Production Supervisor - Blending, Encapsulation, and Washroom

SHIFT** 2pm - 10:30pm, Monday - Friday

• •*Please note that this is an Exempt/Salaried position that supports a 24/5 plant, this could exceed 40 hours per business needs
• •Perform supervisory functions with a cGMP dietary supplement manufacturing environment per established procedures.
• •Monitor proper stock levels for expendable supplies and components used within the manufacturing process.
• •Responsible for documenting employee activities in terms of performance, corrective action, and attendance.
• •Review and sign off work orders (e.g. cleanings, set-up, beginning of runs, ends of runs, etc.…)
• •Review batch records and associated documentation for completeness, legibility, and correctness.
• •Work with quality control to effectively identify, document, and help resolve quality and production issues as needed.
• •Accurately document any out of specification conditions per established procedures.
• •Accurately track work orders internally during the production process.
• •Monitor and verify completeness of all logs for accuracy, completeness, and legibility.
• •Monitor and communicate any changes to production orders including quantities or changes in schedule.
• •Constantly monitor their production environment for compliance to cGMP requirements.
• •Continually assess safety and ensure production employees are working in a safe environment.
• •Report and monitor any unsafe condition.
• •Punctual and Consistent Attendance
• •Support their team to achieve the objectives of the shift.
• •Monitor and support all training activities with their team.
• •Identify and leads in continuous improvement initiatives in their area
• •Complete and verify documentation with accuracy
• •Ability to be at the physical location of the job at the designated shift assigned.
• •Will be asked to train someone and/or participate in a task force to improve company procedures or operations.
• •Ability to be at the physical location of the job for the designated work schedule
• •Will be asked to train someone and/or participate in a task force to improve company procedures or operations.
• •Ability to effectively problem-solve
• •Ability to work collaboratively and maintain effective working relationships with co-workers.
• •Must be able to successfully pass all job-related tests and certifications required for working in a cGMP, quality environment including but not limited to: inspections and GMP

• •College Degree OR 5 years’ experience in a supervisory role in a manufacturing environment in lieu of degree
• •Computer skills including experience with Microsoft Office and ERP systems
• •Highly organized and detail oriented.
• •Ability to work in a fast paced, results oriented environment.
• •Ability to read and write & communicate in English.
• •Experience with FDA/cGMP compliance is preferred
• •Familiar with Microsoft applications such as MS Office
• •Excellent communication and interpersonal skills with proven ability to take initiative and build strong productive relationships
• •Strong organizational and multi-tasking abilities
• •A legal right to work in the United States
• •Must pass a drug screen and a background check in accordance with HWP standards.

• •Possess ability to quickly identify deficiencies and implement corrective action
• •Ability to work well both independently and within a close knit team environment
• •Good communication, interpersonal and customer service skills. Able to effectively communicate with all levels of management and functional areas.
• •Positive Demeanor
• •Dependable, exemplifying this through attendance and job duties
• •Constantly seeking better processes and challenging status quo: Continuous Improvement
• •Clear focus on High Quality Production
• •Commitment to high ethical standards and integrity
• •Works well Independently and in a Team setting
• •Inspires collaborative thinking and team building

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