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Remote Api 653 Inspector Jobs in Union, NJ (NOW HIRING)

... fully remote office. They receive an average of 5 new FDA client inquiries per week ... 503B o Bulk API suppliers and repackagers o FDA audits/investigations • Drug supply chain ...

QA Analyst

New York, NY · On-site +1

$59K - $96K/yr

Familiarity with cross-browser testing tools, web service validation, and log inspection methods ... Proficiency in database queries, database testing, and API/web service testing. * Familiarity with ...

Remote Api 653 Inspector information

What are the key skills and qualifications needed to thrive as a Remote API 653 Inspector, and why are they important?

To thrive as a Remote API 653 Inspector, you need in-depth knowledge of tank inspection standards, welding, and corrosion, alongside an active API 653 certification. Competence in using inspection tools, digital reporting systems, and remote inspection technologies is typically required. Strong attention to detail, effective communication, and problem-solving skills help inspectors accurately assess tank integrity and convey findings to stakeholders. These skills ensure that storage tanks meet regulatory compliance and safety standards, minimizing risks and costly failures.

What is a Remote API 653 Inspector?

A Remote API 653 Inspector is a certified professional who inspects above-ground storage tanks (ASTs) for compliance with the American Petroleum Institute (API) Standard 653, often performing inspections remotely or at various locations. Their primary responsibilities include evaluating the integrity, safety, and suitability for service of tanks used for petroleum and chemical storage. Remote inspectors may use digital tools, drones, or other technology to assess tanks without being physically present on-site, ensuring safety and efficiency. To become certified, inspectors must pass the API 653 examination and maintain their credentials through ongoing education and experience. Their work helps prevent environmental hazards and ensures regulatory compliance.

What are some common challenges faced by Remote API 653 Inspectors, and how can they be addressed?

Remote API 653 Inspectors often face challenges such as limited on-site access, reliance on digital data transmission, and coordinating with on-site personnel for accurate inspections. To address these issues, inspectors should ensure strong communication with facility staff and utilize reliable remote inspection technologies, such as high-resolution cameras and secure data-sharing platforms. It's also important to stay updated on the latest remote inspection protocols and to participate in ongoing training to maintain proficiency. Building a network with other remote inspectors can also provide valuable support and insight into overcoming common obstacles.

What is the difference between Remote Api 653 Inspector vs Remote API 510 Inspector?

AspectRemote Api 653 InspectorRemote API 510 Inspector
CertificationsAPI 653, API 510, API 570 (preferred)API 510, API 570, API 653 (optional)
Work EnvironmentRefineries, storage tanks, tank farmsPressure vessels, piping, refineries
Industry UsageTank inspection and maintenancePressure vessel and piping inspection

Both roles require API certifications and involve inspection work in the oil and gas industry. The Remote Api 653 Inspector primarily focuses on storage tanks, while the Remote API 510 Inspector specializes in pressure vessels. Their certifications overlap but differ in emphasis, and their work environments are similar but with different equipment focus.

What job categories do people searching Remote Api 653 Inspector jobs in Union, NJ look for? The top searched job categories for Remote Api 653 Inspector jobs in Union, NJ are:
What cities near Union, NJ are hiring for Remote Api 653 Inspector jobs? Cities near Union, NJ with the most Remote Api 653 Inspector job openings:
Infographic showing various Remote Api 653 Inspector job openings in Union, NJ as of July 2026, with employment types broken down into 1% Internship, 1% As Needed, 77% Full Time, 10% Part Time, 1% Temporary, and 10% Contract. Highlights an 87% Physical, 10% Hybrid, and 3% Remote job distribution.

FDA Attorney

The Rockridge Group

Pine Brook, NJ • On-site, Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 8 days ago


Job description

TITLE: FDA ATTORNEY POSITIION: DIRECT HIRE Firm X, established in 2000, is a national boutique law firm focused exclusively on Healthcare and Life Sciences. The Firm draws on its experience representing stakeholders across the entire healthcare spectrum. In the Life Sciences, Firm X, has represented pharmacies of all kinds and assisted with regulatory, transactional, and litigation matters. On the Healthcare side, the Firm's clients have included large physician group practices, hospitals, hospital medical staff, ambulatory surgery centers, laboratory companies, as well as the complete panoply of ancillary service providers. Firm X attorneys are licensed in numerous states. The Firm has offices in Pine Brook, New Jersey, and New York City. A Mid-Level or more senior FDA Attorney (Counsel-level or higher) is sought for Firm X’s Pine Brook, NJ, New York City, or fully remote office. They receive an average of 5 new FDA client inquiries per week. Responsibilities will align with the Attorney’s background, which should include: • Compounding rules, regulations and FDA guidance o 503A o 503B o Bulk API suppliers and repackagers o FDA audits/investigations • Drug supply chain security and track and trace o Trading partner requirements o Unique trading partners (i.e., 3PLs, brokers, etc.) o Serialization implementation requirements o Other drug supply chain considerations • Drug and device manufacturing rules o CGMP compliance o NDA and ANDA filings and evaluation o 510K Premarket Approval Filings and evaluation o OTC filings and evaluation o Advice on manufacturing practices • Clinical trial rules o Structuring and drafting clinical trial agreements, informed consent forms, master service agreements, and related research contracts o Institutional Review Board (IRB) submissions and compliance o Clinical trial design, study initiation, data use, adverse event reporting, and post-trial obligations • Labeling and advertising reviews • FDA registration and annual filings • FDA inspections, 483 responses and warning letters • Drug withdrawals and recalls • FDA importation and exportation rules • Veterinary medicine and veterinary compounding • Dietary supplements • FDA regulated medical devices • Reviews of clinical literature and incorporation into arguments/strategies (access to these clinical literature directories is a plus) Requirements: • 10+ years FDA experience – private law firm experience strongly preferred, but will also consider in-house candidates • Clinical trial experience a plus • Filing copyrights a plus • Filing patents a plus • May work in the Pine Brook or New York City office; will also consider fully remote arrangement if located in other states • Admitted to practice in at least one US state • Experience performing most/all of the job responsibilities of the position (outlined above) • Team-player mindset, and ability to work cohesively and collaboratively with a team of attorneys • Strong work ethic Benefits: Firm X offers a hybrid schedule, competitive salary, and a full range of benefits, including PTO, medical, dental, vision, 401(k) (upon eligibility to participate), on-site gym (Pine Brook), and opportunities for substantial salary progression based on performance and contributions. *The posted salary will depend on years of experience and other factors.