29 Stability Testing Jobs

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.,

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. Additionally, you will be required to mentor junior chemists and maintain detailed documentation of all formulations and trials. To be successful in this role, you must have a relevant degree in Cosmetic Science, Chemistry, Ayurveda, or a related field, along with a strong background in formulating herbal, Ayurvedic, or natural skincare, haircare, and personal care products. Knowledge of Ayurvedic ingredients, essential oils, plant extracts, and cosmetic chemistry is essential, as well as experience in stability testing, preservative efficacy testing, and scale-up processes. The ideal candidate will also be familiar with global clean beauty trends, ingredient safety, and GMP and ISO-certified environments. Strong leadership, project management, and collaboration skills are a must for this position. If you are passionate about developing innovative and effective products in the wellness industry, we encourage you to apply for this challenging and rewarding role.,

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, reports, and batch analysis. Additionally, you will conduct stability testing, report any deviations or non-conformities, and ensure the calibration, cleanliness, and maintenance of laboratory instruments and equipment. It will be essential for you to comply with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will also be required to investigate and document any out-of-specification (OOS) results or product complaints. Collaborating with the production and R&D teams to resolve quality-related issues will be part of your responsibilities. Furthermore, staying informed about relevant quality regulations such as ISO, FDA, BIS, etc., and assisting in internal audits and regulatory inspections will be crucial aspects of your role. This is a full-time position that offers benefits including health insurance and life insurance. The work location is in person, and the application deadline is set for 25/07/2025.,

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).

The QC Microbiologist I position involves performing various microbiological testing activities, such as water testing, environmental monitoring, media preparation, and growth promotion of media, under minimal supervision. In addition to conducting raw material testing, finished product testing, stability testing, antibiotic assay testing, gram staining, and microbial enumeration suitability testing, the role also includes antimicrobial effectiveness testing and other required microbial testing. The position requires maintaining quality and efficiency in all tasks performed. Responsibilities include routine water testing, media preparation, growth promotion of media, and environmental monitoring. The role also involves ensuring cleanliness and organization in shared laboratory areas, participating in stock inventory management, and conducting routine Microbial Examination Testing. Additionally, assisting with microbial suitability testing, antimicrobial effectiveness testing, antibiotic assay testing, gram staining, and other microbial testing is part of the job scope. Adherence to Environmental, Health and Safety policies and procedures is essential, along with flexibility to work overtime or weekends occasionally as needed. The ideal candidate should possess specialized knowledge of aseptic technique, environmental monitoring, and microbial examination methods. Familiarity with FDA, USP, ICH, cGMP, and cGLP requirements in a pharmaceutical quality control laboratory is necessary. Proficiency in LIMS, Microsoft Office Suite, and electronic data management systems is also required. Key qualifications include strong organizational skills, attention to detail, multitasking abilities, adaptability to changing priorities, ownership of tasks, proactive problem-solving approach, interpersonal and communication skills, and effective time management. The role may involve lifting/moving weights up to 10 lbs. and occasionally 25 lbs., handling hazardous and non-hazardous materials, and wearing Personal Protective Equipment as needed. Education requirements include a B.S. in microbiology, biology, or a related life science field. Candidates should have 0-4 years of related pharmaceutical microbiology experience and knowledge of autoclave usage, media preparation, aseptic technique, balance use, pH meter, environmental monitoring, and general plating practices. The ability to independently perform assigned tasks from start to finish without errors, including standard, sample, and reagent preparation through data processing and submission, is essential. This is a full-time position based in USA-650 Cathill Road, Sellersville, PA, 18960, US, with job identification 90441128 in the Quality Control category.,

JOB SUMMARY: To ensure on handling of documents like analytical test procedures, specifications, standard operating procedures from initiation till implementation. To ensure quality control GLP related activities are performed as per SOP for calibration, qualification of instrument and equipment. To ensure sampling activities are performed as per SOP and sample integrity are maintained till analysis completion. To ensure working/reference standards are made available for analysis and timely qualification of standards within due date. To involve in investigations and to collaborate with cross function team for root cause determination and implementation of effective CAPA. To ensure safety and use of required personal protective equipments during day-to-day activities. Responsible for carrying out any other responsibilities assigned from time to time orally or in writing by HOD. To maintain and enhance quality index of the site unit data elements pertaining to QC function. Identify the training need and organize for the training to concerned group in QC to avoid event and unconfirmed OOS due to errors during analysis. ESSENTIAL JOB FUNCTIONS: To ensure stability samples are charged and analysis completed within the due date and stability chambers are monitored and maintained at respective conditions. To ensure effective analytical methodology are placed for testing. To ensure analytical method validation and analytical method transfer activities are completed and validated methods are adopted for testing. To ensure sampling activities of RM/Intermediates/Finished as per approved standard operating procedures. To ensure stability study sampling, stability study chamber monitoring and timely withdrawal and completion of analysis. To review the analytical method validation, method transfer, regulatory submission related documents, working reference standard procurements. To co-ordinate self-inspection (internal audit) and its compliances. To approve the lab event/out of specification/our of trend/our of calibration/CAPA/change control/deviation. Ensure trend of quality control errors and effective CAPA implementation. To monitor the compliance with the requirement of GMP. To participate in the management reviews of process performances, product quality and of the quality management systems and advocating continual improvement. To ensure a timely and effective communication and escalation process exists to raise quality issues to appropriate levels of management. To conduct training program and ensure it effectiveness. To ensure quality control GLP related activities are performed as per SOP for calibration, qualification of instrument and equipment. To follow safety & use of required personal protective equipment during day to day activities. To ensure maintenance of housekeeping at shop floor and reporting day to day activities to QC head and in absence delegate change to second line manager. To participate in laboratory internal audits, customer audits, health authority inspection. Awareness of IMS systems (ISO14001:2015 and ISO45001:2018) Travel Estimate Low Job Requirements Educational Qualification M.Sc Chemistry Experience 15+ years experience

Responsibility for conducting Chemical/Instrumental testing of raw material samples to ensure quality standards are met for products manufactured at Sun Pharmaceutical Industries Ltd, both for the domestic market and export to emerging markets. This includes analyzing and reporting stability and finished goods samples, monitoring gowning and sanitation practices, and ensuring compliance with standard operating procedures for analytical instruments. Responsible for system upgrades in alignment with Corporate Quality (CQ) and regulatory guidelines, operating analytical equipment in quality control during assigned shifts, and maintaining accurate documentation and record-keeping practices following Good Documentation Practices (GDP) and laboratory protocols. Supporting internal audits, regulatory inspections, and FDA audits by adhering to best practices and following all cGMP regulations as per Schedule M. Ensuring safety procedures are followed when handling analytical equipment and hazardous materials, completing assigned trainings to address identified training needs, and calibrating analytical equipment as per calibration procedures. Maintaining analytical equipment and laboratories in optimal working condition, overseeing stock levels of working standards, columns, reagents, chemicals, and glassware, and following procedures for non-conforming results as outlined in Standard Operating Procedures (SOPs) related to Out-of-Trend (OOT), Laboratory Incidents, and Out-of-Specification (OOS) results. Adhering to administrative procedures regarding attendance, leave, and other benefits in compliance with company policies and regulations.,

1- QC Exe-Chemical Testing Raw material Testing, finished product and stability testing 2. QMS Executive -CAPA, Deviations, Change Control 5 years Investigations, risk mgmt, documentation 3.QA Officer I year Support work, document control, audit prep Required Candidate profile 4.QA Exe —Training 3 years Conducting cGMP training, maintaining records 5. QA Exe—Validation 5 years (process, cleaning, equipment, HVAC) FDA Audit must Qualification:- M.Sc /B.Pharma/ M.Pharma

Responsibility for conducting Chemical and Instrumental testing on samples of raw materials. Ensuring the quality of products manufactured by Sun Pharmaceutical Industries Ltd for both domestic and emerging markets. Implementing system upgrades in alignment with CQ and regulatory guidelines. Analyzing and reporting stability and finished goods samples when necessary. Monitoring gowning and sanitation practices within the operational area. Ensuring compliance with standard operating procedures for analytical instrument operation. Operating analytical equipment in quality control as per assigned shifts. Adhering to good documentation procedures and recording results as per SOP on GDP and laboratory practices. Supporting internal audits, regulatory inspections, and FDA audits with best practices. Adhering to cGMP regulations as per schedule M. Maintaining safety protocols for handling analytical equipment and potential hazards. Completing assigned training as per identified training needs through organized sessions or self-study. Calibrating analytical equipment as per calibration procedures for assigned responsibilities. Keeping analytical equipment and laboratories in good operational condition. Managing stock levels of working standards, columns, reagents, chemicals, glassware, etc. Following procedures for non-conforming results as outlined in SOPs for OOT, Lab Incidents, and OOS. Complying with administrative procedures related to attendance, leave, and other benefits.,

You are being hired for the position of QC Head at our company based in Ankleshwar, Gujarat. As the QC Head, you will be responsible for ensuring the quality of all batches manufactured, overseeing the Quality Control department functions, and managing activities related to quality assurance. Your main duties will include sampling, inspection, and testing of raw materials, packaging materials, in-process products, and finished products as per specifications for release or rejection. You will also be in charge of stability chamber handling, stability testing, and evaluation of shelf-life of products, as well as preparing stability testing protocols and reports. In addition, you will conduct microbiological analysis of raw materials, finished products, water, and environmental bio-burden monitoring. You will review monthly trend reports for physicochemical and microbiological data and ensure compliance with predefined specifications. Analytical investigations for complaints, product recalls, out of specification results, and deviations will also fall under your purview. Furthermore, you will be responsible for internal Quality System audits, quality review, analysis of non-conforming products, reference standards, working standards, and solution preparations. You will plan and manage all activities of the Quality Control Department to assure the quality of all products manufactured by the company. Coordinating with the manufacturing department to control processes and products at every stage of manufacturing will also be part of your role. Moreover, you will work on the development of specifications and analytical procedures in coordination with the Quality Assurance Department and R&D. You will review the adequacy and relevance of specifications and analytical procedures, ensure instrument qualification, implement audit trail systems for data integrity and security, and coordinate technical audits of the Quality Control Laboratory. Your responsibilities will also include maintaining Quality Control records, control samples, release records, routine Good Laboratory Practices auditing, organizing training programs, establishing guidelines and procedures on cGMP and Good Laboratory Practice, and evaluating Change Control suggestions for overall reviews and validations. As the QC Head, you will play a key role in upholding quality standards, ensuring compliance with regulations, and contributing to the continuous improvement of quality control processes within the company.,

As a Production Chemist in the nutraceutical industry, you will leverage your 5-7 years of experience to lead the production of various products such as tablets, capsules, proteins, and pre-workout blends. Your responsibilities will include ensuring strict compliance with industry regulations and Good Manufacturing Practices (GMP), guiding formulation and development of new products, monitoring quality control processes, and collaborating with cross-functional teams to enhance manufacturing efficiency. Your expertise in nutraceutical ingredients, manufacturing processes, and quality control standards will be crucial in overseeing the production process and driving process optimization. You will be responsible for ensuring product efficacy, stability, and regulatory compliance through your deep understanding of ingredient functionality and interactions. Your role will also involve troubleshooting and resolving production issues related to blending, mixing, encapsulation, and tableting. Additionally, you will maintain comprehensive records of batch production, train and supervise production staff, and ensure that all raw materials and finished products meet defined specification requirements. To qualify for this position, you should have a Masters degree in Pharmaceutical Sciences or Food Science & Technology, along with hands-on experience in tablet and capsule manufacturing, protein and pre-workout product blending, and knowledge of GMP and regulatory requirements in the nutraceutical sector. Strong leadership, communication, and team management capabilities are essential, along with excellent troubleshooting and problem-solving skills. Preferred skills include experience with sports nutrition and pre-workout formulations, as well as familiarity with stability testing and shelf-life analysis. This is a full-time role with health insurance benefits, requiring a night shift schedule and an expected start date of 20/01/2025.,

Hello Candidates, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd We are hiring for QC Chemist HPLC/Premix Formulator/Biochemist for one of our client. Job Title: QC Chemist HPLC/Premix Formulator/Biochemist Location: Sanghi Nagar Hyderabad Department: Quality Control / R&D Reports To: QC Manager / R&D Manager Employment Type: Full-Time Job Summary: We are seeking a detail-oriented and innovative QC Chemist with expertise in HPLC, UV-Vis Spectroscopy, and Karl Fischer titration to perform analytical testing, ensure batch consistency, and contribute to the development of new premix formulations. The ideal candidate will have a strong background in quality control, formulation science, and regulatory compliance, particularly in the food or feed industry. Key Responsibilities: Analytical Testing: Perform qualitative and quantitative analysis using HPLC, UV-Vis spectroscopy, and Karl Fischer titration . Evaluate raw materials, intermediates, and finished premix products for compliance and stability. Quality Control: Conduct routine QC checks to ensure consistency, safety, and regulatory compliance across batches. Troubleshoot deviations and assist in root cause analysis. Documentation & Compliance: Prepare and maintain Standard Operating Procedures (SOPs) , Certificates of Analysis (COAs) , and batch documentation. Ensure lab practices comply with internal and external regulatory standards (e.g., FSSAI , ISO, etc.). Cross-functional Collaboration: Work with R&D and production teams during pilot batches and scale-up processes. Provide input on formulation improvements and new product development. Instrument Maintenance: Maintain, calibrate, and troubleshoot laboratory instruments as per schedules and SOPs. Formulation Development: Develop and optimize nutritional and functional premix formulations to meet evolving customer and market needs. Stay current with trends in ingredient technology and food/feed safety. Key Skills & Abilities: Proficient in HPLC , UV-Vis spectroscopy , and Karl Fischer titration . Strong understanding of quality control procedures and regulatory standards. Ability to develop and optimize formulations based on scientific and commercial criteria. Experience or familiarity with FSSAI regulations and other relevant certifications is a plus. Excellent skills in technical writing, documentation, and reporting . Strong analytical mindset with excellent data interpretation and problem-solving abilities. Flexible and adaptive to new technologies, trends, and regulatory changes. Qualifications: Bachelors or Masters degree in Biochemistry, Chemistry, Food Technology , or a related field. 1 - 5 years of relevant experience in QC, formulation , or analytical testing , ideally in nutraceuticals , food/feed , or pharma sectors. (Interested candidates can share their CV to aradhana@hungrybird.in or call on 9959417171.) Please furnish the below-mentioned details that would help us expedite the process. PLEASE MENTION THE RELEVANT POSITION IN THE SUBJECT LINE OF THE EMAIL. Example: KRISHNA, HR MANAGER, 7 YEARS, 20 DAYS NOTICE Name: Position applying for: Total experience: Notice period: Current Salary: Expected Salary: Thanks and Regards Aradhana, +91 9959417171

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (01-10 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC ARD - OSD Experience: (02-05 Years) •HPLC/ FG/Analytical Method validation/ Stability/liquid chromatographic PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, PACKING Experience: (02-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer, Jr.Executive, Executive & Sr.Executive INTERVIEW VENUE: Hetero Labs Limited (Formulation Unit). Chakkan Road, Kalyanpur (Vill), Baddi, Solan, H.P, INDIA 173205 CONTACT INFO: E-mail: Harishwar.M@hetero.com & Contact: 8121005416 for further info NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID Proofs

Job Title: QA Assistant / Executive - API Industry Location: Kakinada, AP Company: Lyfius Pharma About Lyfius Pharma is 100% subsidiary of Aurobindo Pharma. Its largest API Unit of Aurobindo. Lyfius spread across 236 acres in Kakinada SEZ and it is second largest API manufacturing facility in ASIA. Qualification: M Sc / B Sc Experience: 2 to 4 Years Job purpose The main responsibility of this position is to generate accurate results while following GMP requirements. Responsible for analyzing laboratory samples using various chemical and instrumental techniques, in accordance with established compendial and in-house testing methods, while under minimum supervision. Duties and responsibilities Testing of raw materials by UV, IR, HPLC and GC and wet chemistry techniques as per SOP. Document test results as per SOP and GMP Recognizes OOS or out of trend results and under the direction of the Supervisor assists in the completion of lab investigations Interpret data, communicate results and complete written reports Complete all GMP documentation correctly and in a timely manner Complete all training assignments and maintain personal training records Conduct (participate or lead) routine laboratory and Non-Conformance Investigations Initiate and follow through with actions required to close Change Controls Evaluate methods and procedures and suggest improvements and changes as required Disposes of waste solvents and orders any chemicals or laboratory supplies as required Flexibility to shift start time and occasional overtime Other duties as assigned Knowledge, Skills and Abilities: Ability to apply knowledge of chemistry, math, instrumentation and statistics to complete tasks Proficiency in various techniques and operation of instrumentation (pH meter, viscometer, Karl Fisher apparatus, UV IR spectrophotometer, Chromatography instruments) Ability to work effectively in a team-based environment Proficiency with applicable software (LIMs and Empower) Strong organizational, analytical and multi-tasking ability Ability to troubleshoot and resolve issues Excellent written and oral communication skills, particularly with analytical records, reports and investigations Understanding of GMPs Problem Solving: Routine problems and decisions. Qualifications B. Sc. or equivalent Minimum 2 - 4 years experience in Pharmaceutical Laboratory environment preferred

Job Responsibilities: 1. Document analysis procedures and the test results mainly bioburden testing, spectrophotometric testing and mechanical studies using UTM machines 2. Document product stability studies are completed satisfactorily and supported by correct product sample analysis 3. Establish a tracking mechanism for customer & field complaints and suggest corrective actions Profile: 1. You have experience of around 3 or more years in pharmaceutical industry 2. Educational Qualification - M.Sc./M.Pharm degree with strong interest in quality control documentation 3. You work accurately, technically minded and able to work independently after training in the matter entrusted to you. Experience in a formulations/ API industry is an asset

integration with labware LIMS, Previous responsibility: *Finished product section head: responsibility were, SFG, FP, Inprocess, cleaning samples planing for analysis, incident, deviations, Investigation, CAPA, Effectiveness monitoring and change management related to finished section. *timely releasing of products. *Raw material and packaging material section head, incident, deviations, Investigation, CAPA, Effectiveness monitoring and change management related RM/PM. *timely releasing of materials. *products validation and method transfer. *Stability section head, stability study protocol prepration, review, stability chamber management, monitoring of samples charging, timely analysis, stability summary report compilation, *Ensure timely closing of OOT, OOS, deviations. *regulatory affairs responce and products submitted queries responce. *Laboratory software audit trail review and compliance, safety management. If interested mail cv at : NeetiJ@selectsourceintl.com

Job Summary: Perform and report the analysis of In-Process samples, finished products, Stability samples and Cleaning Validation. Job Responsibilities: To ensure timely completion of analysis and data completion for the same. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems. To perform the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples and cleaning validation. To Prepare Stability Trend Reports for Laboratory samples. To collect and maintain various laboratory samples. To generate and maintain records related to laboratory samples. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. To assist the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other duties as assigned. Job Requirements: Education M.Sc\BPham or any equivalent degree Knowledge, Skills and Abilities Effective command over verbal and written communication with good interpersonal skills. Command on Microsoft-Office (Word, Excel). Able to prioritize the tasks. Best in effective planning of work activities to meet the time lines. Experience Minimum 3 to 6 years of experience in GMP regulated pharmaceutical industry.

Job Summary: Perform and report the analysis of In-Process samples, finished products, Stability samples and Cleaning Validation. Job Responsibilities: To ensure timely completion of analysis and data completion for the same. To be responsible for all activities in the Quality Control Laboratory, including cGLP, documentation and implementation of departmental quality systems. To perform the in-process/finish product/stability testing of laboratory Batches, Commercial batches, other stability samples and Cleaning validation. To Prepare Stability Trend Reports for Laboratory samples. To collect and maintain various laboratory samples. To generate and maintain records related to laboratory samples. Works as a member of a team to achieve all outcomes. Performs all work in accordance with all established regulatory and compliance and safety requirements. Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion. To assist the Senior Analyst / Team Leader/Group Leader in the day-to-day functioning of the Quality Control Laboratory. Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies. All other duties as assigned. Job Requirements: Education M.Sc\BPham or any equivalent degree Knowledge, Skills and Abilities Effective command over verbal and written communication with good interpersonal skills. Command on Microsoft-Office (Word, Excel). Able to prioritize the tasks. Best in effective planning of work activities to meet the time lines. Experience Minimum 2 to 4 years of experience in GMP regulated pharmaceutical industry.

Department: Quality Control Location: Tehsil Inodra, Kangra (HP). Near by Pathankot Reporting to: QC Manager / Head Quality Department Key Responsibilities: Conduct routine testing of raw materials, in-process materials, and finished products as per approved specifications and standard test procedures (STPs). Perform chemical and instrumental analysis using HPLC, UV, IR, GC, KF, etc. Maintain accurate and up-to-date laboratory records, worksheets, and logbooks. Ensure timely calibration and maintenance of laboratory instruments and equipment. Review and follow Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Assist in method development and method validation activities as required Conduct stability testing and prepare stability summary reports. Ensure compliance with company SOPs, quality standards, and regulatory requirements (such as USFDA, MHRA, WHO, etc.). Participate in internal and external audits and implement corrective and preventive actions (CAPA). Manage sampling, labeling, and storage of test samples as per SOPs. Handle out-of-specification (OOS), out-of-trend (OOT), and deviations according to quality procedures. Coordinate with production, QA, warehouse, and other departments for quality-related issues. Monitor environmental conditions of the lab as per the standard protocol. Desired Candidate Profile: Education: B.Pharm / M.Pharm / B.Sc / M.Sc Chemistry or related field Experience: 2–10 years in QC role within a pharmaceutical formulation plant Skills Required: Proficient in operating analytical instruments (HPLC, GC, etc.) Knowledge of GMP, GLP, ICH guidelines Strong documentation and communication skills Attention to detail and ability to work under pressure Good analytical and problem-solving skills

Role: Voice support Executive Qualification:+2 Pass/Graduate 15k-18k Experience: Fresher Language: Malayalam,Kannada,Telugu,Tamil Location: Shantinagar, Bengaluru Malayalam/Tamil+ English (or) Any 2 South Indian Language Preferred and Basic English

Qualification : M.Sc Microbiology / Biotechnology Experience : 7 to 10 year Location : Manjusar (Vadodara)

Roles and Responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Developed personal care and cosmetics products from concept formulation to final production. Performed stability testing and troubleshooting of unstable formulas. Performed stability testing and troubleshooting of unstable formulas Required Candidate profile B.TEC/M. TEC in Cosmetic from leading Cosmetology College or B.Tec/M.Tec from ICT Mumbai Exp Should have 2-3Yrs of exp in leading Indian MNC/MNC/3rd Party Manufacturing, in Personal care Products