We have an open position for a Production Supervisor for our Manufacturing department located in the Irvine, CA location.

RESPONSIBILITIES:

• Oversees the manufacturing floor, inspects raw materials and in process product to verify conformance to specifications.

• Work closely with QC & QA to ensure raw materials, documents, i.e. MBRs, attachments, labels, and material releases are available for manufacturing.
• Ensures timely closure of open manufacturing process orders and including necessary inventory adjustments and labor postings.

• Performs calculations in Master Batch Records as necessary.
• Reviews batch records for accurate completion and to assure Good Documentation Practices (GDP) are followed in line with Right First-Time Goals.

• Assist Production Manager, R&D and Project Management with updating existing and reviewing new MBR’s as necessary.
• Performs training of production personnel for equipment set-up, Standard Operating Procedures and manufacturing processes as described in Master Batch Records.

• Assists Production Manager with review and update of SOP’s as necessary.
• Recommends measures to improve production methods, equipment performance, and quality of product.
• Coordinate with Maintenance on required equipment calibrations and Preventative Maintenance.
• Assists with manufacturing related Quality Investigations and required CAPAs.

• Responsible for hiring, performance reviews, and disciplinary actions for direct reports.

• Performs other related job functions as assigned.

QUALIFICATIONS:

• Bachelor’s degree desire, or High School Diploma or GED required.
• 5 years’ experience in an FDA cGMP regulated pharmaceutical manufacturing environment.
• 5 years’ experience supervising or leading employees in a pharmaceutical manufacturing environment preferred, or equivalent combination of education and experience.
• Able to read and interpret technical procedures, SOP’s and GMP regulations and guidelines.

• Proven track record of process improvement.
• Strong communication skills, both written and verbal.
• Able to lift up to 25 pounds occasionally. Ability to walk, stand for a prolonged period.
• Proficient with MS Office; SAP MRP system desire.
• Bilingual in Spanish desire

Job Type: Experience 

Schedule: Full-Time 

At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity employer.

All suitably qualified candidates will receive consideration for employment based on objective work-related criteria and without regard for the following: age, disability, ethnic origin, gender, marital status, race, religion, responsibility of dependents, sexual orientation, or gender identity or other characteristics in accordance with the applicable governing laws.