449 Process Validation Jobs - Page 18

Seeking a Process Engineer (Projects & Engineering) , experienced in Designing and optimizing processes, risk assessment, process validation, process improvement, regulatory compliance, data analysis, etc. Required Candidate profile Experience - 14 years and above Location - Ahmedabad Industry - Pharmaceuticals

Set up bolus compression machines acc. to production specifications, Adjust machine settings, Identify & report mechanical issue, Load raw materials (powder/granules) into the machine hoppers, Maintain accurate production logs.

Vibonum Technologies Private Limited conducting a Walk-in interview in Quality Assurance department for its OSD Plant at Nanjangud, Mysore. Kindly carry your, latest 3 Months salary slip, appointment letter with CTC breakup and previous company relieving letters. ----------------------------------------------------------------------------------------------------------- Open vacancies in Quality Assurance for: IPQA Manufacturing : Exe > 08-10 Yrs IPQA Packing & Warehouse : Exp > 8 - 16 Yrs QMS: Exe / Sr. Exe : Exp > 08-10 Yrs CSV / ITQA/ Electronic DI compliance : Exp > 10-12 Yrs Process Validation : Exp > 08-10 Yrs AQA / Lab QA : Exp > 08-10 Yrs Documentation Cell : Exp > 04-08 Yrs AM/DM/Man...

We are Hiring for New product Introduction ( NPI Stamping Component Development ) for our Electronic Component Manufacturing in Oragadam Chennai Job Description: Stamping NPI Quality Engineer Position Overview: We are seeking a highly skilled and detail-oriented Stamping NPI Quality Engineer to join our team. The ideal candidate will play a crucial role in ensuring the successful introduction of new stamped parts, ensuring all products meet the highest quality standards and specifications throughout the product lifecycle. This role involves working closely with design, engineering, and production teams to guarantee that new stamping processes and products are validated for quality, manufactu...

Roles and Responsibilities Develop and implement standardized processes to ensure consistency in manufacturing operations. Improve productivity through effective resource utilization, workflow optimization, and process enhancements. Drive quality improvement initiatives to meet and exceed product standards. Conduct and monitor Run @ Rate trials to validate process capability. Prepare and maintain process flow charts to document manufacturing steps and sequence. Perform PFMEA (Process Failure Mode & Effects Analysis) to identify and mitigate risks. Optimize OEE (Overall Equipment Effectiveness) to maximize machine and manpower utilization. Lead cycle time improvement projects to increase thro...

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 Receiving user indents, verifying with approved budget, and floating RFQ to the vendor (minimum 2 to 3 vendors). Preparing a worksheet to validate supplier quotes based on cost, quality, OEM, and delivery lead time Knowledge of SAP for PO release. Create PSR and follow the PSR approvals stage-wise. PO release. Monitoring material delivery against committed vendor dates. Coordinating with the maintenance team for installation and commissioning. Coordinating with the logistics team. Coordinating material in warding and acceptance, and vendor payment. Asset management and handling the Audits Generating and circulating reports to management. Relevant Experience: Mechanical and Electrical, Co...

We are hiring for the role of QA - Executive at JLL!! Department: Quality Assurance Location: Silvasa Engg. Division, Silvasa Experience Range: 4 to 5 Years Qualification: Post Graduation Diploma in Plastic Processing and Testing from CIPET Role & responsibilities Making the required standard quality documents, reviewing and ensure to implement at Silvasa Engg. Division. Strong technical Process knowledge on Packaging Machines as well as good understanding of mould validations Protocols. Basis coordination with all the QA personnel at all the units and with Corporate QA team. Coordination with Corporate Quality Team for packaging samples for continuous quality evaluation. To handle all marke...

We are hiring for the role of QA - Executive at JLL!! Department: Quality Assurance Location: Silvasa Engg. Division, Silvasa Experience Range: 4 to 5 Years Qualification: Post Graduation Diploma in Plastic Processing and Testing from CIPET Role & responsibilities Making the required standard quality documents, reviewing and ensure to implement at Silvasa Engg. Division. Strong technical Process knowledge on Packaging Machines as well as good understanding of mould validations Protocols. Basis coordination with all the QA personnel at all the units and with Corporate QA team. Coordination with Corporate Quality Team for packaging samples for continuous quality evaluation. To handle all marke...

Experience in QMS Section. Change Control, Deviations, CAPA, OOS, OOT, Batch Release Audit

As a Solution Tester, you will be responsible for: 1. Designing and automating test suites to ensure reliability of the system z(s390x) platform technology 2. Having a client-first mindset to test at scale and imitate customer-like environments 3. Creating strategies and scripts to test new features and functionalities 4. Contributing and reviewing code for internal and external repositories 5. Documenting processes (Test plans) and procedures for clarity and reproducibility 6. Interacting with counterparts in US/Germany teams and Red Hat Required education Bachelor's Degree Required technical and professional expertise Required Technical and Professional Expertise with relevant experience o...

Work in an agile, collaborative environment to understand requirements, design, code and test innovative applications, and support those applications for our valued customers Automate testing in both on premise and cloud environments Build and manage testing environments, assisting in debugging application issues Contribute to our continuous improvement and continuous delivery while increasing maturity of our agile adoption practices Perform exploratory testing, discover defects/bugs and works with coders to determine root cause and how to prevent similar issues from happening in the future Required education Bachelor's Degree Preferred education Master's Degree Required technical and profes...

Major purpose of the job : • To ensure compliance of procedure and practices in line with GMP guidelines and regulatory expectations for concerned manufacturing facilities and products of Biotech division, Cadila Pharmaceuticals Ltd. • To coordinate and ensure execution of validation/qualification activities Principal Tasks and Responsibilities: Ensure timely release of Drug Substance (Bulks) manufactured in Biotech Division Managing, mentoring and tracking activities of team, Troubleshooting of key issues and reporting to HOD and management Managing External as well as Internal Audit and Audit compliance related activities Ensure Training index/training needs and completion of Team Ensure t...

Responsibilities: Participate in management review meetings. Review of department trend analysis reports and internal studies or investigations. Ensure corrective action is initiated when required. Provide complete analysis of test results, investigation or information studies. Be capable of assuming study director responsibilities for all routine testing as well as certain advanced or specialized studies as requested by clients. Duties may include test scheduling, test preparation, proper application of test method(s), data collection, data review, and approval of final report of analysis. Maintain thorough knowledge and understanding of all SOPs pertaining to microbiology/sterility assuran...

Responsibilities: Preparation, Review and Issuance of Departmental Sops, Guidelines and Policies. LNB's and Logbooks Issuance and Checking for daily entries in Logbooks. To Review various Documents like Change controls, Incident Reports, CAPA, OOS Results, Deviations, Issuance Records and Internal Audit Reports. Prepare, Review and Maintain Qualification Documents, Review Instrument Calibration Reports QMS activities Training of New Employees, Preparation of Job Description, maintaining Training Files. Issuance of various documents like LNBS, Logbooks, Formats, Register, Sops, Lists, Job Descriptions etc. Allocation of Equipments /Instrument Numbers, Product and employees Code, Register and ...

Job Overview TE Connectivity's Quality Control and Reliability Teams ensure product and / or product components comply with specifications and quality standards. They test and inspect products against performance and integrity criteria to ensure product quality and reliability, and to determine the suitability of product release. Responsibilities The AQE team leader will be responsible for leading and managing a team of 4 - 5 advanced quality engineers on the Quality system activities in APQP & PPAP. Understand Customer drawings, Technical requirements, Quality requirements, CSR and cascade the requirements to CFT Exposure to Design and process validation testing and understanding test speci...

Ensure compliance with cGMP guidelines Batch Manufacturing Record preparation Packaging Material Specification Preparation APQR New drug application Batch card preparation Endorse documents preparation Required Candidate profile Experience in Quality Assurance of 5 years Gender Male

Job Responsibilities: To ensure implementation of cGMP norms in manufacturing areas To give line clearance in dispensing, manufacturing and packaging To monitor dispensing, manufacturing and packaging Sampling of In-process, finished stage and process validation batches and forwarding the same to Quality Control department for analysis To ensure that gowning and entry/ exit procedures are followed as per standard procedures Monitoring of environmental conditions (temperature, humidity & pressure differential) in manufacturing areas To carry out IPQA checks in manufacturing and packaging areas To ensure online documentation To verify that the appropriate qualification, calibration and prevent...

Analyze quality standards for components, materials or services. Apply measures, sampling methods, testing methodology and other procedures that ensure that quality standards are met. Apply quality principles, analyze quality records, prepare reports and recommend improvements. Conduct inspection, verification and validation of components or materials used in development processes. Identify and address recurring problems either with the quality of the product or the reliability of testing procedures. Document quality issues and performance measures for management review. May liaise with external vendors. This is an individual contributor role that requires the use of judgement in applying pr...

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary A role-holder to handle/supervise the manufacturing activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation. Job Responsibilities Works in a safe manner collaborating as a team member to ach...

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary A role-holder to handle/supervise the manufacturing activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation. Job Responsibilities Works in a safe manner collaborating as a team member to ach...

Job Title: Executive Formulation Research & Development Orals Business Unit: R&D1 Regulatory Affairs Job Grade G12A Location : Baroda At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Job Description: Literature search, product...

1.To Initiation , review and conduct Calibration of IPQA Instruments. 2.To review all usage logs of Manufacturing and Packing Area. 3.To review and follow up for Annual Maintenance Activity of IPQA Instruments. 4.To fill and review IPQA instruments log books. 5.To review and provide Line Clearance for Manufacturing Equipments / Packing Equipments.

ApoPharma, a member of the Apotex group of companies, is a pharmaceutical company devoted to the discovery, development and provision of new medicines to help improve the quality of life of patients with debilitating and life-threatening diseases. Investigation into the pathological role of iron in human disease, and how to use novel medicines to treat conditions created or worsened by iron, is a major research focus of ApoPharma. Job Summary A role-holder to handle/supervise the Manufacturing activities and to ensure the on-time production and delivery of product with quality compliance and cost improvisation. Job Responsibilities Works in a safe manner collaborating as a team member to ach...