6078 Qms Jobs - Page 22

Job Responsibilities: 1. Review of Analytical Method Validations/ Verifications protocol/ reports 2. Review of Analytical Method Transfer protocol/ reports 3. Review & release of Reference standard characterization data 4. Review of R&D data and Lab note book for regulatory submission 5. Review of Instrument/Equipment Qualification & Calibration reports 6. Review of CSV (Software Qualification) documents (Protocol &Reports) 7. Review of DS & DP STPs (Reference standard, Raw Material, Intermediate, In process, Semi finished & Finished product). 8. Preparation, Review & training of CQA SOP (Related to R&D Labs) 9. Review of SOPs for R & D function (Analytical Research Laboratory, DDRL (Pilot L...

Job Title: Executive 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: - Method development & Validation by using sophisticated...

Dear Candidate , we are hiring for QC Jr Executive ,Down stream process executives & Operators. Open Positions-50 Down Stream Process Executives & Operators Required • Qualification: Bsc/Msc/ITI/B Pharmacy Experience in handling the following Equipment 1 Chromatography column and system handling. 2 Column Packing (BPG And Chromoflow) 3 TFF System 4 Centrifuge system 5 Filtration, Filter Integrity,Buffer Preparation,CIP_SIP PRODUCTION-DS M Pharmacy/Diploma/B tech/Any Degree 6 Expertise in documentation QMS/GMP Compliance / Process Awareness Biologics Company's only Preferable. • Experience: 2 to 6 years in Total Downstream CTC :up to 5.0 LPA. IMMEDIATE JOINERS ARE PREFERABLE" Interested candi...

Dear Candidate, WE ARE HIRING Department: - Production- DS Designation: - Dy Manager / Manager Qualification: - Preferably Post Graduation in Science Experience: - 15+ Years Age: - Between 35- 40Years Mandatory: - Should come in all shifts, including Night shifts Role: Shift-in-charge for entire DS floor Job Description: > Strong Functional knowledge of DS Biologics (Chromatography and related purification experience protein/ Insulin handling experience preferable). Capable of handling large teams as we have around 45 members in each shift, around 50% of contractual staff. Strong administration / team management capabilities to streamline GMP across the floor. Monitoring the efficiency of em...

KnJ Projects Private Limited is looking for Material cum Quality Expert to join our dynamic team and embark on a rewarding career journey. Develop and implement quality assurance policies and procedures. Conduct quality audits and inspections. Analyze data to identify areas for improvement. Provide training on quality standards and processes. Ensure compliance with regulatory requirements. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Flexinovus is looking for Functional/QA team members to join our dynamic team and embark on a rewarding career journey. Assist in software testing, quality assurance, and validation processes by creating test plans, executing test cases, and documenting results. Collaborate with development teams to identify and fix bugs, ensuring product stability and performance. Participate in requirement analysis and maintain detailed QA documentation. Support continuous integration and improvement initiatives. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourage job seekers to verify all details d...

KGVK (NGO & CSR Arm of Usha Martin Limited) is looking for Quality Control/Assurance Professional to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control systems to ensure products meet regulatory and customer standards. Conduct inspections, audits, and testing to identify deviations or defects. Collaborate with production and R&D teams to address quality issues and implement corrective actions. Maintain documentation and compliance with ISO and GMP standards for continuous improvement. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourag...

KGVK (NGO & CSR Arm of Usha Martin Limited) is looking for Quality Control/Assurance Professional to join our dynamic team and embark on a rewarding career journey. Develop and implement quality control systems to ensure products meet regulatory and customer standards. Conduct inspections, audits, and testing to identify deviations or defects. Collaborate with production and R&D teams to address quality issues and implement corrective actions. Maintain documentation and compliance with ISO and GMP standards for continuous improvement. Disclaimer : This job description has been sourced from a public domain and may have been modified by Naukri. com to improve clarity for our users. We encourag...

Job Description JOB Responsibilities: - Location: Ahmedabad 1. Ensuring the GMP compliance at CMO and Release of batch manufactured for US market at CMU. 2. Monitoring of process starting from dispensing to packing including witness analysis of Lupin products manufactured at CMO for US market and Domestic market. 3. Handling of market complaint with root cause identification and ensuring the CAPA implementation. 4. New product review to be carried out at manufacturing site after availability of all the documents. 5. Review and authorize Master Batch Records, stability protocol, process validation protocol, temperature cycling protocol, specification of in-process, intermediate and finished p...

Experience : 12-15 Years in the role of SQA, SEPG and Metrics Function Skills : Expert knowledge of CMMI SVC & DEV, ISO 20K and ISO 27K, ISMS, PIMS, HIPAA, Software Quality Assurance, Process Improvement & Definition, Data Privacy - GDPR & Six Sigma Green/Black belt would be added advantage. Expertise Skills: Experience in implementing various improvement standards like ISO, Models like CMMI SVC/DEV model till Maturity Level 5 Added advantage if performed ATM role in at least one CMMI Appraisal Experience in implementing ISO 20K & 27K, PIMS, Data Privacy standards and managing, conducting & reporting internal audits results Process definition Process implementation & facilitation Process Imp...

Reviewing advertisements as per code of advertisement Coordinating with Exchanges and Internal Stakeholders for the purpose of advertisements Reviewing content ofcommunication Digital and non-digital posted on social media Submissions of variousregulatory reporting to Regulators.

Responsibilities: * Drive end-to-end enterprise sales in pharma/life sciences. * Own lead generation, client pitching, pilot-to-deal conversion, and multi-site expansion. * Ideal for those with LIMS, QMS, or compliance software sales experience. Health insurance Sales incentives Performance bonus

WhatsApp 7483236645 for complete Job Description Required Candidate profile Must have knowledge of Machine & Components Inspection. 5 yrs as Quality MR must.

As a GSS Direct Procurement Specialist at Alstom, your primary focus will be on being the key Supplier Quality Development referent for the given scope. You will influence both Commodity strategy and suppliers to enhance the quality performance level of purchased parts and services through the qualification and development of suppliers. Your responsibilities will include driving systematic and continuous Suppliers Quality Performance analysis, supporting the procurement organization in all related processes, and conducting regular reviews at Commodity level to ensure the deployment of Supplier Development strategy. Key Responsibilities: - Deploy the Supplier Quality Development (SQD) strateg...

Duties & Responsibilities Execution of production plan Batch preparation and exchange as per the plan ,communication with shift leaders (shift reliving), Allocation of jobs in the respective shift,, Plan & execute fixture maintenance, Ensure process are inline with standards (QMS,EMS,Internal operation standards), Preventive maintenance of coaters, cleaning machine, Blasting machines, stripping equipment, Identify training needs of shift team members, plan and conduct trainings, Evaluate the effectiveness of the training Inform PM on trainings out of his scope, Communicate to service and plant manager in case of machine troubles/errors, Adhere and ensure everyone in the department follows to...

The jobholder acts as a member of Teva External Manufacturing and Supply Operations (EMSO), Jobholder closely interacts with the Team, the CMO Manager and QRM and if required other departments such as Operations, Procurement, Supply Chain, MS&T, and Regulatory Affairs and provides complete support from quality perspective, The position is to review the QMS documents like change controls, deviations, OOS/OOT, batch records associated with formulations that include various dosage forms of products supplied to EMSO The market is primarily for US, EU, UK and Canada, The jobholder will be responsible for review of QMS documents and ensuring that the supply is not interrupted due to the delay and ...

"QMS Knowledge of Regulatory standards CFR820 , ISO 13485 & 14971, 60601 Hands on experience on Risk Management Good understanding of Post Market Survey and complaint handling Design plan Medical Process DQC Deviation and CAPA preferred " " Be a part of core project team and support the quality engineering across the entire development cycle Lead product risk management, usability, reliability and design validation efforts for new product development and design change projects, Lead the development and implementation of design verification and validation plans with project design lead, Lead the development of Critical to Quality (CTQs), design input and output documents, Lead the fixture qua...

We are looking for skilled QA / QC Engineers to join our team at Rcad Solutions, playing a crucial role in ensuring the quality and reliability of our engineering and construction projects. The ideal candidate will have a strong background in quality control and assurance, with excellent analytical and problem-solving skills. Roles and Responsibility Develop and implement comprehensive quality control plans to ensure compliance with industry standards and regulations. Conduct regular site inspections to monitor progress and identify potential quality issues. Collaborate with cross-functional teams to resolve quality-related problems and improve overall project efficiency. Analyze data and pr...

Selection & Recommendation of inspection equipment. Overall responsibility for inspection and testing activities of products. Disposition of nonconforming products. Knowledge of SPC, APQP, PPAP, and 4M changes daily. Layered Process Audits. Quality Management System (ISO-TS 16949) Customer audits/visits and third-party audits. Lean manufacturing principles and methods Proactive process improvements focused on prevention (control plan) Ability to effectively communicate with suppliers and team members Ability to demonstrate leadership potential through a strong data focus and results orientation, and exceptional problem-solving. Strong organisational and project management skills, as well as ...

Candidate should be B.Pharm Candidate should have regulatory exposure/ in previous organisation Candidate should have well command on IPQA activities Candidate should have Command on packaging operations Candidate should be able to work in shift well aware with regulatory requirement

Handling of Manufacturing Compliance i.e. IPQA Activity Handling of QMS Documents like CAPA, and OOS and Change control Handling of APQR Handling of Batch release activity Good in communication skills Exposure of Regulatory audit

Jindal Advance Materials is looking for Quality - QMS Associate - Patherheri (- yrs) to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Assistance to Lead discipline engineer. Adherence to committed schedule and preparation ofmonthly progress report. Quality assurance: Adhere to QMS norms / maintainrequired documents as required for project scope of work. Preparing / checking of designs & MTO Checking and issue of IFC drawings pertaining to hisproject. Regularly checking and reviewing 3D model, throughSPR/other model reviewer to make it clash- free. Compilation of Data Bank/Documents. Field Engineering. Perform and produce Engineering deliverables bycarrying out analysis and design calculations using appropriate software. Maintenance of record prints, check prints, commentedprints and drawings/checklists. Upload the native f...

Define deliver a migration Charter and/or Statement of Work which fully articulates the optimum migration approach through partnership with a variety of stakeholders subject matter experts Lead migration meetings/forums, including Steering Committees and Working Groups to ensure consistent stakeholder understanding of migrations versus the demands of the business

Job Title : Reporting Analyst Location: Kochi Terms: Full Time Requirement : Need to work in nightshift and Weekend if applicable About the Role : An Underwriter is the person who decides whether or not to insure risks for which request has been submitted Underwriter s task is to evaluate a risk and make decision whether or not to provide the proposal for insurance after review the document which has been shared along with submission Responsibilities : Assign tasks need to finish within deadline Maintain the quality in each task