9 Qms Software Jobs

As a skilled Computer System Validation (CSV) Specialist at Avon Quality Management, you will play a crucial role in assisting clients in validating quality management system (QMS) software within the life sciences industry. Your main focus will be on ensuring that the QMS software solutions meet regulatory requirements and industry standards, thus supporting clients in achieving compliance with Good Manufacturing Practices (GMP), FDA, EMA, and other applicable regulations. **Core Responsibilities:** - Lead the validation of QMS software for clients, including planning, execution, and documentation of validation activities. - Develop and review validation deliverables such as Validation Plan...

Who We Are Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with. Ho...

As a QA Validation Specialist at Quascenta, you will play a crucial role in providing technical support for software products such as ValDoc Pro, eLog Pro, and QMS Pro. Your responsibilities will include: - Assisting companies with uploading SOPs and managing qualification in the application - Executing qualification scripts (IQ/OQ/PQ) online - Writing and executing test scripts - Opening bug tickets when necessary Qualifications required for this role: - Prior experience in using QMS software - Experience in equipment/instruments qualification - Experience in process validation will be an added advantage - Fluency in Hindi is a mandatory requirement Quascenta is a leader in offering validat...

As an individual with prior work experience in the Pharmaceutical Industry in a QA role, you are ideally suited for the following role at Quascenta: Role Overview: You will be providing technical support on software products such as ValDoc Pro, eLog Pro, and QMS Pro to companies within the pharmaceutical manufacturing sector. Your primary responsibilities will include: - Assisting customers with SOP uploads - Managing qualifications in the application - Executing qualification scripts (IQ/OQ/PQ) online - Writing and executing test scripts - Opening bug tickets when necessary Key Responsibilities: - Provide technical support on ValDoc Pro, eLog Pro, and QMS Pro - Assist customers with SOP upl...

Leadership Position to head Corporate Quality and report into the COO Lead Quality for 5+ Manufacturing Sites for a leading Automo Component Suppl About Our Client Our client is a leading Automotive Component Supplier headquartered in Delhi-NCR and has multiple plants across India in addition to dedicated R&D Centres Job Description Strategic Leadership Define and implement a unified Quality Vision and Strategy across all plants. Align quality goals with corporate objectives, customer expectations, and regulatory requirements. Lead cross-functional quality governance for new product development, launch, and lifecycle management Multi-Plant Oversight Oversee Quality Assurance and Control acro...

As a QA Chemist at Sinterx Pharma Private Limited, you will play a crucial role in ensuring that all API intermediate manufacturing operations adhere to established quality standards, GMP requirements, and regulatory guidelines. Your responsibilities will include: - Reviewing and approving GMP documentation such as BMRs, BPRs, SOPs - Overseeing batch records, managing deviations, and CAPA - Conducting internal audits and ensuring compliance throughout the production lifecycle Qualifications required for this role include: - Bachelor's or Master's Degree in Chemistry, Pharmaceutical Sciences, or Life Sciences - 5 to 8 years of experience in Quality Assurance within the API or API Intermediate...

We are seeking a skilled Computer System Validation (CSV) Specialist to join our team and assist clients in validating quality management system (QMS) software within the life sciences industry. Your main focus will be to ensure that the QMS software solutions meet regulatory requirements and industry standards, supporting clients in achieving compliance with Good Manufacturing Practices (GMP), FDA, EMA, and other applicable regulations. This client-facing role requires strong technical expertise, regulatory knowledge, and excellent communication skills. In this role, your responsibilities will include leading the validation of QMS software for clients, encompassing planning, execution, and ...

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 requi...

Identify/implement process improvement initiatives using Lean,Six Sigma,Kaizen methodologies. Analyze performance metrics/lead root cause analysis (RCA)/corrective action plans. Collaborate cross-functionally to reduce waste/increase efficiency. Required Candidate profile 3--7 years of experience in a quality or process engineering role. Strong understanding of ISO 9001, IATF 16949, and APQP. Hands-on experience with quality tools (5 Why, Fishbone, SPC, MSA, etc.).