2096 Hplc Jobs - Page 16

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Position : Research Analyst or Sr Research Analyst Experience : 3 - 8 Yrs Job Description: Responsible for Analytical Method Development activities solid orals and injectables Responsible for Responsible for Planning and Monitoring of Method development activities and Regular Analysis for solid orals and Injectables. Responsible for Routine and Stability analysis activities for solid orals and injectables. Responsible for the Review of documents generated in Method development activity. Responsible for the Preparation and Review of Tentative method of analysis and Method development Reports. Responsible for the review of Routine samples documents, Preformulations documents for the Solid oral products and Parental products. Responsible for the Review of Calibrations documents (i.e Dissolution, HPLC, UV and balance). Knowledge on ICH guidelines and all Regulatory guidelines Ref to Friends or colleagues Please share resume: careers@biophore.com at below mentioned address (Interview Date 29-08-2025-30-08-2025) Biophore India Pharmaceuticals Pvt Ltd. Plot# 231, IDA Phase -II, Pashamylaram, Biophore Road, Patancheru (M), Hyderabad. Sangareddy District Telangana 502307

Design and perform efficacy and safety studies of herbal and plant-based formulations using standard pharmacological models. Conduct bioassays, toxicity tests, and mechanism of action studies using in vitro and/or in vivo techniques. Analyze and interpret pharmacodynamic and pharmacokinetic data. Prepare technical reports, research papers, and regulatory documentation as needed. Assist in developing protocols for standardization and quality control of herbal products. Preferably 1- 2 years of experience in pharmacological evaluation of herbal formulations, plant-based extracts, or natural products. Familiarity with in vitro/in vivo testing methods and pharmacological screening protocols for herbal compounds. Candidates with knowledge of Ayurvedic formulations, traditional medicine, or toxicological studies will be given preference. Proficiency in pharmacological testing equipment and techniques (e.g., ELISA, HPLC, GC-MS, cell culture, animal studies). Sound understanding of herbal pharmacology, phytochemistry, and drug development pipelines. Strong analytical and critical thinking skills. Good scientific writing and documentation skills.

Job description Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration schedule Required Candidate profile Preparation and review of Specifications, Method of analysis procedures and Analytical development reports

Job description Perform the testing of Raw Material/Finished goods/In process materials & report the results. Handle the analytical instruments like HPLC, UPLC, GC, ICP, DSC, XRD, PSA Calibration of the Analytical instruments as per the master calibration schedule Required Candidate profile Preparation and review of Specifications, Method of analysis procedures and Analytical development reports

Job Description: Plan, setup, monitor, and work up chemical reactions independently Monitor progress of reactions using standard analytical techniques (TLC, GC, HPLC, LCMS, etc.) Isolate products and optimize reaction conditions for improved yields and output Required Candidate Profile: Industry experience in leading Pharma, CRO (Contract Research Organization), Agrochemicals

Job Description: Plan, setup, monitor, and work up chemical reactions independently Monitor progress of reactions using standard analytical techniques (TLC, GC, HPLC, LCMS, etc.) Isolate products and optimize reaction conditions for improved yields and output Required Candidate Profile: Industry experience in leading Pharma, CRO (Contract Research Organization), Agrochemicals

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC Qualification & Experience: (02 - 06Years) B.Sc, B.Pharma & M.Sc with relevant experience Designations: Jr. Officer, Officer & Jr.Executive PRODUCTION: Compression, Granulation, Auto Coating. Qualification & Experience: (01 - 07Years) ITI, Diploma & B.Sc with relevant experience Designations: Jr. Operator, Operators & Sr. Operator INTERVIEW VENUE: Hotel: HOTEL LE MARIET 9th Km Milestone, Kishanpura. Baddi Nalagarh Highway (NH-105), Dist. Solan Himachal Pradesh. (India)- 174101 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates oInstrument experience in HPLC /GC is mandate. Work experience in formulation only oPreferred for Male Candidates CONTACT INFO: E-mail: Harishwar.M@hetero.com & Cont: 8121005416 for further info.

Job description Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation Troubleshoot as appropriate for successful execution with intimation to supervisor Scale up of R&D developed products to kg scale and then technology transfer to pilot plan Required Candidate profile Preparation and review of Specifications, Method of analysis procedures and Analytical development reports

Job description Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation Troubleshoot as appropriate for successful execution with intimation to supervisor Scale up of R&D developed products to kg scale and then technology transfer to pilot plan Required Candidate profile Preparation and review of Specifications, Method of analysis procedures and Analytical development reports

Job description Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation Troubleshoot as appropriate for successful execution with intimation to supervisor Scale up of R&D developed products to kg scale and then technology transfer to pilot plan Required Candidate profile Preparation and review of Specifications, Method of analysis procedures and Analytical development reports

You will be responsible for performing chemical and instrumentation analysis for various materials such as in-process, raw materials, intermediates, and finished products according to the monthly schedule provided by PPL. This includes utilizing instruments like ICP-MS and LC-MS to ensure analysis is completed within the dispatch timeline. Additionally, you will be involved in developing, validating, transferring, and verifying analytical methods using ICP-MS and LC-MS/MS. Your role will also entail preparing and reviewing protocols, worksheets, and reports related to method developments, validations, verifications, and transfers. Allocating work to chemists, performing instrument calibrations, maintaining documentation online, and ensuring sufficient stock of standards, chemicals, and reagents for analysis are also part of your responsibilities. Furthermore, you will be required to monitor and analyze data in real-time, review analytical data from external labs, maintain calibration certificates and records, investigate deviations, implement corrective actions, review SOPs, conduct training on GLP/GMP, release batches, control costs, and ensure instruments are well-maintained. Collaboration with QA, production, warehouse, and other departments for smooth dispatches, training contract personnel, adhering to safety practices, and upholding clean working conditions are crucial aspects of your role. Your qualifications should include a Bachelor's degree, and proficiency in LCMS/MS and HPLC is essential. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that offers comprehensive services across the drug life cycle. As part of Piramal Group, we are committed to inclusive growth and ethical practices, providing equal employment opportunities based on merit. Join our team at Piramal Enterprises Limited in Digwal, Medak, Telangana, IN, and contribute to our mission of delivering high-quality pharmaceutical solutions globally.,

The Quality Control Specialist in our pharmaceutical company located in Thanjavur plays a crucial role in ensuring that all products adhere to quality standards and regulatory requirements before being released to the market. You will be responsible for conducting a variety of testing and analysis procedures on raw materials, in-process materials, and finished products. Your collaboration with the production team to identify and resolve quality issues will contribute to the continuous improvement of our quality systems and processes. Your key responsibilities will include performing routine and non-routine testing using various analytical techniques like HPLC, GC, and UV/VIS spectroscopy. Additionally, you will conduct microbiological testing, stability testing, and environmental monitoring as necessary. Recording and analyzing test results to ensure compliance with specified standards and regulatory requirements, maintaining detailed records, preparing Certificates of Analysis (COAs), and identifying deviations from standard specifications are essential aspects of this role. You will work closely with the production, research and development, and quality assurance teams to implement corrective and preventive actions, review production batch records, and participate in the development and validation of new analytical methods. Your involvement in internal audits and inspections to ensure compliance with quality systems and regulatory standards, along with recommending continuous improvements to enhance product quality and efficiency, will be paramount. To qualify for this position, you should hold a Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or a related field, with an advanced degree being preferred. A minimum of 2-5 years of experience in quality control within the pharmaceutical industry is required. Proficiency in analytical techniques like HPLC, GC, FTIR, and spectrophotometry, familiarity with GMP, GDP, and regulatory requirements, and strong attention to detail are crucial technical skills. Moreover, possessing excellent problem-solving skills, the ability to work collaboratively in a team environment, and relevant certifications such as Certified Quality Auditor or Six Sigma will be advantageous. Staying current with industry trends, regulatory updates, and advancements in analytical techniques will also be expected in this role.,

As a Senior Manager in Research and Development at a reputed Chemical Manufacturing Company located in Vadodara, Gujarat, your primary responsibilities will include conducting Organic Synthesis with a strong background in analytical tools. You will be tasked with Route Scouting, focusing on cost reduction strategies, and effectively leading and managing teams of chemists. Your role will require hands-on experience in a Good Laboratory Practice (GLP) environment, along with the ability to work with analytical instruments such as NMR, GCMS, and IR for accurate data interpretation. Proficiency in the basics of Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC) is essential for this position. This position demands a candidate with a minimum qualification of M. Sc in Organic Chemistry, preferably holding a Ph.D., and possessing a substantial experience of 10-15 years in the field. The salary range for this role is between 16.00 to 20.00 Lacs per annum. If you meet the specified qualifications and have the requisite experience, we encourage you to apply for this full-time, permanent position by visiting our website at https://www.crownhrservices.com/job-opening. For further inquiries, you can contact us via mobile at 8511522332. As part of the benefits package, you will be entitled to Provident Fund contributions. The work schedule will be during day shifts, and the work location is in person at our facility in Vadodara, Gujarat.,

You will be joining Kenvue as an Associate Scientist, Analytical Chemistry based in Mumbai. At Kenvue, we are passionate about everyday care and science, with a global team of diverse individuals dedicated to delivering the best products to our customers. As a Kenvuer, you will have the opportunity to impact the lives of millions of people every day. We prioritize people, care, trust, and courage, offering brilliant opportunities for you to shape our future and yours. In this role, you will be responsible for various analytical deliverables in new product development projects, supporting changes to commercial products, and specific research-based activities as part of Global operations. Your key role will involve conducting analytical testing, documentation activities, and ensuring compliance under the supervision of the team leader. Your responsibilities will include qualification on assigned analytical technologies, conducting testing using instruments like HPLC/UPLC, GC, IC, AAS, executing stability testing, method validation activities, and participating in method transfer processes. You will also be responsible for calibration activities, technical documentation, following lab processes and quality systems, and collaborating with cross-functional teams for assigned deliverables. To succeed in this role, you should have a minimum of MSc, B Pharm, M. Pharm, Ph.D., or equivalent in a science stream, along with 1 to 3 years of work experience in Analytical development, Quality Control, or related functions in the healthcare/pharma/FMCG sector. Proficiency in MS Office and a good understanding of GMP, 21 CFR Compliance, and Quality environment are preferred. As part of our team, you will have access to a competitive benefits package, paid company holidays, vacation time, learning and development opportunities, employee resource groups, and more. Join us at Kenvue and be a part of our mission to provide exceptional care through science.,

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Phenomenex, one of 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the which makes everything possible. The is responsible for This position reports to the and is part of the l ocated in and working remotely to cover In this role, you will have the opportunity to: In depth knowledge of Chromatography market, industry trends, challenges, and needs with respect to application support and method development. Deep understanding of Chromatography Market in India. Should be able to show path to sales team to develop new market segments, Flexible in approach to work on more chromatography products based on market growth trends and business growth. Work with Application Lab, Sales and Marketing to provide input for relevant content for brochures, websites, technical training, participating in events, customer visits and relation building with top leaders of the industry and performing webinars and seminars. Assist in developing and implementing GTM strategies and action plans that will generate sales growth in the relevant Industry segment, increasing market share and brand awareness Responsible for exploring new markets with adding more incremental business opportunities, delivering regular data reports and updates including key performance indicators such as sales performance, key actions and general results of activities, perform other job-related duties as requested The essential requirements of the job include: Master's degree in chemistry, Biology or other related Science required. PhD is preferred (relevant HPLC, UHPLC, SFC, Flash, LC-MS/MS experience in Pharmaceutical Industry.) 8-10 years working knowledge of consumables sales into target industry growth market with/or similar experiences from Analytical Lab background Prior experience working in the Chromatography field is a must, Hands on experience in market vertical and/or technique focus preferred Strong support at lab on challenges of applications and product suggestions, assist in method development and trouble shootings of the same Highly developed interpersonal and relationship-building experience, excellent presentation skills (seminars, webinars) to target key opinion leaders in the Chromatography market Ability to analyze, facilitate a dialogue across a group or team, communicate difficult concepts and negotiate with others to adopt a new or different point of view Extensive travel maybe required willing to travel up to 60% domestically. Travel, Motor Vehicle Record & Physical/Environment Requirements: Phenomenex, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at . At Phenomenex we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Phenomenex can provide. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit .

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Phenomenex, one of 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the which makes everything possible. The Account Manager is responsible for maintaining and managing allocated territory by meeting and exceeding sales goals. Engaging with customers, providing them with sales and technical support, Build professional relations with key people at customer accounts. Work in cohesion with other functions of company to drive growth strategies and profit margins. This position reports to the and is part of the Sales team located in and will be working remotely to cover the assigned territory. In this role, you will have the opportunity to: Ensure that assigned account territory meets sales and unit goals. Develop relationships with new and existing customers. Provide updates to Sales Manager regarding achievement of goals, trends and competition Implement account action plans, review performance and improve current account sales & support programs for the territory Manage and maintain information in customer database system (MSCRM) The essential requirements of the job include Bachelor's or Master's degree, in any Life Science stream required. At least 8 years of experience in Sales. Advanced knowledge of sales principles and methods of negotiation, and demonstrated advanced capability to identify business opportunities Good knowledge of Chromatography. Pharma & Non-Pharma Market & workflow understanding A proven track record of success in Sales/Customer Service type roles preferred Travel, Motor Vehicle Record & Physical/Environment Requirements: Willingness to travel as per customer engagement needs. It would be a plus if you also possess previous experience in: Laboratory with Hands on experience in chromatography using HPLC Phenomenex, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at . At Phenomenex we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Phenomenex can provide. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit .

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Phenomenex, one of 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the which makes everything possible. The is responsible for T his position reports to the and is part of the l ocated in a nd working remotely to cover In this role, you will have the opportunity to: In depth knowledge of Chromatography market, industry trends, challenges, and needs with respect to application support and method development. Deep understanding of Chromatography Market in India. Should be able to show path to sales team to develop new market segments, Flexible in approach to work on more chromatography products based on market growth trends and business growth. Work with Application Lab, Sales and Marketing to provide input for relevant content for brochures, websites, technical training, participating in events, customer visits and relation building with top leaders of the industry and performing webinars and seminars. Assist in developing and implementing GTM strategies and action plans that will generate sales growth in the relevant Industry segment, increasing market share and brand awareness Responsible for exploring new markets with adding more incremental business opportunities, delivering regular data reports and updates including key performance indicators such as sales performance, key actions and general results of activities, perform other job-related duties as requested The essential requirements of the job include: Master's degree in chemistry, Biology or other related Science required. PhD is preferred (relevant HPLC, UHPLC, SFC, Flash, LC-MS/MS experience in Pharmaceutical Industry.) 8-10 years working knowledge of consumables sales into target industry growth market with/or similar experiences from Analytical Lab background Prior experience working in the Chromatography field is a must, Hands on experience in market vertical and/or technique focus preferred Strong support at lab on challenges of applications and product suggestions, assist in method development and trouble shootings of the same Highly developed interpersonal and relationship-building experience, excellent presentation skills (seminars, webinars) to target key opinion leaders in the Chromatography market Ability to analyze, facilitate a dialogue across a group or team, communicate difficult concepts and negotiate with others to adopt a new or different point of view Extensive travel maybe required willing to travel up to 60% domestically. Travel, Motor Vehicle Record & Physical/Environment Requirements: It would be a plus if you also possess previous experience in: Phenomenex, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at . At Phenomenex we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. Additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Phenomenex can provide. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit .

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Phenomenex, one of 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact. You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life. Phenomenex isn't your typical scientific company. Founded nearly 40 years ago, Phenomenex is a global technology leader committed to developing novel analytical chemistry solutions that solve the separation and purification challenges of researchers, advancing the future of scientific analysis and investigation, ensuring the quality of essentials like your food, water, shampoo, and even cold medication. Be part of our global success and together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. Learn about the which makes everything possible. Do you want to work in Sales Do you like to use your scientific background to help customers in solving their analytical challenges We are currently seeking an Account Manager - Mumbai Territory , who will be responsible to maintain and manage the allocated territory by meeting and exceeding sales and unit goals. Provide sales and technical support to customers on a regular and ongoing basis. Location/Region: Mumbai - India / Region-2 Reports to: District Sales Manager What we'll get you doing: Willingness for travelling in allocated territory up to 100% (outside) Originate phone calls, respond to incoming calls, and provide technical information with regards to chromatography related products and services. Ensure that assigned account territory meets sales and unit goals. Develop relationships with new and existing customers. Develop business plans, and sales strategies for Pharma & Non-Pharma accounts. Provide updates to Sales Manager regarding achievement of goals, trends and competition Implement account action plans, review performance and improve current account sales & support programs for the territory Consistently maintain a positive attitude, be a team player and strive to learn and contribute to company culture. Manage and maintain information in customer database system (MSCRM) Perform other job-related duties as requested by customers and management. Building referral and lead generation networks, addressing client concerns and handling calls that require manager involvement. The essential requirements of the role include: Bachelor's Degree or Master's degree, in any Life Science required. At least three (3) years of experience in Sales Advanced knowledge of sales principles and methods of negotiation, and demonstrated advanced capability to identify business opportunities Good knowledge of Chromatography. Pharma & Non-Pharma Market knowledge & workflow understanding A proven track record of success in Sales/Customer Service type roles preferred Very good interpersonal skills as well as listening and communication skills. Motivation and desire to be successful with a can do approach, maintaining a positive attitude, being a Team player, striving to learn and to contribute to company culture It would be a plus if you also possess previous experience in: Ability to work in cross-functional teams and matrices . Laboratory with Hands on experience in chromatography using HPLC Consistently maintain a positive attitude, be a team player and strive to learn and contribute to company culture Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit .

Role & responsibilities 1. Microbiological Analysis - Conduct microbial limit test, sterility test, endotoxin testing, and bioburden analysis on raw materials, in-process, and finished products. - Perform water testing for purified water and potable water systems as per pharmacopeial standards. - Conduct environmental monitoring of cleanrooms and controlled areas, including settle plates, active air sampling, and surface monitoring. 2. Documentation & Compliance - Prepare and review analytical reports, logbooks, and records in line with GDP (Good Documentation Practices). - Ensure compliance with GMP, WHO, USFDA, MHRA, and other regulatory guidelines. - Handle SOP preparation, revision, and adherence for microbiology operations. 3. Equipment Handling & Calibration - Operate and maintain autoclaves, LAF, incubators, BOD chambers, particle counters, and microbiological instruments. - Ensure timely calibration and qualification of instruments. 4. Quality & Investigation - Support OOS (Out of Specification), OOT (Out of Trend), and deviation investigations related to microbiological testing. - Assist in CAPA implementation for microbiology-related observations. 5. Training & Safety - Provide training to junior team members on microbiology practices and SOPs. - Follow and enforce safety guidelines for handling microbial cultures and hazardous materials. Key Skills & Competencies: - Strong knowledge of pharmacopeial methods (IP, BP, USP, EP) and cGMP guidelines. - Hands-on experience with microbial testing techniques and environmental monitoring. - Good understanding of sterile and non-sterile product testing requirements. - Analytical mindset, attention to detail, and good documentation skills. - Ability to work in team environment and handle regulatory audits confidently.

Responsibilities: * Manage routine QC activities, handling of HPLC, GC, and other instruments. * Ensure compliance with regulatory requirements through quality control procedures. Conduct method validations and prepare report and protocol. Annual bonus Provident fund

The Opportunity: . Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. B. Sc. / M. Sc. (Chemistry) 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Knowledge of Quality Control in Fine Chemicals and pharmaceutical company. Experience of cGMP Willingness to learn Team Player Good communication skills How you will thrive and create an impact :- Give timely reports to SAP for result recording. Fill and update all documents. Zero accidents in the Quality operations. Achieving batch wise timelines, quantity and quality. Will train & supervise the working of all operators working in his dept. Will monitor the waste generated during operation. Will be member of the Emergency response team and will guide & train other team members in case of Emergency. Maintain ISO 9001:2015, SAP, and other Quality system into department. Will maintain the analytical records / log sheets as per GMP & ISO guidelines. Disclaimer: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer. Why Avantor Dare to go further in your career. Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science. The work we do changes people's lives for the better. It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor. We are committed to helping you on this journey through our diverse, equitable and inclusive culture which includes learning experiences to support your career growth and success. At Avantor, dare to go further and see how the impact of your contributions set science in motion to create a better world. Apply today! EEO Statement: We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religious creed, national origin, physical or mental disability, protected Veteran status, or any other characteristic protected by federal, state/province, or local law. If you need a reasonable accommodation for any part of the employment process, please contact us by email at and let us know the nature of your request and your contact information. Requests for accommodation will be considered on a case-by-case basis. Please note that only inquiries concerning a request for reasonable accommodation will be responded to from this email address. 3rd party non-solicitation policy: By submitting candidates without having been formally assigned on and contracted for a specific job requisition by Avantor, or by failing to comply with the Avantor recruitment process, you forfeit any fee on the submitted candidates, regardless of your usual terms and conditions. Avantor works with a preferred supplier list and will take the initiative to engage with recruitment agencies based on its needs and will not be accepting any form of solicitation

1. Handle collections for the assigned area and achieve collection targets on various parameters like resolution, flows, credit cost and roll rates (depending on the bucket) 2. Ensure that the NPA's are kept within assigned budget and active efforts are made to minimize it. 3. Increase the fee income / revenue and develop initiatives to control and reduce the amount of vendor payouts 4. Conduct asset verifications and possession as per SARFESI / Section 9 process through court receivers. 5. Track & control the delinquency of the area (Bucket & DPD wise) and focus on nonstarters 6. Ensure customer satisfaction by ensuring quick resolution of customer issues within specified TAT 7. Build relationships with key clients to ensure timely collections are made and monitor defaulting customers by ensuring regular follow with critical/complex customers to identify reasons for defaulting 8. Represent the organization in front of legal/ statutory bodies as required by the legal team and ensure that the collection team adheres to the legal guidelines provided by the law in force 9. Allocate work to the field executives and ensure that all the agencies in the location perform as per defined SLA, ensuring payments and audit receipts get deposited within the defined SLA. 10. Ensure that there is adequate Feet on Street availability area-wise /bucket-wise/ segment-wise and obtain daily updates from all collection executives on delinquent portfolio & initiate detailed account level review of high-ticket accounts 11. Ensure compliance to all Audit / Regulatory bodies as well as policies and procedures of the company Educational Qualification: Post Graduate/ Graduate in any discipline

Oppurtunity for Quality Control Officer at Pharmaceuticals Manufacturing Company in Vapi, Gujarat. Minimum 3 years of experience required Qualification - B.Sc / M.Sc degree preffered Attractive Salary Interested candidates can share their updated CV at [HIDDEN TEXT] OR Call/ Whatsapp on +918882212450.

You will be responsible for analyzing Vendor Approval samples and preparing Standardization of Solutions as needed. You will also need to implement GLP/GMP requirements and analyze Raw Materials, Finished Products, Stability samples, and Packing materials. Ensuring samples and related documentation meet cGMP requirements is crucial. Additionally, you will need to oversee the analysis of Raw Materials, Finished Products, and Stability Samples from outside commercial labs. Reviewing laboratory chemicals, calibrating instruments such as HPLC, UV, IR, Dissolution, KF Potentiometer, and performing Working standard qualification are part of your duties. Maintenance of Stability Incubators, loading and removing samples from Incubators, and documenting these actions will also be required. Lastly, you will review Analytical data, calibration data, qualification data, etc. Requirements: - Minimum 1-3 years of experience in the Quality Control Department - Willingness to work in shifts - Ability to relocate to the Plant location Qualifications: - B.Sc/M.Sc/B.Pharm,

You will be responsible for providing routine analytical support to the synthetic team for reaction monitoring by HPLC/GC and analysis of intermediates and API. In this role, you will perform wet analysis including LOD, IR, Residue on Ignition, KF determination, and Titrations. Additionally, you will be involved in the calibration of instruments such as UV, IR, HPLC, GC, Autotitrator, polarimeter, etc. Ensuring compliance with 21 CFR requirements, you will also be responsible for LNB writing and all related documentation. Furthermore, you will prepare the necessary documents for PDR. To excel in this role, you should possess good communication skills and be an effective team player capable of working on multiple projects. A robust knowledge of the principles and working of application techniques such as HPLC, GC, Autotitrator, UV spectrophotometer, and other laboratory instruments is essential for success in this position. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that provides end-to-end development and manufacturing solutions across the drug life cycle. With a globally integrated network of facilities in North America, Europe, and Asia, PPS offers services including drug discovery solutions, process & pharmaceutical development, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products are also provided. Additionally, PPS offers development and manufacturing services for biologics, including vaccines, gene therapies, and monoclonal antibodies, facilitated by Piramal Pharma Limited's investment in Yapan Bio Private Limited. The company's reputation as a trusted service provider with extensive experience across various technologies makes it a preferred partner for innovators and generic companies worldwide. Piramal Group is committed to inclusive growth and ethical practices, offering equal employment opportunities based on merit and without discrimination. Employment decisions are made considering qualifications, skills, performance, and achievements to ensure that all applicants and employees receive fair treatment in personnel matters, including recruitment, selection, training, promotion, compensation, and working conditions. Reasonable accommodation is provided for qualified individuals with disabilities and those with needs related to religious observance or practice.,