MCS Manufacturing (Process) Technician

Summary:
We are seeking a dedicated Manufacturing (Process) Technician to provide critical cleaning and sanitation support within an FDA-regulated manufacturing environment. This role requires a hands-on approach, ensuring cleanliness and compliance within production areas. The ideal candidate brings experience in pharma or medical device settings with an aseptic background and familiarity with cGMP Grade 8 or lower environments.

Responsibilities:

• Adhere to Good Manufacturing Practices (GMPs) and Code of Federal Regulations (CFRs).
• Report any discrepancies or quality concerns to the Team Leader or Production Supervisor.
• Ensure quality compliance with a "Right First-Time" mindset.
• Receive and prepare components for manufacturing, feed components into equipment, and perform sanitation tasks.
• Maintain and document accurate records, monitor performance metrics, and participate in daily performance meetings.
• Operate pallet jacks, wrap pallets manually, and use computer systems to manage material inventory and electronic batch records.
• Collaborate with cross-functional teams to identify and implement process improvements.
• Maintain availability of components and products to support continuous operations.

Additional Requirements:

• Team Collaboration: Work effectively in teams to complete operational tasks and contribute positively to the work environment.
• Initiative and Compliance: Take direction well, follow all policies and procedures, and demonstrate initiative in task completion.
• Physical Requirements:
• Regularly lift up to 35 lbs and push/pull objects requiring up to 50 lbs of force.
• Stand for long durations and perform physical activities including bending, reaching, climbing, squatting, and kneeling.
• Ability to work on portable stairs or ladders up to 6 feet.

Requirements

Qualifications:

• Basic Qualifications:
• Associate degree with 2 years of experience, OR
• Technical school training with 2 years of hands-on experience, OR
• High school diploma/GED with 4 years of experience in a relevant field.
• Experience:
• Previous experience as a technician in medical devices or pharmaceutical environments.
• Familiarity with aseptic techniques and component preparation.
• cGMP experience in Grade 8 or lower environments is highly preferable.

Shift:

• Day Shift (7:00 am - 4:00 pm), with potential future shift adjustment to split shift (3:00 pm - 12:00 am).
• Flexibility for overtime is required.