Factors Group of Nutritional Companies
QA Inspector
Factors Group of Nutritional Companies, Monroe, Washington, United States, 98272
Job Title: US QA Inspector
Department: Quality Assurance
Business Unit: Factor Group
Reports to: US QA Inspector Supervisor
Location: 14224 167th Avenue SE, Monroe, WA 98272
Schedule: Monday to Friday, 2:00pm - 10:30pm
Job Class: Hourly/Non-Exempt
This position pays: $23.77 - $26.88
Organizational Summary:
Factors Group of Nutritional Companies Inc. is a leading manufacturer of nutritional supplements and other health-building products. We are dedicated to enhancing the wellbeing of our customers through research, development, and delivery of effective nutritional products. It is our mission to contribute to the lives of our customers, employees, suppliers, and the communities we serve in a cooperative and sustainable manner.
Job Summary:
The US QA Inspector ensures that products conform to specifications and quality standards set by internal quality and current regulatory Good Manufacturing Practices (cGMP) standards, during in-process inspections and prior to release. The US QA Inspector also ensures that production staff and the facility comply with GMP standards, while taking into consideration the company's commitment to our seven Core Values such as Sustainability (people, planet, and profit) in the planning and implementation of all actions related to the area of responsibility.
Job Description: Perform in-process manufacturing and packaging inspections Perform finished product inspections, work order review, and release of finished packaged products using Warehouse Management System (WMS) software Assist with planned process deviation review, non-conformance investigations, and corrective actions Create rework and sorting instructions, documentation, and reinspection forms Review and release incoming labels and other printed materials used in packaging Perform routine and periodic GMP inspections and participate in internal audit program Support pest control program activities Perform site datalogger downloads to support reporting initiatives Assist with procedure review and updating in area of expertise Track and compile daily output to contribute to monthly departmental key performance indicators (KPIs) Adhere to and enforce all given instructions including work procedures, standard operating procedures (SOPs), and cGMP Strictly adhere to and enforce all safety policies as outlined in the company policies and training sessions Provide absence coverage for other QA Inspection staff across shifts Provide QA Inspection coverage for occasional overtime in packaging and manufacturing, including weekends Other duties as assigned Requirements:
Technical
Two years' experience in a pharmaceutical, natural health, or food product manufacturing environment preferred High School diploma or GED required Demonstrated knowledge of cGMP as outlined by the FDA Familiarity with Lean Six Sigma methodology an asset Excellent command of the English language, both written and verbal Proficiency with Microsoft Office applications and data entry Experience with Syspro, WMS, and Quality Management System (QMS) software an asset Attributes
Able to build and maintain positive, productive relationships with individuals of diverse backgrounds across the organization Takes initiative on daily tasks, projects, and problem-solving; seeks continuous improvement opportunities, and is accountable for results Demonstrated attention to detail, time management, and follow-through Able to work effectively both independently and in a collaborative team environment Adaptable to change and flexible to work different shifts as required Regular, predictable attendance is an essential function of this job Availability for occasional overtime is an essential function of this job Physical
Regular standing/walking, up to 8 hours day Spending up to 50% of workday sitting at a computer Occasional stooping, kneeling, or crawling Occasional pushing, pulling, lifting, or carrying up to 50lbs Occasional ascending or descending on ladders or stepstools Environment
Frequently required to wear personal protective equipment (PPE), including masks, gloves, hairnets, lab coats, eye protection, etc. Moderately noisy work environment Fast-paced and cleanliness-focused environment Moderate temperature condition
This position is open to all qualified applicants who are legally entitled to work in the country in which this job is located. Only electronic applications can be accepted. This position will close when a competitive candidate pool has been identified. We thank you all for your applications and a member of our team will contact you soon. All the best!
All Internal applicants will be given priority for consideration for the first five business days that this position is posted. After that five days, Internal applicants will be considered along with all other applicants; however, are guaranteed at minimum a call from the Talent Acquisition team.
Department: Quality Assurance
Business Unit: Factor Group
Reports to: US QA Inspector Supervisor
Location: 14224 167th Avenue SE, Monroe, WA 98272
Schedule: Monday to Friday, 2:00pm - 10:30pm
Job Class: Hourly/Non-Exempt
This position pays: $23.77 - $26.88
Organizational Summary:
Factors Group of Nutritional Companies Inc. is a leading manufacturer of nutritional supplements and other health-building products. We are dedicated to enhancing the wellbeing of our customers through research, development, and delivery of effective nutritional products. It is our mission to contribute to the lives of our customers, employees, suppliers, and the communities we serve in a cooperative and sustainable manner.
Job Summary:
The US QA Inspector ensures that products conform to specifications and quality standards set by internal quality and current regulatory Good Manufacturing Practices (cGMP) standards, during in-process inspections and prior to release. The US QA Inspector also ensures that production staff and the facility comply with GMP standards, while taking into consideration the company's commitment to our seven Core Values such as Sustainability (people, planet, and profit) in the planning and implementation of all actions related to the area of responsibility.
Job Description: Perform in-process manufacturing and packaging inspections Perform finished product inspections, work order review, and release of finished packaged products using Warehouse Management System (WMS) software Assist with planned process deviation review, non-conformance investigations, and corrective actions Create rework and sorting instructions, documentation, and reinspection forms Review and release incoming labels and other printed materials used in packaging Perform routine and periodic GMP inspections and participate in internal audit program Support pest control program activities Perform site datalogger downloads to support reporting initiatives Assist with procedure review and updating in area of expertise Track and compile daily output to contribute to monthly departmental key performance indicators (KPIs) Adhere to and enforce all given instructions including work procedures, standard operating procedures (SOPs), and cGMP Strictly adhere to and enforce all safety policies as outlined in the company policies and training sessions Provide absence coverage for other QA Inspection staff across shifts Provide QA Inspection coverage for occasional overtime in packaging and manufacturing, including weekends Other duties as assigned Requirements:
Technical
Two years' experience in a pharmaceutical, natural health, or food product manufacturing environment preferred High School diploma or GED required Demonstrated knowledge of cGMP as outlined by the FDA Familiarity with Lean Six Sigma methodology an asset Excellent command of the English language, both written and verbal Proficiency with Microsoft Office applications and data entry Experience with Syspro, WMS, and Quality Management System (QMS) software an asset Attributes
Able to build and maintain positive, productive relationships with individuals of diverse backgrounds across the organization Takes initiative on daily tasks, projects, and problem-solving; seeks continuous improvement opportunities, and is accountable for results Demonstrated attention to detail, time management, and follow-through Able to work effectively both independently and in a collaborative team environment Adaptable to change and flexible to work different shifts as required Regular, predictable attendance is an essential function of this job Availability for occasional overtime is an essential function of this job Physical
Regular standing/walking, up to 8 hours day Spending up to 50% of workday sitting at a computer Occasional stooping, kneeling, or crawling Occasional pushing, pulling, lifting, or carrying up to 50lbs Occasional ascending or descending on ladders or stepstools Environment
Frequently required to wear personal protective equipment (PPE), including masks, gloves, hairnets, lab coats, eye protection, etc. Moderately noisy work environment Fast-paced and cleanliness-focused environment Moderate temperature condition
This position is open to all qualified applicants who are legally entitled to work in the country in which this job is located. Only electronic applications can be accepted. This position will close when a competitive candidate pool has been identified. We thank you all for your applications and a member of our team will contact you soon. All the best!
All Internal applicants will be given priority for consideration for the first five business days that this position is posted. After that five days, Internal applicants will be considered along with all other applicants; however, are guaranteed at minimum a call from the Talent Acquisition team.