Administrative Support- Carolina

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    "description_html": "<p><strong>Mentor Technical Group (MTG)</strong> provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.</p><h3><strong>Position Overview</strong></h3>The Clerk responsible for the control, organization, tracking, and archiving of regulated documents in compliance with current Good Manufacturing Practices (cGMP), FDA regulations, and company quality standards. This role ensures accuracy, traceability, and integrity of documentation to support regulatory compliance and product quality. Key Responsibilities Document Control & Management • Maintain and manage controlled documents including: • Logbooks • Issue, retrieve, and reconcile controlled copies of documents. • Ensure proper version control and archival of obsolete documents. • Monitor document review and revision cycles. Key Competencies • Strong attention to detail • Organizational and time management skills • Knowledge of document control systems • Understanding of cGMP principles • Data integrity awareness (ALCOA+ principles) • Proficiency in Microsoft Office<br><br>Education • High School Diploma or GED (required) • Associate degree in Business Administration, Life Sciences, or related field (preferred) Experience • 1–3 years of experience in: • Document control • Administrative support • Regulated industry (pharmaceutical, biotechnology, medical device, or food manufacturing preferred) • Experience working in a cGMP-regulated environment strongly preferred • Familiarity with controlled documentation systems Skills & Competencies • Strong attention to detail and accuracy • Excellent organizational and filing skills • Ability to manage multiple tasks and meet deadlines • Clear written and verbal communication skills • Ability to handle confidential and sensitive information • Strong time-management and prioritization skills.<p><br />\n<strong>Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.</strong></p>\n\n<p><em><strong>Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.</strong></em></p>",
    "description_text": "Mentor Technical Group (MTG)  provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.\n Position Overview\nThe Clerk responsible for the control, organization, tracking, and archiving of regulated documents in compliance with current Good Manufacturing Practices (cGMP), FDA regulations, and company quality standards. This role ensures accuracy, traceability, and integrity of documentation to support regulatory compliance and product quality. Key Responsibilities Document Control & Management • Maintain and manage controlled documents including: • Logbooks • Issue, retrieve, and reconcile controlled copies of documents. • Ensure proper version control and archival of obsolete documents. • Monitor document review and revision cycles. Key Competencies • Strong attention to detail • Organizational and time management skills • Knowledge of document control systems • Understanding of cGMP principles • Data integrity awareness (ALCOA+ principles) • Proficiency in Microsoft Office\nEducation • High School Diploma or GED (required) • Associate degree in Business Administration, Life Sciences, or related field (preferred) Experience • 1–3 years of experience in: • Document control • Administrative support • Regulated industry (pharmaceutical, biotechnology, medical device, or food manufacturing preferred) • Experience working in a cGMP-regulated environment strongly preferred • Familiarity with controlled documentation systems Skills & Competencies • Strong attention to detail and accuracy • Excellent organizational and filing skills • Ability to manage multiple tasks and meet deadlines • Clear written and verbal communication skills • Ability to handle confidential and sensitive information • Strong time-management and prioritization skills.\n Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.\n Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.",
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      "datePosted": "2026-05-26",
      "description": "<p><strong>Mentor Technical Group (MTG)</strong> provides a comprehensive portfolio of technical support and solutions for the FDA-regulated industry. As a world leader in life science engineering and technical solutions, MTG has the knowledge and experience to ensure compliance with pharmaceutical, biotechnology, and medical device safety and efficacy guidelines. With offices in Caguas, PR, Boston, MA & San Francisco, CA, we serve life sciences clients in six global markets: United States, Puerto Rico, Dominican Republic, Mexico, Germany, Canada, and South America.</p><h3><strong>Position Overview</strong></h3>The Clerk responsible for the control, organization, tracking, and archiving of regulated documents in compliance with current Good Manufacturing Practices (cGMP), FDA regulations, and company quality standards. This role ensures accuracy, traceability, and integrity of documentation to support regulatory compliance and product quality. Key Responsibilities Document Control & Management • Maintain and manage controlled documents including: • Logbooks • Issue, retrieve, and reconcile controlled copies of documents. • Ensure proper version control and archival of obsolete documents. • Monitor document review and revision cycles. Key Competencies • Strong attention to detail • Organizational and time management skills • Knowledge of document control systems • Understanding of cGMP principles • Data integrity awareness (ALCOA+ principles) • Proficiency in Microsoft Office<br><br>Education • High School Diploma or GED (required) • Associate degree in Business Administration, Life Sciences, or related field (preferred) Experience • 1–3 years of experience in: • Document control • Administrative support • Regulated industry (pharmaceutical, biotechnology, medical device, or food manufacturing preferred) • Experience working in a cGMP-regulated environment strongly preferred • Familiarity with controlled documentation systems Skills & Competencies • Strong attention to detail and accuracy • Excellent organizational and filing skills • Ability to manage multiple tasks and meet deadlines • Clear written and verbal communication skills • Ability to handle confidential and sensitive information • Strong time-management and prioritization skills.<p><br />\n<strong>Mentor Technical Group es un empleador que ofrece igualdad de oportunidades y todos los solicitantes calificados recibirán consideración para el empleo sin importar raza, color, religión, sexo, orientación sexual, identidad de género, información genética, origen nacional, estado de veterano protegido, estado de discapacidad o cualquier otro grupo protegido por ley.</strong></p>\n\n<p><em><strong>Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.</strong></em></p>",
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