565 Chromatography Jobs - Page 3

Core Purpose of the Role: Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently designing the synthetic scheme for any target and solve chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene. Role Accountabilities: Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy. The candidate should be well versed in using literature search engines and predictive synthesis tools Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipments Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. The candidate should be capable of meeting Syngene s productivity expectations (# of compounds/month, # of steps/month and productivity index of around 1. 5) without compromising on safety and quality. The candidate should be capable of synthesizing the final compounds at a faster turnaround time The candidate should have excellent analytical interpretation and purification skills Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality

Designation: Assistant Manager Job Location: Bangalore Job Grade: 8-II The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1. 9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Result Areas Role-specific: Maintain good aseptic behavior inside BMP4 facility. Perform all the Downstream activities like Assembly preparation, accessories arrangement for step, Dispensing of raw materials and consumables, Reconciliation of excess and unused raw materials and consumables Buffer Preparation, Harvest Clarification, Chromatography operation, Low pH and Intermediate depth filtration, Viral filtration, TFF Operation and 0. 2 filtration. Operating and cleaning of downstream equipment(s) as per standard operating procedures and EOP. Monitoring and process control of the specific Operations of the Downstream. Maintenance of Quality records. Perform In-process product sampling, sample submission and storage. Perform room owner responsibility for the assigned DSP area. Perform equipment/instrument ownership related responsibilities related to DSP. Initiate Complaint Slips (work orders) for DSP related areas and equipment. Coordinate with QA for line clearance. Maintaining process area All-time ready for Inspection/ audit purpose. Maintain facility and assigned zone all-time ready for visit and audit. Involve and support in execution of batches as and when required and perform error free operation as per Batch Manufacturing Record (BMR). Involve in shipment of samples / final product as per packing and dispatch record. Work proactively to meet all document(s) on time closure requirement. Execute the protocols related to Downstream related activity and equipment / instrument qualification. Involve in Shipment of samples /final product as per packing and dispatch record. Execute the batch activity as per BMR and report nonconformity to the supervisor. Issuance of annexures, RM, consumables and BMRs. Track the work order status and ensuring timely closure. Education and Experience Education Master s degree in Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or related field. Industry Experience Minimum 9-12 years of relevant practical experience in Downstream Manufacturing for biopharmaceuticals, specifically with CHO cell lines for monoclonal antibodies, fusion proteins, etc. 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. Pls visit us at https://syngeneintl. com/ to know more about us and what we do.

Description: Responsible for ensuring the accuracy and reliability of laboratory instruments through regular calibration and preventive maintenance. This role involves the daily verification of key instruments, such as balances, pH meters, and Milli-Q water systems, as well as monitoring environmental conditions like temperature. The analyst will perform chemical and instrumental analyses (including Wet Chemistry, HPLC, GC, AAS, etc.) to support R&D and production processes, ensuring product quality at various stages of development and manufacturing. Ensuring data integrity in all laboratory activities. Essential Functions: Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hygro meters, Refrigerator temperature monitoring . Perform the in-process/ intermediate/ finished products analysis by Wet/ Chromatography techniques for R&D/ Plant support. Chemical/ instrument analysis (i.e. Wet/ HPLC/ GC/ AAS/ ICP-MS, etc.) Perform the Impurity standard/ working standard/ primary reference standards To maintain cGMP and Data integrity. Additional Responsibilities: Activities other than the defined in the Job Responsibility are to be done, as per the requirement of HOD Education: Bachelors Degree (BA/BS) B. Sc - Required Bachelors Degree (BA/BS) B. Pharma - Preferred Master Degree (MS/MA) M. Sc - Preferred Master Degree (MS/MA) M. Pharma - Preferred Experience: 3 years or more in 3-8 Yrs Skills: Calibration & Preventive Maintenance - Intermediate Instrument Verification & Monitoring - Advanced In-Process & Product Analysis - Advanced Chemical & Instrumental Analysis - Advanced Standard Preparation - Intermediate cGMP & Data Integrity Compliance - Intermediate Specialized Knowledge: Licenses: Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 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. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Field Service Engineer position will report into the Area Service Manager and will be part of the India Field Service Organization. This role will be located in Ahmedabad working remotely to cover the West-II region. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Responsible for installing, trouble-shooting, planned maintenance of the various range of Equipments sold by CYTIVA to the customers in Academic institutes, Research Institutes, Biopharmaceutical Industries. Required to attend and close the service calls as per CYTIVA Service Quality. Assist in growing the service business by selling the AMC, Spares, Validation & Automation solutions to the customers Collect the payments from the customers for the services rendered and solutions sold. Adhere to the Key Performance Index of Service Operation. with adherence to the EHS norms of the company and customers. Who you are: Mechanical/Electronics/Electrical & Tele-Communications Engineering with minimum 4 years' experience in equipment and associated devices related to Biopharmaceutical Industry in the production/research department or in Service/Maintenance dept. of the Biopharmaceutical Industry or as a service provider to Biopharmaceutical industry. Ability to install, service and troubleshoot the equipment like Upstream Bio-reactors & Downstream Liquid Chromatography systems. Should have knowledge about validation services as per industry norms. Fluency in English language and Exposure to Microsoft Office. The job involves travel needs and extended out location stays – willingness to this need is desired. 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 www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

COMB Discovery Services is a Chemistry Services Provider with expertise in Organic Synthesis / Process Research and Development of Pharmaceuticals and Chemicals related to diverse segments viz. API intermediates, Dyes, Agrochemicals, Energy Materials etc. We are looking for highly motivated and dynamic young Research Chemist. Position : Trainee - Research Chemist Education Qualification : Master of Science – Chemistry Work Experience: Fresh Pass out from College / university. Job Responsibilities: · Independently responsible for the execution of Synthesis project in a timely manner under guidance of Senior Research Chemist. Carry out literature search and propose synthesis plan for discussion and approval. Resolve problems faced during synthesis and purification. · Adept at factual documentation of experiments as per GLP guidelines. · Eager to Learn, update and practice futuristic organic synthesis skills under the supervision of Senior Research Chemist. · As a member of synthesis team participate in all synthesis and scale up activities related to successful completion of project. · Follow good laboratory practices and safety protocols in a disciplined manner under guidance of Senior Colleague. Desired Skills: · Good knowledge of Organic Chemistry and Synthesis. · Interpretation of Characterisation data for structural elucidation viz. HNMR, 13C NMR, IR and Mass. · Knowledge of In-process control techniques viz. Chromatography (TLC, GC, HPLC etc.) · Self-Motivation to Work Hard and Desire to learn for the success of the Team. · Be a Positive and Supportive Team Member. Job Types: Full-time, Permanent, Fresher Pay: ₹10,000.00 - ₹20,000.00 per month Benefits: Health insurance Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Apply now » Operator III - TAPI Date: Jul 23, 2025 Location: Gajraula, India, 244235 Company: Teva Pharmaceuticals Job Id: 62854 Who we are TAPI is the leading international supplier of active pharmaceutical ingredients (APIs). With the industry's broadest portfolio including over 350 API products. We are the go-to global supplier for APIs, supporting 80% of top 50 global pharmaceutical companies. We are proud of our reliable history in the generic API industry dating back over 80 years, and the fact we are considered to be one of the most trusted API suppliers, these enable TAPI to lead the industry, based on our experience, expertise, technologies, and exceptional customer service. Our employees are at the core of our success. Our Headquartered is in Israel, TAPI employs more than 4,000 professionals at 14 sites worldwide. Our state-of-the-art production facilities are located in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico and India. Our significant ongoing investment in R&D generates a steady flow of APIs, enabling timely introduction of new products to market. How you’ll spend your day Carrying out dispensing activities as per applicable procedure. Carrying out process and sampling activities during the production of Intermediate /API’s according to approved batch cards. Responsible for recording the observations of reaction parameters on the batch card as per approved procedure. Filling of all the batch cards (production cleaning) as per approved instructions. Ensure verification of pH meters and weigh balances as per applicable procedures. Maintain work procedure, safety precaution and cGMP. Contributes to the development of new concepts, techniques, and standards including expert knowledge of cGMP standards . Coordination of production tasks to meet assigned schedule Knowledge of Liquide chromatography Operations. Your experience and qualifications 3-5 Years – M.SC 0.5 to 3 years - B.Tech / B.E (Chemical) 24/7 Shift Already Working @TEVA? If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner. Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience. Apply now »

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials Job Description About Chromatography & Mass Spectrometry Division! From sample to knowledge to results, the Chromatography and Mass Spectrometry business develops and manufactures leading-edge chromatography and mass spectrometry instruments, consumables, and software solutions for customers working in the analytical sciences (routine testing markets) and scientific research. Our complete workflow solutions enable productivity and efficiency for customers performing food and beverage testing and manufacturing, environmental and industrial testing, biopharma QA/QC, toxicology, and anti-doping. For scientific research customers, our products support a range of focus areas, including proteomics, metabolomics, drug discovery and clinical research. Roles and Responsibilities: 1.Support Thermo Fisher customers through technical service, installation, operation, training and repair of specialized – Analytical equipment like Ion chromatograpy and have excellent technical competency if the HPLC product line. 2. Undertake product installation on client premises and demonstrate the features related to 21 CFR compliance. In the CDS software. 03.Provide training and technical advice on instrument use, both in person and by phone by sharing Dos and Don’ts for optimum performance of the system. 04.Investigate difficulties and solve faults arising from operation or utilization. 05. Rectify problems or suggest solutions or arrange for repairs to be made. 06.Provide an important link between customers and Sales and Marketing. 07. Provides a communication link between the customer and the company to help ensure that effective service is provided to the customer. 08. Monitor repairs in terms of the organization’s service / warranty cover and making suggestions as to product improvements. 09. Carry out planned maintenance calls and perform regular customer visits. 10. Make recommendations about spare parts requirement and assisting with monitoring equipment. 11.Achieve the assigned spares and Service revenue targets by prompting PM kits, instrument upgrade, software upgrades and calibration the systems. 12. Role requires extensive travelling within the territory and may call for travel outside territory if need arises Knowledge, Skills, abilities Candidate should have minimum 3 to 4 yrs experience in Analytical equipment like Ion chromatograpy and have excellent technical proficiency if the HPLC product line. 1. Bachelor of Technology (Biotechnology/ Electronics 2. Fluent written and verbal communication 3. Interpersonal skills suitable for a people-oriented job, requiring interactions with many people both inside and outside the organization 4. Ability to prioritize service requests and produce clear and concise documentation 5. Self-motivated and proactive in technical and support approach. 6. Closely work with customer in understanding customer pain areas and be consultant between organization and the customer thereby helping the customer and organization to achieve our regional commercial goals. 7. Build good rapport with customer and educate the customer reg. procurement of PM kits annually and reduce DT of the system.

About the Company: PCI Analytics Pvt. Ltd. is an ISO 45001:2018 certified, CRISIL rated company established in the year 1994. It is a leading manufacturer, supplier & exporter of a wide range of Laboratory, Scientific and Speciality equipment for application scope in Analytical instrumentation. We serve the Analytical Instrumentation market globally, working closely with all major OEMs and their partners in providing Pre-site requirement / Speciality gas facilitation services, Sample Preparatory support systems, Accessories and Consumables for Gas Chromatography, Liquid Chromatography, Mass spectrometry, AAS, ICP, FTIR, TOC Analyzers and Allied Analytical techniques. Sales Executive/Engg. Roles and Responsibility – · Business development · Product demonstration · Target Achievement and Revenue Generation · Maintain relation with existing client and vendor · To coordinate with back-office people · To participate in industrial exhibitions Required Experience, Skills and Qualifications – Experience - 1 to 6 Years Technical Knowledge Target Achievement Ready to travel Qualification - B.Sc – Chem/Electronics, Dip. / BE – Mechanical /Instrumentation/Electronics Location – Mumbai, Maharashtra

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 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. Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. The Field Service Engineer position will report into the Area Service Manager and will be part of the India Field Service Organization. This role will be located in Ahmedabad working remotely to cover the West-II region. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery. What you will do: Responsible for installing, trouble-shooting, planned maintenance of the various range of Equipments sold by CYTIVA to the customers in Academic institutes, Research Institutes, Biopharmaceutical Industries. Required to attend and close the service calls as per CYTIVA Service Quality. Assist in growing the service business by selling the AMC, Spares, Validation & Automation solutions to the customers Collect the payments from the customers for the services rendered and solutions sold. Adhere to the Key Performance Index of Service Operation. with adherence to the EHS norms of the company and customers. Who you are: Mechanical/Electronics/Electrical & Tele-Communications Engineering with minimum 4 years' experience in equipment and associated devices related to Biopharmaceutical Industry in the production/research department or in Service/Maintenance dept. of the Biopharmaceutical Industry or as a service provider to Biopharmaceutical industry. Ability to install, service and troubleshoot the equipment like Upstream Bio-reactors & Downstream Liquid Chromatography systems. Should have knowledge about validation services as per industry norms. Fluency in English language and Exposure to Microsoft Office. The job involves travel needs and extended out location stays – willingness to this need is desired. 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 www.danaher.com. At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

Company Description YMC India Pvt. Ltd., a subsidiary of YMC Co. Ltd, Japan, was established in 2008. Headquartered in Noida, YMC India serves a wide range of pharmaceutical and biopharmaceutical industries across the country with regional offices in Hyderabad, Bangalore, and Pune. The company specializes in Analytical and Process Chromatography, providing products such as HPLC/UHPLC Analytical columns, Preparative columns, and packing materials. YMC India is recognized for its comprehensive solutions and customer-centric approach in the chromatography field. Role Description This is a full-time on-site role for a Scientist Executive Preparative ARD at YMC India Pvt. Ltd. located in Hyderabad. The candidate will be responsible for conducting preparative chromatography, method development and validation, analytical testing, data interpretation, and ensuring compliance with regulatory requirements. The Scientist Executive will also collaborate with cross-functional teams and contribute to the development and optimization of chromatographic methods for various applications. Job Title: Scientist / Executive – Preparative ARD Department: Analytical Research & Development (Preparative) Location: Hyderabad Experience: [ 2–4 years] Qualification : M.Sc. / M. Pharm in Analytical Chemistry, Organic Chemistry, or related field Job Responsibilities : Perform preparative chromatography for isolation and purification of active pharmaceutical ingredients (APIs), intermediates, and impurities. Develop and optimize preparative HPLC/LC methods for scale-up and purification. Support method development and validation for impurity profiling and characterization. Operate and maintain preparative instruments including HPLC, flash chromatography systems, and associated software. Collaborate with process R&D and formulation teams to support product development. Document experimental procedures, results, and observations in lab notebooks and reports. Ensure compliance with cGMP, GLP, and safety protocols during laboratory operations.

Kenvue Is Currently Recruiting For a Senior Scientist, R&D Analytical What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To 研发分析经理 Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What You Will Do The Senior Scientist, R&D Analytical is responsible for supporting New Product Development/ Life Cycle Management projects for the Asia Pacific market by providing guidance to staff, conducting advanced research programs, and developing research proposals to meet exploratory objectives in product discovery: Key Responsibilities Lead and manage analytical research projects in R&D department Develop, optimize, validate and transfer analytical methods to support product development and life cycle management projects Collaborate with cross-functional teams to drive scientific advancements Provide technical expertise in analytical instrumentation and data analysis Stay current with industry trends and technologies to drive innovation Lead and oversee chemical analyses to support product discovery objectives Provide expert guidance to staff members on analytical test evaluations and analyses and other projects Required Qualifications What we are looking for Minimum BA/ BS in Chemistry or equivalent science (e.g. Biochemistry, Pharmaceutical Chemistry) with 6 years of proven working experience in Analytical Chemistry and/or Medicinal chemistry Proven track record of leading successful scientific projects Strong knowledge of Asia Pacific Analytical and Stability requirements to support product launches, including EP, ChP, USP compendia requirements and ICH guidelines. Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health or pharmaceutical environment Strong knowledge in UPLC, HPLC, and GC to execute Analytical test method development, validation and optimization. Solid understanding of analytical and physical testing capabilities Desired Qualifications Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment Excellent communication and collaboration skills Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems. Master’s or PhD (Doctor of Philosophy) in chemistry or a closely related field with a deep understanding of medicinal chemistry principles Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Kenvue Is Currently Recruiting For a Principal Scientist, R&D Analytical What We Do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here. Role Reports To 研发分析经理 Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What You Will Do The Principal Scientist, R&D Analytical is responsible for supporting New Product Development/ Life Cycle Management projects for the Asia Pacific market by performing chemical analysis, providing guidance to staff, conducting advanced research programs, and developing research proposals to meet exploratory objectives in product discovery: Key Responsibilities Lead and manage analytical research projects in R&D department Develop, optimize, validate and transfer analytical methods to support product development and life cycle management projects Collaborate with cross-functional teams to drive scientific advancements Provide technical expertise in analytical instrumentation and data analysis Stay current with industry trends and technologies to drive innovation Provide expert guidance to staff members on analytical test evaluations and analyses and other projects Required Qualifications What we are looking for Minimum BA/ BS in Chemistry or equivalent science (e.g. Biochemistry, Pharmaceutical Chemistry) with 8 years of proven working experience in Analytical Chemistry and/or Medicinal chemistry Proven track record of leading successful scientific projects Strong knowledge of Asia Pacific Analytical and Stability requirements to support product launches, including EP, ChP, USP compendia requirements and ICH guidelines. Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health or Pharmaceutical environment Strong knowledge in UPLC, HPLC, and GC to execute Analytical test method development, validation and optimization. Desired Qualifications Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment Excellent communication and collaboration skills Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems. Master’s or PhD (Doctor of Philosophy) in chemistry or a closely related field with a deep understanding of medicinal chemistry principles Note: Total Rewards at Kenvue include salary, bonus (if applicable) and benefits. Your Talent Access Partner will be able to share more about our total rewards offerings and the specific salary range for the relevant location(s) during the recruitment & hiring process. Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Designation: Executive/Senior Officer/ Officer Department: Manufacturing - Antigens (Production) Educational Qualification: M.Sc/ B.Sc/ Diploma (Any Life Sciences background) Experience: 1-7 years Location: Biological E. Limited (Vaccine Division), Kolthur, Hyderabad Roles & Responsibilities: Execution of Upstream & Downstream production batches. Focus on timely execution, to ensure that the process is carried out as per GMP and batch timelines. To execute planned Upstream & Downstream activities to ensure high degree of confidence that the process is delivering a product that meets its target specifications. Routine monitoring of the equipment, Facility and utilities for GMP compliance Execution of documentation activities of liaison with QA and QC for GMP compliance. Participate and execute compliance of validation/ Qualification documents. Participate in execution the various compliance from the different cross functional team for QMS compliance Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months' pay slips on Thursday, 24th Jul'25 & Friday, 25th Jul'25 from 10:00 AM to 01:00 PM at Biological E. Limited (Vaccine Division). Address: Plot No.1, Phase-II, Near MN Park, Genome Valley, Kolthur (V), Shameerpet (M), Dt. Medchal Malkajgiri, Hyderabad Land Mark - A road opposite to Honey burg Resort on Karimnagar Highway. (Beside Venkateshwara Swamy Temple) Interested candidates unable to attend the walk-in can send in their CVs by mention subject as Applying for Department Name to "careers@biologicale.com"

Kenvue is currently recruiting for a: Senior Scientist, R&D Analytical What we do At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Who We Are Our global team is ~ 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. Role reports to: 研发分析经理 Location: Asia Pacific, India, Maharashtra, Greater Mumbai Work Location: Fully Onsite What you will do What you will do The Senior Scientist, R&D Analytical is responsible for supporting New Product Development/ Life Cycle Management projects for the Asia Pacific market by providing guidance to staff, conducting advanced research programs, and developing research proposals to meet exploratory objectives in product discovery: Key Responsibilities Lead and manage analytical research projects in R&D department Develop, optimize, validate and transfer analytical methods to support product development and life cycle management projects Collaborate with cross-functional teams to drive scientific advancements Provide technical expertise in analytical instrumentation and data analysis Stay current with industry trends and technologies to drive innovation Lead and oversee chemical analyses to support product discovery objectives Provide expert guidance to staff members on analytical test evaluations and analyses and other projects What we are looking for Required Qualifications Minimum BA/ BS in Chemistry or equivalent science (e.g. Biochemistry, Pharmaceutical Chemistry) with 6 years of proven working experience in Analytical Chemistry and/or Medicinal chemistry Proven track record of leading successful scientific projects Strong knowledge of Asia Pacific Analytical and Stability requirements to support product launches, including EP, ChP, USP compendia requirements and ICH guidelines. Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health or pharmaceutical environment Strong knowledge in UPLC, HPLC, and GC to execute Analytical test method development, validation and optimization. Solid understanding of analytical and physical testing capabilities Desired Qualifications Experience working in Analytical Chemistry supporting new product development and life cycle management projects in a Consumer Health environment Excellent communication and collaboration skills Strong experience with Empower chromatography data system, using electronic laboratory notebooks (ELN), and LIMS systems. Master’s or PhD (Doctor of Philosophy) in chemistry or a closely related field with a deep understanding of medicinal chemistry principles Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.

Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials About Chromatography & Mass Spectrometry Division! From sample to knowledge to results, the Chromatography and Mass Spectrometry business develops and manufactures leading-edge chromatography and mass spectrometry instruments, consumables, and software solutions for customers working in the analytical sciences (routine testing markets) and scientific research. Our complete workflow solutions enable productivity and efficiency for customers performing food and beverage testing and manufacturing, environmental and industrial testing, biopharma QA/QC, toxicology, and anti-doping. For scientific research customers, our products support a range of focus areas, including proteomics, metabolomics, drug discovery and clinical research. Roles and Responsibilities: Support Thermo Fisher customers through technical service, installation, operation, training and repair of specialized – Analytical equipment like Ion chromatograpy and have excellent technical competency if the HPLC product line. Undertake product installation on client premises and demonstrate the features related to 21 CFR compliance. In the CDS software. Provide training and technical advice on instrument use, both in person and by phone by sharing Dos and Don’ts for optimum performance of the system. Investigate difficulties and solve faults arising from operation or utilization. Rectify problems or suggest solutions or arrange for repairs to be made. Provide an important link between customers and Sales and Marketing. Provides a communication link between the customer and the company to help ensure that effective service is provided to the customer. Monitor repairs in terms of the organization’s service / warranty cover and making suggestions as to product improvements. Carry out planned maintenance calls and perform regular customer visits. Make recommendations about spare parts requirement and assisting with monitoring equipment. Achieve the assigned spares and Service revenue targets by prompting PM kits, instrument upgrade, software upgrades and calibration the systems. Role requires extensive travelling within the territory and may call for travel outside territory if need arises Knowledge, Skills, Abilities Candidate should have minimum 3 to 4 yrs experience in Analytical equipment like Ion chromatograpy and have excellent technical proficiency if the HPLC product line. Bachelor of Technology (Biotechnology/ Electronics Fluent written and verbal communication Interpersonal skills suitable for a people-oriented job, requiring interactions with many people both inside and outside the organization Ability to prioritize service requests and produce clear and concise documentation Self-motivated and proactive in technical and support approach. Closely work with customer in understanding customer pain areas and be consultant between organization and the customer thereby helping the customer and organization to achieve our regional commercial goals. Build good rapport with customer and educate the customer reg. procurement of PM kits annually and reduce DT of the system.

Let s do this. Let s change the world. In this vital role you will be part of the Chromatography Data Systems (CDS) Product Team working on computerized systems validations (CSV) and GAMP (Good Automated Manufacturing Practice). This vital role ensures Amgen systems remain aligned with industry standards and align with all regulatory requirements. Roles & Responsibilities: Advising clients on how to meet compliance requirements using a risk-based approach. Develop validation documentation and standard operating procedures for various GxP applications. Develop test protocols that thoroughly test business requirements. Provide test execution oversight and assist with deviation recommendations as required, work with clients to develop validation plans to ensure that, at the end of the project, the system meets GxP requirements. Work with client business functions and domain experts to develop User Requirements Specification, Functional Requirements Specification, and/or Design Specifications as required Development of test / validation scripts based on software design and configurations. Develop IQ/OQ scripts as required. What we expect of you We are all different, yet we all use our unique contributions to serve patients. Doctorate degree OR Master s degree and 4 to 6 years of Life Science / Biotechnology / Pharmacology / Information Systems experience OR Bachelor s degree and 6 to 8 years of Life Science / Biotechnology / Pharmacology / Information Systems experience OR Diploma and 10 to 12 years of Life Science / Biotechnology / Pharmacology / Information Systems experience Preferred Qualifications: Functional Skills: Must-Have Skills: Demonstrated experience with minimum of 3 to 5 years in pharmaceutical industry, focusing on Computer Systems Validations / GAMP Experience with regulatory agencies - FDA, EMEA, CFDA, and other regulatory agencies Proven leadership skills with the ability to multitask and lead multiple validation projects Thorough understanding of the principles of GAMP, SDLC methodologies and testing standard methodology. Ability to understand existing and new business processes and requirements to ensure proper implementation and validation of systems. Expertise with ALM testing and ALM software (HP) Expertise in use - Veeva (all modules - CDocs, QMS, RIM, DocuSign, etc) Fluent knowledge of rules and regulations: GAMP 5, 21 CFR Part 11 Compliance and CFR Part 210, 211 Compliance. Good-to-Have Skills: Ability to work independently, excellent problem solving and professional written communications skills. Fluent in Microsoft Office suite Including (Excel, Power Point, Visio, Project), Experience with Smartsheets, Salesforce, Tableau a plus FDA Audit experience a plus & working with regulatory agencies Experience with enterprise CDS platform software (Empower/Chromeleon/Unicorn) Soft Skills: Excellent leadership and team management skills. Strong transformation and organizational change experience. Ability to work effectively with global, virtual teams. Excellent analytical and solving skills. Ability to prioritise successfully. Strong presentation and public speaking skills. Strong verbal and written communication skills. High degree of initiative and self-motivation. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers driven and comprehensive Total Rewards Plans that are aligned with local industry standards.

Let s do this. Let s change the world. In this vital role you will be part of the Chromatography Data Systems (CDS) Product Team and will be responsible for driving Life Cycle Management of Empower, Chromeleon, Unicorn and other CDS applications, including GxP validation, testing, and compliance activities, remediation of software vulnerabilities, and managing backup and disaster recovery plans for CDS applications. You will work closely with Lab Scientists, Benchtop Technicians, Product owners, and Business analysts following SAFe Agile methodologies to drive Platform and Product Innovation beyond the KTLO activities to help accelerate Operational Business Goals and advance Amgen s mission of serving every patient every time Roles & Responsibilities: Oversee the software, hardware, and firmware development lifecycle for CDS application, ensuring standard methodologies in development, testing, and deployment across the Global Process Development Organization Work within the framework of SAFe product team, participating in requirements gathering, design discussions, development, implementation, testing, and software validation. Ensure the quality, reliability, and scalability of the CDS applications, following the standard methodologies of software engineering, testing, and documentation. Research and evaluate new technologies and frameworks that can enhance the capabilities and performance of the software solutions. Remain accountable for ensuring overall organizational compliance with quality and GxP in technology services Monitor emerging technologies and trends to find opportunities for platform growth and expansion Apply machine learning and Gen AI techniques to accelerate operational business process flows associated with CDS applications and leverage CDS data to generate insights and provide recommendations for process improvement. What we expect of you We are all different, yet we all use our unique contributions to serve patients. Doctorate degree OR Master s degree and 4 to 6 years of Life Science / Biotechnology / Pharmacology / Information Systems experience OR Bachelor s degree and 6 to 8 years of Life Science / Biotechnology / Pharmacology / Information Systems experience OR Diploma and 10 to 12 years of Life Science / Biotechnology / Pharmacology / Information Systems experience Preferred Qualifications: Functional Skills: Must-Have Skills: Demonstrated experience of owning business applications in a Life Sciences, Pharmaceutical, Biotech company or equivalent industry or knowledge of the pharmaceutical industry GxP system qualification and validation processes for computer related systems Strong knowledge of COTS (Commercial-off-the-shelf) Validations on HPLCs, UPLCs, CEs, GCs, and other standalone systems Proven leadership skills with the ability to lead projects and work closely with a team of hard-working technology professionals Build a culture of innovation and continuous improvement within the team to deliver powerful solutions and platform improvements Solid skills in collaborating and communicating with multi-functional teams, business collaborators, and executives to ensure alignment of platform initiatives with business outcomes, handling expectations, and ensuring successful delivery of projects. Experience with Advancing Capabilities and Delivering Innovative Technology Solutions in a Pharma/Biotech environment Degree in Computer Science, Information Systems, Engineering, or Life Sciences Good-to-Have Skills: At least 5 - 8 years of domain knowledge in health and/or life sciences combined with Information Technology Extensive experience in software development lifecycles Experience using and adoption of Scaled Agile Framework (SAFe) Understanding of ITIL processes and implementation Experience handling vendor relationships and working with external partners or consultants to ensure optimal performance, support, and development of digital products Soft Skills: Excellent leadership and team management skills. Strong transformation and change management experience. Ability to work effectively with global, virtual teams. Excellent analytical and troubleshooting skills. Ability to manage multiple priorities successfully. Strong presentation and public speaking skills. Strong verbal and written communication skills. High degree of initiative and self-motivation. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Let s do this. Let s change the world. The role is responsible for leading and charting the course for the Quality Control Global Technology product teams that builds and transforms capabilities that positively impacts business outcomes. Specifically, this individual will be responsible for planning, design, configuration, deployment, and support of Quality Control Platforms including the Laboratory Information Management System (LIMS), Electronic Lab Notebook, and Chromatography Data Systems. The ideal candidate will have a consistent track record of leadership in technology-driven environments for the Information Systems area and has a passion for fostering innovation and excellence in the biotechnology industry. Additionally, collaboration with multi-functional and global teams is required to ensure seamless integration and operational excellence. The candidate will have a solid background in the end-to-end software development lifecycle and a Scaled Agile practitioner, coupled with leadership and transformation experience. This role demands the ability to drive and deliver against key organizational critical initiatives, foster a collaborative environment, and deliver high-quality results in a matrixed organizational structure Lead a team responsible for the ongoing 24/7 management, optimization and innovation of Quality Control Digital Platforms Collaborate with SAP, MuleSoft and AWS technical teams to design system configurations, data mappings, and integrations between systems. Ensure data integrity by defining data quality standards, monitoring data quality issues, and working with data stewards to address discrepancies. Support the validation processes defined by Amgen, ensuring compliance with regulatory standards (e.g., FDA, GxP) throughout the implementation and ongoing usage. Responsible for leading, growing, and developing the Amgen Technology team in India, ensuring global ways of working are imbedded in the local organization Work with Product Owners, Service Owners and/or delivery teams to ensure that delivery matches commitments, acting as a partner concern point and facilitating communication when service commitments are not met Develop talent, motivate the team, delegate effectively, champion diversity within the team and act as a role model of servant leadership. Maintain strategic relationships and good communication with the leadership team about IS services and service roadmaps to ensure that all the collaborators feel informed and engaged Lead and manage large, diverse teams within a matrixed organization. Collaborate with geographically dispersed teams, including those in the US and other international locations. Oversee the software development lifecycle Develop and implement strategic plans for technology and workforce. Develop a culture of collaboration, innovation, and continuous improvement. Understand the decision-making process, workflows, and business and information needs of business partners and collaborators Contribute and define business outcomes + requirements, technology solutions, and services Improve activities being measured by crafting, monitoring, and optimizing relevant feedback loops through test & learn activities Ensure communication of key performance metrics and analysis of unmet needs Participate in partner and other leadership meetings, working with other parts of the organization, and functional groups to ensure successful delivery Ensure ongoing alignment with strategy, compliance, and regulatory requirements for technology investments and services Ensure alignment of Technology service plans across organization Provide education to new partners with regards to IT service offerings Remain accountable for ensuring overall organizational compliance to quality/compliance requirements such as GXP and Privacy What we expect of you We are all different, yet we all use our unique contributions to serve patients. Basic Qualifications: Doctorate Degree and 2 years of experience in Business, Engineering, IT or related field OR Master s degree with 8 - 10 years of experience in Business, Engineering, IT or related field OR Bachelor s degree with 10 - 14 years of experience in Business, Engineering, IT or related field OR Diploma with 14 - 18 years of experience in Business, Engineering, IT or related field Solid understanding of operations GMP laboratory sample management process, including, data collection, data management, and regulatory requirements Expertise in Quality Control systems, including data entry, data review and reporting Experience with business analysis methodologies including requirements gathering, documentation, and process mapping Demonstrated experience in leading technology initiatives and teams with a track record of successful innovation Exceptional collaboration, communication and interpersonal skills to effectively manage partner relationships and build new partnerships. Experience in applying technology standard process methodologies: Scaled Agile (SAFe), ITIL, etc. Preferred Qualifications: Experience in a leadership role within a pharmaceutical or technology organization Extensive experience in the software development lifecycle in particular with technology used in a GxP environment. Experience using and adoption of Scaled Agile Framework (SAFe) Strong analytic/critical-thinking and decision-making abilities. Ability to work effectively in a fast-paced, dynamic environment. Established business partnerships and IS governance practices involving senior business partners Broad working knowledge of key IS domains and layers Scaled Agile Framework (SAFe) for Teams required Soft Skills: Excellent leadership and team management skills. Strong transformation and organisational change experience. Exceptional collaboration and communication skills. High degree of initiative and self-motivation. Ability to manage multiple priorities successfully. Team-oriented with a focus on achieving team goals. Strong presentation and public speaking skills. Excellent analytical and troubleshooting skills Strong verbal and written communication skills Ability to work effectively with global, virtual teams What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Let s do this. Let s change the world. In this vital role you will be part of the Chromatography Data Systems (CDS) Product Team working on the lifecycle of the CDS platforms which includes refreshing of all software/hardware within the enterprise CDS platforms. This vital role ensures the CDS platforms remain up to date and ensure all systems remain available for business. Roles & Responsibilities: Work with the CDS product team to support the lifecycle of CDS platform software (Empower/Chromeleon/Unicorn) Develop documentation and standard operating procedures for various lifecycle processes Work with vendors to secure the latest version of CDS software, driver packs, patches and other software packages Work with other Amgen infrastructure teams to stand up various infrastructure environments (DEV/TEST/PROD) in the cloud or on-prem Provide support and fix for all CDS platforms Perform testing and develop migration strategies for all CDS platforms CDS software patching and compliance - ensure CDS platforms are secure and patched What we expect of you We are all different, yet we all use our unique contributions to serve patients. Master s degree and 1 to 3 years of Life Science / Biotechnology / Pharmacology / Information Systems experience OR Bachelor s degree and 3 to 5 years of Life Science / Biotechnology / Pharmacology / Information Systems experience OR Diploma and 7 to 9 years of Life Science / Biotechnology / Pharmacology / Information Systems experience Preferred Qualifications: Functional Skills: Must-Have Skills: Demonstrated experience with minimum of 3 to 5 years in systems administration and infrastructure Experience with - Networking, DNS, Firewalls, Security, Patching, AWS, VMWare Proven leadership skills with the ability to multitask and lead simultaneous software/hardware lifecycle projects Create infrastructure requirements for various server types Thorough understanding of Windows and Linux OSes Ability to understand vendor requirements against business needs Develop and maintain various scripts for server task automation Partner with vendors and other team members to solve problems, test new software versions, and secure long-term solutions against the CDS platforms Good-to-Have Skills: Ability to work independently, excellent problem solving and professional written communications skills. Experience with Smartsheets/Excel/Tableau Strong customer focus with ability to work closely with business Experience with enterprise CDS platform software (Empower/Chromeleon/Unicorn) Soft Skills: Excellent leadership and team management skills. Strong transformation and organizational change experience. Ability to work effectively with global, virtual teams. Excellent analytical and solving skills. Ability to manage multiple priorities successfully. Strong presentation and public speaking skills. Strong verbal and written communication skills. High degree of initiative and self-motivation. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.

Good technical knowledge of analytical techniques and instrumentation: Chromatography technique like High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC), Spectroscopy technique like UV-Vis and Infrared (IR), KF titration, zettaliter, Osmometer and Dissolution etc Skills in developing, optimizing, and validating analytical methods to ensure accuracy, precision, and reliability. Understanding of Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), Data integrity and relevant regulatory guidelines (e.g., ICH, FDA, EP) to ensure compliance. Should have strong strong understanding & experience in injectables is mandatory Immediate joiners preferred Email : monisha.lahiri@randstad.in

Execute and supervise Batch activities in accordance with BMRs and established protocols. Prepare, revise, execute, and review Batch Manufacturing Records (BMRs)/PDR/SOPs/Protocols Having strong knowledge of Chromatography techniques, UFDF, Column packing-unpacking. Should be well versed with continuous centrifugation, Homogenizer, and single-use technology. Collaborate with Process Development, MSAT, and Operational Excellence teams for process scale-up and technology transfer activities. Prepare and review qualification documents as per SOPs, ensuring timely review and approval with cross-functional teams. Execution of Installation, Operational, and Performance Qualification (IQ/OQ/PQ) for downstream equipment. Coordinate Commissioning & Qualification activities through collaboration with internal and external cross-functional teams and subject matter experts (SMEs). Coordinate with the maintenance department for the upkeep of operational equipment. Ensure all operational documents, batch records, and checklists are compliant with cGMP Should have good knowledge about process mapping and equipment mapping as per project requirements. Coordination with the client for finalization of process requirements and address client quarries related to project. Manage the stock of required consumables for batch activities and ensure timely procurement. Prepare and review quality protocols and investigate any batch failures in operations. Support the facilitys readiness for regulatory inspections. Having strong knowledge of QMS activities (Change Control, Deviation, CAPA, Investigation, etc.) Report deviations and manage change controls, collaborating with QA to implement corrective actions. Carry out additional tasks as assigned by the HOD.

Execute and supervise BMP4 batch activities in accordance with BMRs and established protocols. Prepare, revise, execute, and review Batch Manufacturing Records (BMRs)/PDR/SOPs/Protocols Having strong knowledge of Chromatography techniques, UFDF, Column packing-unpacking. Should be well versed with continuous centrifugation, Homogenizer, and single-use technology. Collaborate with Process Development, MSAT, and Operational Excellence teams for process scale-up and technology transfer activities. Prepare and review qualification documents as per SOPs, ensuring timely review and approval with cross-functional teams. Execution of Installation, Operational, and Performance Qualification (IQ/OQ/PQ) for downstream equipment. Coordinate Commissioning & Qualification activities through collaboration with internal and external cross-functional teams and subject matter experts (SMEs). Coordinate with the maintenance department for the upkeep of operational equipment. Ensure all operational documents, batch records, and checklists are compliant with cGMP Should have good knowledge about process mapping and equipment mapping as per project requirements. Coordination with the client for finalization of process requirements and address client quarries related to project. Manage the stock of required consumables for batch activities and ensure timely procurement. Prepare and review quality protocols and investigate any batch failures in operations. Support the facilitys readiness for regulatory inspections. Having strong knowledge of QMS activities (Change Control, Deviation, CAPA, Investigation, etc.) Report deviations and manage change controls, collaborating with QA to implement corrective actions. Carry out additional tasks as assigned by the HOD.

GMH Organics( EU- GMP) Injectable Plant is a leading pharmaceutical company dedicated to delivering high-quality products and innovative solutions. We are currently seeking a skilled and detail-oriented QC Analyst with expertise in HPLC to join our Quality Control team. Experience :- 03-05 years Key Responsibilities: Perform routine and non-routine analysis of raw materials, in-process samples, and finished products using HPLC and other analytical instruments. Prepare and execute analytical methods in compliance with GMP and regulatory standards. Document all test results and observations accurately in laboratory notebooks and electronic systems. Conduct method validation, verification, and transfer as required. Investigate and troubleshoot out-of-specification (OOS) results and instrument issues. Maintain and calibrate laboratory instruments in accordance with SOPs. Support stability testing and data review activities. Participate in audits and contribute to continuous improvement initiatives. Qualifications: Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or a related field. 3–5 years of experience in QC laboratory work with hands-on experience in HPLC. Solid understanding of GMP, GLP, and regulatory requirements (e.g., FDA, ICH). Experience with Empower, Chromeleon, or similar chromatography software is a plus. Strong analytical and problem-solving skills. Excellent attention to detail and documentation skills. Ability to work independently and as part of a team. To Apply: Send your resume to (rahul@gmh.co.) and Also You can share on WhatsApp directly 7876456719 Job Types: Full-time, Permanent Pay: ₹22,000.00 - ₹35,000.00 per month Benefits: Commuter assistance Food provided Health insurance Leave encashment Life insurance Paid sick time Paid time off Provident Fund Work Location: In person Application Deadline: 25/07/2025

We are seeking a detail-oriented and experienced Quality Control (QC) Analyst with a strong background in High-Performance Liquid Chromatography (HPLC) to join our analytical team. The QC Analyst will be responsible for testing raw materials, in-process samples, and finished products in compliance with cGMP and regulatory requirements. Key Responsibilities: Perform routine and non-routine analysis using HPLC, UV-Vis, IR, and other instrumentation. Prepare and standardize reagents, solutions, and mobile phases. Interpret and document analytical results accurately in laboratory notebooks, LIMS, or other systems. Conduct method validation and transfer activities under supervision. Ensure compliance with all relevant SOPs, cGMP guidelines, and safety standards. Troubleshoot instruments and report equipment malfunctions. Participate in laboratory investigations (OOS, OOT, deviations). Support continuous improvement of lab practices and documentation. Qualifications: B.S.C or M.S.C in Chemistry, Pharmaceutical Sciences, or a related field. 1–3 years of hands-on HPLC experience in a regulated QC lab (pharmaceutical, biotech, or similar). Working knowledge of USP/EP/ICH guidelines and cGMP. Familiarity with analytical software (e.g., Empower, Chromeleon) is a plus. Strong attention to detail, documentation, and organizational skills. Ability to work independently and as part of a team. Interested Candidates Share me your Cv on WhatsApp 7876456719 Job Type: Full-time Pay: ₹20,000.00 - ₹30,000.00 per month Benefits: Flexible schedule Food provided Health insurance Internet reimbursement Leave encashment Life insurance Paid sick time Paid time off Provident Fund Work Location: In person Application Deadline: 25/07/2025

Roles & Responsibilities: Build and maintain strong relationships with key clients in assigned regions. Deliver product demonstrations and presentations to prospective customers. Develop and implement sales strategies to achieve and surpass sales targets. Collaborate with the Technical team to design and execute impactful marketing campaigns. Requirements: Experience: 4–8 years in sales, ideally in chromatography, biochromatography, or related sectors. Bachelor’s or Master’s degree in a relevant discipline. Demonstrated success in achieving and exceeding sales goals. Preferred familiarity with chromatography columns, vials and septa. Excellent communication and negotiation abilities. Ability to work independently and as part of a team. Willingness to travel within the assigned regions. Job Types: Full-time, Permanent Pay: ₹30,309.63 - ₹100,609.41 per month Benefits: Cell phone reimbursement Education: Bachelor's (Preferred) Experience: total work: 1 year (Preferred) Sales: 1 year (Preferred) Management: 1 year (Preferred) Work Location: In person Application Deadline: 31/07/2025 Expected Start Date: 01/08/2025