Total Quality Manager jobs in Thousand Oaks, CA
Total Quality Manager manages the implementation, administration and measurement of total quality management programs, including Six Sigma initiatives. Leads teams to provide training, tools, and logistical assistance for quality initiatives. Being a Total Quality Manager oversees development of new testing tools, and measurement methods and systems to ensure products and services meet quality standards. Requires a bachelor's degree. Additionally, Total Quality Manager typically reports to a senior manager. The Total Quality Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Total Quality Manager typically requires 5 years experience in the related area as an individual contributor. 1 - 3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Total Quality Manager jobs
Quality Assurance Manager - (JP9589)
- 3 Key Consulting
-
Thousand Oaks, CA
FULL_TIME
-
Job Title: Quality Assurance Manager - (JP9589)
Location: Thousand Oaks, CA. or Cambridge
Employment Type: Contract
Business Unit: Final Product Technology Quality
Duration: 1 years (with likely extensions and/or conversion to permanent)
Posting Date: 12/28/21
Notes: Remote pending lift of COVID restrictions
3 Key Consulting is hiring a Risk Management Senior Associate for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
These roles will start out remote due to COVID and then will go to onsite, M-F. Can sit in Thousand Oaks or Cambridge.
Provide quality oversight with regards to the development and lifecycle management of test and inspection methods and fulfillment of regulatory commitments. Potential scope of products with regards to test and inspection methods includes a wide range of devices, raw material components, and constituent parts, such as: needle protection systems, fluid transfer devices, pen injectors, automatic pen injectors, and micro-infuser delivery pump systems. The qualified candidate will both lead and/or support technical teams to ensure successful method development or remediation and/or fulfillment of regulatory commitments. The role of the Senior Quality Engineer is to provide quality oversight to one or more cross-functional teams to utilize technologies and methodologies that support short-cycle robust development, accelerated compliance efforts, and/or remediation/improvement opportunities.
Work cross-functionally and globally with individuals and project teams within Final Product Technologies Quality and the Final Product Technologies Engineering groups and their stakeholders in Marketing, Operations, and Development; Ensure compliance to design controls and fulfillment of user needs during test or inspection method development or design changes, including proper and compliant integration of different subsystems as required. – Provide quality oversight and guidance regarding the development of process control plans and implementation of process improvements/changes. – Work with cross-functional teams to develop, qualify, and transfer physical test or inspection methods. - Provide comprehensive quality guidance and advice to counterparts and stakeholders.
Why is the Position Open?
Supplement additional workload on team.
Top Must Have Skills:- Quality Assurance experience.
- Experience with technical methods.
- Experience with combination products.
Day to Day Responsibilities:- Review and approve FP Mechanical/Physical methods, method development reports, user requirements, method validation reports and method transfer reports.
- Provide oversight to ensure accuracy and precision of methods to measure final product specifications.
- Review material characterization data, work with Regulatory to inform teams of any regulatory requirements that must be met.
- Facilitate PAI readiness for notified bodies and act as escort.
- Review method transfers across sites and suppliers to provide quality perspective and approval.
- Provides advice to regulatory on submission strategies associated with platforms and physical methods.
- Inform other Quality functions of any material requirements.
- Provide quality expertise and technical knowledge to Final Product Key External Initiative (KEI).
- Co-develop training materials for method transfers and stability method transfers with FPT Core Technologies.
- Co-develop training materials for stability method transfers with FPT Core Technologies
Basic Qualifications:- BS or BE in Engineering and previous experience in the medical device and/or pharmaceutical industries.
- 8 years current experience with engineering processes/procedures and quality tools.
- Major contributions to or the leadership of projects from development through the 510k and PMA approval process.
- Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification/validation, DOE/SPC process optimization & validation (IQ, OQ, PQ), P/DFMEA.
- Product design/development (design control) from concept to post product launch for Europe (EMEA/CE Mark) & US (FDA/PMA/510k) submissions.
- Experience in test or inspection method design and development.
- Small scale device assembly and/or benchtop testing experience..
- Experience with Automated Test Equipment (ATE).
- Experience with regard to Measurement Systems Analysis/GRR principles, including study design/execution/troubleshooting.
- Strong critical thinking, problem solving, risk assessment, and risk management skills.
- Must be capable of working on multiple projects in a deadline driven environment.
Employee Value Proposition:
Working at a great biotech/pharma company, working with a dynamic team on challenging concepts, growing your skill set in the role.
Red Flags:
No and or minimum QA experience.
Interview process:
Video Skype Panel Interview
We invite qualified candidates to send your resume to resumes@3keyconsulting.com. If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.
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Quality Engineering Manager
- Regal Rexnord Corp
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FULL_TIME
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- JobsRus.com Formerly CorTech
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- Guitar Center
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Quality Assurance Manager, Biopharma (JP10285)
- 3 Key Consulting
-
Thousand Oaks, CA
FULL_TIME
- Job Title: Quality Assurance Manager, Biopharma (JP10285) Location: Thousand Oaks, CA Employment Type: Contract Business Unit: Combination Products Operations Quality Control Duration: 6 months with l...
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0 Total Quality Manager jobs found in Thousand Oaks, CA area
Manufacturing Production Supervisor
- Intellyk Inc
-
Simi Valley, CA
- Job Description Job Description Title: Production Team Supervisor Job type: Full time Location: Simi Valley, CA 93063 Jo...
- 4/17/2024 12:00:00 AM
Quality Assurance Supervisor
- Hiring Now!
-
Santa Monica, CA
- Baked Goods Manufacturing Company seeking an experienced and detail-oriented QA Team Supervisor to join our dynamic team...
- 4/17/2024 12:00:00 AM
Quality Assurance Supervisor
- Hiring Now!
-
Torrance, CA
- Baked Goods Manufacturing Company seeking an experienced and detail-oriented QA Team Supervisor to join our dynamic team...
- 4/17/2024 12:00:00 AM
Head Start - Quality Assurance Specialist
- Crystal Stairs
-
Los Angeles, CA
- Crystal Stairs, Inc. Improving the Lives of Families through Child Care Services, Research, and Advocacy Head Start - Qu...
- 4/17/2024 12:00:00 AM
Manufacturing Engineer
- Belcan
-
Simi Valley, CA
- Job Title: Manufacturing Engineer Pay Rate: $130K annually Location: Simi Valley, CA Area Code: 805 ZIP Code: 93063 Star...
- 4/16/2024 12:00:00 AM
Demand Planner
- Pair Of Thieves
-
Culver City, CA
- About the company: Pair of Thieves is a basics brand that takes pride in creating high-quality, freshly designed, multi-...
- 4/16/2024 12:00:00 AM
Director, Production
- Wasserman
-
Los Angeles, CA
- Wasserman powers the business of sports, music, entertainment and culture. We serve clients with exceptional insight, in...
- 4/15/2024 12:00:00 AM
Quality Assurance Assistant
- Gategroup
-
Los Angeles, CA
- We're looking for motivated, engaged people to help make everyone's journeys better. This position is responsible for th...
- 4/15/2024 12:00:00 AM
About Thousand Oaks, California
Thousand Oaks is the second-largest city in Ventura County, California, United States. It is in the northwestern part of Greater Los Angeles, approximately 40 miles (64 km) from Downtown Los Angeles and is less than 15 miles (24 km) from the Los Angeles neighborhood of Woodland Hills. It is named after the many oak trees present in the area, and the city seal is adorned with an oak.
The city forms the central populated core of the Conejo Valley. Thousand Oaks was incorporated in 1964, but has since expanded to the west and east. Two-thirds of neighboring Westlake Village and most of Newbury Pa...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Total Quality Manager jobs
$137,981 to $188,967
Thousand Oaks, California area prices
were up 2.5% from a year ago
were up 2.5% from a year ago
What does a Total Quality Manager do?
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Business marketers need to emphasize on quality of their brands over quantity to survive the cut throat competition.
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Total Quality Management is focused on ensuring that process standards ensure a great customer experience, while Six Sigma is designed to reduce defects.
February 13, 2020
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Total Quality Management (TQM) is an approach that organizations use to improve their internal processes and increase customer satisfaction.
January 14, 2020