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Fujifilm Quality Control Associate Operations in Thousand Oaks, California

Overview

The work we do at FUJIFILM Diosynth Biotechnologies (FDB) changes lives, and our united passion for advancing tomorrow's medicines - our Genki - will always be our driving force. While working as a Quality Control Associate Operations with our Thousand Oaks team, you'll be joining other motivated individuals who fuel one another's passions and embrace every day as an opportunity. We am to foster a collaborative, innovative and rewarding environment, where diverse perspectives and people come together united by a common purpose and shared values. We pursue our fullest potential as individual contributors and team members. We strive to be the employer of choice and offer a competitive compensation and benefit package.

External US

QC Associate Operations

Job Type: Full Time

City: Thousand Oaks (Los Angeles)

Reports to: Supervisor, Quality Control

Position Summary:

The QC Associate Operations position is responsible for executing sample management activities, which include control, receipt, and distribution of product, intermediates, raw materials samples, sample retention, reference samples, and stability samples at Fujifilm Diosynth Biotechnologies California (FDBC). The QC Associate Operations position will interact regularly with internal QC, Quality Assurance, Manufacturing, Warehouse and Facilities groups.In addition to external Quality representatives supporting client requests and/or notifications.

This position is expected to carry out all their activities in compliance with FDBC Quality processes, the requirements of the Quality Management System, and in compliance with regulation requirements governing laboratory controls and manufacturing.Individuals in this role are customer service-oriented, demonstrate fundamental awareness ofverbal and written communication, problem solving, critical thinking, and time management. And role model company core values of trust, delighting our customers, Gemba, and Genki.

Primary Responsibilities:

  • Responsible for receipt and entry of samples in the inventory management system.

  • Performs any combination of sample management tasks, including label, prepare for shipping, transfer to labs, inventory, and disposal.

  • Reviews and verifies sample documents against samples to ensure accuracy and communicate discrepancies. Distributes sample information and documents.

  • Verifies data entry completed by others.

  • Work on LIMS system to support sample management activities.

  • Assists with management of samples in stability studies as needed and directed. Including removal of samples from stability and verification of information.

  • Properly handles, stores, and disposes of hazardous materials according to site procedures.

  • Ensures all work performed strictly adheres to cGMP and FDBC documents.

  • Performs and documents equipment management tasks to maintain QC equipment, which include LN2 freezers, refrigerators, and freezers.

  • Performs document management tasks for sample documents, such as uploading of data reports/data packets into the document management system (Veeva).

  • Performs document management tasks for writing procedures and work instructions.

  • Attends work center team meetings and provides project updates.

  • Perform review of logbook data which includes overall documentation.

Skills and Abilities:

  • Experience working in laboratory environment.

  • Experience with cGMP and QC Sample Management in the pharmaceutical industry preferred.

  • Knowledge of cell-based bioassay and cell culture is a plus.

  • Experience working in LIMS application.

  • Working in shift schedules. (Morning/Afternoon shifts)

  • Working in a flexible and dynamic environment.

Physical Requirements:

  • Subject to extended periods of sitting and standing, vision to monitor and moderate noise levels.

  • Work is performed in a laboratory environment andincludes use of LN2 freezers and lifting/movement of racks of sample boxes.

Education and Professional Experience:

  • High School diploma with 6+ years of experience; or Associates degree with 4+ years of direct laboratory experience; or Bachelor’s degree with 0-3 years of experience.

Travel:

  • Not applicable

Salary and Benefits:

  • $30.50 to $36.50 per hour, depending on experience

  • Medical, Dental and Vision

  • Life Insurance

  • 401k

  • Paid Time Off

Join us! FDB is advancing tomorrow’s medicine, impassioning employees to chase the impossible and continually expand their potential. We are a company of emboldened goal seekers – driven by an innate desire to better ourselves, our families, our workplace, our company, our community and the world at large.

FDBC is an equal opportunity employer to all, regardless of age, ancestry, color, disability (mental and physical), exercising the right to family care and medical leave, gender, gender expression, gender identity, genetic information, marital status, religious creed, sex (includes pregnancy, childbirth, breastfeeding, and related medical conditions), and sexual orientation and any other status protected by state or federal law.

To all agencies: Please, no phone calls or emails to any employee of FUJIFILM about this requisition. All resumes submitted by search firms/employment agencies to any employee at FUJIFILM via-email, the internet or in any form and/or method will be deemed the sole property of FUJIFILM, unless such search firms/employment agencies were engaged by FUJIFILM for this requisition and a valid agreement with FUJIFILM is in place. In the event a candidate who was submitted outside of the FUJIFILM agency engagement process is hired, no fee or payment of any kind will be paid.

Job Locations US-CA-Thousand Oaks

Posted Date 2 weeks ago (11/20/2024 12:21 PM)

Requisition ID 2024-32622

Category Quality Control

Company (Portal Searching) FUJIFILM Diosynth Biotechnologies

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