Quality/Regulatory Support 1st Shift

Job Description Pay Range from $20 to $23 per hour Day Shift  Works under FSQA management guidance to ensure compliance with Foster Farms, FSIS/USDA, and customer requirements.  Monitor the production process and perform routine Food Safety and Quality Assurance (FSQA) checks in accordance with the food safety and quality programs at the manufacturing...

With a robust set of core principles and a well-defined roadmap for sustained expansion, the company is seeking a CMC Regulatory Professional. The ideal candidate will possess:Offering regulatory guidance and assistance product manufacturing, emphasizing Chemistry, Manufacturing, and Controls (CMC) for approved NADA and ANADA products.Aid in executing...

Job Description Pay Range from $20 to $23 per hour Works under FSQA management guidance to ensure compliance with Foster Farms, FSIS/USDA, and customer requirements.  Monitor the production process and perform routine Food Safety and Quality Assurance (FSQA) checks in accordance with the food safety and quality programs at the manufacturing site. ...

The Director, Regulatory Affairs’ primary responsibility is to lead the Regulatory Affairs team in developing and implementing regulatory strategies and procedures. This role will lead regulatory strategy and submissions and provide regulatory guidance to the research and development teams during product development to ensure compliance with regulatory...

**Position Summary**: The Quality Assurance Manager is responsible for the whole oversight of the Quality Assurance, and floor quality at both manufacturing and packaging sites. They are to appropriate, delegate, and review Quality Assurance operations and related tasks to ensure the company’s full Quality Assurance support as well as quality operational...

Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. **Summary**: Quality Assurance Manager is...

Job Description Purpose: AbbVie is dedicated to delivering a consistent stream of innovative, safe, and effective quality medicines and products that solve serious health issues and have a remarkable impact on people’s lives. As a quality organization in research & development, R&D Quality Assurance (RDQA) is committed to driving quality excellence...

About Allogene: Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of...

Shift Digital is the leader in digital marketing program optimization. Established in 2008 and headquartered in Birmingham, Michigan, our comprehensive solutions help national brands and their local retailers measure, manage, and improve the performance of their digital marketing and sales initiatives. The Senior Program Manager is responsible for owning and...

Job Description Pay Range from $20 to $23 per hour 2nd shift  Works under FSQA management guidance to ensure compliance with Foster Farms, FSIS/USDA, and customer requirements.  Monitor the production process and perform routine Food Safety and Quality Assurance (FSQA) checks in accordance with the food safety and quality programs at the manufacturing...

Summary: Our client, a clinical stage biopharmaceutical company based in California, is seeking an experienced and highly motivated, hands-on regulatory affairs leader to join their team. The successful candidate will be responsible for developing and implementing effective regulatory strategies to support the development of innovative cell...

Job Description Block is looking for an experienced Regulatory Licensing Manager with relevant international regulatory lending experience. This is a great opportunity to join a growing legal team, working on exciting issues. As we expand our offerings, your ideas and contributions will make an immediate impact. The core mission of this role is to uphold...

POSITION SUMMARY The primary responsibility of the Senior Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies. The Sr. RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications. Supports necessary regulatory activities required for product...

Job Description Key Responsibilities   Responsible for providing regulatory strategy & support for global development. Responsible for supporting teams & efforts around major filing activities & Regulatory Health Authority (RHA) interactions & meetings, attending & providing regulatory support to other departments, project teams & committees. Organize...

The Senior Director, Quality manages the development, implementation, and maintenance of Quality System processes. This position will interface with cross-functional departments facilitating resolution of events in compliance with divisional and corporate requirements. As a leader, the candidate is expected to effectively lead and mentor. Essential Duties...

Overview: What you can expect!    Find joy in serving others with IEHP! We welcome you to join us in “healing and inspiring the human spirit” and to pivot from a “job” opportunity to an authentic experience!   The Regulatory Production Specialist II will be responsible for managing day-to-day operations of a portfolio of regulatory member...

Job Description Key Responsibilities   Support the development of medical devices and/or device components of combination products by providing support on applicable design control, human factors/usability engineering, and risk management processes. Support implementation of assurances, process controls, and Corrective Actions/Preventative Action (CAPA)...

**Date Posted**: 2024-02-13 **Country**: United States of America **Location**: HCA21: Aerostructures - Chula Vista 850 Lagoon Blvd, Chula Vista, CA, 91910 USA **Position Role Type**: Onsite Collins Aerospace is looking for a **Master Tech, Quality Compliance** at our Chula Vista, CA location who possesses a deep knowledge and highly developed technical...

Job Description Position Summary: The individual is responsible for activities that lead to, and maintain compliance to/with Cutera’s Quality Management System and maintains regulatory approval to market devices. Additionally, the individual is responsible for the assessment of device changes for quality and regulatory implications and developing...

Overview:We are seeking an experienced and visionary Director of Quality to lead our organization's quality assurance and quality control efforts. The Director of Quality will be responsible for developing and executing a comprehensive quality strategy, driving continuous improvement initiatives, and ensuring adherence to regulatory requirements and industry...