5.0 - 9.0 years

0 Lacs

andhra pradesh

On-site

Job Description: To apply to a Varex Imaging position, please create an account and sign-in. CURRENT VAREX IMAGING EMPLOYEES: Please apply by logging into your internal Workday Account. Varex Imaging, headquartered in Salt Lake City, USA, is a leading innovator, developer, and manufacturer of X-ray imaging component solutions, which includes X-ray tubes, digital flat panel detectors, software, and other key components of X-ray imaging systems. Your Role: Performs product inspection and/or audits of quality control programs. Performs packaging line and manufacturing inspections, and sampling and testing of incoming components and raw materials. Ensures raw materials, in-process and finished products meet company standards. May apply approval or rejection labels to bulk raw materials once analytical data is evaluated. May draft procedures and assist with validating or troubleshooting testing methods, including assays. May assess draft and final label copy, using knowledge of labelling regulations. Minimizes downtime by reducing production rework and recalls. Your Profile: - Bachelors degree in mechanical engineering - Possess in-depth knowledge about the IQC Equipments, CMM, Calipers, Height Gauge, Image Dimension Measurements etc. - Expertise in CMM (Mitutoyo) - Interpret and apply GD&T (Geometric Dimensioning and Tolerancing) to validate parts. - Ability to read Engineering drawings and create inspection Plans and Programs. - Conduct hands-on inspection of machined parts, ensuring high accuracy measurements and adherence to quality standards. - Incoming Quality Checks Background - ISO-13485 desired - Experience with SAP software desired. - 5+ years of related experience What we offer: - A unique opportunity to become part of a growing organization in India being a part of a global market leader in X-ray imaging components. - Excellent development potential. - An international work environment with global teams collaborating on various projects across several countries. - Competitive compensation package including participation in Varex incentive plans. - Corporate Health Benefits. - Additional benefits will be added as we grow. Time Type: Full time Job Type: Regular Work Shift: N/A,

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Senior Executive - Regulatory Affairs Labelling Piramal Enterprises

4.0 - 6.0 years

0 Lacs

Mumbai, Maharashtra, India

On-site

Job Description : Business: Piramal Critical Care Department: Regulatory Affairs Location: Kurla Travel: Low Job Overview Responsible for all artworks and labeling components of Piramal Critical Care Products Worldwide with adherence to the labeling processes, ensuring compliance with innovator labeling, internal & external partners, and GMP standards and specifications. Participate in a cross-functional team environment as necessary to ensure labeling documents and associated change requests are medically and scientifically accurate and that they comply with regulatory standards, meet company needs and accurately assess current strategy and global regulations Key Stakeholders: Internal Cross-Functional: Sales, Marketing, Manufacturing, Supply Chain, Medical Affairs, Quality Assurance, Quality Control, Pharmacovigilance, Planning, Project Management, Senior Leadership team Key Stakeholders: External Country Distributors, Health Authority (HA), CMOs and external partners Reporting Structure Reports to: Manager - Labelling ESSENTIAL QUALIFICATION: Bachelor degree or Master's degree in Pharmaceutical sciences or equivalent Experience 4 years relevant regulatory experience (Global experience including US, EU and major Rest of World markets preferred) Roles and Responsibilities: Global labeling details (labels, cartons, package inserts, patient package inserts) to ensure quality and accurate compliance, evaluations, maintenance, reviews and approvals with cross-functional teams for regulatory submissions Preparation of Labelling related documents ex: SmPC, PIL and Labelling texts for submission in EU region. Coordinating with the different stakeholders for timely labeling related submission/approval and query solving. Proofreading all types of label copy/annotation/etc. at all developmental stages as well as final label copy to ensure accuracy of labeling Creation of SPL for US Human and Vet product submissions, drug listing, annual establishment registration and annual self-identification for GDUFA Monitor and process innovator-labeling updates for existing generic products and ensure compliance with innovator updates, including side-by-side comparison with RLDs Responsible for coordination of CCDS development and updates of PCC products and coordination of local labeling updates Contribute to the development and/or review of all labeling aspects included in Promotional Material. Development and maintenance of a central repository for all labeling components Competencies Must have solid interpersonal and organization skills for interfacing with others. Knowledge of Health Authority labeling regulations and requirements. Self-directed, motivated, organized, flexible and accountable. Excellent work ethic with a positive, can-do attitude to succeed in a fast-paced environment. Project management skills is a plus

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