125 Stability Testing Jobs - Page 4

Responsible for test creation, testing a large module or a large component and designing a feature, set of features, or whole feature area independently, Contributing to the immediate team and to other teams across business; Leading software quality engineering discussions and mentoring of other junior quality engineers. Roles and Responsibilities In this role, you will: Apply principles of SDLC and methodologies like Lean/Agile/XP, CI, Software and Product Security, Scalability, Documentation Practices, refactoring and Testing Techniques. Integrate project testing with continuous-integration process. Lead and manage team members to diagnose bugs and formulate solutions. Provide expertise in...

As a Pharma Subject Matter Expert (SME) Trainer, you will be responsible for training candidates in various aspects of Quality Control (QC), Cell Culture Techniques, and Laboratory Procedures. Your role involves providing hands-on experience in analytical testing, microbiological testing, and pharmaceutical laboratory operations. It is essential to educate candidates on method validation, stability testing, and data integrity while ensuring compliance with FDA, USP, and cGMP regulations. Additionally, you will train individuals in utilizing HPLC, GC, UV-Vis, FTIR, PCR, ELISA, and Spectroscopy techniques. Your responsibilities include conducting mock interviews, assisting with resume preparat...

Role & responsibi The Head of QA/QC will be responsible for establishing, implementing, and maintaining quality management systems across the cosmetics manufacturing value chain. This role ensures that all products meet regulatory, customer, and company standards for safety, efficacy, and consistency. The incumbent will lead both Quality Assurance (QA) and Quality Control (QC) teams to achieve compliance with cGMP, ISO, and cosmetic industry regulations. lities Key Responsibilities Quality Assurance (QA): Develop, implement, and maintain Quality Management Systems (QMS) aligned with cosmetic industry standards (ISO 22716, GMP, FDA, BIS, EU Cosmetics Regulations, etc.). Establish and monitor ...

To perform analysis of finished Products and in-process samples. Proficiency in using analytical instruments such as UV/VISIBLE and IR, HPLC Handling of laboratory incidents and deviation. Extensive knowledge of GMP regulations in cGMP Manufacturing Environment. Chemical and Instrumental analysis of In process and finished products. To perform analysis of stability samples. To perform the calibration of instruments like HPLC, Dissolution tester, UV Spectrophotometer. Analysis of OOS/OOT

The Manager - Quality Control (QC) will be responsible for ensuring that all products manufactured for third-party clients meet quality standards, regulatory requirements, and client specifications. You will oversee all QC activities in the production process, lead a team, manage testing procedures, and ensure adherence to quality guidelines for skincare, hair care, body care, and personal care products. Your key responsibilities will include developing, implementing, and maintaining QC processes to ensure products meet quality and safety standards. You will monitor production processes, work closely with the production and R&D team to identify and resolve any quality-related issues, and ove...

You are required to join our team as an R&D Executive (Food Technologist) in Mohali, Punjab. Your main responsibilities will include leading and managing New Product Development projects, ensuring compliance with FSSAI Nutraceutical Regulations, selecting ingredients based on scientific research, developing taste-masking strategies, conducting trials, coordinating with cross-functional teams, and maintaining thorough documentation for regulatory submissions. The ideal candidate must possess a B.Tech in Food Technology with a minimum of 3 years of experience in the industry. You should have expertise in Nutraceuticals, Sports Nutrition, and Health Supplements. It is essential to have knowledg...

The primary responsibility of this role involves early detection, mitigation, and prevention of potential production issues. You will be required to learn and comprehend product features in order to develop a clear, detailed understanding of product testing requirements. Your tasks will include performing various regression testing processes such as feature QC, platform QC, bulk test, completeness test, interruption test, resource usage test, network connection test, and translation testing among others. Collaborating with leads and team members to determine testing priorities, effort estimates, and tracking and reporting progress will be essential. You will also be responsible for writing r...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC Qualification & Experience: (02 - 06Years) B.Sc, B.Pharma & M.Sc with relevant experience Designations: Jr. Officer, Officer & Jr.Executive PRODUCTION: Compression, Granulation, Auto Coating. Qualification & Experience: (01 - 07Years) ITI, Diploma & B.Sc with relevant experience Designations: Jr. Operator, Operators & Sr. Operator INTERVIEW VENUE: Hotel: HOTEL LE MARIET 9th Km Milestone, Kishanpura. Baddi Nalagarh Highway (NH-105), Dist. Solan Himachal Pradesh. (India)- 174101 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Doc...

The Quality Control Specialist in our pharmaceutical company located in Thanjavur plays a crucial role in ensuring that all products adhere to quality standards and regulatory requirements before being released to the market. You will be responsible for conducting a variety of testing and analysis procedures on raw materials, in-process materials, and finished products. Your collaboration with the production team to identify and resolve quality issues will contribute to the continuous improvement of our quality systems and processes. Your key responsibilities will include performing routine and non-routine testing using various analytical techniques like HPLC, GC, and UV/VIS spectroscopy. Ad...

You will be joining Kenvue as an Associate Scientist, Analytical Chemistry based in Mumbai. At Kenvue, we are passionate about everyday care and science, with a global team of diverse individuals dedicated to delivering the best products to our customers. As a Kenvuer, you will have the opportunity to impact the lives of millions of people every day. We prioritize people, care, trust, and courage, offering brilliant opportunities for you to shape our future and yours. In this role, you will be responsible for various analytical deliverables in new product development projects, supporting changes to commercial products, and specific research-based activities as part of Global operations. Your...

You will be joining Vimson Derma, a renowned contract manufacturer of cosmetic and medicated products located in Ahmedabad with over 45 years of experience in the cosmetics and dermatology industry. As a trusted name in the field, Vimson Derma holds certifications such as GMP, GLP, and ISO 9001:2015, ensuring the highest quality standards. The company's product range includes dusting powders, talcum powders, shampoo, conditioner, cream, gel, lotions, oil, soaps, sunscreen, serums, and more. With a substantial client base of over 200 companies across India, Vimson Derma is committed to delivering excellence in the products they manufacture. As the R&D Senior Executive in Cosmetics, your prima...

Job Title: In-Process Quality Assurance (IPQA) Specialist ???? Location: Ahmedabad ???Company: Dermatouch Indias Fast-Growing Dermo-Cosmetic Brand About Dermatouch: Dermatouch is a fast-growing dermo-cosmetic skincare brand trusted by thousands of dermatologists and over 2 million customers across India Our clinically tested formulations solve real skin concerns, and we are committed to delivering safe, high-efficacy skincare solutions Job Overview: We are looking for an In-Process Quality Assurance (IPQA) Specialist to ensure that all manufacturing, packaging, and formulation processes meet the highest quality standards This role is crucial to maintaining product integrity, compliance with ...

As an In-Process Quality Assurance (IPQA) Specialist at Dermatouch, you will play a vital role in ensuring that all manufacturing, packaging, and formulation processes adhere to the highest quality standards. Your responsibilities will be essential in maintaining product integrity, ensuring compliance with regulatory guidelines, and guaranteeing that every batch of Dermatouch products meets stringent quality benchmarks. Your main duties will include conducting real-time quality checks during manufacturing, filling, and packaging processes, as well as ensuring adherence to Good Manufacturing Practices (GMP) and regulatory guidelines. You will also be responsible for monitoring and verifying r...

Looking for Freelance - Food Technologist / Product Development Specialist About Us Were an early-stage food startup building a new-age functional snack brand in India. Our focus is on high-protein, clean-label products designed for modern lifestyles. Were looking for a Food Technologist who can help us take our concept from idea ? lab ? shelf. Responsibilities Develop and optimize recipes/formulations for a new line of nutrition/snack products (bars & related categories). Ensure recipes are scalable from kitchen samples to pilot production to commercial manufacturing . Define and document Standard Operating Procedures (SOPs) for production, quality control, and hygiene. Work on ingredient s...

1) Quality Control (IPPT/FP, RM/PM/ Stability/LIMS/HPLC/Lab Support/Micro) Designation: - Process Incharge Experience : - 2 to 7 Years Qualification : - B.Sc. / M.Sc. / B. Pharm/ M. Pharm * Also we have opening for Fresher (Trainee for) B.E/ B.Tech as mentioned below; 2) B.E- Civil Engineer Fresher (Trainee) Qualification: - B.E./B.Tech in Civil Engineering We are seeking a motivated and detail-oriented Civil Engineering Fresher (Trainee) to join our team. As a Civil Engineer, you will assist senior engineers in the planning, design, and execution of civil engineering projects in commercial, and infrastructure developments. Preferred candidate profile 1) Interested candidates have to bring t...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC Qualification & Experience: (02 - 05Years) •B.Sc, B.Pharma & M.Sc with relevant experience Designations: Jr. Officer, Officer & Jr.Executive • PRODUCTION: Compression, Granulation, Coating. Qualification & Experience: (01 - 04Years) •ITI, Diploma & B.Sc with relevant experience Designations: Jr. Operator, Operators & Sr. Operator INTERVIEW VENUE: Hotel: HOTEL EVERGREEN oAmbala - Chandigarh Expy, Near Bus stand, Bhagat Singh Nagar, Dera Bassi, Sheikhpur Khurd, Punjab 140507 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documen...

Test raw materials, fragrance oils, and finished perfume products for quality compliance. Conduct routine laboratory analysis (e.g., GC, stability testing, pH, density, refractive index). Check and approve incoming raw materials before production. Monitor in-process quality during manufacturing and filling stages. Ensure finished products meet fragrance, color, and appearance specifications. Maintain proper documentation of test results and quality records. Assist in investigating quality issues and implementing corrective actions. Follow safety, hygiene, and GMP (Good Manufacturing Practices) guidelines in the lab. Collaborate with production and R&D teams to maintain product standards. Cal...

You should have a good understanding of product development activities for various injectable dosage forms intended for the regulated market, including general injectable and onco products. Knowledge of ANDA and 505b2 product filing is essential. Familiarity with a wide range of dosage forms such as liquid solution, lyophilized, suspension, and emulsion is required. You should also be well-versed in drug device combination products and understand regulatory expectations. Experience with equipment like high shear homogenizer, high pressure homogenizer, lyophilizer, microfluidizer, and nano mill is preferred. Your responsibilities will include preparing and reviewing product development report...

As an Analyst or Senior Analyst in Bioanalytical Research at Veeda Lifesciences, you will play a crucial role in conducting bioanalytical research activities. This includes method development, validation, and sample analysis utilizing a variety of techniques such as HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Your responsibilities will also involve developing and validating methods for bioanalysis of biologics and biosimilars in compliance with regulatory requirements, such as those set by the USFDA. Collaboration with cross-functional teams will be essential to ensure the timely delivery of high-quality results. Additionally, you will be tasked with perf...

Role & responsibilities Ensuring the cleanliness and housekeeping activities in the laboratory. Ensuring the laboratory safety. Calibration of analytical instruments like High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). Analysis of raw material, in-process, finished product and stability samples using HPLC & GC. Analysis of vendor samples as part of vendor qualification. Analysis of cleaning samples using UV & HPLC. Analytical method validation, method transfer and verification analysis as per protocol. Analytical column performance and maintenance. Temperature and humidity daily check in HPLC room. Preferred candidate profile Analytical Chemistry Documentation skil...

As an R&D Executive (Food Technologist) at our Mohali-based company, you will play a crucial role in leading New Product Development (NPD) and Technology Transfer projects with a specific focus on Nutraceuticals, Sports Nutrition, and Health Supplements. Your expertise in formulation, process innovation, and regulatory compliance will be vital in bringing science-backed products from the lab to the market. Your responsibilities will include managing NPD projects, ensuring compliance with FSSAI Nutraceutical Regulations, selecting ingredients based on scientific research, developing taste-masking strategies, conducting compatibility studies, validating nutritional information, and overseeing ...

The role of Quality Control Manager in Critical Care Business at Bethlehem, PA involves overseeing all Quality Control functions to ensure alignment with core values and ethical practices. Your primary responsibility is to ensure that the Quality Control department meets the needs of both internal and external customers by delivering services and products on time. You will collaborate with various internal stakeholders such as API Manufacturing, Packaging, Quality Assurance, Engineering, Regulatory Affairs, EHS, Supply Chain and Logistics, as well as external stakeholders including Auditors, Customers, Regulatory Agencies, and External Suppliers. Reporting directly to the Senior Manager of Q...

The company is looking for a skilled R&D Chemist Manager with 10+ years of experience in the Herbal Skincare, Haircare, Ayurvedic & Clean Beauty Products industry. As an R&D Chemist Manager, you will be responsible for overseeing the entire product development process, from concept to production, ensuring that the products meet quality standards and regulatory requirements. Your main responsibilities will include leading the R&D team in developing formulations based on Ayurvedic principles and modern cosmetic science, identifying new trends and ingredients in the market, and working closely with production and quality control teams to ensure smooth scale-up and manufacturing processes. Addit...

As a diligent and detail-oriented Quality Control Analyst, you will be an integral part of our QC team. Your primary responsibility will involve conducting various tests on raw materials, in-process samples, and finished cosmetic products to ensure they adhere to predefined quality and safety standards. Your role will be crucial in upholding compliance with regulatory guidelines and maintaining consistent product quality. Your key responsibilities will include performing physical, chemical, and microbiological testing on raw materials, packaging materials, bulk, and finished products. You will also be accountable for preparing, reviewing, and maintaining accurate records of test results, rep...

Oversees QC activities, staff training, SOPs, calibrations, GLP compliance, audits, records, and lab investigations (OOS/OOT) and aligns QC goals with production and ensures lab standards (candidates having approval from Raj. FDA will be preferred).