107 Validation Jobs - Page 4

Oracle CPQ Cloud module Pricing, Quotation Configuration, Product Management-Items, BOMs, and System Configuration, Document Engine and (BML), Utilities Libraries, Validation/Hiding/Constraint rules, Layout editor, Commerce layout, XML, XML-Schema.

Basic Qualifications: Bachelor of Science in Applied Physics, Mechanical Engineering, Electrical Engineering or equivalent (Materials /Chemical/ Civil/ Aerospace/Computer) from an ABET accredited university. Have known the knowledge of classic and adaptive AUTOSAR Demonstrated ability to develop AUTOSAR based systems. Demonstrated competency in dSPACE tools like System desk, Control desk, VEOS, Automation desk and SYNECT. Knowledge on Functional Mockup Interface Knowledge on AI Agents and LLMs. Ability to develop scripts for automating tasks using GenAI. Demonstrated competency in creating virtual ECU’s Demonstrated competency in connecting virtual ECU’s using BUS manager Trained in both VEOS and Control Desk test layout creation. Working experience in Continuous Integration and Continuous Delivery (CI/CD) environment Experience with statistical analysis of data to establish pass/fail criteria Good problem-solving skills Good communication and interpersonal skills Preferred Qualifications: Master’s degree in Applied Physics, Mechanical, Electrical, Aerospace or Computer Engineering from an ABET accredited university A minimum of 3 years within the area of Virtual or Hardware validation using dSPACE tools like System desk, Control desk, VEOS, Automation desk and SYNECT Related engineering experience Understanding of virtual validation process

Role & responsibilities Job responsibilities comprise carrying out of Quality Assurance functions in day-to-day activities. JOB RESPONSIBILTY 1. Responsible for review, approvals and close outs of change controls, deviations, CAPA, incident reports and any other quality system documents 2. Develop, manage and improve Quality Systems and procedures to ensure compliance with all applicable laws, regulations and company quality standards in support of CGxP activities 3. Review and approvals of analytical and formulation development Master documents. 4. Review and approval of analytical activities protocols and reports 5. Submitting whole set of documents required for regulatory submissions for new products 6. Supporting for any regulatory queries from QA perspective 7. Review and approval of validation, qualifications protocols and reports, 8. Monitoring day to day activities in Analytical development and Formulation development in compliance to the GMP 9. Preparation, review and approval of SOPs 10. Conducting training on SOPs, quality management systems and GMP in all aspects including procedural updates 11. Control of documents includes documents storage, issuance, distribution, retrieval and destruction 12. Performing vendor audits of API and Excipients (where necessary) and handling of all activities related to vendor audits 13. Conduct periodic audits of CMOs and Althera affiliate facilities. Participate in the vendor Qualification programme as and when needed. 14. Review and approve change control initiated at CMOs and co-ordination with European QA, RA aid customers and keep track till all the relevant activities are completed 15. Planning and conducting of self-inspection, preparing and sending self-inspection reports to concerned departments. Verifying the self-inspection compliance report for correctness and completion 16. Oversight and coordination with the Contract Manufacturing Organization (CMOs) on batches manufacturing activities as well Quality Management functions for Althera products 17. Coordination with the European QA team on supplying necessary QMS documents as required 18. Responsible for review, approvals and close outs of deviations, CAPA, OOS, OOT and incident reports raised by the CMOs. Timely review of effectiveness of CAP As. 19. Participate in investigations at the CMOs where necessary, review and ensure the investigations are conducted in line with the current regulatory expectations. 20. Applying risk management tools wherever applicable in accordance with current regulatory requirements 21. Handling of Market complaints and to co-ordinate with respective CMOs to get the investigation done on timely manner with appropriate root causes and CAPAs identified. 22. Track all the QMS status of Althera products at CMOs are timely concluded, and reports are shared 23. Coordinate with CMOs in any Regulatory and customer audits at their site, track all the observations and the CAPAs are completed timely as per the commitment. 24. Review and approve of CMOs validation and master documents (BMRs, BPRs, MFR, PVPs, PVRs etc) and Protocols (Validation, Qualification, cleaning, stability etc) 25. Oversee, support and coordinate with Althera affiliate manufacturing and Testing sites and the RnD site. 26. Preparation, Review of the PQRs for Althera products. 27. Ensure quality / technical agreements with contract manufacturing organizations (CMOs)are available and updated within timelines. Preferred candidate profile Perks and benefits best in the industry

Job Description Manages the accounts payable invoice processing including validation, reconciliation and final payments. Job Description - Grade Specific Operating as a Finance specialist Will be building skills for a more specialized Finance service.

Exemplary teaming skills. Youll work with technical leaders providing the certification evidence for projects that will deliver best in class, safest and highest quality software on the planet. These projects can come from multiple industries such as Aerospace and Defense, Industrial, Medical and Automotive verticals and will follow Wind Rivers proven processes Your Role Helping to develop test strategies and cases for VxWorks as well as HVP helping Wind River to grow in its role in new embedded and enterprise market segments. Take initiative to improve features and processes. Contribute ideas for product improvements and iterations. Collaborate effectively with global software engineering teams. At least 8+ years of experience in development of test infrastructure and executing/integration of firmware tests for Embedded devices Driver and board-level system software test development and integration Developing test frameworks using C, C++, Python and Object-Oriented Programming Experience in testing and automation in agile and continuous delivery models. Ability to develop test cases based on high level requirements, low level requirements and test strategies possessing knowledge of input test variations. Strong experience in using LDRA, Polarian, DOORS, Git, Jira, Linux environment. Knowledge on standards DO178B/C, ISO26262, ASPICE. Knowledge on architectures ARM/RISCV/PPC based processors and micro-controllers Your Background BE/BTech or ME/MTech degree in Computer Science, Electronics Engineering, or equivalent. 8+ years of software development, verification & validation experience Experience with Firmware design, specification, and implementation Strong in C, C++, Python (Design Patterns), RTOS Fundamentals. Good understanding of automation tools, technology landscape, and OOPS concepts. Experience in testing and automation in agile and continuous delivery models Excellent English communication skills, both written and verbal Ability to develop test cases based on high level requirements, low level requirements and test strategies possessing knowledge of input test variations. Excellent analytical and debugging skills. Good experience in developing testing automation framework / Test Manager Experience in working with FPGA, Emulators, Simulators for Chip development Familiarity with CI/CD pipelines Strong experience in using LDRA, Polarian, DOORS, Git, Jira, Linux environment. Experience in scripting language e.g., Python Successfully delivered to NA & EMEA customers Lead the agile team using Agile methodology and scrum practice. Certified Scrum Master, experience in a scrum master role. Why join us? You can grow at Aptiv. Aptiv provides an inclusive work environment where all individuals can grow and develop, regardless of gender, ethnicity or beliefs. You can have an impact . Safety is a core Aptiv value; we want a safer world for us and our children, one with: Zero fatalities, Zero injuries, Zero accidents. You have support . We ensure you have the resources and support you need to take care of your family and your physical and mental health. Your Benefits at Aptiv: Hybrid and flexible working hours; Higher Education Opportunities (UDACITY, UDEMY, COURSERA are available for your continuous growth and development) Life and accident insurance Sodexo cards for food and beverages Well Being Program that includes regular workshops and networking events EAP Employee Assistance Access to fitness clubs (T&C apply) Creche facility for working parents

1 attend the breakdown activity and maintain records 2 Support onsite projects 3 Inspection and testing 4 Operation and documents filling and checking of Filter cleaning booth and scrubbers. 5 Supervise maintenance in continuous running machines.

Analog Validation/Characterization Engineer/Lead

Role & responsibilities You shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company. Key Deliverables: 1. Ensure manufacturing practices as per cGMP and GLP standards. 2. Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc. 3. Applications for AHC to AQCS, EIA and Capexil and coordinate related activities. (AHV/SPD: This is exclusive knowledge related to Capsule and companies manufacturing animal origin products. We have mentioned this as the candidate on joining will be responsible for this work though he/she may not be having exposure to same.) 4. Organize internal and external audits for ISO, GMP+, FDA, Capexil, GMP+, EIA and others. Maintain the documents required for those audits. 5. Ensure all personnel are trained on requirements for GMP, GLP, GDP, applicable regulatory issues and other procedures related to their work area. (SBG) 6. Evaluation and approval of Suppliers for RM, PM, testing labs and service providers. 7. Assisting HOD in customer complaint analysis and preparation of customer complaint report. 8. Investigation of incidents, deviations, OOS and ensure corrective actions in place. 9. Reviewing the daily availability of operators and allocating work to them. 10. Maintaining and review BMR documents, guide for relevant changes if required. 11. Label artwork review and management. Technical Competencies: a) Analytical skills (spotting trends and patterns) b) Report writing skills c) Problem solving abilities d) GMP and GDP knowledge e) Good English communication skills (verbal & written). Behavioural Competencies: a) Quality and Service Orientation b) Delivering consistent results c) Ability to prioritize, organize, manage work and time. d) Customer Centric e) Cross Functional Team Working Preferred candidate profile B. Pharma, B.Sc./M.Sc. (Chemistry/Microbiology) 8+ Years of experience in QA process in Pharmaceutical / food processing / cosmetics / chemical industries. Perks and benefits 1. Opportunity to be part of a growing organization offering niche products to Pharma industry. 2. Opportunity to work at Head Office location. 3. Intimate small company culture with MNC professionalism. 4. Company value programs TrANSSCEnD. 5. Employee events like festival celebrations, family fun events etc. 6. Five days working (alternate weeks). 7. Medical Insurance for your immediate family. 8. Housing accommodation for Bachelors & family.

AUTOMOTIVE EMBEDDED TECHNOLOGY PRODUCT LIKE: ECU, TCU, CONTROLLES, ON/OFF BOARD CHARGER. ANALOG, DIGITAL, MCU, SENSORS, POWER, SUPPLIERS AND POWER AND POWER ELCTRONICS. HARDWAREAND SOFTWARE REQUIREMENT UNDERSTANDING AND PRODUCT ARCHITECTURE. Required Candidate profile PLAN, DEVELOPED AND PERFORM TESTING ON THE BENCH VEHICLES IN ALIGNMENT EMI/EMC I/O TESTING, DVP TESTING. ACCOUNTABLE FOR RFQ HANDLE & CONVERSION, VA/VE CONTINUOUS APPROACH. DEVELOP NEW FUNCTION MODULE

Incedo is hiring!! Position Title: Associate/Management Trainee Business Function : Operations Department: Banking Treasury Operations Validating & Remediating data extracted from Signer documents RESPONSIBILITIES: 1. Ensuring quality and time efficient production of documents 2. Ensure all process tasks are completed 4. Ensure self and team is escalating critical issues to Department Head/Lead thereby ensuring a seamless process flow 5. Provide ideas to remove complexity and increase productivity by process improvement/lean processes. 6. Contribute actively in documenting procedures and work instructions. 7. Actively ensure that team always engages positively with any stakeholders and maintain a high service level 8. Ensure data integrity and strict adherence to SLAs 9. Own, coordinate and delegate work as required 10. Work across functions to identify root cause to breaks and contribute to find resolutions 11. Support team members in the completion of assignments. 12. Back-up in all other areas as needed. Qualifications & Experience: Bachelor's degree in Accounting, Finance or a business-related field, or equivalent work experience 0 - 2 yrs of related experience, preferably in Retail/Commercial Banking operation, Treasury operations or Account opening and maintenance. Excellent written and verbal communications Ability to manage multiple tasks and deadlines simultaneously Ability to identify and resolve exceptions Strong personal computer skills and knowledge of other office equipment We offer: 1. Chance to join a truly growth-embracing culture, which will commit to helping you grow personally and professionally. 2. An opportunity to work as part of a dynamic, ambitious and international team in an informal and pleasant working environment. Regards, HR Team

Experience in multi-core controllers Experience in Embedded C Experience in writing and understanding tests for SoCs Experience in test automation (Python knowledge preferred)

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client: Industrial membranes manufacturer Position: Sr. Design Engineer - Mechanical Location: Vadodara Job Profile: Technical Selection & Detailed Design Engineering of EPC Projects. Preparation of Material Requisition, Technical Bid Evaluation, checking and validation of engineering documents. Participate Design Input Review, conduct meeting with client, Value Engineering Prospects for equipments/packages of Projects. Customer & Vendor Coordination for technical discussion and quarry resolution, Vendor Document Review. Preparation of Engineering Documents, Review of Drawings, Data Sheets, PFD, P&ID, Mass Balance, Process Calculations, Piping & Valve selection etc. Desired Profile: Diploma Mechanical / BE / B.Tech (Mechanical Engineering) with 5+ years of experience especially in Mechanical Design with Water & Waste Water Solution, Oil & Gas Industry, Turnkey Engineering Design or EPC company. Experience in Design Software. Experience in Water Treatment company background preferable. Experience in Design Software like AutoCAD, Plant 3D etc. Excellent expertise in Engineering Design. Should have capability to lead the mechanical design engineers of company. Excellent problem solving and time management skills. Product & Product documents standardization. Candidate who can join immediately would be added advantage. Must have very good communication skills in English. Interpersonal Skill. Good Team Handling Ability and Good Team Player. Recruiter Profile: BEST - FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India E-Mail: hrd@bfrr.in Website: www.bestfitrecruitment.co.in

Greetings! & very warm welcome to BEST-FIT Recruitment Riders, We are BEST-FIT Recruitment Riders feel immense pleasure to search and provide you with better carrier opportunities to aid you in achieving your aspirations. BEST-FIT Recruitment Rider is a highly specialized Recruitment & Executive Search Partner for Pharmaceutical, Biotech, CRO, Chemicals, Medical Devices & Turnkey Pharma Projects Engineering-Construction Design Sectors. We are searching & recruiting highly qualified professionals for Middle-Senior-Upper-Management and Executive jobs. (Eg: Managers, VP, President, CFO & CEO). Also offering customized recruitment services by Headhunting & Executive Search for Middle & Top management level professionals according to clients specific needs. We are BEST-FIT Recruitment Riders do exactly what our name tells. To know more about us please visit our website: www.bestfitrecruitment.co.in We would like to inform you that presently we have professional career opportunity matching to your profile with one of our esteemed client. Please see the following position summary: Client: Subsidiary of the American MNC Pharma Company Position: Assistant Manager - QA (Green Field Project) Location: Dahej, Gujarat Job Profile: Projects Cycle management for Validation & Qualification of Green Field Projects. Document Preparation of all phases of Validation of major from scratch. Conducting QA validation lifecycle documentations. Preparing & reviewing of documentations related to URS, DQ, IQ, OQ & PQ Preparation & Reviews of documents related to Validation Master Plan & Project Validation Plant, Validation Protocol & Reports, and Qualification related documents. Assist in the monitoring and periodic revalidation of equipment and processes. Follow all regulatory guidelines & cGMP guidelines, as required by the job function. Liaise with key personnel within project teams to ensure validation tasks are completed in a timely manner Work to create an environment of open communication, participation and information-sharing within and between teams within QA and throughout facility. Desired Profile: Graduate Engineer in any Discipline with 5 to 7 years experience in QA documentations especially in Green Field Projects. Preferably worked in Pharma with experience in Documentation related to URS, DQ, IQ, OQ & PQ. Exposure to Green field Projects would be first preference. Expertise in preparing documentations related to green field projects with Parma. Extremely meticulous, methodical & process oriented Stay informed about advancements in QA, regulatory requirements, & industry trends. Continuously expanding knowledge & skills to enhance performance and contribute to continuous improvement initiatives. Recruiter Profile: BEST - FIT Recruitment Riders G-7, Amrit Complex, Opp: Mahavir Jain Vidhyalaya & Jain Derasar, R.V. Desai Road, Near Goyagate Circle, Vadodara-390001, Gujarat, India E-Mail: hrd@bfrr.in Website: www.bestfitrecruitment.co.in

B.Sc. / M.Sc. with 3 to 4 years of experience in pharmaceutical industry. Experience of CAPA, change control, QMS, Documentation, SOP Preparation, IPQA, BMR issuance and review, Equipment qualification, GMP/GDP documents, etc. Required Candidate profile To ensure Q. A. activities are carried out as per set procedures and ensure to record in respective documents. Preparation and review of equipment and utility qualifications documents. Perks and benefits Negotiable - Depending Upon Candidate & Experience

About Us: Unison Pharmaceuticals Private Limited (Formerly known as Unison Pharmaceuticals) was established in 1981 with a vision of providing quality & most affordable medicines across the nation. The company is having 1st Rank (Unit wise sales) in Gujarat state since more than 17 consecutive years as per ORG IMS. In addition to this, the company is ranked 82 among top companies of India (Rupee wise sales) MAT December 2021. Website : www.unisonpharmaceuticals.com We are seeking specialists for multiple roles into Quality Assurance at our EU Approved OSD Manufacturing facility at Unit I Moraiya, Ahmedabad. Company : Unison Pharmaceuticals pvt ltd. Location : Unit I (Moraiya, Ahmedabad) - Transportation provided from Ahmedabad routes (1) Quality Assurance - Validation Designation: Sr. Executive /Assistant Manager /Dy. Manager Education Qualification: B.Pharm/M.Sc/M.Pharm Experience Required: 8 to 12 years Job Exposure required: Must Have : Process Validation, Cleaning Validation Preferred to have: QMS, Risk Management, Qualification (2) Quality Assurance - Compliance & Training Management Designation: Executive / Sr. Executive Education Qualification: B.Pharm/M.Sc/M.Pharm Experience Required: 6 to 10 years Job Exposure required: Must Have : Audit Compliance, Training Management (3) Quality Assurance - Documentation Designation: Officer / Sr. Officer / Executive Education Qualification: B.Pharm/M.Sc/M.Pharm/B.Sc Experience Required: 4 to 7 Years Job Exposure required: Must Have : APQR or IPQA & Batch Record Preparation (4) Quality Assurance - Process Validation Designation: Officer / Sr. Officer / Executive Education Qualification: B.Pharm/M.Sc/M.Pharm/B.Sc Experience Required: 5 to 8 Years Job Exposure required: Must Have : Process Validation, Hold Time Study (5) Quality Assurance - IPQA - Packing Designation: Officer / Sr. Officer / Executive Education Qualification: B.Pharm/M.Sc/M.Pharm/B.Sc Experience Required: 4 to 8 Years Job Exposure required: Must Have : In process QA , Line clearance of Packing area Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career.

We are hiring IT Recruiter professionals for Bangalore location at BTM layout. Responsibilities: Should have experience on end-to-end recruitment process Experience on IT contract staffing Expertise on Sourcing, screening skills & validation process Exposure on all the IT technologies Should be ready to work from office Should have excellent communication skills Sourcing work experience on recruitment portals & social networks

Hi, We are hiring for ITES Company for Validation Associate Role. Job description ***Minimum 3 years as Validation Associate is required.*** 1. Data validation test script creation: Create necessary validation scenarios needed to ensure checks are functioning as required and document scenarios in the Data Validation Specification(DVS). Document expected results for each testing scenario. Feedback to the clinical Data Scientist (CDS) any ambiguities in logic that require clarification for testing scenario creation. 2. Data validation test script execution: Entry of test data as specified in each testing scenario Compare the result obtained through entry of the test data to the expected result. Re-execute all checks that do not pass to ensure they are actual failure. Document validation failures. For validation failures due to incorrect testing scenarios, update DVS and re-execute testing scenario. Re-execute and document within the DVS validation results for checks that required programming updates. 3. Validation of the SI data set creation process: Enter data into all study visits and forms. Extract data from InForm into SI datasets Generate list of data within InForm Generate list of data contained within SI datasets Compare InForm listing to the SI dataset listing. Document unexpected inconsistencies between listing. Review time slicing specification against the SI data sets to ensure time slicing variables are being accurately populated. Document incorrect/unexpected time slicing variable assignments. Compare the pre-defined variable values as specified in the DVS against the SI data sets. Document inconsistencies To Apply WhatsApp 'Hi' @ 9151555419 and Follow the Steps Below: a) For Position in Mumbai Search : Validation Associate Mumbai (Job Code # 171) b) For Position in Pune Search : Validation Associate Pune (Job Code # 172) C) For Position in Indore Search : Validation Associate Indore (Job Code # 174)

Invoice processor: execute tasks, quality control, mentor, troubleshoot, process improvement, expertise in AP/AR, resolve email queries. Contribute to ad-hoc reports, error tracking, Root Cause Analysis, preventive measures, and daily metrics. Required Candidate profile Grad/Postgrad in finance/accounting/management Strong written and verbal communication Data entry skills Interpersonal skills for teamwork Proficient in MS Office AP & AR Keen attention to detail

review and execution of SOP, Master BMR and BPR, Qualification document and Validation document.Responsible for review of Executed BMR/BPR.monitoring, verification and review of IPQA activities on shop floor of Injectable Department, as applicable Required Candidate profile Deviation, Market complaint& OOS related to shop floor. QA SOPs & IPQA , Calibration& Preventive maintenance Line clearance, IPQA Activity, BMR checking, BPR Verification, Sampling activity

Focus on APPLICATION ENGINEERING, PRODUCT DEVELOPMENT, VALIDATION, TESTING, RFQ REVIEW, PRODUCT DESIGN, CAD PACKAGING, DEVELOP PROTOTYPES, TEST PROTOTYPES, PREPARE DFEMA, TEST PROCEDURE, ENGINEERING SPECIFICATION, RECOMMEND DESIGN CHANGES, WARRANTY Required Candidate profile BE EEE/ECE/MECHATRO 10+yrs exp with AUTOMOTIVE/ COMMERCIAL VEHICLES / ENGG MNCs into APPLICATION ENGINEERING, PRODUCT DEVELOPMENT, VALIDATION, TESTING etc FEMALES preferred Must relocate to CHENNAI Perks and benefits Excellent Perks. Send CV to cv.ch2@adonisstaff.in

Dear Respect Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation QA Department Job description -4 -7 Yrs Development Quality Assurance / Formulation Quality Assurance R&D: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs,BDRs, PDRs, MFRs and MPR) SOP’s and Guidelines Preparation and Review and Approval of SOP’s. Responsible for conducting Internal Audits/External Audits for Cross functional Departments in Formulation Division and External Division. Conducting and Coordinating Employee Trainings. Responsible for Review and Approval of Vendor Qualification Please Share update resume: careers@biophore.com Ref to Friends or colleagues. Total Exp: Current CTC: Exp CTC : Notice Period: Designation:

Alembic Pharmaceuticals Ltd is looking for a Regulatory Affairs professional for the position of Assistant Manager/ Deputy Manager based at our Corporate Office - Vadodara, Gujarat. Job Criteria: B.Pharm or M.Pharm qualification having experience between 10 - 15 yrs. with dossier filling experience in MEXICO Countries. Knowledge for review of quality documents like executed batch documents, method validation, change Good communication skill Job Responsibility: Should have through knowledge of Mexico submission. Should have understanding for requirements of Mexico. Should have understanding for review of regulatory documents like batch record, specifications, COAs, stability data, change control, process validation report etc. Should have knowledge of review of method validations, chromatograms, dissolution profile, raw data etc. Interested candidate can share cv on creyesha.macwan@alembic.co.in

Roles and Responsibilities: Responsible for capturing additional detail information needed for the testing the backend APIs and integration points Responsible for the documentation of test scenarios, deployment of builds in lower environments on AWS Participates in estimation and planning of Testing, validations, deployment and operation activities. Responsible for effort estimation of overall testing activities for all software units based on provided functional specification Responsible for working closely with developers and business analysts. Tools Required: Performance tools - JMeter, Gatling, scala Version control knowledge - Git - Subversion Continuous integration experience - Jenkins Experience & Skills: Testing - Experience and a strong interest in system testing - Junit/TestNG - XPath - RestAssured - mock framework Request response (Must have) - Message Queue REST Certifications (Good to have): • ISTQB Foundation or similar

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities QUALITY ASSURANCE IPQA (Injectable), IPQA (OSD) & QMS / Documentation / Validation and Qualification (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. Injectable Manufacturing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI OSD Manufacturing / Dispensing / QMS (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification B Sc / M Sc / B. Pharmacy/ M Pharmacy / Diploma Time and Venue : 17th May 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in.

Qualification : Bachelor's degree in a related field or equivalent work experience. Years of experience : 1 to 4 Years relevant experience Required skills : Proven experience in technical document control or a related field. Strong knowledge of document management software and tools. Attention to detail and the ability to work with complex technical documents. Familiarity with project management Familiarity with industry standards and regulations related to documentation. Roles & Responsibilities Manage and control all technical documents, including engineering drawings, manuals, specifications, and procedures Ensure that all technical documentation adheres to regulatory and quality standards. Facilitate the retrieval of technical documentation Collaborate with subject matter experts to review and validate technical documents Ensure that all technical documentation adheres to regulatory and quality standards.