83 Adl Jobs

Product Development: Assist in the design, formulation, and testing of new products or services, ensuring they meet quality and performance standards.

Planned purchase to maintain stock. Having knowledge in IT Hardware & Software Procurement. Creating PO & Buying Activities. Having a good Knowledge in material Follow-up with Vendor & Supplier.

Role Overview: At Kimia Biosciences, we value our people and prioritize a people-first approach. As a dynamic API manufacturing company based in India, we pride ourselves on being world-class in innovative technology. Our growth from 2012 to 2020 is attributed to the commitment, ability, and relentless efforts of our employees. We have a team of committed, high-performing, passionate, and excellent professionals who have contributed significantly to our development and growth. Our management style combines wisdom with excellent Human Resource practices to compete in the pharmaceutical market by attracting top talent and fostering a corporate culture of equality and growth. Key Responsibilities: - Must have experience in various analytical method transfers from ADL to QC - Preparation of Analytical method validation protocols and reports - Experience in analytical method validation and reviewing of Analytical method validation reports - Familiarity with published guidelines on analytical method validation and transfer - Awareness of data integrity issues Qualifications Required: - Relevant experience in analytical method transfer and validation - Knowledge of published guidelines on analytical method validation - Understanding of data integrity issues (Note: No additional details of the company were provided in the job description),

The candidate in this position is responsible to - Drive and execute New Product Design and Development, VAVE, B&P, and Sustaining Engineering through Eaton PROLaunch / PreLaunch / ACES Engineering processes and CI mindset Create Product Concepts & Architecture ideas and demonstrate, expertise at STEM - Science Technology Engineering Mathematics basics for demonstrating the feasibility of designs through relevant Engineering calculations/predictions Has proficiency with CAD, Analytical Tools (CATIA, CREO, AutoCAD, MathCAD, Matlab/Simulink, CfX, ADL, etc.), Limits, Fits & Tolerancing, GD&T Apply basics of DfX - DFSS, DFMA, DfR, and DFE. Apply Robust design methodologies/tools for decision making - DFSS, LEAN, DMAIC Execute technical, schedule, cost, and quality commitments for every deliverable as per project scope. An additional responsibility of managing the project/program financials as appropriate. Execute IPT leadership across the Project. Seek team input to promote a rapid resolution to issues. Provides feedback on performance indicators. Establish objectives and goals and provide direction to the project teams in areas of customer concerns, potential changes in scope, and risk assessment. Manage effective customer communications. Improve organization responsiveness to customer requirements. Communication & managing customer expectations and contractual commitments internal to the business. Ensure standard program management processes are utilized and adequate support to the project team by coordinating PM reviews, and preparing & publishing PM metrics and reports. Provide monthly project updates (Project Status Report - Green/Yellow/Red) of the current situation relating to milestones and problem/high-risk areas (e.g., technical, cost, and schedule). Provide updates to the business units as well as divisional, and group levels. Play a key role in developing business proposals and executing the overall program plan. Handle RFI/RFP/RFQ process by providing engineering inputs to customer inquiries, creating solutions and estimating materials, testing costs, and Engineering NRE In-depth know-how of Digital tools and capabilities including but not limited to - Python Programming, Advance Excel, PowerBI, VB and/or similar equivalent etc. to drive Continuous Improvement (Digital mindset) and Digitalization strategies across technical, Project execution, and functional productivity domains Know-how of Aerospace Product Testing and Qualification - DO160 and failure investigation, FRACA (RCA, FTA, 8D), Authoring Qualification Artifacts (QPP, ATP, QTP, QSAR, QTR) Qualifications: Post Graduate Bachelor s and/or Bachelors degree in Engineering (Mechanical, Hydro-Mechanical, Electro-Mechanical or Mechatronics Domain) Masters degree - 0-2 years or Bachelors degree - 3-5 years experience, Overall 3-5 years of experience, Min 3 years of Product Engineering, Design, Development and Validation of Hydraulics, Hydro-Mechanical, Electro-Mechanical products. Skills: Portfolio, Program & PM methodologies, Project Engineering, processes and tools, DFSS, Analytical Thinking, Aerospace Products (Electro-Hydro-Mechanical) Drive for Results, Analysis-First and Digital Mindset, Organizational Savvy, Strong Communications and Influencing skills Mechanical/Mechatronics Engineering - Project Engineer - New Product Design/ NPI - Design and Analytical Calculations - Actuators, EMA, Electromechanical Actuators, Gear train, transmission, gearbox, gears, Electrical motor selection/design - Electro-Mechanical Products

About the Team At Nutanix Cloud Manager, we are trying to build the next generation platform to help enterprises model, develop and manage applications. We want to give them the ability to encapsulate not only infrastructure but even the application its architecture and deployment as code. You will be reporting to the Senior Manager Engineering, QA - NCM Team. Your Role As the gatekeeper of our product quality, you would be required to ensure that product releases adhere to the highest quality norms. You will design and develop a testing framework for our products and be part of a ruthless quality team. You will develop test tools, test cases, maintain test beds, and provide metrics and test/quality status. What You Will Bring: Be a self-starter who can flourish in a fast-paced technology company Be the owner of our automation and delivery systems Be actively participating in Coding & Code reviews Have expertise in languages like Python, JAVA Have expertise with automation and building tools such as Selenium, JMeter and Jenkins Strong systems background (Linux systems with exposure to Process, Memory and IO Management tools You will enable our engineers to generate known-quality releases with every commit, discover defects early and iterate fast. Thrive on working on open-source technologies. Excellent programming and scripting capabilities to develop code for automated tests. Should have an extremely good problem-solving approach with good hands-on knowledge of Algorithms & Data Structures.

We are seeking a talented and motivated R&D Executive specializing in synthesis to join our Agrochemical research and development team. The ideal candidate will be responsible for developing, optimizing

We are seeking a talented and motivated R&D Executive specializing in synthesis to join our Agrochemical research and development team. The ideal candidate will be responsible for developing, optimizing,

We are seeking a talented and motivated R&D Executive specializing in synthesis to join our Agrochemical research and development team. The ideal candidate will be responsible for developing, optimizing,

Plan, setup, monitor, and workup chemical reactions Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Isolate product and Optimize reaction conditions for improved yields and output.

Qualification: MSc. Biotechnology (If Phd then industrial exp can be little less) Keywords: mAbs, Method development, HPLC Thorough knowledge of HPLC based analysis of recombinant proteins. Viz. RP-HPLC, SE-HPLC, glycan analysis etc. Independently design method development of proteins, qualification, transfer following ICH/USP/EP/IP guidelines, including the writing and review of protocols, transfer plans, and reports. Carry out day-to-day analytical work and working in co- ordination with the Cell culture and downstream teams in Biotech R&D. Set-up product related test/ release specifications and analytical protocols Biotech products. Design inhouse /outsource methods for Physico-chemical characterization of biological products. Co-ordination with QC for smooth implementation of new methods. Maintenance of equipment logs and documentation in the lab. Maintaining and monitoring stability of various products in Biotech. Responsible for preparation of lab related documents, regulatory submission documents and QC supports (SOP, STP, COA, MOA, Specification). Interpret data and write reports in support of regulatory submissions Reviewing of analytical data for in-process & stability related activities.

Please walk in to the interview on SUNDAY 13th Sep 2025 b/w 10:00 AM to 3:00 PM at below mentioned venue. Venue: Unison Pharmaceuticals Pvt. Ltd. Block A, Office Number: 905,6,7,8 Safal Pegasus, 100 Feet Anand Nagar Rd, Chinar Bungalows, Prahlad Nagar, Ahmedabad, Gujarat 380015 Apply now to become a part of a growing team!! 1) Analyst: ADL - Routine Analysis Experience: 2 to 8 years Job Role: ADL - Sample Analyst Markets: Domestic & Regulatory Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) Designation: Officer / Sr. Officer No. of vacancies: 05 Roles and Responsibilities : Perform chemical, physicochemical and wet analysis as per product requirements. Routine In-process, Finished product (Initial & Stability samples) analysis. Data reporting with good documentation practice and presenting results in informative report format. 2 ) Analyst: - ADL - LCMS Experience: 2 to 8 years Job Role: ADL - LCMS Analyst Location: Moraiya, Ahmedabad (Transportation is available from specific routes of Ahmedabad) Designation: Officer / Sr. Officer No. of vacancies: 05 Roles and Responsibilities : Method development of nitrosamine impurities/NDSRI/genotoxic impurities on LCMS/MS with proper documentation and prepare Analytical test procedure & worksheet. Routine API & Finished product (Initial & Stability samples) analysis like Nitrosamine impurities, Genotoxic impurities, NDSRI, related substances Method validation for analytical method on LCMS/MS Responsible to Stability data compilation for finish product as per requirement. Follow GLP in the laboratory. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen Facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive Regards, Team HR Unison Pharmaceuticals Pvt Ltd

Role & responsibilities Provide Support to routine analysis of API Synthesis R&D and Stability samples. Documentation of Daily analysis in corresponding product LNB. Development of analytical methods for drug substances, raw materials and intermediates. Perform AMV, AMDR, AMT activities. Preparation of Analytical method validation / AMT protocol & report. Preparation of Tentative STP/MOA during Development. Trouble shooting at the time instrument operation and analytical method related problem. Preparation of COA, MOA and provide to LIMS. HPLC and GC Calibration and Documentation and provide GLP for the same. Prepare method development report. Analytical method transfers and Documentary Methods Transferring new analytical techniques to Quality control. Development and validation of cleaning method for drug substance

IITR is currently looking for a highly skilled ADL Officer for one of the pharmaceutical Co. Location - Vapi, Gujarat. If you are interested and for further information, please share your updated CV to talent@hireindians.com/call on 8700944544. Required Candidate profile Min Exp - 2-4 yrs of experience. Qualification - BSc/MSc in pharma

The ideal candidate will be responsible for method development and validation, as well as routine and stability analysis utilising a variety of analytical techniques, including HPLC, GC, Dissolution testing, and Karl Fischer titration.

The ideal candidate will be responsible for method development and validation, as well as routine and stability analysis utilising a variety of analytical techniques, including (HPLC), GC), Dissolution testing, and Karl Fischer titration.

As an AM Research and Development, you will be responsible for planning, setting up, monitoring, and working up chemical reactions independently. You will need to monitor the progress of reactions using standard methods and analytical techniques such as TLC, GC, HPLC, LCMS, etc. It will be your duty to isolate products, optimize reaction conditions for improved yields, and purify compounds using chromatography, distillation, and crystallization methods. Additionally, you will be required to characterize and identify compounds using UV, IR, NMR, LCMS, and GCMS techniques. Ensuring the parallel execution of multiple reactions conducted by both yourself and the team will be essential. You will also be involved in scaling up R&D developed products to kg scale and then facilitating technology transfer to the pilot plant. Furthermore, troubleshooting as appropriate for successful execution with intimation to the supervisor will be part of your responsibilities. If you believe you are suitable for this position, please submit your resume mentioning details such as Present CTC, Expected CTC, Company Name, Current Location, Notice Period, and Native Place to the provided email address. This role requires a qualification of MSc in Organic Chemistry with first class, along with a minimum of 4 years of experience in Research and Development within the leading pharma, CRO, or Agrochemicals industry. If you have the relevant skills and experience, we encourage you to apply for this exciting opportunity.,

As a member of our team, you will be responsible for the synthesis and purification of assigned molecules/experiments. You will also actively participate in process development activities for the assigned molecule, as well as provide support for scaling up developed processes in the pilot plant and large-scale manufacturing processes. Your role will be crucial in ensuring complete support for Tech Transfer activities by closely collaborating with cross-functional teams. An essential aspect of your responsibilities will be to add value to processes through innovation. You will be expected to understand and analyze reports received from the Analytical department, which may include NMR, Mass Spectrum, IR, HPLC, GC, among others. Additionally, you will work closely with the Analytical Development Laboratory (ADL) to process samples for analysis as per the project requirements. Your expertise and dedication in these areas will be pivotal in contributing to the success of our projects and the overall efficiency of our operations.,

As an M. Sc Analytical Chemistry professional with 2-4 years of experience in method development and validation in Analytical Development Laboratory (ADL), you will be responsible for ensuring the accuracy and reliability of analytical methods used in the testing of chemical substances. Your expertise in chemical analysis will be crucial in supporting research and development efforts within the organization. You should have a strong foundation in analytical chemistry principles and techniques, as well as hands-on experience in method development and validation. Your attention to detail and problem-solving skills will be essential in identifying and resolving any issues that may arise during the analytical process. A background in the chemical industry is a must for this role, as it will provide you with the necessary knowledge and understanding of the various chemical compounds and processes involved in method development and validation. Additionally, you must be prepared to work in shifts to support the operational needs of the laboratory and ensure continuous testing and analysis of samples. Your dedication to quality and precision in analytical work, coupled with your ability to adapt to changing priorities and work effectively in a team environment, will make you a valuable asset to the ADL team.,

JOB OVERVIEW Executes complex simulations in CFD and Thermal to optimize design and manufacturing. Develops complex Multiphysics simulation methods that meets design requirements in thermal management of Electronic Systems, especially in high-speed transceivers, connectors, and their assemblies. KEY RESPOSBILITIES: 5 to 8 years of industry experience. Expertise in Ansys Workbench. Experience on connector products (Plastic and Sheet Metal parts). Knowledge on material science (Metals, Resins & hyper elastic material) and implement for simulation. Expertise on CAE tools, Optimization techniques, and testing methods. Development & execution of complex Thermal simulation models to optimize manufacturing, designs or processes for high-speed IO products in data center, telecom and allied applications. Perform calculation & simulation on temperature distribution over system. Proficient in simplifying complex CAD geometries for efficient structural and thermal simulation analyses In-depth knowledge of mechanical design, conductive, convective, & radiation heat transfer, and fluid flow mechanics. Collaborate with designer, manufacturing, and testing teams to correlate CFD & Thermal Simulation results with physical testing Experience with DOE (Design of Experiments) and optimization techniques Ensuring the maintenance and updating of simulation models to achieve optimal accuracy and relevance. Execute CFD Techniques steady, transient, conjugate heat transfer, internal & external flows, electronics cooling, electro-thermal analysis using Software tools like Ansys Work Bench, Fluent, CFX, Icepak, AEDT, Q3D etc. Translate actual problem to Thermal model, interpret analysis results and select best solution. Monitor and evaluate simulation software capabilities and industry trends. Collaborate with design & validation teams to enhance the design optimization. Understanding the influence/impact activities on financial decision.

The role involves synthesizing and purifying assigned molecules and conducting experiments. You will be responsible for the process development activities of the assigned molecule, as well as supporting the scaling up of developed processes in pilot plants and large-scale manufacturing processes. Additionally, you will provide complete support for Tech Transfer activities by closely collaborating with cross-functional teams. Your role will also include adding value to processes through innovation. It is essential to understand and analyze reports received from the Analytical department, including NMR, Mass Spectrum, IR, HPLC, GC, etc. You will partner with the Analytical Development Laboratory (ADL) to process samples for analysis as per the requirement.,

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

Division Department Sub Department 1 Job Purpose Provide analytical support to API R&D, Regulatory Affairs, Manufacturing units and other analytical laboratories by method development of raw materials, intermediates and final API in order to ensure the drug development is carried out as per the project timelines and adheres to all regulatory requirements Key Accountabilities (1/6) Provide method development and routine analysis under GLP environment to finalise the specification for standardization of the molecule and for final DMF submission Conduct extensive literature search Analyse raw materials, intermediates, final API, forced degradation samples, stability samples, GTIs on different analytical instruments under GLP environment Conduct Fate and Purge studies/carryover studies Perform method validation Prepare specification based on carryover studies Perform method transfer to manufacturing units for routine QC analysis Key Accountabilities (2/6) Investigate plant queries like OOS, OOT for quality control of drug substance and products in order to provide corrective actions and check samples for impurities Review the entire process to identify the source of impurities Perform degradation study to identify impurities Analyse packing material in case of leachable and extractable Key Accountabilities (3/6) Characterise final API and impurities to prepare the test or working standards for routine laboratory purpose Perform chemical and physicochemical analysis to arrive at the purity, potency and structural identity of the molecule Store impurities as per chemical properties Key Accountabilities (4/6) Conduct the incubation and perform complete analysis of stability samples to conclude the storage, shelf life and packing conditions of the final API Incubate samples at various conditions Select packing material Perform analysis of stability samples Compile trend and identify degrading impurity Evaluate shelf life of the drug substance for expiry conclusion Key Accountabilities (5/6) Keep track of the latest innovation and applications which can be used with the existing techniques to investigate / resolve critical issues Attend various webinars, conferences Evaluate various demo datas generated by instrument manufacturers at their demo labs Compare various parameters like shorter run time, solvent consumption, cost factor and environment safety Key Accountabilities (6/6) Major Challenges Changes in the Regulatory guidelines: Keeping abreast with latest regulatory guidelines and interaction with RA department Conflict regarding the priorities of samples: Interaction with cross-functional team along with the managers to prioritise the samples Delay in cross-functional activities: Interaction with immediate supervisor for clarity of responsibility Difference in instrument compatibility for analysis: Escalated to supervisors Key Interactions (1/2) API R&D/ F R & D for planning, product information and result discussion (daily) RA for regulatory discussion for Deficiency, DMF filing (as per need basis) IP or patenting any product or getting information of any known patent (as per need basis) Units for sample requirement, Method transfer, Method validations, investigations (weekly) Purchase & Imports for impurities/chemicals, instrument and Equipment (as per need basis) HR for Personal discussion and organisation rules and regulation, company policy discussion (as per need basis) Key Interactions (2/2) Outsource Labsfor external analysis (weekly) Vendors-Instruments/Equipment for service and support (as per need basis) Application specialists for application support to resolve any challenging queries (as per need basis) Dimensions (1/2) Minimal error for lab compliance and maximise output Maximise instrument utility by working in shifts Online delivery of analytical data to R&D Ensuring 100% compliance with the regulatory Meet the turnaround times for projects Publish two papers in a year Dimensions (2/2) Number of trials on various techniques during development stages Key Decisions (1/2) Result discussion for online monitoring of samples with R&D Change in method of analysis with supporting analytical data to the respective Group Leader Key Decisions (2/2) Education Qualification Sc Relevant Work Experience Minimum 15 years of experience in pharmaceutical industry with analytical experience Good presentation and communication skills are preferable Show

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

Analytical Development Laboratory Associate Male Min 2-5 Exp only API Co Salary: 2-3 LPA Location: Vadodara( Nandesari ), Gujrat

Business - Research & Development Department - ADL ( API ) Position - Research associate to Team Lead Qualification - M.Sc./M.Pharm Experience - 3 to 8 Years Contact - Sharad Yadav ( HR ) - sharad.yadav@cadilapharma.com