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Java Developer Night Shift Jobs in Missouri (NOW HIRING)

The Underground Mine Night Shift Electrician is responsible for inspecting, troubleshooting ... Our team of dedicated electricians, engineers, and technicians provides electrical, data, security ...

The Underground Mine Night Shift Electrician is responsible for inspecting, troubleshooting ... Our team of dedicated electricians, engineers, and technicians provides electrical, data, security ...

3rd Shift Mine Electrician

Randolph, MO ยท On-site

$45 - $55/hr

The Underground Mine Night Shift Electrician is responsible for inspecting, troubleshooting ... Our team of dedicated electricians, engineers, and technicians provides electrical, data, security ...

Night Shift 7p-7a M-F Location: Washington, MO Job Duties and Responsibilities * Perform preventive ... Diagnose and repair programmable logic controllers (PLCs), electronic circuits, motors, and control ...

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Java Developer Night Shift information

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$14

$53

$72

How much do java developer night shift jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for java developer night shift in Missouri is $53.18, according to ZipRecruiter salary data. Most workers in this role earn between $46.01 and $59.52 per hour, depending on experience, location, and employer.

What is a Java developer night shift?

A Java Developer Night Shift job involves designing, developing, and maintaining Java-based applications while working during nighttime hours. This role is often required by companies that operate globally, support international clients, or manage critical systems that need 24/7 monitoring. Responsibilities include writing clean code, debugging issues, collaborating with teams remotely, and ensuring system stability outside regular business hours. Night shift developers may also handle urgent issues, deploy updates, and provide support to maintain smooth operations.

What are the key skills and qualifications needed to thrive as a Java developer night shift?

A successful Java Developer Night Shift requires strong proficiency in Java programming, problem-solving abilities, and typically a degree in computer science or related field. Familiarity with tools such as Eclipse or IntelliJ IDEA, version control systems like Git, and frameworks such as Spring Boot is often essential, while certifications like Oracle Certified Java Programmer can be beneficial. Excellent communication skills, self-motivation, and the ability to work autonomously during non-standard hours set top candidates apart. These skills ensure effective system maintenance, timely issue resolution, and reliable performance even with minimal direct supervision overnight.

What are some common challenges faced by Java developers working the night shift, and how are they addressed?

Java Developers working the night shift often handle live support, system monitoring, and urgent bug fixes when fewer staff are present, which can require greater independence and problem-solving skills. Adapting to the night schedule and ensuring effective collaboration with daytime teams are also common challenges. Most organizations support night shift developers with clear escalation procedures, comprehensive documentation, and scheduled handover meetings to facilitate smooth communication. This setup helps ensure that all critical updates and issues are efficiently managed across different shifts, allowing developers to maintain high standards of reliability and code quality.

What are popular job titles related to Java Developer Night Shift jobs in Missouri?

For Java Developer Night Shift jobs in Missouri, the most frequently searched job titles are:

What job categories do people searching Java Developer Night Shift jobs in Missouri look for?

The top searched job categories for Java Developer Night Shift jobs in Missouri are:

What cities in Missouri are hiring for Java Developer Night Shift jobs?

Cities in Missouri with the most Java Developer Night Shift job openings:

GMP Manufacturing Support Supervisor-Night Shift

Merck Group

Saint Louis, MO โ€ข On-site

$85K - $149K/yr

Full-time

Medical, Retirement, PTO

Posted 3 days ago

New


Job description

Work Your Magic with us! Start your next chapter and join MilliporeSigma.
Ready to explore, break barriers, and discover more? We know you've got big plans - so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.
This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.
Your Role:
At MilliporeSigma, the GMP Manufacturing Support Supervisor -Night Shift at our Cherokee site/3300 S. Second Ave, St Louis, will play a key role within our GMP Operations Systems & Support team. This team supports Manufacturing through various functions including buffer manufacturing, training, compliance, equipment and facility cleaning, and raw material coordination. Expectations of the GMP Operations System & Support team are to ensure compliance and readiness within our GMP Manufacturing teams, ultimately enabling high manufacturing success. Job duties include:
  • Shift Details: This role will support 24/7 manufacturing operations and work 12-hour shifts from 6:00pm - 6:30am including a 20% shift differential
  • Lead production scientists and operators in the scale-up, technology transfer, and execution of cGMP buffer manufacturing.
  • Lead Facility Operators in supporting Manufacturing through maintaining cleanliness of manufacturing facilities and equipment, staging of equipment and supplies, waste disposal, and other various manufacturing support activities.
  • Develop employees' knowledge and skills to improve performance and expand abilities as well as to coordinate the group's efforts to assist meeting the departmental, company, and customer's objectives. Oversee the manufacturing of processing aids and excipients, regulated by the Food and Drug Administration and other regulatory bodies.
  • Adhere to protocols consistent with, and established according to, current Good Manufacturing Practices.
  • Work cross-functionally with Project Management, Technical Operations, Process & Analytical Development, Quality Control, Quality Assurance, Packaging, Materials Management, Engineering, and Maintenance.
  • Interact with our customers' project management, technical and quality teams.
  • Maintain departmental goals and objectives in a safe manner and in compliance with all applicable federal, state, and company regulations (OSHA, EPA, FDA, EMA etc.).
  • Responsible for the management of capital for equipment and facility improvements, including balancing the departmental budget.
  • Support department efforts toward Process Improvement and company goals.
  • Revise and approve procedures, batch records, and other documentation to ensure compliance with cGMP guidelines.
  • Ensure employees remain current with all department and site training requirements.
  • Lead root cause investigations and implement effective corrective and preventative actions related to manufacturing deviations.
  • Provide leadership and support of safety initiatives within production operations to ensure compliance to OSHA requirements.
  • Ensure tasks are done in accordance with approved site procedures, batch records and protocols.

Physical Attributes:
  • Stand for extended periods of time
  • Lift, push, and or pull up to 35lbs.
  • Wear mask, safety shoes, gloves, Tyvek suits, respirator, and related personal protective equipment

Who You Are
Minimum Qualification:
  • Bachelor's Degree Chemistry, Biology Biochemistry or other Life Science field OR in Chemical Engineering, Mechanical Engineering or other Engineering fields
  • 2+ years of life science manufacturing experience in a cGMP setting
  • 1+ year of Management, Supervisory, or Lead experience

OR
  • High School Diploma or GED
  • 6+ years of life science manufacturing experience in a cGMP setting
  • 1+ year of Management, Supervisory, or Lead experience

Preferred Qualifications:
  • 3 + years of Management, Supervisory or Lead experience in GxP environment
  • Customer interfacing audit experience
  • Knowledge of Six Sigma concepts/Lean Manufacturing or process improvement
  • Familiarity with buffer manufacturing, facility and equipment cleaning, and raw material management
  • Strong Microsoft Office experience for Manufacturing/Operating procedure writing, technical report generation, product tracking and trending data analysis and Operational Excellence reports
  • Strong interpersonal skills, conflict resolution experience, written, and verbal communication skills

RSREMD
Pay Range for this position: $85,700.00 - $149,400.00
The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here.
What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!