GOOD KIND
DOCUMENT CONTROL
GOOD KIND, Round Rock, Texas, us, 78682
About The Goodkind Co
Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora.
Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place.
OverviewReporting to the Quality Assurance Supervisor, the Document Control Specialist is responsible for oversight activities specific to documentation control, and is focused on maintenance and processing of document workflows for the facility, including document management system, batch and process documentation (issuance and control), and document storage (physical and electronic).
What You'll Do
Manage the document lifecycle including preparation, routing, review, approval, distribution, and archival.Review documents submitted to ensure the correct use of templates correctly entered data and document types.Maintain documentation and records including audit reports, SOPs, regulatory documents, batch records, etc.Create and manage approval workflow for final procedures, documents, records, specifications, etc.Maintain audit training records to ensure records are complete and accurate before filing.Perform advanced word processing.Publish weekly reports and logs identifying open workflows, submittals, and other documents.Assist in developing document control related procedures and implementation.Organize and ensure accurate and reliable filing systems for all paper-based GMP documents.Work with team members to ensure proper maintenance and retention of all qualifying documents and information.Ensure that document retention and review systems are compliant with internal and external standards, including ISO 22716 and FDA.Maintain flexibility to provide additional support as requested or required based on individual production and manufacturing needs.Provide support in external and internal audits.Prepare finished goods COAs, and Spec Sheets for new productsExperience with issuing and reviewing change management documentation.Perform other duties as assigned.What We Require
Bachelor's degree in Library Science, Communications, or Business Administration preferred.Minimum of 3 years of technical writing/document control experience in the personal care/cosmetics/contract manufacturing industry.Fast, efficient, high-level user of Google Suite tools.Innovative, Open-Minded, Collaborative, and Team-Oriented attitude.Experience with Electronic Document Management systems, Microsoft Office Suite, and Adobe Acrobat.Experience with maintaining and reporting for a Quality Management System (QMS)Detail oriented with exceptional organizational, time management and interpersonal skills.Team player with the ability to work across multiple functions, cultures, and disciplines.Positive and constructive attitude.Demonstrated problem-solving ability in a cross-functional environment.GMP / ISO 22716 experience a plus.Ability to sit and/or stand for extended periods of time.Knowledge, Skills, and Abilities
Master Complexity: Competently handle day to day work challenges; thrive in uncertain circumstances; adapt to changes in the work environment; manage multiple tasks and competing demands; change approach or method to best fit the situation.Commitment: Strive to attain quality results on time; convey a sense of urgency and drive issues to closure; earn a reputation for reliability and dependabilityAnalytic Skills: Ability to anticipate problems and offer potential solutionsCustomer Focus: Understand the company's customer demographics and objectivesInnovation: Develop and champion unique ideas and solutions; find new ways to use technology more effectively; promote continuous learningInterdependent Partnering: Contribute to a productive and cooperative atmosphere; show commitment to team objectives; contribute own fair share of effort; available to work outside of standard business hours if needed.
Founded in 2010 and based in the Austin area, Goodkind is a leading manufacturer of clean and green personal care and beauty products. Goodkind specializes in natural deodorant, skincare, and facial care products. The company has a wealth of experience in the formulation of these products and can develop according to a variety of guidelines from consumer organizations such as Ecocert to EWG, to retailers such as Credo or Sephora.
Goodkind is a certified B Corporation. As such, we balance purpose and profit, considering the impact of decisions across associates, customers, suppliers, community, and the environment. Goodkind believes by following this central multi-stakeholder approach, we are creating optimal value for each stakeholder while leaving the world a better place.
OverviewReporting to the Quality Assurance Supervisor, the Document Control Specialist is responsible for oversight activities specific to documentation control, and is focused on maintenance and processing of document workflows for the facility, including document management system, batch and process documentation (issuance and control), and document storage (physical and electronic).
What You'll Do
Manage the document lifecycle including preparation, routing, review, approval, distribution, and archival.Review documents submitted to ensure the correct use of templates correctly entered data and document types.Maintain documentation and records including audit reports, SOPs, regulatory documents, batch records, etc.Create and manage approval workflow for final procedures, documents, records, specifications, etc.Maintain audit training records to ensure records are complete and accurate before filing.Perform advanced word processing.Publish weekly reports and logs identifying open workflows, submittals, and other documents.Assist in developing document control related procedures and implementation.Organize and ensure accurate and reliable filing systems for all paper-based GMP documents.Work with team members to ensure proper maintenance and retention of all qualifying documents and information.Ensure that document retention and review systems are compliant with internal and external standards, including ISO 22716 and FDA.Maintain flexibility to provide additional support as requested or required based on individual production and manufacturing needs.Provide support in external and internal audits.Prepare finished goods COAs, and Spec Sheets for new productsExperience with issuing and reviewing change management documentation.Perform other duties as assigned.What We Require
Bachelor's degree in Library Science, Communications, or Business Administration preferred.Minimum of 3 years of technical writing/document control experience in the personal care/cosmetics/contract manufacturing industry.Fast, efficient, high-level user of Google Suite tools.Innovative, Open-Minded, Collaborative, and Team-Oriented attitude.Experience with Electronic Document Management systems, Microsoft Office Suite, and Adobe Acrobat.Experience with maintaining and reporting for a Quality Management System (QMS)Detail oriented with exceptional organizational, time management and interpersonal skills.Team player with the ability to work across multiple functions, cultures, and disciplines.Positive and constructive attitude.Demonstrated problem-solving ability in a cross-functional environment.GMP / ISO 22716 experience a plus.Ability to sit and/or stand for extended periods of time.Knowledge, Skills, and Abilities
Master Complexity: Competently handle day to day work challenges; thrive in uncertain circumstances; adapt to changes in the work environment; manage multiple tasks and competing demands; change approach or method to best fit the situation.Commitment: Strive to attain quality results on time; convey a sense of urgency and drive issues to closure; earn a reputation for reliability and dependabilityAnalytic Skills: Ability to anticipate problems and offer potential solutionsCustomer Focus: Understand the company's customer demographics and objectivesInnovation: Develop and champion unique ideas and solutions; find new ways to use technology more effectively; promote continuous learningInterdependent Partnering: Contribute to a productive and cooperative atmosphere; show commitment to team objectives; contribute own fair share of effort; available to work outside of standard business hours if needed.