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2 - 6 years

8 - 12 Lacs

Nasik, Navi Mumbai

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Role & responsibilities:- Design and develop concepts for New Products under development. Provide design output/ Specifications in both 2D and 3D format Validate and test the samples/ prototype as per the design specifications and standards. Also, ensure new product features/ function are met as per marketing specification. Make changes/ improvements in Design based on the testing results and ensure that the product is functioning as per its features and specifications. Creation of Item codes, Engineering BOM. Collaborate with cross functional teams - R&D Industrialization, CPD, QA and ME teams for new product development and qualification. Support R&D Industrialization and Process department to develop and qualify tools, Jigs and fixtures. Work on continuous product enhancements and life cycle management of all products. Initiate and implement change management processes and achieve more than 90% completions before due dates. Preferred candidate profile:- Expertise in Designing through design software. Core design experience for products ACB/MCCB/MCB/RCCB/Controlgear is essential. Highly proficient in using MS Office applications like Excel, word and power-point and enterprise application software, Cero, ProE AutoCAD, Solid Works, CATIA, etc.) Excellent communication and presentation skills Perks and benefits:- As per company norms

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2 - 4 years

3 - 6 Lacs

Bengaluru

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Role & responsibilities 1. Analytical Testing and Analysis : a. Analyze samples from various sources (raw materials, intermediates, finished products, and stability samples) to determine compound composition and quantities. b. Perform routine and complex analyses using HPLC, Prep HPLC, LCMS, UPLC, and Flash chromatography. c. Interpret analytical data and provide comprehensive reports of scientific results, including trend analysis and data summaries. d. Conduct testing, release, and documentation of raw materials, intermediates, and finished products, adhering to established specifications. e. Perform stability studies and analyze degradation products. 2. Method Development and Validation: a. Develop and validate HPLC, LCMS, and other analytical methods for various drug products and chemical compounds, including forced degradation studies. b. Ensure methods are robust, reliable, and compliant with regulatory requirements (ICH guidelines, etc.). c. Write and review method validation protocols and reports. 3. Instrument Management and Documentation: a. Perform routine calibration, maintenance, and troubleshooting of HPLC, LCMS, GC, and other analytical instruments. b. Prepare and maintain Standard Operating Procedures (SOPs) and Instrument Operating Procedures (IOPs). c. Maintain accurate and detailed documentation of all analytical activities, including raw data, instrument logs, and reports, in accordance with GLP/GMP. d. Participate in instrument qualification. 4. Quality Control and Compliance: a. Ensure all analytical activities comply with established quality control procedures and regulatory guidelines. b. Maintain awareness of and adhere to health and safety regulations, including chemical handling and waste disposal. c. Validate methods and equipment to ensure accuracy and reliability, participating in audits as needed. d. (Optional) Ensure compliance with cGMP and GLP guidelines. e. Participate in investigations of out-of-specification (OOS) results. 5. Collaboration and Communication: a. Work collaboratively in cross-functional teams, including R&D, formulation, and regulatory affairs. b. Liaise with customers, staff, and suppliers as needed. c. Report scientific results effectively to stakeholders, including presentations and written reports. d. Participate in project meetings. Preferred candidate profile Technical Skills: a. Extensive hands-on experience with HPLC, Prep HPLC, LCMS, UPLC, and Flash chromatography. b. Proven experience in developing and validating HPLC and LCMS methods. c. Knowledge of instrument calibration, maintenance, and troubleshooting. d. Proficiency in data interpretation, statistical analysis, and documentation. e. Knowledge of stability testing. Knowledge: a. Strong understanding of analytical chemistry principles and techniques. b. Knowledge of raw materials, intermediates, finished product, and stability testing. c. Knowledge of preparing SOPs, IOPs, validation protocols, and reports. d. Knowledge of regulatory guidelines (ICH, etc.). e. (Optional) Knowledge of cGMP and GLP compliance. Soft Skills: a. Excellent analytical and problem-solving skills. b. Strong attention to detail and ability to maintain meticulous records. c. Excellent communication skills (both written and verbal). d. Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint). e. Ability to work independently and manage multiple tasks effectively. f. Strong team player Key Attributes: a. Accuracy and reliability in analytical work. b. Commitment to quality, compliance, and safety. c. Proactive and adaptable to new challenges and technologies. d. Strong organizational and time-management skills. e. Ability to learn and keep up to date with new analytical techniques and regulatory requirements. f. Ethical conduct. Perks and benefits

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6 - 11 years

3 - 8 Lacs

Mumbai, Kalyan/Dombivli

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Job title ADL executive Division phrama Function Analytical method validation Location dombivali Designation ADL executive Job Grade Reporting to (position) ADL Head Direct Reportees (Nos) Company Name Aart industries limited Key Role & Responsibilities 1)Able to performed method validation on GC HS 2)analytical method transfer 3) Able to performed method validation on GCMS 4)method development on GC 5)Handling incident and deviation 6) online review of system,log books 7)Aware of 21 CFR part 11 guidlines ICH and Anvisa Guidlines 8) GC MS and LCMS Linkages within / outside the organisation Internal External Job specification Experience min 9 years Qualification MSc CTC Range as per company based on skill and knowlage Target Company if Any Certifications/Trainings Skills / Competencies Have good knowledge of GC gcms Awareness 21 CFR part 11 knowledge of GMP and GDP handled OOS,OOT incident deviation able to work in shifts. analytical method validation FDS study and photostability Role & responsibilities Preferred candidate profile Perks and benefits

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3 - 5 years

6 - 8 Lacs

Noida

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OGA Instructional Designer is responsible to engage or collaborate with appropriate stakeholders and SMEs to identify business content needs and create content working closely with onshore SMEs/ Trainers and Stakeholders. They will apply knowledge of appropriate instructional design tools and resources used to develop training or process content and create engaging and effective learning experiences Primary Responsibilities: Engage or collaborate with appropriate stakeholders and SMEs to identify business content needs and create content working closely with onshore SMEs or Trainers and Stakeholders Conduct task analysis or research to identify the specific knowledge, skills, behaviors needed to achieve desired performance levels Analyzes, updates, and refines existing online content Develop learning objectives based on appropriate analyses (e.g., business analysis, task analysis, audience analysis) Develop appropriate learning activities based on training designs and learning objectives Identify and implement appropriate instructional design theories for developing interactive and learner friendly trainings Apply principles of adult learning and training best practices to create effective and innovative training design solutions Research or identify appropriate delivery approaches or media or methodologies (e.g., ILT, eLearning, webinar, virtual training) and obtain required approvals Demonstrate and apply knowledge of appropriate instructional design tools and resources used to develop training content Designs learning activities, assignments, and assessments. Creates computer-based training (CBT) modules, instructors manuals, and storyboards Identify and communicate appropriate solutions needed to address identified business issues and needs (e.g., training, coaching, policy changes, system changes, process or procedure changes, compliance issues, documentation issues, incentive issues, leadership issues, organization structure) Determine project goals or milestones based on identified business needs or timelines, and obtain appropriate approvals (e.g., go or no-go decisions, checkpoints) Identify measurement approaches and mechanisms to evaluate success of the solution (e.g., quality scores, conversion rates, call volumes, order volume) Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regards to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so Your primarily responsible will be for the effective delivery and design of training programs and materials across the organization from an individual who will keep abreast of various training delivery techniques, business processes, products and systems in several functional areas. This will be done in accordance with management and functional leaders to gather information on business needs to design instructor led, Web-based and e-learning training including training processes and procedures. Identifying training needs for facilitator guides as wells as train the trainer sessions by gathering Web-based techniques and interactive learning strategies. As a key resource to others you must maintain a high degree of accuracy along with attention to detail, excellent oral and written communication skills, strong interpersonal skills and the ability to always meet deadlines. Required Qualifications: Graduate 3+ years of hands-on experience with online learning including tools such as Captivate, Articulate Storyline, RISE, Snag IT, Camtasia and others Hands-on experience of making videos using any of these tools - Camtasia, Video Scribe, Vyond, Powtoon, etc. Awareness of LMS and LCMS standards Thorough exposure to ID tools (Articulate Suite, Camtasia, Snag IT, Vyond, Captivate, Adobe Photoshop, etc.) Proficient computer skills including MS Word and PowerPoint Process Specific Skills Proven experience with designing and developing online learning solutions, both synchronous and asynchronous Knowledge of basic ID principles such as ADDIE, Blooms taxonomy, Adult Learning Principles, Gagnes 9 events etc. Solid analytical skills, attention to detail, problem-solving and fact-based decision-making abilities Ability to design curriculum Ability to design or develop serious games (game-based quizzes) Awareness of gamification frameworks Soft skills: Good written and spoken communication skills Time management and multitasking skills Highly motivated Creative bent of mind

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2 - 7 years

4 - 9 Lacs

Udaipur

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Reporting to (Title) Sr. Team Leader Process Innovation Level E1 E4 Position Purpose The role holder shall report to the Sr. Team Leader Process Innovation and shall perform research activities as designing and conducting scientific experiments, analyzing and interpreting results leading to significant value to the business of PI by Process Innovation. Strategic Responsibilities Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of CreAgro Chemistry by driving innovation and team performance according to objectives and targets being set by the Director and Head of Chemistry. Fullfilling requirements as set by Group Leader and Team Leader, e. g. within specific Research Projects Ensuring the security of intellectual property for CreAgro (patent applications, ensuring freedom-to-operate) Updating self with respect to chemistry knowledge through literature scanning to foster innovation Support the Team Leader with special focus on target setting and constantly seek functional feedback Operational Responsibilities Work with the Team to achieve and exceed targets within the frame given by the Group Leader and Team Leader of Process Innovation Keep self updated on the state of the art in synthetic chemistry development and techniques, while putting specific focus on innovative process research Continuous documentation and reporting of all research results obtained within the area of responsibility as defined in the SOP / guideline Seek functional support actively from Team Leader Carrying out literature search by use of available tools (Reaxis/Scifinder/Patents etc.) Carrying out synthetic experiments safely, efficiently, capturing all the experimental procedures and data effectively Updating the Team Leader on the functional progress/issues of the project on a regular basis Constructive and active particiption in all technical and functional meetings of the Team People Responsibilities Support Team members by providing peer feedback Foster an environment of knowledge sharing within the Team Additional Accountabilities: Maintain healthy working relationships with the related teams and departments in Process Innovation Responsible for individual safety Education Qualification MSc/PhD in Organic Chemistry from a reputed University / Institute from India or overseas with excellent academic credentials Work Experience Good experimentalist with experience in industry for 2-7 years, preferably from Contract Research Organization (CRO) & Contract Research and Manufacturing Services (CRAMS). Experience of working in process research Industry to be Hired from Pharmaceutical/ Agrochemical Functional Competencies Knowledge of Organic Chemistry Ability to efficiently use search engines like Scifinder / Reaxys, etc. Lab Experience Ability to interpret analytical data such as NMR Good experimentation skills MS Office Skills Interaction Complexity and Team Work Internal Other Chemistry/Analytical Chemistry Team members Process R&D chemists and engineers SCM Team Other support functions External: Chemical Logistics Service Engineers

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3 - 7 years

7 - 11 Lacs

Udaipur

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Level: Executives Reporting to (Title): Group Leader - Analytical Position Purpose The incumbent would provide support to the Process Research team by providing assistance in reaction monitoring on (HPLC, GC, NMR, IR, LCMS), characterization and data generation of submitted compounds, final product assay method development. Analysis of impurities, physical characterizations, residue content, stability studies, etc. Strategic Responsibilities Actively imbibing the values and philosophy of PI Industries Efficient contribution to the overall success of CreAgro Analytical Chemistry through scientific contribution and supporting team performance according to objectives and targets being set by the leadership team Remain at the cutting edge of knowledge required for the new a.i. discovery activity in crop protection through constant updating of personal knowledge and own skill-sets Operational Responsibilities Experimental determination of several phys-chem parameters like Small molecules Aqueous solubility, Solubility in different solvents, pKa, logP, Henrys Law constant as per OECD guidelines Strong theoretical back ground on the aforesaid phys-chem parameters Analysis of the phys-chem experimental results using Microsoft Excel and GraphPad Prism Good knowledge of statistical analysis like paired student t-test and others Conducting Photo Stability and hydrolytic stability studies Operational skill in Spectroscopic & Chromatographic Techniques Evaluate different equipments required for the work and operation of the same Prepare the Study Strategy and implement as per SOP Documentation and reporting of analytical results Comply to all safety requirements of the role Financial Responsibilities Work with in the limit of budgets Suggest cost improvement areas to the Team Leader / Group Leader People Responsibilities Collaborate with team members and cross functional teams to ensure meeting research objectives Ensure team harmony through collaboration and active participation in all team discussion Education Qualification MSc/Organic Chemistry/Analytical Chemistry/Agriculture from a reputed University / Institute with excellent academic credentials Work Experience 2-5 years of hands on experience on Assay of a.i. by potentiometry, HPLC, GC, impurity purification/analysis Experience in chromatography method validation is an added advantage Industry to be Hired from Agro Chemical / Pharma Generics / Research Universities or Institutes Functional Competencies Scientific Knowledge_O Research Approach Data Analysis Experimental Skills Interaction Complexity and Team Work Interaction Frequency Purpose of Interaction Internal : Team Members , Group Leader As and when required Planning work, discussing results of experiments, resolving doubts, for hiring and HR related issues, for reimbursement claims.

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1 - 6 years

2 - 6 Lacs

Udaipur

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Key Responsibilities: Strategic Actively imbibing the values and philosophy of PI Industries. Efficient contribution to the overall success of product innovation (PRI) through scientific contribution to objectives and targets being set by the leadership team. Fullfilling requirements and achieveing goals set by the Team Leader and Group Leader Working as a team member, contributing to the team objective with special focus on achiving and exceeding the set target. Development of individual & team strengths by attending trainings based on the regular feedback as an individual and as a team Operational Monitoring reaction masses using LCMS/GCMS. Execution of purity assessment and assay determination of samples using GC/HPLC/UFLC. Able to carry method development for challenging compounds through GC/GCMS/HPLC/UFLC Developing methods on Prep HPLC for purification/isolation of impure compounds. Elucidating and confirming structures using NMR, FTIR and LCMS/MS Ensure the scheduled performance of calibrations, Preventive maintenance and troubleshooting of core analytical instrument. Following the set instrument maintenance practices like periodic solvent changes, system flushing, etc. Assist the other team members in day to day activities like sample preparation, method developments, report generation and data management. Following safety practices with out fail. Financial Planning the activities with existing resources and infra structure. Suggesting the cost-effective areas to the Team Leader / Group Leader Developing methods to improve the environment safety and to reduce the cost. People Collaborate with team members and cross functional teams to meet research objectives. Develop and foster positive relationships with other teams and support groups to maximize cooperation and consequent benefit to objective delivery Should be able to work in multitasking environment Ensure team harmony through collaboration and active participation in all team discussion Apart from the above responibilities, specific responsibilities of Research scientists Note : The Associate would in any of the areas listed below based on the requirement and should have sufficient knowledge and expertise in the area alloted as listed below 1. HPLC/UFLC Candidate should be well versed with normal and reverse phase chromatography techniques. Able to optimize chromatographic methods Keen knowledge on low level analyte-impurities quantification by HPLC. 2. LCMS SQD & TQD Well versed with operations of one or more makes of LCMS-SQD & TQD instruments. Aware of basic principles related to mass spectrometry, sources, analysers and detectors. Hands on experience in analysis of compounds using LCMS instrument and releasing the mass confirmation reports. Keen knowledge on ppb / ppm level quantification of analytes from AI, formulations, various matrices like microsomes, soil, plant extracts by LCMSMS. Perform possible structural elucidation/Identification of degradants/metabolites/impurities using LCMS/MS 3. NMR Perform suitable 1D/2D NMR experiments based on the requirement and confirm one among proposed structures or propose a new structure. Manage the NMR activities viz, perform routine NMR (1D&2D) analysis, QNMR, cryogen replenishing. Keen knowledge of NMR technology & instrument maintenance. 4. Physchem assays Have hands on knowledge of various in vitro ADME/ physchem assays like solubility, LogP, pKa and in vitro Metabolic stability assay. Able to develop methods, check method compatibility for accuracy, precision, matrix effect and apply it further for the quantification of formulations, plant extracts, various matrices like soil, microsomes etc. Perform the microsomal stability experiments to determine half-life and Clint. Awareness about Met ID using various scans, fragmentation tree & HRMS will be an added advantage. Knowledge about sample preparation and analysis of photo stability and hydrolytic stability. 5. Prep-HPLC Able to develop a robust chromatographic method both at analytical and preparative scale, by designing cost effective methods for chiral and achiral molecules. Knowledge of chiral chromatography and isolation of enantiomers using preparative HPLC. Please share updated resume on e-mail id Shubhi.chandnani@piind.com

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1 - 4 years

3 - 6 Lacs

Ahmedabad

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MD/MV Roles and Responsibilities:- MD/MV group does assay method development and validation for various drug and their metabolites in biological fluids like plasma serum or urine by using LC/MS/MS. During method validation precision, accuracy, stability of drug/metabolite in biological fluid as well as after extraction is evaluated. The validated methods are then followed for the analysis of subject samples analysis for doing bioequivalence study.

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8 - 12 years

6 - 13 Lacs

Mahad, Raigad, Ratnagiri

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Role & responsibilities Experience in operation and trouble shooting of process in plant. Isolation and purification of different organic compound using column chromatographic and crystallization techniques. Optimize the process parameters, what-if studies, holding studies etc. for scale up. Investigation of OOS/OOT and stability related issues. Analytical development In R&D department Reactions performed like Hydrogenation, Brominating, Oxidation, Reduction and condensation. Handling of Moisture sensitive reactions. Study and understand the project requirements, identifying and collection of suitable literature. Support lab manager to prepare weekly technical reports and other project related technical documents (impurity profile tables, Plant batch data, developmental reports) Executing assigned reactions of project. • Looking after the Safety equipment's management and maintaining it as per regulatory requirement in R&D lab. • Study the MSDS of each chemical using in every new project and make arrangement of Safety equipment's accordingly. Handled HPLC system of Agilent technologies Eriochrome (A.04.07) and version Open Lab cds2.4 • Good in Thin layer chromatography & Column chromatography. • Polymorph characterization with the aid of XRD, DSC, TGA and IR Techniques. • Having good ability to interpret analytical results like NMR, HPLC, GC, LCMS, MASS, IR & UV. Preferred candidate profile Perks and benefits

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2 - 7 years

2 - 6 Lacs

Hyderabad

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Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-03-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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.

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3 - 5 years

3 - 8 Lacs

Hyderabad, ECIL Cross Roads

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Analysis of samples by using HPLC (Open Lab Solutions).Wet Analysis by using IR, UV, pH, etc.Quality Control Documentation. Responsibilities: Conducting Laboratory Experiments: Plan and execute a variety of chemical experiments, including synthesis, analysis, and characterization. Operate and maintain laboratory equipment such as spectrophotometers, chromatographs, and titrators. Collect and record experimental data accurately and meticulously. Data Analysis and Interpretation: Analyze experimental data using statistical and other relevant methods. Interpret results, draw conclusions, and prepare technical reports and presentations. Identify and troubleshoot problems encountered during experiments. Research and Development: Conduct literature reviews and stay abreast of the latest advancements in chemistry and related fields. Contribute to the development of new products, processes, and formulations. Participate in brainstorming sessions and contribute creative ideas. Laboratory Maintenance: Maintain a clean, organized, and safe laboratory environment. Ensure compliance with safety regulations and laboratory protocols. Order and maintain laboratory supplies and equipment.

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5 - 10 years

4 - 9 Lacs

Valsad

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Role & responsibilities Implement norms for safety culture and 5S in laboratory Provide support and execute analytical method development and validation Coordinate for analytical testing and reporting Execute calibration of various analytical instruments as per schedule Adhere to ADL department policies and SOPs Comply with statutory and regulatory requirements Eligibility Individuals who have cleared 10th and 12th in first attempt (50% and above) MSc (50% and above), with no academic gap. Interested candidates can share their CV to juhi_bhavsar@atul.co.in or call on 81605 01583

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2 - 5 years

0 - 3 Lacs

Bengaluru

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Role : Analyst LCMS/HRMS Key Job responsibilities Analyst should able to carryout testing in method transfer and method verification activities. Subject matter expert on analysis of HPLC, LCMS, GCMS for both assay and impurities routine samples of in process, cleaning validation, SFG & Stability. Subject matter expert in analysis of nitrosamine impurities. Subject matter expert calibration of instrument and its management.

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2 - 6 years

3 - 8 Lacs

Navi Mumbai

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Job Title: Senior Research Associate / Executive Analytical Laboratory Location: Rabale, Navi Mumbai Department: Analytical Method Validation/Analytical Method Development Reports to: Manager/Senior Manager Position Type: Full-time Position Summary We are looking for a skilled and detail-oriented Senior Research Associate/Exectuive to join our dynamic team at Fusion Scientific Laboratories, a leading USFDA and EMA accredited pharmaceutical laboratory. The successful candidate will play a key role to operate and maintain advanced analytical instruments such as HPLC/GC/GC-MS/ ICP-MS/ IC/ LC-MS/HR-MS. The ideal candidate will support method development and validation, and ensure accurate and timely data reporting. This role is crucial for delivering high-quality analytical results to support research, product development, and quality control initiatives. Key Responsibilities: Operate and maintain analytical instruments including HPLC/GC/GC-MS/ ICP-MS/ IC/ LC-MS/HR-MS. Perform routine and specialized analyses on various samples in compliance with established protocols and regulatory requirements. Support method development, optimization, and validation for new and existing analytical procedures. Prepare samples, reagents, and standards for analysis, ensuring accuracy and consistency. Perform data acquisition, processing, and interpretation, and compile results into detailed reports. Maintain detailed laboratory records and ensure compliance with GLP/GMP, ISO, or other applicable standards. Conduct regular instrument calibration, performance checks, and maintenance to ensure precision and reliability. Stay updated on advancements in analytical techniques and instrumentation. Adhere to all safety and regulatory requirements within the laboratory environment. Collaborate with cross-functional teams to support research and development, quality control, and other organizational needs. Qualifications: Masters degree in Chemistry, Analytical Chemistry, Biochemistry, or a related field. 2–6 years of experience in operating analytical instruments such as HPLC, GC, GC-MS, ICP-MS, IC, and LC-MS. Technical expertise in analytical method development and validation. Proficiency in data interpretation and reporting, with attention to detail. Familiarity with GLP, GMP, and other relevant regulatory standards. Problem-solving and time management skills. Ability to work independently and collaboratively in a team-oriented environment. Knowledge of software used in analytical instrumentation (e.g., Chromeleon, Analyst, Lab solution, Empower software would be added advantage). Work Environment: Laboratory-based role with adherence to SOPs and safety protocols. May require occasional extended hours to meet project deadlines. Fusion Scientific Laboratories is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

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2 - 7 years

3 - 7 Lacs

Bengaluru

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Candidate should have hands on experience by analysis In-process and routine samples using Gas chromatograph, High performance liquid chromatograph, Ion chromatograph, and IR Candidate should have hands on experience in qualitative and quantitative analysis using GCMS, LCMS and HRMS Candidate should have adequate knowledge on Pharmacopeias and working standard and impurity standard qualifications. Candidate should have adequate knowledge on quality guidelines from ICH Candidate should have hands on experience in good documentation practices and communications skills by Vocal and writing.

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0 - 2 years

2 - 4 Lacs

Bengaluru

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Greetings from Atria Power!! (www.atriapower.com). We are hiring for B.Tech Mechanical or Chemical Engineering Graduate with 5 + years of Experience in Bio Mass Power Plant for Atria Power. About Atria Group. Atria Group was established in 1950. We are one of the most eminent business groups in South India. Atria Group is with business verticals which includes Power(Atria Power), Internet Technology(ACT Broadband), Media Services(ACT cable TV), Hospitality (Atria Hotels), Education (Atria Institute of Technology & Xceler) and Real Estate. Should be capable of first principles design of Biomass based power plants including fuel handling system and boilers. Should generate Specification and RFQ for procurement of Biomass system. Proficient in Testing and Acceptance of Biomass systems. Requirements. Tech Graduate Mechanical or Chemical Engineering. 5+ years of Relevant Experience. Hands on Experience in AutoCAD. Proficient in MS project. Proficient in MS Office. Fluent communication skills both verbal and written. Sujitha Balan. 073386 99681 (ref:mfg.careers). Show more Show less

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1 - 5 years

2 - 7 Lacs

Navi Mumbai

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Job Title : Analytical Chemist Qualification: M.Sc. in Organic Chemistry/Analytical chemistry Experience : 1-5 years of relevant experience in CRO, Discovery R&D, API, and Agrochemicals at Analytical R&D lab. Location : Dev Research Centre (SML Ltd), Nerul, Navi Mumbai-400706 Vacancies : 2 Roles and Responsibilities: To perform analytical method development and validation activities using GC, HPLC, LCMS & Chemical analysis. Performing analysis of NCE, raw material, in-process, intermediate, Stability studies & finished product. To maintain and update analytical records with complete data derived from analysis. Preparation and maintaining Lab notebooks, Training Records, and other logbooks. Ensure the work environment is clean and safe complying with safety and as per GLP. Operation and calibration of various analytical instruments. Excellent knowledge in wet chemistry instruments like Balance, pH meter, Melting point, UV, polarimetry, IR, Moisture balance analyser and keeping instruments calibration and maintenance records. Share your CV on careers@sml-ltd.com

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3 - 6 years

4 - 7 Lacs

Petlad

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Job Description Job Title: R&D (Peptide chemistry) JRS/RS/SRS (Nutraceutical Industry) Job Location: - Plot No. 214, Borsad - Tarapur Road, Ta: Petlad, Dist: Anand, Gujarat, India. Department: Research and Development Reports To: Manager R&D Job Type: Full-TimeCompany Profile: -Pharmanza Herbal Pvt. Ltd. is one of the few companies, which is focusing on standardizing and proving the efficacy of Herbal products. Our strong supplier base, fully equipped R&D facility, FDA approved manufacturing facility, infrastructure for conducting human trials as well as our formulations unit provides a one stop solution to our valued customers. Pharmanza Herbal Pvt Ltd. is one of the leading research-oriented companies, manufacturing herbal extracts used in the Ayurvedic and nutraceutical segment. Our journey began in 1997 with Pharmanza India, our group company located in Khambhat, India, where we started producing herbal extracts. While Pharmanza India primarily focuses on veterinary allopathic formulations, we leveraged its facilities to manufacture herbal products such as Garcinia cambogia, Commiphora mukul, and Withania somnifera from 1997 to 2004. As the business expanded, and we began exporting our products to countries like the US, Japan, and Germany. Pharmanza Herbal was established in Dharmaj, India, to continue our commitment to quality and innovation in herbal solutions. The facility is certified by Food safety authority of India (FSSAI), Food and drug Administration, India (Gujarat office) with NSF-GMP International. Current certifications include ISO9001:2015, ISO22000:2018, NSF-GMP, NSF-SPORT,USP-GMP,USP-Ashwagandha,Bosewelia with Kosher and Halal and USDA/APEDA organic certifications for products. Additionally, we are also certified SEDEX 4 Pillers and ECOVADIS. Job Overview: - Seeking a skilled JRS/RS/SRS with 4-5 years of experience in peptide synthesis, purification, and characterization for nutraceutical applications. Responsibilities include developing innovative peptide formulations, optimizing processes, ensuring regulatory compliance, and collaborating with cross-functional teams for product development and quality enhancement. Responsibilities and Duties: - Participate in R&D teams associated with process development and characterization for peptides and other modalities. Develop and characterize peptide processes in the laboratory and translate them to scalable processes. Proactively advise and share knowledge and expert opinions with peers, project leaders, and senior management. Mentor staff in troubleshooting strategic and experimental issues. Review key regulatory documents and author technical memos and reports. Identify and nurture ideas for continuous improvement activities and initiatives within the department. Collaborate with organic chemists, analytical chemists, clinicians, engineers, drug product development, and project management. Qualifications: - Education level: - M. Pharm., M.Sc. (Chemistry/ Biotechnology/ related specialization) / Ph.D. Experience: - 04 to 05 yrs. Gender: - Any. Salary Range: - Competitive. Skills: - Expertise in the isolation and characterization of peptide molecules from plant materials. Strong troubleshooting skills and ability to develop methods for special functionalized peptides. Proficiency in analytical data analysis to identify isolated/ synthesized targets and key intermediates. Adherence to laboratory safety and industrial hygiene practices. Well versed with instruments and related techniques like UV, HPLC, LCMS, Electrophoresis, NMR etc.. Benefits: Competitive salary package. Subsidized food facility. Free Transportation facility from Vadodara location. Medi-claim facility. Opportunities for professional development and growth. A dynamic and collaborative work environment committed to sustainability. Join our team of passionate professionals and contribute to the growth and success of our nutraceutical product portfolio. If you have the required expertise and are ready to take on this exciting challenge, we encourage you to apply now. Company Website: - www.pharmanzaherbal.com Company Email id: - hrm@pharmanza.com

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3 - 5 years

3 - 4 Lacs

Navi Mumbai, koparkhairane

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Role & responsibilities Job Profile: Conducting literature survey on new product. Preparation of standard operating procedure (SOP), and protocol for bio-study and conduct the training for same. Assisting in developing bio-analytical method, as per the regulatory guidelines, on LC-MS/MS platform for quantitative determination of drugs in human matrices. Validating the bio-analytical method, as per the regulatory guidelines, on LC-MS/MS Conducting routine bio-analysis of clinical samples on LC-MS/MS along with recording raw data as per GLP. Preparing spread sheet for spiking solution, calibration curve standards and quality control samples. Processing of clinical samples by various samples clean up techniques like solid-phase extraction, liquid-liquid extraction and protein precipitation methods. Compilation of raw data in data sheet, laboratory logbooks and its submission to quality control department. Maintenance and calibration of various analytical instruments and equipments used in the bio-analytical section.

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1 - 6 years

3 - 4 Lacs

Navi Mumbai

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Interested candidates share your resume to sanjay.behera@thyrocare.com or whatsapp to 8928285213 Key Responsibilities: Sample Preparation and Handling: Prepare and process samples (e.g., liquids, solids, environmental samples) for ICPMS and LCMS analysis. Prepare standards, reagents, and calibration solutions as needed for ICPMS and LCMS analyses. Ensure accurate and thorough labeling, storage, and disposal of samples, chemicals, and waste in compliance with safety regulations. ICPMS & LCMS Operation: Operate, calibrate, and maintain ICPMS and LCMS systems, ensuring high-quality data output. Perform routine analyses using ICPMS and LCMS techniques for the detection of metals, ions, and compounds in a variety of sample types. Prepare and run samples using ICPMS and LCMS, ensuring accuracy, precision, and efficiency. Troubleshoot instrument-related issues, optimizing performance as needed. Data Analysis and Reporting: Analyze data generated from ICPMS and LCMS instruments, ensuring accuracy and completeness of results. Interpret complex analytical data and compile reports for review by senior laboratory staff or clients. Document and track results in laboratory information management systems (LIMS) or appropriate software. Quality Control and Compliance: Ensure quality control standards are maintained throughout testing, including calibration, validation, and cross-checking results. Follow established laboratory protocols and regulatory guidelines (e.g., GLP, ISO standards) to ensure accurate and reliable data. Maintain and manage calibration standards, quality control samples, and blank samples to meet the required analytical accuracy. Instrumentation Maintenance and Troubleshooting: Conduct routine maintenance and calibration of ICPMS and LCMS instruments, ensuring they are functioning optimally. Troubleshoot and resolve instrument issues, collaborating with engineers or senior lab staff when necessary. Monitor instrument performance, ensuring that diagnostic or preventative maintenance is conducted according to schedules.

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0 - 4 years

1 - 6 Lacs

Ahmedabad

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MD/MV group does assay method development and validation for various drug and their metabolites in biological fluids like plasma serum or urine by using LC/MS/MS. During method validation precision, accuracy, stability of drug/metabolite in biological fluid as well as after extraction is evaluated. The validated methods are then followed for the analysis of subject samples analysis for doing bioequivalence study. Candidates must experience in MD-MV onto LC/MS/MS for drugs and their metabolites in various biological fluids. Well versed in operating and trouble shooting LC/MS/MS instruments. Well versed in literature search, basic computer knowledge and MS-office. Aware of recent trends in regulated bioanalysis and regulatory guidelines Perform the extraction of samples using wet chemistry. Centrifuges, evaporators, freeze specimens as required. Performs aliquots of samples for wet chemistry. Performs wet chemistry according to study protocol guidelines and/or SOPs. Completes QC sheets and makes log book entries as required by protocol and/or SOP. Operate HPLC, LC/MS/MS and ICP-OES; troubleshoots problems and performs minor repairs

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3 - 7 years

4 - 5 Lacs

Hosur, Berigai

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Job Profile The job position "Analytical Method Development" is to support the plant operation team by 1. Sustaining Quality Management and Quality system 2. Implementation of IMS 3. Ensuring Customer Satisfaction 4. Timely response to Production Team. 5. Ensuring Quality assurance at all stages of production 6. "People Development ." Role & responsibilities 1. To carry out testing and inspection in shifts of incoming raw materials, in-process reaction monitoring 2. Samples and finished products. Inspection and testing would encompass both wet analysis and instrumental 3. Methods of analysis. To maintain all testing records in line with ISO-9001 and cGMP requirements. 4. facilitate clearance of finished products from production shop floor to finished goods. 5. Analysis and advice / instruction required to address specific customer requirements. 6. Should have experience in HPLC, GC and preferably in ICP OES & LCMS , GCMS, NMR 7. Should be aware of Chemical Safety, GLP practice & documentation. 8. Review of finished product report and release 9. Follow Instrumentation calibration , AMC, CMC 10.Knowledge on SAP activities preferred 11. follow of Outsource analysis and get the timely report from the testing lab Preferred candidate profile Post Graduate in Chemistry / Analytical Chemistry 3 to 7 Years Experience in Checmical & Pharma Industry with method Development Interested candidate can share their resume to STK3@sanmargroup.com

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7 - 12 years

6 - 12 Lacs

Bengaluru

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Dear All, Greeting from Falcon services! JD for Assistant Manager/ Manager PS-Food Chemical for our Bangalore lab. Summary- We are looking for an Assistant Manager/ Manager with experience in residue analysis of foods, feed & water using GC-MS/MS and LC-MS/MS. The person will have adequate knowledge of extraction of pesticide residues, aflatoxins, antibiotic residues, dyes, melamine, hydrogen phosphide, inorganic bromide, dioxins from food & feed. The person will also be responsible for the laboratory operations of residues lab focused on ensuring maintaining TAT, responsible for implementation of accreditation requirements and optimization and validation of test methods as per requirements . Position Assistant Manager/ Manager PS Food - ChemicalJob Description: Testing of various agriculture, food products and water for residue testing by standard and in-house methods. Monitoring the turnaround time of the sections / reports as per the given schedule. Ensure on-time training of respective team as per training planner, mentor / train analysts/Jr. Analysts. Extraction of pesticide residues, antibiotic residues, toxins from food and feed samples as per applicable SOP. Handling, maintenance and troubleshooting of LC-MS/MS or GC-MS/MS. Ensure on time method development / verification and validation. Ensuring purity and validity of CRMs Preparation of standard solutions. Daily maintenance of lab equipment. Coordinate and ensure Calibration / Preventive Maintenance / repair schedule with adequate documentation. Equipment /method troubleshooting / repairs. Supporting lab manager for RCA and CAPA. Following good laboratory practices. Following disposal process for samples & solutions as per SOP. Accurate analysis and interpretation of test results. Maintenance of laboratory documents and records. Validation of methods and calibration/verification of instruments. Immediate response to the internal or external enquiries.Communications with cusotmer for technical support . Additional Knowledge : Awareness of NABL norms. Thorough knowledge of ISO 17025: 2017 Quality Management System. Adequate knowledge in operating, troubleshooting and maintenance of LCMS, GCMS, UPLC and other analytical equipment. Adequate knowledge of validation guidelines such as SANTE, AOAC, EC 657, etc Exposure to regulatory requirements such as FSSAI, EIC, APEDA, etc and validations guidelines and regualtion as per EIC, APEDA and other regualtory requirment. Knowlegde of the Regualtions and Guidelines for the residue analysis. Experience 8 to 12 Years Qualification M.Sc Chemistry

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2 - 5 years

3 - 6 Lacs

Hyderabad

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Knowledge on how to develop the LCMS / HPLC suitable method from the GCMS method.Preferable to handling of LC-HRMS instrument and technical knowledge on E & L studies.Method development for GTIs and Nitrosamines by LCMS.Collect the literatures.

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6 - 10 years

15 - 25 Lacs

Noida

Remote

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SDG is a global cybersecurity, identity governance, risk consulting and advisory company that advises and partners with clients to address their complex security, compliance and technology needs and delivers on strategy, transformation, and long-term management of their cybersecurity and IAM programs. We help some of the largest brands in the world realize their business vision through a mix of strategic advice, expert systems integration, relevant technology recommendations and smart managed services. Our value proposition to our customers is that we bring thought leadership to the table in each of our domains, a passion for customer success, and an eye to risk management in everything we do. We are looking for you to join our SDG family! We are seeking a highly skilled and experienced IdentityNow Engineer to join our team. As an IdentityNow Engineer, you will be responsible for designing, implementing, and maintaining the identity and access management (IAM) infrastructure. You will collaborate with cross-functional teams to ensure the secure and efficient management of identities, access rights, and application onboarding processes. Looking for notice serving candidates or immediate available. Position: SailPoint Senior Tech Lead Experience: 6 to 9yrs Location: Noida OR Work from Home (Both options are available) Shift Timing: 2PM to 11PM Roles & Responsibilities Responsible for development and deployment of solutions within Identity and Access Management (IAM) domain majorly SailPoint. Design & develop custom tasks as per client requirement. Designing custom screens for requesting additional access, approvals. Configuration includes (but is not limited to): JML, workflows, triggers, application connection and configuration of identity/role/entitlement modelling, custom reports, provisioning. Conduct impact assessments, and communicate impacts and develop mitigation strategies. Develop additional code and/or supporting modules to integrate external systems or processes into IdentityIQ processes. Designing & implementing the out-of-the-box and custom connectors. Lead and participate in project meeting that include project resources to achieve project objectives. Preparing & reviewing the design and deployment guide documents. Requirements: At least 5 years of experience in SailPoint IdentityIQ designing, development, configuration, testing, integration, and deployment. SailPoint connector development experience with both out-of-the-box and custom connectors. Experience in any other IDM suite is an added advantage.Sound experience in developing applications using Java, J2EE components. Should have a very good understanding of information security concepts with in-depth knowledge of IAM solutions and latest trends. Understanding of SailPoint deployment architecture and ability to design based on client requirements.

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