Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations. Role Description This is a full-time on-site role for a Pharmaceutical Validation SME located in Chennai. The candidate will be responsible for providing technical support to companies on the following software products: ValDoc Pro - Qualification lifecycle management software eLog Pro - Electronic logbook QMS Pro - Quality Management system software You will also be responsible for the following: Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online Write test scripts and execute them. Open bug tickets where required. Qualifications BPharm or Biotechnology degree Will be expected to serve minimum 2 years with the company if offered a position. Show more Show less
IMPORTANT NOTE: Candidate should have prior work experience in Pharmaceutical Industry in QA role in Validation. Do NOT apply if you have software testing experience Company Description Quascenta specializes in offering comprehensive validation lifecycle management software solutions to empower pharmaceutical manufacturing sites. Our flagship products, eResidue Pro, eProcess Pro, ValDoc Pro, QMS Pro and eLog Pro, are designed to streamline QMS, product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. We provide innovative solutions tailored to meet unique requirements, with experienced Subject Matter Experts (SMEs) analyzing data and recommending improvements. Role Description This is a full-time on-site role. The candidate will be responsible for providing technical support to companies on the following software products: ValDoc Pro - Qualification lifecycle management software eLog Pro - Electronic logbook QMS Pro - Quality Management system software You will also be responsible for the following: Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online Write test scripts and execute them. Open bug tickets where required. Qualifications Prior experience using a QMS software Experience in qualification of equipment/instruments Experience in process validation a plus Fluency in Hindi a must. Show more Show less
Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations. Role Description You will also be responsible for the following: Understand what process validation, cleaning validation, qualification, quality managements means. Write test scripts and execute them. Open bug tickets where required. Qualifications BPharm or Biotechnology degree Will be expected to serve minimum 2 years with the company if offered a position. Show more Show less
Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations. Role Description This is a full-time on-site role for a Pharmaceutical Validation SME located in Chennai. The candidate will be responsible for providing technical support to companies on the following software products: ValDoc Pro - Qualification lifecycle management software eLog Pro - Electronic logbook QMS Pro - Quality Management system software You will also be responsible for the following: Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online Write test scripts and execute them. Open bug tickets where required. Qualifications BPharm or Biotechnology degree 2-5 yrs experience in QA or Production in Pharma Will be expected to serve minimum 2 years with the company if offered a position. Show more Show less
Key Responsibilities Review and analyze software requirements and functional specifications. Design, develop, and execute manual test cases and test plans. Identify, document, and track software defects clearly and accurately. Collaborate with developers and business analysts to understand new features and resolve issues. Perform regression, integration, and system testing across web/mobile applications. Create and maintain detailed documentation for testing activities and findings. Participate in periodic reviews and workflow improvement sessions Required Skills Proficient in manual testing methodologies and best practices. Good understanding of SDLC, STLC, and bug life cycle. Experience with defect tracking tools (such as JIRA or similar). Strong analytical skills and attention to detail. Effective verbal and written communication skills. Preferred Qualifications Bachelor’s degree in Computer Science, Information Technology, or a related field. Prior experience (3-7 years) in manual software testing. Familiarity with web technologies and user interface validation. Exposure to vendor management or workflow automation software is a plus. About Us Quascenta specializes in providing comprehensive validation lifecycle management software solutions for the pharmaceutical industry. Their mission centers on empowering pharmaceutical manufacturing sites with digital tools to streamline product manufacturing and cleaning processes, ensuring strict compliance, increased efficiency, and measurable cost savings
Looking for local candidates from Chennai/Tamilnadu Salary: 3-6 Lacs CTC based on experience Key Responsibilities Review and analyze software requirements and functional specifications. Design, develop, and execute manual test cases and test plans. Identify, document, and track software defects clearly and accurately. Collaborate with developers and business analysts to understand new features and resolve issues. Perform regression, integration, and system testing across web/mobile applications. Create and maintain detailed documentation for testing activities and findings. Participate in periodic reviews and workflow improvement sessions Required Skills Proficient in manual testing methodologies and best practices. Good understanding of SDLC, STLC, and bug life cycle. Experience with defect tracking tools (such as JIRA or similar). Strong analytical skills and attention to detail. Effective verbal and written communication skills. Preferred Qualifications Bachelor’s degree in Computer Science, Information Technology, or a related field. Prior experience (3-7 years) in manual software testing. Familiarity with web technologies and user interface validation. Exposure to vendor management or workflow automation software is a plus. About Us Quascenta specializes in providing comprehensive validation lifecycle management software solutions for the pharmaceutical industry. Their mission centers on empowering pharmaceutical manufacturing sites with digital tools to streamline product manufacturing and cleaning processes, ensuring strict compliance, increased efficiency, and measurable cost savings
Note: This position is based out of Chennai. No remote option available. Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations. Role Description This is a full-time on-site role for a Pharmaceutical Validation SME located in Chennai. The candidate will be responsible for providing technical support to companies on the following software products: ValDoc Pro - Qualification lifecycle management software eLog Pro - Electronic logbook QMS Pro - Quality Management system software You will also be responsible for the following: Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online Write test scripts and execute them. Open bug tickets where required. Qualifications Prior experience using a QMS software Experience in qualification of equipment/instruments Experience in process validation a plus Fluency in Hindi a must.
We are looking for candidates with Good command of English to write technical articles on pharmaceutical validation. Refer Destin's memo section on cleaningvalidation.com to understand the requirement Knowledge of Photoshop a plus Company Description At Quascenta, we specialize in comprehensive validation lifecycle management software solutions for the pharmaceutical manufacturing industry. Our flagship products—eResiduePro, eProcessPro, and eLogBook—are designed to streamline processes related to product manufacturing and cleaning, ensuring compliance, efficiency, and cost savings. Each product brings unique capabilities: eResiduePro simplifies residue calculations, eProcessPro tracks critical parameters through the lifecycle, and eLogBook organizes validation records. Our experienced SMEs provide data analysis and improvement recommendations tailored to your needs.
Note: This position is based out of Chennai. No remote option available. Salary: 5-8 lacs CTC based on validation experience Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites with the software tools they need to streamline their product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, including eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions support organizations in meeting regulatory requirements while optimizing operations. Role Description This is a full-time on-site role for a Pharmaceutical Validation SME located in Chennai. The candidate will be responsible for providing technical support to companies on the following software products: ValDoc Pro - Qualification lifecycle management software eLog Pro - Electronic logbook QMS Pro - Quality Management system software You will also be responsible for the following: Assist customers with uploading their SOPs and managing qualification in the application. Of interest to the customer will be the ability to execute qualification scripts (IQ/OQ/PQ) online Write test scripts and execute them. Open bug tickets where required. Qualifications Prior experience using a QMS software Experience in qualification of equipment/instruments Experience in process validation a plus Fluency in Hindi a must.
Role Description This is a full-time on-site role for a Digital Social Media Content Creator located in Chennai. The Content Creator will be responsible for creating image and short video digital content across social media platforms - Linkedin, Facebook, Instagram and Tiktok. Daily tasks will include content creation, social media management, engagement with the pharmaceutical manufacturing community, and analyzing social media performance metrics. Qualifications Minimum 2 years experience with Adobe Photoshop Minimum 2 years experience with Premiere Pro, Final Cut Pro, or CapCut Social Media Management, Community Engagement, and Trend Analysis skills Proficiency with social media platforms, Tiktok, Linkedin, Facebook Ability to develop and execute social media strategies Company Description Quascenta specializes in providing comprehensive validation lifecycle management software solutions for pharmaceutical manufacturing sites. Our mission is to streamline product manufacturing and cleaning processes to ensure compliance, efficiency, and cost savings. Our flagship products, eResiduePro, eProcessPro, and eLogBook, are designed to simplify and optimize lifecycle management. Our experienced SMEs analyze data and recommend improvements, ensuring tailored solutions for each customer's unique needs.
Role Description This is a full-time remote role for a Blog Content Writer based in Chennai. The Blog Content Writer will be responsible for creating engaging web content, developing content strategies, conducting research, writing, and proofreading articles. The role involves collaborating with the President Qualifications Web Content Writing and general Writing skills Experience in developing Content Strategies and conducting Research Proofreading skills Excellent written and verbal communication skills Ability to work independently Bachelor's and/or Masters degree in Biology or related fields a plus Experience with Adobe Photoshop Company Description Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored to the pharmaceutical manufacturing industry. Our mission is to empower manufacturing sites with tools to streamline processes, ensuring compliance, efficiency, and cost savings. Flagship products like eResiduePro, eProcessPro, and eLogBook are designed to revolutionize the management of product, process, and cleaning lifecycles. We offer more than software by providing expert analysis and recommendations for improvements based on our extensive industry experience.
As a candidate for the position at Quascenta, you will be required to demonstrate a strong command of English for writing technical articles on the software products offered by the company. Your responsibilities will include leveraging your SEO experience to develop and execute strategies aimed at enhancing organic search performance. Additionally, you will be tasked with optimizing website content to align with Google ranking factors and generating engaging content for social media channels and the company's blog. To assist with content creation, you will utilize AI tools such as Perplexity. Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored for the pharmaceutical manufacturing sector. The company's flagship products, namely eResiduePro, eProcessPro, and eLogBook, are designed to streamline manufacturing and cleaning processes, ensuring compliance, efficiency, and cost savings. Each product offers unique capabilities aimed at simplifying residue calculations, tracking critical parameters, and organizing validation records. To excel in this role, you should possess proven experience in SEO content writing and website optimization. Familiarity with tools like Google Analytics and SEMrush is essential, and the ability to leverage AI tools for research and content planning will be beneficial. As part of a dynamic team, you must demonstrate adaptability and a startup mentality, enabling you to iterate quickly and document processes effectively. Strong analytical skills will be crucial for measuring content performance and adjusting strategies to drive continuous improvement.,
You will be responsible for writing technical articles on pharmaceutical validation with a strong command of English. It is essential to refer to Destin's memo section on cleaningvalidation.com to understand the specific requirements. Additionally, having knowledge of Photoshop will be considered a plus for this role. Quascenta specializes in offering comprehensive validation lifecycle management software solutions for the pharmaceutical manufacturing industry. Our primary products, eResiduePro, eProcessPro, and eLogBook, are meticulously designed to enhance the efficiency of manufacturing processes and cleaning operations. These products not only ensure compliance with industry standards but also contribute to cost savings for our clients. As part of our team, you will have the opportunity to work with experienced subject matter experts who provide valuable data analysis and improvement recommendations customized to meet the unique needs of our clients. Your role in creating technical content will play a crucial part in supporting pharmaceutical validation processes and enhancing overall operational effectiveness within the industry.,
The position is based out of Chennai and does not offer a remote work option. The salary offered is between 5-8 lacs CTC based on validation experience. At Quascenta, we specialize in providing comprehensive validation lifecycle management software solutions. Our mission is to empower pharmaceutical manufacturing sites by offering software tools to streamline product manufacturing and cleaning processes, ensuring compliance, efficiency, and savings. Our flagship products, such as eResiduePro, eProcessPro, and eLogBook, aim to transform how companies manage their product, process, and cleaning lifecycles. With over 20 years of experience, our solutions help organizations meet regulatory requirements while enhancing operations. This full-time on-site role is for a Pharmaceutical Validation Subject Matter Expert (SME) based in Chennai. The selected candidate will offer technical support on software products like ValDoc Pro, eLog Pro, and QMS Pro to client companies. Responsibilities include assisting customers with uploading SOPs, managing qualifications in the application, executing qualification scripts (IQ/OQ/PQ) online, writing and executing test scripts, and opening bug tickets when necessary. Qualifications for the role include prior experience with QMS software, equipment/instrument qualification, and process validation. Fluency in Hindi is a mandatory requirement.,
Role Description Quascenta is seeking a social media content creator who will be responsible for contributing engaging content that helps drive awareness of our brand worldwide to customers working in pharmaceutical manufacturing. This role will have a strong emphasis on animation (explainer videos), reels, static visuals, live streams, memes, case studies, etc. The candidate should be able to work with above noted media forms. The idea is to use Instagram, Linkedin and TikTok content for this purpose. Key responsibilities Design and animate explainer videos, motion graphics, and animated infographics. Shoot, edit, and optimize short-form videos for Instagram Reels, TikTok, and Stories. Create visually striking static assets—carousels, infographics, branded graphics. Develop engaging live stream and webinar content (Q&A sessions, demos, case studies). Produce and edit audio snippets, such as micro-podcasts and audiograms. Develop interactive posts—polls, quizzes, Q&As—using platform-native features. Monitor and engage with user-generated content and collaborate with clients for testimonials and success stories. Craft memes, relatable content, and leverage trending formats/audios (especially for Instagram and TikTok). Essential Skills & Qualifications Strong portfolio demonstrating animation, video editing, and graphic design. Proficiency in multimedia tools (Adobe Creative Suite, After Effects, Premiere Pro, Canva, etc.). Deep understanding of social media content trends and best practices for LinkedIn, Instagram, and TikTok. Ability to script, storyboard, and present visual stories clearly. Excellent communication, time management, and project coordination skills. Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions to pharmaceutical manufacturing sites. Our mission is to empower these sites with tools that streamline product manufacturing and cleaning processes, ensuring compliance, efficiency, and cost savings. Our flagship products, eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of industry expertise, our solutions combine cutting-edge software with experienced Subject Matter Experts who recommend practical improvements, making compliance simpler and operations smoother.
Role Description The Javascript automation tester role involves writing and executing automated test scripts, create and maintain test cases, and ensure the reliability and performance of the software developed by Quascenta. The role requires collaboration with development teams to identify and resolve issues and ensure that the products meet the highest standards of quality and compliance. We will train you on the tools to be used. Qualifications Proficiency in JavaScript for handling test scripts Fast learner Should be able to write test scripts Ability to work independently Salary : Rs 25,000 - Rs 35,000 Company Description Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored for pharmaceutical manufacturing sites. Our flagship products, eResiduePro, eProcessPro, and eLogBook, revolutionize product, process, and cleaning lifecycle management, ensuring compliance, efficiency, and cost savings. With products designed by industry experts, we not only provide software but also offer expert analysis and recommendations to improve your workflows. Our solutions help simplify residue calculations, track critical processes, and maintain organized validation records. Experience innovative tools designed to meet your unique needs and reach out to learn more.
Role Description This is a full-time remote role for a Blog Content Writer based in Chennai. The Blog Content Writer will be responsible for creating engaging web content, developing content strategies, conducting research, writing, and proofreading articles. The role involves collaborating with the President Qualifications Web Content Writing and general Writing skills Experience in developing Content Strategies and conducting Research Proofreading skills Excellent written and verbal communication skills Ability to work independently Bachelor's and/or Masters degree in Biology or related fields a plus Experience with Adobe Photoshop Company Description Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored to the pharmaceutical manufacturing industry. Our mission is to empower manufacturing sites with tools to streamline processes, ensuring compliance, efficiency, and cost savings. Flagship products like eResiduePro, eProcessPro, and eLogBook are designed to revolutionize the management of product, process, and cleaning lifecycles. We offer more than software by providing expert analysis and recommendations for improvements based on our extensive industry experience.
Role Description Quascenta is seeking a social media content creator who will be responsible for contributing engaging content that helps drive awareness of our brand worldwide to customers working in pharmaceutical manufacturing. This role will have a strong emphasis on animation (explainer videos), reels, static visuals, live streams, memes, case studies, etc. The candidate should be able to work with above noted media forms. The idea is to use Instagram, Linkedin and TikTok content for this purpose. Key responsibilities Design and animate explainer videos, motion graphics, and animated infographics. Shoot, edit, and optimize short-form videos for Instagram Reels, TikTok, and Stories. Create visually striking static assets—carousels, infographics, branded graphics. Develop engaging live stream and webinar content (Q&A sessions, demos, case studies). Produce and edit audio snippets, such as micro-podcasts and audiograms. Develop interactive posts—polls, quizzes, Q&As—using platform-native features. Monitor and engage with user-generated content and collaborate with clients for testimonials and success stories. Craft memes, relatable content, and leverage trending formats/audios (especially for Instagram and TikTok). Essential Skills & Qualifications Strong portfolio demonstrating animation, video editing, and graphic design. Proficiency in multimedia tools (Adobe Creative Suite, After Effects, Premiere Pro, Canva, etc.). Deep understanding of social media content trends and best practices for LinkedIn, Instagram, and TikTok. Ability to script, storyboard, and present visual stories clearly. Excellent communication, time management, and project coordination skills. Company Description At Quascenta, we specialize in offering comprehensive validation lifecycle management software solutions to pharmaceutical manufacturing sites. Our mission is to empower these sites with tools that streamline product manufacturing and cleaning processes, ensuring compliance, efficiency, and cost savings. Our flagship products, eResiduePro, eProcessPro, and eLogBook, are designed to revolutionize how companies manage their product, process, and cleaning lifecycles. With over 20 years of industry expertise, our solutions combine cutting-edge software with experienced Subject Matter Experts who recommend practical improvements, making compliance simpler and operations smoother.
NOTE: Please send hr@quascenta.com a date and time this week you are free to take a test on JavaScript. Role Description The Javascript automation tester role involves writing and executing automated test scripts, create and maintain test cases, and ensure the reliability and performance of the software developed by Quascenta. The role requires collaboration with development teams to identify and resolve issues and ensure that the products meet the highest standards of quality and compliance. We will train you on the tools to be used. Qualifications Proficiency in JavaScript for handling test scripts Fast learner Should be able to write test scripts Ability to work independently Salary : Rs 25,000 - Rs 35,000 Company Description Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored for pharmaceutical manufacturing sites. Our flagship products, eResiduePro, eProcessPro, and eLogBook, revolutionize product, process, and cleaning lifecycle management, ensuring compliance, efficiency, and cost savings. With products designed by industry experts, we not only provide software but also offer expert analysis and recommendations to improve your workflows. Our solutions help simplify residue calculations, track critical processes, and maintain organized validation records. Experience innovative tools designed to meet your unique needs and reach out to learn more.
NOTE: You have to come to our office for a test on Javascript. No online option. Send an email to hr@quascenta.com confirming one of the options listed below: Friday 22, 2025: 3-4pm Monday 25, 2025: 3-4pm Role Description The Javascript automation tester role involves writing and executing automated test scripts, create and maintain test cases, and ensure the reliability and performance of the software developed by Quascenta. The role requires collaboration with development teams to identify and resolve issues and ensure that the products meet the highest standards of quality and compliance. We will train you on the tools to be used. Qualifications Proficiency in JavaScript for handling test scripts Fast learner Should be able to write test scripts Ability to work independently Salary : Rs 25,000 - Rs 30,000 Company Description Quascenta specializes in providing comprehensive validation lifecycle management software solutions tailored for pharmaceutical manufacturing sites. Our flagship products, eResiduePro, eProcessPro, and eLogBook, revolutionize product, process, and cleaning lifecycle management, ensuring compliance, efficiency, and cost savings. With products designed by industry experts, we not only provide software but also offer expert analysis and recommendations to improve your workflows. Our solutions help simplify residue calculations, track critical processes, and maintain organized validation records. Experience innovative tools designed to meet your unique needs and reach out to learn more.