Label Printing Supervisor

(www.lso-inc.com) is in North Orange County in the city of Brea, California. Life Science Outsourcing, Inc (LSO) is a contract manufacturer of medical devices with in-built capabilities to offer clients full-service solutions through our six divisions. Clients rely on LSO to perform all activities required to introduce their products to market, from sourcing to drop shipping.

We are looking for a proactive and enthusiastic Label Printing Supervisor with a good positive energy to join our team. In this role you will be responsible for creating, planning and managing the label printing function. Maintain accurate inventory of blank labels & ribbons and report any adjustments to affected departments. Assist LSO to produce Quality Products, on time and within budget. 

We encourage you to submit a resume with salary requirements.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

• Reviews label procedures to ensure compliance of regulatory requirements.
• Create, set up and update all labels per customer’s requirements.
• Generate a Label Approval form.
• Manages label printing department and overall expectations pertaining to setting accurate schedules and allocating resources.
• Ensures label printing staff are trained to perform jobs effectively.
• Ensure label printing staff activities are in compliance with documented procedures.
• Ensure material is issued in Deacom in a timely manner
• Ensure label printing staff reports labor hours are allocated in Deacom
• Ensure staff prints label reports on time for each order produced in Deacom within the established time
• Maintain label printing area in accordance with GMP.
• Manages the maintenance of the computers, printers, and scanners. 
• Other duties may be assigned.

The requirements listed below are representative of the knowledge, skill and/or ability required. 

• Experience using ZEBRA, Quicklabel printers is required 
• Proficient using Labelview and Bartender printing systems 
• Strong computer skills (Microsoft Office Suite – Word, Excel, and Outlook) required.
• Possesses strong verbal and written communications.
• Knowledge of documentation control requirements for cGMP regulated industries to meet FDA and ISO regulations is desired.
• Excellent attention to detail – must be detail-oriented and possess strong organizational skills.
• Ability to work with cross-functional teams.

SKILLS

• Highly skilled in problem solving and analysis.
• Considerable amount of leadership and communication skills.
• Able to work with all departments.

PHYSICAL DEMANDS – Reasonable accommodations may be made to enable individuals with disabilities to perform the following essential physical demands:

• Physically able to sit, stand and walk for extended periods of time.
• Able to move about on foot; walk up and down stairs repeatedly as needed.
• Clarity of vision at 20 inches or more; able to view a computer monitor for extended periods of time.
• Able to work in an area with ambient temperature (hot or cold) according to the season

All your information will be kept confidential according to EEO guidelines.