17 Stability Testing Jobs

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

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

Knowledge of proper operation and cleaning of Machine & Area related to Granulation, Compression, Coating and Capsule Filling Knowledge of BMR/BPR preparation and SOP preparation Knowledge of Equipment and area qualification and validation activity

JOB DESCRIPTION Department : Quality Control Chemical Designation : Manager – Stability Reporting To : Head – Quality Control Educational Qualification : M. Pharma / M.Sc. (Chemistry/Pharmaceutical Sciences) Job Responsibilities 1.Responsible for preparation and review of Stability Study Protocols, Stability Study Reports, and Stability Summary Sheets for all products (General Injectables and OSD). 2 Responsible for initiation, monitoring, and timely execution of stability studies for registration batches, validation batches, and commercial batches as per ICH guidelines. 3 Responsible for managing stability chambers, their qualification, calibration, and monitoring as per regulatory and internal guidelines. 4 Responsible for monitoring pull-out schedules, analysis of stability samples, and ensuring timely reporting. 5 Responsible for statistical analysis, trending, and evaluation of stability data, including identification and investigation of Out of Trend (OOT) and Out of Specification (OOS) results. 6 Responsible for preparation, review, and approval of analytical reports for Finished Products, In-process materials, Raw Materials, Packaging Materials, Water and Steam (Condensate) samples, including stability samples. 7 Responsible for preparation, review, and execution of Analytical Method Transfers and Method Validations related to stability and routine testing. 8 Responsible for preparation and review of Standard Operating Procedures (SOPs), Analytical Test Data Sheets, General Test Procedures, Specifications, and Calibration Data Sheets. 9 Responsible for review and handling of laboratory incidents, Out of Calibration (OOC) reports, deviations, OOS, OOE, OOT events, Change Controls, and Corrective and Preventive Actions (CAPA). 10 Responsible for Good Documentation Practices (GDP) and Good Laboratory Practices (GLP) implementation and compliance across the team. 11 Responsible for preparation/review of Qualification Reports/Protocols for instruments and equipment used in the QC Laboratory. 12 Responsible for preventive maintenance schedules, calibration schedules, and management of instruments, including handling of breakdowns. 13 Responsible for management of Working Standards, Reference Standards, and Impurity Standards, including procurement, qualification, issuance, and maintenance. 14 Responsible for allocation of work, supervision, and review of activities performed by the QC team members and ensuring section-wise coordination. 15 Responsible for providing GMP/SOP/Analytical training to QC personnel and ensuring compliance to safety practices within the QC department. 16 Responsible for acting as Section Head and taking charge in the absence of the QC Head to ensure continuity and compliance. 17 Responsible for executing and monitoring QC activities related to the General block and Oncology block (ADL, R&D) at BDR Pharmaceuticals International Pvt Ltd, Baska Site. 18 Responsible for self-training and tracking of training status for self and team members on all applicable SOPs and protocols. 19 Responsible for cross-functional communication with R&D, QA, Production, and Regulatory Affairs teams for new product stability requirements, troubleshooting, and regulatory submissions. 20 Additional responsibilities shall be assigned as per organizational requirements based on operational needs.

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

Role & responsibilities 1. Product Formulation & Innovation: Develop and optimize cosmetic formulations for skincare, haircare, personal care, and other beauty products. Conduct research on new ingredients, technologies, and trends in the cosmetics industry. Work on clean beauty, sustainable, and herbal formulations to align with market demand. Ensure stability and compatibility of formulations through rigorous testing. 2. Process Development & Scale-up: Develop lab-scale formulations and guide the scale-up process for commercial production. Optimize process parameters for better efficiency, yield, and cost-effectiveness. Collaborate with production and quality teams to ensure smooth product transfer from R&D to manufacturing. 3. Regulatory & Compliance: Ensure compliance with BIS (Bureau of Indian Standards), FDA, AYUSH, FSSAI , and other regulatory bodies. Prepare technical documentation, PIF (Product Information File), and dossier submissions for product approvals. Keep updated with global cosmetic regulations (EU, US FDA, ASEAN, etc.). 4. Quality Assurance & Testing: Conduct stability studies, microbiological tests, and performance evaluations. Collaborate with third-party labs for dermatological and clinical testing. Work closely with QA/QC teams to maintain high product standards. 5. Cross-functional Collaboration: Work with marketing & branding teams to develop consumer-centric products. Collaborate with procurement & supply chain for sourcing raw materials and packaging. Coordinate with manufacturing teams for large-scale batch production trials. Preferred candidate profile Expertise in cosmetic formulation techniques (emulsions, surfactants, active delivery, etc.). Strong knowledge of raw materials, excipients, and actives used in cosmetics. Familiarity with analytical and stability testing methods . Understanding of GMP, ISO 22716 (Cosmetic GMP), and regulatory standards . Ability to innovate and create unique, market-driven formulations . Strong project management, leadership, and problem-solving skills.

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

Job Title: Formulation and Development Executive Experience Required: Minimum 3 years Key Responsibilities: Develop and formulate cosmetic products across various categories such as skincare, hair care, and grooming products, ensuring high-quality formulations. Facilitate the successful transfer of formulations from R&D to production, ensuring seamless scaling up of manufacturing processes. Collaborate with production and manufacturing teams to ensure efficient and accurate technology transfer. Prepare and manage all necessary documentation related to technology transfer. Conduct stability testing to ensure the shelf life and quality of products under various environmental conditions. Analyze and interpret stability test results and recommend improvements to formulations. Maintain proper documentation of all stability testing and product evaluation data. Maintain well-organized records of formulations, test results, and production processes. Key Skills & Qualifications: A degree in pharmaceutical sciences, chemistry, cosmetology, or a related field. Minimum of 3 years within the cosmetic or pharmaceutical industry. Strong knowledge of formulation techniques, stability testing methodologies, and technology transfer processes. Proficient in preparing, maintaining, and reviewing technical documentation in line with industry standards. Familiarity with regulatory requirements for cosmetic products (e.g., FDA, EU Cosmetics Regulation, etc.). Ability to analyze and interpret data from stability testing, raw material testing, and formulation trials.

Job Responsibilities: 1. Perform analysis procedures mainly bioburden testing, spectrophotometric testing and mechanical studies using UTM machines 2. Ensure product stability studies are completed satisfactorily and supported by correct product sample analysis 3. Also, whenever required provide support to Marketing by educating customer 4. 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 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

Job description RESPONSIBILITIES Ensure that quality control laboratory is ready all time for any regulatory inspection. To ensure this by continuous monitoring of GLP practices. Co-ordinate for internal & external calibrations of QC instruments. Ensure analyst validations are as per the SOP. Co-ordinate with service providers for breakdown and preventive maintenance of instruments. Calibration of QC instruments as per defined schedule. Analysis of finished products and raw material samples. Perform analytical method verification / validation of finished product samples. Prepare working standards. Reference & working standard issuance / discard / maintenance (reconciliations, procurement, and validity check of reference standards). Ensure compliance to good documentation practices & good laboratory practices. Comply and ensure the implementation of safety practices. WORK RELATIONS Interfaces: Internal Quality Assurance, Quality Control, EHS, HRA, Warehouse, Engineering Interfaces: External External Vendors. DESIRED SKILLS Must have experience in Quality Control department in reputed pharma organizations. Should have hands on experience of Instrument Handling Strong knowledge of operating HPLC, GC, KF, IR, pH Meter etc. One Should Manage day to day Planning One should Timely review of logbook entries & daily monitoring activities.

Job description Performance Test Engineer Job Description: Skills and Experience Requirement: At least 3 to 8 years of experience in Performance Testing and Engineering activities Must have knowledge on Performance Testing Life Cycle Significant experience in performance test planning, workload modelling, capacity planning, scalability and stability testing, and stress testing of small to large scale applications Extensive experience in creating Jmeter script and designing scenarios. Expertise in performance test scripting, execution, monitoring, analysis reporting. Expertise in developing dynamic performance testing suites using any of these performance test tools like Apache JMeter (Mandatory), Blazemeter, Performance Centre, Microfocus LoadRunner (Added Advantage). Ability to work within Pace team collaborating with Product owners/business analysts and developers to understand requirements. Working experience in an Agile and/or Pace delivery framework. Extensive experience in any one of APM tools like AppDynamics, Dynatrace Splunk. Good to have knowledge on using Atlassian JIRA Confluence. Good to have understanding about the AWS cloud and concepts. Your tasks responsibilities includes but not limited to: Own delivery of performance test phase from specification to design, prep, execution through to test closure Provide accurate estimates for delivery of performance test tasks scripting, execution, analysis and reporting. Create reusable performance test scripts and assets using toolsets including Apache Jmeter. Maintain existing and new performance test scripts to make sure scripts are reusable for release activities. Create performance test data via NFT scripts and maintaining test data repo. Develop and execute component and system level performance tests Analyse performance results to identify bottlenecks and optimisations Work with distributed team resources, developers, DBAs, SMEs to analyse, identify and resolve performance test issues. Create detailed performance test reports to appropriate levels, depending on audience (eg. Interim test reports, Test Summary Report) Analyse metrics and trends to highlight performance opportunities for improvements Work with delivery stakeholders to define Performance test engineering requirements, scope, workload models recommended testing frameworks Assist stakeholders with identifying and understanding performance risks and recommending mitigation strategies and approaches. Effectively manages risks, issues, dependencies, and stakeholders throughout the delivery Setting up monitoring and dashboards or ability to monitor using any one of the APM tools like Appdynamics, dynaTrace and data management tools like Grafana, Splunk and other cloud native tools Excellent verbal and written communication skills Participates in and contributes to all Pace team activities and events Having automation and engineering mind-set and up-skill team members in the domain of testing and continuous integration capabilities Integrate performance and quality engineering frameworks with CI/CD, infrastructure as code, DevOps, automation, and various cloud technologies Undertake any other tasks assigned by your lead/manager that you have the capability to perform safely in line with relevant internal Group policies and external regulatory requirements. Adhere to the Code of Conduct. The Code of Conduct sets the standards of behavior, actions and decisions we expect from our people.

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

Develop and optimize cosmetic formulations, conduct trials, ensure regulatory compliance, maintain documentation, evaluate raw materials, optimize processes, collaborate with teams, troubleshoot challenges, and stay updated with industry trends. Required Candidate profile Minimum 3 years of experience in cosmetics or pharmaceutical sector Bachelors or master’s degree in Cosmetic Science, Chemistry, Pharmaceutical Sciences, or a related field

Vacancy - Stability Team Lead/Manager - Investigational analysis in Analytical Department (formulation) Experience in years : 14 to 16 years in Regulated and Emerging markets Educational qualification : M.Sc Analytical chemistry Dosage forms : Oral solids, Liquid orals, Ophthalmic and injectable products Job description : 1) Will be responsible and accountable for the trouble shooting and investigational analysis of R&D stability samples 2) Sound technical and scientific knowledge for investigation of anomalies. 3) Root cause identification and CAPA for OOT and OOS for developmental stability samples 4) Online review of HPLC and UV raw data of stability 5) Well versed with operation of Empower 3.0 and Chromeleon 7.2 software 6) Has experience in handling a team of 4 to 5 members 7) Should have exposure to Assay, Dissolution, preservative content and related substances testing Candidates with prior experience in investigational and trouble shooting analysis is preferable.