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Temp Medical Device Startup Jobs in Indiana (NOW HIRING)

Support 24x7 site-based operations after startup. Write/revise accurate operational procedures ... Previous pharmaceutical or medical device experience is preferred. Completed training in ...

CNC Machinist 2nd Shift

Warsaw, IN · On-site

$18 - $30/hr

... within the medical device industry. This role is responsible for setting up, operating, and ... Temp-to-Hire * Compensation: $18.00 - $30.00 per hour, based on shift and experience * Application ...

... within the medical device industry. This role is responsible for setting up, operating, and ... Temp-to-Hire * Compensation: $18.00 - $30.00 per hour, based on shift and experience * Application ...

Document Controller

Indianapolis, IN · On-site

$72K - $85K/yr

... or medical device environment (GxP). * Technical Proficiency: Required hands-on experience with ... For temporary assignments lasting 13 weeks or longer, AllSTEM Connections is pleased to offer major ...

We provide commissioning, qualification, validation, startup, project management, and other ... medical device In-depth understanding of GAMP guidelines and FDA regulations (21 CFR 11, 210, 211 ...

We provide commissioning, qualification, validation, startup, project management, and other ... medical device In-depth understanding of GAMP guidelines and FDA regulations (21 CFR 11, 210, 211 ...

Experience in medical device, aerospace, automotive, or precision manufacturing environments ... A leader in contingent and permanent workforce solutions, we also provide temp-to-hire staffing ...

Showing results 21-40

Temp Medical Device Startup information

What are some typical challenges faced by temp employees at a medical device startup, and how can they successfully adapt?

Temp employees at medical device startups often encounter fast-paced environments with evolving priorities and limited onboarding time. They may need to quickly familiarize themselves with complex products, regulatory standards, and cross-functional teams. Successful adaptation involves being proactive in asking questions, embracing flexibility, and staying organized to manage shifting tasks. Building strong communication with permanent staff can also help temp employees integrate smoothly and deliver impactful results.

What is a temp medical device startup?

A Temp Medical Device Startup is a temporary or short-term company focused on developing, testing, or launching new medical devices. These startups often form to rapidly innovate or address specific healthcare needs, sometimes as part of a contract or pilot project. Temporary startups may operate only for the duration of a specific development cycle or clinical trial, after which they may dissolve or be absorbed by a larger company. Working at such a startup typically involves fast-paced, cross-functional teamwork and the opportunity to contribute to cutting-edge healthcare solutions.

What are the key skills and qualifications needed to thrive as a temp at a medical device startup?

To thrive as a Temp at a Medical Device Startup, you need a background in life sciences or engineering, familiarity with regulatory standards, and the ability to rapidly learn new processes. Experience with tools like CAD software, laboratory equipment, or project management systems is often required, along with knowledge of FDA or ISO compliance. Strong problem-solving skills, flexibility, and effective communication help you adapt to the fast-paced and evolving environment of a startup. These competencies are crucial for ensuring product quality, meeting deadlines, and supporting innovation in a highly regulated and competitive field.

What is the difference between Temp Medical Device Startup vs Medical Device Quality Assurance Technician?

AspectTemp Medical Device StartupMedical Device Quality Assurance Technician
CredentialsTypically requires a degree in engineering, biology, or related field; certifications varyRequires a degree in life sciences or engineering; often holds certifications like CQE or ISO auditor
Work EnvironmentFast-paced, dynamic startup setting, often temporary or project-basedStructured environment within established companies, focusing on compliance and quality control
Employer & Industry UsageCommon in early-stage startups developing new medical devicesFound in established medical device companies ensuring product quality and regulatory compliance

While both roles involve working with medical devices, a Temp Medical Device Startup typically focuses on supporting early-stage product development in a dynamic environment. In contrast, a Medical Device Quality Assurance Technician works within established companies to ensure products meet quality standards and regulatory requirements.

What are the most commonly searched types of Medical Device Startup jobs in Indiana?

The most popular types of Medical Device Startup jobs in Indiana are:

What are popular job titles related to Temp Medical Device Startup jobs in Indiana?

For Temp Medical Device Startup jobs in Indiana, the most frequently searched job titles are:

What cities in Indiana are hiring for Temp Medical Device Startup jobs?

Cities in Indiana with the most Temp Medical Device Startup job openings:

Maintenance Technician

Novartis

Indianapolis, IN • On-site

$47K - $88K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 14 days ago


Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 rated pharmaceutical


Job description

Job Description Summary

The Maintenance Technician is responsible for performing corrective and preventative maintenance and support services for the building(s) and all equipment for a GMP Radioligand Therapies Production Facility. Responsible for reliable, efficient, and sustained operation of the facility and all equipment. Additionally supports current project operations and site goal objectives and ensures compliance with regulatory, corporate, and site requirements related to their functional area.
Location: Onsite
Please note this is a 2nd shift position (6pm - 6am; 2x2x3)


Job Description

Major accountabilities:

Adhere to Novartis Quality Policies and procedures as they pertain to the position to ensure that all products are safe, pure, effective and of the highest quality.
Perform a wide range of maintenance repair activities on production equipment, lab equipment and building management systems.
Assist in troubleshooting and repair of process equipment (example: containment isolator systems, filling line equipment and associated utility connections) which may include mechanical, electrical wiring, pneumatics, motors, pumps, vacuum systems, HVAC, control systems, compressed gases, filling line, under little to no supervision.
Interpret P&IDs, equipment/system layouts, wiring diagrams, and specifications in planning and performing maintenance and repairs.
Support 24x7 site-based operations after startup.
Write/revise accurate operational procedures, training documents and maintenance procedures for various production and utility systems.
Provide radiation safety program support, responsible for calibration and functionality of all radiation detection equipment
Completes Equipment Work Order Thoroughly, and Accurately and Documents them in the System
Supply information and technical data for securing spare parts.
Provide responsive customer support with emphasis on customer satisfaction.
Perform startup and commissioning activities as required.
Support and/or perform investigations / deviations from an engineering/maintenance perspective and help with data for timely closure of deviations and CAPAs
Perform preventative and corrective maintenance on manufacturing process related equipment within a cleanroom environment.
Complete and provide accurate documentation, as required in cGMP operations.
Oversee work and provide training of less experienced maintenance technicians and/or new technicians.
Other related duties as assigned.
Use of CMMS system for documentation of relevant work.

The salary for this position is expected to range between $47,500 and $88,300 per year.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

Minimum Requirements:

High School diploma or equivalent is required; Bachelor's Degree is preferred.
1+ years of relevant hands-on plant maintenance experience in a regulated GMP environment is required.
Previous aseptic fill/finish and/or radio pharmacy experience is preferred.
Previous pharmaceutical or medical device experience is preferred.
Completed training in radioactive or hazardous materials environment is preferred.
Must be able to adhere to all applicable procedures, company policies and any other quality or regulatory requirements. (For example: OSHA, DEA, FDA, EMEA, ANVISA, HS&E, etc.)
Experience working in a team environment, with excellent communication and organizational skills.
Proficient computer skill utilizing MS Office suite applications, Building Management Systems, and Computerized Maintenance Management Systems (CMMS) or similar system.
Ability to climb ladders and lift up to 50 lbs.
Wear and work in protective clothing, including respiratory protection, confined space entry and clean room environments.
Must be flexible to work nights, weekends, and holidays as required.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$47,500.00 - $88,300.00


Skills Desired

Control Systems, Engineering Technical Expertise, GDP Knowledge, gmp knowledge, HSE Knowledge, Knowledge Of Relevant Tools And Systems, Manufacturing Process (Production), Operational Excellence, Total Productive Maintenance

What Novartis employees say

Pay

Benefits

Hours and flexibility

Workplace

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