98 Spectrophotometer Jobs - Page 3

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India Show more Show less

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India Show more Show less

Position Title: Executive – Quality Control Qualification And Experience M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India Show more Show less

About Company House of Spices is a leading South Asian Food manufacturer and distributor in North America (USA & Canada) and has been delivering pure and quality products for over 50 years with 9 distribution centers throughout North America. We have our own brands and have exclusivity for distributing our partner brands in US / Canada. Our vision is to bring our culture alive through the celebration of authentic ethnic food, flavor and families. Our mission is to provide consumers easy access to all authentic ethnic food and flavors across the North American marketplace with a will to win. Visit www.hosindia.com to know more. JOB DESCRIPTION This position will be responsible for developing and scaling recipes for South Asian ready-to-eat food products, ensuring that formulations can be successfully commercialized in collaboration with vendors and manufacturing partners. The ideal candidate must have expertise in global food safety systems, international regulatory affairs, new product development (NPD), and quality management systems (QMS) , with hands-on experience in USA, Canada, and other global regulatory frameworks . Key Responsibilities: Product Development & Innovation Developing new recipes for ready-to-eat South Asian food products, including gravies, pickles, sweets, parathas, naan, and more. Modify and scale recipes for large-scale production while ensuring consistency in taste, texture, and shelf stability. Stay ahead of global food trends and introduce innovative, clean-label, and consumer-friendly food products. Work closely with the marketing and sales teams to align product innovation with market demand . Process & Production Scale-up Collaborate with vendors, co-packers, and manufacturers to scale up R&D formulations into full-scale production . Ensure process optimization, ingredient sourcing, and cost efficiency without compromising quality. Conduct pilot plant trials and oversee first production runs to maintain product integrity. Food Safety & Regulatory Compliance Ensure full compliance with USA, Canada and FSSAI regulations . Implement and maintain HACCP, BRC, and FSSC standards to meet global food safety requirements. Work with regulatory teams to obtain necessary product approvals and certifications for international markets. Quality Assurance & Sensory Evaluation Establish and oversee sensory testing panels to ensure products meet consumer expectations. Utilize advanced analytical instruments like HPLC, spectrophotometer, rapid-visco analyzer, and microscopy for product evaluation. Troubleshoot and resolve product quality issues in collaboration with QA teams. Cross-functional Collaboration & Project Management Lead cross-functional teams across R&D, operations, and marketing to ensure product launches meet business objectives. Develop and manage timelines for new product development projects , from ideation to market launch. Prepare technical documentation, SOPs, and reports for R&D projects. Supervisory Responsibility This position has no direct supervisory responsibilities but does serve as a coach and mentor for other positions in the department. Position Type/Expected Hours of Work This is a full-time position. Days and hours of work are Monday through Friday. Travel Extensive travel is expected for this position. Preferred Education and Experience Bachelor’s/Master’s/PhD in Food Science, Food Technology, or a related field. 8+ years of experience in R&D, food product development, or food technology, preferably in South Asian cuisine and ready-to-eat food segments. Hands-on experience with global food regulatory standards (USA FDA, CFIA Canada, and FSSAI). Expertise in commercial food production processes, ingredient functionality, and sensory science. Experience with HACCP, BRC, FSSC certifications, and food safety audits. Ability to scale recipes from lab to commercial production with a focus on quality, efficiency, and cost-effectiveness. Strong project management skills with experience in cross-functional team leadership. Knowledge of packaging technologies and shelf-life extension techniques. AAP/EEO Statement House of Spices Inc; provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, national origin, disability, veteran status, or any other characteristic protected by state, federal, or local law. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. Show more Show less

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 2 - 6 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

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

We are seeking a dedicated Service Engineer with experience in the pharmaceutical industry to handle installation, commissioning, maintenance, and technical support of our equipment and systems. Your role is critical in ensuring customer satisfaction and compliance with industry standards. Role & responsibilities : Perform installation, commissioning, and preventive maintenance of pharmaceutical machinery and cleanroom systems. Troubleshoot technical issues on-site and remotely, ensuring minimal downtime for clients. Provide technical training and support to customers and internal teams. Maintain service documentation, reports, and customer logs. Ensure all work complies with GMP, safety, and regulatory standards. Preferred candidate profile : - Qualifications Required: BE/BTECH in ( Instrumentation / Electronics and Telecommunication) , BSC (Physics) - 1-6 years of field service experience, preferably in pharmaceutical or healthcare environments. - Familiarity with pharmaceutical equipment such as PLC, SCADA,HVAC systems, cleanroom equipment, isolators, or processing machines (preferred). - Strong problem-solving and customer service skills. - Willingness to travel extensively to client sites. What We Offer: Competitive salary + high-performance incentives Learning & development opportunities Career growth opportunities in a fast-growing sector A collaborative environment with innovative technologies Training and development opportunities How to Apply: If you're passionate about pharma instrumentation and sales leadership, wed love to hear from you! Apply directly via LinkedIn or send your CV to : HR Sonica : Technohr@technovalue.in / 88797 73091 Subject Line: "Application Service Engineer Pharma Instruments"

Roles and Responsibilities Operate laboratory equipment such as GC-MS, FTIR, HPLC, UV Spectrometer, Polarimeter, Viscometer, etc. to analyze samples and gather data. Develop new methods for analyzing complex chemical compounds using various analytical techniques like spectroscopy (FTIR), chromatography (HPLC), mass spectrometry (GC-MS). Collaborate with cross-functional teams to troubleshoot issues related to product quality control and process optimization. Desired Candidate Profile 1-2 years of experience in an R&D environment handling chemicals & performing analytical work. MS/M.Sc(Science) degree in Chemistry or equivalent qualification from a recognized university. Strong understanding of chemistry principles including organic chemistry, physical chemistry, biochemistry etc. .

Position: QC Chemist Location: Ahmedabad Experience: 4 - 6 Years Industries: Chemical Responsibilities: To conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods or stability samples. To calibrate, validate, or maintain laboratory equipment. To compile laboratory test data and perform appropriate analyses. He should able to handle Quality Control related Instruments like HPLC, GC, UV spectrophotometer, autotitrator, Karl Fischer, etc. To complete documentation needed to support testing procedures including data capture forms, equipment logbooks / inventory forms. To interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release. Monitor testing procedures to ensure that all tests are performed according to established item specifications, standard test methods and protocols. Preparation of Certificate of analysis (COA) and reporting to QC Manager. Knowledge of Oracle Documentation is preferable. Required Skills Must have 4 to 6 years of experience in Quality Control Laboratory in chemical industry. Must be excellent in written and spoken English; net savvy and adept at computer skills Attention for detail Team player Good in communication Required Qualification: - B.Sc/M.Sc- Chemistry Salary :- Upto 4.00 LPA Job Types: Full-time, Permanent, Fresher Pay: ₹300,000.00 - ₹400,000.00 per month Benefits: Food provided Health insurance Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Overtime pay Yearly bonus Work Location: In person

Maintenance and Calibration and maintenance of electronic field instruments for flow, level, pressure, temperature transmitter, QAL instruments Hands on experience of maintenance / configuration of DCS/ PLC, SCADA control systems General Description: Reporting to the Maintenance Supervisor, the Maintenance Technician is responsible for performing all-around maintenance and repair services to increase the availability and reliability of the facility and its assets. The role requires collaboration and coordination with maintenance planners/schedulers, parts storeroom attendants and other site functions such as Production, Technical Services, and Contractors (not limited to those). The Maintenance Technician is an active participant in creating, cultivating, and embedding a culture of Continuous Improvement to further the ION chemical Brand promise and Operational Excellence. An Ion Chemicals Maintenance Technician is also responsible for participating in developmental activities designed to stimulate individual and organizational growth. Maintenance Technician Functional Role Preventive, predictive maintenance of Instruments such as Flow, Level, Pressure transmitters of various make e.g. Emerson, Yokogawa, Siemens, E&H etc., Calibration of temperature transmitter for RTD, Thermocouples, pH transmitters, radar level, mass flow meters, vortex, magnetic, orifice type flow meters. Maintenance & troubleshooting of electronic, mechanical weighing scales, bagging machine, bulk loading systems, Gas analyzer, moisture analyzers systems. Maintenance and calibration of various type of control valves, Shutoff valves, Pressure regulating valves Maintenance and calibration of Utility instruments for steam boilers, hot oil furnaces, air compressors, chilling plant, DM plant, cooling towers, power plant instrumentation. Maintenance and Calibration of analytical instruments like GC, titrators, Karl fisher, Spectrophotometer, Colorimeter, Portable meters like pH, Conductivity, Explosive meter etc. Hands on experience of maintenance / configuration of DCS/ PLC, SCADA control systems. Able to read and understand P&ID, hook-up drawings, panel drawings, control circuit diagrams, cable scheduling, JB scheduling, tray work, instrument tubing work is necessary Ensures daily work meets EHS compliance and builds continuous improvement in EHS performance Responsible for performing technical diagnosis and technical repair of site assets Responsible for conducting preventive maintenance to increase asset uptime and reliability Responsible for conducting reliable asset repair in the most cost-efficient manner Ensures tools, parts, and all equipment are safe and in effective working order Responsible for the identifying and securing parts, tools, and inventory to complete work orders Responsible for communicating and securing work permits and associated safety equipment to perform work Acts as mentor for less-skilled, less tenured maintenance technicians Provide guidance and direction for contractors when needed Accountable for parts checked out inventory, salvage of good parts and proper disposal of bad parts Ability to use computer and accurately input data at an efficient pace to meet the and complete work order responsibilities Consults with engineers and vendors as necessary to complete work order requirements and work order closeout Job Type: Full-time Pay: Up to ₹550,000.00 per month Benefits: Provident Fund Schedule: Morning shift Supplemental Pay: Yearly bonus Work Location: In person

Post for QC Chemist in Pharma Formulation Unit - based at Vatva, Ahmedabad, Gujarat. Sections - Tab, Cap, Syp, Cream, Mouthwash, Dry Powder, SoftGels Required Work Experience - Testing of Finished Formulation, API & Excipients Testing on Instruments like HPLC, Spectrophotometer, Dissolution Test Apparatus, Karl Fischer, Potentiometer, Titration, PH Meter, Analytical Balance, Hot Air Oven, etc. Work Experience - Required of QC Lab of Pharma Formulation Unit or FDA Approved Drug Testing Labs of Public or Private Sectors. Candidates (Do not apply for this job post) - with work experience from Other sectors like API, Dyes & Chemicals, Water Purification, Cosmetics, etc. Job Type: Full-time Benefits: Flexible schedule Paid sick time Schedule: Day shift Supplemental Pay: Overtime pay Education: Bachelor's (Required) Experience: Quality control of Formulation Testing: 3 years (Preferred) Work Location: In person

Hiring Alert: Analytical Chemist – Dairy/FMCG We are hiring a passionate and detail-oriented Analytical Chemist to join our team. This is a great opportunity for freshers or experienced professionals (0–5 years) looking to build or advance their career in the Dairy or FMCG industry. Job Details: Position: Analytical Chemist Industry: Dairy / FMCG Location: Jagdalpur, Chhattisgarh (Relocation required) Experience Required: 0 to 5 years Salary: No salary barrier for the right candidate Employment Type: Full-time, Permanent Key Responsibilities: Conduct chemical and microbiological analysis of raw materials, in-process samples, and finished products Operate laboratory instruments such as HPLC, GC, UV-Vis Spectrophotometer, etc. Maintain accurate lab records, test reports, and documentation as per regulatory standards Ensure product compliance with quality and safety norms (FSSAI, ISO, BIS) Support R&D and product development teams with analytical data Identify deviations and assist in corrective and preventive action (CAPA) Adhere to Good Laboratory Practices (GLP) and company SOPs Candidate Requirements: B.Sc. / M.Sc. in Chemistry, Analytical Chemistry, or a related discipline 0–5 years of relevant laboratory or industrial experience Knowledge of analytical instruments and quality standards is preferred Fresh graduates with strong academic background are welcome to apply Willingness to relocate to Jagdalpur, Chhattisgarh Strong attention to detail, communication, and documentation skills Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹30,000.00 per month Schedule: Day shift Evening shift Fixed shift Night shift Work Location: In person

Analytical QA Reviewer - Officer: Looking for a candidate with 2 to 4 years of work experience as QC analyst / AQA reviewer in reputed pharma companies. Should have Knowledge of handling/ analytical data review of HPLC , FTIR , UV spectrophotometer , KF Autotitrator , Dissolution apparatus. Have Basic knowledge of CGMP , GDP , Data integrity . Should have Basic knowledge of OOS (Out of specification), OOT, OOC

Work Profile: Production Chemist pesticides Company: Ankita Organics Private Limited Location: Faridabad, Haryana Industry: Agrochemicals / Pesticides Manufacturing Job Type: Full-time Qualification: Minimum B.Sc. in Chemistry Experience: 2–5 years in agrochemical manufacturing preferred Key Responsibilities: Manage day-to-day operations of the production unit for pesticide formulations including: Emulsifiable Concentrates (EC) Suspension Concentrates (SC) Soluble Liquids (SL) Water-Dispersible Granules (WDG) Independently oversee and execute batch manufacturing as per standard operating procedures (SOPs) and safety protocols. Ensure accurate weighing, mixing, and formulation processes while maintaining batch integrity and product consistency. Monitor production timelines and ensure compliance with regulatory standards (CIBRC guidelines). Maintain production records, batch manufacturing records (BMR), and other statutory documentation. Coordinate with procurement and inventory teams for timely availability of raw materials and packaging materials. Supervise workers and operators on the shop floor; ensure discipline, hygiene, and adherence to safety standards. Preferred Skills and Knowledge: Strong understanding of formulation chemistry related to agrochemicals. Ability to troubleshoot formulation and stability issues. Knowledge of Good Manufacturing Practices (GMP) and Environment, Health & Safety (EHS) norms. Capable of independently managing the production floor and small-to-medium scale plant operations. Additional Advantage (Preferred but Not Mandatory): Working knowledge of analytical laboratory equipment such as: HPLC (High Performance Liquid Chromatography) GLC (Gas-Liquid Chromatography) UV-Vis Spectrophotometer Ability to coordinate with QC/QA teams for product validation and sample testing. Key Attributes: Self-motivated, disciplined, and proactive. Strong leadership and team management skills. Attention to detail with excellent record-keeping ability. Willingness to adapt and grow with a fast-paced and expanding company. Job Type: Full-time Pay: From ₹30,000.00 per month Benefits: Cell phone reimbursement Health insurance Schedule: Day shift Evening shift Weekend availability Work Location: In person Expected Start Date: 01/06/2025

Role & responsibilities Preferred candidate profile Perks and benefits

Role & responsibilities 1. Testing of Ores and Minerals, heavy metal, coal etc. 2. Perform accreditation procedure from NABL & MOEF &CC (application, MU, calibration, all applicable relevant records) 3. Environmental monitoring and testing 4. Handling & working with testing equipment AAS, Hg-Analyser, spectrophotometer, bomb calorimeter, Gas Chromatography and other basic equipment. 5. Thorough knowledge of microbiological Testing Desirable: ISO 17025 training (4 days) Preferred candidate profile 1-5years experienced in industrial mineral testing & analysis Must have exposed in NABL Labs B.sc /MSc Chemistry preferred Willing to relocate to Udaipur,Rajasthan Male candidate preferable with good communication skills Interested candidates can either apply here or can share CV at pooja.relhan@golcha.com

Testing of products - salt, protein,Enzyme,Mineral,Vitamins, Nondairy creamer, FatPowder. New Product development. Analytical instruments handling. stability testing.Titrations, Microbiological testing of R&D products. Support in Product Formulation. Required Candidate profile M.Sc Chemistry ( Analytical, Organic and inorganic chemistry) with relevant knowledge

Ensure that the manufactured products consistently meet established standards, customer specifications, and industry regulations Optimize processes and drive continuous improvement initiatives Product Modification/ Development as per customer need Required Candidate profile B. Sc Chemistry with M. Sc Polymer Science mandatory 12+ years' experience in Quality Assurance & Control in a chemical/ polymer manufacturing company (preferably in polystyrene manufacturing)

Are you ready for a new beginning? We need your talent, knowledge and dedication to better our world with biology. Our purpose points the way In Novonesis, we know that solutions rooted in biology can help solve humanity’s biggest challenges. Since we began more than a century ago, this has been our guide. It’s how we've gotten so far. And it’s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. We’re here to better our world with biology. Job Description The Research Associate will perform routine operations required in the laboratory involved in grain processing, starch, fermentation and distilling, follow directions and procedures and maintain accurate up-to-date records of all work performed. The duties involve (but not limited to) Prepare and carry out experimental work to meet specific project goals. Interpret and summarize results within the context of the specific experiment. Use and maintenance of the laboratory equipment. Understand and implement the technical methods and procedures. Participate in lab activities like inventory management, data capture, safety, quality. Qualification and Experience M.Sc/ B.Tech/M. Tech in Chemical Sciences/ Biotechnology/ Chemical Engineering with 2 years’ experience in starch and distilling process and technology. Knowledge of lab scale fermentation protocols. Handling of analytical instruments like HPLC, GC, Spectrophotometer, Microscope. Good at data compilation and interpretation. Knowledge of Grain processing and enzyme application would be an added advantage. Curious, self-driven and a strong team player. Strong experimental skills, with a talent to apply scientific findings to solve practical problems. Excellent interpersonal, written, and verbal communication skills Could our purpose be yours? Then apply today! At Novonesis we commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We recommend you not to attach a cover letter to your application. Instead, please include a few sentences in your resume/CV about why you are applying. To ensure a fair recruitment process, please refrain from adding a photo in your resume/CV. Novonesis is committed to creating a diverse environment and is proud to be an equal opportunity and affirmative action employer. All employment decisions are based on business needs without regard to race, color, ethnicity, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, disability, or veteran status. Want to learn more? Learn more about Novonesis, our purpose, and your career opportunities at novonesis.com Not the right fit for you? Even if this job isn't the right fit for you, perhaps you know someone who might find it interesting. If so, please feel free to share the job link and encourage them to apply. Thank you for your referral! Please check out our other open positions. The right fit for you could just be a few clicks away.

Are you ready for a new beginning? We need your talent, knowledge and dedication to better our world with biology. Our purpose points the way In Novonesis, we know that solutions rooted in biology can help solve humanity’s biggest challenges. Since we began more than a century ago, this has been our guide. It’s how we've gotten so far. And it’s how we'll impact the future. Now, more than ever, the world needs change. And with biosolutions, the possibilities for transformation are endless. We’re here to better our world with biology. Job Description and Responsibilities The Research Associate will be traveling to industrial plants and perform experiments, collect and analyse data to support the implementation of Novonesis technologies at the plant scale. The candidate is expected to work under the direction of senior staff, carry out experimental work involving established methods to meet specific team/project goals and maintain accurate up-to-date records of all work performed. The candidate must ensure that all work is performed in accordance with the quality and safety guidelines. The duties involve (but not limited to) Traveling to customers’ location to support the implementation of Novonesis technologies at the plant scale. Prepare and carry out experimental work to meet specific project goals. Interpret and summarize results within the context of the specific experiment. Use and maintenance of the laboratory equipment. Understand and implement the technical methods and procedures. Required Education and Experience M.Sc/ B.Tech/M. Tech in Chemical Sciences/ Chemical Engineering with 2 years’ experience in analytical methods related to starch and distilling industry. Handling of analytical instruments like HPLC, GC, Spectrophotometer, Microscope. Good at data compilation and interpretation. Knowledge of enzyme application would be an added advantage. Curious, self-driven and a strong team player. Strong experimental skills, with a talent to apply scientific findings to solve practical problems. Excellent interpersonal, written, and verbal communication skills Could our purpose be yours? Then apply today! At Novonesis we commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We recommend you not to attach a cover letter to your application. Instead, please include a few sentences in your resume/CV about why you are applying. To ensure a fair recruitment process, please refrain from adding a photo in your resume/CV. Novonesis is committed to creating a diverse environment and is proud to be an equal opportunity and affirmative action employer. All employment decisions are based on business needs without regard to race, color, ethnicity, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, disability, or veteran status. Want to learn more? Learn more about Novonesis, our purpose, and your career opportunities at novonesis.com Not the right fit for you? Even if this job isn't the right fit for you, perhaps you know someone who might find it interesting. If so, please feel free to share the job link and encourage them to apply. Thank you for your referral! Please check out our other open positions. The right fit for you could just be a few clicks away.

Position: Astt Manager - QA Qualification: B.Sc / M.Sc in Chemistry Experience: 6 years to 10 years in QA CTC can go maximum to Rs 9 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API PHARMA ONLY Responsibility: Support MR in QMS Responsible for driving Quality Mindset. Support IMS Audits, FDA , Vendor Audits. Strong in Document Control and Process Documentation. Should have supported US FDA Inspections and Audits KEYWORDS: GMP, FDA, IMS, QMS, AUDITS

Role & responsibilities Literature search using various search engines. Analytical Method Development of raw materials, active substances and Finished product. Analysis of raw materials, active substances and finished products. Preparation of test protocol. Experience in handling instruments like spectrophotometer, HPLC, and GC. Knowledge of analytical method validation. Knowledge of natural chemistry background and its analysis.

Key Responsibilities:Quality Control (QC): ✅ Conduct analysis of raw materials, in-process samples, and finished products using approved test methods. ✅ Operate laboratory instruments (e.g., HPLC, UV spectrophotometer, FTIR) as per SOPs. ✅ Ensure proper sampling, labeling, and storage of materials and retain samples. ✅ Maintain calibration and qualification records of lab instruments. ✅ Conduct stability studies and maintain related data. ✅ Review and approve test results; report deviations or non-conformances. ✅ Manage laboratory reagents, reference standards, and consumables. Quality Assurance (QA): ✅ Review and approve batch manufacturing and packing records (BMR/BPR). ✅ Oversee compliance with GMP, SOPs, and regulatory requirements. ✅ Coordinate and participate in internal audits, vendor audits, and regulatory inspections. ✅ Handle deviations, change controls, CAPA (Corrective & Preventive Actions), and complaint investigations. ✅ Manage document control: issuance, review, and archiving of SOPs, policies, and records. ✅ Conduct training for plant personnel on quality systems and GMP. ✅ Perform periodic review and qualification of equipment, processes, and cleaning validation. Required Qualifications: Education: B.Sc. / M.Sc. in Chemistry, Microbiology, Biotechnology, or B.Pharm / M.Pharm Experience: 2–5 years in QC/QA within the pharmaceutical or nutraceutical industry Key Skills and Competencies: Strong knowledge of nutraceutical regulations (FSSAI, WHO-GMP, USFDA, etc.) Hands-on experience with analytical techniques and equipment Excellent understanding of documentation practices and quality systems Good communication and interpersonal skills Attention to detail, problem-solving ability, and proactive approach Familiarity with software like LIMS, ERP, or electronic documentation systems (if applicable) Performance Metrics: Compliance rate with regulatory and internal standards Accuracy and timeliness of testing and documentation Number of deviations, CAPAs, and their timely closure Successful audit outcomes (internal and external) Training compliance of plant personnel Job Type: Full-time Pay: ₹15,000.00 - ₹30,000.00 per month Benefits: Paid sick time Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person