Supv II, Manufacturing

Baxter International Inc., assists healthcare professionals and their patients with the treatment of complex medical conditions, including cancer, hemophilia, immune disorders, kidney disease and trauma. The company applies its expertise in medical devices, pharmaceuticals and biotechnology to make a meaningful difference in patients' lives.
1) Supervisor is expected to provide guidance, support, direction and leadership through positive interactions with all personnel during daily operations.
2) 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.3) 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.4) Review, approve, and manage documentation for batch and system records. Assist in release of product for distribution. Assist in meeting product release time goals.5) Emphasize training programs designed to enable staff to consistently execute all manufacturing processes with strict compliance to cGMPs and EHS regulations.6) 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.7) Perform/lead technical reviews, investigations and process improvement projects. Provide manufacturing input into integration and validation of new equipment and processes.8) Resolves technical, material and cGMP problems that may impact project deadlines. Provide guidance and troubleshooting assistance as needed during a deviation in the process.
9) Represent the company during FDA inspections. Provide information as necessary to FDA that establishes credibility and demonstrates compliance with cGMPs.10) Provide a positive and equitable working environment emphasizing the Baxter Shared Values: Respect /Responsiveness / Results.Qualifications
1) Demonstrated interpersonal and leadership skills with ability to interface well with other departments, and lead effectively and efficiently in a team environment.2) In-depth process knowledge of related manufacturing equipment and processes.
3) Ability to manage multiple priorities in a manufacturing plant setting.4) Ability to analyze and interpret scientific, and statistical data.5) Strong professional writing skills and ability to prepare technical reports.6) Experienced understanding of cGMPs and other regulatory guidelines applicable to the medical/pharmaceutical industry.7) Strong assessment and troubleshooting skills.8) Ability to respond to detailed inquiries, and present information to groups and senior management.9) May be required to supervise multiple groups/shifts.10) Overtime may be required at times.
11) Good computer skills.12) BS degree in a scientific or engineering discipline with 3-5 years of manufacturing experience or AA degree and/or equivalent manufacturing experience.
13) Plus 4-6 years supervisory related experience required.14) Demonstrated knowledge and application of world-class business systems such as TPS (Toyota Production System), Lean Manufacturing and Six Sigma is a plus.As a global leader dedicated to building the best team in health care, Baxter offers competitive compensation and full benefits. To view other opportunities at Baxter, please visit our Careers@Baxter site. EOE M/F/D/V
REQUIREMENTS
Please see Job Description