Quality Specialist - Brunswick
2 weeks ago

Job summary
Your Job Georgia-Pacific Cellulose LLC is seeking a dynamic and motivated individual to join our Corporate Quality team as an experienced Quality Specialist. This key role supports Quality Operations across Brunswick Cellulose, Alabama River Cellulose, and Leaf River Cellulose locations. We are looking for a proactive self-motivated team member who embodies our Principle-Based Management approach driving continuous improvement operational excellence and alignment with customer needs all while fostering collaboration and integrity.This is a hybrid position that will require at least 2 days of work onsite at Brunswick Cellulose.
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
We re a fast-growing startup operating in specialized alternative markets where every detail matters Our team is small agile and focused on building operations that are reliable disciplined and scalable Were looking for someone who takes pride in precision thrives in structured e ...
1 week ago
We are recruiting Quality/Compliance Specialist for one of our clients. · ...
2 weeks ago
We're looking for someone who takes pride in precision, thrives in structured environments, and enjoys ensuring that systems and processes perform exactly as intended.About this role: · Verify workflows and task completion against established SOPs · Conduct pre- and post-executio ...
1 month ago
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. · We offer a wide variety of competitive benefits services and programs that provide employees with resources to pursue goals both at work personal lives Read more: · ...
1 month ago
We are seeking a Senior Specialist in Documentation Management to join our team. This role is responsible for ensuring compliance within the organization as it pertains to documentation and records management. The ideal candidate will have a minimum of 4 years of quality experien ...
2 weeks ago
Provides Quality support to Contract Manufacturing Operations (CMOs) within a cross functional team and Product Disposition reviews for drug products manufactured/packaged by CMOs. · In addition, to ensure that products released from CMOs comply with Client internal and governmen ...
2 weeks ago
The Quality Assurance Specialist will oversee manufacture, testing and distribution of clinical supplies to assure quality and compliance with Good Manufacturing Practices (GMP/GDP) and other applicable regulations. · Batch disposition (release/reject decision) · Audit of interna ...
2 weeks ago
Ensure that products manufactured at packaging facilities are manufactured tested released according to established specifications. · ...
2 weeks ago
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. · Bristol Myers Squibb is anything but usual. · Here, uniquely interesting work happens every day, · in every department.From optimizing a production line to the latest breakthrough ...
1 month ago
This role will develop processes and procedures for the supplier quality management system. · B.S. in Natural Sciences, Chemistry, Microbiology, Biology or Pharmacy · ...
2 weeks ago
Challenging. Meaningful. Life-changing. · Bachelor of Science degree in chemistry, pharmacy or biology or a related pharmaceutical science. · ...
1 month ago
This role involves providing quality oversight during Clinical Supply Operations drug product and packaging manufacturing activities. · Provide Quality on the floor in-Process support during manufacturing operations. · Assure the quality of manufactured products complies with all ...
4 weeks ago
This role will focus on the facilitation and execution of data quality (DQ) assessment and issue remediation activities for enterprise systems, · Perform data quality profiling and assessment to identify anomalies and data quality issues/gaps that require remediation in technical ...
2 weeks ago
Provides quality support to contract manufacturing operations within a cross-functional team and product disposition reviews for drug products manufactured/packaged by CMOs. · ...
2 weeks ago
This is a Quality Documentation (QC) Specialist role responsible for managing commercial specifications and methods, reviewing change proposals, and performing quality approval of GTS documents. · ...
1 month ago
Global Pharma company looking to hire experienced quality professional to assist with SAP projects of full end to end system lifecycle. · SAP Quality Management consultant · ...
2 weeks ago
Challenging. Meaningful. Life-changing. · Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. · ...
3 weeks ago
We are looking for an experienced quality professional to assist with SAP projects of full end-to-end system lifecycle in our Global Pharma company. · SAP Quality Management consultant to support SAP projects of full end-to-end system lifecycle; including analysis, testing, proce ...
3 weeks ago
The candidate will manage commercial specifications and methods to ensure clear, correct concise consistent compliant documentation. · Manage commercial specifications and methods to ensure clear correct concise consistent compliant documentation. · Review and execute change prop ...
1 month ago
Bristol Myers Squibb is seeking a Quality Assurance Validation Specialist to perform independent review and approval of initial Commissioning, Qualification, and Validation lifecycle documents. · ...
3 days ago
+The candidate will manage commercial specifications and methods to ensure clear documentation. · Review change proposals for GTS documents. · Perform quality approval of GTS documents. · +Manage commercial specifications and methods. · +Qualifications + Bachelor degree requiredB ...
1 month ago