565 Chromatography Jobs - Page 6

As a Chemical Laboratory Technician, you will be responsible for preparing test solutions, compounds, and reagents for conducting tests and coordinating test procedures. You will be tasked with determining the chemical and physical properties, compositions, structures, relationships, and reactions of both organic and inorganic compounds. Utilizing chromatography, spectroscopy, and spectrophotometry techniques will be a key aspect of your role. Your duties will also include the development, improvement, and customization of products, equipment, formulas, processes, and analytical methods. Collaboration with scientists and engineers to analyze, interpret, and develop tests will be essential. Additionally, you will introduce heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Furthermore, you will be responsible for writing technical papers and reports, as well as preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and procuring new laboratory supplies will also fall under your purview. Evaluating and ensuring compliance with laboratory safety procedures and standards will be a critical part of your responsibilities. This is a full-time, permanent position with benefits such as health insurance and Provident Fund. The work schedule includes day and morning shifts, with additional perks like performance bonuses and yearly bonuses. The work location is in person.,

The role involves conducting water quality testing for various projects, performing laboratory experiments to isolate and maintain microbial cultures, and documenting microbiology laboratory processes. You will be responsible for developing and maintaining Standard Operating Procedures (SOPs), calibrating lab instruments periodically, and preparing standard solutions and specifications for tests. Additionally, you will oversee laboratory inventory management and ensure compliance with safety procedures and standards. Familiarity with chromatography and spectrophotometry techniques is required. Proficiency in MS Office tools is essential for this position. The ideal candidate should possess a degree in microbiology, biochemistry, or analytical chemistry, along with 1-2 years of experience as a microbiologist or lab analyst. Post-graduation in microbiology, biochemistry, analytical chemistry, or related fields, or a B.Tech. in Chemical Engineering, Materials Science & Engineering, or Environmental Engineering, is preferred. Candidates should have knowledge of laboratory tests used in microbiology and analytical chemistry, excellent laboratory skills, and proficiency with computers and scientific equipment. Strong problem-solving, critical thinking, and analytical skills are necessary, along with a willingness to learn and effective communication skills.,

Please call 9947350555 more details Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Candidate will be qualified MSc chemistry . This job will prefer male candidate. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety Job Type: Full-time Pay: ₹16,500.00 - ₹17,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Rotational shift Education: Master's (Preferred) Language: Malayalam (Preferred) Work Location: In person Speak with the employer +91 9947350555

Company Description S.K. Traders is one of the largest distributors of lab chemicals, glassware, chromatography consumables, and more in Central India, serving cities such as Indore, Bhopal, Pithampur, Dewas, Ratlam, Nagda, Jabalpur, Sagar, Bina, and Ujjain. Established in 1993, we have built strong relationships with major pharma, chemical, institutional, and research customers. We proudly hold authorized dealerships for top brands including Merck Specialities, Sigma Aldrich, Borosil, Hi-Media Labs, Thermo Fisher Scientific, and Waters India. Role Description This is a full-time remote role for a Business Development Executive. The Business Development Executive will be responsible for identifying new business opportunities, generating leads, managing accounts, and maintaining effective communication with clients. Daily tasks include developing strategies for business growth, nurturing client relationships, and working closely with the sales team to achieve targets. Qualifications Proficiency in New Business Development and Lead Generation skills Strong Business and Account Management abilities Excellent Communication skills Strong analytical and problem-solving skills Ability to work independently and remotely Experience in the lab chemicals and life sciences industry is a plus Bachelor's degree in Business, Marketing, or related field

Nano Micro is a technology startup recognized globally for its leadership in producing spherical, monodisperse particles through proprietary manufacturing processes. These methods enable high-yield, cost-effective production across diverse industries and applications. Meeting purification needs from laboratory to manufacturing scale in both small molecule pharmaceuticals and biopharmaceuticals requires ongoing integration of advancements in chromatography and resin technology, as well as adept management of continually evolving business and scientific challenges. We deliver comprehensive purification solutions for both small molecule and biopharmaceutical sectors, including: · Small molecule therapeutics · Antibody and protein therapeutics · Peptide therapeutics · Oligonucleotide therapeutics · Vaccine discovery and development · Plasma proteins, among others Nano Micro swiftly established itself as an OEM supplier for chromatography vendors worldwide, supporting pharmaceutical and biopharmaceutical purification under various brands. The company has since introduced its own brand internationally, with a strategic focus on India, where it has made considerable market advances and successfully expanded operations within major accounts. This is perfect time a larger team dedicated to increasing market share by penetrating and ramp up volumes within all areas of biopharmaceutical purification. Opportunities at Nano Micro Nano Micro welcomes candidates from a broad range of disciplines, including sales, business development, and scientific research mainly focusing on application support and scaling up in biopharmaceutical space. Commitment to Continuous Improvement At Nano Micro, employees are encouraged to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners. Collaborative Environment Our workplace fosters cooperation and mutual respect, with a strong emphasis on diversity and inclusivity. Professional Development Nano Micro prioritizes employee growth by supporting professional development and skill enhancement and provides opportunities throughout the organization. We recognize that learning from setbacks is intrinsic to progress and actively encourage staff to engage in new experiences beyond conventional roles. At Nano Micro, business growth and career development are aligned as employees work to deliver effective resin solutions in all application areas. The company offers competitive pay, performance-based bonuses, and comprehensive benefits in line with startup industry standards. Application Scientists (Multi Location) We are looking for a motivated life science scientists to join our India Field Applications Scientist team focused on Biopharmaceuticals. The ideal candidate is outgoing, confident, and has strong communication and presentation skills. You should be able to work independently and as part of an energetic sales team that supports research in life sciences, and instrumentation – such as protein purification, and separation devices, molecular synthesis, and Organic slime resistant nano filtration solutions. Our team provides scientific expertise to researchers, labs, and manufacturing sites across India, prioritizing customer needs with our Chromatography Resin portfolio. We foster an interactive and supportive nationwide culture. Primary Responsibilities: · Deliver both field-based and remote scientific engagement with customers across pre- and post-sales functions, including tailored 1:1 consultation, product demonstrations, application-focused training, and assay optimization. · Develop in-depth expertise with protein filtration, purification and separation instrument hardware and software while staying current on existing assays, workflows, and emerging applications. · Effectively communicate customer perspectives and feedback to product management, fostering innovation and supporting evolving market demands. Qualifications · Master’s or PhD (preferred) in Chemistry, Immunology, Bioengineering, or related field · Field Application Scientist experience strongly preferred · 5+ years in advanced academic or industry settings · Experience in applications such as vaccines, insulin, plasma proteins, mAbs, oligonucleosides, immunomodulators, GLP-1 peptides, etc. · Strong written, verbal, public speaking, interpersonal, and organizational skills · Willing to travel 40–60% within the country Apply: send your resume to srinivas@nanomicrotech.com

Date: 8 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Discovery Services Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene’s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time 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 solving 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 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 and # of steps/month) 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 Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience Up to 5 years Skills And Capabilities Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms Candidate should be capable of solving synthetic problems independently Should be excellent in purification and analytical interpretation skills. Familiar with operations of relevant apparatus - instrument / equipment. Education M.Sc in general or organic chemistry

NanoMicro is a technology startup recognised globally for its leadership in producing spherical, monodisperse particles through proprietary manufacturing processes. These methods enable high-yield, cost-effective production across diverse industries and applications. Meeting purification needs from laboratory to manufacturing scale in both small molecule pharmaceuticals and biopharmaceuticals requires ongoing integration of advancements in chromatography and resin technology, as well as adept management of continually evolving business and scientific challenges. We deliver comprehensive purification solutions for both small molecule and biopharmaceutical sectors, including: · Small molecule therapeutics · Antibody and protein therapeutics · Peptide therapeutics · Oligonucleotide therapeutics · Vaccine discovery and development · Plasma proteins, among others NanoMicro swiftly established itself as an OEM supplier for chromatography vendors worldwide, supporting pharmaceutical and biopharmaceutical purification under various brands. The company has since introduced its own brand internationally, with a strategic focus on India, where it has made considerable market advances and successfully expanded operations within major accounts. This is perfect time a larger team dedicated to increasing market share by penetrating and ramp up volumes within all areas of biopharmaceutical purification. Opportunities at NanoMicro NanoMicro welcomes candidates from a broad range of disciplines, including sales, business development, and scientific research mainly focusing on application support and scaling up in biopharmaceutical space. Commitment to Continuous Improvement At NanoMicro, employees are encouraged to seek innovative approaches and embrace new working methods, ensuring continuous advancement for colleagues, clients, and partners. Collaborative Environment Our workplace fosters cooperation and mutual respect, with a strong emphasis on diversity and inclusivity. Professional Development NanoMicro prioritises employee growth by supporting professional development and skill enhancement, and provides opportunities throughout the organisation. We recognise that learning from setbacks is intrinsic to progress and actively encourage staff to engage in new experiences beyond conventional roles. At Nano Micro, business growth and career development are aligned as employees work to deliver effective resin solutions in all application areas. The company offers competitive pay, performance-based bonuses, and comprehensive benefits in line with startup industry standards. India Sales Leader - key responsibilities : · Develop and execute business plans to grow the Biopharmaceutical market. · Identify and manage new business opportunities. · Maintain strong relationships with customers and team members. · Work with cross-functional teams to align and implement strategies. · Monitor market trends and competitors for growth opportunities. · Represent the company at industry events to promote products. · Present business development updates and analysis to senior management for decision-making. Qualifications: · A Master's degree in Life Sciences is required; a PhD is preferred. · Demonstrated success in business development within the biopharmaceutical sector. · In-depth knowledge of both upstream and downstream workflow processes. · Exceptional communication, negotiation, and interpersonal abilities. · Capacity to work autonomously as well as collaboratively within a fast-paced and evolving environment. · Flexibility and willingness to travel as necessary to achieve business goals. Experience: 10+ years of experience with minimum of 4 years driving pan India sales team. Candidates with 5-6years can be considered for Business Manager role. To Apply: send in your resume to srinivas@nanomicrotech.com

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 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. 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 Danaher Business System which makes everything possible. The Business development Manager is responsible for District -2 -Karnataka, Tamilnadu and Kerala This position reports to the National Business Development Manager and is part of the Business Development Team located in Bengaluru and working remotely to cover District -2 -Karnataka, Tamilnadu and Kerala region. 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: if applicable for role Ability to travel – 70 % travel, overnight, within territory or locations Must have a valid driver’s license with an acceptable driving record 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 Danaher Benefits Info. 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 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.

Please call 9947350555 more details Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures. Candidate will be needed Qualification MSc chemistry MALE candidate will prefer. Determining chemical and physical properties, compositions, structures, relationships, and reactions of organic and inorganic compounds. Using chromatography, spectroscopy, and spectrophotometry techniques. Developing, improving, and customizing products, equipment, formulas, processes, and analytical methods. Conferring with scientists and engineers to analyze, interpret, and develop tests. Introducing heat, light, energy, and chemical catalysts to chemical substances to induce reactions. Writing technical papers and reports, and preparing standards and specifications for processes, tests, and products. Maintaining laboratory instruments, troubleshooting malfunctions, and purchasing new laboratory supplies. Evaluating and ensuring compliance with laboratory safety procedures and standards. Job Type: Full-time Pay: ₹16,000.00 - ₹18,000.00 per month Benefits: Food provided Health insurance Provident Fund Schedule: Day shift Education: Master's (Preferred) Language: Malayalam (Preferred) Work Location: In person

At SCIEX, our work at one of Danaher's 15 operating companies plays a vital role in saving lives. We are driven by a shared commitment to innovate for real-world impact. As a global leader in mass spectrometry, SCIEX provides cutting-edge solutions for precise detection. With a history spanning over 50 years, SCIEX has been at the forefront of developing revolutionary technologies and solutions in mass spectrometry and capillary electrophoresis. Our products empower customers to swiftly address environmental threats, gain deeper insights into disease-related biomarkers, enhance patient care in clinical settings, expedite the introduction of relevant drugs to the market, and ensure the safety and healthiness of food. Joining SCIEX means embarking on a fulfilling role that magnifies your contribution to the world and enables you to unlock the potential of life. SCIEX, a part of Danaher's 10 Life Sciences companies, collaborates to expedite the exploration, advancement, and delivery of solutions that protect and enhance human health. **Field Service Engineer** As a Field Service Engineer within the Western Service Team based in Pune, you will be reporting to the Service Manager in Mumbai. This role is completely remote. **Responsibilities** The Field Service Engineer will have the following key responsibilities: - Successfully completing assigned training tasks on designated products and duties. - Conducting top-notch installations, repairs, and maintenance on mass spectrometry instruments and managing escalation calls. - Addressing critical calls and prioritizing customer satisfaction. **Essential Requirements** The essential requirements for this position include: - A Bachelor's Degree in Engineering. - A minimum of 3 years of experience with instruments such as GC, HPLC, and Mass Spectrometer. - Profound expertise in analytical instrumentation in Service, particularly in the realm of mass spectrometry, and relevant experience in Mass Spec and HPLC. - Proficiency in computer operation and MS Office. - Proficient in English (both written and verbal). **Travel, Motor Vehicle Record & Physical/Environment Requirements:** - Willingness and ability to travel, including overnight or outstation calls on short notice, if necessary. - Capability to handle, transport, or carry equipment as needed. **Preferred Qualifications** Having prior experience in the following areas would be advantageous: - Chromatography - Mass Spectrometry Join our exceptional team today. Together, we will expedite the practical impact of future science and technology. We collaborate with customers worldwide to help them surmount their most intricate challenges by crafting solutions that bring the force of science to life. To learn more, please visit www.danaher.com. At Danaher, we cherish diversity and the presence of both similarities and differences, whether visible or not, within our workforce, workplace, and the markets we serve. Our team members, customers, and shareholders bring distinctive and diverse perspectives due to these varied attributes.,

At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Common Responsibilities: Follow the established Environment, Occupational Health, Safety and Sustainability (EHSS) practices for safe work environment and adhere to the highest standards of quality, integrity & compliance for every work activity. Complete the assigned trainings in a timely manner and comply with the training procedure & training calendar. Attend all assigned mandatory trainings related to data integrity, health, and safety measures. Compliance to Current Good Manufacturing Practices and Good Documentation Practices. Adherence to Standard Operating procedures, Operational control Procedures. Participate in & support the trainings on procedures, protocols, and On-the-Job activities. Follow the discipline of reporting structure at times of escalation. Report nonconformities & deviations to the respective supervisor(s) and/or line manager(s). Participate in & support for on-time initiation & closure of deviations, investigations, CAPA and change controls. Safety and DI Responsibilities: Adhere to organizational policies & procedures on EHSS, POSH, Data Integrity and IT security. Always wear the applicable PPEs and adhere to any other Environment, Health, and Safety (EHS) requirements in the workplace for individuals & lab/plant safety. Understand all necessary safety protocols and always follow the same to ensure safety for all. Proactively identify near-misses & potential incidents and communicate to supervisor and/or line manager or through the respective web portals. Specific Responsibilities: Maintain good aseptic behavior inside Biologics operations 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. Preparation and review of operation related documents. 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. Preparation of general Downstream related procedures, protocols, risk assessment and BMRs. 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. Preparation and periodic revision of equipment cleaning checklist (ECC)as ad when required. Execute the batch activity as per BMR and report nonconformity to the supervisor. Review of executed Documents on time. Issuance of annexures, RM, consumables and BMRs. Track the work order status and ensuring timely closure. Involve in upstream related activities under supervision of upstream supervisor.

Walk-in @ Indore We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume. *Job Location: Matoda, Ahmedabad, Gujarat. Engineering (Instrumentation / QMS / Process Equipment maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech with relevant functional experience in Calibration / Instrumentation / QMS activities QUALITY ASSURANCE QMS / Documentation / Validation and Qualification / IPQA (OSD) (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. QUALITY CONTROL (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M.Sc. (Organic Chemistry / Analytical Chemistry) B. Pharmacy / M Pharmacy MICROBIOLOGY (Officer / Senior Officer/ Executive) Experience - 02 to 07 Years Education - B.sc / M. Sc (Microbiology) Injectable Manufacturing (Executive/Senior Officer / Officer / Associate) Experience - 01 to 06 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma with relevant functional experience in injectable manufacturing/ Aseptic area operations / Visual inspection / QMS activities OSD Manufacturing (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing operations / QMS activities Time and Venue : 20th July 2025 09:30 Hrs to 18:00 Hrs ______________________________________________________ PAPAYA TREE Group of Hotels - Indore, Address: AB Road , Near Dr. Hardia Eye Clinic, Rau, Indore, MP ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. Note: Having relevant qualification only can attend the scheduled walk-in.

Job Title: Research Associate Trainee Job Location: Hyderabad/Bangalore Department : Discovery Chemistry About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Role Accountabilities Attend training on environment, health, and safety (EHS) measures. Follow environment, health, and safety (EHS) requirements always in the workplace ensuring individual and lab/plant safety 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. Ensure that the instrument / equipment is calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately. Ensure that they know the MSDS 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. Leadership Capabilities Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Specific requirements for this role Experience 0-3 Years Education MSc General/Organic Chemistry Equal Opportunity Employer .

JOB DESCRIPTION Designation: Executive Job Location : Bangalore Reporting to : Deputy Manager Job Grade : 9-I 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 BMP1 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 0-4 years of relevant practical experience in Downstream Manufacturing for biopharmaceuticals, specifically with CHO cell lines for monoclonal antibodies, fusion proteins, etc. Other competencies required for the role NA Equal Opportunity Employer NA Pls visit us at https://syngeneintl. com/ to know more about us and what we do.

Job description Horizon Biolabs Pvt Ltd. is a Pharmaceutical Analytical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices Industries . We are Looking for candidates with BSc/MSc/Bpharm/Mpharm and having 3-5 years of experience in Quality Control environment to conduct daily analysis activities involving Wet lab, HPLC and Gas Chromatography (GC) systems . Analyse various raw materials/Finished Pharma products and substances using a range of analytical instrumentation and techniques such as high-performance liquid chromatography (HPLC), gas chromatography (GC) and electrochromatography. Record data and interpret findings to produce scientific reports of results, making sure that everything complies with guidelines. Exposure to Analytical Methos Validation and Analytical Methos Development of HPLC/GC-based methods desirable. Exposure with Protocol and AMV Report preparations desirable. HPLC,SOR,IR Water content and stability. Timely execution of assigned responsibilities. Job Type: Full-time Pay: ₹16000.00-18000.00 per month Benefits: Provident Fund Schedule: Day shift Application Question(s): Immediate Joiner Education: Bachelor's (Preferred) Experience: total work: 2-3 years (Required) Location: Hyderabad, Telangana (Required) Job Type: Full-time Pay: ₹20000.00 - ₹25,000.00 per month Benefits: Provident Fund Schedule: Day shift Candidates from Hyderabad only Work Location: In person Application Deadline: 15/04/2025 Job Type: Full-time Pay: ₹18,000.00 - ₹20,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Are you from Hyderabad?Having min.exp.of 2 years in HPLC,GC tests,are immediate joiner?(7-10 days) Location: Hyderabad, Telangana (Required) Work Location: In person Application Deadline: 05/07/2025 Expected Start Date: 14/07/2025

Job description Horizon Biolabs Pvt Ltd. is a Pharmaceutical Analytical Testing Laboratory located in Hyderabad , India . We are industry-leading global provider of laboratory testing services in Chemical and Microbiological segments across the pharmaceutical , Biotech , medical devices Industries . We are Looking for candidates with BSc/MSc/Bpharm/Mpharm and having 3-5 years of experience in Quality Control environment to conduct daily analysis activities involving Wet lab, HPLC and Gas Chromatography (GC) systems . Analyse various raw materials/Finished Pharma products and substances using a range of analytical instrumentation and techniques such as high-performance liquid chromatography (HPLC), gas chromatography (GC) and electrochromatography. Record data and interpret findings to produce scientific reports of results, making sure that everything complies with guidelines. Exposure to Analytical Methos Validation and Analytical Methos Development of HPLC/GC-based methods desirable. Exposure with Protocol and AMV Report preparations desirable. HPLC,SOR,IR Water content and stability. Timely execution of assigned responsibilities. Job Type: Full-time Pay: ₹16000.00-18000.00 per month Benefits: Provident Fund Schedule: Day shift Application Question(s): Immediate Joiner Education: Bachelor's (Preferred) Experience: total work: 2-3 years (Required) Location: Hyderabad, Telangana (Required) Job Type: Full-time Pay: ₹20000.00 - ₹25,000.00 per month Benefits: Provident Fund Schedule: Day shift Candidates from Hyderabad only Work Location: In person Application Deadline: 15/04/2025 Job Type: Full-time Pay: ₹18,000.00 - ₹20,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Hyderabad, Telangana: Reliably commute or planning to relocate before starting work (Preferred) Application Question(s): Are you from Hyderabad?Having min.exp.of 2 years in HPLC,GC tests,are immediate joiner?(7-10 days) Location: Hyderabad, Telangana (Required) Work Location: In person Application Deadline: 05/07/2025 Expected Start Date: 14/07/2025

🔯 Position:- CHEMICAL LAB OFFICER 🔯 Location:- SARIGRAM 🔯 Salary:- UPTO 40K 🔯 Experience:- 3-5 YEARS 🔯 Qualification:- MSc chemistry organic, inorganic, analytical chemistry Required Skills :- Wet analysis Titration of inorganic materials, acid base, complexometric titration, balancing of equations, basic concepts of chemistry; instrument calibration, creative, innovative and out of the box thinking. Making standard solutions. Maintaining Raw and Rough lab registers and note books. Experience in carrying out instrumental method of analysis, like Flame photometry, refractive index, Gas Liquid chromatography ( GLC). Creating COA, specification, CAPA Should have experience in QA and SOP, making BMR Should have good background of GLP/GMP and maintaining good documentation. Handling e-mail communication, inter and intra departmental interaction and knowledge of Microsoft tools like, word, excel and PPT mandatory. A flexible mind set of multitasking is an advantage. Skills: instrument calibration,wet analysis,making standard solutions,capa,titration,qa and sop,gas liquid chromatography,glp/gmp,refractive index,titration of inorganic materials

Key Responsibilities: • Perform qualitative and quantitative analysis of fragrance samples using GC and GC-MS techniques. • Interpret chromatograms and identify volatile compounds using spectral libraries and retention indices. • Support fragrance development and quality control by providing analytical data and reports. • Maintain and troubleshoot GC instruments (Agilent/PerkinElmer/other systems) and related equipment. • Prepare samples and maintain sample logs, reference standards, and calibration data. • Work closely with perfumers, evaluators, and R&D teams to support innovation and quality initiatives. • Ensure all laboratory practices comply with internal SOPs, industry standards, and safety guidelines. • Document results accurately in lab notebooks and digital systems; prepare technical reports and presentations as required. Qualifications: • Bachelor’s or Master’s degree in Chemistry, Analytical Chemistry, or related field. • 2–5 years of hands-on experience in Gas Chromatography, preferably in fragrance, essential oils, or related industries. • Knowledge of GC-MS, method development, and compound identification techniques. • Proficiency in chromatographic software. • Strong analytical thinking, problem-solving, and communication skills. • Attention to detail with the ability to work independently and collaboratively. Preferred Qualifications: • Experience in the fragrance or flavor industry. • Familiarity with international fragrance regulations and quality standards (e.g., IFRA, ISO). • Basic knowledge of olfactory science or interest in perfumery.

Responsibilities: * Collaborate with cross-functional teams on project delivery. * Conduct research analysis using chromatography techniques. * Prepare protein purifications and demonstrate products. Annual bonus

Date: 10 Jul 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Manufacturing Services Job Description Designation: Executive Job Location: Bangalore Reporting to: Deputy Manager Job Grade: 9-I 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 BMP1 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 µ 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 0-4 years of relevant practical experience in Downstream Manufacturing for biopharmaceuticals, specifically with CHO cell lines for monoclonal antibodies, fusion proteins, etc. Other Competencies Required For The Role NA Equal Opportunity Employer NA Pls visit us at https://syngeneintl.com/ to know more about us and what we do.

JOB DESCRIPTION Job Title: Research Associate Trainee Job Location: Hyderabad/Bangalore Department : Discovery Chemistry About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Role Accountabilities Attend training on environment, health, and safety (EHS) measures. Follow environment, health, and safety (EHS) requirements always in the workplace ensuring individual and lab/plant safety 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. Ensure that the instrument / equipment is calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately. Ensure that they know the MSDS 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. Leadership Capabilities Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Specific requirements for this role Experience - 0-3 Years Education - MSc General/Organic Chemistry Equal Opportunity Employer .

Core Purpose of the Role: Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant notebooks. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner. Role Accountabilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment s 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. Ensure that the instrument / equipment is calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately Ensure that they know the MSDS 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

JD FOR OLIGO PRD Designation : Purification Scientist Job Location: Bangalore Department : Chemical Development - Oligonucleotide About Syngene At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards always Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Job Purpose: The key objective of the role is to support the oligonucleotide development activity in a PRD facility at Syngene. The candidate is expected to generate engineering data in the laboratory and provide technical inputs and hands on support to ongoing projects, based on thorough literature information or evaluation of available experimental data. Having good knowledge in the documentation like, Technology transfer document, risk assessment, and Investigation report. Knowledge of optimization and scale-up of anion exchange chromatography and ultrafiltration is essential. Support for the manufacturing activity. Having previous oligonucleotide/peptide synthesis knowledge is a plus. Key Responsibilities: Purification of MAbs, Peptides, Oligonucleotide and ADCs Experience with AKTA Systems: AKTA Pure, AKTA Pilot, and AKTA Bioprocess, AKTA Process & also worked with Continuous Chromatography. Support R&D for the development of the processes feasible to execute at the manufacturing facility. Perform a chromatography and ultrafiltration processes for the development activity. Maintain the raw material inventory and instrument spare part inventory. Interpretation and compilation of analytical data. Follow environment, health, and safety (EHS) requirements always in the workplace ensuring individual and lab/plant safety. Support manufacturing team at all stages of the execution of Oligonucleotide batches, this involves Synthesis, C & D process, Chromatography, Ultrafiltration, lyophilization and other daily activities. Follow up with Cross functional teams to complete the activities. Adhere to the Safety, Quality, Data Integrity norms as per policy. Prepare project related documents like, Process development report, Technology Transfer Document and weekly updates. Educational Qualification: M. Sc. , Biochemistry/Chemistry Technical/functional Skills: Experience in working in a Peptide/Oligonucleotide/ Biological upstream/downstream laboratory. Experience in setting up experiments and generate data suitable for technology transfer and execution at large scale. Experience in handling the automated instruments. Basic understanding of organic chemistry reaction principles. Basic understanding and knowledge on ion exchange chromatography, column purification and membrane filtration. Experience: 5-8 years post qualification Behavioural Skills: Should have the capability to work in a team and ability to handle demonstrate a good team spirit. While possessing a good ability to follow instruction should also demonstrate innovative in his/her approach, good communication skills. Should be proactive while working on allotted responsibility. Flexibility to work on shifts and staggered weekends depending on work responsibility. Equal Opportunity Employer: .

Designation: AQA Reviewer Job Location: Bangalore Department: Analytical Quality Assurance About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scienti fi c services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scienti fi c problems, improve R&D productivity, speed up time to market and lower the cost of innovation . Key Responsibilities: Review of analytical raw data (through ELN / manual) generated by analyst, protocols/ reports pertaining to the section as per the standard operating procedure and speci fi cation. Ensuring, verifying, and reviewing the instrument usage log periodically and accordingly checking the labels as per SOP. Review of Outsourced analytical report. Review of logbooks with respect to all activity performed in the lab. Responsible for taking any other job allocated by Department Head / Department In charge. Review of technical data in analytical document viz. Calculations, Chromatograms, method parameters, integration, logbook entries, WS/RS and Column usage records, method parameters, reconciliation, vendor COA and other technical data in analytical document. Responsible to ensure review and release of raw material and packing material in LIMS/SAP. Responsible to ensure review and release of cleaning samples, inprocess samples, calibration reports and standard qualification reports. Reviewer shall ensure the documents physically for availability of all the pages of ODS and supporting documents. Review the documents for completeness, compliance to good documentation practices, test results against specification limits or acceptance criteria as mentioned in protocol and reconciliation of forms issued as applicable Review of all the tests as specified in the specification/Request for analysis /validation protocol/sampling protocol have been carried out Review of all supporting documents like chromatograms, balance print outs, Instrument printouts are enclosed in sequential manner to the parent report with signature as applicable Review of the test results in COA against specification along with other relevant sample information before approval. In case of any discrepancy, immediately notify to the reporting manager or his designee or Head or designee GMP Analytical Laboratory. Ensuring of conducting regular GMP rounds at Quality Control Laboratory. Involving in the Laboratory incident investigation, review, and approval. Educational Quali fi cation: M. Sc (Life science / Chemistry)/ M. Pharm Technical/functional Skills: Good exposure in Enterprise Applications like SAP, Learning Management Systems, Trackwise, and Analytical laboratory Applications like Chromatography and Non-chromatography data Management. Well versed in electronic data audit review. Good Knowledge on handling the application software. Establish good Interpersonal skills with cross-functional teams. Experience: 9 to 12 Years experience in life science industry. Behavioural Skills: Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team. Good speaking-listening-writing skills, attention to details, proactive self-starter. Ability to work successfully in a dynamic, ambiguous environment. Ability to meet tight deadlines and prioritize workloads. Ability to develop new ideas and creative solutions. Should be able to work in team and flexible for working in shifts. Should be a focused employee. Equal Opportunity Employer: .

Job Summary We are seeking a highly skilled Analytical Scientist to join our Research and Development team. The successful candidate will be responsible for developing, validating, and implementing analytical methods for the quantification and identification of genotoxic impurities in pharmaceutical products. This role will involve extensive use of chromatography techniques and adherence to regulatory standards. The ideal candidate should have a strong background in analytical chemistry, method development, and data analysis, with a keen eye for detail and a commitment to ensuring the highest quality standards. Roles & Responsibilities You will be responsible to review relevant Literature and stay updated with the latest research and scientific literature relevant to the field of genotoxic impurities and chromatography methods. You will be responsible to develop and optimize chromatography-based methods for accurately quantifying genotoxic impurities in various samples. You will be responsible to address regulatory deficiency queries concerning the analytical methods and data related to genotoxic impurities. You will be responsible to ensure the quality and accuracy of reference standards and working standards used in analytical testing and method development. You will be responsible to develop analytical methods, conduct validation studies to ensure the accuracy and reliability of the methods, and transfer validated methods to the Quality Control (QC) department. You will be responsible to prepare comprehensive reports documenting method development, validation results, and any forced degradation studies performed. You will be responsible to conduct forced degradation studies to identify potential impurities and establish their chemical nature and behaviour. You will be responsible to perform real-time analysis of samples during product development stages to ensure product quality and consistency. You will be responsible for compilation of Stability Data to assess the stability profile of the products under various conditions. You will be responsible to evaluate the effectiveness of the product development strategy and identify any cross-functional issues affecting the process. You will be responsible to identify and plan for the developmental needs of the product, considering factors such as scale-up and potential process improvements. You will be responsible to source and manage the procurement of necessary chemicals, solvents, columns, and other laboratory equipment. You will be responsible to ensure proper maintenance of laboratory equipment as per Good Laboratory Practices (GLP) standards to guarantee accurate and reliable results. You will be responsible to calibrate instruments as per the calibration schedule and strictly follow Standard Operating Procedures (SOPs) to maintain consistency and accuracy. You will be responsible to maintain a clean and organized work area, and ensure that the laboratory environment is controlled at the required temperature for optimal analytical conditions. You will be responsible to keep all relevant documents well-maintained and organized for easy access and compliance with internal and external auditing requirements. Qualification Educational qualification: Masters in Science/ Organic chemistry Minimum work experience: 5 years of experience in analytical method development Skills & attributes: Technical Skills Have work experience on Process scale up of Active Pharmaceutical Ingredients. Experience in Process Optimization (Manufacturing) Experience in the development and regular analysis in Wet analysis-IR, Ultra Violet, Moisture analysis, Chromatographic techniques Strong understanding of regulatory guidelines and industry standards related to pharmaceutical product development and analysis. Proven experience in method validation and documentation in compliance with regulatory requirements. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/