Manufacturing Technician - 2nd Shift

Bio-Techne; Wallingford (CT); On-site; USD 26,000 - 36,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

401k plan

ESPP

Job summary

Bio-Techne in Wallingford, CT is seeking an entry-level manufacturing associate to support the consumables production team. You will operate semi-automated equipment to coat capillaries and fabricate cartridges in an ISO 13485 environment.

The role emphasizes attention to detail, adherence to SOPs, and teamwork with engineers and scientists. Prior manufacturing exposure is valued; training is provided, and safety is a priority.

Qualifications

• High School Diploma and 2+ years 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.

Responsibilities

• Operate semi-automated equipment and software.
• Perform entry-level functions within the manufacturing department.
• Perform in-process QC inspection and documentation.
• Assist engineers and scientists with improvements and troubleshooting.
• Follow SOPs, WIs, and regulatory documents.
• Meet quality and productivity expectations.

Skills

Hand-eye coordination

SOP adherence

Troubleshooting

Measurement tools

Documentation

Safety compliance

Detail oriented

Teamwork

Organization

Communication

Education

High School Diploma

Tools

Microscope

Microsoft Office

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

Qualifications

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.

Bio-Techne is an E-Verify Employer in the United States.

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.