Supv II Manufacturing
Hayward, CA
Req ID 51471BR
Business Title
Supv II, Manufacturing
Business
BioScience
Sub-Business
Manufacturing
Country
US
State/Province
California
Location of Position
Hayward, CA
Shift_
1st
Job Description
The production supervisor position is responsible for implementing and supervising all activities in the production area to ensure manufacturing goals and project deadlines are met while maintaining compliance with current good manufacturing practices (cGMPs), environmental health and safety (EHS) guidelines and any other regulations that could apply. Focus is on optimization for the use of raw materials, equipment and personnel in producing quality products. May monitor and control labor and capital expenditures. May assist in developing budgets. Recommends manufacturing policies, procedures and programs. Supervisor is expected to provide guidance, support, direction and leadership through positive interactions with all personnel during daily operations.
Responsible for supervising the day-to-day production, scheduling, staffing, material management, compliance, training and auditing activities - to meet customer requirements including deadlines and quality standards.
Interview, hire, coach, motivate, develop and discipline staff. Conduct annual performance reviews for all direct reports. Assist in setting performance objectives and development plans. Monitor progress.
Review, approve, and manage documentation for batch and system records. Assist in release of product for distribution. Assist in meeting product release time goals.
Emphasize training programs designed to enable staff to consistently execute all manufacturing processes with strict compliance to cGMPs and EHS regulations.
Develop and implement performance measurement and internal auditing programs in order to routinely evaluate operation efficiency and quality. Implement changes as needed based on assessments.
Perform/lead technical reviews, investigations and process improvement projects. Provide manufacturing input into integration and validation of new equipment and processes.
Resolves technical, material and cGMP problems that may impact project deadlines. Provide guidance and troubleshooting assistance as needed during a deviation in the process.
Represent the company during FDA inspections. Provide information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs.
Provide a positive and equitable working environment emphasizing the Baxter Shared Values: Respect /Responsiveness / Results
Job Requirements
• In-depth process knowledge of related manufacturing equipment and processes.
• Ability to manage multiple priorities in a manufacturing plant setting.
• Ability to analyze and interpret scientific and statistical data.
• Strong professional writing skills and ability to prepare technical reports.
• Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.
• Strong assessment and troubleshooting skills.
• Ability to respond to detailed inquiries, and present information to groups and senior management.
• May be required to supervise multiple groups/shifts.
• Overtime may be required at times .
Good computer skills.
BS degree in a scientific or engineering discipline with 3-5 years of manufacturing experience or AA degree or equivalent manufacturing experience. Plus 4-6 years supervisory related experience required.
Doing Work that Matters
Baxter provides its employees with comprehensive compensation and benefits. To view additional opportunities at Baxter and to learn more about the company, please visit our Web site at company website. EOE M/F/D/V.
