Manufacturing Technician - 2nd Shift

CyVek, Inc.; Wallingford (CT); On-site; USD 26,000 - 36,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

Short-term disability

Long-term disability

401(k) with company match

ESPP

HSA

Job summary

Bio-Techne is seeking an entry-level manufacturing associate to support capillary coating and cartridge fabrication in an ISO 13485 environment. The role involves operating semi-automated equipment, performing QC inspection, and assisting engineers to implement improvements.

Strong attention to detail, quick learning, and clear communication are essential as you follow SOPs, complete documentation, and ensure quality and productivity targets are met.

Qualifications

• High School Diploma required with 2+ years in manufacturing environment.
• Experience with manufacturing, medical device manufacturing is a plus.
• Experience working with a microscope daily is a plus.

Responsibilities

• Operate semi-automated equipment and software.
• Perform entry-level manufacturing tasks.
• Conduct in-process QC inspection and documentation.
• Support process engineers and multidisciplinary teams in improvements and troubleshooting.
• Follow SOPs, WIs, and regulatory documentation.
• Maintain ISO 13485 quality compliance.

Skills

Hand-eye coordination

SOP adherence

Troubleshooting

Measurement & inspection

Documentation & record-keeping

Safety & compliance

Detail-oriented

Teamwork

Organization

Verbal & written communication

Education

High School Diploma

2+ years in manufacturing

Tools

Microscope

Job description

By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range: $19.20 - $26.40

Position Summary

The successful applicant will work with other members of the consumables production team to support and sustain manufacturing activities for capillary coating and cartridge fabrication in an ISO 13485 environment.

Key Responsibilities

• Operate semi-automated custom equipment and software
• Perform entry-level functions and jobs within the manufacturing department
• Perform in-process QC inspection and documentation
• Perform tasks to assist process engineers and a multidisciplinary team of engineers and scientists to implement improvements and troubleshooting issues
• Must be detail-oriented, learn quickly, respond to feedback, and communicate clearly
• Responsible for continual ISO 13485 quality compliance
• Read and follow SOPs, WIs, and regulatory documentation
• Excellent written and spoken communication skills (English)
• Safety-minded, disciplined workmanship
• Familiar with basic computer software: Microsoft Office
• Capable of basic ERP functions
• Able to learn new skills, concepts, and tasks as required
• Follow priorities per the supervisor
• Understand and follow appropriate standard operating procedures for Regulatory awareness of chemical handling and hazards
• Work may change from day to day within reasonable and expected boundaries and qualifications
• Complete all compliance training as assigned
• Meets quality and productivity expectations
• Participate in continuous process improvement efforts by assisting with the efforts under the guidance of leads and supervisors
• Works independently with minimal supervision on routine tasks

Education and Experience

High School Diploma and 2+ years’ experience in a relevant manufacturing environment. Experience with manufacturing, medical device manufacturing is a plus. Working with a microscope daily and understanding the use of space under a microscope is a plus.

Knowledge, Skills, and Abilities

• Strong hand-eye coordination and manual dexterity.
• Ability to follow SOPs, work instructions, and quality procedures.
• Basic troubleshooting and problem-solving skills.
• Proficient in the use of measurement and inspection tools.
• Accurate documentation and record-keeping skills.
• Commitment to workplace safety and compliance requirements.
• Strong attention to detail and quality focus.
• Ability to work effectively in a team environment.
• Strong organizational skills with the ability to manage multiple priorities.
• Effective verbal and written communication skills across all levels of the organization.

Working Conditions

Work performed in a laboratory and production environment with exposure to chemicals, reagents, and standard lab equipment. Standard schedule hours with occasional variation depending on production needs. Onsite work required during standard business hours.

Physical Requirements

Ability to lift and handle materials weighing 5–50 lbs. Ability to stand, walk, and perform repetitive laboratory tasks for extended periods. Manual dexterity required for laboratory equipment and fine measurement techniques.

Why Join Bio-Techne

We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

EEO statement

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Resume Policy

To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

Work Authorization

This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status).

Accommodations

If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact [e-mail] for assistance.

About Bio-Techne

Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services. Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.