About Aerol Aerol Formulations P. Ltd is an ISO 9001 & ISO 45001 certified, family run MSME and a leading manufacturer of Industrial and automotive use Aerosols (Lubricants, Cleaners, Coatings, Mold Release Spray etc.), Specialty Lubricants & multi-functional chemical preparations. Operational since 1989, Aerol holds a leading market position in most of the verticals with a pan India sales network. Aerol has been consistently making profits and is now poised for high trajectory growth with the help of qualified professionals. Aerol has a modern, well equipped manufacturing facility in Bahadurgarh, Haryana with licenses to store Petroleum solvents, LPG and mandatory permissions from Industrial Health & Safety Department, Pollution Control Department etc. For more information on the Company, please log on to www.aerolgroup.com. Job Title: Manager Quality Operations Location: Asaudah, Bahadurgarh, Dist. Jhajjar, Haryana Key Responsibilities Quality Control & Assurance Monitor and control all activities carried out by the Quality Control Team, ensuring safe and efficient operations in the factories. Oversee and manage documentation as per regulatory and organizational requirements. Ensure that all Standard Operating Procedures (SOPs) are available and consistently followed for raw materials, finished products, and in-process materials. Assist in ensuring that quality-critical activities are performed as outlined in planning documentation. Participate in reviewing and authorizing changes in processes, specifications, procedures, and test methods that may impact quality. Inspect and verify the availability and accuracy of all reports and certifications before shipment. Compliance & Audits Oversee QMS compliance. Ensure the smooth execution of internal and external audits, conducting Management Review Meetings (MRMs) within the specified timeframe. Develop and implement a self-inspection program for continuous improvement of the Quality Management System (QMS). Ensure the implementation and follow-up of Root Cause Analysis (RCA) and Corrective & Preventive Actions (CAPA) for customer complaints and non-conformities (NCs). Verify the implementation of CAPA through periodic spot audits. Assist in fulfilling responsibilities as prescribed under the Factories Act, Pollution Regulations, HWRA, Hazardous Waste Management, Plastic Waste Management & Legal Metrology act and rules. Lead the Safety Committee and ensure safety practices in all stages of manufacturing, material handling and storage. Ensuring compliance with PESO norms for storage of LPG & Petroleum solvents. Technical & Process Support Provide technical support to the Production Department for major and recurring issues, assisting in the implementation of approved improvement plans. Support vendor development initiatives to enhance service quality and the standard of supplied products. Provide technical support to the Sales Department and Customers with updated Technical Data-sheets, Material Safety Data Sheets and coordination with QC & QA departments of customers. Laboratory & Equipment Management Ensure proper procurement and monitoring of laboratory chemicals, glassware, apparatus, and instruments including Calibration records Oversee the maintenance of all instruments and apparatus, coordinating with manufacturers and service providers when required. Coordinate testing services at Third Party labs and maintaining records and reports Education B. Sc. / M.Sc. (Chemistry preferred) Experience 10–12 years of relevant experience in the QC & QA operations in chemicals petroleum , or pharmaceuticals industry, along with a minimum of 1-2 years of department leadership experience. Skills Authoritative leadership with team building/team work skills Articulate and respectful towards colleagues Excellent English & Hindi communication skills (Both written and spoken) Computer literate with expertise in MS Office Ability to deal with Government departments and regulatory authorities. Preferences Staying close to factory location or willing to relocate nearby Owning conveyance 35-45 year old age group Good health Interested candidates please share your cv on -9818769511 Job Type: Full-time Pay: ₹55,000.00 - ₹65,000.00 per month Benefits: Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person

Responsibilities for Mechanical Engineers: Maintain and upgrade equipment for smooth operations. Ensure machinery runs efficiently through proper design and upkeep. Troubleshoot mechanical issues and improve system performance. Responsibilities for Production/Industrial Engineers: Analyze production workflow to improve efficiency. Optimize workforce and resources for better productivity. Implement process improvements to reduce costs and waste. Please Note: We have partnerships with multiple international employers and recruitment firms in Canada, Australia, and the United Kingdom. Your profile will be screened to determine the most suitable country based on eligibility.

Job Description Creation of LOD 100 to LOD 400 models of infrastructure projects using different BIM Softwares such as (AutoCAD Civil3D, InfraWorks or Revit ) . Creating custom structure using part builder. (Gravity Networks) Adding pipes and fittings to the content catalogue (Pressurized Networks). Must have skills in Drafting/Modelling skills in Civil 3D such as Earthworks, Grading, Roads & Utilities (Electrical, Telecom and streetlight, Sewerage, Stormwater, Potable water, Firefighting, and irrigation etc.). Good knowledge of Autodesk Navisworks, with experience in clash detection & resolution, Experience in analyzing & producing of clash reports is preferrable. Work closely with BIM Lead and Design Leads to ensure the project’s compliance with the given policies and processes, and to ensure timely implementation and completion. Generate construction drawings, profiles, cross-sections, and quantity take-offs from 3D models. Review each drawing for readability, presentation, and adherence to standards, in accordance with the company QA/QC process. Collaboration and coordination with other disciplines on design changes and model development tasks. Qualifications Bachelor’s degree in civil engineering or Diploma. 5+yrs experience as a Civil 3D Modeler in infrastructure projects. Proficiency in AutoCAD Civil 3D and other relevant design software. Show more Show less

Designation - BIM Coordinator (Architectural/Structural) (5+ yrs) Responsibilities Assist project team adherence to BIM Implementation Plan (BIP), including model submittal schedule and updates of the models to reflect as-built conditions for submittal. Assist teams to deliver client BIM requirements for Architectural and Structural services. Perform QA/QC on Autodesk Revit models. Preparation of drawing packages. Technical capability of BIM LOD 300 with knowledge of 400 and 500. Coordination and development of the design to Construction through BIM processes such as 5D/4D. Manage the 3D models, review model quality and technical content including clash detection and compliance with the BIM Execution Plan. Analyze models provided by Architects, Engineers, subcontractors and consultants to identify coordination and constructability issues. Knowledge of parametric and non-parametric family creation. Experience in Scan to BIM & PDF to CAD projects. Software Proficiency Autodesk Revit Autodesk AutoCAD Navisworks Dynamo Recap Show more Show less

Specialist - Logistics Job Id: 11094 City: Pune, Maharashtra, India Department: Logistics Function: SCM Employee Type: Permanent Full Time Seniority Level: Mid-Senior level Description: Required knowledge of: 1. Knowledge of Exim Policy, Incoterms, Payment Terms, UCP Rules 2. Conversant with Customs Rules and regulation for import & export 3. knowledge of the International Logistic & transportation industry. 4. Conversant with handling of hazardous cargo shipment 5. Complete knowledge of export-import shipment process ( Air, rail, Ocean) Primary Responsibilities: Responsible for complete export shipment planning process as per incoterms and customer orders – right from cargo readiness to shipment and b/l release - from multiple loading ports in India Achieving Monthly export dispatch targets – from multiple manufacturing plants in India Follow up - with shipping companies and forwarding agents for bookings Follow up - with forwarding agent and CHA's for timely gate in the port and advance loading list send to shipping co. Responsible for timely updation of shipment status in SAP. Coordination with Customer service teams for shipment updation to customers Coordination with planners , dispatch teams, QC teams at plants. Coordination with CHAs, transporters, freight forwarders, shipping lines, third party inspection agencies. Resolution of issues related to shipments with customs, shipping lines, CFS, other allied agencies. Responsible for MIS reporting. Ensure export/import laws and regulations in the importing ports at respective destination countries are adhered to. Responsible for KPIs related to timely delivery and shipment costs. Provide advance container volume forecast to shipping lines, CHAS, Transporters Involvement in Global Logistics for respectives given region like - NAM, EU, APAC, LATAM etc. Would be also responsible for Pre-shipment & post- Shipment whenever required. Total Experience in Yrs. (Minimum required) 08-12 years Qualification MBA in SCM/IB/Operation Specific or Additional Certifications (if Any) required Diploma in EXIM /SCM /logistics Technical Skills Requirement Material management / import export management / Supply chain management / Proficient in Excel /Profcient in English & quality communication Behavioral Skills Requirement People management, computer skills with SAP, Strong Communication and Co-ordination & Interpersonal Skills, Time management , focused to work.

Position Title: Executive – Quality Control Qualification and Experience: M. Sc (Organic / Analytical Chemistry) / B. Pharm with 5 - 8 years of Experience as an analyst in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Implement quality control activities at Ankleshwar, adhering to regulatory/global quality Directives and HSE guidelines with optimum utilization of resources to ensure consistent good quality of products to meet customers’ requirements. Responsibilities: Analysis: Performing timely sampling and analysis of raw material, bulk product, intermediates, finished goods, and other samples. Performing analysis of Stability, process validation samples, and Cleaning Validation. Handling of sophisticated laboratory instruments viz., HPLC, GC, UV & IR spectrophotometer, Dissolution tester, auto-titrator, polarimeter, etc. Good Laboratory Practice Performing calibration & maintenance of the lab. Equipment and assistance for the qualification of laboratory equipment. Knowledge on the preparation of SOPs and Formats and Analytical Test records. Managing reference standards, working standards, laboratory reagents & chemicals. Arranging and observing Control Samples and maintaining the record. Participating in the Investigation of out-of-specification results. Maintaining laboratory raw data related to testing activity. Validation Performing Analytical Method validation, cleaning validation as per the protocol. Other Coordinating with production and the warehouse for analytical activities Compliance to HSE Requirements for QC laboratory. Identifying and correcting unsafe conditions or behaviours, and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instructions of the Department. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge Good coordination & communication skills. Analytical ability Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in GMP/ GLP environment. Location information: Ankleshwar, Gujarat, India

Job ID R-228851 Date posted 06/11/2025 About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Job Description / Capsule Detailed Roles & Responsibilities: Works in close collaboration with the external service provider (CRO) and Investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner. Responsible for ensuring that the study is conducted in accordance with AZ Procedures/ Applicable SOP’s & Guidelines, such as ICH and GCP as well as relevant local regulations. Ensure delivery of the projects according to the commitment & set timelines. Initiate, conduct and deliver non interventional studies (local, regional and global) across TAs, External Service Provider Identification, Selection, and Work in close collaboration Initiate ESP contact (CRO, DM and Laboratory), exchange contracts and negotiate costs along with purchase team for DM, monitoring, central lab, translation, printing service, as applicable. Prepare clinical trial budget and get management approval after discussion. Assist in designing of study Protocol, CRF, ICF and other study related documents. Prepare Monitoring Plan, SDV and QC plan for the study. QC review of study documents, CRO and ASV along with CRO person to check QC Budget Preparation & approval. Work with medical colleagues on study protocol and related documents. Ensure quality conduct of the trial/study. Oversee site/Investigator identification and selection and SDV. Ensure Timely delivery of project from study start-up to DBL & CSR. Ensuring compliance with the Protocol, SOPs, ICH-GCP and other applicable regulatory requirements. Regular coordination with CROs to track progress of trial with target and actual milestones. During the trial, to take CAPA to ensure GCP compliance and reliability of data. Publication Management, Adherence to Publication Policy Essential Degreeorequivalentprofessionalqualificationin related field Pharm D ExperienceinhandlingClinicaltrials,observational studies,PublicationandESR Desirable Post-graduatequalification Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. Project Manager Posted date Jun. 11, 2025 Contract type Full time Job ID R-228851 APPLY NOW Why choose AstraZeneca India? Help push the boundaries of science to deliver life-changing medicines to patients. After 45 years in India, we’re continuing to secure a future where everyone can access affordable, sustainable, innovative healthcare. The part you play in our business will be challenging, yet rewarding, requiring you to use your resilient, collaborative and diplomatic skillsets to make connections. The majority of your work will be field based, and will require you to be highly-organised, planning your monthly schedule, attending meetings and calls, as well as writing up reports. Who do we look for? Calling all tech innovators, ownership takers, challenge seekers and proactive collaborators. At AstraZeneca, breakthroughs born in the lab become transformative medicine for the world's most complex diseases. We empower people like you to push the boundaries of science, challenge convention, and unleash your entrepreneurial spirit. You'll embrace differences and take bold actions to drive the change needed to meet global healthcare and sustainability challenges. Here, diverse minds and bold disruptors can meaningfully impact the future of healthcare using cutting-edge technology. Whether you join us in Bengaluru or Chennai, you can make a tangible impact within a global biopharmaceutical company that invests in your future. Join a talented global team that's powering AstraZeneca to better serve patients every day. Success Profile Ready to make an impact in your career? If you're passionate, growth-orientated and a true team player, we'll help you succeed. Here are some of the skills and capabilities we look for. 0% Tech innovators Make a greater impact through our digitally enabled enterprise. Use your skills in data and technology to transform and optimise our operations, helping us deliver meaningful work that changes lives. 0% Ownership takers If you're a self-aware self-starter who craves autonomy, AstraZeneca provides the perfect environment to take ownership and grow. Here, you'll feel empowered to lead and reach excellence at every level — with unrivalled support when you need it. 0% Challenge seekers Adapting and advancing our progress means constantly challenging the status quo. In this dynamic environment where everything we do has urgency and focus, you'll have the ability to show up, speak up and confidently take smart risks. 0% Proactive collaborators Your unique perspectives make our ambitions and capabilities possible. Our culture of sharing ideas, learning and improving together helps us consistently set the bar higher. As a proactive collaborator, you'll seek out ways to bring people together to achieve their best. Responsibilities Job ID R-228851 Date posted 06/11/2025 About AstraZeneca AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies. Job Description / Capsule Detailed Roles & Responsibilities: Works in close collaboration with the external service provider (CRO) and Investigators to ensure quality and quantity commitments are achieved in a timely and efficient manner. Responsible for ensuring that the study is conducted in accordance with AZ Procedures/ Applicable SOP’s & Guidelines, such as ICH and GCP as well as relevant local regulations. Ensure delivery of the projects according to the commitment & set timelines. Initiate, conduct and deliver non interventional studies (local, regional and global) across TAs, External Service Provider Identification, Selection, and Work in close collaboration Initiate ESP contact (CRO, DM and Laboratory), exchange contracts and negotiate costs along with purchase team for DM, monitoring, central lab, translation, printing service, as applicable. Prepare clinical trial budget and get management approval after discussion. Assist in designing of study Protocol, CRF, ICF and other study related documents. Prepare Monitoring Plan, SDV and QC plan for the study. QC review of study documents, CRO and ASV along with CRO person to check QC Budget Preparation & approval. Work with medical colleagues on study protocol and related documents. Ensure quality conduct of the trial/study. Oversee site/Investigator identification and selection and SDV. Ensure Timely delivery of project from study start-up to DBL & CSR. Ensuring compliance with the Protocol, SOPs, ICH-GCP and other applicable regulatory requirements. Regular coordination with CROs to track progress of trial with target and actual milestones. During the trial, to take CAPA to ensure GCP compliance and reliability of data. Publication Management, Adherence to Publication Policy Essential Degreeorequivalentprofessionalqualificationin related field Pharm D ExperienceinhandlingClinicaltrials,observational studies,PublicationandESR Desirable Post-graduatequalification Why AstraZeneca? At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare. AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements. APPLY NOW Explore the local area Take a look at the map to see what’s nearby. Reasons to Join Thomas Mathisen Sales Representative Oslo, Norway Christine Recchio Sales Representative California, United States Stephanie Ling Sales Representative Petaling Jaya, Malaysia What we offer We're driven by our shared values of serving people, society and the planet. Our people make this possible, which is why we prioritise diversity, safety, empowerment and collaboration. Discover what a career at AstraZeneca could mean for you. Lifelong learning Our development opportunities are second to none. You'll have the chance to grow your abilities, skills and knowledge constantly as you accelerate your career. From leadership projects and constructive coaching to overseas talent exchanges and global collaboration programmes, you'll never stand still. Autonomy and reward Experience the power of shaping your career how you want to. We are a high-performing learning organisation with autonomy over how we learn. Make big decisions, learn from your mistakes and continue growing — with performance-based rewards as part of the package. Health and wellbeing An energised work environment is only possible when our people have a healthy work-life balance and are supported for their individual needs. That's why we have a dedicated team to ensure your physical, financial and psychological wellbeing is a top priority. Inclusion and diversity Diversity and inclusion are embedded in everything we do. We're at our best and most creative when drawing on our different views, experiences and strengths. That's why we're committed to creating a workplace where everyone can thrive in a culture of respect, collaboration and innovation.

Job description Overview The Operations Support Specialist plays a crucial role in ensuring the efficient operation of our business processes. This position involves a combination of administrative, logistical, and technical support to enhance productivity and streamline operations across various departments. Key Responsibilities: Order Management & Data Entry Enter and manage customer and dealer orders in internal systems. Generate invoices and shipping labels via platforms like Eshipz and BlueDart. Maintain clean and accurate data across all platforms. E-Commerce Platform Operations Handle Amazon FBA, EasyShip, and Seller Flex order processes, including booking, uploading invoices, label generation, and monitoring shipment statuses. Track Safe-T claims, initiate return/refund/exchange processes on Amazon and the website. Coordinate with internal teams for Quality Check and inventory updates for returns. Returns, Refunds, Exchanges Track return shipments across channels, perform necessary follow-ups. Liaise with the QC team for inspection status and update stock on internal CRM (Tigersheet). Coordinate internally with the sales team for exchanges/repairs for customers based on SOPs. Reporting & Accuracy Support the team with regular inventory checks and physical stock counts. Maintain records of return claims, pending shipments, or damaged/missing items. Flag discrepancies proactively and support resolution. Any other duties that may be assigned These may include but are not limited to pick & pack for dealer/customer orders. Helping in the production department for stock transfer to the warehouse. Requirements: 1–3 years of experience in e-commerce operations or sales back-end support. Familiarity with Amazon Seller Central (FBA, EasyShip, Safe-T claims, etc.) is a must. Working knowledge of order management tools (like Eshipz & CRM like ZOHO preferred). Strong attention to detail, especially with data and documentation. Comfortable handling spreadsheets, system-based work, and multi-platform coordination. Good written communication and basic customer handling skills are a bonus. What We Offer: Competitive salary & benefits package. Opportunity to work with a passionate & innovative team. Professional development & learning opportunities. Industry Type: Internet (E-Commerce) Employment Type: Full Time, Permanent About company ViaTerra Gear is one of India's leading brands in motorcycle touring accessories. Incorporated in 2010, the company has an extensive portfolio of products in luggage, apparel and hard part categories. We have an in-house team that designs and tests the products, and the products are manufactured at company facilities in Nashik, Maharashtra and Chennai, Tamil Nadu. We also source some products from manufacturing partners in Asia and Europe. The ViaTerra brand is trusted by customers in India and in over 60 countries around the world. Company Info Link: https://viaterragear.com Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Leave encashment Provident Fund Schedule: Day shift Morning shift Application Question(s): Can you start immediately ? Work Location: In person Expected Start Date: 14/06/2025

Flowserve is a world-leading manufacturer and aftermarket service provider of comprehensive flow control systems. Join a company whose people are committed to building a more sustainable future to make the world better for everyone. With 16,000+ employees in 50+ countries, we combine our global reach with local presence. Our team challenges themselves to approach each situation with ingenuity and creativity to help provide our customers with the most innovative flow control products and services. We support 10,000+ customers worldwide, creating products to meet the needs of our customers who are supplying energy, fresh water, pharmaceuticals and other essentials to consumers, businesses and governments globally. We invite you to put your talents and career in motion at Flowserve. Company Overview: If a culture of excellence, innovation and ownership is what you’re searching for, consider putting your experience in motion at Flowserve. As an individual contributor, or as a leader of people, your enterprise mindset will ensure Flowserve’s position as the global standard in comprehensive flow control solutions. Here, your opportunity for professional development and industry leading rewards will be supported by our foundational commitments to the values of people first, integrity and safety. Thinking beyond opportunity and reward, at Flowserve, we are inspired by working together to create extraordinary flow control solutions to make the world better for everyone! Job Summary: In this role you will perform documented inspections in the verification of conformance of parts to applicable drawings, procedures, specifications and all applicable statutory and regulatory requirements. The QC Inspector is responsible for the content of the Inspection Test Plan (ITP) and project quality plan according to customer’s and Flowserve’s specifications and international standards. Besides, the QC Inspector is responsible for defining, advising and controlling all project required QC documents. The QC Inspector reports directly to the QC Supervisor/Manager. Responsibilities & Requirements: Documenting dimensional and visual inspections to the drawing or applicable procedures Documenting non-conforming material utilizing an NCR (nonconforming materials) process Reviewing and verify internal and external qualifications of suppliers, welders, NDE personnel with regard to Non-Destructive Examinations (NDE), welding procedures and/or other applicable requirements. Reviewing and approve supplier’s manufacturing and testing documents/procedures and to take care for approval (when required) of these documents by the customer, his customer and the authorized inspection body Preparing and define test and inspection requirements for the required projects such as ITP and procurement specifications Diploma or BE with 3-5 years relevant experience And any other duties assigned Preferred Experience / Skills: Knowledge of welding, NDE and quality systems Knowledge of the established quality standards, laws and regulations of national and international authorities Must have knowledge of inspection equipment generally found in machining, assembly and test operations Effective utilization of CMMs is a plus Flexible, eager to learn, accurate, analytical with positive, can-do attitude Flexibility and willingness to travel Good interpersonal, communication, negotiation, analytical and presentation skills Problem solving skills Operational Excellence & High Level of Customer Service Standard Req ID : R-15042 Job Family Group : Operations Job Family : OP Quality Assurance EOE including Disability/Protected Veterans. Flowserve will also not discriminate against an applicant or employee for inquiring about, discussing or disclosing their pay or, in certain circumstances, the pay of their co-workers. Pay Transparency Nondiscrimination Provision If you are a qualified individual with a disability or a disabled veteran, you have the right to request a reasonable accommodation if you are unable or limited in your ability to use or access flowservecareers.com as result of your disability. You can request a reasonable accommodation by sending an email to employment@flowserve.com. In order to quickly respond to your request, please use the words "Accommodation Request" as your subject line of your email. For more information, read the Accessibility Process. Show more Show less

Job Title: Officer – Quality Control (Microbiology) Department: Quality Control – Microbiology Reporting To: QC Microbiology Manager / Quality Head Employment Type: Full-time Salary: ₹20,000 per month Experience Required: Minimum 2 YearsQualification: M.Sc. / B.Sc. (Microbiology or related life sciences field) Job Summary: We are looking for a dedicated and detail-oriented Officer – QC Microbiology to join our Quality Control team. The selected candidate will be responsible for performing microbiological testing of raw materials, finished products, water, and environmental monitoring to ensure compliance with quality and regulatory standards. Key Responsibilities: 1. Microbiological Testing: Conduct routine microbiological analysis of raw materials, finished products , and in-process samples . Perform water testing (WFI, Purified Water, RO Water) for microbial limits. Execute sterility testing, BET (Bacterial Endotoxin Test) , and Microbial Limit Testing . 2. Environmental Monitoring: Carry out environmental monitoring of production and sterile areas , including air, surface, and personnel monitoring. Maintain and review EM records, trends, and reports. 3. Media Preparation & Validation: Prepare, sterilize, and validate media for microbiological testing. Perform growth promotion tests and media control checks. 4. Documentation & Compliance: Ensure timely and accurate documentation of all microbiological activities as per cGMP and GLP . Maintain logbooks, worksheets, test reports, and analytical records as per SOPs. 5. Instrument Handling: Operate and maintain laboratory equipment such as Incubators, LAF, Autoclave, pH meter, Conductivity meter, and Particle counter . Ensure instruments are calibrated and maintained as per schedule. Candidate Requirements: Education: M.Sc. / B.Sc. in Microbiology or Life Sciences Experience: Minimum 2 years in pharmaceutical QC microbiology Knowledge Required: Strong understanding of microbiological techniques and regulatory standards. Familiarity with GMP , GLP , and ISO guidelines. Skills: Good observation and documentation skills. Ability to follow SOPs and work in a sterile environment. Basic computer proficiency for record-keeping and reporting. Work Schedule: 6 days working Job Types: Full-time, Permanent Pay: ₹216,000.00 - ₹240,000.00 per year Benefits: Flexible schedule Food provided Health insurance Paid time off Provident Fund Schedule: Day shift Morning shift Weekend only Supplemental Pay: Overtime pay Performance bonus Yearly bonus Location: Baddi, Himachal Pradesh (Required) Work Location: In person

Company Description ClinFocus empowers life sciences organizations to accelerate clinical trials through technology-driven solutions. Our services include EDC Development, Systems Integration, AI Deployment & Enablement, Clinical Data Science, Project Management, and Development of Integrated Dashboards. As an ISO-certified organization and partner of Medidata Rave, we are committed to excellence and trust in clinical research. We are seeking a highly motivated and skilled Clinical Statistical Programmer to join our dynamic Biometrics team. In this role, you will be instrumental in the development, validation, and maintenance of programs used for the analysis and reporting of clinical trial data. You will work closely with biostatisticians, data managers, and clinical scientists to ensure the accurate and timely delivery of high-quality statistical outputs. Responsibilities: Develop, validate, and maintain SAS programs for the creation of SDTM and ADaM datasets, tables, listings, and figures (TLFs) according to statistical analysis plans (SAPs) and programming specifications. Ability to contribute to the development and implementation of Statistical Analyses Plan Perform quality control (QC) of programs and outputs generated by other statistical programmers to ensure accuracy, consistency, and adherence to company standards and regulatory guidelines. Collaborate with biostatisticians to clarify programming requirements, resolve data issues, and ensure the accurate implementation of statistical methodologies. Contribute to the development and review of programming specifications, mock TLFs, and other study-related documentation. Ensure compliance with regulatory requirements (e.g., FDA, EMA, ICH-GCP) and internal Standard Operating Procedures (SOPs). Participate in team meetings and contribute to discussions regarding study design, data analysis, and reporting strategies. Proactively identify and implement process improvements to enhance efficiency and quality of programming deliverables. Maintain comprehensive documentation of programming activities and version control. May contribute to the development and maintenance of programming standards and macros. Qualifications: Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, Mathematics, or a related scientific field. Minimum of3] years of experience in clinical statistical programming within the pharmaceutical, biotechnology, or CRO industry. Proficiency in SAS programming (Base SAS, SAS/STAT, SAS/GRAPH, SAS Macro Language). Strong understanding of CDISC standards, including SDTM and ADaM. Experience with regulatory submissions (e.g., NDA, BLA) is highly desirable. Solid understanding of clinical trial processes, ICH-GCP guidelines, and relevant regulatory requirements. Excellent attention to detail and strong problem-solving skills. Ability to work independently and as part of a collaborative team. Strong written and verbal communication skills. Experience with other programming languages (e.g., R, Python) is a plus. Knowledge of industry best practices for statistical programming. What We Offer: Opportunity to work on innovative clinical trials across diverse therapeutic areas. A collaborative and supportive work environment. Opportunities for professional growth and development. Competitive salary and benefits package. Show more Show less

Responsibilities Design, develop, and execute comprehensive test plans to ensure all aspects of the product are validated. Review and analyse requirements, specifications, and technical design documents, ensuring thorough understanding and providing timely, actionable feedback. Perform functional, regression, and integration testing to verify software functionality and stability. Drive product quality within agile environments, ensuring that testing is efficient and effective even in short release cycles. Identify and report issues through clear documentation and verify that they are resolved effectively. Maintain detailed documentation of testing processes, findings, and solutions for team-wide reference. Collaborate closely with the development team and QA/QC members to troubleshoot, enhance testing efficiency, and support quality improvement across all stages of the product lifecycle. Skills & Qualifications Strong understanding of the testing lifecycle. Proven ability to work independently with minimal supervision. Effective communicator with excellent documentation skills. Strong analytical and problem-solving abilities. Experience in automated testing using Selenium with Java and Playwright with TypeScript or JavaScript. Team player with the ability to collaborate effectively across QA and development teams. What We Offer Attractive base salary with performance-based bonuses. Work on diverse projects spanning various industries and technologies. Opportunities to work with new technologies and grow within the company. Supportive remote work culture and focus on work/life balance. Enjoy the flexibility of remote work from anywhere in India. (ref:hirist.tech) Show more Show less

Key Job Requirements Has good knowledge of popular Automation tools. Has proficient knowledge in programming languages such as java. Creating, Modifying, Debugging and Executing Test scripts for web/mobile applications using Java and Selenium Web driver tool. Defect Reporting and Tracking using any Defect Management Tool. Test Management using any Test Management tool like Zephyr/Jira / MF ALM QC / TFS Involvement in Framework creation. Reporting Test results and status reports on a regular basis to Team Lead. Good Understanding of methodologies such as Agile and Waterfall. Hands on experience of working with at least one of GUI based Test Automation tools for desktop and/or Mobile Automation using Appium. Experience on other tools like Appium testing will be an added advantage. Hands-on experience in different test frameworks like Robot, TOSCA, Rest Assured, TestNG, Maven, Capgemini ADAPT etc. and device farm solutions like Perfecto / Experitest / AWS frameworks will be a big plus. Preferred Skills Knowledge of version management tools and repository tools like Git and GitHub, Bit Bucket, CI & Build tools such as, Junit Jenkins, Gradle, etc. Knowledge to create/manage execution pipeline on Azure Devops, Browser stack. Should be able in the modern Agile practices such as BDD/Cucumber, DevOps. Familiarity with process of Test Automation tool selection & test approach. Strong hands-on experience in the implementation of various Automated Testing Solutions including Selenium, Cucumber, SoapUI, Postman and LoadRunner. About Company CresTech is a specialized software testing and QA services provider spread across its 4 delivery centers at Noida (India), Gurugram (India), Bangalore (India) and California (USA). We are the first (India headquartered) Independent software testing company to be assessed at CMMI Level 3 SVC. CresTech works with its global clients in the areas of test automation, mobile QA transformation, cloud migration testing, and end user experience management that includes performance and security testing. Leveraging innovation at its core (with 3 provisional patents to its credit), CresTech is trusted by Fortune 500 enterprises and start-ups alike to help them in their QA programs worldwide. Our solution spectrum spreads across Insurance, Travel, E-Commerce, Telecom (VAS), Print & Media and Mobile Application space. Visit us at www.crestechsoftware.com (ref:hirist.tech) Show more Show less

Job Role: Lab Officer- TermOps Job Role ID: SECTION I: BASIC INFORMATION ABOUT THE JOB ROLE Outlines the count of employees reporting and financial and geographic scope of the role Job Role Variant: Analyst QA/QC Manager Job Position: Chemist Job Position ID: 81173751 Value Stream: Asset Operations Quality Management: Sub-Job Family SECTION II: PURPOSE OF THE ROLE A two to three line statement outlining the objective or the reason for which the job exists. To carry out analysis of process, product, and other samples by using standard and other test methods as per product specification/sample schedule/supervisor instructions, in order to perform & ensure validity of calibration, verifications, standardization, and quality control data & update results in LIMS while adhering to safe work practices & guidelines. List of responsibilities attached to the role are documented below. These responsibilities are representative and the role holder is also responsible for any other job assigned by the superior authorities from time to time. This section is not intended to be an exhaustive listing of all activities done by the role holder. It should capture only the key responsibilities of the role. SECTION III: KEY RESPONSIBILITIES AND ACCOUNTABILITIES OF THE ROLE Responsibilities Policies, Procedure and Process Adherence - Adhere to standard test methods or work instructions and compliance to Quality system procedures - Follow applicable HSEF procedures/practices with awareness about environmental statutory regulations - Keep self abreast with leading practices & trends and contribute to the identification of continuous improvement of systems, processes, and procedures. Undertake/participate in trainings to enhance competencies and knowledge Quality Assurance Operations - Conduct inspection of received routine samples and distribution of samples as per type of analysis to the different sections of the laboratory. Raise concerns with shift in charge in case of abnormal samples or delay of routine sample delivery as per schedule - Conduct required tests and confirm test results by using validation techniques prior to reporting to ensure test result reliability - Report deviations in test results to concerned stakeholders - Perform on-spot mitigation in emergency situations under the guidance of the shift in charge - Conduct effective sample management and disposal of leftover samples - Maintain good housekeeping and availability of analytical gears for next experiments - Make proper entries of results recording in the raw data book/LIMS/process register/and also maintain the same in the individual raw data book Metrics that are used to evaluate the success/performance of the role; specific targets do not need to be included as those would change from Y-o-Y SECTION IV: SUCCESS METRICS (TOP 3-5 KPI's) Compliance to ISO 17025 Quality Management System Adherence to various standards and compliances (e.g. ISO 9001, ISO 18001, ISO 45001, AS 9100D) Compliance to safety guidelines and instructions Quality audit score Timely completion of schedule analysis & report release Timely completion of product analysis and report release within stipulated time limit Timely implementation of LIMS and SAP-QM SECTION V: OPERATING NETWORK Key Interactions Internal: Site teams, PC&I, etc. External: NA SECTION VI: KNOWLEDGE AND COMPETENCIES Education Qualifications: Bachelor's Degree in Science with specialization in Chemistry (preferred)/Master's Degree in Science with specialization in Chemistry (preferred) FUNCTIONAL COMPETENCIES BEHAVIORAL COMPETENCIES Experience (Must Have & Good to Have) Must have: 2 years of experience in QA/QC discipline Good to have: Experience in a similar field will be preferred Functional/Behavioral Competencies Required To Execute The Role - Knowledge of the test procedure and results reporting - Knowledge of sample handling - Knowledge of process stream samples - Product classification and certification - Method development and validation - Complaint handling & feedback analysis - LIMS & SAP-QM Show more Show less

We are looking for a Quality Analyst to write and execute manual tests to ensure product quality. As a QA engineer, you will be designing and implementing tests, debug and make corrective actions. You play a vital role in the companys application development process. You will be responsible for testing the product before launches to ensure that the product is free from errors and reliable. What You'll Be Doing Manage own productivity, learning and utilization of hours. Collaborate with team members to understand project requirements/SOW. Understand and adapt workflow for QA project based on sprints and milestones. Managing QC & UAT for each projects and ensuring deliverables as per scope. Making test plan, test cases for the assigned projects and manage results for them. Perform Functional and Non-Functional Testing. Identify and report defects or issues in the project. Work closely with the dev team and certify each build as part of internal/external UAT. Supporting other team members to achieve project objectives, customer delight and process compliance. In the case of crisis, or breakdown, work along with the tech team to identify the root cause and assist in resolving them. Follow QA standards, policies, and procedures. Accountable for the code quality, and bug-free delivery of development. Managing documentation for QA department & Reporting in desired format. Adhere to QA procedures and policies. Develop and execute performance and load-testing scripts. What We'd Love To See Proven 3 to 4 years of experience and expertise in quality assurance. Strong knowledge of software QA methodologies, tools and processes. Experience in Magento E-Commerce domain is must. (B2B, B2C), Shopify and mobile application testing [android,ios]. Experience in writing clear, concise, and comprehensive test plans and test cases. Hands-on experience with automated testing tools, JMeter Load testing. Experience working in an Agile/Scrum development process and managing tasks defects using tools such as JIRA. Able to work on dedicated projects/multiple projects as an individual QA or with team. Be familiar with testing tools and methodologies. Must be able to clearly describe and discuss problem and work towards finding solution. Certification is add on. BS/MS degree in Computer Science, Engineering or a related subject. Itd Be Great If You Had Strong writing and communication skills. Automation Testing experience. (ref:hirist.tech) Show more Show less

Global Sales Strategy & Operations (GSSO) is the team that helps shape Gartner's mission-critical sales priorities and works with sales leaders to drive tactical and analytical insights. As an associate on the GSSO team, you'll be at the forefront of the ongoing transformation of Gartner's sales force, which delivers approximately $4.9B in annual revenue and working to drive sustained double-digit growth. You will partner with business leaders across Gartner to support a global sales force comprised of more than 5,000 associates who sell to every major function, industry and market sector around the world. About this Role: The Senior Specialist role is part of the Territory Planning & Analytics (TP&A) team in GSSO. The TP&A team is focused on designing the optimal territory investment, design and alignment strategy to maximize Sales (and Services) productivity. The Senior Specialist will join the Territory Contact & Enrichment Team in TP&A that use various tools and platforms driven by automation and analytics to empower sellers with high quality bullseye prospect contacts quickly, pro-actively, accurately and at scale in a prioritized and streamlined manner. What you will do : Operational Excellence Actively work on completing the prospects research life cycle within timelines & provide timely and accurate output. Work on ad-hoc operational projects with minimal guidance Manage and resolve assigned tasks end to end within service level agreements. Drive operational excellence – incremental improvement in process across prospecting– reduced steps, intuitive and simpler process design/interfaces. Implement best practices/tested solutions across processes to maximize effectiveness Stakeholder Management and Collaboration Engage with stakeholders and partners with members across functions to deliver value. Partner within and across teams to Identify gaps, problem solve and improve processes. Embrace collaboration, improve ideas, and apply analytical thinking to drive impact. Perform manual workstreams to deliver the output and act as a champion mindset to provide solutions on automating manual workstreams Own and drive execution of assigned work streams independently. Project Management Ensure data integrity by identifying discrepancies and updating datasets regularly. Manage data tools and internal applications including automation tools, Excel, Power BI, prospecting tools etc. Successfully drive high complexity projects with minimal guidance Gain strong understanding of internal systems and processes such as Bulls eye, title QC, deduplication etc. Mentor and train other team members on processes/tools What you will need : Bachelor’s degree with 3 years of relevant experience in global organization Proficiency in Microsoft Office, especially Excel and PowerPoint; Knowledge of third-party prospecting tools is a plus Excellent oral and written communication skills Ability to thrive in a fast-paced, deadline-driven, and dynamic team environment. Experience communicating complex data through relevant means to senior leaders Experience applying various analytic techniques (segmentation, regression, forecasting, etc.) is a plus Excellent interpersonal skills, a team player and quick learner What you will get: Competitive salary, generous paid time off policy and more! India: Group Medical Insurance, Parental Leave, Employee Assistance Program (EAP) Collaborative, team-oriented culture that embraces diversity Professional development and unlimited growth opportunities #GSSO Who are we? At Gartner, Inc. (NYSE:IT), we guide the leaders who shape the world. Our mission relies on expert analysis and bold ideas to deliver actionable, objective insight, helping enterprise leaders and their teams succeed with their mission-critical priorities. Since our founding in 1979, we’ve grown to more than 21,000 associates globally who support ~14,000 client enterprises in ~90 countries and territories. We do important, interesting and substantive work that matters. That’s why we hire associates with the intellectual curiosity, energy and drive to want to make a difference. The bar is unapologetically high. So is the impact you can have here. What makes Gartner a great place to work? Our sustained success creates limitless opportunities for you to grow professionally and flourish personally. We have a vast, virtually untapped market potential ahead of us, providing you with an exciting trajectory long into the future. How far you go is driven by your passion and performance. We hire remarkable people who collaborate and win as a team. Together, our singular, unifying goal is to deliver results for our clients. Our teams are inclusive and composed of individuals from different geographies, cultures, religions, ethnicities, races, genders, sexual orientations, abilities and generations. We invest in great leaders who bring out the best in you and the company, enabling us to multiply our impact and results. This is why, year after year, we are recognized worldwide as a great place to work. What do we offer? Gartner offers world-class benefits, highly competitive compensation and disproportionate rewards for top performers. In our hybrid work environment, we provide the flexibility and support for you to thrive — working virtually when it's productive to do so and getting together with colleagues in a vibrant community that is purposeful, engaging and inspiring. Ready to grow your career with Gartner? Join us. The policy of Gartner is to provide equal employment opportunities to all applicants and employees without regard to race, color, creed, religion, sex, sexual orientation, gender identity, marital status, citizenship status, age, national origin, ancestry, disability, veteran status, or any other legally protected status and to seek to advance the principles of equal employment opportunity. Gartner is committed to being an Equal Opportunity Employer and offers opportunities to all job seekers, including job seekers with disabilities. If you are a qualified individual with a disability or a disabled veteran, you may request a reasonable accommodation if you are unable or limited in your ability to use or access the Company’s career webpage as a result of your disability. You may request reasonable accommodations by calling Human Resources at +1 (203) 964-0096 or by sending an email to ApplicantAccommodations@gartner.com. Job Requisition ID:100271 By submitting your information and application, you confirm that you have read and agree to the country or regional recruitment notice linked below applicable to your place of residence. Gartner Applicant Privacy Link: https://jobs.gartner.com/applicant-privacy-policy For efficient navigation through the application, please only use the back button within the application, not the back arrow within your browser. Show more Show less

Selected Intern’s Day-to-day Responsibilities Include Labeling and annotating datasets—text and images—with precision following project guidelines. Maintaining high accuracy and implementing quality control (QC) measures to meet defined standards. Reviewing and verifying annotations, flagging inconsistencies, and ensuring inter-annotator agreement benchmarks are met. Using industry tools like Labelbox and Label Studio to perform annotation tasks and participate in automated QC workflows. About Company: Ideas to Impacts Innovations Private Limited (I2I) is in the business of promoting innovative ideas that can create significant positive impacts for both customers and the non-metros of India. Our 'small town' model is the logical next step of Indian off-shoring. By providing cutting-edge technology services and products from the small towns of India, we go beyond the cost and social impact benefits, and work towards 'Distributing The Future Evenly (TM)'. Show more Show less

Ensure Quality of products, processes & services r established,monitored & maintained & against defined Goals.Establish Strong Customer Base while performing Internal/External Audits & Plant Improvements.Ensure people/process adhere 2 Co's norms Required Candidate profile Develop & maintain Quality Standards/check procedures throughout.Analyzing rejections/rework/statistical data to take CAPA to eliminate root cause of problems in order to prevent recurrence of problem

Company Description we required QC head for our group company for the manufacturing of Transformers at POr, Vadodara location. Role Description This is a full-time, on-site role located in Vadodara for the position of Quality Control Head. The Quality Control Head will be responsible for overseeing quality control processes, ensuring quality assurance and quality management, for the transformers manufacturing upto 50 MVA, 66 KV class. Daily tasks include conducting analytical tests, quality assessments, and implementing quality control standards to meet company and client requirements. Experience : 10+ years experience in the transformers industry Qualifications Quality Control, Quality Assurance, and Quality Management skills Strong Analytical Skills Excellent problem-solving and leadership abilities Good communication and team management skills Bachelor’s degree in Engineering, Quality Management, or a related field Experience in the transformer industry is a plus Show more Show less

About This job is provided by apna.co About the Role: As a Quality Auditor you will be responsible for evaluating, monitoring, and assessing the performance of Assissted Growth (Telesales) representatives to ensure adherence to company standards, policies, and customer service protocols. The role involves conducting regular audits of recorded calls/chats, reviewing sales processes, identifying areas for improvement, and providing constructive feedback to help optimize sales effectiveness, compliance, and customer satisfaction. Role Responsibilities Review and audit recorded calls/ chats to ensure adherence/compliance with established internal control procedures by examining centres, reports, operating practices, and documentation Deliver detailed and actionable feedback to telesales agents, highlighting strengths and areas for improvement. Communicate the audit findings by preparing a final report; identify and promote continuous improvement opportunities in training, process, policies and facilities Enforce adherence to requirements; advising management on needed actions Prepare special audit and control reports by collecting, analysing, and summarising operating information and trends Contribute to team effort by accomplishing related results as needed Maintain focus on data integrity, customer safety and producing work of the highest quality Identify barriers to customer success wherever they originate (tools, training, etc) Become an "expert" on support processes and make recommendations towards next steps based on customer experience Collaborate with training teams to identify training needs based on audit results. Work closely with team leaders, supervisors, and managers to ensure alignment on performance expectations and the implementation of corrective actions when necessary. Qualifications Any Bachelor's degree At least 1-2 years of prior experience in telesales, customer service, or a related field. 1-2 years of prior experience in quality management roles Six Sigma Certification is an added advantageSkills: Basic proficiency in productivity tools (email, calendar), Microsoft Suite (excel, PowerPoint), Google sheets, Google docs Proficiency in Hindi and Regional language is an added advantage Self motivated, ability to prioritize and manage multiple tasks effectively while meeting deadlines.and reliable to meet deadlines Proven ability to work in a fast-paced team setting Strong problem-solving and data analysis skills to assess trends and performance metrics Ability to work cross functionally with other departments Working Conditions The role is based in the office The workweek is Monday to Saturday Show more Show less

Raw Material TestingPerform identification, assay, and purity tests for herbal powders, extracts, oils, and excipients. Ensure compliance with API, FSSAI, BIS, or AYUSH standards. Maintain raw material specifications and COAs (Certificate of Analysis). 🧴 2. In-Process Quality ChecksMonitor pH, viscosity, microbial limits, moisture content, etc., during shampoo, cream, syrup, and capsule production. Record and correct deviations in real-time with production teams. ✅ 3. Finished Product AnalysisConduct quality checks as per IP/USP/AYUSH pharmacopoeial guidelines. Maintain batch-wise quality records and approve or reject finished goods. Validate label claims: preservatives, actives (like curcumin, aloin, glycyrrhizin), shelf life tests. 🧪 4. Microbiological & Stability TestingEnsure freedom from pathogens (E. coli, Salmonella, Yeast/Mold) in products. Conduct accelerated & real-time stability studies as per AYUSH/FDA norms. 📋 5. Documentation & ComplianceMaintain GLP (Good Lab Practices) and GDP (Good Documentation Practices). Prepare COAs, QC reports, batch release documents, and SOPs. Support regulatory inspections (FDA, AYUSH, FSSAI, ISO, GMP audits). 🛠 6. Calibration & MaintenanceCalibrate pH meters, balances, spectrophotometers, incubators, etc. Ensure proper functioning and documentation of all lab equipment.

Production ChemistDepartment: Manufacturing / Production Location: [Specify Location] Reporting To: Production Manager / Plant Head Job Type: Full-Time 🧭 Roles & Responsibilities🔧 1. Batch Manufacturing & SupervisionExecute and supervise batch manufacturing of Ayurvedic formulations: syrups, churnas, vatis, capsules, oils, creams, shampoos, etc. Ensure accurate weighing, mixing, blending, granulation, filtration, and filling as per BMR/BPR (Batch Manufacturing/Packaging Records). Follow SOPs and maintain hygiene and GMP compliance on the shop floor. 📋 2. Documentation & ComplianceMaintain all production-related documentation: Batch Manufacturing Records (BMR) Equipment cleaning logs Daily production reports In-process control logs Ensure traceability of every batch produced as per AYUSH / GMP standards. 🧴 3. Equipment Operation & MaintenanceOperate and monitor equipment like mixers, pulverizers, coating machines, capsule filling machines, homogenizers, and shampoo/cream mixers. Coordinate preventive maintenance and calibration with the engineering team. ⚖ 4. Coordination with DepartmentsCoordinate with QC, QA, Store, and Packing departments for raw materials, samples, approvals, and timely execution of production schedules. Report material shortages, production delays, or deviations proactively. ✅ 5. Regulatory & Safety ComplianceAdhere to safety norms and Good Manufacturing Practices (GMP). Ensure cleanliness of production areas as per Schedule-T (AYUSH GMP). Participate in internal and external audits. 🧑‍🎓 Qualifications & Skills 1–3 years of experience in Ayurvedic / Cosmetic / Herbal / Pharma production Knowledge of GMP, AYUSH Guidelines, Schedule-T Ability to manage manpower and maintain production discipline Strong observation, process understanding, and documentation skills

Piscium Health Sciences Pvt Ltd is a Nano technology based medical devices company based out of Navi Mumbai. The position of Quality Manager involves checking of incoming raw material, in process checks and outgoing material Final Inspection. Candidate should be a graduate, preferably experienced for 2 years in QC . The candidate will also assist in ISO led processes and documentation.

Interior Designer Location: Kochi Qualifications: Bachelor’s or Master’s Degree in Interior Design / Interior Architecture from a reputed institution Strong portfolio demonstrating a range of high-quality interior design projects Minimum XX+ years of experience in an architectural or interior design studio Proficiency in AutoCAD, SketchUp, Revit, Adobe Suite, and rendering tools such as Enscape / V-Ray / Lumion Working knowledge of design documentation, FF&E specifications, and project coordination Key Responsibilities Work alongside the Principal Architect and Senior Designers in developing concept-driven, high-end interior design solutions Lead interior design packages from concept to execution for residential, commercial, hospitality, and institutional projects Prepare detailed mood boards, material palettes, 3D presentations, and FF&E documentation aligned with project narratives Collaborate with clients to understand their vision, lifestyle, and spatial needs and translate that into thoughtful, user-centric designs Participate in project kickoff meetings, site surveys, and ongoing coordination with architecture, MEP, and structural teams Review and refine design intent during all phases: concept, schematic design, detailed drawings, and tender documentation Ensure that all design work aligns with F+A’s design philosophy, aesthetic direction, and quality benchmarks Liaise with vendors, fabricators, and product suppliers to source and curate materials, finishes, and furniture pieces Provide support in BOQ preparation, cost estimation, and procurement documentation for interior elements Oversee site implementation, mockups, and final styling, ensuring execution matches design intent Maintain compliance with project timelines, client expectations, and QA/QC standards Keep abreast of emerging trends, materials, and technologies in interior design and integrate them into ongoing work Other design and coordination duties as assigned from time to time What We’re Looking For: Strong creative thinking with attention to detail and spatial storytelling Ability to balance aesthetics with practicality and cost-conscious design Excellent communication and presentation skills (written, spoken, and visual) Capable of handling fast-paced design environments with multiple ongoing projects Passionate about design excellence and contributing to a collaborative studio culture If interested, please send your CV's and Portfolio to careers@fahedarchitects.com Show more Show less

Skill required: Regulatory Services - Life Sciences Regulatory Affairs Designation: LifeScience Regulatory Svs Associate Qualifications: Bachelor of Pharmacy/Master of Pharmacy Years of Experience: 1 to 3 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song— all powered by the world’s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world’s leading biopharma companies bring their vision to life – enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The incumbent will perform the regulatory operations tasks of bookmarking and hyper linking for granular components (documents) of submission in accordance with ICH guidelines and other Health Authorities, review and transform Source Documents. Perform Quality Control (Document QC) checks for all submission components. Collect, collate and evaluate the scientific data gathered as part of R & D. Advise on legal and scientific restraints and requirements. Ensure the organization`s products comply with current regulations. Example; Build regulatory submission strategy, author CMC documents, and health authority packages etc. What are we looking for? Ability to meet deadlines Ability to perform under pressure Ability to work well in a team Adaptable and flexible Agility for quick learning Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Show more Show less