1376 Hplc Jobs - Page 3

Role Name In Community Title Senior Executive Department Sales Hiring Manager Deepak Subramanian Brief Role Description Narayana One Health is in the process of setting up a strategic team tasked with bringing health and insurance closer to patients. The initiative involves setting up primary and secondary care services that are easily accessible to patients and are supported by hyper-responsive processes built to keep patient needs and satisfaction at the center of focus. The initiative aims to bridge the gap between Narayana One Health’s in-hospital offering and patient’s everyday healthcare needs and provide patients access to a continuum of care tailored to their specific healthcare needs. Narayana One Health is looking for Senior Executives for Bangalore, India. This is an individual contributor role in an employee-oriented, high-performance environment that emphasizes spreading Nayana One Health Care Benefits in Bangalore (Karnataka). Your role will entail, Qualification of Leads (via various channels), by calling them, meeting face to face and selling Narayana Arya insurance plans to customers and briefing them about the HealthCare benefits of Arya Insurance via individual reach and through a referral channel model known as One to Many. Responsibilities: 1. Identify Engage and build relationships with Key Community Leaders of Cultural Associations, RWAs etc. 2. Manage Engagement with Community by executing agreed formats of events and sponsorships 3. Generate Interest for Arya Insurance Plans 4. Carry out Right Execution Daily (RED) and adhere to P-100 Program Guidlines 5. Ensure correct Activation and closures at Individual and at channel level. 6. Deliver Monthly targets on Inputs and Outputs Requirements and skills 1. Graduate Degree with Minimum 3-4 years' experience in sales (B2C, B2B or both)- preferred experience in Insurance or financial products and services. 2. Keen Interest in Healthcare and Health Insurance. 3. Passion for new Business Initiatives. 4. A knack for sales and positioning an idea. 5. Highly creative with experience in identifying target audience. 6. Good Communication Skills. 7. Proficient in using CRM, Analytical Tools. Location – Bangalore

Role & responsibilities Analytical test including physical and wet analysis. Expertise in handling of HPLC, GC , UV and IR Knowledge on OOS and OOT Calibration of laboratory Instruments. Preparation and standardization of Reagents/Volumetric solutions. To ensure cGLP compliance and Data Integrity Note : Candidate who can Join Immediately are preferred and willingness to work in Shift basis. Candidate should have experience in Pharmaceutical Formulation - OSD - Tablets Manufacturing facility

We're Hiring! Assistant Manager Quality Control Location: Hosur | Company: Global Calcium Unit III Experience: 712 years | Full-time | On-site Global Calcium is looking for a passionate and experienced Assistant Manager – Quality Control to join our team at Unit III in Hosur. In this role, you'll be responsible for leading day-to-day QC operations — from testing and inspecting materials to ensuring regulatory compliance, analyzing trends, and driving quality improvement initiatives. You’ll collaborate with production teams to proactively address and resolve quality issues. What We’re Looking For: Strong background in Quality Control with leadership experience Knowledge of regulatory standards and QMS (Area Qualification, Analytical Method Validation, Instrument Qualification) Hands-on experience with instruments like ICP-MS and AAS Excellent analytical, documentation, and problem-solving skills Proficiency in team communication and management Master’s degree in Chemistry, Pharmaceuticals, or related field Prior experience in the pharmaceutical or manufacturing industry is a strong plus Interested candidates can share their profiles at: dhanushkumar@globalcalciumpharma.in Join us at Global Calcium and be a part of a company committed to quality, innovation, and growth.

Exp. in ARD/AMD of minimum -15 to 20 years Lead the development and validation of analytical methods Prepare and review technical documentation Drive analytical strategy in global or cross-functional project teams

Quality officer Male Instrument Analysis GC/HPLC Min 2-5 only API CO 2 to 35year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

The role offers you the opportunity to complete product quality checks under close supervision. You will be responsible for conducting routine testing and analysis of production work, ensuring accuracy in quality checks and documenting quality control issues as needed. Your essential functions will include timely analysis of samples under test, coordinating with production for quality-related issues, sampling and analyzing RM/Intermediate/Finished Goods, ensuring compliance of ATR, assisting in ISO implementation, and possessing knowledge of calibration, standard preparation, standardization, and relevant documentation. Furthermore, you will need to have expertise in handling HPLC, GC, and wet analysis. As part of your department-specific and ongoing functions, you will be required to provide timely reports to SAP for result recording, fill and update all relevant documents, maintain zero accidents in quality operations, achieve batch-wise timelines, quantity, and quality, train and supervise operators in your department, participate in the Emergency response team, and maintain ISO 9001:2008 and ISO/IEC 17025:2005, SAP, and other Quality systems. To qualify for this position, you must hold an M. Sc. in Chemistry and have 3-4 years of experience in Quality, including cGMP, ISO, and regulatory audits, as well as laboratory safety. Preferred skills and qualifications include knowledge of Quality Control in Fine Chemicals and pharmaceutical companies and experience of cGMP. Desired skills and competencies for this role include willingness to learn, being a team player, and possessing good communication skills. Please note that the above statements are a general description of the nature of work performed in this classification and are not exhaustive. Avantor is an equal opportunity employer committed to diversity and inclusion. Join our global team of 14,000+ associates at Avantor and make a difference in people's lives through life-changing science. Dare to go further in your career, contribute your talents, learn new skills, and grow with us. Apply today and be part of a culture that supports your career growth and success. If you require a reasonable accommodation during the employment process, please contact us at recruiting@avantorsciences.com to discuss your needs. Requests for accommodation will be considered on a case-by-case basis. By submitting candidates without a formal assignment or contract from Avantor, you forfeit any fee, as per our 3rd Party Non-solicitation Policy. Avantor engages with recruitment agencies based on its needs and does not accept unsolicited solicitations.,

As a Peptides Production Executive at Piramal Pharma Solutions (PPS), your primary responsibility will be to learn and assist in the production of peptides following established protocols and quality standards. This role is designed to provide hands-on training in peptide synthesis, purification, and related processes. Your key responsibilities will include understanding and adhering to standard operating procedures (SOPs) for peptide synthesis, assisting in the preparation of reagents, solutions, and equipment, executing peptide synthesis under the guidance of experienced personnel, and learning and performing purification techniques such as HPLC, chromatography, and filtration. You will also be expected to maintain accurate records of production and testing activities, follow Good Manufacturing Practices (GMP) and safety guidelines, operate and maintain peptide production equipment, and report any equipment malfunctions promptly. Additionally, you will be required to maintain detailed records of all production activities, compile data, assist in preparing production reports, communicate effectively with team members and supervisors, contribute to process improvements, provide feedback on procedures to enhance efficiency and quality, attend training sessions to enhance knowledge and skills, and actively participate in professional development opportunities. The preferred candidate profile for this role includes a basic understanding of peptide synthesis principles, strong attention to detail, commitment to quality, ability to work in a team-oriented environment, good communication and interpersonal skills, and willingness to learn and adapt to new processes. To be considered for this position, you should have a minimum of 2 years of experience in peptides production. Piramal Group values inclusive growth and ethical practices, and as an equal employment opportunity employer, bases its decisions on merit, considering qualifications, skills, performance, and achievements. The organization strives to ensure that all applicants and employees receive equal opportunities in personnel matters, including recruitment, selection, training, placement, promotion, compensation, and benefits, among others.,

We are looking for a Chemistry Research Intern who is eager to learn best laboratory practices, assist in ongoing research activities, and contribute to experimental workflows to drive innovation at altM. The candidate will get hands-on exposure to organic synthesis, characterization techniques, and cross-functional research environments, working closely with senior scientists and engineers. Responsibilities include supporting lab-scale synthesis and formulation activities, assisting in purification and characterization of compounds using instruments such as NMR, GC-MS, HPLC, and IR, helping prepare reagents, setting up reactions, and monitoring experimental progress. The role also involves maintaining accurate lab records, inventory, and data logs, staying curious and engaged, with support provided for literature review, method development, and data interpretation over time, as well as adhering to safety protocols and best practices in lab settings. Requirements for the role include being a student or recent graduate with a Bachelors or Masters in Chemistry (preferably Organic or Applied Chemistry), with prior lab and project experience and internships being a nice-to-have. Strong theoretical and practical knowledge of organic chemistry principles and techniques, proficiency in using lab equipment and analytical instruments, excellent problem-solving skills, attention to detail, strong communication and interpersonal skills, with the ability to collaborate effectively in a team, commitment to safety, compliance, and ethical conduct in scientific research, and the ability to work from our lab in Bangalore with a willingness to travel for fieldwork or partner projects. The compensation and benefits offered include competitive cash compensation, negotiable for the right talent and qualifications.,

Experince in HPLC & GC will be preffered Quality Control Inspection Sampling, inspection and testing of material (Analysis of material) Analytical method validation Conduct test such as Tests: GC, HPLC QC Documentation Male Candidates can apply

Responsible to work as per the organizational compliance requirement. Responsible to develop the method for different quality attributes for complex injectable drug products like Liposomes, Ophthalmic Drug product. Responsible to perform method validation & verification Responsible to perform analysis of drug product by using different analytical techniques like HPLC, GC, UV, and other relevant techniques. Responsible to perform Identification, Investigation and troubleshooting task. Responsible to perform chemical analysis like, Extraction, Refluxing, Residue on ignition, Centrifuging & Evaporation etc. Responsible to prepare the study template, analytical method validation & verification reports & protocols.

Role: To execute activities related to R&D Peptide Process Development & Scale-ups, along with a group comprising of Research Officers/ Research Assistants in co-ordination with Team/Group Leader Details of Previous Work Experience (Mandatory Requirement) Literature search and ROS (Route of Synthesis) finalization Basic knowledge of Orthogonal protected amino acid and Peptide Solid phase peptide Synthesis/Oligonucleodtide Synthesis Handling of hazardous chemical like Trifluoroacetic acid Knowledge of handling of analytical HPLC/Oligo Synthesis Purification using Preparative HPLC Preparative column packing and usage. Computer literacy etc. Knowledge of Phosphoramidalin /handling/storage Job Description: Literature search with respect to assigned project and finalizing the non-infringing synthetic route Experimentation (Process development, DoE study, optimization and validation). Purification of Peptide and knowledge of lyophilisation of pure solution. Handling of analytical HPLC and preparation of buffer. Characterisation of Peptide using HRMS,2D NMR, IR, Peptide mapping and sequencing. Preparation of Technology transfer documents. Scaling-up of process developed at R&D. Assisting to RA in filing DMF. General Laboratory Management etc.

JOB DESCRIPTION Designation: Senior Analyst Special Instrumentation and Method validation Job Location: Bangalore Department: Analytical Development About Syngene 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 company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times 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 Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Role Purpose: Job Description: Performing analytical method validations and related documentation, as well as analysis of RM, PM, Intermediates, API, and Finished products. Key Responsibilities: 1) Following Good Laboratory Practices while working in the QC Laboratory. 2) To maintain and clean the responsibility allotted for individual instruments. 3) Use required safety apparel while sampling, analyzing, and working in the laboratory. 4) Carry out the analysis of validation samples as per the protocol. 5) Initiation of laboratory incidents and deviations. 6) Preparation of calculation sheets and making draft reports. 7) Disposal of the sample for analysis after use. 8) Taking any other job that the HOD or the Section Head allocates. 9) Analysis of Intermediate, finished product, and working standard qualification per specification. 10) Ensure that the instrument usage log is verified and reviewed periodically, and check the labels accordingly as per SOP. 11) Preparation of protocols and Observation data sheets. 12) Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, etc... 13) Being well-versed in the Chromeleon data management application and LIMS will be advantageous . To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc (Analytical/General Chemistry) Technical/Functional Skills: 1) Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc... 2) Being well-versed in the Chromeleon data management application and LIMS will be advantageous . Experience: 3- 6 years Behavioral Skills: Should be an adaptive learner. Should demonstrate practical Communication skills. Organization and ability to balance work and Life. Should possess good Time Management abilities. 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 regarding 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

JOB DESCRIPTION Designation: Analyst - Stability and EGMP Job Location: Bangalore About Syngene 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 company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times 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 Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Description: Performing analytical method validations and related documentation, as well as analysis of RM, PM, Intermediates, API, and Finished products. Key Responsibilities: Performing Chromatographic and Non-chromatographic analysis for Drug substances, Drug products, Intermediates, Excipients, etc ). Conduct the analysis on qualified techniques per the approved specification / protocol / procedures , interpret the data from analytical instruments, report the results, and promptly submit the completed documents for review within the established window. Recording of analytical observations/findings, reporting of data and results in observation data sheets, forms, logbooks, LIMS, and ELN application software, and support in preparing stability summary reports and review of final documents. Responsible for timely intimation/investigation of any events or deviations to the Department Head, QA function, supporting the related investigations to the clients, and timely closure. Instrument calibration as per schedule, hot water flushing of HPLC, and general preventive checks for laboratory instruments. Perform validation activities and method transfers for multiple client projects. Actively participate in client and regulatory audits. Ensure to follow cGMP and GDP. Preparing the certificate of analysis for standards and impurities and Reports for Analytical Method Validation and Analytical Method Transfer. Support in performing Qualification and Calibration of assigned Instruments and Equipment. Create/prepare documents, master data, and static data in LIMS, ELN, and LMS software as applicable. Outsourcing of sample testing is based on requirements and updating in respective logbooks. Coordination with engineering & maintenance and external vendors for preventive maintenance and calibration activity. Support in preparation of instruments URS, DQ, and IOP. Supported preparing standard operating procedures and uploading data in LIMS and other relevant activities per departmental requirements. Use of required safety PPE while sampling, analyzing, and working in the Laboratory. Individuals working in the GMP environment are responsible for documenting/recording the activities contemporaneously and accurately as per good documentation practices. Ensure safety compliance as per Syngene policy and EHSS requirements. Taking any other jobs by the Head QC/Group Leader/Designee. To ensure safety compliance as per Syngene policy and EHSS requirements. Educational Qualification: M Sc / M Pharma (Analytical/General chemistry) Technical/Functional Skills: Should be well versed with the latest analytical techniques like HPLC/GC, KF/KFC, IR/UV, LC-MS, GC-MS, IC, ICP-OES/ICP-MS, DSC, TGA, etc... Being well-versed in the Chromeleon data management application and LIMS will be advantageous . Experience: 3- 6 years Behavioral Skills: Should be an adaptive learner. Should demonstrate effective Communication skills. Organization and ability to balance work and Life. Should possess good Time Management abilities. 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 about public assistance, veteran status, or any other characteristic protected by applicable legislation or local law.

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

Role & responsibilities Production chemist and QC chemist Preferred candidate profile HPLC,GC wet lab,BPR,BATCH PLAN,REACTORS,ANALYSIS,WET LAB,INSTRUMENTATION, Perks and benefits As per company norms

• Perform sampling, testing, and analysis of raw materials, in-process materials, and finished products as per approved specifications . • Operate and maintain laboratory instruments like HPLC, UV-Vis Spectrophotometer, pH meter, etc.

Applications are invited for the Post of Junior Research Fellow ( JRF ) for the ANRF Funded Project in the Department of Physics, School of Advanced Sciences (SAS), at Vellore Institute of Technology (VIT), Vellore, T.N, India. Title of the Project : “Development of cost-efficient and scalable perovskite based colloidal nanoparticles for high performance plastic scintillators” Qualification : M.Sc./ M.Tech. in Physics/ Materials Science or related fields from recognized universities/institutes with a minimum of first class and with GATE / CSIR-UGC JRF / NET-LS qualification. Mandatory Skills : Candidates should have a strong research background in synthesis and characterization of nanomaterials. Experience with colloidal semiconductor nanomaterials and related photo physics is desirable. Stipend : Rs. 37,000 p.m. + 8% HRA for the first two years (JRF); Rs. 42,000 p.m.+ 8% HRA for the third year (SRF) will be as per Institute norms. No. of Vacancies : 01 Post (ONE) Age Limit (if any) : Not exceeding 30 years i.e. Age must be from 18 to 30 years Sponsoring Agency : ANRF, PMECRG program, New Delhi, India Duration : 36 Months Principal Investigator : Dr. Abhinav Anand, Assi stant Professor, Department of Physics School of Advanced Sciences, Vellore Institute of Technology (VIT) Vellore - 632 014, Tamil Nadu. Interested candidates with the above-mentioned qualifications can send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before ( 18/08/2025) through the website: http://careers.vit.ac.in No TA and DA will be paid for appearing the interview. Shortlisted candidates will be called for an interview at a later date which will be intimated by email. The selected candidate will be expected to join at the earliest.

Role & responsibilities Preferred candidate profile

Job Title: Quality Control Chemist Job Location - Bathinda/ Rajpura, Punjab Job Purpose and Impact The Chemist - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines. Key Accountabilities Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module. Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up. Perform method validation and verification to roll out new testing method in the lab. Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system. Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports. Maintain systems and techniques for reporting data across functional areas. Organize and participate ring tests with the goal to check and control methods and equipment. Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff. Other duties as assigned Qualifications Minimum Qualifications Bachelor's degree in a related field or equivalent experience Preferred Qualifications "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively" Necessary English reading capacity Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc. Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing Minimum of Three years of working experience in the Food industry Lab

We are conducting Walk-in Interview at Indore for our OSD manufacturing Facility based out of our Ahmedabad (SEZ-II), please find the below details. Date : 27th May 2025 (Sunday) Interview Location: Ahmedabad Timings: 9:00 am 5:00 pm Interview Venue: PTC-Sigma Block No. 2, 3, 4, 5, Sigma Commerce Zone,Nr Iskon Mandir BRTS Bus Stand, Ambli Bopal Road, Ahmedabad – 380015 ? Job Location: Ahmedabad Education Qualification: ITI/Diploma/BSC/ /B.Pharma Departments are as follows : Production- OSD : Plant Operator/ Technical Assistant : ITI / Diploma having 3 - 8 years of experience in operating machines like Granulation (ACG, Glatt, Tapasya, GEA), Fitzpatrick Roll Compactor, Compression machines (Fette), Wurster Coater (ACG, Glatt, Anish), imprinting, Visual Inspection. Perform line clearance, operation and cleaning of equipment / instrument / auxiliary items Executive/ Sr Executive: B. Pharma with 3 - 8 years of experience in Tablet/ Capsule department with experience in Granulation, Compression, Coating, Inspection . Responsible to plan for the manufacturing of batches in coordination with PPMC. To monitor line clearance, cleaning of equipment, instrument, auxiliary items. To carry out qualification activities. To initiate QMS activities (Change control, deviation, CAPA, investigation) and E-BMR. To handle manpower and allocate daily activities.. Engineering: Technician : Diploma / ITI with 3- 8 years of experience in plant maintenance & Process Equipment (Electrical/ Instrumentation) and Instrumentation . Candidates should have experience in Plant maintenance, preventive maintenance and breakdown maintenance of OSD plant equipment. Troubleshooting of mechanical and electrical equipment . Instrument and calibration of OSD plant equipment. They should have knowledge and experience in instruments sensors, PLC, HML, SCADA, and experience in calibration activities. Quality Assurance (Qualification) Assistant Manager / Deputy Manager / Associate Manager: B.Pharm with 10-20 years QA & MFG – Qualification. Candidates should have experience in Qualification, Validation. They would have to prepare, execute and review of equipment/ instrument/ system /utility /area qualification program. Review of data backup activity, data restoration and its compliance. QMS documentation exposure is required. completion of CAPAs and to perform change control/CAPA effectiveness. Associate Manager: CSV B.Pharm with 15-20 years with experience in Issuance and retrieval of documents. Candidate should have experience in Review of various Qualification and CSV Documents. Review of system audit trail, system security user privileges and ensure the compliance. Review of data backup activity, data restoration and its compliance. To ensure timely completion of CAPAs and to perform change control/CAPA effectiveness. For all the positions, candidate should have exposure in pharmaceutical company and exposure to regulatory requirements of documentation and cGMP will be added advantage. Interested candidates Please Walk-in for an interview along-with their Aadhar Card, Passport size Photograph, updated CVs, Salary Structure, Salary Slip and relevant documents(original as well as Photocopies) as per the schedule.

Location: Ankleshwar Department: Quality Control Experience: 4 to 7 years Position : Executive Job Description: We are looking for a skilled HPLC Analyst (Executive QC) who will be responsible for ensuring quality compliance in laboratory testing of pharmaceutical raw materials, intermediates, finished goods, and stability samples. Key Responsibilities: Adhere to GLP (Good Laboratory Practices) and laboratory safety protocols . Perform routine and stability analysis of raw materials, intermediates, finished products, in-process samples , returned goods, hold time studies using HPLC . Maintain online documentation and ensure CFR 21 Part 11 compliance. Record and maintain analytical results in worksheets and LIMS modules. Conduct analysis as per current STP, SOPs, and specifications . Prepare and standardize reagents, solutions, and mobile phases as per requirement. Ensure column performance is tracked and updated in column logbooks . Maintain instrument logbooks , calibration schedules, and instrument history records . Participate in analytical method transfer (AMT) with A.R. laboratory teams. Prepare stability protocols and reports , and perform stability sample analysis . Monitor temperature & humidity of laboratory, refrigerators, and working standard chambers. Report and initiate investigations for OOS, OOT, Deviation, QI, NQI, and discrepancies in analysis. Follow Good Chromatographic Practices for integration and review of chromatographic data. Ensure data integrity and compliance during all analytical activities. Communicate and coordinate with stores for urgent material analysis. Avoid solvent/chemical wastage and ensure clean laboratory operations. Interested candidate please fill the below given link: https://docs.google.com/forms/d/e/1FAIpQLScDxs_rRkTFo3l4kQNsy9oij5XXDEi4ztPPsIbwxHvGaLaKbA/viewform?usp=header

You will be part of the Formulation Development team, contributing your expertise in Biologic Formulations and pharmaceutical sciences. Your responsibilities will include conducting literature reviews, formulating biological products, designing and executing experiments, analyzing data using various techniques, calibrating instruments, performing proof-of-concept studies, conducting stability studies, writing scientific reports, and collaborating with cross-functional teams. To excel in this role, you should hold a minimum of a Postgraduate degree (MTech, MPharm) in Pharmaceutical Sciences, Chemistry, or a related field. Proficiency in analytical techniques like HPLC, GC, pH, Osmolality, KF, and UV spectroscopy is essential. Effective communication, strong analytical and research skills, teamwork abilities, and knowledge of pharmaceutical excipients and raw materials will be key to your success in this position.,

As an ADL Officer/Executive at our Analytical Development Laboratory (ADL) located in Changodar, Ahmedabad, Gujarat, India, you will be an integral part of our team dedicated to developing, validating, and executing analytical methods to ensure the quality and compliance of our pharmaceutical products. Your key responsibilities will include developing, optimizing, and validating analytical methods for raw materials, intermediates, and finished products using techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy while adhering to ICH guidelines. You will also be responsible for conducting routine quality control tests on pharmaceutical products, analyzing raw materials, in-process samples, and finished products for various physical and chemical parameters. In addition, you will play a crucial role in maintaining accurate and detailed laboratory records, preparing and reviewing standard operating procedures (SOPs) and analytical method documents, and ensuring regulatory compliance with GMP and GLP regulations. You will also be involved in the calibration, maintenance, and troubleshooting of laboratory equipment and collaborate closely with formulation, R&D, and production teams to support product development and troubleshooting. To be successful in this role, you should possess a Bachelor's or Master's degree in Science (Chemistry, Biochemistry) or Pharmacy, proficiency in analytical techniques such as HPLC, GC, FTIR, and UV-Vis spectroscopy, familiarity with regulatory guidelines (e.g., ICH, FDA, EMEA), strong attention to detail, excellent organizational skills, effective communication, and teamwork abilities. Both freshers and experienced candidates are encouraged to apply. Joining our team will offer you the opportunity to be part of a dynamic environment committed to excellence in the pharmaceutical industry. We provide opportunities for professional growth, continuous learning, and the chance to make a meaningful impact on healthcare. This is a full-time, permanent position with benefits including commuter assistance, life insurance, and provident fund. The work location is in person. If you have 2 years of experience in pharmaceuticals and 1 year of experience in analytical chemistry, we welcome your application to join our team and contribute to our mission of ensuring quality and compliance in pharmaceutical product development.,

You will be responsible for liaising between various departments such as Planning, Production, Technical Services, Marketing, and Exports. Your roles and responsibilities will include the preparation, review, and implementation of SOPs and STPs. You will be checking all QC related records like analytical reports and logbooks. Additionally, you will be involved in planning and distributing samples for the analysis of Raw Materials, Intermediates, and finished products. You will design and conduct Stability studies as per ICH Guidelines and develop and validate analytical testing methodology used to control raw materials, production intermediates, and final products. Your tasks will also include the preparation and maintenance of working standards with documents, as well as the operation and calibration of laboratory instruments like HPLC, GC, and Spectrophotometer. You will review and approve Raw material, finished product, and Packaging material specifications. Furthermore, you will be responsible for handling customer audits and regulatory authority audits and preparing compliance reports. Troubleshooting of HPLC, GC, and other instruments will be part of your responsibilities. You will manage the laboratory and work towards analytical laboratory improvement, cGMP and GLP compliance, and problem resolution. As the QA/QC Manager, you will be solely responsible for exports and quality-related issues for the unit. You will supervise QC chemists to ensure the smooth working of the department and to guarantee the best quality of products from the production. This is a Full Time position located in Byrathi, Bangalore.,

Perform Calibration and Instrumental analysis of Raw Material, In process samples and finished product. Hands on experience on HPLC, GC, FTIR, Polarity meter & UV spectrophotometer. Good knowledge of software specially Empower. Able to do trouble shooting on instrumentation & able to resolve problem on line. Sound Knowledge of investigation and handling OOS/OOT/Deviation & Lab incident. Perform qualification of working standard and its management.