2096 Hplc Jobs - Page 9

About Us HCP Wellness Private Limited is a leading manufacturer of Skin Care, Cosmetics, and Oral Care products, committed to delivering innovative, high-quality solutions that combine science, safety, and customer trust. At HCP Wellness, we believe in teamwork, ownership, discipline, cleanliness, and safety values that guide every process from lab to shelf. Position Overview The QC Chemist Vacancy will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Email career@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

About Us HCP Wellness Private Limited is a leading manufacturer of Skin Care, Cosmetics, and Oral Care products, committed to delivering innovative, high-quality solutions that combine science, safety, and customer trust. At HCP Wellness, we believe in teamwork, ownership, discipline, cleanliness, and safety values that guide every process from lab to shelf. Position Overview The QC Analytical Chemist will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

The Chemist Quality Control will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

The Job For QC Chemist will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry.

About Us HCP Wellness Private Limited is a leading manufacturer of Skin Care, Cosmetics, and Oral Care products, committed to delivering innovative, high-quality solutions that combine science, safety, and customer trust. At HCP Wellness, we believe in teamwork, ownership, discipline, cleanliness, and safety values that guide every process from lab to shelf. Position Overview The QC Chemist Jobs will be responsible for ensuring that all raw materials, in-process materials, and finished products meet the highest standards of quality, safety, and compliance. This role requires strong technical knowledge, keen attention to detail, and adherence to GMP, GLP, and regulatory guidelines to maintain product integrity. Key Responsibilities Conduct quality control testing of raw materials, bulk, and finished goods as per SOPs. Perform physicochemical, instrumental, and microbiological analysis using methods such as HPLC, GC, UV, FTIR, pH meter, viscometer, and titrations. Ensure compliance with cGMP, GLP, and regulatory requirements (FDA, ISO, WHO-GMP). Prepare and review analytical reports, COAs, stability study data, and batch release documents. Monitor in-process quality at various manufacturing stages to prevent deviations. Collaborate with QA, R&D, and Production teams to resolve quality issues. Participate in internal audits, CAPA, and continuous improvement initiatives. Maintain proper documentation and ensure calibration, safety, and cleanliness of instruments and lab areas. Qualifications & Skills Education / Certifications B.Sc. / M.Sc. in Chemistry, Pharmaceutical Chemistry, Cosmetics, or related field. Additional certification in Quality Control / GMP / GLP preferred. Hard Skills Proficiency in analytical techniques (HPLC, GC, UV, FTIR, Titrations, etc.). Knowledge of stability studies, specifications, and pharmacopeia (IP, USP, BP, EP). Strong understanding of cosmetics, oral care, and skincare formulations. Hands-on experience with documentation, SOPs, and COA preparation. Familiarity with regulatory guidelines (FDA/ISO/WHO-GMP). Soft Skills Strong attention to detail and accuracy. Good communication and teamwork skills. Ability to troubleshoot and solve problems effectively. Discipline, ownership, and commitment to safety and cleanliness. Experience 2 3 years of experience in Quality Control within the Cosmetics, Skincare, Oral Care, or Pharmaceutical industry. Why Join HCP Wellness? Opportunity to work with a fast-growing, innovation-driven personal care manufacturer. Exposure to state-of-the-art laboratories and advanced testing techniques. Work culture built on teamwork, ownership, discipline, cleanliness, and safety. Growth opportunities within R&D, QA, and global compliance roles. Apply Now WhatsApp Apply Now WhatsApp Job Location : Bavla On Call Assistance: Email career@hcpwellness.in Job Type: Full-time Perks: Team Outings Cafeteria Soft Skill Training Job Training Health Insurance Office cab/shuttle

Roles and Responsibility Develop and implement quality control processes to ensure high standards of coding services. Conduct regular audits to identify areas for improvement and provide recommendations for enhancement. Collaborate with cross-functional teams to resolve quality-related issues and improve overall performance. Analyze data to identify trends and patterns, and develop strategies to address them. Develop and maintain quality control documentation, including policies and procedures. Provide training and coaching to team members on quality control best practices. Job Requirements Strong knowledge of quality control principles and practices, particularly in the healthcare industry. Experience with coding systems and software applications is desirable. Excellent analytical and problem-solving skills, with attention to detail and the ability to work independently. Strong communication and interpersonal skills, enabling effective collaboration with cross-functional teams. Ability to work in a fast-paced environment, prioritizing tasks and managing multiple projects simultaneously. Familiarity with CRM/IT enabled services/BPO industry operations and regulations is an asset.

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on life-critical solutions we are deeply immersed into the worlds of Transmission, Distribution, Asset Management and Market Management making sure we shape how the energy landscape looks today and tomorrow. Our teams breathe software-life into R&D, Services and Support for GE Vernova Electrification Softwares products while liaising with stakeholders and customers all around the globe. GE Vernova is a global provider of software, hardware, services, and expertise in automation and embedded computing. We offer a unique foundation of agile and reliable technology providing customers a sustainable competitive advantage in the industries they serve, including energy, water, consumer packaged goods, oil & gas, government & defense, and telecommunications. The activity within this office consists of development and implementation of: Energy Management Systems (EMS) Distribution Management Systems (DMS) Different specialized teams for distinct technical fields contribute to the realization of these systems. (hardware, communications, databases, HMI, applications). One of the activities, carried out in the mentioned context, is engineering for specific monitoring and control of power systems applications (power flow, short-circuit calculation state estimator, contingency analysis, optimization in power systems, voltage control, load frequency control, power reserve management, load forecast, stability analysis, transient regimes, modeling of the equipment, of the automation and protection systems in power plants and of the power grids, energy market models). Main job responsibilities: Development of the mathematical models of the physical phenomena in the power systems Software development for real-time applications (code, testing) Carrying out the analysis to define the specifications for the real time monitoring and control systems Commissioning of the EMS, DMS systems Engineering and code development for the EMS, DMS systems that meets the high standards. Parameterization, optimization, testing of EMS, DMS systems Databases management Good technical background is required. The development of professional skills is achieved, in time, by involvement in the team activities and by trainings. Knowledge of the power systems phenomena and processes and related mathematical models(power flow, state estimator, short-circuit analysis, contingency analyst, voltage control, load-frequency control, power systems optimal regimes, load forecast, stability analysis, transient analysis, modeling of equipment and of automation and protection systems in power plants and power grids, DTS, models for the energy market) C C ++ programmer skills or similar Exposure in Modelling of SCADA and Power System Analyst Applications Familiarity or development experience on Windows OS or UNIX OS Qualifications Requirements Master's degree in Power Systems with 2 to 5 years of experience in the PSA Domain Troubleshooting skills Fluent in English Ability and willingness to travel Desired Characteristics Technically good performer who can integrate and test complex software systems to completion with a minimal supervision Excellent communication skills (verbal and written) Rigorous, methodical, well organized and self-disciplined Take initiatives, good trouble-shooter and autonomous Adaptability, reactivity and Availability Ability to analyze complex topics and make a verbal/written synthesis Ability and willingness to travel Network & Links Internal: Operations, Product Development, Tendering, and Maintenance & Support External: Customers, Partners Performance Measurement On Time Delivery Costs deviation + Committed budget (effort) deviation Software Delivery Processes Compliance Customer Satisfaction In collaboration with Methods & Tools Drive excellence in execution through continuous improvement and change management to implement competitiveness improvement initiatives (costs base reduction, lead time reduction, DevOps framework, productivity improvement, quality improvement) Monitor the efforts performance measurement indicators In collaboration with Maintenance & Support Ensure a smooth transfer to maintenance of ending projects through coordinated knowledge transfer. Can be solicited to provide some back-end support to maintenance team as part of the maintenance contract Customer Management Comply and contribute to elaboration of relevant Quality Procedures, work instructions and Processes in Quality Management System Report or resolve any process non-conformances in a timely manner Health and Safety Sets the example by demonstrating the proper acts and actively observes work conditions. Routinely observes routines and behaviors of others and provides immediate feedback regarding unsafe behavior and celebrates achievements or safe behaviors. Actively and routinely promotes the identification of hazards and near misses. Additional Information Relocation Assistance Provided: Yes

Hi we are hiring Position;- QC Officer & Executives QC Officer & Executives Location- Baddi Experience- 2-6 years (HPLC analyst ) Salary Range- 20-30 K Interested candidate Apply Mail ;-Tisha.singh@unitedgroupmail.com Contact No;- 9041666549

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on life-critical solutions we are deeply immersed into the worlds of Transmission, Distribution, Asset Management and Market Management making sure we shape how the energy landscape looks today and tomorrow. Our teams breathe software-life into R&D, Services and Support for GE Vernova Electrification Softwares products while liaising with stakeholders and customers all around the globe. GE Vernova is a global provider of software, hardware, services, and expertise in automation and embedded computing. We offer a unique foundation of agile and reliable technology providing customers a sustainable competitive advantage in the industries they serve, including energy, water, consumer packaged goods, oil & gas, government & defense, and telecommunications. The activity within this office consists of development and implementation of: Energy Management Systems (EMS) Distribution Management Systems (DMS) Different specialized teams for distinct technical fields contribute to the realization of these systems. (hardware, communications, databases, HMI, applications). One of the activities, carried out in the mentioned context, is engineering for specific monitoring and control of power systems applications (power flow, short-circuit calculation state estimator, contingency analysis, optimization in power systems, voltage control, load frequency control, power reserve management, load forecast, stability analysis, transient regimes, modeling of the equipment, of the automation and protection systems in power plants and of the power grids, energy market models). Main job responsibilities: Development of the mathematical models of the physical phenomena in the power systems Software development for real-time applications (code, testing) Carrying out the analysis to define the specifications for the real time monitoring and control systems Commissioning of the EMS, DMS systems Engineering and code development for the EMS, DMS systems that meets the high standards. Parameterization, optimization, testing of EMS, DMS systems Databases management Good technical background is required. The development of professional skills is achieved, in time, by involvement in the team activities and by trainings. Knowledge of the power systems phenomena and processes and related mathematical models(power flow, state estimator, short-circuit analysis, contingency analyst, voltage control, load-frequency control, power systems optimal regimes, load forecast, stability analysis, transient analysis, modeling of equipment and of automation and protection systems in power plants and power grids, DTS, models for the energy market) C C ++ programmer skills or similar Exposure in Modelling of SCADA and Power System Analyst Applications Familiarity or development experience on Windows OS or UNIX OS Qualifications Requirements Master's degree in Power Systems with 2 to 5 years of experience in the PSA Domain Troubleshooting skills Fluent in English Ability and willingness to travel Desired Characteristics Technically good performer who can integrate and test complex software systems to completion with a minimal supervision Excellent communication skills (verbal and written) Rigorous, methodical, well organized and self-disciplined Take initiatives, good trouble-shooter and autonomous Adaptability, reactivity and Availability Ability to analyze complex topics and make a verbal/written synthesis Ability and willingness to travel Network & Links Internal: Operations, Product Development, Tendering, and Maintenance & Support External: Customers, Partners Performance Measurement On Time Delivery Costs deviation + Committed budget (effort) deviation Software Delivery Processes Compliance Customer Satisfaction In collaboration with Methods & Tools Drive excellence in execution through continuous improvement and change management to implement competitiveness improvement initiatives (costs base reduction, lead time reduction, DevOps framework, productivity improvement, quality improvement) Monitor the efforts performance measurement indicators In collaboration with Maintenance & Support Ensure a smooth transfer to maintenance of ending projects through coordinated knowledge transfer. Can be solicited to provide some back-end support to maintenance team as part of the maintenance contract Customer Management Comply and contribute to elaboration of relevant Quality Procedures, work instructions and Processes in Quality Management System Report or resolve any process non-conformances in a timely manner Health and Safety Sets the example by demonstrating the proper acts and actively observes work conditions. Routinely observes routines and behaviors of others and provides immediate feedback regarding unsafe behavior and celebrates achievements or safe behaviors. Actively and routinely promotes the identification of hazards and near misses. Additional Information Relocation Assistance Provided: Yes

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on life-critical solutions we are deeply immersed into the worlds of Transmission, Distribution, Asset Management and Market Management making sure we shape how the energy landscape looks today and tomorrow. Our teams breathe software-life into R&D, Services and Support for GE Vernova Electrification Softwares products while liaising with stakeholders and customers all around the globe. GE Vernova is a global provider of software, hardware, services, and expertise in automation and embedded computing. We offer a unique foundation of agile and reliable technology providing customers a sustainable competitive advantage in the industries they serve, including energy, water, consumer packaged goods, oil & gas, government & defense, and telecommunications. The activity within this office consists of development and implementation of: Energy Management Systems (EMS) Distribution Management Systems (DMS) Different specialized teams for distinct technical fields contribute to the realization of these systems. (hardware, communications, databases, HMI, applications). One of the activities, carried out in the mentioned context, is engineering for specific monitoring and control of power systems applications (power flow, short-circuit calculation state estimator, contingency analysis, optimization in power systems, voltage control, load frequency control, power reserve management, load forecast, stability analysis, transient regimes, modeling of the equipment, of the automation and protection systems in power plants and of the power grids, energy market models). Main job responsibilities: Development of the mathematical models of the physical phenomena in the power systems Software development for real-time applications (code, testing) Carrying out the analysis to define the specifications for the real time monitoring and control systems Commissioning of the EMS, DMS systems Engineering and code development for the EMS, DMS systems that meets the high standards. Parameterization, optimization, testing of EMS, DMS systems Databases management Good technical background is required. The development of professional skills is achieved, in time, by involvement in the team activities and by trainings. Knowledge of the power systems phenomena and processes and related mathematical models(power flow, state estimator, short-circuit analysis, contingency analyst, voltage control, load-frequency control, power systems optimal regimes, load forecast, stability analysis, transient analysis, modeling of equipment and of automation and protection systems in power plants and power grids, DTS, models for the energy market) C C ++ programmer skills or similar Exposure in Modelling of SCADA and Power System Analyst Applications Familiarity or development experience on Windows OS or UNIX OS Qualifications Requirements Master's degree in Power Systems with 2 to 5 years of experience in the PSA Domain Troubleshooting skills Fluent in English Ability and willingness to travel Desired Characteristics Technically good performer who can integrate and test complex software systems to completion with a minimal supervision Excellent communication skills (verbal and written) Rigorous, methodical, well organized and self-disciplined Take initiatives, good trouble-shooter and autonomous Adaptability, reactivity and Availability Ability to analyze complex topics and make a verbal/written synthesis Ability and willingness to travel Network & Links Internal: Operations, Product Development, Tendering, and Maintenance & Support External: Customers, Partners Performance Measurement On Time Delivery Costs deviation + Committed budget (effort) deviation Software Delivery Processes Compliance Customer Satisfaction In collaboration with Methods & Tools Drive excellence in execution through continuous improvement and change management to implement competitiveness improvement initiatives (costs base reduction, lead time reduction, DevOps framework, productivity improvement, quality improvement) Monitor the efforts performance measurement indicators In collaboration with Maintenance & Support Ensure a smooth transfer to maintenance of ending projects through coordinated knowledge transfer. Can be solicited to provide some back-end support to maintenance team as part of the maintenance contract Customer Management Comply and contribute to elaboration of relevant Quality Procedures, work instructions and Processes in Quality Management System Report or resolve any process non-conformances in a timely manner Health and Safety Sets the example by demonstrating the proper acts and actively observes work conditions. Routinely observes routines and behaviors of others and provides immediate feedback regarding unsafe behavior and celebrates achievements or safe behaviors. Actively and routinely promotes the identification of hazards and near misses.

Overview This role will assist the AMESA Supplier Quality Assurance team by conducting re-approvals annually for low risk designated suppliers located in AMESA that supply ingredients to Pepsico. This role will contact suppliers, request, and review returned pre-requisite data and documents, and re-approve the supplier site (3-year reapproval cycle). The role will update the required database(s) to support the re-approval. The expectation is ~200 supplier sites per year. The role will also support ancillary programs in AMESA SQA such as gathering program evidence from suppliers and brokers related to Food Fraud, Quality and Food safety Certifications and Contaminants programs as well as updating the Master Supplier Ingredient database when new ingredients are added to existing supplier sites or when ingredients or supplier sites are obsoleted. In addition, the role may be required to create short PowerPoint reviews of supplier non conformances from specified material groups on a quarterly basis (~ 5) to support the AMESA SQA agenda. There will be an ongoing requirement to cleanse and update supplier/ingredient data in the data base /portals with information supplied by Suppliers or GP or Pep manufacturing facilities. Responsibilities Functional Responsibilities Utilize SQA Trackwise database to determine Supplier site re-approvals required over a defined time (12 months). SQA AMESA team can construct a list/query to enable this and have specific records can be assigned to a named person. Using a pre-determined script by Material class/Sub class of materials, and/or a specific questionnaire to use send a request by email to the supplier requesting documentation and certifications to support the re-approval. The pre-determined documents are listed on script and in the body of the specific questionnaire. The process can benefit from having a brief zoom call with the supplier to re-educate the supplier on the request. This has proven to assist the agility of receiving all the documentation at once and avoids re-connecting / follow up on missing documentation. Typical documents requested are quality and food safety certifications (GFSI/ISO9001/Others), 3rd party audit reports, process flow diagrams, HACCP plans, specific contaminants data, pathogen sensitive ingredient program etc. Because the re-approval frequency for low-risk suppliers is approx. 3 years, it is likely that the supplier contacts may have changed, so it may be necessary at times to find a new contact by connecting with GP or pep site representative to determine who buys the material and ascertaining a new contact. Review all documents received from supplier site and create an Audit record in Trackwise database, complete the requisite record fields based on the information supplied. Carry out a check on FDA data base or horizon scanning data base also is required. Attach all the received Supplier site documents and questionnaire, and assign a status, and next audit date, and complete the audit verifying materials are correct. The person will also update progress metrics monthly showing number of sites completed/ sites outstanding/ overdue / sites on plan for balance of year. This can be a simple Dashboard. Maintain data governance of the information supplied by the R&D /specifications teams to update all Ingredient records in the Global Trackwise Database (additions/changes ~5-10 per week) cross checking the data base and if needed the specifications. In addition, continue to cleanse Supplier -Ingredient Master data in Trackwise data to ensure records are in correct status and are complaint, as required. e.g., Update any supplier site name changes or contact name changes etc. These are ad hoc and not frequent but important to update. Add GFSI certificates to supplier audit record when received, upload certificates to TW site audit record from Portal. Support the Supplier Performance Management agenda. (primarily supplier non-conformance incidents registered by plants and in a database). The task primarily would be to the preparation of short presentations for cross functional meetings held quarterly targeting ~ 5 material category metrics. Help prepare data for Europe sector manufacturing sites GFSI audits. The request is generally to check supplier data and documents received before an audit to ensure it is all present and correct or collect data during the audit if we find issues on conformance. This may be one or twice per month. Support ancillary programs in SQA such as food fraud questionnaire sending and reviewing to suppliers, request for contaminants data, creating ad-hoc requests from suppliers resulting from an incident of regulatory affairs requests, sending and reviewing/ aligning Pathogen Sensitive Ingredient (PSIP) Questionnaires as part of a formal AMESA PSIP program. Some of these requests in the medium term may be automated but still requires governance to check compliance and close out requests/ follow up on outstanding information yet to be furnished. Qualifications Bachelors degree in a science discipline (e.g Food Science, Food Engineering, Food Chemistry, Microbiology, Biochemical Engineering or Chemical Engineering or equivalent relevant experience required.) Lead Auditor training is a requirement, and the person will need to complete training either in advance, or shortly afterward joining the team. SQA Europe team can act as proxy to quicky review and approve the records in the interim and Europe SQA can assist in organizing the training as applicable. 1-2 years of experience on Regulatory, QA/QC, or other Food related FMCG in a technical role Ability to interpret technical information, escalate issues and seek alignment towards workable solutions. Proficient with Microsoft Office Suite Ability to rapidly learn computer applications/programs / interrogate databases such as specification /SAP & navigate systems. Basic understanding of Food Safety, Microbiology and Regulatory Affairs Collaborative skills and strong interest in working with others across time zones; Ability to build relationships and work closely with both internal and external partners. Good communication skills oral and written (e.g. communication on telephone, external and internal to PepsiCo, managing with other support group functions, etc.) Ability to manage time effectively across multiple priorities and projects requiring a high degree of organizational and communication skills to ensure requests are delivered in a timely manner. Self-motivated & demonstrated ability to take initiative on projects. Fluent in English (HBS)

Role and Responsibility: Technical Support: Provide expert technical support to customers and field personnel on HPLC troubleshooting, and resolving application issues. Application Development: Develop and optimize analytical methods and applications using HPLC for various industries, including pharmaceuticals, industrial, environmental, food, and life sciences. Customer Training: Conduct customer training sessions, webinars, and workshops to enhance user proficiency and satisfaction. Collaboration : Work closely with the sales and marketing teams to identify customer needs and develop tailored solutions. Collaborate with R&D to provide feedback on product performance and enhancements. Documentation: Prepare and maintain application notes, technical documents, and reports to support customer applications and product development. Innovation: Stay updated with the latest advancements in HPLC and contribute to the development of new applications and methodologies. Aware of calibration and operation procedure for instruments ( balance, K.F, HPLC. UV, refractometer and viscometer etc,) Experience of QC software like Empower, LIMS, Tiamo 3.0, Lab solution, SCM etc. Preparation of documents ( SOP, protocol etc) related to Quality control.Role & responsibilities Preferred candidate profile Qualification : B.Sc (chemistry)./ B.Pharma candidates only. Experience: 4-10 years experience working with HPLC/wet finish/Sampling is compulsory. Interested candidates can sent their CV to jagpal.dewal @ipca.com

Title Manager - Revenue, Sales & Assets Reporting Department Revenue, Sales & Assets COE Location Gurugram Level Level - 5 About your team Finance is a global function at Fidelity International, with close to 300 dedicated employees and offices across 12 locations including UK, Germany, Bermuda, Australia, India and China. The Finance Department supports the management of the business in the achievement of business goals and objectives, and improves shareholder value by ensuring the timeliness, accuracy, integrity, consistency and relevance of financial information, in relation to the business decision-making process. The role is with Revenue Centre of excellence (COE) and the primarily responsibility revolves around providing financial support, analysis and management information to the Board, the Global Operating Committee (GOC) and other senior members of FIL management including distribution and investment teams. A large proportion of the teams activity is focused on: Continuously striving to make our regular reporting as informative as possible. Supplying valuable analysis to support debate and decision-making at GOC and other senior management meetings. Co-ordinating FILs quarterly forecast process. Ownership of the management reporting hierarchy. In addition to these group-wide responsibilities, we provide decision support to the onshore distribution finance and IM finance teams. This support majorly includes Revenue, AuM, Sales & Assets reporting, forecasting together with a significant amount of ad hoc analysis. About your role This role is an excellent opportunity to gain a broad understanding of the Distribution Reporting function and its role in FILs Financial Services business, and to support the relevant stakeholders. Need a highly motivated Individual, who will be managing critical reporting for FILs senior management , handling day to day data issues and acting upon various ad-hoc requests under tight timeframes. He/she would also be responsible for providing technical, systems and data support, working closely with India technology teams, business finance teams and regional sales teams across geographies. He/she would have to ensure compliance to all agreed internal and external SLAs and requirements. Shall also be responsible for end to end support on global projects, changes and system enhancements within the agreed timelines. To this end, the individual will perform a variety of tasks including coordinating with various technology teams and stakeholders, planning and setting out data requirements, summarizing and communicating progress and status. This demanding role would perfectly suit a dynamic individual looking to work in a fast paced environment to ensure the smooth running of business critical reporting.This person will be responsible for overall business management of a large account/process or multiple small accounts/processes. He/She will be responsible for identifying functional linkages across the organization and developing appropriate processes and road map for the function and managing the work activities of a dept/function through junior team members. He/She will also be responsible for capability development of the team/ unit and contributes to development plans for the entire organization, will be responsible for conducting appraisals, feedback & handling work allocations for direct reports and reviewing the same for indirect reports. Key Responsibilities Partners with leadership, BU and sales leaders to synthesize and deliver key KPI reporting requirements related to Sales, assets and Revenue. Identifying, maintaining and developing new reports required by Business teams using OBIEE and Power BI; Gathering, transforming, and storing data through data acquisition, metadata management, data cleansing, data transformation and data distribution. Ensuring timely provision of key sales & assets metrics to senior management across FIL; Reviewing and analysing the sales, assets and revenue numbers to ensure accurate internal & external reporting; Liaise with stakeholders and counterparties to resolve exceptions in a timely and pro-active manner; Managing monthly stakeholder calls, sharing functional updates and resolving issues raised; Maintaining and developing new reports required by Business teams using OBI/Tableau/Power BI; Ensuring accurate recodes and adjustments are placed to the back-end, internal EDW system; Providing ad hoc analysis, reports and presentations to the business under challenging time frames; Working with various tech teams to provide business requirements, identify solutioning, testing and operational readiness. Participation in projects as required & performing periodic general administrative tasks. Leading global projects and driving both system and process change proactively. Leveraging data for decision making purposes. Participating in meetings with various teams to determine upcoming tech changes impacting the team/process. About you Technical Functional skills Graduate or Post Graduate/CA degree from a recognised university, preferably in engineering or finance; 8 -10 years experience in a similar position, preferably within a global and or a financial services company; Preference to candidates with techno-functional and change management skillset. Ability to understand multiple systems and underlying data. Knowledge of OBIEE or similar BI tool. Visualization experience with Power BI (good to have). Understanding of Oracle and MS Access databases Knowledge of writing MS-SQL extraction queries (good to have). Sound analytical skills with an eye for details and an appetite to dive into issues in depth as needed; High numeracy and able to co-relate data/ information Proven Project and Program management skills Ability to work with large and complex data sets Essential skills Experience in managing the expectations of senior stakeholders Ability to complete multiple tasks against tight deadlines, able to prioritise and organise effectively Able to cope with sustained pressure Ability to embrace change and adapt quickly Keen to review processes and drive improvements. Ability to manage a high functioning team. Awareness of risk and controls framework to ensure adequate controls in the BAU process. Business Facing Responding to the expectations of senior stakeholders in a timely manner; Strong written and verbal communication skills; Willingness to work additional hours and bank holidays as per business requirements; Ability to challenge conventional ideas/ status quo. Teamwork Ability to work as part of a team and contribute towards team goals, but equally able to work independently and deliver results; Ability to grasp new concepts, assimilate information and deliver high quality solutions at speed; Flexible and adaptable, responds rapidly to change.

Job Description Summary Come Join Our Software Integration Team!! Our main activity consists in setting up GE Vernova software in different environments for internal and external customers, supporting project activities and providing expertise in tailoring the components based on requirements. We have a hybrid work environment as we work from home, the office and travel to customer sites as needed. The integration engineer is a key member in all projects, being engaged throughout the full lifecycle (Development, Factory Acceptance Tests, Site Acceptance Tests, Cutover, Support). Job Description GE Vernova allows us to bring a significant contribution to the Worldwide Electrical Energy context. Delivering on life-critical solutions we are deeply immersed into the worlds of Transmission, Distribution, Asset Management and Market Management making sure we shape how the energy landscape looks today and tomorrow. Our teams breathe software-life into R&D, Services and Support for GE Vernova Electrification Softwares products while liaising with stakeholders and customers all around the globe. GE Vernova is a global provider of software, hardware, services, and expertise in automation and embedded computing. We offer a unique foundation of agile and reliable technology providing customers a sustainable competitive advantage in the industries they serve, including energy, water, consumer packaged goods, oil & gas, government & defense, and telecommunications. The activity within this office consists of development and implementation of: Energy Management Systems (EMS) Distribution Management Systems (DMS) Different specialized teams for distinct technical fields contribute to the realization of these systems. (hardware, communications, databases, HMI, applications). One of the activities, carried out in the mentioned context, is engineering for specific monitoring and control of power systems applications (power flow, short-circuit calculation state estimator, contingency analysis, optimization in power systems, voltage control, load frequency control, power reserve management, load forecast, stability analysis, transient regimes, modeling of the equipment, of the automation and protection systems in power plants and of the power grids, energy market models). Main job responsibilities: Development of the mathematical models of the physical phenomena in the power systems Software development for real-time applications (code, testing) Carrying out the analysis to define the specifications for the real time monitoring and control systems Commissioning of the EMS, DMS systems Engineering and code development for the EMS, DMS systems that meets the high standards. Parameterization, optimization, testing of EMS, DMS systems Databases management Good technical background is required. The development of professional skills is achieved, in time, by involvement in the team activities and by trainings. Knowledge of the power systems phenomena and processes and related mathematical models(power flow, state estimator, short-circuit analysis, contingency analyst, voltage control, load-frequency control, power systems optimal regimes, load forecast, stability analysis, transient analysis, modeling of equipment and of automation and protection systems in power plants and power grids, DTS, models for the energy market) C C ++ programmer skills or similar Exposure in Modelling of SCADA and Power System Analyst Applications Familiarity or development experience on Windows OS or UNIX OS Qualifications Requirements Master's degree in Power Systems with 2 to 5 years of experience in the PSA Domain Troubleshooting skills Fluent in English Ability and willingness to travel Desired Characteristics Technically good performer who can integrate and test complex software systems to completion with a minimal supervision Excellent communication skills (verbal and written) Rigorous, methodical, well organized and self-disciplined Take initiatives, good trouble-shooter and autonomous Adaptability, reactivity and Availability Ability to analyze complex topics and make a verbal/written synthesis Ability and willingness to travel Network & Links Internal: Operations, Product Development, Tendering, and Maintenance & Support External: Customers, Partners Performance Measurement On Time Delivery Costs deviation + Committed budget (effort) deviation Software Delivery Processes Compliance Customer Satisfaction In collaboration with Methods & Tools Drive excellence in execution through continuous improvement and change management to implement competitiveness improvement initiatives (costs base reduction, lead time reduction, DevOps framework, productivity improvement, quality improvement) Monitor the efforts performance measurement indicators In collaboration with Maintenance & Support Ensure a smooth transfer to maintenance of ending projects through coordinated knowledge transfer. Can be solicited to provide some back-end support to maintenance team as part of the maintenance contract Customer Management Comply and contribute to elaboration of relevant Quality Procedures, work instructions and Processes in Quality Management System Report or resolve any process non-conformances in a timely manner Health and Safety Sets the example by demonstrating the proper acts and actively observes work conditions. Routinely observes routines and behaviors of others and provides immediate feedback regarding unsafe behavior and celebrates achievements or safe behaviors. Actively and routinely promotes the identification of hazards and near misses.

IITR is currently looking for a highly skilled ADL Officer for one of the pharmaceutical Co. Location - Vapi, Gujarat. If you are interested and for further information, please share your updated CV to talent@hireindians.com/call on 8700944544. Required Candidate profile Min Exp - 2-4 yrs of experience. Qualification - BSc/MSc in pharma

About The Role Role Finance and Administration CSR: 360 degree CFO Like responsibility in running functions and entities Will be responsible for managing accounts, compliances and Tax for ~ 3 not for profit entities Will support financial reporting for CSR Hybrid work structure for work life balance Requirement CA with 5-7 years of experience Deep understanding of financial, legal, tax and compliances matter .

JOB DESCRIPTION Job Title: Research Associate ( Level 9-I) Job Location: Bangalore Department : Discovery Chemistry - Analytical About Syngene: Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Ensure personal and team adherence to safe practices, procedures, and Syngene s quality standards at all times. Contribute to the development and continuous improvement of systems, procedures, and practices that uphold safety, integrity, and compliance. Foster a workplace culture that prioritizes Environment, Health, and Safety (EHS) and operational discipline. Maintain a safe lab/plant environment by strictly following EHS protocols and safety guidelines. Ensure timely completion of all mandatory trainings related to data integrity, health, and safety for self and team members. Hold self and team accountable for achieving safety goals and maintaining compliance. Regularly review and govern safety metrics to drive continuous improvement. Core Purpose of the Role: Perform analysis and documentation in compliance with established procedures. Upload analytical data to SAP and update sample status accordingly. Self-approve identification tests including LC-MS, GC-MS, IR, NMR, SOR, MR, MC, and UV. Prepare samples and load them into the autosampler. Conduct instrument calibration and maintain records as per the defined schedule. Ensure compliance with product specifications, SOPs, and laboratory standards. Maintain accurate records of solvents and consumables for smooth lab operations. Role Accountabilities: Proficient in analytical method development using HPLC, LC-MS, GC, GC-MS, and Preparative HPLC. Hands-on experience with key analytical instruments including HPLC, LC-MS, GC, GC-MS, and Preparative HPLC. Strong theoretical foundation in analytical techniques with proven skills in data interpretation. Demonstrates accountability for personal and team safety by strictly following Syngene s safety protocols. Consistently adheres to Environment, Health, and Safety (EHS) policies and standards. Always Ensures proper use of Personal Protective Equipment (PPE). Complies with Syngene s data integrity procedures and quality standards. Reviews and verifies daily/monthly equipment monitoring, calibration, and documentation records. Leadership Capabilities Clear Communication Convey ideas effectively and actively listen to others. Problem-Solving Identify issues and propose practical, actionable solutions. Emotional Intelligence Understand and manage personal emotions while empathizing with others. Initiative Take proactive actions without waiting for instructions. Adaptability Respond effectively to changing environments and challenges. Team Collaboration Work productively within diverse teams. Feedback Receptiveness Seek, accept, and apply constructive feedback. Time Management Prioritize tasks and meet deadlines efficiently. Conflict Resolution Address disagreements constructively and professionally. Self-Motivation Maintain drive and focus to achieve goals independently. Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Education M. Sc. (Chemistry/Analytical Chemistry) Experience 0-3 years Skills and Capabilities Able to work follow instructions and perform the tasks under the supervision of the reporting manager. Fair interpersonal skills. Undertake relevant safety and quality trainings Equal Opportunity Employer .

Roles & Responsibilities Quality Control Analyst Prepare and review Standard Test Procedures (STPs) , analytical protocols, and reports. Perform Analytical Method Validation, Process Validation , and prepare validation protocols as per regulatory requirements. Conduct testing and quality control activities for raw materials, bulk, in-process, finished goods, and stability samples. Operate and maintain analytical instruments and techniques including HPLC, UV-Vis Spectrophotometer, Karl Fischer, and other QC equipment . Perform calibration, qualification, and preventive maintenance of analytical instruments and ensure proper documentation. Maintain accurate and complete laboratory records in compliance with cGMP, US FDA regulations, and ICH guidelines . Ensure adherence to Good Laboratory Practices (GLP) , data integrity, and documentation practices. Support laboratory audits and regulatory inspections by ensuring compliance with GMP and safety standards . Collaborate with cross-functional teams for investigations, deviations, OOS/OOT results, and CAPA implementation . Provide training to team members on laboratory practices, instrument handling, and regulatory guidelines.

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

Primary Responsibilities: * Exposure for Analysis and documentation of tablets, capsules, Liquid/Cream. * Developing and validating analytical test methods for the testing of pharmaceutical products for manufactured to GMP and ICH requirements. * Developing and validation of Cleaning Method validation. * Transferring and documentation new analytical techniques to the Quality Control (QC) laboratory. * Controlling laboratory chemicals required for analytical activities. * Planning and organizing stability testing. * Writing/reviewing specifications and methods of analysis. * Writing/reviewing of Standard Operating Procedures (SOPs) as per regulatory requirement. * Participating in self-inspections and regulatory inspections. * Sample management and Documentation of RM and PM. * Preparation and review of all analytical related documents. * Working standard management. * Handling of QC Instrument operation and Calibration related activity. * Handling of OOS / OOT and Lab related incident / Investigation. * Planning of daily activities of the laboratory. * Must have skill of handling of HPLC Independently.

Conduct literature survey, analyze samples (innovator, developmental, stability), Method Development & Validation, Product analysis, documentation, reports, instrument handling & troubleshooting. Required Candidate profile . M.Pharm/ M.Sc./ Skilled in LNB/logbook documentation, test methods, validation/verification, instrument calibration, troubleshooting & data review.

Job Requirements Ensuring the timely release of the PDIS for introduction of New products as per Category requirements for both DEC and Vendor Pick-up. Validation of GC & AMC-Crafting Charges for all new products Coordinate with NPI & Factory NPD teams for Timely completion of proto products Dashboard maintenance and tracking the stage gate completion of designs and effectively communicating to all relevant stakeholders NPD spoc of Brief to PDIS release for DEC designs and co-ordinate with category managers for vendor pick-ups. Ensuring proto bin liquidation through periodic inputs to the category teams Ensure the smooth implementation of newly developed NPD portal across vendors for both plain & Studded Creation of an intelligent framework for systematic capturing of CatPB, CFA, Complexity and design attributes for all Product groups Extended support for all kind of NPIM activities. Behavioural Skills Customer orientation Drive for outputs Networking ability Detail orientation KnowledgeVendor management experience

Manage & guide team, coordinate with all concerned department, supervise method development/validation, review data/docs, oversee calibration, method transfers, customer calls & team training. Required Candidate profile M.Pharm/ M.Sc with team management skills in AR&D. Strong in method development/validation, data review, calibration, training juniors, client coordination.

Role & responsibilities : Person would be team leader. Person would be responsible for managing 6-10 people from sr. scientist to interns. Candidate would be responsible for planning of work for direct reportees, reviewing of their timesheets. Candidate would be responsible for coordination with cross functional team and AAT team. Person would be responsible for representing AAT in internal meetings Person should be experienced for HPLC, CE, SoloVPE related techniques, trouble shooting , data review and data interpretation Knowledge in characterization methods such as Mass analysis, CD, Flr, DSC, MALS would be an additional advantage. Person should know method qualification for HPLC, CE, SoloVPE related techniques Person would be involved in document preparation and review of MQP, MOA, MQR, Specification, analytical similairty studies Experience in analytical section related sourced document preparation for EMA and USFDA would be an additional advantage Person would be responsible for preparaing client query response and timely communication to cross functional team Technical Skill Requirement: Knowledge for HPLC based methods such as SE HPLC, CEX HPLC, Poly 20 measurement, RP HPLC, Capillary Electrophoresis related based techniques such as CE SDS R & NR, cIEF. CE analysis on Maurice system would be an added advantage SoloVPE analysis Soft Skill Requirement: Fluent in English, Should be approachable Able to present technical data in internal meeting Able to faciliate required work by coordinating with cross funcational team Technical review of the the data and ensuring timely communication to cross funcational team Able to resolve/disucss with manager if any conflicts within team is oberved

Roles and Responsibilities Conduct quality control activities such as raw material inspection, finished product testing, and sample analysis using HPLC and other relevant methods. Ensure compliance with USFDA regulations by performing chemical testing and material verification. Develop and implement quality control procedures to maintain high-quality standards in the manufacturing process. Collaborate with cross-functional teams to resolve quality issues and improve overall process efficiency. Maintain accurate records of all quality-related activities, including test results, inspection reports, and documentation. Desired Candidate Profile 9-14 years of experience in Quality Control or related field (Pharmaceutical industry). B.Sc degree in Any Specialization; MS/M.Sc(Science) preferred but not mandatory. Strong knowledge of Chemical Analysis, Chemical Testing, HPLC, Material Testing, Materialize CSS, Raw Material Inspection, Sample Inspection, Quality Inspection & Quality Control principles.