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Overnight Eu Jobs (NOW HIRING)

Must have overnight availability, including weekends, and some holidays. More details upon interview. * Requirement : Must have professional cooking experience, including large-scale production, and ...

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Overnight Eu information

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$13

$52

$70

How much do overnight eu jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for overnight eu in the United States is $52.19, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $63.46 per hour, depending on experience, location, and employer.

What is an Overnight EU?

Overnight EUs typically refer to employees who work overnight shifts in environments such as warehouses, hospitals, hotels, or retail stores within the European Union. These roles often involve tasks that need to be completed outside regular business hours, such as stocking inventory, cleaning, or providing essential services. Overnight positions require adaptability to non-traditional hours and may offer higher pay rates or shift differentials. Working overnight can impact sleep schedules and work-life balance, so it’s important to consider these factors before applying. These jobs are essential for businesses that operate around the clock or require overnight maintenance.

What skills and qualifications are needed to thrive as an Overnight EU?

To excel as an Overnight EU Operations Specialist, you typically need strong analytical skills, attention to detail, and familiarity with EU compliance regulations, often supported by a relevant degree or operational experience. Knowledge of enterprise resource planning (ERP) systems, Microsoft Office Suite, and possibly certifications in supply chain or logistics are commonly expected. Excellent communication, problem-solving abilities, and the capacity to work independently during non-traditional hours are standout soft skills for this position. These skills ensure smooth overnight operations, regulatory compliance, and effective issue resolution across European markets.

What are the unique challenges faced by an Overnight EU, and how can I best prepare for them?

Working as an Overnight EU team member often involves managing tasks during non-standard hours, which can present challenges such as maintaining effective communication with daytime colleagues and adapting to a nocturnal schedule. You may also need to handle urgent issues independently, as immediate support resources could be limited overnight. To succeed, it's important to develop strong self-management skills, proactively document your work for smooth handovers, and prioritize your well-being by establishing a healthy sleep routine. Collaboration tools and clear communication processes are essential for staying aligned with your team across different shifts.

What is the difference between Overnight Eu vs Warehouse Associate?

AspectOvernight EuWarehouse Associate
Required CredentialsHigh school diploma or equivalent; forklift certification often preferredHigh school diploma or equivalent; basic warehouse safety training
Work EnvironmentNight shifts in distribution centers or warehousesDay shifts in warehouses or retail stores
Employer & Industry UsageLogistics, shipping, and distribution companiesRetail, manufacturing, and logistics companies
Common Search & ComparisonOvernight Eu vs Warehouse Associate

Overnight Eu roles typically involve night shifts focused on logistics and distribution tasks, often requiring certifications like forklift operation. Warehouse Associates work during daytime hours, handling inventory and order fulfillment. Both roles are essential in warehouse environments but differ mainly in shift timing and specific duties.

More about Overnight Eu jobs

What cities are hiring for Overnight Eu jobs?

Cities with the most Overnight Eu job openings:

What are the most commonly searched types of Eu jobs?

The most popular types of Eu jobs are:

What states have the most Overnight Eu jobs?

States with the most job openings for Overnight Eu jobs include:

Infographic showing various Overnight Eu job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 21% Part Time, and 1% Contract. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $108,557 per year, or $52.2 per hour.

$98K - $123K/yr

Full-time

Medical, Dental, Life, Retirement, PTO

Re-posted 2 days ago


Job description

We exist to create positive change for people and the planet. Join us and make a difference too!
Job Title: Medical Device QMS Auditor
Location: Candidates must reside in one of the following states: IL, MN, WI, IN, NJ, MA, PA, OH.
BSI (British Standards Institution) is the global business standards company that equips businesses with the solutions to turn standards of best practice into habits of excellence.
Our Medical Devices (or Regulatory Services) team ensures patient safety while supporting timely market access for our clients' medical device products globally. BSI is an accredited ISO 13485 Certification Body recognized in many global markets.
This is a travel based position with extensive travel to medical device manufacutering sites. Candidate must be comfortable with overnight travel of 13-15 days out of every month.
Essential Responsibilities
  • Analyze and assess quality management systems with emphasis on design controls, manufacturing controls, production processes, process validation, verification/validation, and testing activities, ensuring compliance with ISO 13485, CE Marking, and MDSAP schemes.
  • Assess manufacturing processes including production controls, process validation, risk management, supplier controls, and design transfer activities.
  • Prepare assessment reports and communicate findings to clients, providing clear direction for corrective actions where appropriate.
  • Recommend the issue, re-issue, or withdrawal of certificates in accordance with BSI policies and procedures.
  • Lead assessment teams, ensuring quality of service and effective working relationships with clients and team members.

Education & Technical Qualifications
  • Technical degree (Bachelor's, or higher) in Engineering, Science, or a related technical discipline required. Relevant fields include Biomedical, Mechanical, Electrical, or Chemical Engineering; Materials Science; Biology; Microbiology; Chemistry; or related technical fields applicable to medical devices, SaMDs, or IVDs.
  • Minimum of 4 years' experience in the medical device, SaMD, or IVD fields with direct, hands-on involvement in designing, manufacturing, validating, inspecting, testing, or clinically evaluating devices. Candidates must have personally worked with devices, specifications, or code, indicate the types and classifications of devices, and demonstrate their level of involvement on their CV. Regulatory or audit experience only is insufficient.
  • Detailed hands-on experience with design and manufacturing/production controls, including process validation (IQ/OQ/PQ), risk management, supplier controls, CAPA, nonconforming product management, and change control.
  • Knowledge of regulatory requirements and quality management standards including ISO 13485, MDSAP, FDA QSR (21 CFR 820), and EU MDR/IVDR are a plus

Core Competencies
  • Strong verbal and written communication skills, and attention to detail.
  • Ability to work under pressure and meet deadlines.
  • Self-motivated, flexible, and excellent time management/planning skills.
  • Willingness to travel extensively.
  • Enthusiastic, committed team player.
  • Business development and public speaking skills are considered advantageous.

Preferred Qualifications
  • Experience with process validation, equipment qualification, and manufacturing process development.
  • Experience in design and development activities, including design controls and design transfer.
  • Hands-on experience with software-controlled medical devices, SaMD, or automated manufacturing systems.
  • Experience auditing or assessing quality management systems compliant with ISO 13485, CE Marking, and MDSAP.
  • Experience with risk management (ISO 14971), sterile medical devices, aseptic processing, or cleanroom manufacturing.
  • Experience leading hands-on teams in manufacturing, testing, or validation.
  • Lead Auditor certification (ISO 13485, MDSAP, or equivalent) preferred.
  • Previous experience working for a Notified Body, Regulatory Body, or Certification Body preferred.
  • Advanced degree (MS, PhD) in engineering, science, or related technical discipline preferred.

The salary for this position can range from $98,100 to $123,860 annually; actual compensation is based on various factors, including but not limited to, the candidate's competencies, level of experience, education, location, divisional budget and internal peer compensation comparisons. BSI offers a competitive salary, group-sponsored health and dental, short-term and long-term disability, a company-matched 401k plan, company paid life insurance, 11 paid holidays and 4 weeks paid time off.
#LI-REMOTE
#LI-MS1
About Us
BSI is a business improvement and standards company and for over a century BSI has been recognized for having a positive impact on organizations and society, building trust and enhancing lives.
Today BSI partners with more than 77,500 clients in 195 countries and engages with a 15,000 strong global community of experts, industry and consumer groups, organizations and governments.
Utilizing its extensive expertise in key industry sectors - including automotive, aerospace, built environment, food and retail, and healthcare - BSI delivers on its purpose by helping its clients fulfil theirs.
Living by our core values of Client-Centricity, Agility, and Collaboration, BSI provides organizations with the confidence to grow by partnering with them to tackle society's critical issues - from climate change to building trust in digital transformation and everything in between - to accelerate progress towards a better society and a sustainable world.
BSI is an Equal Opportunity Employer dedicated to fostering a diverse and inclusive workplace.