Operator, 12hr shift Jobs

Operator, 12hr shift

The Blood Pressure Cuff Operator is responsible for operating and maintaining bl...

Location

United States , Skaneateles Falls

Salary:

21.00 USD / Hour

Baxter

Expiration Date

Until further notice

Requirements

High School Diploma or GED equivalent required
demonstrated experience in a manufacturing or production setting is preferred
strong attention to detail and ability to follow established procedures accurately
excellent communication and interpersonal skills, with the ability to work collaboratively with team members and supervisors
basic computer skills, SAP experience is a plus
strong organizational skills and ability to manage multiple tasks efficiently
ability to maintain a clean and safe work environment
experience with quality control procedures and documentation is a plus
good mechanical dexterity/eyesight, be able to read, write and use basic math
maintain a high degree of accuracy in performing repetitive tasks

Job Responsibility

Responsible for reading, understanding, and following assembly processes
can inspect, fold, label and box product
utilize basic computer skills, such as SAP to download labels
use the auto bagger as needed
package blood pressure cuffs according to procedures
document and record production data accurately and securely, adhering to confidentiality and data management policies
work in various positions: standing, sitting and repetitive jobs
consistently meet all productivity and quality requirements
adhere to all safety protocols and regulations, including proper handling and disposal of materials and waste.

What we offer

Medical and dental coverage
insurance coverage for basic life, accident, short-term and long-term disability
business travel accident insurance
Employee Stock Purchase Plan (ESPP)
401(k) Retirement Savings Plan
Flexible Spending Accounts
educational assistance programs
paid holidays
paid time off ranging from 20 to 35 days based on length of service
family and medical leaves of absence

Fulltime

Paste Plant Operator

We are seeking a Paste Plant Operator to join an innovative and award wining com...

Location

Australia , Various Sites

Salary:

Not provided

Quattro Project Engineering

Expiration Date

Until further notice

Requirements

Experience preferred however not essential as on the job training is provided
Current Police Clearance or willingness to obtain
Current Manual Drivers License
Ability to be in a team whilst maintaining a high standard of work quality and housekeeping
Strong work ethic and punctual
Ability to work in a safe and efficient manner
Willing to undergo a full pre-employment medical including an instant drug and alcohol screen
Able to work 12hr shifts

Job Responsibility

Operation of a Paste Backfill Plant and associated tailings filtration system
Sampling paste, tailings, and filter cake product for testing
Surface management of the underground reticulation system including flushing and remote actuation of paste diverters for dumping
Performing all duties with a priority on all aspects of safety
Other duties as directed by Leading Hand or Paste Fill Coordinator

What we offer

Agile Innovation: Operate in a flexible, start-up-like environment backed by the strength of a global mining leader
Career Growth: Enjoy direct access to senior management in a flat organisational structure where your contributions are visible and valued
Comprehensive Benefits: Quattro offers a range of benefits, including health and entertainment discounts, as well as a generous parental leave policy with 12 weeks of paid leave
Variety of Roster Options: 14 days on / 14 days off, 8 days on / 6 days off, 7 days on / 7 days off
5 weeks annual leave
Onsite camp facilities, accommodation and messing provided
Employee Assistance Program

Fulltime

Production Technician I

The technician will be responsible for assembling, operating, and monitoring sta...

Location

United States , Melrose Park

Salary:

24.00 USD / Hour

HonorVet Technologies

Expiration Date

Until further notice

Requirements

Have a minimum of a High School Diploma, GED, or equivalent education with one year of experience in a relevant work environment
Able to work 12hr shifts on a 2-2-3 schedule
Able to stand on concrete floors for an extended period of time
Able to lift up to 35 pounds by bending and lifting
Able to move heavy equipment and components as needed
Able to work with hazardous materials including antineoplastic products and raw materials that could lead to serious illness/injury
Able to wear required personal protective equipment (eye protection, safety shoes, gown, gloves)
Must be able to understand, speak, and write English in order to comply with necessary SOPs, SPECs, Job-specific training materials, GMPs, and other manuals

Job Responsibility

Assembling, operating, and monitoring state-of-the-art, aseptic equipment following applicable Standard Operating Procedures and current Good Manufacturing Practices
Practice good aseptic techniques to minimize the potential for product contamination
Understand advanced computerized systems through HMI
Ability to operate advanced HMI applications
Perform basic level machine operation, set-up and troubleshooting of all state-of-the-art equipment in their area
Load Parts Washer, Component Sterilizer, Vial Washer, Filling Machine and Capping Machine with raw materials and format parts
Maintains a down qualification if required by their area
Perform microbiological monitoring within the Filling Machine, ALUS, and Capping Machine
Assist other departments including MQA, Maintenance, Metrology, Engineering, Validation, Tech Transfer and Microbiology, with tasks on the equipment in their area General
Clean and sanitize equipment and Production areas per SOP

Fulltime

New

Audit Experienced Staff

At EY, you’ll have the chance to build a career as unique as you are, with the g...

Location

Bahamas , Nassau

Salary:

Not provided

ACCA

Expiration Date

January 08, 2026

Requirements

A bachelor’s degree in an accounting, finance or a business discipline
Confidence in your ability to prioritize when managing multiple projects simultaneously

Job Responsibility

Performing audit procedures, while developing effective, client-focused audit strategies
Proactively building relationships that support our ability to provide tailored services that meet a wide range of assurance needs and contribute to new business development
Identifying and reacting to potential risks and developing new ways to improve our products and processes that promote growth and increase revenue
Continually updating your understanding of business trends and emerging technologies to maintain your reputation as a trusted business advisor

What we offer

medical, dental and vision coverage
competitive pension plan
generous vacation and leave entitlement(s)
a range of programs and benefits designed to support your physical, financial and social well-being
Continuous learning
Success as defined by you
Transformative leadership
Diverse and inclusive culture

New

Full Stack Software Engineer

As (Senior) Full Stack Software Engineer with a passion for Agile in Brainlab’s ...

Location

Germany , Munich

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

Education in Computer Science, Mathematics, Physics, Engineering or related discipline, or equivalent working experience
Several years of professional experience in full stack development
Expertise in C++
Experience with automated testing and building CI/CD pipelines
Natural Team player, strong communication skills and ability to work cross-functionally
Fluent in written and spoken English

Job Responsibility

Working in a LeSS environment as part of a cross-functional team, collaborating closely with Product Owners and departments such as Quality Assurance, Usability, and other teams involved in the solutions
Design, develop, integrate, test, release and maintain applications that are used to plan and perform spinal surgical interventions to deliver innovative, user-centered solutions that improve patient care
Take ownership in building and evolving our BDD, TDD practices and our CI pipelines
Create systems that are scalable, maintainable with clean, readable code in C++, HTML5 (Python, Rust, ...)
Work according to medical software development standards
Stay informed on emerging technologies, industry trends, and healthcare developments

What we offer

30 vacation days, plus December 24th and December 31st
Flexible working hours
Bike leasing via cooperation partner "BikeLeasing"
Parking garage and safe underground bike storage
Award-winning subsidized company restaurant and in-house cafes
Variety-rich fitness program in our ultra-modern 360m2 company gym
Regular after work, team, and company events
Comprehensive training and continuing education opportunities

Fulltime

New

Employee in quality management and/or regulatory affairs

As a professional QM/RA associate, you will be responsible for tasks in Quality ...

Location

Austria , Salzburg

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

Experience or training in Quality Management, preferably in the medical device sector (ISO 13485) or any industry with high regulatory standards
Knowledge of EU MDR (Medical Device Regulation) and experience with Class II or higher medical devices is an advantage
Familiarity with clinical evaluations and post-market surveillance processes under MDR guidelines is highly desirable
Knowledge of international regulations and certifications for medical devices is a plus
Fluent in German and English (written and spoken)
Flexible, team-oriented, and eager to work in an international environment

Job Responsibility

Support and collaborate across all areas of Quality Management (QM)
Ongoing control, improvement, and optimization of quality management processes and standards
Assist in creating and reviewing deviation reports, risk management plans, and CAPA (Corrective and Preventive Actions), ensuring thorough monitoring of corrective actions
Ensure the implementation and monitoring of regulatory requirements for medical devices
Assist with international product certifications and approvals
Liaise with regulatory bodies and authorities, including correspondence with notified bodies (globally)
Support clinical evaluations, ensuring that medical devices meet clinical safety and performance requirements in accordance with regulatory standards
Participate in post-market surveillance activities, including monitoring product performance in the market and managing feedback loops to continuously improve device safety and effectiveness
Support internal and external audits as well as supplier audits
Assist R&D with documentation and support the development process

What we offer

A motivating work atmosphere in a young, dynamic team
An exciting and varied scope of assignments customized for your skills and interests
The opportunity to grow with us, be directly involved and participate in our company’s success
A secure, permanent full-time contract
Generous social benefits within our culturally diverse enterprise
Freshly-cooked meals and healthy snacks provided daily
Good public transport connections and parking facilities available
Flexible working hours
Support for daily obligations (childcare, etc.)

Fulltime

New

Audit Senior

At Deloitte, we believe in the power of curiosity, a sense of purpose, and a gro...

Location

Bahamas

Salary:

Not provided

ACCA

Expiration Date

January 22, 2026

Requirements

A bachelor’s degree or equivalent post-secondary/qualification (i.e., ACCA)
An internationally recognized professional accounting qualification (CPA, CA, ACA, ACCA) or are currently on track to complete designation requirements
2-3 years of relevant audit experience in a public practice firm including knowledge of US GAAP or IFRS reporting standards

Job Responsibility

Help lead, plan, and execute high quality audit engagements from start to finish and assist clients with complex accounting matters and identifying business and financial risk
Leverage audit tools and new technologies
Develop and mentor junior audit team members
Engage in well-being and sustainability initiatives, a variety of social and community events, and other programs aligned with Deloitte's Shared Values

What we offer

Relocation packages for international candidates
Comprehensive total compensation and rewards package that includes a focus on learning, skills development and well-being

Fulltime

New

R&D Process Engineer - Software Development

We are seeking a dedicated and experienced (Senior) Process Engineer for softwar...

Location

Germany , Munich

Salary:

Not provided

Brainlab

Expiration Date

Until further notice

Requirements

University degree Computer Science or equivalent
Knowledge of IEC 62304 and its successful implementation in organizations
Knowledge of other medical device software related standards and regulations such as FDA 21 CFR Part 820 and ISO 13485 desired
Solution orientation and a structured nature
Strong communication and documentation skills and ability to work cross-functionally
Experience in software development in a regulated industry (medical devices preferred)
Basic to intermediate proficiency in programming languages (e.g. Python, Java) and/or experience with scripting and automation tools to enhance process efficiency
Fluent in written and spoken English, German is a plus

Job Responsibility

Design, implement, and optimize software development processes within R&D in accordance with relevant medical device standards (e.g., IEC 62304, ISO 13485, ISO 14971, MDR/FDA)
Work cross-functionally with R&D, Quality Management, Quality Assurance to maintain a compliant yet efficient development environment
Ensure audit readiness and support internal and external audits related to R&D processes
Align software development processes within the Brainlab agile methodology
Provide process training and coaching to R&D colleagues and facilitate knowledge sharing across the organization
Align and integrate tools that support process automation and collaboration within R&D

What we offer

30 vacation days, plus December 24th and December 31st
Flexible working hours
Hybrid work model within Germany
Bike leasing via cooperation partner "BikeLeasing"
Parking garage and safe underground bike storage
Award-winning subsidized company restaurant and in-house cafes
Variety-rich fitness program in our ultra-modern 360m2 company gym
Regular after work, team, and company events
Comprehensive training and continuing education opportunities

Fulltime

Operator, 12hr shift

Baxter

Location:
United States , Skaneateles Falls

Category:
Manufacturing

Contract Type:
Employment contract

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 20, 2025

Looking for more opportunities? Search for other job offers that match your skills and interests.

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Operator, 12hr shift

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Location:United States , Skaneateles Falls

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Job Description:

Job Responsibility:

Requirements:

Nice to have:

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Job Posted:March 20, 2025

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