25 Uv Spectrophotometer Jobs

Job Description Handling of Potentiometer titration, Karl-Fisher , Calibration of Potentiometer titration , Karl Fischer , Handling of Polarimeter, Handling of UV Spectrophotometer, Handling & Calibration of PH meter, Show more Show less

Role & responsibilities Planning and Carrying out trials as per guidance and instructions of seniors. Tracking environmental microorganism development. Growing microbe cultures. Recording, analyzing and interpreting data. Perform laboratory analysis on all materials after appropriate sterilization. Perform tests on component samples, identify any contamination, conduct an analysis and initiate corrective measures. Study various cultures of microorganisms in isolation according to standard. Develop various testing processes for all new raw materials, finish product. Handling of basic instruments such as UV Spectrophotometer, pH meter, moisture balance etc. Media Preparation and fair knowledge in handling of microbes. Preferred candidate profile 1-2 years of experience in Microbiology B.Sc. / M. SC. / B. Tech ( Microbiology/ Bio-Technology/ Bio-Chemistry) Strong troubleshooting and Analytical Skills. Freshers with relevant educational qualification may also apply.

Job Opportunity at Natco Pharma Limited (Formulation Unit) Department: Quality Control Position: Chemist / Officer / Executive Qualification: B. Pharmacy / M. Pharmacy / M. Sc Experience: 3 to 5 Years Location: Kothur, Telangana Key Responsibilities: Analysis of finished products, raw materials, and in-process samples Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus Testing of Packing Materials Adherence to GLP, GDP, cGMP, and ALCOA+ standards Assay and dissolution testing using HPLC Regulatory exposure in formulation is mandatory Interested candidates may share their CVs at jaganmohan.p@natcopharma.co.in

You will be joining the VTC MFG. QC Department as a Probationer-HO Staff, with a primary responsibility of ensuring the quality control of manufacturing processes. The ideal candidate should hold a M.Sc. degree in Biotechnology, Biochemistry, or Microbiology and have at least 3-7 years of hands-on experience in a relevant field, preferably with a background in the pharmaceutical industry. Your role will involve conducting various analytical tests and procedures such as RP-HPLC, SEC-HPLC/SE-HPLC, Dionex, IC/Ion Chromatography, Biochemical analysis, UV spectrophotometer, Protein, O-acetyl. It is essential to have a good understanding of these techniques and equipment to perform accurate quality assessments. As a member of the VTC MFG. QC team, you will play a crucial role in upholding the quality standards of the manufacturing processes. Your expertise and attention to detail will contribute significantly to ensuring the production of high-quality products that meet regulatory requirements and customer expectations.,

Role & responsibilities Perform the calibration and preventive maintenance of the instruments as per the respective schedules. Analysis of raw material / finished products / stability samples / Dissolution profiling for R&D/ Plant support. Analytical Method Development /Verification Assay, Related substances, Dissolution etc . Perform the determination of KF factor, Daily verification of Balances, pH meter, Milli-Q water system, Hot Air Oven, Refrigerator temperature monitoring. Develop/ optimize the analytical methods by Chemical/ instrument analysis Verify/ validate the analytical methods by Chemical/ instrument analysis Preparation / Revision of Specification and Method of analysis for Raw materials / Finished Product / Inactive / Excipients etc Appropriate documentation of results and calculations, preparation of SOPs, specifications and test methods. Interpret results, evaluate data, draw relevant conclusions and give timely feedback to concerned Departments. Analytical Technology transfer of analytical methods by Chemical/ instrument analysis Perform the Impurity standard/ working standard/ primary reference standards. Receiving and filling controlled copy of specifications / method of analysis / SOP / STP etc Operation of various software like Oasis LIMS, Q Edge TMS, Chromeleon etc Preferred candidate profile Qualification: B. Pharm / M.Pharm / M. Sc Experience: Minimum 2 years in HPLC Analysis Development and Validation Perks and benefits Mediclaim

As an Analytical Chemist at our leading Contract Research Organization (CRO), you will have the opportunity to assist in conducting analytical testing of samples using instruments such as HPLC, GC, LC-MS/MS, and UV Spectrophotometer under supervision. You will play a crucial role in preparing reagents, solutions, and standards following Standard Operating Procedures (SOPs) with precision and attention to detail. Your responsibility will include accurately recording and maintaining raw data, logs, and reports in compliance with GLP/GMP standards. By ensuring proper documentation, you will play a pivotal role in meeting regulatory and internal audit requirements. You will provide essential support in method development and validation for pharmaceuticals and biologics. Under the guidance of senior analysts, you will contribute to stability studies and impurity profiling, gaining valuable hands-on experience in the field. Learning and assisting in calibrating and maintaining analytical instruments will be part of your routine tasks. Following preventive maintenance schedules diligently and promptly reporting any malfunctions will be essential in ensuring the smooth functioning of instruments. Adhering to GLP, GMP, and regulatory guidelines while performing your assigned tasks will be crucial. Your active participation in audits and commitment to maintaining compliance with safety and quality standards will be highly valued. You will have the opportunity to enhance your proficiency in analytical techniques through active participation in training sessions. Staying informed about new methodologies, instruments, and advancements in the field will be key to your professional development. We are looking for candidates with a background in M.Sc. (Analytical Chemistry, Organic Chemistry, or related field), M.Pharm, or B.Pharm with practical academic experience. A basic understanding of analytical techniques and foundational knowledge of instruments like HPLC, LC-MS, or GC is desirable. Familiarity with GLP and GMP guidelines will be an advantage. Strong analytical and critical thinking abilities, effective communication and teamwork skills, and enthusiasm for learning and adapting to new challenges are essential soft skills we are seeking in potential candidates. Joining us will provide you with the opportunity to kickstart your career in a structured training environment, tailored to help freshers transition into a professional analytical setting. You will gain hands-on experience with advanced analytical instruments and methodologies, along with clear career progression paths and professional development programs.,

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Role Description: Quality control executive Location: Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 Experience: 5 to 6 years Roles Responsibilities:- To perform all the testing related to RM, bulk, FP and stability samples To perform all the testing of packaging materials Handling of QMS documents like SOP, CAPA, repeat analysis, Deviation etc. To manage and lead the team To perform analytical method validation To prepare specifications for different materials New vendor approval Should have working experience of HPLC, GC, UV spectrophotometer, centrifuge etc. What will you need to be successful Preferred experience in sterile pharma plant. Extensive understanding of sterile and disinfectant products, GMP and GLP Should have faced and experienced regulatory audits Positive attitude, problem solving and time management hould have a knowledge of ICH guidelines and other standards Interested Relevant can share profiles to

You will be responsible for providing routine analytical support to the synthetic team for reaction monitoring by HPLC/GC and analysis of intermediates and API. In this role, you will perform wet analysis including LOD, IR, Residue on Ignition, KF determination, and Titrations. Additionally, you will be involved in the calibration of instruments such as UV, IR, HPLC, GC, Autotitrator, polarimeter, etc. Ensuring compliance with 21 CFR requirements, you will also be responsible for LNB writing and all related documentation. Furthermore, you will prepare the necessary documents for PDR. To excel in this role, you should possess good communication skills and be an effective team player capable of working on multiple projects. A robust knowledge of the principles and working of application techniques such as HPLC, GC, Autotitrator, UV spectrophotometer, and other laboratory instruments is essential for success in this position. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) that provides end-to-end development and manufacturing solutions across the drug life cycle. With a globally integrated network of facilities in North America, Europe, and Asia, PPS offers services including drug discovery solutions, process & pharmaceutical development, clinical trial supplies, commercial supply of APIs, and finished dosage forms. 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 are also provided. Additionally, PPS offers development and manufacturing services for biologics, including vaccines, gene therapies, and monoclonal antibodies, facilitated by Piramal Pharma Limited's investment in Yapan Bio Private Limited. The company's reputation as a trusted service provider with extensive experience across various technologies makes it a preferred partner for innovators and generic companies worldwide. Piramal Group is committed to inclusive growth and ethical practices, offering equal employment opportunities based on merit and without discrimination. Employment decisions are made considering qualifications, skills, performance, and achievements to ensure that all applicants and employees receive fair treatment in personnel matters, including recruitment, selection, training, promotion, compensation, and working conditions. Reasonable accommodation is provided for qualified individuals with disabilities and those with needs related to religious observance or practice.,

Eurofins is the world leading Food Testing laboratory group, deploying a comprehensive range of state-of-the-art analytical techniques in order to support its clients' increasingly stringent quality and safety standards. We are present in India as Eurofins Analytical Services India Pvt Ltd and provide a comprehensive and one-stop testing service to businesses and organizations involved in food and feed processing, Agro products, Export, Hospitality and Retail chains. About The Role Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for record control, measurement traceability and testing results review and approve the testing reports. Maintenance of Standard Reference Materials, Chemicals, Reagents, and Glassware used in the laboratory. To support the installation of additional analytical equipment, methods for the analysis of all kinds of food/feed/water matrices based on the transfer of existing methods and knowledge form the Eurofins Group Preparation of standard operating procedures. Validation of non-standard test methods and non-routine test methods. Be responsible for skill training, reviewing, and appraising the laboratory staff. Be responsible for configuring and monitoring the instrument, equipment, and its environment conditions. Organize and supervise confirmation and verification of the testing methods. Estimation of measurement uncertainty for test parameters Scope preparation for new parameters Be responsible for control of nonconformity work, complaint, Retest request etc Reliable, independent, and service oriented approach to work Qualifications 8-10 years experience of working in food testing laboratory. Strong understanding of ISO 17025 implementation and accreditation process. Proficient in analytical techniques of wet chemistry, proximate analysis, heavy metals analysis. Should have strong leadership skills to handle team of analysts, allotting and supervising the task to team and also monitoring and evaluating the work done. Preferrably a food analyst Graduate in B.Sc / M.Sc in Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Position Overview We are seeking a dedicated and skilled Organic Chemist to join our dynamic team in Jaipur. This full-time position offers an exciting opportunity to contribute to innovative projects in the field of organic chemistry. The ideal candidate will possess a strong foundation in organic chemistry principles and methodologies, along with practical experience in quality assurance and testing. If you are passionate about advancing your career in a collaborative environment, we encourage you to apply. Key Responsibilities Conduct research and experiments in organic chemistry to develop new products and processes. Perform quality assurance (QA) analysis and testing to ensure compliance with industry standards. Utilize various QC tools and techniques to monitor and improve product quality. Develop and optimize analytical methods using techniques such as Gas Chromatography (GC), High-Performance Liquid Chromatography (HPLC), and UV Spectrophotometry. Document and report findings, ensuring accurate record-keeping and adherence to regulatory requirements. Collaborate with cross-functional teams to support product development and troubleshooting efforts. Stay updated with the latest advancements in organic chemistry and related fields. Qualifications The successful candidate will possess the following qualifications: Bachelor's or Master's degree in Organic Chemistry or a related field. 1 to 5 years of relevant work experience in a laboratory setting. Strong knowledge of organic chemistry principles and laboratory techniques. Proficiency in QA analysis, QA testing, and the use of QC tools. Hands-on experience with GC, HPLC, and UV spectrophotometer. Excellent problem-solving skills and attention to detail. Ability to work independently and as part of a team in a fast-paced environment. Strong communication skills, both written and verbal. This position is based in Jaipur and follows a day schedule with an on-site work mode. We are looking to fill one position, and the annual salary for this role is 4,50,000. If you meet the qualifications and are eager to make a significant impact in the field of organic chemistry, we invite you to submit your application.

Job Description Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. Having analytical knowledge of Nasal/Derma products. 3. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 4. Ensuring data integrity policy, GDP and its effectiveness up to compliance 5. To maintain the stability chamber and tracker. 6. To maintain the stability chamber and tracker. 7. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Role & responsibilities Responsible for analysis and documentation of in-process, finished products and stability samples. Handling of QMS, Preparations of Protocols and analytical documents. Preferred candidate profile Biological (Therapeutical Protein) sample Plate based analysis such as ELISA techniques (HCP, HCD, Protein A leachates), PCR, RT-PCR and SDS-PAGE methods. Bioassay analysis for finished products and stability samples by using Gen5 and PLA software. Maintenance of cell lines, Cell culture media and Revival of cell lines. Responsible for analysis of in-process, finished products and stability samples. Preparation of certificate of analysis. Preparation of standard operating procedures, specifications, Protocols and standard testing procedures Operation of UV spectrophotometer, pH Meter, gel power pack, Plate reader and RT-PCR. Initiation of QMS events like lab event, Deviation, OOS, CAPA and Change controls Daily Maintenance of QC laboratory as per GMP requirement. Supervision of AMC and CMC activities for all instruments in the QC. Calibration of instruments and equipment as per the SOP. Work in Shifts

Role & responsibilities Analysis of Routine and Stability samples using instruments like HPLC , UHPLC (Shimadzu), GC.UV spectrophotometer, IR, KF titrator and Dissolution tester. Having Experience in handling of Instruments, Like Analytical Balance, pH meter, KF Titrator, UV spectrophotometer, HPLC, UHPLC, Dissolution tester, GC is preferable Perform Calibration of instruments or equipment Like HPLC, Dissolution. Understanding of wet chemical analysis like: Titration, LOD, KF , IR, UV etc. Maintain analytical documentation records and online documentation of experiments. Understanding of analytical method development Activity. Execute routine Analytical research activities of drug products Follow GLP and safety in the laboratory as per regulatory guidelines. Responsible for any other assignment allocated by the Department Head.

As a Quality Control Chemist at our company, you will be responsible for conducting various tests using equipment such as HPLC, IR, UV Spectrophotometer, etc. You should have a deep understanding and hands-on experience with these instruments. Your primary duty will be to handle Quality Control tests for raw materials, packing materials, SFP, and Finished OSD Formulations. We are specifically looking for candidates residing in the vicinity or able to commute daily to Kerala GIDC. It is essential that you meet the criteria mentioned above to be considered for this role. If you meet these requirements and are confident in your ability to manage the entire functions of Quality Control testing, we encourage you to apply for this position.,

: (In Scope of Position based Promotions (INTERNAL only) Job Title Risk Specialist - Controls Gatekeeper LocationMumbai, India Corporate TitleAssociate Role Description The purpose of the Non-Financial Risk Management (NFRM) function is to ensure that the banks Non-Financial Risk (NFR) exposure is adequately managed in-line with the group wide risk appetite and NFRM framework. To achieve this the NFRM function requires: Risk Managers with experience, seniority, and tools to assess complex risks and intervene where they lie outside the banks risk appetite. A comprehensive, integrated, simple, and easy to use NFR Framework with supporting technology that assists risk identification, assessment and remediation. Strong understanding of the businesses combined with regular engagement which would allow NFRM to provide support, review and challenge in line with the 3 Lines of Defense Model Close coordination with all 2nd Line of Defense (LoD) Risk Type Controllers to facilitate the production of a holistic view of NFR. Proper consideration of emerging risks, rather than just current issues Effective governance combined with supporting MI that facilitates decision-making. NFRM is a matrix organization with business/region and functional specialist axes. The role a business aligned NFR manager has within NFRM is to work with a specific business area and manage NFR according to the 3 LoD model and the NFR mandate. Specifically, they perform independent oversight of the implementation of the Group's NFRM Framework within the Business Divisions and Infrastructure Functions and independently assess material risks and/or key controls (as required), providing challenge, approval, or veto as appropriate. What well offer you . 100% reimbursement under childcare assistance benefit (gender neutral) Sponsorship for Industry relevant certifications and education Accident and Term life Insurance Your key responsibilities This role in the NFR Mumbai Risk Centres Controls Gatekeeper team will be expected to effectively perform 2nd LoD responsibilities to include the independent advice, facilitation, and monitoring and assessment activities on a risk-basis for the underlying business units. Monitor banks controls environmentidentify areas of enhanced Risk Management based on read across of underlying information (e.g. Controls, loss themes, metrics, Findings/SIIs and other contextual information). Review requests for amendments to Control Inventory and ensure theyre in alignment with Operational Risk Controls Procedure Framework. Collaborate with key 1st LoD stakeholders through periodic touchpoints to ensure effective and demonstrable challenge to Divisional Control Officers is made where required. Contribute to Projects/Working Groups relating of NFR Framework or identified NFR risk issues. Monitor key metrics through internal reports and systems and flag issues and breaches; collaborate with 1st LoD stakeholders as the issues and breaches evolve and help provide a link to the wider NFR landscape. Assist in the preparation of decision-making material (such as reports, dashboards, etc.) for the effective 2nd Line of Defense monitoring and challenge of operational risk management. Assess key risks and controls e.g. review lessons learned, deep dives, scenario analysis/emerging risk discussions. Your skills and experience A robust understanding of Non-Financial Risk Management principles and practices with minimum 5-8 years experience in Operational Risk Management Candidates with qualification of Chartered Accountant (CA), Master of Business Administration (MBA), Certification on Risk Management will be preferred. Strong Controls framework background with 2nd LOD and Audit experience in key controls identification, Assurance and Challenge. Business Analyst and Financial Controller with relevant exposure to various Automation tools like VBA Macros, Alteryx, QlikView and SQL etc. Demonstrable experience of developing strong working relationships with business areas to facilitate successful risk management within the 3 LoD model. Advanced user of MS Excel / Access database/VBA Macros/VBA Form Design with experience of data aggregation and manipulation to produce meaningful MI. Worked with Senior Stakeholders within a high-pressure dynamic environment. Ability to demonstrate effective challenge to divisions with regards to risk identification and risk mitigation; identifying material themes and being able to influence business areas to focus on those areas. How well support you . . . About us and our teams Please visit our company website for further information: https://www.db.com/company/company.htm We strive for a culture in which we are empowered to excel together every day. This includes acting responsibly, thinking commercially, taking initiative and working collaboratively. Together we share and celebrate the successes of our people. Together we are Deutsche Bank Group. We welcome applications from all people and promote a positive, fair and inclusive work environment.

Job Title Junior Chemist / Chemist Location - Dhayari, Pune, Maharashtra Qualifications M.Sc. - Soil Chemistry Experience 1 to 4 Yrs. Exp. Pref Industry – Agriculture / Chemical/ Fertilizers/ FMCG/ Pharmaceutical / Biotechnical Key Skills - Good communication Skills Documentation Time management Continual Improvement Process Previous hands-on experience of analytical instruments Knowledge of Soil chemistry and organic manure testing Knowledge of water sample testing Knowledge of good laboratory practices Self-motivated and organized individual with excellent communication skills Roles & Responsibilities- Responsible for Raw material chemical testing Responsible for Finished Product Testing: Organic manure, Bio stimulant, Bio fertilizer, Bio pesticides, etc. Responsible for testing nutrient contents in soil samples. Responsible for calibration and operation of analytical instruments like pH Meter, atomic absorption spectrophotometer, Conductivity meter, HPLC, Flame photometer, UV spectrophotometer, kelplus Kjeldahl unit. Data entry and record keeping as per quality norms. Independent handling of chemistry lab and equipment

Candidate should have a B.Sc or M.Sc in Analytical Chemistry, Food Technology, or Food Chemistry. Preferred to have some knowledge of proximate analysis and water analysis. Willing to learn handling laboratory instruments like AAS, UV Spectrophotometer, HPLC, GC, and FTIR. Open to training and skill development as per laboratory requirements. Should demonstrate enthusiasm for laboratory work and scientific procedures. Eurofins offers international growth opportunities for high-performing individuals.

1) Testing in-coming raw materials material (Non ferrous Metals) and finished product (Non-ferrous oxide) for all parameters. 2) Data entry and record keeping as per quality SOPs and ISO standards 3) Reporting to the QC Head on analysis results Required Candidate profile BSc (minimum) with 4-5 minimum years of experience in analytical chemistry and lab testing, lab instrument handling.

KRA: To provide routine analytical support to the synthetic team for reaction monitoring by HPLC/GC, analysis of intermediates and API. Perform wet analysis as LOD, IR, Residue on Ignition, KF determination, Titrations etc. Calibration of instruments such as UV, IR, HPLC, GC, Autotitrator, polarimeter etc. LNB writing and all documentation as per 21 CFR compliance. Preparation of required documents for PDR. Skills required: Good communication skills, and effective team player with the ability to work on multiple projects. Robust knowledge of principles, working of applications techniques such as HPLC, GC, Autotitrator, UV spectrophotometer and other laboratory instruments. Responsibilities Qualifications M.sc Analytical chemistry/ M-Pharma

Responsible to develop, implement and be responsible for the production plan for their respective departments. To deliver timely and accurate analysis of samples to meet customer commitments. Be responsible for record control, measurement traceability and testing results review and approve the testing reports. Maintenance of Standard Reference Materials, Chemicals, Reagents, and Glassware used in the laboratory. To support the installation of additional analytical equipment, methods for the analysis of all kinds of food/feed/water matrices based on the transfer of existing methods and knowledge form the Eurofins Group Preparation of standard operating procedures. Validation of non-standard test methods and non-routine test methods. Be responsible for skill training, reviewing, and appraising the laboratory staff. Be responsible for configuring and monitoring the instrument, equipment, and its environment conditions. Organize and supervise confirmation and verification of the testing methods. Estimation of measurement uncertainty for test parameters Scope preparation for new parameters Be responsible for control of nonconformity work, complaint, Retest request etc Reliable, independent, and service oriented approach to work Qualifications 8-10 years experience of working in food testing laboratory. Strong understanding of ISO 17025 implementation and accreditation process. Proficient in analytical techniques of wet chemistry, proximate analysis, heavy metals analysis. Should have strong leadership skills to handle team of analysts, allotting and supervising the task to team and also monitoring and evaluating the work done. Preferrably a food analyst Graduate in B.Sc / M.Sc in Chemistry Additional Information Good interpersonal and communication skills. Energetic, flexible and innovative. Able to work independently and to coordinate several activities simultaneously. Good in communication, read and write in English and local language. Acts quickly and decisively. Knowledge in Microsoft Office (such asMicrosoft Word, Excel, Power Point, & etc.),

Long Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Competencies Education Others Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs.

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

Hello, We have urgent opening for the below profile Designation :- Technician / Operator Experience :- 3-5 Years Qualifications :- Diploma in instrumentation Job Responsibilities :- 1) Manage and maintain analytical instruments which includes HPLC, Dissolution, UV Spectrophotometer , GC, Particle size, Milli Q water purification system, Analytical/Precision balance etc. 2) Co-ordination with service engineer for breakdown and preventive maintenance 3) Oversee repair and calibration of instruments/equipments 4) Ensuring adherence to quality standards and best practices to ensure zero downtime 5) Co-ordination with CFT team for PO and spares If you think that you fit the role, please share your updated copy of resume with notice period, Current CTC, Expected CTC. We would divulge more information regarding the position. Please share your resume on jobs.hr@ipca.com

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 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