165 Spectrophotometer Jobs - Page 7

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

Position: QC Officer Qualification: B.Sc / M.Sc in Chemistry Experience: 3 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 4.5 Lacs per Annum. Location: Ankleshwar / Panoli. It's a Shift Working job Transport Provided. Industry: API PHARMA ONLY Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

Position: QC Executive Qualification: B.Sc / M.Sc in Chemistry Experience: 5 years to 7 years in QC / Analytical Development labs CTC can go maximum to Rs 6.5 Lacs per Annum. Location: Ankleshwar / Panoli. Transport Provided. Industry: API / Bulk Drugs / Pharma. Those working in Crop Sciences, Fertilisers are not eligible. Responsibility: T o follow Good laboratory Practices (GLP). Should be working on HPLC, GC and other Lab Testing Equipments To follow the procedures mentioned in SOP's and General test Procedures To monitor periodic calibration of instruments as per the schedule To follow all safety standards while working. To ensure documentation of QC / analytical activities as per Co. policy To provide complete support for internal & external Audits at your location. Analysis of plant related samples for any customer related query. To prepare and review Certificate of analysis and Analytical Test Reports. KEYWORDS: GCMS, LCMS, HPLC, GLP, NABL, FDA

Perform sampling and testing of raw materials, packaging, and finished products. Maintain QC records and documentation as per SOPs. Ensure compliance with GMP, ISO, and regulatory standards. Report quality issues and support corrective actions. Required Candidate profile B.Sc./M.Sc. in Chemistry 2+ years in Quality Control, preferably in cosmetic or chemical ind Know of analytical instruments Strong attention to detail and understanding of quality standards.

Job Title: Junior Chemist – Agrochemical Industry Location: [Insert Location] Department: Quality Control / R&D / Production Lab Reports To: QC Manager / Lab Head / Plant Manager Experience Required: 0–2 years Employment Type: Full-time Job Summary: We are seeking a detail-oriented and enthusiastic Junior Chemist to join our agrochemical division. The role involves supporting the quality control and formulation teams by performing chemical tests on raw materials, technicals, and finished formulations under supervision. The candidate will work with common lab instruments and follow industry regulations and SOPs. Key Responsibilities: Assist in the analysis of technicals, formulations (EC, SC, WP, WG, etc.), and raw materials as per standard methods. Perform routine tests such as pH, specific gravity, viscosity, emulsion/stability, active ingredient content . Operate basic instruments like UV-Vis spectrophotometer, Karl Fischer, GC, HPLC (training will be provided if needed). Prepare reagents, standardize solutions, and maintain lab records as per SOPs. Ensure all samples are labeled, tested, and recorded accurately. Help with stability studies and maintain sample retention records. Support senior chemists in method development, pilot trials, and new formulation evaluations. Adhere to GLP, safety norms, and environmental standards during lab work. Required Qualifications & Skills: Education: B.Sc. / M.Sc. in Chemistry, Agrochemical Science, Industrial Chemistry, or related discipline. Experience: 0–2 years (freshers with internships in QC/R&D labs welcome). Skills: Basic knowledge of agrochemical formulations and testing procedures. Familiarity with laboratory safety and chemical handling. Willingness to learn analytical instruments and quality control documentation. Good observation, teamwork, and communication skills. Growth Opportunity: Exposure to QA/QC, R&D, regulatory documentation, and formulation technology . Hands-on training with industry-standard equipment and advanced lab techniques. Opportunity to grow into roles such as QC Chemist, Formulation Chemist, or Regulatory Analyst. Agrochemical Product Types You’ll Work With: Herbicides, Insecticides, Fungicides Liquid and Solid Formulations (EC, SC, WP, WG, SL, etc.) Job Type: Full-time Pay: ₹9,866.11 - ₹20,000.00 per month Benefits: Health insurance Paid sick time Schedule: Day shift Fixed shift Supplemental Pay: Yearly bonus Work Location: In person

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 We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performing the PM. To ensure that the instruments / equipment are used with utmost care and as instructed in the relevant SOP. To attend the breakdown's and close notification or order of the instrument /equipment after the Completion of breakdown maintenance. To be a part of investigating the incidence related to instrument Responsible for the maintaining of required spares for all instruments in warehouse. To get the quotations for the required spares and services for the maintenance of the instruments. To generate the purchase requisitions for the required spares and services. To perform the PM in the given frequency within the given period. Adhering to the allotted shift schedule with right time. If any changes prior permission shall be taken from Group leader. Qualifications Educational qualification: An B.Tech. or any Degree in Instrumentation, Mechanical, Electronics, Electrical. Required Work experience: 3 to 6 years Skills & attributes: Technical Skills Hands-on Experience on maintenance of Waters HPLC (Arc, e2695), Agilent HPLC (1200, 1260 Infinity), Agilent GC-HSS (7890, 8890, 7897, G1888), Dissolution Testers (Electrolab, Sotax), Metrohm Titrators. Working experience in a cGMP (Current Good Manufacturing Practice) environment, with a special emphasis on Good Documentation Practices (GDP). Basic knowledge in SAP usage Behavioural Skills Prioritizes effective communication and demonstrates a performance-oriented mind-set. Effective verbal and written communication skills. Performance-oriented approach, consistently striving for high standards. Demonstrates flexibility in working shifts and a clear understanding of team dynamics. Additional Information About the Department Quality Control Formulations For more details, please visit our career website at https://careers.drreddys.com/#!/

Mission As Quality Assurance Officer will be the responsible to ensure right quality of the products as per Stanley Stella standards by proper monitoring, inspecting & guiding before they reach to consumer. Your purpose will also be to implement the right SOP in each area which will help to preserve our reputation by ensuring that our product & services are capable to drive sustainable growth. Main responsibilities Yarn quality check. Printability check. Maintain Mini bulk file properly. Risky point analysis for any new styles & feedback to BLO PD and HQ before approval. Greige Fabric quality check & monitoring the Knitting parameter randomly. Recipe & process route check. Ensure Finished Fabric quality parameters with relevant fabric test reports as per quality manual. Approve finished fabric shade of each batch by visually & spectrophotometer. Check bulk Accessories on garments, trim cards. Cut panel check & keep record. Samples check before shipment at different stages of production and some special projects samples. Conduct PP Meeting Ensure all quality parameters from Cutting, Sewing, Finishing & Packing as per company’s technical information manual/standard. Be present at the production line set up /first product flow, for new styles. In-line inspection & Final inspection. Keep record from the washing plant for all the panel wash garments. Dealing with vendors on quality issues and give solutions. Packing accuracy check on a daily basis (Mixed boxes/Missing pcs/sticker info vs content, etc.). Production line status update to line manager on a daily basis and update the OT status in common portal. Daily follow up C.S.R point in the production floor & make a report (monthly) and send to line manager. ETP PH Test (weekly) & make report. Weekly update of the factory’s quality situation to line manager. Guide the supplier in STST expectations and requirements. Your profile Graduate/ Masters. Educational Background on Textile Technology will be added advantage for the positions 5years of relevant work experience, good product and production knowledge with inspection criteria, AQL, shade and defects type, etc Strong leadership skill and teamwork mentality Exposure in Quality Assurance Excellent communication both verbal and written, analytical and interpersonal skills Computer literacy is must, especially strong skill to work in Excel. Flexible on working hours, Ability to work under pressure Ability to work with smart technology i.e., Tablet/Laptop for various reporting About us Stanley/Stella is the European leader in premium, sustainable blank apparel. Over the past decade, we’ve built the strongest brand in our industry — driven by a deep sense of purpose and a clear vision for the future of fashion. As a global company with multiple entities worldwide, we operate with integrity and care at every level. Sustainability is embedded in every decision we make — from the way we design our products to the long-term partnerships we build across our supply chain. We hold ourselves accountable not only for what we create, but how we create it. Excellence is our standard — from product quality to customer experience. We are uncompromising when it comes to detail, consistency, and delivering on our promises. And as the world evolves, so do we. Innovation fuels our ambition, inspiring us to challenge the norm, explore new ideas, and keep moving forward. At Stanley/Stella, we’re not just shaping the future of responsible fashion — we’re doing it together, with intention and heart. Ready to be part of the journey? Learn more: careers | Stanley/Stella