MCS Manufacturing (Process) Technician - BioPharma Consulting JAD Group
Thousand Oaks, CA
About the Job
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:
- 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.
Skills and Abilities:
- 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.
Requirements
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.
Source : BioPharma Consulting JAD Group