449 Process Validation Jobs - Page 14

Job Description Officer/Executive- Packaging Development 1. Design, preparation, review and approval of documents - OPMLs, BPRs, Specifications for Packaging materials, In-house Labels and Pallet Matrix. Checking of Artworks and Shade Cards for labels, Primary Secondary packing materials. 2. Execution and coordination for SAP related activities like loading of master recipes and Bill of Materials (BOMs) for Finished Goods (FGs). 3. Conducting different Trials for Packing Materials, 4. Monitoring and technical support for execution of Packing equipment qualification/ Trial / Scale up / exhibit / commercial process validation batches on packing lines and handling of investigations, if any duri...

Works independenly on creating test plans, executing tests, troubleshooting the issues, automating test cases, reporting bugs with all the required details, reviewing the tests, providing the test reports, analying test failures Capable of analyzing moderately complex challenges using analytical tools and data interpretation. Applies critical thinking to assess problems with relevant data independently to evaluate potential solutions after considering various possibilities. Engages in independent analysis and collaborates with others to gather insights and develop recommendations including challenging existing processes. Capable of working independently while actively contributing to team an...

As a QA (Quality Assurance) /Test Developer you will be designing better ways to identify potential weak spots, inefficiencies, and issues within software systems. This position will work closely with development teams and other test engineers in the implementation and delivery of software products that meet rigorous quality standards, budgets, and timelines. You will play a key role by delivering quality functions for development teams within test driven framework. Your scope will include Test Plan Development, Test Case Execution, Automation Testing, Data Creation, API Validation and incorporating test automation in the CI/CD pipelines. Your primary responsibilities include: Selenium Test ...

Hiring Sr. Quality Engineer to lead QA processes in automotive & assembly line. Handle PPAP, MSA, SPC, 8D analysis, QMS audits, and support production with corrective actions and quality system improvements. Required Candidate profile Diploma/B.Tech with 5+ yrs quality exp. in automotive. Hands-on in 8D, PPAP, MSA, SPC, and QMS. Strong in audits, documentation & RCA. Experience with suppliers, customer handling preferred.

Job Description Labware 7. LIMS implementation, Master data creation, Validation. Caluculation configurations. CSV documentations, Test Script review, Instrument integrations. LIMS trouble shooting and resolutions. QAMS activities, CCP, CAPA, Deviation investigation. Work Experience 4-7 years of experience in QC and LIMS Implementation Education Post Graduation in Analytical Chemistry or Analytical Chemistry Graduation in Pharmacy or Pharmacy Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

Responsibilities: * Conduct BPR reviews, process validations & batch manufacturing oversight. * Ensure compliance with industry standards through IPQA practices.

Job Description: We are looking for a dynamic and experienced Production Officer to oversee day-to-day production activities in our API manufacturing plant . The ideal candidate should have a strong understanding of batch processing, GMP compliance, equipment operation , and regulatory documentation . Key Roles & Responsibilities: Execute production activities as per batch manufacturing record (BMR) and standard operating procedures (SOPs) . Handle and operate plant equipment such as reactors, centrifuges, ANFD, FBD, dryers , etc. Ensure timely charging and discharging of materials and maintain strict compliance with process parameters . Perform in-process checks and report any deviation or ...

Will be responsible for Dossier preparation, review submission in ACTD/CTD/Country Specific format for Product registration. Review technical documents like process validation, AMV, Stability and composition etc, labeling, batch records, specification sheets. Co-ordinate with Plant / ADL / RD for documents samples. Co-ordination with API / PM vendors to resolve technical queries w.r.t. regulatory requirements. Assisting Export Manager in marketing business development activities. Candidate Criteria: Bachelor s degree in Pharmacy or other Life Science with excellent communication skills in English. Minimum 2 years of experience in regulatory affairs or in pharmaceutical formulation.

Overview Lead - Testing & Validation Responsibilities Design & process validation for all type of EM EGR. Basic knowledge of engine and its subsystem testing. Understanding of testing setup requirement of mechatronic components and EM EGR and Pneumatic EGR. Knowledge of mechanical testing setup and testing equipment\u2019s. Analysis of customer return parts and analysis. Support to application engineers to resolve customer queries. Mechanical Testing set up as per testing requirements. Analysis of customer returned samples & report generation Qualifications B Tech./ Diploma in Mechanical Engineering Essential skills Leakage measurements Flow Measurements Vibration Measurements Vibration data...

A.1 Job Purpose 2.1 Ensuring Procurement at optimum cost by partnering with procurement team in contracting and procurement 2.2 Ensuring Tax optimisation, Suppliers Credit financing and protection of Group’s Interest 2.3 To Lead Integration of RIL system with PMC’s and/or EPCM’s system and seamless data flow Insurance Adequacy at optimized cost and adherence of RIL SOP’s in contracting and procurement. A.2 Job Accountabilities 2.1 Contracting and Process Validation - Term Sheet Validation, Exhaustive POs Validation including Commercial terms, Insurance, Cost, Taxes, GCP/SCP, Suppliers Credit financing etc. 2.2 Certifications QSD Certification of Manpower billing of Contractors, Payroll & oth...

Develop thorough test plans and document the results and progress Develop in-depth functionality and stability automatic tests that will map customer use cases Research the right set of workloads and benchmarks Develop automated test scenarios and environments for End2End automatic evaluation Collect test evidence measurements to ensure system functionality, stability and scalability Establish automatic measures to assess the accuracy Analyze results to find ways to improve functionality coverage Analyze root causes and identify areas for improvement Collaborate with development teams to drive resolution for issues and improvement Generate test automation summary reports for stakeholders rev...

Description: Manager QC, is responsible for Managing the activities of the quality control laboratory to ensure timely delivery of materials for use in production and releases of finished products from the laboratory as committed, ensure testing of stability samples within structure of timelines identified in relevant SOP, ensure laboratory activities on par with compliance expectations, and provide top notch inter- and intra-department customer service. Essential Functions: Manage the day-to-day operations of the Quality Control laboratory including setting and communicating priorities based on the production schedule. Maintain knowledge of the potential impact of Quality Control activities...

Hiring Production Chemist for nutraceuticals. Must have experience in tablet, capsule & liquid formulation, scale-up, BOM management & regulatory compliance. Pharma degree required. Strong knowledge of production & quality processes essential.

Knowledge of Machine Programming with Macros & Can understand Virtual Tool Path Knowledge of Auto Cad Basic Knowledge of Sliding Head Machines Knowledge of Machine setting & Troubleshooting, tool selection Knowledge of CNC Jaw formation Required Candidate profile Core Tools knowledge (APQP, PPAP, FMEA, SPC & MSA) Knowledge of Process Design & Part Feasibility Knowledge of Process Validation Knowledge of ECN handling

Dear All, We are conducting Walk-In Interview on 13th June 2025(Friday) for Quality Assurance and Quality Control( Formulations ) departments. Quality Assurance: AQA - 6-8 Years of experience in Analytical QA IPQA - 2-4 Years of experience in Line Clearance activities for Production, Warehouse and Dispensing of Raw Materials Quality Control: IPFP - 4-5 Years of experience in HPLC, GC, UV, Dissolution and RS. Stability - 4-6 Years of experience in Dissolution, GC, UV and Sample management Raw Materials - 2-3 Years of experience in sampling of Raw and Packing materials Analytical Method Validations - 3-5 Years of experience in Method validations, HPLC and Dissolution instruments Microbiology -...

Sr. Executive AM- Hot Refining: CMR GreenTechnologies Limited CMR Group is India's largest producer ofAluminium and zinc die-casting alloys. With 13 state-of-the-art manufacturingplants across the country, CMR has become the preferred supplier for many ofIndias largest automotive industry leaders. Since its inception in 2006, CMRhas consistently outpaced competition by focusing on delivering superior valueto its stakeholders. This value is driven by a strong commitment to technicaladvancements, quality enhancement, sustainability, and people-centric practices.We believe in an " Employee First " philosophy, ensuring that our people are at the core of our success. Our dedication tofostering an...

Role & responsibilities 1) To perform line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labeling and packing 2) To perform Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. 3) To issue and control of SOPs, BMRs, BPRs, BCRs and also finished product label/product container seals /sealing of the containers as the part of IPQA activities. Preferred candidate profile

Job Summary: We are seeking a highly skilled and detail-oriented Quality Control (QC) Engineer with 35 years of experience in quality inspection, process validation, and compliance monitoring. The ideal candidate will ensure that our products meet internal and external standards and comply with regulatory and customer requirements. You will work closely with cross-functional teams, including Production, R&D, and Supply Chain, to drive continuous quality improvements in a high-performing, fast-paced environment. Key Responsibilities: Perform inspections of incoming materials, in-process items, and finished products to ensure compliance with specifications and industry standards. Develop and i...

Responsibilities: Performing requirements analysis to develop overall testing strategy & individual test cases & protocols. Identify testing requirements & dependencies Work with relevant experts for generating testing Jigs and dependencies Performing unit testing, integration testing, and pilot unit verification and validation for all Electronic/Hardware/Embedded/Mechanical/Optical subsystems. Handle all V&V documentation including creating and maintain verification test plans & generating final reports. Work with design team to debug issues and perform root cause analysis. Coordinate with regulatory teams for identifying & performing 3rd party tests. Perform Component level validation and ...

Audit verified statements processed by KPO Associates to ensure accuracy. Validate that mismatches and discrepancies have been correctly identified and classified. Provide detailed feedback and highlight errors or inconsistencies for corrective action. Prepare comprehensive quality reports and recommend process improvements. Ensure compliance with Standard Operating Procedures (SOPs) and regulatory guidelines. Participate in calibration exercises and training sessions to maintain quality standards. Required Skills: Audit, Quality Assurance, Process Validation, Reporting, Compliance, Analytical Skills Qualifications: Bachelor's degree in any discipline (Finance or Commerce preferred) 5+ years...

Role & responsibilities • You will be responsible for documentation and execution of qualification activities. This includes preparation, review and execution of URS (User Requirement Specification), DQ (Design Qualification), FDS (Functional Design Specification), UTM (User Traceability Matrix), IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), RQ and (Requirement Qualification) documents. • Your responsibilities include review of miscellaneous qualification documents and preparation and review of risk assessments for equipment and systems. • You will be responsible for new project related FAT (Factory Acceptance Test) and SAT (Site Acceptance ...

Role & responsibilities Preparation & review Protocol & Reports of Process validation, cleaning validation, CEHT/DEHT study and wet cake hold time study. Preparation, review and tracking of periodic evaluation of validated process. Review of Qualification documents like URS, DQ, IOQ, PQ, Requalification, Verification Qualification, temperature mapping, etc. Monitoring the validation (Process/Cleaning) activities. Verification of Analytical records, Executed Batch Production Record and Equipment Cleaning Record as a part of Process Validation and Cleaning Validation. Please share profiles with job title on gaurangikudavkar@lupin.com

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 3-10 yrs in API Location - Mysore Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical/BSC Chemistry Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental pro...

Must to have experience on new product development, technology transfer, and process validation from R&D to pilot scale and further to commercial production. Develop BFD, PFDs, and P&IDs for new products and process trials.

Role & responsibilities Aurobindo Pharma Ltd. Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Assurance (Market Complaints / QMS / Validation / IPQA) Quality Control (GMP / GC / LCMS / HPLC) 3 Experience Required: 2 7 years (pharmaceutical manufacturing) Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Quality Assurance Key Scope • Handle Market Complaint investigations, trend analysis and regulatory responses • Maintain site QMS: Deviations, CAPA, Change Control, Audit readiness • Execute and review Equipment / Process / Cleaning Validation documentation • Perform IPQA activities: line clearance, in-process checks, batch recor...