QA Technician

Food manufacturing company in Carson is looking for a QA Technician to join their second shift team! Opportunity to work overtime and gain experience within QA! WHAT'S IN IT FOR YOU:

OT opportunities

Work in a fast-paced manufacturing environment

Opportunity for permanent hire

REQUIRE EXPERIENCE:

Food manufacturing

HACCP

Ability to work 2nd shift

SCHEDULE:

Monday-Friday, start time between 12pm and 2pm (8 hour shift from there)

Flexibility to work OT

Flexibility to work Saturdays

Description: Conducts appropriate analytical testing of materials, work in progress (WIP), finished goods (FG), and equipment to assure compliance with product quality standards as required by GMP, HACCP, and standard specifications. Practices proper chemical, physical, microbiological, and sensory testing procedures. Inspects incoming goods to meet quality standards defined by ingredient specifications. Oversees processing/manufacturing practices; such as Critical Control Points (CCP) and Control Points (CP), and derive raw data for appropriate documentation. Collects and organizes retained, shelf-life, and microbiological test samples per production. Reviews and organize processing documentation to assure products are within respective standard specification, and report any deviations to the Quality Assurance Supervisor, while placing the products on Hold. Enforces and comply with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), safety guidelines, and quality assurance and food safety programs Carries out routine audits throughout the facility, document the findings and corrective actions, and issue maintenance/safety tags where needed. Informs the Quality Assurance team of significant issues or developments identified during regular work. Participates in Quality Assurance training and validation as defined by management. Represents the department in continuous improvement teams and other cross-functional departments. Uses proper documentation and generates accurate records according to process control and QA programs. Review records after end of shift/day. Represents the department in continuous improvement teams and other cross-functional teams. Monitors and report manufacturing and materials deviations from product and materials standards. Evaluates line operations to assure compliance with GMPS and report deviations to operations and QA Management. Keeps Quality Assurance Team informed of significant issues or developments identified during daily activities and actions taken to improve the situation. Skills:Quality Assurance, Microbiology, HACCP, inspection, GMP, productionExperience Level:Entry LevelDiversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

Actalent is an equal opportunity employer.About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.