449 Process Validation Jobs - Page 17

Role & responsibilities Skills : Candidates should have thorough exposure and proficient knowledge in the following areas at a minimum: Cleaning validations Process validations and continuous process verification Investigations of Out-of-Specifications (OOS)/deviations Review of all documentation (i.e. batch records, test results, deviation, LIR, OOS, CAPA, validation, COA, Change Controls, etc.) prior to disposition (release or rejection) of batch. Review of executed document like batch record etc. and also to ensure on time compliance of errors/deviations identified (if any). Review of step-by-step performance and compliance to batch manufacturing and packaging record requirements and reso...

Key Roles Responsibilities: 1. Oversee and support the overall activities during the product development life cycle from quality perspective in RD (API and intermediates). 2. To understand the site needs with respect to system establishment and sustainability. 3. Author/ Review and approve the SOPs/work directions required for implementing the Quality systems in RD activities as per GLP and regulatory requirements. Ensure effective implementation of SOPs/ work directions. 4. Review and approve Lab Familiarization Reports (LFR), Product development reports (PDR), Technology transfer, product specifications STPs, analytical method validation, method transfer, qualification, calibration, proces...

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 Notice Period - 1 month ( maximum) Location - Mysore ( Nanjangud) Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical Salary- 20% to 30% hike on current ctc 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 instr...

We are seeking a highly skilled and motivated Process Engineer to join our team at Morepen Laboratories Ltd, a leading organization dealing in manufacturing of home diagnostics medical devices. The Process Engineer will play a crucial role in optimizing manufacturing processes, ensuring product quality, and driving continuous improvement initiatives. This role requires a strong understanding of manufacturing principles, medical device regulations, and process improvement methodologies. Role & responsibilities Process Optimization: * Analyze and optimize manufacturing processes to improve efficiency, reduce costs, and enhance product quality. * Develop, implement, and validate process improve...

Hikal Ltd is looking for Assistant Manager to join our dynamic team and embark on a rewarding career journey Supervises daily operations and team performance Assists in strategic planning and business development Ensures compliance with company policies and procedures Supports senior management in decision-making

Msc in Chemistry, Synthetic R&D, Organic Chemistry, API industry, Process development, Process validation

Key Responsibilities: Technology Transfer: Lead the transfer of pharmaceutical formulations, processes, and technologies from R&D to commercial production. Develop and execute technology transfer protocols and ensure successful execution of transfer to manufacturing sites. Troubleshoot and resolve technical issues during the transfer process. Collaborate with both internal teams and external contract manufacturing organizations (CMOs) to ensure smooth transfer of knowledge and materials. Formulation Development (FD): Participate in the development and optimization of formulations for drug products, focusing on scalability and manufacturability. Work on the scale-up of formulations from lab t...

Job Location: Bhavnagar Navi Mumbai Company description Diversity Statement About the Role: Ferrero is manufacturing surprises and KJ packing at supplier end, to ensure quality supplies this post is required, below are the details of objectives for this position. Implementation and Ensuring that Ferrero quality standard and protocol are well practiced and followed at vendors producing surprises and packing. Performing supervisions providing guidelines for continuous improvements on quality, safety and hygiene standards. Coordination with the supplier, taking follow ups and guiding the supplier for to meet the other compliance audits like CCC, TISI, Disney etc. Main Responsibilities: Supervis...

business development - Warehouse PPC/BD-W/1312211 Contract Logistics PPL Head Office Posted On 16 Apr 2025 End Date 31 May 2025 Required Experience 3 - 5 years ShareApply Basic Section No. Of Openings 1 Designation Grade Assistant Manager - M3 Freshers/Experience Experience Employee Bonus One Month Organisational GPCOMP Pon Pure Chemicals Group Company Name Pon Pure Logistics Private Limited Department Contract Logistics Country India State Tamil Nadu Region Chennai Branch PPL Head Office Skills Skill Sales & Marketing Skills Communication skills Customer Data Minimum Qualification Under Graduate CERTIFICATION No data available Working Language English Hindi Tamil About The Role Person shoul...

Apply now » .buttontext67bbcd0b84b126cf a{ border1px solid transparent; } .buttontext67bbcd0b84b126cf a:focus{ border1px dashed #00a3e0 !important; outlinenone !important; } Currently at TechnipFMC? Apply here. Intern/Apprentice Subsea/Surface Engineering Location: Hyderabad, IN #job-location.job-location-inline {displayinline;} Employment type: Employee Place of work: Office Offshore/Onshore: Onshore .buttontext3b34abe12d83182e a{ border1px solid transparent; } .buttontext3b34abe12d83182e a:focus{ border1px dashed #5B94FF !important; outlinenone !important; } .buttontexta77353c8ab1a0824 a{ border1px solid transparent; } .buttontexta77353c8ab1a0824 a:focus{ border1px dashed #5B94FF !importan...

Project Role : Data Platform Engineer Project Role Description : Assists with the data platform blueprint and design, encompassing the relevant data platform components. Collaborates with the Integration Architects and Data Architects to ensure cohesive integration between systems and data models. Must have skills : Graph Databases Good to have skills : Life Sciences, Autosys Minimum 7.5 year(s) of experience is required Educational Qualification : BE Summary :As a Data Platform Engineer, you will be responsible for assisting with the blueprint and design of the data platform components. Your typical day will involve collaborating with Integration Architects and Data Architects to ensure coh...

Manufacturing Engineering Design Manager Job Title: Manufacturing Engineering Manager Location: Mysore Karnataka Industry: Consumer Appliances / Food Tech Reporting To: Operations Head Job Summary The Manufacturing Engineering Design Manager will be responsible for overseeing the process development and manufacturing engineering of product at a contract manufacturer (CM). This role will ensure the successful transition of product design to scalable and cost-effective manufacturing, maintaining high quality and reliability standards. The candidate will collaborate with design, quality, and supply chain teams to establish robust production processes and drive continuous improvement. Key Respon...

QA & QC Executive Job Description Position Overview The QA & QC Executive is responsible for ensuring that products meet quality standards and regulatory requirements through systematic inspections, testing, and process monitoring. This role involves collaboration with production teams to implement corrective actions and continuous improvement initiatives. Key Responsibilities Quality Control & Inspection Conduct inspections on raw materials, in-process products, and finished goods to identify defects or deviations from quality standards. Utilize measurement tools and testing instruments to verify dimensions and other quality criteria. Monitor all operations that affect quality and report ma...

Role & responsibilities Conduct in-process checks during various stages of sterile injectable manufacturing, including dispensing, compounding, filtration, filling, and sealing. Perform line clearance and area clearance before the start of manufacturing and packaging operations. Monitor aseptic practices and personnel hygiene compliance inside cleanrooms and controlled areas. Verify critical process parameters and environmental conditions during batch processing. Ensure compliance with SOPs, batch manufacturing records (BMR), and batch packaging records (BPR). Participate in visual inspection activities and oversee container-closure integrity checks. Monitor the usage and replacement of ster...

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...

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety, and quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Job Description Preparation & Review of SOP’s of QA system and review / approval of SOP’s of other departments. Review of master BMR/BPR of commercial and exhibit batches. Review of BMR / BPR, scale-up and placebo batches. Review of executed BMR/BPR of commercial and exhibit batches for batch release. Issuance, Retrieval & Destruction of SOP’s, STP, specification, BMR/BPR, annexures & other formats. Login and review of quality system documents such as Deviation and IPOOS. In-process Quality Assurance during Production / Packing activities. Sampling at different stages of manufacturing / packing as per the requirement (In-process, BU, CU, finished, control, QP, Hold Time & stability etc.) Rev...

Hii, Greetings from Avani consulting ! We are hiring for Production Officer/associate for a leading Pharma API Manufacturing company Position- officer/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...

You will be part of a strong, modern team culture driven to create world-class development and deployment environments, delivering an industry leading user experience for our customers. Working out of a modern office in the heart of the city, you will be valued for your contributions in a rapidly growing organization with dynamic opportunities. Each day, you will attend daily team scrums and project meetings to make important contributions in the development, test and architecture of automated solutions to continue building and optimizing our cloud and deployment infrastructure. The Cloud QA Tester is a key role in the growing and dynamic IBM Automation organization. As a QA Tester for Cloud...

Department: Quality AssuranceReporting To: Quality Assurance Manager / Team LeadJob Summary: We are looking for a detail-oriented and proactive Senior Executive Quality Assurance to ensure our products and processes consistently meet quality standards. The role involves conducting inspections, supporting quality control processes, identifying defects, and assisting in continuous improvement initiatives. Key Responsibilities: Perform quality inspections and tests to ensure products and processes meet defined standards. Monitor production processes for compliance with quality specifications and identify areas for improvement. Document and report non-conformities and assist in root cause analys...

Office Administration HO Asset Tracking, asset allocation and Records1) 0 Gap 2) No Policy Violation 3) No Customer GrievanceCheck all AIS Admin on-line portals as a checker and escalate deviations to Sr Executive Admin1) No Gap 2) Maximum 1 working day to escalate gapsBooking of Hotels, Guest House, Taxi for outstation employees, expats etc1) 0 Gap 2) No Policy Violation 3) No Customer GrievanceVehicle Fuel, R&M and Trackers1) 0 Grievance 2) No SOP violation 3) Within budgeted costMISAll Corp Admin MIS except MIS handled by Unit Head Admin for specific office1) Maximum 3 working days gap to updatation 2) No Policy Violation Location Issue Logs- Plan, execute, Record and share MoM1) No Gap 2...

Role & responsibilities 1. Preparation of Drug Master File for US, EU and Row countries according to year plan. 2. Preparation and submission of Annual Reports, Amendments and updates to filed DMFs. 3. Preparation and Submission of responses to queries from customer and regulatory authorities. 4. Preparation of Technical information package (TIP) based on customer requirement. 5. Adequacy review of documents required for Drug Master File & TIP preparation like BMR, process validation reports etc. 6. Coordination with R&D, Quality Control and Quality Assurance to collect required documents. 7. Evaluation of impact of changes to the submitted DMF’s. Preferred candidate profile Only API - Indus...

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...

Novo Nordisk Global Business Services (GBS) India Department Commercial DD&IT, GBS Are you passionate about IT validation and compliance? Do you want to play a pivotal role in ensuring regulatory adherence and driving innovation in a global pharmaceutical company? If you have the expertise and enthusiasm to lead in this critical area, we want to hear from you! Read on and apply today. The position As a Lead IT Validation & Compliance at Novo Nordisk, you will be entrusted with the following responsibilities: Ensure IT compliance by monitoring adherence to regulations like GDPR and GxP, aligning systems with evolving standards, and enforcing internal policies. Lead IT system validation by man...

Job Description QA-Qualification Injectable /Parenteral (Officer/Senior Officer/ Executive) Job Location Sanand, Ahmedabad (Injectable Facility) No of Position - 03 Total Experience - 2-7 Years in Injectable Manufacturing Education B. Pharmacy/M. Pharmacy Will appreciate immediate joiner for this role Oversight and Governance QA ensures that all qualification activities (DQ, IQ, OQ, PQ) follow Good Manufacturing Practices (GMP) and regulatory guidelines (e.g., US FDA, EU GMP, WHO). Participates in project planning for qualification activities. Reviews and approves Qualification Master Plan (QMP). Document Review and Approval: QA is responsible for reviewing and approving all qualification do...