Process Leader, Bio Production 2nd Shift Mon-Fri 3:00PM - 11:30PM
- Location
- Saint Joseph, MO · On-site
- Job type
- Full-time
- Level
- Senior
- Listed
- 8 days ago
About the role
Apply now »
About the role
As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people.
We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
Provides technical direction and supervision in their assigned biological production area according to company policies and corporate business plans. Ensures technical competence through proper selection and training of the work force, ensuring a safe work place. Implements and maintains compliance status (cGMP,OSHA) within the department.
Manages the documentation flowing in/out of the production floor including, but not limited to, batch records, equipment logbooks, etc. Assist in developing a continuous improvement philosophy within the work force. Implement new technologies. Assist in maintaining the lowest cost of production possible.
Duties & Responsibilities
- Supervise personnel to include communicating to management the status and/or progress of departmental concerns, issues, employee actions, new ideas, and all other relevant information to ensure success within the department.
- Hire, train, coach and develop personnel within the department in accordance with polices and procedures.
- Coordinate the activities and schedules of the department.
- Prepare and/or manage departmental budget and monitor departmental expenses and capital projects.
- Responsible for purchase of operating supplies to include recommendations new or replacement equipment. Coordination of cycle counts in the Department to control inventory in production areas.
- Accurate business function documentation management: Organize/prioritize batch record reviews as defined by Management for completed production items.
- Create, review and approve relevant SOPs, Controlled Forms and other business function documents to support regulatory compliance, change controls and company driven initiatives.
- Manage and maintain tracking system for department key performance indicators. Provide data/metrics to Management regarding individual, equipment, production trends; provide recommendations to resolve errors.
- Analyze production problems, document findings, and implement solutions to resolve problems
- Investigate production process deviations.
- Ensure compliance with cGMP, APHIS, OSHA, EPA, EU, and JP regulations pertaining to production process.
- Direct engagement in process execution including performing, supervising and supporting process steps ensuring safe, compliant and reliable outcomes.
Requirements
High School Diploma. Bachelor's Degree in related business or scientific field preferred.
- In addition to Bachelor's degree, 2 years professional experience.
- 6 years relevant experience in lieu of degree.
- Experience must be inclusive of 1 year leadership experience.
- Demonstrated ability to train others and complete OJT assessments.
- Demonstrates the ability to follow systematic continuous improvement methodologies and the willingness to identify, define, and implement process improvements.
- Experience must be inclusive of managing and auditing master receipts, batch records and process order data within relevant SAP/ERP software systems.
- Experience with word processing, spreadsheets, and database management required.
- Must be detail oriented, able to work with minimal supervision and self-motivated to utilize resources to troubleshoot as needed.
- Ability to manage multiple on-going projects with aggressive deadlines.
- Strong proofreading skills along with excellent communication and written capabilities.
- Must be proficient in MS office applications such as Word, Excel, Outlook, etc.
- Experience in ERP inventory control system(s)is preferred but not necessary.
- Must be able to readily learn and quickly become proficient in all software applications utilized for packaging equipment and operations.
Eligibility Requirements
- Must be legally authorized to work in the United States without restriction.
- Must be willing to take a drug test and post-offer physical (if required)
- Must be 18 years of age or older
- Apply now »
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From Boehringer Ingelheim's careers page, first listed on Rolev.ai on November 5, 2026. Rolev.ai is not the employer.
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Common questions
Where is the Process Leader, Bio Production 2nd Shift Mon-Fri 3:00PM - 11:30PM job at Boehringer Ingelheim located?
This Process Leader, Bio Production 2nd Shift Mon-Fri 3:00PM - 11:30PM position at Boehringer Ingelheim is located in Saint Joseph, MO (On-site). Always check Boehringer Ingelheim's application page for specific state eligibility or relocation policies.
How do I apply for the Process Leader, Bio Production 2nd Shift Mon-Fri 3:00PM - 11:30PM position at Boehringer Ingelheim?
This listing links directly to Boehringer Ingelheim's application page. You can apply directly on Boehringer Ingelheim's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.