BD · 1 day ago
QC Supervisor
San Diego, CA
Full-time
Onsite
Mid, Senior Level
$96K/yr - $158K/yr
6+ years expBD is one of the largest global medical technology companies in the world, dedicated to advancing the world of health. The QC Supervisor is responsible for leading the day-to-day activities of the QC team, managing productivity, training associates, and ensuring compliance with quality control processes.
Health CareMedical DeviceTechnical Support
Responsibilities
Manage departmental work schedule to ensure timely and effective execution of all QC testing and daily operational objectives
Participate in the development and initiation of business strategies for the QC department to meet the goals and objectives of the business including staffing, equipment and space requirements
Proficient in prioritization of group workload and assignment of testing, communicates effectively with other departments on status updates
Create and prepare daily/weekly/monthly reports to include required corporate metrics, project timelines and productivity measurements
Develop and implement new or revise current department policies and procedures including departmental SOPs and Batch Records for all QC functions
Review and approve all required documentation, including QC Batch Records, change notifications and SOPs
Perform, maintain and document routine training program for departmental employees
Lead human resource management requirements including the interviewing, hiring, and training of all departmental Associates as well as preparation and review of departmental employee annual performance appraisals, goal assignments and career development planning
Direct departmental projects and initiatives to include cost savings and process optimization directives and process improvements
Initiate and lead the departmental continuous improvement programs (i.e. Lean, Six Sigma, etc.) by providing the tools, resources and support needed
Participate in the development and optimization of manufacturing processes and procedures to optimize departmental efficiencies and maintain good product quality
Responsible for equipment and supplies ordering, including new equipment onboarding activities, test method development, and/or validation support including protocol/report writing
Oversee equipment calibration, equipment logs and required documentation as necessary. Work with instrumentation department for onboarding and troubleshooting of equipment
Manage inventories of reference materials or other assay standards including supplies and reagents used in QC assays
Ensure a high level of customer service to all internal and external customers including responsiveness and clearly managing expectations
Receives minimal direction on routine work, general instructions on new assignments, issue resolution, projects, and other assignments
Performs Other Tasks Assigned By Management As Required
Implements the company’s Affirmative Action Plan as it applies to the function supervised. Monitors conduct and relationships among the associates supervised to prevent discriminatory acts or comments
Keeps abreast of U.S. and non-U.S. regulations affecting own area of supervision / management and complies with those regulations, practices and procedures to support regulatory compliance requirements. Communicates the need for compliance to members of own functional area. Brings regulatory compliance questions/issues to the attention of the next level of management
Ensures Environmental Health and Safety (EH&S) training through facilitating the development and implementation of safety awareness programs
Qualification
Required
Minimum of a BA/BS Degree in science, engineering, or other relevant discipline, with a minimum of six years relevant technical experience within medical, pharmaceutical or Life Science industry
A minimum of 6 years' experience in related aspects of quality, manufacturing or production processes is necessary
A minimum of 2-year managerial experience required, or equivalent experience in leading projects
Knowledge of the FDA medical device quality system regulations and international quality system standards/regulations (e.g. ISO 9001, ISO 13485) as it relates to the design and continued support of BD products
Can develop strategy, plan projects, and drive the completion of long-term goals and objectives
Able to use judgement to influence within and across functions to drive impact on the business/function
Demonstrated ability to exercise independent judgement by utilizing strong analytical and tactical skills supported by facts and data
Ability to effectively work with peers
Effective communication (written, verbal and listening) and prioritization skills, with special attention to detail, while maintaining overall perspectives
Preferred
Prior project management is highly desirable
Experience in immunology is a plus
TrackWise, SAP, technical writing, auditing experience preferred
Advanced proficiency in data analysis tools such as Excel or MiniTab preferred
Benefits
Valuable, competitive package of compensation and benefits programs
Rewards and recognition opportunities that promote a performance-based culture
Company
BD helps advance clinical therapy with the process for patients and health care providers with innovative technology services and solutions.
10001+ employees
H1B Sponsorship
BD has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (66)
2022 (4)
2021 (3)
Funding
Current Stage
Public CompanyTotal Funding
$540MKey Investors
Steris
2023-08-02Post Ipo Equity· $540M
1962-04-23IPO
Leadership Team
Tom Polen
Chairman, CEO and President
Maureen Mazurek
Chief Sustainability and EHS Officer
Recent News
EIN Presswire
2026-01-09
Company data provided by crunchbase