Quality Associate II
Job Location:
Summerville, SC - USA
Monthly Salary:
Not Disclosed
Posted on:
7 hours ago
Vacancies:
1 Vacancy
Job Summary
At Thorne we work to deliver high-quality science-backed solutions to empower individuals to take a proactive approach to their well-being. Each day begins with a mission to help others discover and achieve their best health. We count on our team members to challenge and push the boundaries to make that happen. At Thorne youll be joining a team of more than 750 passionate individuals committed to our cause of providing superior health solutions at every age and life stage.
The Quality Associate is responsible and accountable for various quality tasks and operations.
Possesses and applies a broad knowledge of Quality principles practices and procedures. Manages product certification process and supports the following process: Change Control Corrective and Preventive Action (CAPA) system deviation process customer complaints nonconforming material process and internal audit process. Coordinates with third party
certifying bodies internal resources and outside contract manufacturers on product information and certification testing. Must be able to lead and work with cross-functional teams and track projects to completion.
The Quality Associate is responsible and accountable for various quality tasks and operations.
Possesses and applies a broad knowledge of Quality principles practices and procedures. Manages product certification process and supports the following process: Change Control Corrective and Preventive Action (CAPA) system deviation process customer complaints nonconforming material process and internal audit process. Coordinates with third party
certifying bodies internal resources and outside contract manufacturers on product information and certification testing. Must be able to lead and work with cross-functional teams and track projects to completion.
RESPONSIBILITIES
Build a strong working relationship with third party certification entities and manage certification program. Coordinate information between third party certification entities internally at Thorne and outside contract manufacturers to certify products.
Provide and maintain status reports.
Assist with customer complaint investigations as necessary. Become thoroughly knowledgeable of the applicable portions of Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs) and maintain knowledge base on an ongoing timely basis as procedural changes occur without relying on management intervention or direction.
Manage the Deviation and the Nonconforming Material process through EtQ.
Support the stability program by coordinating sample submission to the lab for internal and/or external addition coordinate meetings and approvals for review of stability data. Create and compile stability data results and final reports.
Proactively initiate the development of streamlined systems to effectively identify and resolve quality problems and process improvement opportunities.
Participate in internal audits and inspections of various departments/processes.
Write revise and review SOPs controlled forms and related documents to ensure best practices and current operations.
Demonstrate knowledge of department procedures and company policies pay attention to detail in all aspects and complete all paperwork accurately neatly and fully.
Participate on process improvement teams to provide quality input and direction. Ensure that documentation of improvements is completed and approved as needed.
Provide quality review and feedback on new products and processes.
Provide ongoing support to all employees on quality system requirements and problem solving.
Compile and create monthly KPI reports and/or periodic reports for management.
Complete ERP functions as related to the NCM process.
Ensure compliance with GMP FDA OSHA and all other regulatory requirements in accordance with company policy.
Adhere to company safety requirements.
Demonstrate initiative and job knowledge by suggesting ideas discovering new and better ways of accomplishing goals and finds innovative well thought-out solutions to problems.
Take initiative and makes sound decisions within the guidelines provided and is willing if necessary to stop a procedure or process when SOP or product quality is in question.
Promote the Companys Mission and Values including an accountable innovative and results-oriented culture promoting customer service openness teamwork mutual trust and respect.
Actively participate in all required training and development programs and electives as may suit ones needs and support colleagues trainers and management as appropriate with these efforts.
Ability to be available for other duties as assigned.
Seek formal and informal performance assessments of self including performance versus expectations and goals behaviors and leadership potential.
Provide and maintain status reports.
Assist with customer complaint investigations as necessary. Become thoroughly knowledgeable of the applicable portions of Standard Operating Procedures (SOPs) and Good Manufacturing Practices (GMPs) and maintain knowledge base on an ongoing timely basis as procedural changes occur without relying on management intervention or direction.
Manage the Deviation and the Nonconforming Material process through EtQ.
Support the stability program by coordinating sample submission to the lab for internal and/or external addition coordinate meetings and approvals for review of stability data. Create and compile stability data results and final reports.
Proactively initiate the development of streamlined systems to effectively identify and resolve quality problems and process improvement opportunities.
Participate in internal audits and inspections of various departments/processes.
Write revise and review SOPs controlled forms and related documents to ensure best practices and current operations.
Demonstrate knowledge of department procedures and company policies pay attention to detail in all aspects and complete all paperwork accurately neatly and fully.
Participate on process improvement teams to provide quality input and direction. Ensure that documentation of improvements is completed and approved as needed.
Provide quality review and feedback on new products and processes.
Provide ongoing support to all employees on quality system requirements and problem solving.
Compile and create monthly KPI reports and/or periodic reports for management.
Complete ERP functions as related to the NCM process.
Ensure compliance with GMP FDA OSHA and all other regulatory requirements in accordance with company policy.
Adhere to company safety requirements.
Demonstrate initiative and job knowledge by suggesting ideas discovering new and better ways of accomplishing goals and finds innovative well thought-out solutions to problems.
Take initiative and makes sound decisions within the guidelines provided and is willing if necessary to stop a procedure or process when SOP or product quality is in question.
Promote the Companys Mission and Values including an accountable innovative and results-oriented culture promoting customer service openness teamwork mutual trust and respect.
Actively participate in all required training and development programs and electives as may suit ones needs and support colleagues trainers and management as appropriate with these efforts.
Ability to be available for other duties as assigned.
Seek formal and informal performance assessments of self including performance versus expectations and goals behaviors and leadership potential.
WHAT YOU NEED
Experience and/or Education: By training education and/or experience must be able to perform the essential duties of their job. Minimum of a high school diploma required with a preference of a college degree.
Language Ability: Employee is able to read and understand at a highly technical and proficient level. The employee follows instructions both verbal and written and communicates effectively with supervisors and fellow employees.
Computer and Technical Skills: Employee can use the equipment and software required to accomplish the responsibilities of the position.
Ability to effect change in a positive environment. Must be able to provide constructive arguments and sound justification as it pertains to technical and supplier requirements.
Initiate and complete reports in a timely manner.
Work independently with little direction in a fast-paced environment.
Possesses good interpersonal skills and engages with others in a positive manner.
Schedule projects and meet tight deadlines.
Develop and deliver on assigned objectives within requested timeframes.
Possess strong attention to detail.
Possess strong verbal and written communication skills.
Raise issues and concerns promptly and offers pragmatic solutions for consideration.
Document and present work in a clear accurate and concise manner.
Quality Associate levels: Associates must be able to complete all tasks listed above with no assistance or guidance from others to advance to a Quality Associate II.
The levels are as follows:
Quality Associate I
Quality Associate II
PHYSICAL DEMANDS Being able to meet the Physical Demands of the job is an essential duty of the job.
Employees at Thorne Research perform the Responsibilities of their jobs in various manufacturing warehousing and administrative areas. The various departments at Thorne Research include Production Operations Quality Accounting/Finance Medical Affairs Administration Information Technology Maintenance Engineering Customer Service and Sales.
Must be able to work in a stationary position as well as move about unassisted. Must be able to hear and converse with supervisors and other employees. Must be able to read large volumes of printed material. Must be able to work in a moderate noise level environment.
Language Ability: Employee is able to read and understand at a highly technical and proficient level. The employee follows instructions both verbal and written and communicates effectively with supervisors and fellow employees.
Computer and Technical Skills: Employee can use the equipment and software required to accomplish the responsibilities of the position.
Ability to effect change in a positive environment. Must be able to provide constructive arguments and sound justification as it pertains to technical and supplier requirements.
Initiate and complete reports in a timely manner.
Work independently with little direction in a fast-paced environment.
Possesses good interpersonal skills and engages with others in a positive manner.
Schedule projects and meet tight deadlines.
Develop and deliver on assigned objectives within requested timeframes.
Possess strong attention to detail.
Possess strong verbal and written communication skills.
Raise issues and concerns promptly and offers pragmatic solutions for consideration.
Document and present work in a clear accurate and concise manner.
Quality Associate levels: Associates must be able to complete all tasks listed above with no assistance or guidance from others to advance to a Quality Associate II.
The levels are as follows:
Quality Associate I
Quality Associate II
PHYSICAL DEMANDS Being able to meet the Physical Demands of the job is an essential duty of the job.
Employees at Thorne Research perform the Responsibilities of their jobs in various manufacturing warehousing and administrative areas. The various departments at Thorne Research include Production Operations Quality Accounting/Finance Medical Affairs Administration Information Technology Maintenance Engineering Customer Service and Sales.
Must be able to work in a stationary position as well as move about unassisted. Must be able to hear and converse with supervisors and other employees. Must be able to read large volumes of printed material. Must be able to work in a moderate noise level environment.
WHAT WE OFFER
- Competitive compensation
- 100% company-paid medical dental and vision insurance coverage for employees
- Company-paid short- and long-term disability insurance
- Company- paid life insurance
- 401k plan with employer matching contributions up to 4%
- Gym membership reimbursement
- Monthly allowance of Thorne supplements
- Paid time off volunteer time off and holiday leave
- Training professional development and career growth opportunities
Required Experience:
IC
About Company
We believe good health could always be made better. Shop Thorne's complete line of integrated health solutions