Remote E-Commerce Associate
Delegate CX
Build and maintain online stores for U.S. promotional products clients from a home-based role in the Philippines. Manage products, orders, integrations, and e-commerce support.
खोलें
PerkinElmer फार्मास्यूटिकल्स, स्वास्थ्य सेवा, खाद्य और पेय पदार्थ, पर्यावरणीय विश्लेषण तथा औद्योगिक परीक्षण जैसे क्षेत्रों में उपयोग किए जाने वाले विश्लेषणात्मक और परीक्षण समाधान विकसित करता है। इसके पोर्टफोलियो में मास स्पेक्ट्रोमीटर, क्रोमैटोग्राफी उपकरण, स्पेक्ट्रोस्कोपी प्रणालियाँ, प्रयोगशाला उपकरण और उपभोग्य सामग्री शामिल हैं, जो संगठनों को सामग्रियों का मूल्यांकन करने, वैज्ञानिक अनुसंधान में सहायता देने, उत्पाद की गुणवत्ता बनाए रखने और अनुपालन मानकों को पूरा करने में मदद करते हैं। 1938 से चली आ रही विरासत के साथ, PerkinElmer दुनिया भर की प्रयोगशालाओं और औद्योगिक टीमों के साथ खाद्य सुरक्षा, पर्यावरणीय परीक्षण, स्वास्थ्य सेवा और औद्योगिक गुणवत्ता नियंत्रण जैसे क्षेत्रों में काम करता है।
Lead Validation Engineer – cGMP
Lead validation engineering work for PerkinElmer’s Project Farma life-sciences projects. Deliver CQV, system validation, and technical project support across client sites.
विवरण
- Complete technical work across validation and life-sciences projects
- Deliver CQV activities, including protocol development and equipment testing
- Document technical issues and help drive their resolution
- Verify that deliverables satisfy client specifications, regulatory obligations, and industry standards
- Prepare SOPs, requirements specifications, testing protocols, and summary reports
- Carry out system and process validation protocols in accordance with GxP practices
- Troubleshoot equipment and manufacturing processes through hands-on technical support
- Surface project roadblocks, escalate them appropriately, and develop practical solutions
- Support project controls and scheduling across budgets, timelines, milestones, risks, forecasts, and cost reporting
- Share technical expertise and coach less experienced team members
- Complete Project Farma’s internal qualification training program
- Support site strategy and develop and execute CQV protocols
- Build effective working relationships with project teams and client contacts
- Help advance project-level business development, proposals, and client deliverables
- Maintain full individual billability and escalate issues that could affect billable targets
आवश्यकताएँ
- Bachelor’s degree in life science, engineering, or a related field, or equivalent experience in capital project engineering, pharmaceutical cGMP facility start-up, CapEx/OpEx project management, or comparable military work
- Up to eight years of experience in consulting and/or engineering services
- Ability to travel as required for client project assignments
- Ability to travel up to 100% or as required
- Authorization to work full-time in the United States
- This role does not offer current or future work visa sponsorship
- Valid driver’s license
- Knowledge of cGMP, GxP, FDA requirements, and applicable industry standards
- General familiarity with Earned Value Analysis and project management tools
- Technical expertise in CQV, system and process validation, protocol development, equipment testing, SOPs, requirements specifications, and summary reports
लाभ
- Full-time presence at client sites
- Travel opportunities supporting client projects and business needs
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