1074 Glp Jobs - Page 10

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

Job Title Manager / Sr.Manager Micro Lead Job Grade G10 / G9B Function Global API Business Sub-function Manager's Job Title: Skip Level Manager's Title Function Head Title: Location: Ahmednagar No. of Direct Reports (if any) Areas of Responsibility To plan, review and monitor overall activities in Microbiology and lead the department. Co-ordination with other departments for priorities and provide the timely support/testing to avoid delay due to analysis. Review of all departmental related documents and review results in LIMS system in microbiology section. Ensure all documents are complete in time. To review the lysate sensitivity test, Bacterial endotoxin test of WFI and API products. To c...

About Us Zapcom is a global Product Engineering and Technology Services company, specializing in bespoke, customer-centric solutions across industries like BFSI, e-commerce, retail, travel, transportation, and hospitality. Headquartered in the US, with a presence in India, Europe, Canada, and MENA, we excel in transforming ideas into tangible outcomes using AI, ML, Cloud solutions, and full-stack development. At Zapcom, we value accountability, ownership, and equality, empowering you to excel. We listen to your aspirations and provide the support needed to achieve them. Our diverse, collaborative culture ensures every voice is heard, driving innovation and business value. With global opportu...

1.Monitoring of cGMP and GLP compliance and compliance to applicable regulatory requirement and filing commitments. 2.Resopnsible for investigation of LIR (Incident / OOS/ OOE). 3.Analysed data review. 4.Analysis of Finished, In process, Process validation, Cleaning Validation samples.

1.Preparation and standardize of volumetric solutions and maintaining its record. 2.Preparation of standard solutions and reagents and maintaining its record. 3.Water Analysis and data punching in SAP. 4.Analysis of Raw Material and Miscellaneous samples as per GTPs/ SOPs/ Spec & MOAs. 5.Raw materials Control sample management.

Roles & Responsibilities for Analyst 1. Understanding and maintenance of Quality Management System. 2. Performing the analysis as per the guidelines under supervision of Senior Analyst/ Lab manager. 3. Instrument operation and calibration on regular interval for Analytical balance, pH meter, HPLC, LCMS, etc. 4. Maintenance of the technical records, certificate of analysis as per requirement. 5. Recording Initial observations, necessary data, and calculations. 6. Inform the lab manager for any kind of equipment breakdown, fault or any kind of irrelevant test results (Preventive maintenance). 7. Perform method development, method validation and project related activities as per SOP/ Protocol. ...

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,

QC planning; GLP/QMS; chemist schedule/qualification Plan/review validation, calibration -AMC/CMC; audits; SOP/STP prep/training; COAs; stability loading/protocols prep Compile batch analysis data Indent materials Internal/External Mail coordination Required Candidate profile QC lead(GMP pharma—oral solids). GLP/QMS docu; ICH method & process validation HPLC/GC/UV, dissolution stability; OOS & CAPA-change control; monthly SOP/STP prep/review-mentoring, working std dev,

Roles and Responsibilities Conduct analytical testing using various instruments such as GC, HPLC, spectrophotometer, etc. Prepare samples for analysis and record results accurately. Maintain laboratory equipment and ensure proper functioning of instruments. Develop and validate new methods for analyzing chemicals and materials. Collaborate with cross-functional teams to resolve issues related to product quality. Should be familiar with software Caliber LIMS To analyze AMV, IP, CV, PV, FP stability products Worked in CGMP, GLP and GDP maintained environment in laboratory Who can Apply : Candidates with core Injectables experience

HOW MIGHT YOU DEFY IMAGINATION Youve worked hard to become the professional you are today and are now ready to take the next step in your career. How will you put your skills, experience and passion to work toward your goals At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Come do your best work alongside other innovative, driven professionals in this meaningful role. What you will do The Quality Compliance Senior Manager is a global role and part of the Clinical & Research Quality (CRQ) team for the R&D Quality Organization. CRQ organization plays a cr...

Associate Scientific Business Analyst Biological Studies (LIMS) What you will do In this vital role you will be working closely with Amgen Research partners and Technology peers to ensure that the technology/ data needs for drug discovery research are translated into technical requirements for solution implementation. The role leverages scientific domain and business process expertise to detail product requirements as epics and user stories, along with supporting artifacts like business process maps, use cases, and test plans for the software development teams. This enables the delivery team to estimate, plan, and commit to delivery with high confidence and identify test cases and scenarios ...

Join a globally recognized CRO and be part of cutting-edge research and work with advanced technologies and contribute to high-impact pharmaceutical innovation Department: Analytical Services (Biologics) Position: Senior Chemist/Junior Research Associate Location: Hyerabad Qualifications: M.Sc. / M. Pharm / M.Sc. in Biotechnology or Equivalent Qualification 1-3 years of relevant experience in pharmaceutical industry or CRO environment. Proficiency in mass spectrometry and chromatographic techniques for biologics. Knowledge of cGMP/GLP and instrument qualification processes. Strong communication and independent working skills. Roles and Responsibilities Develop analytical methods and for biol...

Quality Compliance Manager Process Excellence, Continuous Improvement & Innovation What you will do l The Quality Compliance Manager is a global role and part of the Continuous Improvement & Innovation team for the R&D Quality Organization. This role will support processes and efforts related to continuous improvement and change management. They will be a vital part of Amgen's Quality Management System, providing expert support to create and manage R&D controlled processes aimed at continuous improvement through the application of standard methodologies (Lean, DMAIC, Six Sigma). The Quality Compliance Manager will contribute to implementing strategies and providing leadership to ensure excel...

Walk-in drive: Senior Chemist / Junior Research Associate - HPLC Analytical Method Validations Work Location: Hyderabad Eligibility: Must have 1 to 3 Years of experience in Analytical Method Validations by using HPLC for Formulation products. M.Sc. / M-Pharmacy or Equivalent Qualification. Job Description : Analytical method validations and method transfer as per cGMP requirements for drug products. Strong experience in handling various analytical instruments like HPLC, UPLC, UV and Dissolution USP type-I and II and type-IV. Dissolution, Assay and Related Substances method validationand method development of finished products like Tablets, Capsules, Pellets, oral suspensions and Injectables ...

Position Title: QC Chemist (Team Member) Company name : Sinterx Pharma Private Limited. Location: Valigonda, Choutuppal. Position Description: The QC Chemist with 5 to 8 years of experience is responsible for leading and executing complex analytical testing of API intermediates to ensure compliance with predefined quality standards and regulatory guidelines. This role includes conducting advanced testing, reviewing analytical data, supporting investigations, mentoring junior analysts, and contributing to continual improvement initiatives. The QC Chemist plays a key role in maintaining product quality throughout the production lifecycle by collaborating closely with Quality Assurance, Product...

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,...

Role Overview: As a member of the ANKLESHWAR QC -U1 department, you will be responsible for handling HPLC systems and GC instruments. Your main duties will include maintaining instrument usage logs, training records, and following SOPs for various types of samples. Additionally, you will be required to adhere to GMP and safety norms, attend training programs, and ensure timely reporting of results. Key Responsibilities: - Handle HPLC system and GC instruments - Maintain instrument usage log, inward register, and training records - Follow SOPs, specifications, and STP for different types of samples - Utilize LIMS for sample receiving and testing - Adhere to GMP, safety norms, and company poli...

As an Officer in the Quality Control department at German Remedies Pharmaceuticals Pvt Ltd., your role will involve the following key responsibilities: - Raw Material sampling and analysis of both raw materials and finished samples - Analysis of Finished Products - Planning work based on priority - Reviewing documents - Working in the GLP section - Handling HPLC equipment To qualify for this position, you should meet the following requirements: - Qualification: M.Sc in Chemistry & B. Pharma - Total Years of Experience: 2-4 Years - Experience in Zydus: Minimum One Year - Department from which people can apply: Quality Control,

Division Department Sub Department 1 Job Purpose Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards. Key Accountabilities (1/6) Analyse and review samples based on work allocation to meet the service level agreement Analyse samples as per priority and work allocation Review the data as per respective specification, Microbiological Methods and results obtained Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLA Key Accountabili...

Division Department Sub Department 1 Job Purpose Execute analysis of allocated samples and Produce reliable and reproducible results in order to ensure their compliance to the microbiological quality parameters and predefined specifications and standards. Key Accountabilities (1/6) Analyse and review samples based on work allocation to meet the service level agreement Analyse samples as per priority and work allocation Review the data as per respective specification, Microbiological Methods and results obtained Prepare, review and submit reports to Team leader within stipulated timelines in order to support individual sample release within stipulated timelines to achieve SLA Key Accountabili...

The individual will play a crucial role in analytical research focused on flavor chemistry for process research initiatives that deliver on the innovation business KPIs/needs. This role requires deep expertise in advanced analytical techniques to identify, quantify, and understand the flavour compounds that define our ingredients, process intermediates, and products. The ideal candidate will drive analytical deliverables in process projects and contribute significantly from concept to completion, all the while broadening experience via project work in different disciplines and research programs. ROLE REQUIREMENTS: Qualifications Education: PhD in Analytical Chemistry/ Flavor Chemistry/ Food ...

Bachelors degree in engineering / science. 3+ years of experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. Experience with the implementation of Quality Management systems (Track wise/ Master control / ETQ/ CEBOS) Should be able to Develop validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Should be able to create project Deliverables which will encompass validation plans, specifications, test protocols and standard operation procedures Good communication and technical writing skills are a must. Should be able to work Independently. Should be Flexible to han...

Proactively work with Tech-Ops & Planning team to ensure minimization of Material expiry at Plant level. Lunch of the NPD/EPD in their respective cluster with RFT, enabling the zero loss to Business Growth. Effectively Manage the QA budget approved for the Cluster. Customer Service Regular visit of Market and ensure Product Integrity (Product Quality Index & Packaging Quality index) at Consumer Level as per Design Quality. Collaborate with Supply-chain team in addressing the Internal Complaints with high sense of urgency. Collaborate with Procurement/Planning team in resolving the Incoming Materials Challenges with stipulated timeline. Collaborate with TechOps in reviewing the root cause ana...

Lead synthesis, purification, and characterization of agrochemical intermediates and actives. Optimize reactions, processes, and formulations for efficiency, yield, and cost-effectiveness. Support scale-up from lab to pilot plant and transfer processes to manufacturing. Mentor and guide junior chemists, review experimental plans, and ensure scientific rigor. Collaborate with analytical, quality, regulatory, and manufacturing teams. Contribute to product lifecycle management and IP documentation (patents, innovations). Ensure strict adherence to GLP, EHS, GMP, and laboratory safety protocols. Drive innovation by suggesting new synthetic routes, formulations, or process improvements. Key Skill...

Lead and oversee synthesis, process development, and formulation projects for agrochemical products. Mentor, train, and manage a team of Junior and Senior chemists, fostering a collaborative and high-performance environment. Drive technology transfer and scale-up from lab to pilot plant and support manufacturing integration. Collaborate with cross-functional teams including manufacturing, analytical, regulatory, and quality for successful product delivery. Define and execute R&D strategies and roadmaps , aligned with business objectives and market needs. Ensure compliance with GLP, EHS, GMP, and other applicable regulatory standards. Identify new opportunities for innovation, cost optimizati...