Advanced Medical Device Assembler & QC Specialist

Biopharma Careers; Pittsburgh (Allegheny County); On-site; USD 37,000 - 45,000; Full time

Benefits offered by this job

Vacation time

Holiday time

Sick time

Medical, dental, vision

Educational assistance

Annual bonus

Job summary

Bayer in Pittsburgh, PA is seeking an experienced Manufacturing Associate II to support advanced assembly and quality processes in a fast-paced FDA-regulated environment. You will assemble circuit boards and mechanical components, apply SPC/GMP principles, and collaborate with engineers and leaders to meet quality and productivity goals.

Prior experience and teamwork are essential. The role includes training, mentoring production staff, and data recording to ensure traceability and continuous

Qualifications

• High School Diploma or GED required.
• Minimum 1 year experience in medical device assembly or technical assembly.
• Must understand or quickly learn Bayer's quality systems policies.
• Ability to perform technical writing.
• Ability to adapt in fast-paced environments.
• Demonstrated teamwork and problem-solving.
• Ability to read technical drawings and visual work instructions.

Responsibilities

• This role assembles and supports various medical device manufacturing processes in an FDA-regulated facility.
• Support quality control inspections and participate in continuous improvement.
• Collaborate with leadership to train and mentor production staff.
• Collect data, maintain records related to quality and production metrics.
• Interact across departments to communicate information and resolve issues.

Skills

Medical device assembly

Quality systems knowledge

Technical writing

Teamwork

Adaptability

Education

High School Diploma/GED

Associate's Degree

Tools

Blueprints/Technical drawings

Job description

Bayer in Pittsburgh, PA is seeking an experienced Manufacturing Associate II to support advanced assembly and quality processes in a fast-paced FDA-regulated environment. You will assemble circuit boards and mechanical components, apply SPC/GMP principles, and collaborate with engineers and leaders to meet quality and productivity goals.

Prior experience and teamwork are essential. The role includes training, mentoring production staff, and data recording to ensure traceability and continuous