What are the responsibilities and job description for the MCS Manufacturing (Process) Technician position at BioPharma Consulting JAD Group?
The Manufacturing (Process) Technician is responsible for facility and equipment cleaning and sanitation in support of FDA-regulated manufacturing areas. The role ensures minimal impact on production while adhering to Current Good Manufacturing Practices (cGMPs), Standard Operating Procedures (SOPs),
Responsibilities:
Qualifications:
Responsibilities:
- Perform facility/equipment cleaning and sanitation to support FDA-regulated manufacturing areas
- Follow Good Manufacturing Practices (GMPs) and applicable Code of Federal Regulations (CFRs) standards
- Ensure compliance and quality by maintaining a "Right First-Time" approach
- Receive, prepare, and feed components into equipment for use in manufacturing operations
- Sanitize equipment and production areas, documenting all work according to cGMP standards
- Report discrepancies or issues to the Team Leader or Production Supervisor to ensure safety and quality standards are maintained
- Use pallet jacks and manually wrap pallets for material handling
- Utilize computer systems for material inventory management and electronic batch recordkeeping
- Partner with cross-functional teams to drive continuous improvement opportunities
- Participate in daily performance meetings, ensuring components and products are available for uninterrupted operation
- Must be able to work on your feet for long durations and perform physical tasks such as lifting up to 35 lbs, pushing/pulling objects that require up to 50 lbs of force
- Ability to perform movements like bending, reaching, climbing, kneeling, squatting, stooping, and standing on ladders or portable stairs up to 6 feet
- Strong verbal and written communication skills to effectively convey information and document work
- Problem-solving skills to identify and resolve issues efficiently
- Strong teamwork and collaboration skills to foster a positive and productive work environment
Qualifications:
- Education & Experience:
- Associate degree and 2 years of relevant experience OR
- 2 years of hands-on technical school experience OR
- High school diploma/GED and 4 years of experience in manufacturing or related fields
- 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
