68 Analytical Testing Jobs

Role Overview: As a Quality Control Officer, your primary responsibility is to ensure the best quality of products and minimize customer complaints by conducting stringent online quality control checks and finished product inspections. You will be responsible for implementing the right quality control systems and standards for processes, physical systems, and the environment. Troubleshooting during online production to minimize wastage and ensure quality will be a key aspect of your role. Additionally, you will be expected to maintain GMP, GHK GLP, and conduct internal/external audits. Key Responsibilities: - Conduct online quality checks in the process area to ensure FLI standards of quality are followed - Conduct visual inspections on key operating parameters of machines - Peelers, Fryers, Slicer, Chip Conveyors, Seasoning Tumbler - Check potatoes in the trim and pare area for proper peeling - Monitor slice thickness and free surface moisture periodically - Decide on introducing anti-foaming agent in the process - Record dwell time from operators logbook - Check seasoning level and conduct analytical tests as required - Optimize utilization of fryer oil and conduct regular checks - Compare test results against gold standards and adjust oil blend as needed - Monitor fried chips for various parameters - Conduct analytical tests for blanching requirements and fryer oil usage - Take corrective actions based on test results and provide feedback to operators - Communicate process requirements to shift in-charge and production manager - Inform Quality Manager of crisis situations for appropriate decision-making - Conduct online quality checks and finished product inspection in the packaging area - Ensure compliance with Frito Lay standards of quality in the packaging process - Monitor Quality Checkers for air leakage and other quality parameters - Conduct analytical tests for oxygen percentage in bags and film quality - Address any concerns promptly with operators, shift in-charge, and production manager - Consult with Quality Manager for critical situations and ensure corrective actions are implemented Qualifications: - B.Tech in Food Technology (Note: Any additional details about the company were not provided in the job description.),

Role Overview: As a Senior Executive - API at Dishman Carbogen Amcis Limited in Bavla, Gujarat, you will be responsible for ensuring that analytical methods are validated and verified in compliance with regulatory standards. Your role will involve reviewing and approving validation protocols and reports to ensure accuracy and consistency. Additionally, you will review and evaluate raw data from analytical testing to ensure compliance with specifications and standards. It will be your responsibility to identify trends, deviations, and out-of-specification results in analytical data and recommend corrective actions. Key Responsibilities: - Ensure that all analytical testing is performed according to SOPs (Standard Operating Procedures) and regulatory requirements. - Coordinate with the QC (Quality Control) team to ensure proper execution of tests and maintenance of laboratory equipment. - Review and approve laboratory reports, batch records, and test results. - Maintain accurate records in compliance with GMP (Good Manufacturing Practices) and regulatory guidelines. - Investigate and document any deviations or non-conformances identified during testing. - Participate in root cause analysis and the implementation of corrective and preventive actions (CAPA). Qualifications Required: - Bachelor's or Master's degree in a relevant scientific discipline. - Previous experience in a similar role within the pharmaceutical or chemical industry would be advantageous. - Strong understanding of regulatory standards and compliance requirements. - Excellent attention to detail and analytical skills. - Good communication and coordination abilities to work effectively with the QC team. (Note: No additional details of the company were present in the job description.),

- Lead BD for pharma/analytical testing - Drive domestic & global client acquisition - Handle key accounts & contract negotiation - Develop growth strategies & manage team - Exp. in lab services - Drive global client growth

As a Pharma Subject Matter Expert (SME) Trainer, you will be responsible for training candidates in various aspects of Quality Control (QC), Cell Culture Techniques, and Laboratory Procedures. Your role involves providing hands-on experience in analytical testing, microbiological testing, and pharmaceutical laboratory operations. It is essential to educate candidates on method validation, stability testing, and data integrity while ensuring compliance with FDA, USP, and cGMP regulations. Additionally, you will train individuals in utilizing HPLC, GC, UV-Vis, FTIR, PCR, ELISA, and Spectroscopy techniques. Your responsibilities include conducting mock interviews, assisting with resume preparation, and providing real-world project training to enhance the skills of the candidates. You will be required to ensure that trainees understand deviation handling, OOS/OOT investigations, CAPA processes, and regulatory audit procedures. Collaboration with the sales team is crucial to ensure that the trainees meet the expectations of their future employers. The ideal candidate should possess hands-on experience in cell culture, microbiology, and analytical laboratory techniques. Proficiency in HPLC, GC, FTIR, UV-Vis, and PCR is essential for this role. A strong understanding of data integrity, compliance documentation, and industry regulations such as cGMP, ICH, USP, and FDA guidelines is also required. Previous experience in stability testing, method validation, and impurity profiling will be beneficial. Your excellent mentoring and training skills, coupled with a passion for upskilling candidates, will be key to your success in this position. In addition to the specific responsibilities mentioned above, you will be expected to conduct one-on-one in-person training sessions, coordinate with internal teams for seamless training execution, and provide support to candidates in resume building, interview preparation, and exposure to real-time projects. Keeping abreast of industry trends and continuously updating training content accordingly is an integral part of this role. Please note that candidates who successfully complete two years with us will be eligible for visa sponsorship. If you are enthusiastic about mentoring and developing future pharmaceutical professionals, we look forward to receiving your application.,

The Manager - Quality Control (QC) will be responsible for ensuring that all products manufactured for third-party clients meet quality standards, regulatory requirements, and client specifications. You will oversee all QC activities in the production process, lead a team, manage testing procedures, and ensure adherence to quality guidelines for skincare, hair care, body care, and personal care products. Your key responsibilities will include developing, implementing, and maintaining QC processes to ensure products meet quality and safety standards. You will monitor production processes, work closely with the production and R&D team to identify and resolve any quality-related issues, and oversee the quality control department's daily operations for smooth workflow and efficient resource utilization. Ensuring compliance with international quality standards and local regulatory requirements will be crucial, along with conducting regular audits of production facilities. You will evaluate team performance, conduct stability, microbiological, and efficacy testing, maintain accurate records, and oversee the preparation of quality control documentation. To qualify for this role, you should have a Bachelor's or Master's degree in chemistry, Pharmacy, Cosmetics, Engineering, or a related field, along with 5-7 years of experience in quality control or quality assurance within the skincare, hair care, body care, or personal care manufacturing industry. Strong knowledge of Good Manufacturing Practices (GMP), ISO 9001, FDA, and other relevant regulatory standards is necessary, as well as proven experience in managing a team and leading quality control functions. Experience with testing methods, product development processes, and quality control tools is essential, along with attention to detail, analytical skills, and problem-solving abilities. Proficiency in Microsoft Office and quality management software is required, and certification in Quality Management is an advantage. This is a full-time position with benefits including health insurance and Provident Fund, requiring a day shift schedule. A question about your background in the Cosmetic Manufacturing Industry will be asked during the application process, with the work location being in person.,

You will be responsible for developing electrochemical sensors for biological and diagnostic applications. This will involve designing and characterizing electrodes, optimizing biochemical assays on disposable electrodes. You will independently design experiments, execute them, analyze the data, and maintain records diligently. Additionally, you will be involved in lab maintenance and organizational activities. As a Research Fellow, you are expected to apply relevant scientific principles and techniques to analytical testing problems. You will also be responsible for drafting and revising process documents, assay methods, and sampling plans. The ideal candidate for this role should have an educational qualification in Chemical Engineering, Material Science Engineering, or MSc Chemistry with an interest in membrane-related work. If you are passionate about research and have the required educational background, this opportunity based in Bangalore could be a perfect fit for you. For further details or to apply for the position, please contact us at career@bigtec.co.in.,

Role & responsibilities Lead and manage the stability study program as per ICH guidelines. Plan, initiate, and monitor real-time, accelerated, and intermediate stability studies for all products. Ensure timely sampling, testing, and data review for all ongoing stability studies. Maintain and review stability protocols and reports, ensuring compliance with regulatory requirements. Handle stability chambers (qualification, calibration, and monitoring) and ensure 21 CFR Part 11 compliance. Provide managerial oversight for instrument calibration, qualification, and maintenance activities in QC lab. Ensure timely availability of reagents, reference standards, working standards, and lab consumables. Support analytical testing of RM/PM/FG and ensure smooth functioning of lab operations. Perform investigation and troubleshooting of analytical issues, OOS, OOT, and lab incidents. Ensure GMP compliance in all QC stability and lab support activities. Prepare and review SOPs, protocols, and laboratory documentation. Support regulatory inspections and audits with necessary documentation and responses. Initiate and review change controls, deviations, and CAPAs related to stability and lab operations. Participate in quality risk assessments, method transfers, and method validations. Drive continuous improvement initiatives for lab efficiency, error reduction, and cost control. Implement systems for improved turnaround time (TAT) for testing and report generation. Oversee and ensure timely calibration, qualification, and preventive maintenance of analytical instruments. Ensure adequate availability and management of laboratory reagents, reference standards, and working standards. Review and approve analytical test data, protocols, and reports ensuring regulatory compliance. Support lab teams during analytical method validation, method transfer, and troubleshooting of technical issues. Train team members on LIMS usage, functionality, and best practices. Interested candidate can share their CV at Anee.Silas@otsukapharma.in

You will be joining Vimson Derma, a renowned contract manufacturer of cosmetic and medicated products located in Ahmedabad with over 45 years of experience in the cosmetics and dermatology industry. As a trusted name in the field, Vimson Derma holds certifications such as GMP, GLP, and ISO 9001:2015, ensuring the highest quality standards. The company's product range includes dusting powders, talcum powders, shampoo, conditioner, cream, gel, lotions, oil, soaps, sunscreen, serums, and more. With a substantial client base of over 200 companies across India, Vimson Derma is committed to delivering excellence in the products they manufacture. As the R&D Senior Executive in Cosmetics, your primary responsibility will be to formulate, develop, and enhance cosmetic products while ensuring compliance with industry regulations and market trends. This role will involve extensive research, product innovation, stability testing, and collaboration with various departments to introduce high-quality cosmetic formulations to the market. Your key responsibilities will include developing and optimizing innovative formulations for skincare, haircare, personal care, and cosmetic products based on market and client requirements. You will need to identify and assess new active ingredients, raw materials, and technologies to improve product efficacy and innovation. Conducting stability studies to evaluate product performance, consistency, and shelf-life under various conditions will also be a crucial aspect of your role. It is essential to ensure that all formulations comply with GMP, BIS, FDA, ISO 9001:2015, and other relevant cosmetic regulations. Collaboration with the production team to streamline formulation processes for scalability, cost efficiency, and production feasibility will be an integral part of your responsibilities. Analyzing competitor products and industry trends to enhance existing formulations and create market-driven innovations will also be expected. Maintaining detailed records of formulation trials, test results, and regulatory documentation, as well as evaluating raw materials for performance and safety, will be essential tasks. Working closely with Quality Assurance, Production, Purchase, and Marketing teams to facilitate smooth product development and launch will be part of your daily activities. To qualify for this role, you should hold a Masters/Bachelors degree in Cosmetic Science, Chemistry, Pharmaceutical Sciences, or a related field, along with at least 5 years of experience in cosmetic product formulation and R&D. Strong knowledge of cosmetic ingredients, emulsions, surfactants, actives, and preservatives is required. Familiarity with GMP, BIS, FDA regulations, ISO standards, and safety guidelines is essential. Experience with stability testing, analytical testing, and product evaluation techniques is advantageous. Proficiency in MS Office (Excel, Word, PowerPoint) and formulation software is expected. Strong problem-solving, analytical, and documentation skills are necessary, along with the ability to manage multiple projects and meet deadlines in a fast-paced environment. This is a full-time position with a work schedule of 6 days per week. The job location is at 816/3 Kothari Industrial Estate, Opp Khodal Lodge, Santej, Kalol, Gujarat 382721.,

Role & responsibilities Only those candidates can apply who: 1. are available for full time (in-office) internship 2. can start the internship between 25th Aug'25 and 29th Sep'25 3. are available for duration of 6 months 4. have relevant skills and interests in Chemistry * Women wanting to start/restart their career can also apply Preferred candidate profile Candidates shall be fresh graduates from the year 2023 and onwards. He, or she shall have good communication skills with good personality and agility to learn in life. The opportunity is in a Japanese MNC and is a wonderful opportunity to kickstart the career.

- Having experience in manufacturing cosmetics related products such as Cream, Lotion, Shampoo, Face Wash, Cleaner, Skincare, Nailpolis etc. - Supervising in-process quality control and managing bulk approvals and finished goods (FG) release. Required Candidate profile - Hands-on experience in instrumental and analytical testing of raw materials (RMs). Maintaining comprehensive records of quality tests, inspections, and other related activities.

Eurofins Consumer Product Testing India provides high standard quality assurance and control services, such as testing, certification, inspection, audits, technical and regulatory services, to manufacturers, brand owners, distributors and trading companies, buying associations, consumer associations, and retailers worldwide. We are dealing with various consumer product testing like: "¢ Fabric and Textiles "¢ Cosmetics "¢ Food contact materials "¢ Toys "¢ Detergents "¢ Apparel "¢ Rubber "¢ Leather "¢ Plastics "¢ Accessories "¢ Footwear "¢ Home Textiles With EUR 4.5 billion in annual revenues and 50,000 employees across over 800+ laboratories across 50 countries, Eurons Scientic is a leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. Roles and Responsibilities Sample control and file keeping to client and follow up to match the TAT Good connect and coordination with external Clients, Sales team & lab team. To ensure to attend and clear the entire query from client and vendor in an efficient manner New on Boarding Vendor Management(NOB) Hold Reduction. Maintaining all the Quality records generated during the process. Ensure confidentiality of information obtained during the course of employment. Closely working with Sales & Operations team Qualifications Graduate or MBA From Textile industry Additional Information Compensation will be between 3 - 8 LPA based on current.

Eurofins Consumer Product Testing India provides high standard quality assurance and control services, such as testing, certification, inspection, audits, technical and regulatory services, to manufacturers, brand owners, distributors and trading companies, buying associations, consumer associations, and retailers worldwide. We are dealing with various consumer product testing like: "¢ Fabric and Textiles "¢ Cosmetics "¢ Food contact materials "¢ Toys "¢ Detergents "¢ Apparel "¢ Rubber "¢ Leather "¢ Plastics "¢ Accessories "¢ Footwear "¢ Home Textiles With EUR 4.5 billion in annual revenues and 50,000 employees across over 800+ laboratories across 50 countries, Eurons Scientic is a leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. "¢ Should be a local candidate from Panipat. "¢ Knowledge of Home textiles products, like kitchen accessories / sheet sets / towels/ Mats etc. "¢ Relevant experience in QA/ QC (Quality Assurance/ Quality Control) "¢ Willing to travel. "¢ Maintain the quality compliance of the customers. "¢ To ensure product delivery on time to meet customer satisfaction. "¢ Should be able to handle day to day activities at production floors. "¢ To carry out all kind of controls/inspections like PPM, Inline, Mid, Final audits etc. as per AQL system & as defined by the buyer in order to get product in right desired quality within the given delivery date. "¢ Good computer and communication skills. "¢ Develop, manage implement, communicate, and maintain a quality plan to bring the Company"™s Quality Assurance Systems and Policies into compliance with quality system requirements. "¢ Effectively interact with the Technical, Development, and Production team to maintain product quality; ensuring that targets are achieved. "¢ Assisting technicians with checking patterns/specification and construction, identifying, and resolving production impracticalities in an appropriately timely manner, and to make a final decision on quality according to company standards and requirements. "¢ Supervise in the handling of sample evaluation and production approval by reviewing the measurement, workmanship, fitting, accessories, etc., and giving comments on the production. "¢ Monitored QA/QC performance by gathering relevant production data and producing statistical reports to be communicated with all related departments. Identifying relevant quality-related training needs and delivering training. "¢ Responsible for each aspect of TQM/Quality Management/Control and product assembly in the factory. "¢ Knowledge of problem-solving quality tools like fishbone, why-why analysis . "¢ Provide enough quality control seminars and coaching for company trainees. "¢ To conduct Risk Analysis and pre-production meeting and to give size set sample approval. "¢ Doing In-line inspection to check the quality/Follow up pre-Final / final inspections. "¢ To keep all necessary documents and quality SOP & ensuring all quality & production issue by Auditing & Controlling. "¢ To be able to provide approval such as print, embroidery, wash & as per required by the MR teams. "¢ To maintain all discipline and compliance issue & able to communicate with overseas customers. Qualifications "¢ Degree/Diploma in Textiles / NIFT graduate is preferred "¢ Minimum 10-15 years' relevant experience "¢ Strong knowledge of quality tools is a must "¢ Able to work under pressure, result oriented, excellent communication skills, self-motivated, responsive and detail minded "¢ Ability to build strong relationships with the team as a good team leader, communication effectively with internal and external parties "¢ Well organized individual, able to manage multiple tasks, strong problem-solving skills, handle multiple priorities in a fast paced and dynamic environment "¢ Excellent command of written and spoken English. Literate in Microsoft office programs If this sounds like you, ! Additional Information Key SkillQA manager, Quality Assurance home textile, Quality Assurance , quality control, ISO 17025 is must

Eurofins Consumer Product Testing India provides high standard quality assurance and control services, such as testing, certification, inspection, audits, technical and regulatory services, to manufacturers, brand owners, distributors and trading companies, buying associations, consumer associations, and retailers worldwide. We are dealing with various consumer product testing like: "¢ Fabric and Textiles "¢ Cosmetics "¢ Food contact materials "¢ Toys "¢ Detergents "¢ Apparel "¢ Rubber "¢ Leather "¢ Plastics "¢ Accessories "¢ Footwear "¢ Home Textiles With EUR 4.5 billion in annual revenues and 50,000 employees across over 800+ laboratories across 50 countries, Eurons Scientic is a leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. Prepare individual sales action plans in line with the overall sales strategy to ensure a targeted and focused approach that consistently contributes to the overall growth aims of the business Materialize current sales opportunities and identify news ones to meet required revenue targets within defined areas of responsibility Sales target of revenue and sales proposal & meetings etc. Identify, research, plan contact potential clients to establish new business in order to achieve targeted revenue growth Anticipate, identify and understand client s needs and pains and translate those into sales opportunities Prepare quotations, service agreements and tenders within set deadlines. Textile experience with TIC industry preferrably. Qualifications Any Graduation with MBA. Pref. B.Tech/Diploma in Textile Additional Information Key SkillSales, Marketing, Negotiation, Business development, BD, Target, Budget

Chemical and physical tests on in-process samples, and finished products using techniques like HPLC, GC, and titrations. Maintaining accurate records of analytical data, preparing reports, and ensuring compliance with GLP and GMP. Required Candidate profile Developing & validating analytical methods and procedures to ensure accuracy Following all safety guidelines, regulatory standards Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

Product Development/Product performance/Process Parameter Knowledge on modification of activated carbon structure Develop specialty carbons for gas phase potable waters Testing as per international testing procedures Establishment of Quality system Required Candidate profile Contact: 8939813208 Mail ID: finadsorbent@carbons.in

Oversee analytical quality control operations. Ensure compliance with regulatory requirements. Maintain accuracy in analytical testing and reporting. QC executive - Should have haandled - pH meter, Osmometer, Conductivity meter, & manage samples

Job description Lead the verification and validation of analytical and microbiological methods, ensuring they meet all regulatory and internal quality requirements. Design, execute, and document method validation protocols, including accuracy, precision, specificity, and robustness studies, in compliance with FDA, TGA, ICH, and EMA guidelines. Review and approve validation protocols and reports, ensuring they are scientifically sound and fully compliant with Good Laboratory Practice (GLP) and other relevant regulatory standards. Analytical and Microbiology Methods: Provide expert review and oversight of analytical and microbiological testing protocols, data, and reports, ensuring compliance with regulatory standards and internal quality systems. Oversee the development, validation, and implementation of new analytical and microbiological methods and, including but not limited to chemical analysis, sterility testing, microbial limits testing, and endotoxin testing. Ensure that all methods are validated to provide reproducible and accurate results, adhering to FDA, TGA, ICH, and EMA requirements Data Review and Integrity: Conduct thorough reviews of raw data and final reports related to analytical and microbiology testing and method validation. Ensure that all data generated during analytical and microbiological testing is accurate, complete, and adheres to the approved protocols and SOPs. Identify and resolve any data discrepancies or deviations from established protocols. Regulatory Compliance: Ensure that all analytical and microbiological methods and validations comply with FDA, TGA, ICH, and EMA regulations. Assist in the preparation of documentation for regulatory submissions, providing quality assurance support for analytical and microbiological data and validation reports. Continuous Improvement: Contribute to the development and continuous improvement of quality systems related to analytical and microbiological methods and validation processes. Participate in root cause analysis of quality issues and support the implementation of corrective and preventive actions (CAPAs). Training and Development: Provide guidance and training to R&D staff on best practices in analytical and microbiological testing, method validation, and quality assurance. Act as a mentor and resource for junior staff in the areas of analytical development, microbiology and quality assurance What you d gain: Invaluable hands-on experience working alongside seasoned developers. Opportunity to learn and grow in a supportive environment. Gain exposure to the entire software development lifecycle. Contribute to real-world software projects and make a positive impact. Qualifications: Bachelor s degree in Chemistry, Microbiology, Biology, Pharmaceutical Sciences, or a related scientific discipline is required. Advanced degree (Master s or Ph.D.) in a related field is preferred. Minimum of 5-7 years of experience in quality assurance with a focus on analytical, microbiology, method verification, and validation within the pharmaceutical, biotech, or life sciences industries. Extensive experience with analytical and microbiological testing methods, including method verification, validation, sterility, microbial limits, and endotoxin testing. Strong expertise in analytical and microbiological methods and their application in product development. Excellent attention to detail and analytical skills with a focus on data integrity and accuracy. Strong written and verbal communication skills, with the ability to document and present complex technical information clearly. Ability to work effectively in a team-oriented environment and collaborate across multiple departments. Proficiency with quality management systems and software tools. This position is remote and may require occasional travel to other sites or meetings. The role may involve working in a laboratory environment with exposure to chemicals and biohazardous materials.

As a Quality Control and Assurance Manager, your main responsibility will be to manage and supervise QC and QA operations to ensure alignment with industry standards and company SOPs. You will be in charge of performing and overseeing analytical testing using advanced laboratory instruments such as AAS, HPLC, and Titration. Your role will also involve ensuring that quality standards are maintained throughout all production stages. Additionally, you will conduct internal and external audits, ensuring the timely implementation of corrective and preventive actions (CAPA) and maintaining documentation in compliance with regulatory requirements. As a leader in the QC/QA team, you will also provide guidance and mentorship to team members. To be successful in this role, you should hold a B.Sc/M.Sc in Chemistry or a related field and have a minimum of 8-12 years of experience in Quality Control & Assurance within the chemical or related industries. Sound knowledge of various analytical techniques and instrument handling is essential, along with proven experience in audit preparation and compliance. Strong communication, leadership, and problem-solving skills are crucial for this position. Candidates who can join immediately will be given preference. This is a full-time, permanent position with benefits including health insurance, paid sick time, and Provident Fund. The work location is in Khanna, Punjab, therefore, reliable commuting or planning to relocate before starting work is preferred. The ideal candidate should have at least 9 years of experience in chemical testing. If you meet the candidate requirements and are ready to take on this challenging role, we encourage you to apply and be a part of our dynamic team.,

The Senior Business Development Executive position at Ribosome Research Center in Kim, Surat requires a candidate with an MBA in Marketing and 5 to 10 years of experience working as a Business Development Executive in a Contract Research Organisation. The ideal candidate should have experience in GLP, Pre Clinical or a well-known CRO Company. As a Senior BD Executive, you will be responsible for developing strategic market positioning and creating market space. You will be expected to generate new leads for contract research services and create effective market campaigns in Preclinical R & D, Pharma R & D, drug testing, toxicology, and analytical testing. Additionally, you will be managing key global strategies and collaborating with the research team to develop services of the Contract Research Organisation aligning to the needs of OECD GLP compliances. Your role will also involve managing existing businesses and creating long-term business opportunities. The benefits of this position include food provided, leave encashment, paid sick time, and paid time off. Key skills required for this role include business development, research, CRO management, toxicology, lead generation, contract research services, pharma R&D, business opportunities, market positioning, OECD GLP compliance, preclinical, drug testing, campaigns, analytical testing, and strategic planning.,

Role & responsibilities Analytical test including physical and wet analysis. Expertise in handling of HPLC, GC , UV and IR Knowledge on OOS and OOT Calibration of laboratory Instruments. Preparation and standardization of Reagents/Volumetric solutions. To ensure cGLP compliance and Data Integrity Note : Candidate who can Join Immediately are preferred and willingness to work in Shift basis. Candidate should have experience in Pharmaceutical Formulation - OSD - Tablets Manufacturing facility

Analytical Development Laboratory Associate Male Min 2-5 Exp only API Co Salary: 2-3 LPA Location: Vadodara( Nandesari ), Gujrat

You will be responsible for liaising between various departments such as Planning, Production, Technical Services, Marketing, and Exports. Your roles and responsibilities will include the preparation, review, and implementation of SOPs and STPs. You will be checking all QC related records like analytical reports and logbooks. Additionally, you will be involved in planning and distributing samples for the analysis of Raw Materials, Intermediates, and finished products. You will design and conduct Stability studies as per ICH Guidelines and develop and validate analytical testing methodology used to control raw materials, production intermediates, and final products. Your tasks will also include the preparation and maintenance of working standards with documents, as well as the operation and calibration of laboratory instruments like HPLC, GC, and Spectrophotometer. You will review and approve Raw material, finished product, and Packaging material specifications. Furthermore, you will be responsible for handling customer audits and regulatory authority audits and preparing compliance reports. Troubleshooting of HPLC, GC, and other instruments will be part of your responsibilities. You will manage the laboratory and work towards analytical laboratory improvement, cGMP and GLP compliance, and problem resolution. As the QA/QC Manager, you will be solely responsible for exports and quality-related issues for the unit. You will supervise QC chemists to ensure the smooth working of the department and to guarantee the best quality of products from the production. This is a Full Time position located in Byrathi, Bangalore.,

Role & responsibilities • The primary task of the Quality Analyst is call monitoring and providing actionable insight To gather information to help improve agent performance in the call center QA have an evaluation form that will be used to capture the information Implement scripts, record actual results and identify defects Suggest creative and active solutions for problem Assist in identifying & reporting of defects and propose resolution Identify training needs and take action to improve performance Prepare, review and present input to quality analysis test cases Identify and bridge gaps, Asses agent performance Ensure call audit targets are met successfully covering the entire team (allocated) Identify the bottom quartile, work with them and show improvement Calibrate with local Operations team to discuss the observations and track the improvement Creating an inspiring team environment with an open communication culture Organize regular, Refresher / Q&A and Call listening session Monitor teams quality performance and report on metrics Discover training needs and provide coaching Capture Customer Voice and propose solution over better call handling Identify process gaps, if any and highlight to operations team Publish Quality score agent wise/team wise/center wise on a regular basis Give process overview to the new team members Monthly assessments to check the knowledge level of the team Preferred candidate profile • Minimum 2 year of Quality Analyst experience and 3 years of overall experience Knowledge of Quality audits and parameters Good PC skills, especially MS Excel Good communication skills verbal and written Organizational and time-management skills Decision-making skills Graduate for recognized university • Good PC skills, especially MS Excel • Good communication skills verbal and written • Organizational and time-management skills • Decision-making skills

Eurofins Consumer Product Testing India provides high standard quality assurance and control services, such as testing, certification, inspection, audits, technical and regulatory services, to manufacturers, brand owners, distributors and trading companies, buying associations, consumer associations, and retailers worldwide. We are dealing with various consumer product testing like: "¢ Fabric and Textiles "¢ Cosmetics "¢ Food contact materials "¢ Toys "¢ Detergents "¢ Apparel "¢ Rubber "¢ Leather "¢ Plastics "¢ Accessories "¢ Footwear "¢ Home Textiles With EUR 4.5 billion in annual revenues and 50,000 employees across over 800+ laboratories across 50 countries, Eurons Scientic is a leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. "¢ Should be a local candidate from Panipat. "¢ Knowledge of Home textiles products, like kitchen accessories / sheet sets / towels/ Mats etc. "¢ Relevant experience in QA/ QC (Quality Assurance/ Quality Control) "¢ Willing to travel. "¢ Maintain the quality compliance of the customers. "¢ To ensure product delivery on time to meet customer satisfaction. "¢ Should be able to handle day to day activities at production floors. "¢ To carry out all kind of controls/inspections like PPM, Inline, Mid, Final audits etc. as per AQL system & as defined by the buyer in order to get product in right desired quality within the given delivery date. "¢ Good computer and communication skills. "¢ Develop, manage implement, communicate, and maintain a quality plan to bring the Company"™s Quality Assurance Systems and Policies into compliance with quality system requirements. "¢ Effectively interact with the Technical, Development, and Production team to maintain product quality; ensuring that targets are achieved. "¢ Assisting technicians with checking patterns/specification and construction, identifying, and resolving production impracticalities in an appropriately timely manner, and to make a final decision on quality according to company standards and requirements. "¢ Supervise in the handling of sample evaluation and production approval by reviewing the measurement, workmanship, fitting, accessories, etc., and giving comments on the production. "¢ Monitored QA/QC performance by gathering relevant production data and producing statistical reports to be communicated with all related departments. Identifying relevant quality-related training needs and delivering training. "¢ Responsible for each aspect of TQM/Quality Management/Control and product assembly in the factory. "¢ Knowledge of problem-solving quality tools like fishbone, why-why analysis . "¢ Provide enough quality control seminars and coaching for company trainees. "¢ To conduct Risk Analysis and pre-production meeting and to give size set sample approval. "¢ Doing In-line inspection to check the quality/Follow up pre-Final / final inspections. "¢ To keep all necessary documents and quality SOP & ensuring all quality & production issue by Auditing & Controlling. "¢ To be able to provide approval such as print, embroidery, wash & as per required by the MR teams. "¢ To maintain all discipline and compliance issue & able to communicate with overseas customers. Qualifications "¢ Degree/Diploma in Textiles / NIFT graduate is preferred "¢ Minimum 10-15 years' relevant experience "¢ Strong knowledge of quality tools is a must "¢ Able to work under pressure, result oriented, excellent communication skills, self-motivated, responsive and detail minded "¢ Ability to build strong relationships with the team as a good team leader, communication effectively with internal and external parties "¢ Well organized individual, able to manage multiple tasks, strong problem-solving skills, handle multiple priorities in a fast paced and dynamic environment "¢ Excellent command of written and spoken English. Literate in Microsoft office programs If this sounds like you, ! Additional Information Key SkillQA manager, Quality Assurance home textile, Quality Assurance , quality control, ISO 17025 is must

Eurofins Consumer Product Testing India provides high standard quality assurance and control services, such as testing, certification, inspection, audits, technical and regulatory services, to manufacturers, brand owners, distributors and trading companies, buying associations, consumer associations, and retailers worldwide. We are dealing with various consumer product testing like: "¢ Fabric and Textiles "¢ Cosmetics "¢ Food contact materials "¢ Toys "¢ Detergents "¢ Apparel "¢ Rubber "¢ Leather "¢ Plastics "¢ Accessories "¢ Footwear "¢ Home Textiles With EUR 4.5 billion in annual revenues and 50,000 employees across over 800+ laboratories across 50 countries, Eurons Scientic is a leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. Roles and Responsibilities Sample control and file keeping to client and follow up to match the TAT Good connect and coordination with external Clients, Sales team & lab team. To ensure to attend and clear the entire query from client and vendor in an efficient manner New on Boarding Vendor Management(NOB) Hold Reduction. Maintaining all the Quality records generated during the process. Ensure confidentiality of information obtained during the course of employment. Closely working with Sales & Operations team Qualifications Graduate or MBA From Textile industry Additional Information Compensation will be between 3 - 8 LPA based on current.