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Entry Level Medical Device Jobs in Enfield, CT (NOW HIRING)

West Shore

Sales Consultant - Paid Training

Hartford, CT · On-site

$80 - $200/hr

Must have a valid smart phone or smart device in order to log into Company required systems using two-factor authentication * Comprehensive Health Insurance options (Medical, Dental, Vision, Accident ...

TRC Companies, Inc.

Distribution Designer I

Windsor, CT · On-site

$20 - $27/hr

Perform field data collection utilizing laptop computer, tablet device, GPS, and other electronic ... Medical, dental, vision, and disability insurance. * 401k package that includes both traditional ...

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Entry Level Medical Device information

What is an entry level medical device job?

Entry level medical device jobs are positions within medical device companies that are designed for individuals who are new to the industry or just starting their careers. These roles can include positions such as sales representatives, quality assurance associates, regulatory affairs assistants, and manufacturing technicians. They typically require a bachelor's degree in a related field, strong communication skills, and a willingness to learn. Entry level employees may assist with product launches, support senior staff, and ensure products meet regulatory standards. These roles offer valuable experience and a pathway to more advanced positions within the medical device industry.

What are the key skills and qualifications needed to thrive as an entry level medical device sales representative?

To thrive as an Entry Level Medical Device Sales Representative, you need a bachelor’s degree (often in life sciences, business, or a related field), strong sales acumen, and a good understanding of medical terminology. Familiarity with CRM systems, sales tracking software, and product-specific training or certifications like the Certified Sales Professional (CSP) can be advantageous. Excellent communication, resilience, and relationship-building skills help you connect with healthcare professionals and navigate complex sales processes. These abilities ensure effective product promotion, customer trust, and success in a competitive, fast-paced market.

What are some common challenges faced by entry-level professionals in the medical device industry?

Entry-level professionals in the medical device industry often face challenges such as adapting to strict regulatory requirements, learning complex product details, and understanding clinical environments. They must quickly develop a strong grasp of medical terminology and device functions to effectively support sales teams or healthcare providers. Collaboration with cross-functional teams—such as engineering, quality assurance, and regulatory affairs—is essential, and strong communication skills help in navigating this dynamic environment. Overcoming these challenges can provide a solid foundation for career advancement within the industry.

What cities near Enfield, CT are hiring for Entry Level Medical Device jobs?

Cities near Enfield, CT with the most Entry Level Medical Device job openings:

Entry Level Medical Device jobs near you
Infographic showing various Entry Level Medical Device job openings in Enfield, CT as of August 2026, with employment types broken down into 77% Full Time, 10% Part Time, and 13% Contract. Highlights an 100% In-person job distribution.

Manufacturing Engineer

Springfield, MA • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

$72K - $93K/yr

Contractor

Re-posted 19 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Manufacturing Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Manufacturing Engineer
Location: USA
Duration: Long Term

Position Overview

We are seeking a motivated Manufacturing Engineer with 0–1 year of experience to support manufacturing operations within the pharmaceutical, biotechnology, or medical device industry. This entry-level role is ideal for recent graduates or candidates with internship or co-op experience who are eager to build a career in regulated manufacturing. The selected candidate will assist with process improvements, manufacturing support, equipment qualification, documentation, and quality compliance while working closely with cross-functional teams.

Key Responsibilities

  • Support daily manufacturing operations to ensure safe, efficient, and compliant production.
  • Assist in monitoring and improving manufacturing processes to enhance productivity and product quality.
  • Support equipment installation, qualification, troubleshooting, and maintenance activities.
  • Assist with process validation, equipment qualification (IQ/OQ/PQ), and manufacturing documentation.
  • Prepare and maintain SOPs, work instructions, batch records, and engineering documentation.
  • Collaborate with Manufacturing, Production, Quality Assurance, Validation, Engineering, and Regulatory teams.
  • Collect and analyze manufacturing data to identify process improvement opportunities.
  • Assist with deviation investigations, CAPA activities, and change control documentation.
  • Ensure compliance with GMP, cGMP, FDA regulations, ISO standards, and company quality procedures.
  • Participate in Lean Manufacturing and continuous improvement initiatives.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or a related engineering discipline.
  • 0–1 year of experience through internships, co-op programs, academic projects, or entry-level roles in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
  • Basic understanding of manufacturing processes and engineering principles.
  • Familiarity with GMP/cGMP, FDA regulations, ISO 13485, or regulated manufacturing practices is preferred.
  • Basic knowledge of process validation, equipment qualification, and quality systems is a plus.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in a cross-functional team environment.
  • Proficiency in Microsoft Office applications.
  • Eagerness to learn and grow in a regulated manufacturing environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/