53 Stability Testing Jobs

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

We seek a passionate Product Development Food Technologist to spearhead the creation of innovative and nutritious food products for babies, pregnant mothers, and new mothers at Rorosaur Foodtech Private Limited. As a key member of our New Product Development department, you will be instrumental in shaping the future of early childhood nutrition in India. This role encompasses the entire product lifecycle, from initial concept and formulation to nutritional and stability testing, label development, and ensuring compliance with FSSAI guidelines. The ideal candidate will possess a strong foundation in food science, a creative mindset, and a commitment to delivering high-quality, safe, and nutritious food products. You will collaborate closely with cross-functional teams, including sourcing, manufacturing, and marketing, to bring innovative products to market that meet the evolving needs of our consumers. Your expertise will be crucial in maintaining the highest standards of quality and safety, aligning with Rorosaur's mission to provide wholesome and convenient nutrition for infants and mothers. Responsibilities Product Formulation and Recipe Development Develop innovative and nutritious food formulations for babies, pregnant mothers, and new mothers, focusing on natural ingredients and optimal nutrient profiles. Design and execute recipe development, ensuring products are both palatable and nutritionally balanced. Optimize existing product formulations based on sensory evaluation, stability testing, and market feedback. Conduct thorough literature reviews and stay updated on the latest research in infant and maternal nutrition to inform product development decisions. Collaborate with the sourcing team to identify and qualify vendors for high-quality raw materials, ensuring compliance with Rorosaur's standards. Document all formulation and recipe development activities meticulously, including ingredient specifications, processing parameters, and nutritional information. Nutritional and Stability Testing Identify and implement improvements to testing methodologies to enhance accuracy and efficiency. Monitor and maintain accurate records of all testing activities, ensuring compliance with quality control procedures. Collaborate with external laboratories and research institutions to conduct specialized testing and analysis. Analyze test results, interpret data, and prepare comprehensive reports summarizing findings and recommendations. Conduct stability studies to determine product shelf life and identify potential degradation pathways. Plan and execute nutritional testing protocols to ensure products meet specified nutritional requirements and regulatory standards. Label Development and Regulatory Compliance Maintain a comprehensive database of all product labels and regulatory documentation. Work closely with legal and regulatory teams to address any compliance-related issues. Prepare and submit documentation for regulatory approvals, ensuring timely and efficient processing. Select appropriate FSSAI categories for new products, based on formulation and intended use. Stay up-to-date on FSSAI regulations and guidelines, ensuring products meet all applicable legal requirements. Develop accurate and compliant food labels, ensuring all required information is included and presented clearly. Manufacturing and Quality Assurance Provide training and support to manufacturing staff on product-specific requirements and quality control procedures. Investigate and resolve any quality-related issues that arise during production. Conduct regular audits of manufacturing processes to ensure compliance with quality standards. Participate in Hazard Analysis and Critical Control Points (HACCP) studies to identify and mitigate potential food safety hazards. Develop and implement Good Manufacturing Practices{GMP) to maintain a safe and hygienic production environment. Collaborate with the manufacturing team to scale up production of new products, ensuring consistent quality and adherence to specifications. New Product Innovation and Market Analysis Contribute to the development of Rorosaur's overall product strategy. Monitor competitor activity and analyze their product offerings to identify opportunities for differentiation. Develop and present product proposals to senior management, highlighting potential benefits and risks. Evaluate the feasibility of new product ideas, considering technical, economic, and regulatory factors. Generate innovative product concepts based on market insights and consumer feedback. Conduct market research to identify unmet needs and emerging trends in the infant and maternal nutrition market.

Sampling and Analysis of Raw Material, In-Process sample, Packaging material and finished products as per approved specification / analytical protocol. Assist and train to supportive and new joining staff related laboratory work. Operation & Calibration of the instrument/ equipment used in analysis as per standard operating procedures. Supervise and perform tests on various microbiological activities (i.e. Finish goods, Packing material, Water, environment monitoring etc.) on a regular basis Manage and oversee laboratory work and Communicate with HOD for required chemical, media, glassware and instrument spare and timely maintain inventory . Communicate with QA department and HOD for complete document work as per approved protocol and SOP. Maintain timely worksheet and accurate record logbook of instruments as per FDA/GMP guideline Prepare and standardization of Analytical solutions and regents to conduct test. Develop various testing processes based on requirement of customer. Maintain good laboratory practice (GLP) in lab Compile and analyze test information to determine process or equipment operating efficiency and to diagnose malfunctions Preparation of SOP, STS and Product Specification and maintain all protocols Investigation of deviations in the analysis . Out of specification investigations for laboratory results. Analytical investigation for complaints and product recalls. Release or rejection of every batch of Products for distribution and sale. Stability testing and evaluation of shelf-life of products

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 the quality engineering, test planning and testing methodology for a software project and keeps abreast of evolving QA industry processes and standards. Develop and execute maintainable automation tests for acceptance, functional, and regression test cases. Master the basics of underlying transmission and distribution software applications domain. Education Qualification For roles outside USA: Bachelor's Degree in Computer Science or STEM Majors (Science, Technology, Engineering and Math) with advanced experience. For roles in USA: Bachelor's Degree in Computer Science or STEM Majors (Science, Technology, Engineering and Math) with minimum years of experience6years Desired Characteristics Technical Expertise: Bachelors Degree in Computer Science or in equivalent. A minimum of 10 to 12 years of Software Testing experience with Web or SaaS Platform based products, Postgress databases. Experience on building Test Automation Frameworks specifically in Java, Javascript Type Script, Selenium. Experience testing web services (SOAP/REST) Experience testing hosted or SaaS-based solutions. Familiar with relational database design and good working knowledge of SQL for querying, updating, and deleting data. Strong proficiency with functional, regression, performance and stability testing techniques. Experience working in a cross-functional development team with the ability to influence quality of products in that environment. Demonstrates the initiative to explore alternate technology and approaches to solving problems. Skilled in breaking down problems, documenting problem statements and estimating efforts. Strong oral and written communication skills. Effective team building and problem-solving abilities. Business Acumen: Understands the technology landscape, up to date on current technology trends and new technology, brings new ideas to the team. Displays understanding of the project's value proposition for the customer. Shows commitment to deliver the best value proposition for the targeted customer. Learns organization vision statement and decision-making framework. Able to understand how team and personal goals/objectives contribute to the organization vision Leadership: Voices opinions and presents clear rationale. Uses data or factual evidence to influence. Learns organization vision statement and decision-making framework. Able to understand how team and personal goals/objectives contribute to the organization vision. Seeks to understand problems thoroughly before implementing solutions. Gide the team with questions to clarify requirements when ambiguities are present. Identifies opportunities for innovation and offers new ideas. Takes the initiative to experiment with new software frameworks Adapts to new environments and changing requirements. Pivots quickly as needed. When coached, responds to need & seeks info from other sources. Additional Information Relocation Assistance Provided: Yes

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 preparation, and providing real-world project training to enhance the skills of the candidates. You will be required to ensure that trainees understand deviation handling, OOS/OOT investigations, CAPA processes, and regulatory audit procedures. Collaboration with the sales team is crucial to ensure that the trainees meet the expectations of their future employers. The ideal candidate should possess hands-on experience in cell culture, microbiology, and analytical laboratory techniques. Proficiency in HPLC, GC, FTIR, UV-Vis, and PCR is essential for this role. A strong understanding of data integrity, compliance documentation, and industry regulations such as cGMP, ICH, USP, and FDA guidelines is also required. Previous experience in stability testing, method validation, and impurity profiling will be beneficial. Your excellent mentoring and training skills, coupled with a passion for upskilling candidates, will be key to your success in this position. In addition to the specific responsibilities mentioned above, you will be expected to conduct one-on-one in-person training sessions, coordinate with internal teams for seamless training execution, and provide support to candidates in resume building, interview preparation, and exposure to real-time projects. Keeping abreast of industry trends and continuously updating training content accordingly is an integral part of this role. Please note that candidates who successfully complete two years with us will be eligible for visa sponsorship. If you are enthusiastic about mentoring and developing future pharmaceutical professionals, we look forward to receiving your application.,

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 SOPs for production, packaging, warehousing, and distribution processes. Oversee validation and qualification activities (equipment, process, cleaning, method validation). Drive regulatory compliance audits and ensure timely closure of CAPA (Corrective and Preventive Actions). Manage risk assessments, deviation handling, OOS (Out of Specification) investigations, and ensure continuous improvement. Ensure compliance with product safety, labeling, and claims regulations in domestic and international markets. Quality Control (QC): Supervise incoming raw material, packaging material, in-process, and finished product testing (physical, chemical, microbiological). Establish and monitor specifications, testing protocols, and acceptance criteria for all products. Oversee calibration, maintenance, and qualification of laboratory equipment. Ensure timely release of raw materials and finished products as per quality standards. Review and approve analytical test results, COAs, and stability studies. Leadership & Strategic Functions: Lead, mentor, and develop the QA/QC team; build a culture of accountability and excellence. Liaise with regulatory bodies, certification agencies, and third-party auditors. Collaborate with R&D, Production, Supply Chain, and Marketing teams to ensure smooth product lifecycle management. Drive continuous improvement projects (Six Sigma, Lean, Kaizen) in quality operations. Provide strategic inputs to management for product recalls, market complaints, and regulatory updates. Key Skills & Competencies Strong knowledge of cosmetic GMP (ISO 22716), FDA guidelines, BIS standards, and international regulations (EU, ASEAN, GCC, etc.). Expertise in formulation, stability testing, microbiology, and packaging validation. Proficiency in quality tools and systems QMS, CAPA, RCA, FMEA, Risk Management. Strong analytical, decision-making, and problem-solving skills. Leadership skills with the ability to manage cross-functional teams. Excellent communication, documentation, and audit management skills. Qualifications & Experience Education: M.Pharm / B.Pharm / M.Sc. (Chemistry, Microbiology, Biotechnology, Cosmetic Science, or related field). Experience: Minimum 5+ years of experience in Quality (QA/QC) within the cosmetics, personal care, FMCG, or pharmaceutical industry, with at least 5+ years in a leadership role. Experience in handling regulatory inspections and certifications. Preferred candidate profile

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 oversee the quality control department's daily operations for smooth workflow and efficient resource utilization. Ensuring compliance with international quality standards and local regulatory requirements will be crucial, along with conducting regular audits of production facilities. You will evaluate team performance, conduct stability, microbiological, and efficacy testing, maintain accurate records, and oversee the preparation of quality control documentation. To qualify for this role, you should have a Bachelor's or Master's degree in chemistry, Pharmacy, Cosmetics, Engineering, or a related field, along with 5-7 years of experience in quality control or quality assurance within the skincare, hair care, body care, or personal care manufacturing industry. Strong knowledge of Good Manufacturing Practices (GMP), ISO 9001, FDA, and other relevant regulatory standards is necessary, as well as proven experience in managing a team and leading quality control functions. Experience with testing methods, product development processes, and quality control tools is essential, along with attention to detail, analytical skills, and problem-solving abilities. Proficiency in Microsoft Office and quality management software is required, and certification in Quality Management is an advantage. This is a full-time position with benefits including health insurance and Provident Fund, requiring a day shift schedule. A question about your background in the Cosmetic Manufacturing Industry will be asked during the application process, with the work location being in person.,

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 knowledge in formulation development, regulatory compliance, process innovation, and technology transfer. Your role will involve working on formulation feasibility, taste-masking strategies, nutritional information validation, label claims, and process flowcharts design. You will also be responsible for sensory evaluation, shelf-life testing, and documentation management. Preferred experience includes working in Sports Nutrition, Infant Nutrition, Dietary Supplements, and exposure to functional claim validation and flavor optimization. This is a full-time position with benefits such as health insurance, yearly bonus, and a day shift schedule. The job requires in-person work at our Mohali location. If you have a passion for developing innovative products in the food industry and meet the qualifications mentioned, we encourage you to apply for this exciting opportunity.,

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 regression test plans, test cases, and usage scenarios for testing purposes, as well as preparing the test environment and test data. Execution of testing and consolidation of test results into clear and concise reports will be part of your routine. Additionally, creating and tracking tickets for any issues related to functionality, usability, performance, reliability, and stability issues will be a crucial aspect of your role. Working closely with software test engineers to verify and report any functional issues revealed during tests will also be part of your responsibilities. To qualify for this position, you must hold a BCA/B.Tech degree. You should be an autonomous thinker capable of managing your own diary while adhering to strict deadlines. A proactive and resilient individual with a positive attitude and motivation to succeed is desired. Strong organizational and time management skills are essential, along with excellent English verbal and written communication abilities. Good analytical and problem-solving skills, accuracy, attention to detail, as well as strong collaboration and teamwork skills are also important for this role.,

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 Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates oInstrument experience in HPLC /GC is mandate. Work experience in formulation only oPreferred for Male Candidates CONTACT INFO: E-mail: Harishwar.M@hetero.com & Cont: 8121005416 for further info.

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. Additionally, you will conduct microbiological testing, stability testing, and environmental monitoring as necessary. Recording and analyzing test results to ensure compliance with specified standards and regulatory requirements, maintaining detailed records, preparing Certificates of Analysis (COAs), and identifying deviations from standard specifications are essential aspects of this role. You will work closely with the production, research and development, and quality assurance teams to implement corrective and preventive actions, review production batch records, and participate in the development and validation of new analytical methods. Your involvement in internal audits and inspections to ensure compliance with quality systems and regulatory standards, along with recommending continuous improvements to enhance product quality and efficiency, will be paramount. To qualify for this position, you should hold a Bachelor's degree in Chemistry, Microbiology, Pharmaceutical Sciences, or a related field, with an advanced degree being preferred. A minimum of 2-5 years of experience in quality control within the pharmaceutical industry is required. Proficiency in analytical techniques like HPLC, GC, FTIR, and spectrophotometry, familiarity with GMP, GDP, and regulatory requirements, and strong attention to detail are crucial technical skills. Moreover, possessing excellent problem-solving skills, the ability to work collaboratively in a team environment, and relevant certifications such as Certified Quality Auditor or Six Sigma will be advantageous. Staying current with industry trends, regulatory updates, and advancements in analytical techniques will also be expected in this role.,

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 key role will involve conducting analytical testing, documentation activities, and ensuring compliance under the supervision of the team leader. Your responsibilities will include qualification on assigned analytical technologies, conducting testing using instruments like HPLC/UPLC, GC, IC, AAS, executing stability testing, method validation activities, and participating in method transfer processes. You will also be responsible for calibration activities, technical documentation, following lab processes and quality systems, and collaborating with cross-functional teams for assigned deliverables. To succeed in this role, you should have a minimum of MSc, B Pharm, M. Pharm, Ph.D., or equivalent in a science stream, along with 1 to 3 years of work experience in Analytical development, Quality Control, or related functions in the healthcare/pharma/FMCG sector. Proficiency in MS Office and a good understanding of GMP, 21 CFR Compliance, and Quality environment are preferred. As part of our team, you will have access to a competitive benefits package, paid company holidays, vacation time, learning and development opportunities, employee resource groups, and more. Join us at Kenvue and be a part of our mission to provide exceptional care through science.,

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 primary responsibility will be to formulate, develop, and enhance cosmetic products while ensuring compliance with industry regulations and market trends. This role will involve extensive research, product innovation, stability testing, and collaboration with various departments to introduce high-quality cosmetic formulations to the market. Your key responsibilities will include developing and optimizing innovative formulations for skincare, haircare, personal care, and cosmetic products based on market and client requirements. You will need to identify and assess new active ingredients, raw materials, and technologies to improve product efficacy and innovation. Conducting stability studies to evaluate product performance, consistency, and shelf-life under various conditions will also be a crucial aspect of your role. It is essential to ensure that all formulations comply with GMP, BIS, FDA, ISO 9001:2015, and other relevant cosmetic regulations. Collaboration with the production team to streamline formulation processes for scalability, cost efficiency, and production feasibility will be an integral part of your responsibilities. Analyzing competitor products and industry trends to enhance existing formulations and create market-driven innovations will also be expected. Maintaining detailed records of formulation trials, test results, and regulatory documentation, as well as evaluating raw materials for performance and safety, will be essential tasks. Working closely with Quality Assurance, Production, Purchase, and Marketing teams to facilitate smooth product development and launch will be part of your daily activities. To qualify for this role, you should hold a Masters/Bachelors degree in Cosmetic Science, Chemistry, Pharmaceutical Sciences, or a related field, along with at least 5 years of experience in cosmetic product formulation and R&D. Strong knowledge of cosmetic ingredients, emulsions, surfactants, actives, and preservatives is required. Familiarity with GMP, BIS, FDA regulations, ISO standards, and safety guidelines is essential. Experience with stability testing, analytical testing, and product evaluation techniques is advantageous. Proficiency in MS Office (Excel, Word, PowerPoint) and formulation software is expected. Strong problem-solving, analytical, and documentation skills are necessary, along with the ability to manage multiple projects and meet deadlines in a fast-paced environment. This is a full-time position with a work schedule of 6 days per week. The job location is at 816/3 Kothari Industrial Estate, Opp Khodal Lodge, Santej, Kalol, Gujarat 382721.,

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 regulatory guidelines, and ensuring that every batch of Dermatouch products meets stringent quality benchmarks Key Responsibilities: ?? In-Process Monitoring & Compliance Conduct real-time quality checks during manufacturing, filling, and packaging processes Ensure adherence to GMP (Good Manufacturing Practices) & regulatory guidelines Monitor and verify raw material, in-process, and finished product specifications ?? Batch Release & Documentation Review and approve batch manufacturing records (BMR) & batch packaging records (BPR) Ensure all deviations, non-conformances, and out-of-specification (OOS) cases are documented and addressed Coordinate with the production and quality control (QC) teams for batch approvals ?? Quality Control & Risk Management Identify and rectify process deviations or defects in real time Conduct sampling & stability testing of in-process materials and finished products Implement corrective and preventive actions (CAPA) to eliminate process flaws ?? Regulatory & Compliance Audits Ensure compliance with FDA, CDSCO, ISO, and other regulatory standards Assist in internal & external audits and prepare required reports Maintain quality assurance logs, reports, and records ?? Continuous Improvement Work closely with the R&D and production teams to optimize formulations and processes Conduct training sessions for production staff on quality assurance protocols Implement best practices in IPQA for enhanced product safety and efficacy Qualifications & Requirements: ??? Education: B Pharm, M Pharm, B Sc, M Sc in Chemistry, Microbiology, or related field ???? Experience: 2-5 years in IPQA / Quality Assurance within the pharma, cosmetics, or FMCG industries ???Knowledge of: GMP, GLP, regulatory audits, CAPA, stability testing, and quality control processes ???Skills: Strong analytical skills, attention to detail, ability to work cross-functionally

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 raw materials, in-process materials, and finished product specifications. Additionally, you will review and approve batch manufacturing records (BMR) and batch packaging records (BPR), documenting any deviations, non-conformances, or out-of-specification (OOS) cases, and coordinating with production and quality control (QC) teams for batch approvals. Identifying and rectifying process deviations or defects in real time, conducting sampling and stability testing of in-process materials and finished products, and implementing corrective and preventive actions (CAPA) to eliminate process flaws will also be part of your role. You will be required to ensure compliance with FDA, CDSCO, ISO, and other regulatory standards, assist in internal and external audits, and prepare necessary reports. Maintaining quality assurance logs, reports, and records will be crucial in this position. Collaborating closely with the R&D and production teams to optimize formulations and processes, conducting training sessions for production staff on quality assurance protocols, and implementing best practices in IPQA for enhanced product safety and efficacy will also be part of your responsibilities. To be successful in this role, you should have a degree in B.Pharm, M.Pharm, B.Sc, or M.Sc in Chemistry, Microbiology, or a related field, along with 2-5 years of experience in IPQA or Quality Assurance within the pharma, cosmetics, or FMCG industries. Knowledge of GMP, GLP, regulatory audits, CAPA, stability testing, and quality control processes is essential. Strong analytical skills, attention to detail, and the ability to work cross-functionally will also be valuable assets for this position.,

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 sourcing (protein bases, binders, natural flavors, stabilizers, etc.) that align with cost, nutrition, and shelf-life requirements. Conduct shelf-life studies, stability testing, and sensory evaluation . Liaise with contract manufacturers/co-packers and ensure smooth scale-up. Ensure compliance with FSSAI and other relevant food safety regulations. Provide nutritional analysis and labeling inputs . Requirements Bachelors/Masters in Food Technology, Food Science, Nutrition, or related fields . 25 years of hands-on experience in R&D or product development (preferably in bars, snacks, functional foods, or health/nutrition categories). Strong understanding of protein systems, binders, natural sweeteners, flavoring, and texture optimization . Familiarity with food regulations (FSSAI) and shelf-life/safety testing. Ability to work with co-packers, suppliers, and external labs . Problem-solving mindset: able to translate product vision into a scalable, commercially viable formula . What We Offer Opportunity to build a product from scratch and see it come alive in the market. Creative freedom to experiment with innovative formulations . Flexible working arrangement. ???? How to Apply Send your CV and a short note on your previous product development experience (what products youve actually created, not just theory) to [HIDDEN TEXT]. Show more Show less

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 their updated CV and pass-port size photo. 2) The above positions are for experienced candidates and for rotational shifts only. 3) Parenteral /Injectable exposure is preferable. 4) Kindly note that candidates having Pharma exposure will only be considered for interview process. 5) Male Candidates would only be preferred due to rotational shift 6) Freshers may email their CV on Anee.Silas@otsukapharma.in Companys Website : www.otsukapharma.in

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 Documents and ID Proofs NOTE: Offering a competitive joining bonus to successfully selected candidates oInstrument experience in HPLC /GC is mandate. Work experience in formulation only oPreferred for Male Candidates CONTACT INFO: E-mail: Harishwar.M@hetero.com & Cont: 8121005416 for further info.

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. Calibrate and maintain laboratory equipment.

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 reports, master formula records (MFR), stability protocols, study protocols, and standard operating procedures (SOP). You should have a basic understanding of Quality by Design (QbD) principles for formulation development, including Quality Target Product Profile (QTTP), Critical Quality Attributes (CQA), Critical Process Parameters (CPP), Critical Material Attributes (CMA), risk assessment, and control strategy. Knowledge of various Quality Management System (QMS) documents like change control, incidents, planned deviations, and unplanned deviations is necessary. A fundamental understanding of API specifications, Drug Master Files (DMF), excipient specifications, in-process specifications, finished product specifications, and shelf-life specifications of injectable products is expected. Additionally, you should be familiar with the preparation and review of necessary documents required for ANDA submission and product approval. Your skills and expertise should be at an advanced level in formulation development for solution-based injectables, while scale-up and process optimization, material science and excipients selection, CoA & analytical data review, and technical troubleshooting should be at an intermediate level. Regulatory affairs and compliance skills are expected to grow over time, along with cross-functional coordination, stability testing, protocol development and documentation, and cross-functional collaboration. Investigation & CAPA management is also at an intermediate level. Qualifications: - M Pharm Amneal is an equal opportunity employer that values diversity and inclusion. The Human Resources team at Amneal plays a crucial role in partnering with all aspects of the organization to drive success through effective people management. They provide high-level input at a strategic level, ensure legal compliance and best practices, offer support and advice to meet organizational objectives, provide expert guidance on workforce management and employee relations, and keep the organization informed about developments impacting employment matters.,

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 performing stability testing of biological products under different conditions. Troubleshooting issues related to instrument calibration, maintenance, and operation will also fall within your scope of duties. The ideal candidate for this role should hold a Bachelor's degree in Pharmacy (B.Pharm) or a Master's degree in Pharmacy (M.Pharm) from an accredited institution, or alternatively an M.Sc. degree. Previous experience ranging from 0 to 4 years is preferred. A strong understanding of analytical instruments like HPLC, UPLC, GC, MS, ICP-MS, and wet analysis is highly desirable for this position.,

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 skills GMP, cGMP/ GLP Skills Interpersonal skills 5S skills( Sort, Straighten, Shine, Standardize& Sustain)

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 technology transfer to the production floor. Collaboration with cross-functional teams for cost optimization, process standardization, and sensory evaluation will be key aspects of your role. Preferred qualifications for this position include a B.Tech in Food Technology with a minimum of 3 years of industry experience in Sports Nutrition, Infant Nutrition, or Dietary Supplements. Proficiency in functional claim validation, regulatory documentation, and flavor optimization will be advantageous. This is a full-time position that offers health insurance, a yearly bonus, and requires fluency in Hindi. Your dedication to product innovation and commitment to quality will contribute significantly to our company's success.,

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 Quality Control, your essential duties and responsibilities include leading a team of QC Analysts, ensuring compliance with quality systems and regulatory requirements, maintaining documentation, coordinating investigations and improvement projects, reviewing and approving test documents, managing quality processes through SAP system, overseeing batch production and testing, participating in product development support, and maintaining lab equipment. To be successful in this role, you must possess strong organizational and communication skills, critical thinking abilities, excellent customer service skills, creativity in problem-solving, energetic and motivational disposition, confidentiality maintenance, coaching skills, proficiency in computer tools, and the ability to lead a team in a fast-paced environment while managing multiple projects effectively. The ideal candidate should have a B.S. in Chemistry or a related discipline, minimum 5 years of experience in a pharmaceutical manufacturing laboratory environment, at least 3 years of supervisory experience, hands-on experience with quality systems in a GxP environment, familiarity with FDA, MHRA, and other health authority inspections, knowledge of international regulations, and audit experience. If you are looking for a challenging opportunity in Quality Control with a focus on pharmaceutical manufacturing, this role at 3950 Schelden Circle, Bethlehem, PA, 18017, US might be the perfect fit for you.,