567 Chromatography Jobs - Page 21

Job Overview JOB DESCRIPTION As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Preferred Candidate Profile Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Experience: Minimum 2 Yrs in peptides production Qualifications Masters/Bachelors degree in Chemistry or a related field. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Show more Show less

Job type Full-time Shift and schedule General shift -Sunday off Location Trichy-Tamil Nadu Summary TNB Analytical Laboratory is currently recruiting for a Laboratory Junior chemist for Pharma Testing services. TNBL Testing Lab provides complete testing services for all types of food,water and pharmaceutical products and other environmental aspects under one roof. We have fulfilled all the requisites to offer a complete testing service to our clients. It is an independent testing body dedicated to provide the highest quality analytical data that meet the needs of our clients and are dependable, ethical, and accurate. We are committed to ensure accurate and timely services for testing activities, and continuously meet or exceed the stated and or implied expectations of our customers. Our testing services cover multiple chemical, microbiological, physical and sensory examinations to analyze the safety and/or quality of samples being tested. Our scientists have comprehensive skills in the fields of analytical chemistry, microbiology and chromatography. Essential Job Functions ● Performs laboratory analytical test procedures on assigned Tablets,syrup,capsules and raw material samples in accordance with Indian Pharmacopoeia guidelines.. ● Prepare samples for analytical testing as stated in Standard Operation Procedures. ● Prepares, maintains, and disposes of various chemical standards, solvents and reagents, test solutions ● Calibrate and perform preventive maintenance on laboratory equipment and instrumentation as required by manufacturer specifications. ● Assists in the preparation and maintenance of all laboratory reports, logs and records on analytical results and quality control. ● Maintains laboratory equipment and supplies. ● Adhere to safety procedures in accordance with laboratory and chemical plans. ● Performs other related job duties as assigned. Qualifications, Knowledge, Skills, and Abilities Education and Experience: Bachelor's/Master degree in Pharmacy/M.Sc Chemistry 1 to 3 years of experience in a similar role, preferably in the chemical or pharmaceutical industry Special requirements Candidates must have sound knowledge in HPLC ,UV, DISSOLUTION, DISINTEGRATION APPARATUS,KF TITRATOR. Preferably candidates with NABL awareness are mostly likely to be hired. Salary As per industrial standards based on experience Contact us TNB Analytical Laboratory Pvt Ltd, 2/3,North Throwpathi Amman Kovil street, Puthur,TRICHY-620017 Tamil Nadu Contact No: 9025533868 Mail @:-tnbanalytical@gmail.com Job Type: Full-time Pay: ₹8,000.00 - ₹10,000.00 per month Experience: total work: 1 year (Preferred) Work Location: In person Expected Start Date: 02/06/2025

Job Title: QC Executive – GC Machine Operator Company: Pharmaceuticals Industry Location: Ahmedabad, Gujarat Job Type: Full-time Salary: ₹5,00,000 – ₹7,00,000 per year Experience: 4–7 years (Required) Job Description We are hiring a Quality Control (QC) Executive – GC Machine Operator for our OSD (Oral Solid Dosage) pharmaceutical manufacturing unit. The ideal candidate will have extensive experience in Gas Chromatography (GC) operations within a regulated pharma environment. Key Responsibilities Conduct GC analysis on raw materials, in-process samples, and finished products. Ensure compliance with cGMP , GLP , and other regulatory requirements. Operate, calibrate, and maintain GC instruments (Agilent/Waters or similar). Prepare and review analytical test reports and documentation. Assist during regulatory inspections (e.g., USFDA, WHO, MHRA). Qualifications B.Sc / M.Sc in Chemistry or B.Pharm / M.Pharm 4–7 years of hands-on GC experience in the pharmaceutical industry Familiar with quality standards and regulatory guidelines Good documentation practices and attention to detail With Regards, Himani(HR) 9377165778 Job Types: Full-time, Permanent Pay: ₹500,000.00 - ₹700,000.00 per year Work Location: In person

Job Overview JOB DESCRIPTION As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Preferred Candidate Profile Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Experience: Minimum 2 yrs in peptides manufacturing Qualifications Masters/Bachelors degree in Chemistry or a related field. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office About Team: Antibody team The antibody team is involved in engineering and development of antibodies, with a deep focus on reagent quality and specificity. The core activities of the team include design, development, purification, conjugation, and testing of antibodies in a variety of immunoassay applications using groundbreaking tools and technologies. The goal of the program is advanced product development and creation of product-specific information to promote research use. Role: To be an integral part of an antibody development team with a focus on performance and specificity using innovative molecular, protein, biochemical, and cell biology methods. Responsibilities: Meticulous experimental planning and execution to meet program goals. Timely record keeping of results into data sheets and laboratory notebooks. Regular mining of literature and keeping oneself up to date with developments in the field. Compilation and presentation of data in written and oral formats. Active participation in team meetings with attention to detail and adherence to schedules. Strong theoretical and proven understanding of protein and antibody conjugation chemistries. Hands-on experience in performing protein or antibody conjugations to dyes, labels, or reporter tags. Experience with the development of new conjugation protocols and the design of site-specific conjugation strategies is desirable. Experience and knowledge in protein purification and analysis technologies such as affinity or ion exchange chromatography, SEC, HPLC, and SDS-PAGE. Experience or familiarity with antibody or protein engineering, rational design of mutants, and molecular biology. Experience with structural biology and protein modeling and visualization tools such as Pymol, Shrodinger, Discovery Studio or other similar programs is desirable. Theoretical or practical experience in antibody development platforms is desirable. Proficient in MS Office applications such as Word, PowerPoint, Excel, and possess a strong statistical knowledge and familiarity with statistical software such as Prism. Seeking self-motivated candidate who excels in learning and applying new concepts for process or product improvements. Must have strong interpersonal skills to connect with peers and leadership. Show more Show less

Job Family: Plant Engineering Sub Job Family: Operation, Repair & Maintenance Preferred type of working: On-Premise Years of Experience: 6 - 12 Business unit: Biologics City- Hyderabad TM - Plant Engineering DS I&A Summary: Experienced Team member to handle Instrumentation & Automation (I&A) function in Drug Substance manufacturing plant. This role plays a critical part in ensuring the smooth operation, efficiency, and regulatory compliance of our biopharmaceutical manufacturing processes. To join a team of technicians responsible for maintaining, troubleshooting, and optimizing a complex network of instrumentation and automation systems. Responsibilities: Implement strategies for the preventative maintenance of all I&A equipment within the Drug Substance manufacturing area. Perform qualification of I&A equipment according to cGMP and regulatory requirements. Troubleshoot and resolve I&A system malfunctions, ensuring minimal disruption to production timelines. Work collaboratively with other engineering personnel, production teams and quality assurance to identify opportunities for process optimization through automation. Stay current on advancements in I&A technology relevant to biopharmaceutical manufacturing. Manage and maintain technical documentation for all I&A systems. Prepare and participate in audits and inspections related to I&A systems. Ensure adherence to all safety regulations and procedures within the manufacturing plant. Qualifications Bachelor's degree in Engineering (in instrumentation/electronics & communication/ electrical/Computer Science) or a related field. Minimum 5 years of experience in a biopharmaceutical or similar aseptic manufacturing environment with a focus on I&A. Proven experience in a technical environment. Strong understanding of cGMP regulations and GAMP® 5 guidelines. In-depth knowledge of biopharmaceutical manufacturing processes and equipment. Experience with common biopharmaceutical manufacturing automation systems (e.g., DCS, SCADA, PLC). Troubleshooting and problem-solving skills. Strong communication, interpersonal, and collaboration skills. Ability to prioritize and handle multiple tasks in a fast-paced environment. TM - Plant Engineering - DS Mechanical Job Description Maintenance and repair of a wide range of biopharmaceutical DS processing equipment, including: Bioreactors Fermentation tanks Tangential Flow Filtration (TFF) systems Chromatography columns Purification skids Aseptic processing equipment Develop and implement preventive maintenance programs to ensure optimal equipment uptime and performance. Troubleshoot equipment malfunctions, diagnose root causes, and implement corrective actions. Manage spare parts inventory and ensure timely procurement of critical materials. Ensure the completion of work orders and ensure adherence to established maintenance procedures and cGMP regulations. Contribute to continuous improvement initiatives by identifying opportunities for equipment optimization and process efficiency. Prepare and maintain detailed maintenance documentation, including logs, reports and procedures. Interface with other departments (e.g., Production, Quality Assurance) to ensure effective communication and collaboration. Training and development of other team members. Ensure a safe work environment for the team by enforcing safety protocols and conducting regular safety training. Qualifications Bachelor's degree in Mechanical Engineering or a related field. Minimum 5+ years of experience in a biopharmaceutical or aseptic manufacturing environment. In-depth knowledge of biopharmaceutical processing equipment and cGMP regulations. Strong understanding of preventive maintenance practices and troubleshooting techniques. Excellent communication, interpersonal, and problem-solving skills. Ability to prioritize tasks, and meet deadlines. Working knowledge of computerized maintenance management systems. Send CV - shrikantsg@drreddys.com Put subject as role above. Show more Show less

Job Description Designation : HPLC Trainee Section : Training Qualification : Ph. D./ M. Tech./ M. Sc./ B. Tech./ B. Sc. Experience : Fresher Employment Type : Short Term / Long Term Location : Gurugram, Haryana Description High-Performance Liquid Chromatography (HPLC) is a widely used analytical technique for separating, identifying, and quantifying components in a mixture. Utilizing high pressure to force a liquid mobile phase through a stationary phase, HPLC effectively separates compounds based on their interactions with both phases. This method is highly versatile, allowing for the analysis of a wide range of substances, including pharmaceuticals, food additives, and environmental samples. HPLC is renowned for its speed, precision, and sensitivity, making it an essential tool in laboratories for quality control, research, and development across various industries. FARE Labs conducts a specialized training on High-Performance Liquid Chromatography (HPLC) tailored for various sample matrices following national/ international standard methodology. This training is aimed at laboratory professionals, researchers, and students interested in analyzing food additives such as antioxidants, synthetic colors, preservatives, artificial sweeteners etc. Objectives Provide a solid understanding of HPLC principles and applications in food safety. Equip trainees with practical skills for operating HPLC systems. Discuss the analysis of specific food additives using HPLC. Familiarize attendees with data analysis and interpretation techniques. What is to learn? Introduction to HPLC Overview of chromatography principles and HPLC components (pumps, injectors, columns, detectors) Instrumentation Pumps: Isocratic vs. gradient systems Injectors: Manual vs. automatic Columns: Selection criteria for food analysis Detectors: UV-Vis, fluorescence, ELSD, and mass spectrometry HPLC Method Development for Food Additives Identification And Quantification Of Various Target Analytes Such As Antioxidants: TBHQ, BHT, BHA etc. Synthetic Colours: eight permitted synthetic colours, banned colours Preservatives: benzoates, sorbates etc. Artificial Sweeteners: Aspartame, saccharin etc. Practical Applications Hands-On Training Instrument setup and calibration for food analysis Preparation and analysis of more than 500 samples of various matrices Running HPLC methods for food additives Data Analysis Understanding chromatograms and quantification methods Software tools for data processing and reporting Troubleshooting Common Issues Resolving baseline noise, peak tailing, and fronting Preventive maintenance tips for HPLC systems Responsibility Adherence to Safety Protocols: Strictly follow all laboratory safety guidelines and protocols to prevent accidents and ensure the well-being of all participants. Active Participation: Engage actively in all training sessions, discussions, and practical exercises. Complete all assigned tasks and projects on time. Respect for Equipment and Facilities: Handle all laboratory equipment and materials with care. Report any damages or malfunctions to the instructor immediately. Collaboration and Teamwork: Work collaboratively with fellow participants, sharing knowledge and supporting each other’s learning. Integrity and Accuracy: Maintain a high standard of integrity in all testing procedures and documentation. Ensure that all results are accurate and reliable. Requirements - Skills, Knowledge And Abilities Commitment to the Program: Participants must demonstrate a commitment to the training program by attending all scheduled sessions, completing all assignments, and actively participating in practical exercises. A signed commitment agreement may be required before the start of the program. Health and Safety Compliance: Participants must comply with health and safety regulations, including wearing appropriate personal protective equipment (PPE) and adhering to all safety protocols. A medical clearance or proof of immunizations may be required for certain training programs. Get in Touch Email at trainings@farelabs.com Show more Show less

Role & responsibilities Downstream process executives & operators Preferred candidate profile should have experience in chromatography ,column packing(BPG and Chromoflow) TFF , centrifuge system, filtration

Company Description Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. " Job Description Job Summary Roles & Responsibilities: Hands on experience of Overall Asset care for Process equipment to take care of the total process equipment health of the plant. For OSD/Encapsulation/Ointment/Liquid/QC OSD: Quadro sifter, ROMACO & FETTE Compression, GFB pro 30, GLATT & ACG Tablet coater, ACG Blister packing machine, IMA Bottle packing machine, JACKSON online conveyor/ Bulk2D, etc. Encapsulation: GIC Engineering Inc, Gelatin mass holding vessel, Romaco Blister machine, KOCH Wallet machine, etc. Liquid Area: Liquid filling machine, Capping machine, Induction cap sealing. Responsible for the Overall Asset care (Electrical / Instrumentation of all process and packing equipment) Ensure that Current Good Manufacturing Practices (cGMP), ATAR (All time audit readiness) checklist, regulatory requirements are being adhered to are being adhered to the Maintenance of Process equipment & other related machinery Ensure that all the safe practices as per SHE process, and protocols are adhered to while working Hands on skill of trouble shooting of all equipment in the above sections for OSD/Encapsulation/Ointment Responsible for identification and closure of all abnormalities in his area of work Co-ordinate with internal customers for routine maintenance issues by providing feedback to the Engineering Head from time to time Responsible for Planning and execution of Preventive Maintenance Program (PMP) for all Process equipment as per schedule Co-ordination with internal and external vendors for Break-down maintenance, routine maintenance issues Hands on experience on breakdown maintenance and followed by root cause analysis (RCA) for every major breakdown of the equipment by identifying and implementing the action plan Execution of all the assigned action plan CAPA (Engineering, QA & Safety) Preparation and review of engineering-based URS, SOP’s, SOI’s, PMP’s , CAPEX and revisions of the same Commissioning FAT, Commissioning and followed by complete Qualification as per procedure Ensure that all the required spares, critical tools and spares are maintained for the process equipment so as to ensure continuous operation & reduce downtime verify all concerned daily log books and ensure documentation is online. Operational knowledge of TPM. Ability to create Equipment Tree, develop Autonomous Maintenance and Preventive Maintenance standards, deeply in understanding of problem statement, RCA and CAPA Hands on experience on various PLC’s (Siemens, Rockwell, Schneider, etc.) Hands on experience on SCADA & HMI (WIN CC Explorer 7.4, 7.5, FT View, IFIX) QC: Fume exhausting unit, Walk in Stability Chamber, High performance liquid chromatography, Verticle Auto clave etc. Qualifications Educational qualification: Diploma in Engineering or Bachelor's Degree in Engineering (Electrical / Instrumentation) Additional preference:: JH & TPM knowledge. Minimum work experience: 3-6 years of experience in the pharmaceutical industry with a focus on maintenance and engineering. Preferable Exp, FMCG with strong TPM background. Skills & attributes Technical Skills Prior experience in maintenance and engineering roles preferred. Good understating on Pharmaceutical Manufacturing and Packing operation Strong understanding & experience in preventive maintenance practices, procedures & engineering solutions. Understanding of Good Engineering Practices. Understanding of relevant regulatory standards. Proficiency in SAP or similar maintenance management systems. Technical knowledge in Facility and Plant Engineering, infrastructure building, contractor management. Knowledge of regulatory requirements, including Good Laboratory Practices, GMP and cGMP standards. Ability to understand the specific requirements of Process team / Delivery teams Behavioral skills: Attention to detail and strong organizational skills. Experience in Engineering, Vendor management, Contractor management and safety requirements. Ability to work collaboratively in a cross-functional team environment. Excellent communication and interpersonal skills. Delivery-oriented mind-set. Behavioural skills: Proactive approach to identifying and solving challenges Collaboration with cross-functional teams, promoting a cooperative and inclusive work environment. Efficient time management to meet production schedules and deadlines without compromising quality. Effective communication and training skills for user departments and service providers. Show more Show less

Job Overview JOB DESCRIPTION As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Preferred Candidate Profile Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Qualifications Masters/Bachelors degree in Chemistry or a related field. About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Show more Show less

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. We are currently seeking a Account Manager who will be responsible to maintain and manage South India territory by meeting and exceeding sales and unit goals. Provide sales and technical support to customers on a regular and ongoing basis. What we’ll get you doing: Originate phone calls, respond to incoming calls, outgoing calls, visiting customers and provide technical information to customers with regards to chromatography related products and services. Monthly and Weekly plan for customer visits to provide technical information, product demonstration and/or technical seminar. Attend local vendor shows and company sponsored trade shows Manage the performance of existing Channel partners and develop strategies to improve their sales and revenue of the assigned territory related accounts. Conduct on-site product demonstrations and/or technical seminars. Develop relationships with new and existing customers. Manage and maintain information in customer database system (MSCRM) Perform other job-related duties as requested by customers and management. Building referral and lead generation networks, addressing client concerns and handling calls that require manager involvement. Willingness for travelling in around respective territory up to 90% (outside), 10% (Inside) The essential requirements of the role include: Master’s degree or Ph. D., in any Life Science required. Minimum Five (5) years of experience in Sales and having Chromatography experience Having Experience of managing and driving Channel partners of the products related to life sciences. Very good interpersonal skills as well as listening and communication skills. Motivation and desire to be successful with a “can do” approach, maintaining a positive attitude, being a Team player, striving to learn and to contribute to company culture Must be able to present clearly and to large groups, i.e., seminars and trainings. It would be a plus if you also possess previous experience in: Ability to work in cross-functional teams and matrices. Laboratory with Hands on experience in chromatography using HPLC 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. Show more Show less

Beckman Coulter LS Beckman Coulter Life Sciences’ mission is to empower those seeking answers to life’s most important scientific and healthcare questions. With a legacy spanning 80+ years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900 associates across 130 countries, you’ll help drive our vision of accelerating answers—and our commitment to excellence. Beckman Coulter Life Sciences is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This role will be an On-site role at our Beckman Coulter Life Science, Bangalore Development Center (BDC) manufacturing facility located in Bengaluru. Do you want to work in Manufacturing Operations Team? Do you enjoy working in a dynamic work force, collaborating with other team members and diverse groups, to meet Organization goal and customer demand? Then read on! We are currently seeking a "Polymer Chemist I" position in Production-Operations who will be primarily responsible for polymer dye synthesis and related manufacturing processes. The company is compliant with ISO 9001: 2015, ISO 13485: 2016 & EN ISO 13485: 2016, MDSAP and Beckman Coulter corporate Quality system requirements. In this role, you will be responsible for: Handing metal catalyst reactions. Performing and optimization of C-N and C-C coupling reactions. Experience in handling air/moisture sensitive reagents and performing of reactions at the temperature range of -78ºC to higher temperatures. Perform purification of the organic compounds using different types of column chromatography techniques and other separation techniques. Responsible for organic synthesis of fluorescent dyes suitable for Flow Cytometry applications. The required qualifications for the job include: M.Sc. in Chemistry/Organic Chemistry/Biochemistry or related discipline. Experience: 3-5 years Demonstrate ability to be flexible and resourceful. Ability to work in a team environment & Excellent communication skill. It would be a plus if you also possess previous experience in: Having polymer chemistry and Conjugation chemistry knowledge with good Hands-on experience on HPLC/UPLC/GPC/TFF/Spectrophotometer/Fluorimeter and Automated purification system. This job is eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical insurance to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law 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. Show more Show less

Work Schedule Standard (Mon-Fri) Environmental Conditions Office About company: Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving sophisticated analytical challenges, delivering efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global teams of more than 100,000 colleagues delivers an outstanding combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com About team: Providing outstanding product development services to Thermo Fisher scientific global business units, is one of the essential functions of the India Engineering Center (IEC). This global research and development center, established in 2009, located at HiTech City, Hyderabad, with over 150 employees. We are a team committed to develop innovative and groundbreaking technologically sophisticated products ranging from laboratory equipment, analytical instruments, remote monitoring solutions, chromatography and mass spectrometry. We are proud of the work that we do at IEC thereby fulfilling our mission of making the world a healthier, cleaner, and safer place: About the Job: Ideal candidate will help bring ownership for a design de-risking of PCBA which may need refresh driven by aging design or supply chain issues. In this position, candidate will work closely with global sites to ensure that Change Management within this portfolio achieves a maturity. Will ensure right design metrics are followed. Role Purpose Summary: The Hardware Engineer III is a professional level member of a global R&D Team. The role is of a hands-on Electrical/Electronic engineer who is motivated & technically competent of the new product design and update of existing products. The person will play key role in demonstrating engineering knowledge to assist team in its PCBA Risk Mitigation strategy. Job Title: Engineer II, Electrical Hardware Roles & Responsibilities: As part of a multi-functional development team, major responsibility will include driving PCBA Risk mitigation strategy and execution of projects for Electronics commodities on product level. Responsible for technical delivery of all Electrical & Electronics related projects. Design and conceptualise to ensure the technical quality of actions. Own & Implement technically sophisticated projects right from scoping to implementation Should have good knowledge on the compliance requirement & should support product regulatory compliance testing. Proficient to synthesise specifications of electronic components into product fitment. Work with cross function team to understand customer requirement, participate in system / subsystem design review, finalize electronics design requirement by reviewing with systems & global engineering teams Design schematic of digital, mix signal & power electronics circuit board that satisfied the design requirement Agility to work on multiple simultaneous projects, tasks & programs to suit business needs Provide Plan A, Plan B. Drive design options & tradeoff analysis meeting diverse product requirements. Build the design documents for design review (HLD, DFMEA, requirements traceability matrix etc.), and verification plan mapping to the key performance & reliability requirement. Verify the design performance qualifying requirements, meeting Manufacturability and Serviceability, and achieve the cost/reliability target. Collaborate closely with multi-domain teams assisting product development meeting regulatory, safety, environmental, reliability, thermal and interface standard (Ethernet, USB, etc.) compliance requirements. To work with the sourcing team and the supplier to coordinate the manufacturing and provide detailed requirement for FCT of PCBA to make sure the PCBA from production line can meet design requirement. Skills and Proficiencies: Excellent understanding of Electrical and Electronics Engineering fundamentals Ability to drive decision through design and simulation tools. Mentor different tools and intent with hands-on experience Can conceptualize design architectures & identify challenges in designs. Applies self-learning to derive component functioning Independently conceptualize and run design calculations to prove design Collaborate & drive concepts, trade off analysis and leads component selection to meet the technical specifications Actively contribute to design analysis and simulation ensuring design optimization and confirmation to requirements Conduct testing as per test plans (including functional and regulatory test cases). Record test results Capture Schematic based on design document and input. Build design documents & artifacts as per design process Ability to efficiently work on the below tasks with mentorship Preferred Qualifications: Bachelor’s degree in Electrical / Electronic Engineering with proven track of over 6 years Knowledge of any Circuit design and Simulation tools. Handle Low to medium complexity projects independently with ability to provide mentorship to early talent. Build work breakdown structure (WBS) of projects with support from senior project managers Engage with project multi-functional teams for reviews to seek inputs under the guidance of Program & design managers Desirable: Acquaintance in Project Management C/C++ Embedded Programming Basic understanding of FPGA based Design and programming using HDL Show more Show less

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. " Job Description Job Summary Roles & Responsibilities: 1. Hands on experience of Overall Asset care for Process equipment to take care of the total process equipment health of the plant. For OSD/Encapsulation/Ointment/Liquid/QC 2. OSD: Quadro sifter, ROMACO & FETTE Compression, GFB pro 30, GLATT & ACG Tablet coater, ACG Blister packing machine, IMA Bottle packing machine, JACKSON online conveyor/ Bulk2D, etc. 3. Encapsulation: GIC Engineering Inc, Gelatin mass holding vessel, Romaco Blister machine, KOCH Wallet machine, etc. 4. Liquid Area: Liquid filling machine, Capping machine, Induction cap sealing. 6. Responsible for the Overall Asset care (Electrical / Instrumentation of all process and packing equipment) 7. Ensure that Current Good Manufacturing Practices (cGMP), ATAR (All time audit readiness) checklist, regulatory requirements are being adhered to are being adhered to the Maintenance of Process equipment & other related machinery 8. Ensure that all the safe practices as per SHE process, and protocols are adhered to while working 9. Hands on skill of trouble shooting of all equipment in the above sections for OSD/Encapsulation/Ointment 10. Responsible for identification and closure of all abnormalities in his area of work 11. Co-ordinate with internal customers for routine maintenance issues by providing feedback to the Engineering Head from time to time 12. Responsible for Planning and execution of Preventive Maintenance Program (PMP) for all Process equipment as per schedule 13. Co-ordination with internal and external vendors for Break-down maintenance, routine maintenance issues 14. Hands on experience on breakdown maintenance and followed by root cause analysis (RCA) for every major breakdown of the equipment by identifying and implementing the action plan 15. Execution of all the assigned action plan CAPA (Engineering, QA & Safety) 16. Preparation and review of engineering-based URS, SOP’s, SOI’s, PMP’s , CAPEX and revisions of the same 17. Commissioning FAT, Commissioning and followed by complete Qualification as per procedure 18. Ensure that all the required spares, critical tools and spares are maintained for the process equipment so as to ensure continuous operation & reduce downtime 19. verify all concerned daily log books and ensure documentation is online. 20. Operational knowledge of TPM. Ability to create Equipment Tree, develop Autonomous Maintenance and Preventive Maintenance standards, deeply in understanding of problem statement, RCA and CAPA 21.Hands on experience on various PLC’s (Siemens, Rockwell, Schneider, etc.) 22. Hands on experience on SCADA & HMI (WIN CC Explorer 7.4, 7.5, FT View, IFIX) QC: Fume exhausting unit, Walk in Stability Chamber, High performance liquid chromatography, Verticle Auto clave etc. Qualifications Educational qualification: Diploma in Engineering or Bachelor's Degree in Engineering (Electrical / Instrumentation) Additional preference:: JH & TPM knowledge. Minimum work experience: 3-6 years of experience in the pharmaceutical industry with a focus on maintenance and engineering. Preferable Exp, FMCG with strong TPM background. Skills & attributes Technical Skills Prior experience in maintenance and engineering roles preferred. Good understating on Pharmaceutical Manufacturing and Packing operation Strong understanding & experience in preventive maintenance practices, procedures & engineering solutions. Understanding of Good Engineering Practices. Understanding of relevant regulatory standards. Proficiency in SAP or similar maintenance management systems. Technical knowledge in Facility and Plant Engineering, infrastructure building, contractor management. Knowledge of regulatory requirements, including Good Laboratory Practices, GMP and cGMP standards. Ability to understand the specific requirements of Process team / Delivery teams Behavioral skills: Attention to detail and strong organizational skills. Experience in Engineering, Vendor management, Contractor management and safety requirements. Ability to work collaboratively in a cross-functional team environment. Excellent communication and interpersonal skills. Delivery-oriented mind-set. Behavioural skills: Proactive approach to identifying and solving challenges Collaboration with cross-functional teams, promoting a cooperative and inclusive work environment. Efficient time management to meet production schedules and deadlines without compromising quality. Effective communication and training skills for user departments and service providers. Show more Show less

Dr. Reddy’s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can’t Wait. We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity – to strengthen our core further (the next steps) and to build the future (the new bets). ‘The Next and the New’ is how we aim to continue to be the partner of choice – purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose – helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparency Dr Reddy’s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization. " Job Description Job Summary Roles & Responsibilities: 1. Hands on experience of Overall Asset care for Process equipment to take care of the total process equipment health of the plant. For OSD/Encapsulation/Ointment/Liquid/QC 2. OSD: Quadro sifter, ROMACO & FETTE Compression, GFB pro 30, GLATT & ACG Tablet coater, ACG Blister packing machine, IMA Bottle packing machine, JACKSON online conveyor/ Bulk2D, etc. 3. Encapsulation: GIC Engineering Inc, Gelatin mass holding vessel, Romaco Blister machine, KOCH Wallet machine, etc. 4. Liquid Area: Liquid filling machine, Capping machine, Induction cap sealing. 6. Responsible for the Overall Asset care (Mechanical of all process and packing equipment) 7. Ensure that Current Good Manufacturing Practices (cGMP), ATAR (All time audit readiness) checklist, regulatory requirements are being adhered to are being adhered to the Maintenance of Process equipment & other related machinery 8. Ensure that all the safe practices as per SHE process, and protocols are adhered to while working 9. Hands on skill of trouble shooting of all equipment in the above sections for OSD/Encapsulation/Ointment 10. Responsible for identification and closure of all abnormalities in his area of work 11. Co-ordinate with internal customers for routine maintenance issues by providing feedback to the Engineering Head from time to time 12. Responsible for Planning and execution of Preventive Maintenance Program (PMP) for all Process equipment as per schedule 13. Co-ordination with internal and external vendors for Break-down maintenance, routine maintenance issues 14. Hands on experience on breakdown maintenance and followed by root cause analysis (RCA) for every major breakdown of the equipment by identifying and implementing the action plan 15. Execution of all the assigned action plan CAPA (Engineering, QA & Safety) 16. Preparation and review of engineering-based URS, SOP’s, SOI’s, PMP’s , CAPEX and revisions of the same 17. Commissioning FAT, Commissioning and followed by complete Qualification as per procedure 18. Ensure that all the required spares, critical tools and spares are maintained for the process equipment so as to ensure continuous operation & reduce downtime 19. verify all concerned daily log books and ensure documentation is online. 20. Operational knowledge of TPM. Ability to create Equipment Tree, develop Autonomous Maintenance and Preventive Maintenance standards, deeply in understanding of problem statement, RCA and CAPA QC: Fume exhausting unit, Walk in Stability Chamber, High performance liquid chromatography, Verticle Auto clave etc. Qualifications Educational qualification: Diploma in Engineering or Bachelor's Degree in Engineering (Mechanical) Additional preference:: JH & TPM knowledge. Minimum work experience: 5-10 years of experience in the pharmaceutical industry with a focus on maintenance and engineering. Preferable Exp, FMCG with strong TPM background. Skills & attributes Technical Skills Prior experience in maintenance and engineering roles preferred. Good understating on Pharmaceutical Manufacturing and Packing operation Strong understanding & experience in preventive maintenance practices, procedures & engineering solutions. Understanding of Good Engineering Practices. Understanding of relevant regulatory standards. Proficiency in SAP or similar maintenance management systems. Technical knowledge in Facility and Plant Engineering, infrastructure building, contractor management. Knowledge of regulatory requirements, including Good Laboratory Practices, GMP and cGMP standards. Ability to understand the specific requirements of Process team / Delivery teams Behavioral skills: Attention to detail and strong organizational skills. Experience in Engineering, Vendor management, Contractor management and safety requirements. Experience in Engineering, Vendor management, Contractor management and safety requirements. Ability to work collaboratively in a cross-functional team environment. Excellent communication and interpersonal skills. Delivery-oriented mind-set. Behavioural skills: Proactive approach to identifying and solving challenges Collaboration with cross-functional teams, promoting a cooperative and inclusive work environment. Efficient time management to meet production schedules and deadlines without compromising quality. Effective communication and training skills for user departments and service providers. Show more Show less

The Company PerkinElmer is a global analytical services and solutions provider with offerings including the leading OneSource Field and Laboratory services business that serve the biopharma, food, environmental, safety and applied end markets to accelerate scientific outcomes. Since 1937, PerkinElmer has served as a trusted partner in laboratory analysis and management and today complements its service offerings with a broad portfolio of atomic spectroscopy, molecular spectroscopy, and chromatography instruments, consumables, and reagents. With a dedicated team of more than 5,000 team members, the Company serves customers in more than 35 countries. Additional information is available at www.perkinelmer.com Purpose As a Senior Procurement Specialist, you will be responsible for managing the procurement process from sourcing to contract management. You will collaborate with various departments to ensure that procurement activities align with the company's strategic objectives. The ideal candidate will have a strong background in procurement, excellent negotiation skills, and the ability to build and maintain vendor relationships. Responsibilities Develop and implement procurement strategies to optimize costs while maintaining quality standards. Identify and evaluate potential suppliers, negotiate contracts, and establish agreements that align with the company's needs and objectives. Monitor supplier performance and conduct regular vendor evaluations to ensure compliance with contractual agreements and quality expectations. Collaborate with cross-functional teams, including finance, operations, and legal, to support procurement initiatives and drive process improvements. Analyze market trends and stay informed about industry best practices to identify opportunities for cost savings and efficiency enhancements. Manage the procurement process for major projects, including RFQ/RFP development, supplier selection, and contract negotiation. Lead supplier relationship management efforts, including resolving disputes, managing supplier risks, and fostering long-term partnerships. Oversee the procurement team and provide guidance and mentorship to junior staff members. Ensure compliance with relevant laws, regulations, and company policies throughout the procurement process. Prepare and present reports and recommendations to senior management to support decision-making and strategic planning efforts. Basic Qualifications Bachelor's degree in business administration, supply chain management, or a related field; Master's degree preferred. At least 5 years of experience in procurement, with a focus on strategic sourcing and contract negotiation. Preferred Characteristics Proven track record of successfully managing procurement projects and achieving cost savings targets. Strong analytical skills and the ability to interpret data and make informed decisions. Excellent communication and interpersonal skills, with the ability to build effective relationships with internal stakeholders and external suppliers. Solid understanding of procurement best practices, industry trends, and relevant regulations. Proficiency in procurement software and tools, such as ERP systems and e-procurement platforms. Certification in procurement or supply chain management (e.g., CSCP, CPIM, CPSM) is a plus. PerkinElmer is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability status, age, or veteran status or any other characteristics protected by applicable law. PerkinElmer is committed to a culturally diverse workforce. Show more Show less

Job description Job Title: GC LCMS Data Analysis Expert – Trainer Location: Bangalore (Remote) Employment Type: Part-time | 5 Days a Week Work Hours - 4.5hrs per Day Salary : Between 25-30k/month About Biotecnika Biotecnika is a pioneer in life science education and research training in India. With over 18 years of trust and innovation, we’re expanding our educational frontier with a new specialized course on GC (Gas Chromatography) and LCMS (Liquid Chromatography-Mass Spectrometry) Data Analysis. Our mission is to equip the next generation of scientists and professionals with cutting-edge analytical skills that are highly valued in pharma, biotech, food, and environmental industries. We’re looking for a passionate and experienced GC LCMS Data Analyst who is excited to share their expertise and train aspiring professionals in this high-demand field. Role Overview As a GC LCMS Data Analysis Expert Trainer, you will be vital in developing and delivering a career-ready training program. Your work will involve theoretical and hands-on training in chromatographic principles, instrumentation, data interpretation, troubleshooting, and industry applications. Key Responsibilities Curriculum Design: Develop comprehensive course modules for GC, HPLC, and LC-MS/MS techniques. Cover principles, instrumentation, method development, calibration, validation, and data interpretation. Design practical assignments, real-life case studies, and recorded sessions for student engagement. Training Delivery: Conduct live online/offline classes and Q&A sessions. Mentor students with practical examples, software walkthroughs (like ChemStation, MassHunter, Xcalibur, etc.). Guide students on compliance with GLP, GMP, FDA, and ICH guidelines related to data analysis. Student Assessment & Feedback: Design assessments and hands-on exercises to evaluate student learning. Offer constructive feedback and support to help them master both fundamental and advanced skills. Industry Relevance: Share insights on real-world data challenges and quality control in analytical labs. Stay up-to-date with evolving techniques and software in chromatographic data processing. Qualifications Education: M.Sc./Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, Biotechnology, or related fields. Experience: Minimum 2 years of hands-on experience in operating and analyzing data from GC, HPLC, LC-MS instruments. Experience in regulated environments (e.g., pharma, CROs, or food testing labs) preferred. Prior teaching/training experience will be an added advantage. Skills: Strong theoretical knowledge and practical command of chromatography and mass spectrometry. Familiarity with data processing tools and instrument software. Effective communication, teaching, and mentorship abilities. Why Join Biotecnika? Make an Impact: Your knowledge will directly empower the next generation of analytical scientists. Career Advancement: Be part of a learning-focused culture with room to grow. Balanced Life: Enjoy a healthy work-life balance with a 5-day workweek. Collaborative Culture: Work alongside experts who are equally passionate about science and education. Stability & Purpose: Join a trusted brand that’s committed to quality education in life sciences. How to Apply Think you’re the one who can decode chromatograms and teach others to do the same? Send your updated CV and a brief cover letter to hr-dept@biotecnika.org with the subject line: "Application for GC LCMS Data Analysis Trainer – Biotecnika" Show more Show less

Key responsibilities of this job role include: Design and execute multistep organic syntheses under the supervision of senior scientists. Having knowledge of enzymatic reactions. Perform compound purification using techniques such as column chromatography, recrystallization, HPLC, etc. Characterize synthesized compounds using analytical techniques (NMR, LC-MS, IR, UV-Vis, etc. ). Maintain accurate and detailed records of all experiments Participate in group meetings and contribute to scientific discussions. Ensure compliance with laboratory safety protocols and chemical handling guidelines. Assist in the preparation of reports, presentations, and research publications. M. Sc. in Organic Chemistry, Medicinal Chemistry with 3-4 years of experiences or fresh Ph. D in organic chemistry.

Role & responsibilities We are seeking a qualified individual with strong expertise in organic chemistry, including in-depth knowledge of chemical reactions and mechanisms. The role involves: Distillation of organic solvents and purification of organic compounds using column chromatography, vacuum distillation, and crystallization. Scaling up chemical reactions from gram to kilogram scale. Conducting experiments for assigned projects and maintaining accurate records of observations in the lab notebook. Proficiency in using online resources, including chemistry-related searches, to support research and project work. Operation and maintenance of laboratory equipment such as round-bottom flasks (RBF), TLC chambers, pH meters (calibration and use), rotary evaporators, Buchner filters, microfilters, vacuum systems, and tray dryers. Candidates should demonstrate hands-on experience and attention to detail in laboratory practices. Preferred candidate profile:- API/CRO- R&D Qualifications:- M.sc Organic Chemistry/Industrial Chemistry / M. Pharma (Medicinal Chemistry)

Engineer should have on site installation, Qualification, repair and preventive maintenance experience on LPLC and HPLC products. Overall chromatography experience will get preference. The Services Technician will be responsible for delivering the desired customer service experience. The goal is to drive service success that improves customer satisfaction, maximizes customer retention and increases profitability. Main Responsibilities & Tasks Engineer should have experience on LPLC and HPLC product segments. Overall chromatography experience will get priority. Provide service and customer support during field and inhouse visits or dispatches. Manage all on site installation, repair, maintenance and test tasks. Diagnose errors or technical problems and determine proper solutions. Produce timely and detailed service reports. Ensure the timely and correct documentation of processes. Operate vehicle in a safely manner and use field automation systems Follow all company's filed procedures and protocols Cooperate with technical team and share information across the organization Comprehend customer requirements and make appropriate recommendations / briefings Contact customers concerning processes of the customer file Build positive relationships with customers Qualification & Skills Engineering degree in chemistry, Electronics, Electrical and Instrumentation or similar 3-7 years of proven field service experience Ability to troubleshoot, test, repair and service technical equipment. Ability to work flexible shifts and to adapt to changing work schedules High customer orientation Team spirit Familiarity with mobile tools and applications Good command of spoken and written English About Sartorius Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide. We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment. Join our global team and become part of the solution. We are looking forward to receiving your application. www.sartorius.com/careers Show more Show less

Job Description Beckman Coulter Life Sciences mission is to empower those seeking answers to lifes most important scientific and healthcare questions. With a legacy spanning 80 years, we have long been a trusted partner to our customers, who are working to transform science and healthcare with the next groundbreaking discovery. As part of our team of more than 2,900 associates across 130 countries, youll help drive our vision of accelerating answersand our commitment to excellence. Beckman Coulter Life Sciences is one of 10 Life Sciences companies of Danaher. Together, we accelerate the discovery, development and delivery of solutions that safeguard and improve human health. This role will be an On-site role at our Beckman Coulter Life Science, Bangalore Development Center (BDC) manufacturing facility located in Bengaluru. Do you want to work in the Manufacturing Operations Team? Do you enjoy working in a dynamic work force, collaborating with other team members and diverse groups, to meet Organization goal and customer demand? Then read on! We are currently seeking a "Polymer Chemist 2" position in Production Operations who will be primarily responsible for polymer dye synthesis and related manufacturing processes. The company is compliant with ISO 9001: 2015, ISO 13485: 2016 & EN ISO 13485: 2016, MDSAP and Beckman Coulter corporate Quality system requirements. In This Role, You Will Be Responsible For Experience in handing metal catalyst reactions. Experience in performing and optimization of C-N and C-C coupling reactions. Experience in handling air/moisture sensitive reagents and performing of reactions at the temperature range of -78C to higher temperatures. Perform purification of the organic compounds using different types of column chromatography techniques and other separation techniques. Having polymer chemistry and Conjugation chemistry knowledge with good Hands-on experience on HPLC/UPLC/GPC/TFF/Spectrophotometer/Fluorimeter and Automated purification system. The Required Qualifications For The Job Include M.Sc. in Chemistry/Organic Chemistry/Polymer chemistry/Biochemistry or related discipline, with minimum of 5 years industrial experience. Demonstrated ability to be flexible and resourceful. Ability to work in a team environment & Excellent communication skill. Previous experience with polymer chemistry and protein conjugation will have an added advantage. It would be a plus if you also possess previous experience in: Organic synthesis of fluorescent dyes suitable for Flow Cytometry applications. This job is eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical insurance to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Companys sole discretion, consistent with the law. Join our winning team today. Together, well accelerate the real-life impact of tomorrows 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. Show more Show less

As a Peptides Production Trainee, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Preferred candidate profile: Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. MSc/BSc Chemistry

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.

Project coordination with inter department and client. Project monitoring & controlling Prepare Project budget Project execution as per budget with cost control. Project closure with analysis & evaluation for continual improvement & development. Generation of project deliverables/ output Project Plan(Project opening) SO punching Material tracking FAT internal/External Monitor and control site activities Installation qualification Interdepartmental document verification and approval Provide regular MIR (Management Information Report). Payment planning and follow up with project coordinator. Incumbent needs to know Experience Project Engineer preferably handling WT projects 1 to 2 years OR Site Engineer handling WT systems - 3 to 5 years Preferably working experience of projects in pharma Educational Qualifications

Design & Detailing of Process Filtration (UF/MF/NF) for Pharma Application, Diary etc Costing of Systems Experience of line Sizing, Responsible for Selection of Membranes Responsible for Preparing detailed BOQ Monitor review and verify stage of design, Upgradation of design system tools, Responsible for Planning & control micro level , Design system output generation on basis of URS & checklist received Responsible for preparing Techno Commercial Offer Must Process of Water System. Computation of line Sizing Experience in Design, Techno commercial proposals for water system (UF/MF/NF).