Production Lead

QuidelOrtho•Carlsbad, CA

5d•Onsite

About The Position

At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Production Lead. This position is responsible for coordinating assembly and/or packaging activities which may include but are not limited to any of the following processes; spotting, lamination, testing (in-process and matrix), filling, lyophilization operation, strip loading and assisting machine operation, inspecting assembled devices and pouches, packaging final kits and following all associated QSRs, manufacturing instructions, operating procedures and drawings. This position will be on 2nd shift: Monday - Friday / 2:00 pm - 10:30 pm. This position will be onsite in Carlsbad, CA.

Requirements

High School diploma or equivalent
Leadership training or experience.
Ability to objectively evaluate performance and provide constructive criticism.
Experience of Senior Production Associate or equivalent
Same as Senior Production Associate with additional ability to coordinate schedule requirements of all processes performed in the department
Must demonstrate knowledge of internal customer/supplier relationships in decision making
Demonstrates consistent and sound judgement
Knowledge of basic Excel and Word
Capable of running area in absence of supervisor

Responsibilities

Carries out duties in compliance with established business policies.
Coordinates all manufacturing line activities including labor and material allocation so that production standards are met.
Ensures the accuracy of material and labor transactions into LN.
Allocates labor based on skill level and employment status (perm/agency).
Adheres to daily production schedule and ensures that production goals are obtained.
Ensures timely start-up, changeovers and shutdown.
Responsible for data integrity and timely tracking of all line measures (yield, scrap, downtime).
Ensures effective shift transition by clearly communicating with leads on all shifts regarding quality, personnel and equipment issues.
Effectively communicates with all support groups (mechanics, engineers, warehouse personnel, quality control, chemistry, planning and management).
Complies with all QSRs.
Ensures that all manufacturing documents are reviewed and completed in an accurate and timely manner.
Responsible for maintaining department attendance records and reviewing employee time cards for accuracy.
Coordinates and participates in staff training.
Ensures that training records are accurately maintained and current.
May write and participate in employee performance evaluations.
Assists with the transfers of new products to manufacturing including validation of equipment and/or processes.
Proactive in working with facilities and maintenance to repair/improve equipment.
Initiates document and procedural changes utilizing the ECO system.
Coordinate processing of experiments for R & D or Chemistry departments.
Perform other work-related duties as assigned