting a Walk-in Interview on October 12th, 2025 to hire Quality Control professionals for its state-of-the-art OSD manufacturing facility in Nanjangud, Mysore . Department: Quality Control Work Location: OSD Plant, Nanjangud, Mysore Interview Date: Oct 12th, 2025 (Sunday) Time: 09.00 am to 05.00 pm Venue: Althera Laboratories India Pvt Ltd, Bangalore (https://maps.app.goo.gl/ozdZFQh9pN3YkYAb) Althera Laboratories India Pvt Ltd No S26, Yarandahalli, Bommasandra-Jigani link road, Hebbagodi post, Bengaluru 560099 Bengaluru, Karnataka 560099 Open Positions in Quality Control- 50 Nos Asst Manager - QC / Sr. Executive - QC / Ex...

About the Function: Our Supply Chain and Manufacturing team are problem-solvers, sourcing, producing, and delivering our much-loved brands to delight customers around the globe. Over half of Diageos 30,000+ people work in Supply Chain and Manufacturing. Its an intricate and sophisticated operation thats the product of logistical, manufacturing, and technical collaborations. Our teams in 100 sites in over 30 countries cover production facilities, supplier relationships, customer collaborations and third-party agreements. Were committed to realising our Society 2030: Spirit of Progress goals, to protect the environment and support our farmers and suppliers. Whatever your skills and experience,...

Job Description Maintenance of GLP in the Laboratory Upkeep of Housekeeping in the Laboratory. Ensuring activity logs are maintained for all critical instruments /equipment’s. Timely preparation of Laboratory Documents. Timely review of analytical data generated in laboratory. Ensuring Analytical Technology transfer from transferring lab as per approved protocol. Review and approval of incident , out of specification ,out of trend report and approval of QC related activities. Involved in QAMS activities such as change control, CAPA , incidents, deviation etc. Approval of stability summery report. Timely review of Quality control procedures and initiation for up gradation of same. Compliance ...

About the role: This role is responsible for executing and managing analytical R&D projects related to alcoholic beverages. It includes conducting precise chemical and instrumental analysis of raw materials, intermediates, and finished liquids in alignment with defined test methods, Good Laboratory Practices (GLP), and ISO 17025 requirements. The position also supports senior analysts in innovation and research initiatives and contributes to technical capability building across stakeholders through training and knowledge sharing. Role Responsibilities: Key Technical Responsibilities: Conduct and support analytical R&D projects for product and process development Perform chemical analysis on ...

As a highly experienced and motivated individual, you will be leading the Analytical Development Laboratory (ADL) team in the Research & Development (R&D) division. Your role will involve developing analytical methods for various dosage forms, managing the ADL team, collaborating with cross-functional teams, ensuring proper documentation, and optimizing processes for efficiency. **Key Responsibilities:** - Lead the development of analytical methods for various dosage forms such as oral solids, oral liquids, topical dosage forms, capsules, etc. - Manage, guide, and lead the ADL team to achieve departmental objectives and ensure high-quality work standards. - Collaborate with cross-functional ...

Role Overview: As a Quality Assurance Specialist focusing on plant quality, your main responsibility will be ensuring the overall quality parameters of raw milk. Key Responsibilities: - Testing of milk and milk products for physico-chemical parameters. - Preparation of chemicals and standardization. - Monitoring GMP practices and process CCPs. - Maintaining GLP requirements. - Keeping all log sheets as per ISO standards and compiling data. - Coordinating with internal quality, production, and finished goods store teams. - Calibrating and verifying equipment, as well as maintaining records. - Monitoring the weight of finished goods packaging. - Updating and coordinating daily activities. - In...

Role Overview: As a Scientist II at USP, you will play a crucial role in supporting the development of reference materials, specifically focusing on analytical method development for in-process samples in the synthetic lab. Your responsibilities will include performing various analytical tests, ensuring a safe and GLP-compliant environment in the lab, evaluating reference standards, developing and validating official methods, conducting stability studies, and contributing to research projects within the analytical department. Key Responsibilities: - Support reaction monitoring, scale up, and final analysis of samples based on monograph/in-house procedures, including method development when n...

Roles and Responsibilities Conduct quality control analysis using HPLC, GC, UV, spectrophotometer, sterile techniques, and other relevant methods. Ensure compliance with USFDA, GMP, GLP regulations during regulatory audits. Develop and maintain SOPs for laboratory operations and testing procedures. Collaborate with cross-functional teams to resolve quality issues and improve processes. Perform stability studies on APIs and finished products as required. Desired Candidate Profile 2-7 years of experience in a pharmaceutical industry setting with expertise in QC analysis. MS/M.Sc(Science) degree in Chemistry or related field; Strong understanding of analytical instruments such as HPLC, GC, UV s...

Roles and Responsibilities Ensure compliance with GLP guidelines, including investigation of OOS/OOT events and vendor qualification. Maintain accurate records of GLP documents, instruments, and equipment through preventive maintenance schedules. Conduct calibrations on instruments according to CGMP requirements and perform spares management tasks. Implement LIMS system for effective inventory control and HPLC analysis. Perform CAPA activities as needed to resolve quality issues. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Organic Chemistry from a recognized university. Minimum 10-15 years of experience in pharmaceutical industry with expertise in GLP practices. Strong ...

Regulatory Affairs Associate Responsible for preparation, review & submission of regulatory documents (US FDA, EMA, ICH), ensuring compliance with guidelines, supporting product approvals, maintaining records & coordinating with authorities. Required Candidate profile BSC/MSC/B.Pharm or Life Sciences graduate with knowledge of regulatory guidelines, dossier prep, submission processes, documentation, compliance, MS Office, attention to detail & communication skills.

Roles & Responsibilities :- Conduct analysis of samples using HPLC, GC, Spectrometer, and other basic analytical instruments of the lab with experience in developing and validating HPLC/GC methods Analysis of Sugars, Alcohols, Antibiotics, enzymes, active ingredients, and raw material using HPLC/GC Providing Technical support for internal and external stake holders Being the clear R&D player by working closely with cross-functional teams to drive execution across multiple projects while maintaining and achieving timelines to ensure speed to market. To conduct analysis of samples and provide inputs to R&D/QC teams Required Skill Sets: Hands on experience on HPLC, GC, Spectrometer, and other b...

Position Title: Executive : Manufacturing Science and Technology (MST) Qualification And Experience POST GRADUATE IN CHEMISTRY/PHARMACY Experience: 0-7 years of Experience as an analyst/Development technologist in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Providing analytical support for Chemistry activities ensuring compliance to regulatory, group directives, quality requirements, safety standards to fulfill the organization's objective, living Group's Values and Code of Ethics Responsibilities Responsibilities: Analytical method validation: Analytical method Development Analytical method transfer, Analytical method validation CMC Activity Sampling & testing of Pr...

Roles and Responsibilities Develop new APIs through organic synthesis, method development, and optimization. Conduct literature reviews to stay updated on latest research trends and technologies. Ensure compliance with GMP guidelines during API manufacturing processes. Collaborate with cross-functional teams for product development, scale-up, and commercialization. Perform impurity analysis using techniques like NMR, DSC, etc. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Ph.D/Doctorate in Chemical Sciences from a recognized university. Strong expertise in areas such as API synthesis, organic chemistry, method development/validation/transfer/methodology. 9-14 years of exp...

Job Title: Executive Analytical Development (Microbiology) Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own SunshineAs you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Job Description: 1. Method development, Method ...

Hi, We have job opportunity with API Manufacturing Pharma Industry for Sr. Associate- Quality Control Profile, Mysuru Location. Job Location: Mysuru Department: Quality Control Qualification: M.Sc Chemistry Open to work in 3 shift operation. Purpose of Job Supporting for Equipment Qualification, Sampling, analysis of in process, finished product and Stability Samples. Key Responsibility Area Handling and troubleshooting of Analytical Equipments like HPLC, LC-MS, GC-HS, FT- IR, UV, Potentiometer, Polarimeter, ICP and KF. Handling of Empower CDS software. Preparation and maintenance of finished product reserve samples Analysis of In process, Stability and FG Samples as per the Specification. O...

Position Summary: Ensure that clients receive high-quality data by reviewing laboratory data for accuracy, clarity, and compliance with GMP and/or GLP regulations. Essential Duties and Responsibilities: Apply GMP/GLP standards in all areas of responsibility, as appropriate. Review laboratory documentation, generated data, calculated results, and final reports to ensure they meet departmental, corporate, and client SOPs. Gain a technical understanding of the analytical techniques relevant to the data being reviewed. Read and interpret analytical procedures accurately. Utilize MS Windows applications including Excel, Word, Access, and Outlook for documentation and communication. Demonstrate an...

Role Overview: Zapcom is a global Product Engineering and Technology Services company that specializes in providing bespoke, customer-centric solutions across various industries. As part of our team, you will have the opportunity to work on impactful projects that transform ideas into tangible outcomes using technologies like AI, ML, Cloud solutions, and full-stack development. We foster a culture of accountability, ownership, and equality, empowering you to excel and grow professionally. Join us now to be part of something extraordinary and shape the future with global opportunities and expansion plans. Key Responsibilities: - Achieve and exceed sales targets by developing a robust sales pi...

In pursuit of future expansion, we need Formulation & Development Officer/ Sr. Officer - 2-4 years in advanced probiotic/ nutraceutical / food supplement /phyto-pharmaceutical formulation development in solid orals (Tablet/Capsule/Granules/Powder) /Liquid Orals (Syrup/Suspension/Liquids) / semi-solid (Cream/ointment/ gel/paste). The candidate should preferably possess one or more of below requisites: 1.Knowledge of steps involves in Formulation and development. 2.Experience in development of Nutraceutical/ advanced probiotic/herbal formulations 3.Knowledge of GMP, GLP, D&C Act, ICH guidelines, FSSAI & AYUSH. 4.Ability to take lab trail and other lab related activity. 5.Ability to prepare the...

Company Description AMN Life is a leading manufacturer and exporter of a wide range of formulations in various therapeutic segments including antibiotics, gastro, anti-inflammatories, cardiology, nephrology, CNS, and oncology. With facilities approved by EU, Health Canada, Brazil - Anvisa, and Philippines situated in Bhilad (Gujarat) and Kala Amb (Himachal Pradesh), AMN Life is equipped to handle large scale production and tech transfer projects. Headquartered in Bandra Kurla Complex, Mumbai, with offices in Singapore, UK, Australia, and Philippines, AMN Life excels in providing quality medicines at affordable prices globally. We are recognized for our strong global presence, innovative R&D,...

M.Sc, Phd/ Doctorate Keyskills Scientific & Technical Leadership. Regulatory and Quality compliance. Ensure cost effective process development. Ensure that laboratory work is carried out in a safe manner. Ensure that the R&D unit complies with relevant statutes. Key roles Lead development of synthetic routes and scale-up processes for APIs and intermediates. Guide polymorphism studies, impurity profiling, and characterization using advanced analytical techniques. Ensure cost effective robust process chemistry and technology transfer to manufacturing units. Manage multiple projects Mentor and develop team members, fostering a culture of scientific rigor and continuous improvement. Ensure adhe...