Cleanroom Supervisor
Full-Time
The Cleanroom Supervisor primary functions include supervising people and processes in order to meet quality and customer requirements. The Cleanroom Supervisor will also work with all functions within the organization to help drive continuous improvement. In addition, this position includes relaying information between their team and upper management, guiding their team through daily work activities and monitoring employee performance to ensure maximum productivity.
Essential Functions:
- Supervise operators in a fast-paced environment
- Adhere to and support cleanroom and safety requirements
- Contributes to creating a culture of continuous improvement and leads by example
- Work with production manager and appropriate department personnel to ensure new procedures are well understood by operators
- Help ensure that business goals, deadlines and performance standards are met
- Ensure that all team members adhere to good manufacturing practices, standard operating procedures and work instructions
- Ensure product output meets quality standards
- Help improve teammate relations, customer quality and operational efficiency
- Help organize and maintain warehouse/facility appearance and functionality
- Support internal and external audits
- Assist with daily production functions such as label printing, label verification, component inspection and processing, packaging, shipping, paperwork review and other functions as needed
- Assist with daily production functions such as label printing, label verification, component inspection and processing, packaging, shipping, paperwork review and other functions as needed
Position Requirements:
- 10+ years of supervisory (direct and/or direct lead experience)
- 10+ years of manufacturing and /or packaging (sterile and non-sterile) experience in a controlled industry, pharmaceutical, medical devices preferred
- Ability to work both independently and as a part of a team
- Knowledge of manufacturing, packaging and cleanroom operations
- Computer literacy in spreadsheets, excel, email, etc…
- Ability to resolve conflicts, meet deadlines, manage production activities and effectively multitask
- Strong organization, documentation and time management skills with the demonstrated ability to meet deadlines
- Strong knowledge of ISO13485
- Experience with key reporting indicators ( KPI’s)
- Experience with inspection methods including but not limited to drawings, overlays, visual aids and hand tools such as calipers and micrometers
To inquire and/or apply for current opportunities, please send resume to Careers@MainstreamMedicalDevices.com
Mainstream stands as an equal opportunity employer and is committed to providing fair and equal treatment to its employees and applicants without regard to race, color, national origin, religion, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal state and/or local laws. Mainstream will make reasonable accommodations that are necessary to comply with disability discrimination laws.