2096 Hplc Jobs - Page 14

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

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 06-09-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to interact with cross - functional and cross - cultural teams. Previous experience of running analytical techniques such as HPLC, Dissolution, KF, IC with the ability to extract and prep various samples in a variety of forms. As this role involves liaising with other departments on a regular basis, you will need good communication skills and the ability to work effectively as part of a team. Note : Formulation Quality Control Candidates also eligible. Interview Date : 06-09-2025 Department : Formulation Analytical Research & Development(FAR&D) Experience : 1 to 6 Years Qualification : M. Pharmacy / M.Sc. / B Pharm Position: Executive Work Location : MSN R&D Center, Pashamylaram, Hyderabad Interview Venue Details MSN Laboratories, R&D Center,Pashamylaram, Hyderabad

Role & responsibilities For QC CHEMIST : BSc or BPharm with min 3 years experience in Cosmetics or Pharma industries. Able to handle all testing equipment s like HPLC, RI, Analytical of RM/PM, test reports preparation Preferred candidate profile B.Sc or B.Pharma Graduate.

Role & responsibilities R&D Synthesis: Experience in API synthesis, process development, and DMF filing. Develop cost-effective, high-quality, and eco-friendly processes as per ICH guidelines. Optimize lab processes, validate products, and transfer technology to pilot plant. Design and propose specifications for KSM, intermediates, and APIs. Proficient in NMR, Mass, IR characterization and troubleshooting synthesis/impurity issues. Prepare documentation for process development and technology transfer. ADL: Method Development by HPLC. Method Validation by HPLC. Preparation, Review, and Technical input for specification and method of analysis. Experience in GLP related activities i.e., calibration, qualification of instruments and standard management.

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.,

Job Title: Quality Control Analyst Formulation (OSD & Injectables) Experience: 2 to 8 Years Work Location: MSN Formulation Unit-II, Kothur , Hyderabad Department: Quality Control - Formulations Employment Type: Full-time Job Posting Purpose: We are looking for an experienced and motivated Formulation QC Analyst with 2 to 8 years of hands-on experience in testing Oral Solid Dosage (OSD) and Injectable formulations . This role involves executing and supporting analytical testing, method validation, and regulatory compliance for pharmaceutical products. The ideal candidate will have a strong understanding of GMP/GLP , be proficient with analytical instruments , and have exposure to regulatory audits (e.g., USFDA, MHRA). Key Responsibilities: Conduct routine and non-routine testing of raw materials , in-process , finished products , and stability samples using HPLC , GC , LCMS , ICPMS , Dissolution , etc. Perform method development, validation, verification , and method transfer in compliance with ICH and regulatory guidelines. Handle and maintain laboratory instruments; ensure equipment calibration , qualification , and preventive maintenance . Record, analyze, and report data in compliance with GMP , GLP , LIMS , and data integrity requirements. Support stability studies , impurity profiling , and E&L (Extractables & Leachables) assessments. Participate in OOS/OOT investigations , root-cause analysis , and implementation of CAPAs . Collaborate with QA, R&D, and manufacturing teams for timely completion of projects. Assist in preparing documentation for regulatory submissions and support during regulatory inspections (e.g., USFDA, MHRA). Provide training and support to junior analysts as needed. Required Skills and Qualifications: B.Pharm / M.Pharm / M.Sc. in Pharmaceutical Sciences, Chemistry, or related field. 2 to 8 years of hands-on QC experience in pharmaceutical formulations (OSD & Injectables). Proficient in analytical techniques: HPLC , GC , Dissolution , LCMS , ICPMS , UV , Karl Fischer , etc. Strong understanding of method development , validation , ICH guidelines , IP/FP testing , and stability protocols . Knowledge of LIMS , 21 CFR Part 11 , GMP , GLP , and data integrity practices. Experience working in regulated environments with exposure to USFDA , EU , MHRA , or other inspections. Preferred Attributes: Good documentation and analytical skills. Ability to work in a fast-paced, deadline-driven environment. Strong team player with good communication skills. Exposure to regulatory submissions , change controls , and SOP writing . Role & responsibilities Kindly send your profile to the following email address: umamaheswari.pasam@msnlabs.com

You will be responsible for planning, setting up, monitoring, and executing chemical reactions independently within the Agrochemical Industry located in Saykha, Gujarat. Your key tasks will include monitoring the progress of reactions using standard methods and analytical techniques such as TLC, GC, HPLC, and LCMS. You will be required to isolate products, optimize reaction conditions to enhance yields, and purify compounds using chromatography, distillation, and crystallization methods. Characterization and identification of compounds using UV, IR, NMR, LCMS, and GCMS will also be part of your responsibilities. In addition, you will need to oversee the parallel execution of multiple reactions, both performed by yourself and the team. Scaling up R&D developed products to kg scale and facilitating technology transfer to the pilot plant will be crucial aspects of your role. Troubleshooting for successful execution, along with regular updates, final reports, PDR preparations, and inter-departmental communications will also fall under your purview. The ideal candidate should have a Master's degree in Science (M.Sc) with 4 to 10 years of experience in R&D Synthesis within the Engineering / Engineering Design / R&D / Quality industry. Key skills required for this position include R&D Synthesis, R&D Chemist, Research & Development Executive, UPLC, HPLC, GC, and chemical and agro expertise. This role offers a salary ranging between 2 Lacs 50 Thousand to 6 Lacs per annum. If you are a proactive and experienced professional in the field of R&D Synthesis, we invite you to apply for this opportunity.,

You will be a Quality Assurance & Analytical Chemist at FMC, where your primary responsibility will be to provide daily analysis support by developing, validating, and applying various modern analytical technologies and approaches for the development and commercialization of agricultural products. You will ensure that FMC quality standards and good laboratory practices are implemented at the Toller site by conducting cross-checks and on-site audits as per business needs. Your role will involve knowing, understanding, and practicing all aspects of laboratory safety and industrial hygiene protocols, developing, validating, and implementing methods for qualitative and quantitative analysis, conducting routine and non-routine analysis, collecting data, generating summaries and reports, supporting investigations of quality incidents, and operating and maintaining various analytical instrumentation. You will work closely with synthetic chemists and engineers to provide structure determinations and analytical results as requested, manage the quality of active ingredients and intermediates with contract manufacturers, review MOA and analytical Teck pack, and perform other tasks assigned by the line manager. To be successful in this role, you should have a Master's degree or above in chemistry/biochemistry or equivalent experience, along with 10+ years of experience and a minimum of 8 years in analytical development/quality control positions. You should have experience with method development and troubleshooting using various lab instruments/techniques and a track record of delivering quality results on time. Strong interpersonal, problem-solving, and troubleshooting skills are essential, along with good written and oral communication and coordination capabilities with different stakeholders. Familiarity with computers and software packages from various instrument manufacturers is also desirable. If you are a motivated leader with a strong technical background and a passion for safety and efficiency, we invite you to apply for this dynamic role and become a part of our team at FMC.,

You are seeking an Assistant General Manager- Research & Development position at an Indian Pharmaceutical MNC located in Thane, Maharashtra. As the Associate General Manager, you will lead the Analytical Method Validation team, overseeing validation activities for various dosage forms and managing a team of 15+ scientists. Your responsibilities include ensuring regulatory compliance, driving quality and efficiency, and fostering collaboration with R&D, Regulatory, and Plant QA/QC teams. Your key responsibilities will involve providing leadership for analytical method validation across different formulations, overseeing RM and PM characterization, managing method validation projects in alignment with regulatory guidelines, and serving as a subject matter expert for analytical lifecycle management. You will also be responsible for interactions with internal regulatory teams, reviewing DMF documentation, defining product specifications and analytical methods, ensuring audit readiness, and providing support to various cross-functional units. To excel in this role, you should hold a degree in Analytical Chemistry or related scientific discipline, possess extensive experience with analytical instrumentation, have knowledge of international regulatory guidelines, understand QMS principles and GLP practices, demonstrate strong leadership skills, and exhibit excellent communication and project execution capabilities. Additionally, you should be willing to work in shifts if required and be open to travel to external sites as needed. If you meet the qualifications and are interested in this opportunity, please share your CV at pooja.j@domniclewis.com.,

This is a full-time on-site role for a Quality Control Officer. As a Quality Control Officer, you will be responsible for ensuring the quality and safety of products through laboratory testing and data analysis. Your primary duties will include conducting analytical tests using instruments such as HPLC, GC, UV, IR, Water content by KF, Auto titrator, and Dissolution Apparatus. Additionally, you will be responsible for quality assurance activities and effectively communicating results with team members and clients. To excel in this role, you should possess strong analytical and laboratory skills, along with hands-on experience in operating various testing instruments. Your ability to follow Standard Operating Procedures (SOPs) and work in a regulated laboratory environment will be crucial. Excellent communication and interpersonal skills are essential for effective collaboration with team members and clients. The ideal candidate should have a Bachelor's degree in Chemistry, Pharmaceutical, or a related field. Previous experience in Quality Control and Quality Assurance, particularly in the pharmaceutical or related industry, will be advantageous. Knowledge of FDA regulations and Good Manufacturing Practice (GMP) guidelines is preferred. This position offers a full-time, permanent opportunity with a work schedule that may include day shifts, morning shifts, and rotational shifts. The work location is on-site, and the employer can be contacted at +91 9624411126 for further discussions. If you meet the qualifications and are looking to contribute your expertise to ensuring product quality and safety, we encourage you to apply for this exciting opportunity as a Quality Control Officer.,

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com . Job Summary Method verification/validation of compendia/pharmacopeial updations, Method verification of SDCs (Supplier Driven Changes) method. Method validation of cleaning verification, Preparation of method verification and validation protocols and reports, Evaluation of SDC, compendial/pharmacopeial updations, Preparation of In-House method and Specification. Analysis of raw material and excipients. Job Responsibilities Analysis of Compendia, raw material samples, Analytical method transfer samples as per method of analysis by adhering to the regulatory procedures. Preparation and review of Memo, Method Verification/ Method validation protocols, Method Verification/Method validation reports, Method transfer summaries. To involve in investigations and excursions as per SOP, to provide technical support during investigations of OOS/OOT results and to identify assignable cause. Compendia changes review, method verification. To perform the cleaning validation as per the protocol. Perform all work in accordance with all established regulatory and compliance and safety requirements. Responsible for preparation and updating of specification and method of analysis as per regulatory requirements and compendia requirements. To be responsible for all activities in the Quality control Laboratory, including cGLP, documentation and implementation of departmental quality system as and when required. To generate and maintain records related to laboratory samples. Works in a safe manner collaborating as a team member to achieve all outcomes. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other relevant duties as assigned. Job Requirements Education MinimumMSc/BPharm or any equivalent degree. Knowledge, Skills And Abilities Command on Microsoft-Office (Word, Excel). Able to prioritize the tasks. Best in effective planning of work activities to meet the time lines. Able to perform multi parameter analysis on HPLC instrument. Experience Minimum 2 to 4 years of experience in GMP regulated Pharmaceutical Industry. At Apotex, we are committed to fostering a welcoming andaccessible work environment, where all everyone feels valued, respected, and supported to succeed. We offer accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation. Show more Show less

This is where your work makes a difference. At Baxter, we believe every person-regardless of who they are or where they are from-deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job-you will find purpose and pride. Essential Duties and Responsibilities: This section contains a list of five to eight primary responsibilities of the work. The incumbent will perform other duties as assigned. To complete the planned work (Method validation/Submission Studies/Regulatory query) in stipulated time frame given by sub-department manager. To perform all the testing and data recording of API samples, Development Product samples, Validation Samples, Stability samples, Bulk hold samples, RLD samples, PDR samples etc. according to draft/approved Method of analysis or current Pharmacopoeia. To operate the different instruments like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter etc. as per approved standard operating procedures. To calibrate the Instruments as and when required (Daily/as per schedule) like HPLC, GC, Balance, Auto titrator, Karl Fisher Titrator, pH meter etc. as per approved standard operating procedures. To use live reference standards, working standards and Impurity Standards for analysis and maintain their records. To verify the shelf life of chemicals and reagents before performing analysis of material or product. To follow good documentation and ALCOA++ practices. To follow the good Laboratory practices in the Department. To follow the instruction and procedure as mentioned in the approved protocol. To keep track of routine requirements. Inform and ensure timely procurements of the same to respective person or Department. To Report and investigate any failure / abnormal observation / deviation / Non-Compliance to sub-department manager and seeking for the solutions. To communicate project related issues to sub-department manager and follow the action plans. To check the trend of results before reporting the results. To keep the status of daily work and report to sub-department manager on daily basis. To prepare standard operating procedures (SOPs) and standard formats for Documentation. To verify the instruments after maintenance of the Instruments. To check preventive maintenance, Breakdown Maintenance and perform risk assessment. To report preventive maintenance and Breakdown Maintenance to sub-department manager. To represent subject matter expertise in the areas of analysis internally and externally as needed. To make Analytical problem-solving efforts to meet urgent business needs. To focus on innovation, process improvement, and/or operational excellence. To execute and manage projects/programs utilize established methods, techniques, or approaches. To Implement new or improved techniques and procedures around specific tasks write and implement SOP's. To complete the training as per the quality matrix targets. To Maintain knowledge of relevant regulatory requirements related to R&D to ensure compliance in all research, data collection and reporting activities. In addition to having an in-depth knowledge and understanding of cGxP and related regulations and guidance. Equal Employment Opportunity Baxter is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic. Reasonable Accommodations Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the here and let us know the nature of your request along with your contact information. Recruitment Fraud Notice Baxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information. To learn how you can protect yourself, review our .

*Sound knowledge of GC, HPLC *Wet Lab Analysis *GDP & GMP. *Monitoring and analyzing processes to identify areas for improvement . *Maintaining accurate documentation and records of quality control activities, test results. Required Candidate profile "Male Candidates, 1 to 3 Years experience only"

Role & responsibilities Assist in routine inspection, calibration, and preventive maintenance of lab instruments and equipment. Support troubleshooting and timely repair of laboratory machinery to minimize downtime. Maintain accurate records of maintenance activities, equipment logs, and service schedules. Ensure compliance with safety, quality, and regulatory standards within the laboratory environment. Coordinate with external vendors and service providers for specialized maintenance and calibration. Monitor lab utilities (like HVAC, water systems, and power supply) critical for lab operations. Assist in maintaining inventory of spare parts and consumables related to lab equipment. Collaborate with the lab team to ensure optimal functioning of all technical instruments.

Role & responsibilities 1) Having sound knowledge about HPLC analysis, Method Validations & Developments 2) Having good knowledge in GLP & GMP, 21 CFR Part 11 compliance 3) Having "Good Documentation Practice". 4) Having knowledge about facing of Regulatory Audits, like USFDA, WHO Preferred candidate profile

1. Execute validation of analytical methods as per ICH guidelines 2. Method Verification 3. Method Transfer 4. Instrument Handling (HPLC,UV-Visible Spectrophotometer) 5. Documentation & Compliance 6. Audit Readiness & Regulatory Support Perks and benefits Bachelor's Accommodation and Travelling facility

Quality Control Dept, ensuring Timely testing & quality check of Raw Materials and Finished Products. Analysis on equipment like HPLC, FTIR, GC etc, all other Q.C. related matters Required Candidate profile Experience in handling HPLC, FTIR, GC etc, for 3 to 7 yrs, Experience in Quality Control dept. of Pharma Company. FDA Approval Required. Perks and benefits Apply with Salary Drawn & Expected Salary

The position of Assistant/Executive in the Analytical PRD department of the R&D Business Division is located in Udaipur. Reporting to the Group Leader - Analytical PRD, you will be responsible for assisting in the analytical method development of assigned projects within the given timeframe while adhering to safety and environmental regulations. Your duties will include raw materials and finished products analysis, generating Certificate of Analysis (COA), and troubleshooting any complexities during analysis proactively. You will play a crucial role in understanding the analytical scope of the assigned projects, providing inputs for analytical support planning, ensuring proper maintenance of laboratory instruments, and timely calibration of assigned instruments. Additionally, you will be responsible for analytical method development on GC, HPLC, and Wet analysis, method validation/verification/evaluations, routine analysis, and preparation of Standard Test Procedures. Characterization of compounds using various spectroscopic techniques, preparation of reference standards, and elemental characterization will also fall under your operational responsibilities. In terms of qualifications, you should hold a Master's or Doctorate degree in Analytical/Organic Chemistry from a reputable University/Institute and possess 2-6 years of industrial experience in industries related to Agrochemicals, Fine Chemicals, Pharma-API, or Specialty Chemicals. Your functional competencies should include analytical skills, practical experience with HPLC/GC, understanding of Health, Safety, and Environment (HSE) practices, data management, and analytical data interpretation. Moreover, you will be expected to actively participate in skill-upgradation opportunities, problem-solving sessions, and training programs, while effectively coordinating and communicating with interdepartmental team members. Time management and adherence to budget proposals and controls within your area of responsibility will also be essential aspects of your role. Your interaction will primarily involve daily reviews with internal stakeholders such as Group Leaders in R&D, AVP Analytical, and Head Process Technology to discuss project progress. Additionally, you may engage with clients or customers for project-related meetings as needed.,

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 Analytical Chemist at our leading Contract Research Organization (CRO), you will have the opportunity to assist in conducting analytical testing of samples using instruments such as HPLC, GC, LC-MS/MS, and UV Spectrophotometer under supervision. You will play a crucial role in preparing reagents, solutions, and standards following Standard Operating Procedures (SOPs) with precision and attention to detail. Your responsibility will include accurately recording and maintaining raw data, logs, and reports in compliance with GLP/GMP standards. By ensuring proper documentation, you will play a pivotal role in meeting regulatory and internal audit requirements. You will provide essential support in method development and validation for pharmaceuticals and biologics. Under the guidance of senior analysts, you will contribute to stability studies and impurity profiling, gaining valuable hands-on experience in the field. Learning and assisting in calibrating and maintaining analytical instruments will be part of your routine tasks. Following preventive maintenance schedules diligently and promptly reporting any malfunctions will be essential in ensuring the smooth functioning of instruments. Adhering to GLP, GMP, and regulatory guidelines while performing your assigned tasks will be crucial. Your active participation in audits and commitment to maintaining compliance with safety and quality standards will be highly valued. You will have the opportunity to enhance your proficiency in analytical techniques through active participation in training sessions. Staying informed about new methodologies, instruments, and advancements in the field will be key to your professional development. We are looking for candidates with a background in M.Sc. (Analytical Chemistry, Organic Chemistry, or related field), M.Pharm, or B.Pharm with practical academic experience. A basic understanding of analytical techniques and foundational knowledge of instruments like HPLC, LC-MS, or GC is desirable. Familiarity with GLP and GMP guidelines will be an advantage. Strong analytical and critical thinking abilities, effective communication and teamwork skills, and enthusiasm for learning and adapting to new challenges are essential soft skills we are seeking in potential candidates. Joining us will provide you with the opportunity to kickstart your career in a structured training environment, tailored to help freshers transition into a professional analytical setting. You will gain hands-on experience with advanced analytical instruments and methodologies, along with clear career progression paths and professional development programs.,

As a Senior Manager in the Research and Development department at Gujarat Fluorochemicals Limited, you will play a crucial role in leading a team to drive innovation and growth. Your main responsibilities will include conducting thorough literature surveys, identifying viable and non-infringing routes for commercializing fluoro-specialty molecules, developing and standardizing industrial processes, and meeting cost targets within specified timelines. Additionally, you will be expected to discover and develop new products, prepare various reports, and scale up lab processes to commercial levels. To excel in this role, you must have strong leadership skills to manage a team of scientists and chemists, possess in-depth knowledge of synthetic and analytical methods, and demonstrate proficiency in interpreting analytical data from various sources such as UV, IR, NMR, GC, GCMS, HPLC, LCMS, and MS. Familiarity with GLP, GMP, IMS guidelines, as well as an understanding of literature and patents, will be essential. Moreover, you should be adept at meeting customer requirements and have a good command of SAP and IMS systems. Ideally, you should hold a Master's or Ph.D. degree in Organic Chemistry and have accumulated 12-13 years of relevant experience in R&D, with a preference for candidates with a background in Fluoropolymers. Your total experience should fall within the range of 12-15 years, with specific expertise in Fluorospecialties. If you are a proactive and results-driven professional with a passion for research and development, we encourage you to apply for this challenging and rewarding opportunity at Gujarat Fluorochemicals Limited.,

You are invited to join Global Calcium Pvt. Ltd., a prominent API manufacturing company located in Bangalore, India, specializing in speciality API's, benzodiazepines, ophthalmics, oncology, chelated minerals, and organic mineral salts. We are currently seeking talented individuals to fill various roles in the QC Department. Open Positions: - QC ICP-MS Analyst (2 openings) - QC DMF Support (2 openings) - QC Analytical Validation Support (2 openings) - QC Wet Analysis (2 openings) Qualifications: - B.Sc./M.Sc. in Chemistry or related fields - 1 to 4 years of relevant pharmaceutical QC experience - Familiarity with cGMP practices and regulatory compliance Responsibilities: - Perform routine and non-routine analyses using analytical techniques and instruments - Develop and validate analytical methods and protocols - Prepare and maintain detailed documentation and reports - Ensure adherence to regulatory guidelines and GMP standards - Collaborate with other departments for cross-functional projects - Participate actively in laboratory investigations and troubleshooting activities Walk-in Interview Details: - Venue: Global Calcium Pvt. Ltd., Unit III, 19 & 19B, Sipcot Industrial Complex, Phase - 1, Dharga, Hosur - Date: 14th June 2025 - Time: 9:30 AM to 11:00 AM Please note that only candidates with relevant experience in the pharmaceutical QC domain will be considered for these positions. Benefits and Perks: - As per industry standards If you possess the required skills and experience in DMF preparation, UV, regulatory documentation, elemental impurity analysis, cGMP practices, HPLC, GC, classical wet chemistry techniques, quality control, ICP-MS, wet analysis, and method validation techniques, we encourage you to attend the walk-in interview and become a part of our dynamic team at Global Calcium Pvt. Ltd.,

Date: 1 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Job Title: Junior Analytical Development Scientist Oral Solids Job Location: Bangalore Department: Analytical Development Drug Product About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to companys integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace always. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always. Core Purpose of the Role: Analytical development supporting Formulation development Routine analysis of samples Method development Instrument calibrations Documentation Report preparation Miscellaneous lab responsibilities Role Accountabilities Candidate should have very good educational and theoretical background. Candidate should have knowledge of theoretical working principle of KF auto titrator, dissolution, spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC Knowledge of any other instruments than the above will be added advantage. Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Experience: 1 to 3 years Skills And Capabilities Technical/functional Skills: Candidate should have good proficiency for MS-office tools Should be able to search scientific literature on-line Behavioral Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Education: M.Pharm / M.Sc Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities. Show more Show less

Job Description Of Lady Security Guard Job Introduction / Roles Responsibilities As a professionally trained Security Guard for G4S, you could be a member of the security team responsible for securing premises, such as building sites, courts, shops, warehouses, banks and factories You would be conducting foot or vehicle patrols, controlling access at points of entry, securing equipment and people, responding to emergency situations, monitoring CCTV, surveillance operative and helping to identify and prevent criminal activity, Protect premises, property, and information Reporting daily to Supervisor with all daily reports as per procedures Ensuring all Policies and Procedures are adhered to at all times All Health, Safety, and Environment instructions are to be adhered to at all times Operating and monitoring security systems Control the entry and exit of individuals, materials, and vehicles Patrol on foot searching for any situations or conditions hazardous to the property or safety of a person at a site Patrol all outside parking areas as required to ensure vehicle safety and to detect an unauthorized person Write appropriate reports as required Benefits And Advantages Of Joining G4S Career growth G4S standard uniform Job training and consistent upskilling Salary on the 7th of every month 27 annual leaves Annual Bonus of max 1-month salary Gratuity (after 5 years of service) Accidental insurance up to INR 3 lakhs EPF 12% from employer and 12% from Employee ESI Health Coverage for self & family Pension applicable after 10 years continues services (Retirement age 58 years) In case of death during the services, pension applicable of nominee and 2 children till 25 years age and INR 75k ex-gratia and INR 3,62000/EDLI benefits Ideal Candidate Minimum Education qualifications is 10th Pass Minimum Height 5 feet and 7 inches (57?) for men and 5 ft for women Age between 18 to 35 for fresher and upto 40 for Experienced Security Guard Physically and Medically fit and look like mature

Job Description Operation & Calibration of the entire instrument like HPLC (W ater 2489 & Isocratic withEMPOW 3 software),( Shimadzu LC2010 CHT, with LC Solution and lab solution software) , Gas chromatographgy (Shimadzu-2010 Pro With HS, GC2014, GC-2030) with Lab Solution, UV Spectrophotometer ( Shimadzu , lab india, systonic and Elico) Dissolution test apparatus Lab India, Electrolab,