Google Ads Manager | Consultant | To The New TO THE NEW

4.0 - 6.0 years

6 - 12 Lacs

Noida

Hybrid

Job Summary/ Your Role in a Nutshell: The ideal candidate will be responsible for setting up and maintaining ad units, configuring line items, and implementing advanced targeting and yield optimization strategies. This role involves close collaboration with content, tech, and product teams to ensure seamless ad delivery, troubleshoot issues, and drive revenue growth. A deep understanding of programmatic advertising, video ad formats (VAST, VMAP, VPAID, SSAI), and performance analysis tools is essential. This is a project-based hiring opportunity with an initial visibility of 3 months, which may be extended based on business requirements and individual performance. What you'll do: Create and manage Google Ad Manager (GAM) inventory: ad units, placements, and line items Video Ad Setup in GAM on VOD and Linear channels Set up and optimize ad unit IDs for web/app environments to ensure maximum fill rates and revenue Configure and manage line items (sponsorship, standard, network, house, etc.) across various priority levels Implement targeting rules including geo, device, browser, audience segments, and custom key-values Collaborate with content, tech, and product teams to ensure correct ad tag integration and delivery Optimize ad yield through header bidding, floor price management, and AdX/AdSense integration Monitor ad performance metrics (e.g., CPM, CTR, Viewability, Fill Rate) and recommend improvements Troubleshoot ad serving and delivery issues using Google Publisher Console, Ad Inspector, and network debuggers Ensure compliance with ads.txt, privacy regulations (GDPR, CCPA), and platform policies Prepare regular performance reports and revenue forecasts What you need: Bachelors degree in Technology/Marketing/Advertising/Business, with 4+ years of experience Strong hands-on experience with Google Ad Manager (GAM 360 preferred), AdSense Knowledge on configuration of Client Side Video Ad using VAST, VMAP, and VPAID, and Server Side ad using DAI, SSA,I etc. Deep understanding of ad serving logic, programmatic ads, and revenue optimization Familiarity with ad trafficking, line item types, targeting capabilities, and DFP tags Proficient in analyzing data via Google Analytics, Ad Manager reports, and other tools Working knowledge of third-party demand partners (SSPs, DSPs, header bidding platforms) Basic understanding of HTML, JavaScript, and debugging tools (Chrome DevTools, etc.)

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Sr Quality Engineer Amgen Inc

4.0 - 6.0 years

6 - 8 Lacs

Hyderabad

Work from Office

The Sr Quality Engineer will be an integral part of the design and development of combination products, providing quality oversight of the processes and deliverables generated throughout development and commercialization. In addition, this role will also support various aspects of the product lifecycle including complaint investigations, expansion and transfer of products to new manufacturing sites, inspection readiness activities, and platform support and improvements. Responsibilities: Provide Quality technical expertise, Quality oversight, and serve as a single point of Quality contact for combination and non-combination products associated with final product activities. Ensure program alignment and proper linkages within the Design and Development Plans, Risk Management Documentation, and Control Plans. Provide oversight and review of Human Factors Engineering (HFE) Protocols and Reports, as well as onboarding and auditing HFE suppliers related to life cycle management of commercial programs. Train and educate key functional partners and management on combination product requirements, standards and regulations Contribute to content and review of regulatory submissions and RTQs, and support audits and inspections for associated projects related to life cycle management of final product programs Scope may include a wide range of products, including but not limited to vial, prefilled syringes, needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, electromechanical on-body injector systems, and accessories. Plan and lead continuous improvements to the quality processes related to devices, combination product, assembly, labeling and packaging. Provide independent design review for other programs Provides quality oversight of the development, qualification, validation, transfer and maintenance of physical test methods including sample selection NOTE: This role may require working in shifts or extended hours within the same shift What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a with these qualifications. Basic Qualifications: Doctorate degree OR Masters degree and 4 to 6 years of Quality experience OR Bachelors degree and 6 to 8 years of Quality experience OR Diploma and 10 to 12 years of Quality experience Preferred Qualifications: 5+ years of quality and manufacturing experience in biotech or pharmaceutical industry (device experience a plus) Bachelors Degree in a Science Field Ability to oversee multiple medium complexity projects simultaneously Working knowledge of quality engineering and/or mechanical engineering Familiar with final products including applicable guidance, regulations and standards (e.g., MDR, ISO 14971, ICH Q9, ICH Q8, ICH Q10, ISO 13485, EU Annex 1, 21 CFR parts 4, 820, 210 and 211) Prior experience working as part of a combination product launch team Able to successfully manage workload to meet timelines Ability to effectively negotiate, articulate, and defend a position after taking feedback from multiple sources Ability to operate in a matrixed or team environment with site, functional, and executive leadership Experience driving decision making by using Decision, Advice and Inform (DAI) principles Understanding of industry requirements/expectations of a Quality Management System (QMS) Understanding of the applicable manufacturing/testing processes (i.e. Active Pharmaceutical Ingredient, Drug Substance, Drug Product, Packaging, Device manufacturing processes) Execution of technical standards, internal requirements, and regulations Comfortable with both drug and device terminology Ability to travel +/- 15-20% of time to domestic and international Amgen sites.

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