Environmental Monitoring and Sampling Services Supervisor - Tercer Turno

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    "heading": "Environmental Monitoring and Sampling Services Supervisor - Tercer Turno",
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    "description_html": "<ol style=\"margin-bottom:8px;\"><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Serves as the subject matter expertise to the EM and sampling activities. Under the direction of the Environmental Monitoring and Sampling Manager, supervise the environmental monitoring program and technicians; serves as a facilitator to the team members.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Participate in the recruitment and selection of staff; provide or coordinate staff training; work with employees to ensure performance is in accordance to expectations; work with manager and human resources department for guidance in managing any performance deviation.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Plan, prioritize, assign, supervise and review the work of staff involved in the collection. Establish schedules for the collection of all EM sampling; implement policies and procedures. Ensure all necessary testing is carried out and in accordance with internal procedures, protocols, and cGMP's.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Conduct performance evaluations for the assigned EM and Sampling Technicians.</span></span></span></span></span></li></ol><ol style=\"margin-bottom:8px;\"><li style=\"margin-bottom:8px;text-align:justify;\"><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">Ensure strict adherence to current Good Manufacturing Practices (cGMPs), established cleaning/preparation practices and procedures, and compliance with quality standards and regulations.</span></span></span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Provide support to Quality Team in internal investigations, deviations or event reports and ensure the closure of such reports for nonconforming results, in a timely manner.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Participates in the drafting and review of technical documents and procedures to ensure compliance in the event that changes are required. </span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Support continuous operations by periodically evaluating workload versus resources to ensure coverage with changing priorities. </span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Support the Environmental Monitoring and Sampling Manager in the development of proposals, as well as in the preparation of consumables and overall budget planning.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Identify and mitigate risks to ensure compliance and escalate any issues with Environmental Monitoring and Sampling Manager.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Monitor and improve key performance indicators (KPIs) related to lab efficiency, safety, quality, delivery, inventory and productivity. </span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Drive continuous improvement initiatives and lead cross-functional projects as a subject matter expert (SME).</span></span></span></span></span></li></ol><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Oversee the Environmental Monitoring and Sampling team and activities when Environmental Monitoring Manager is not available (vacation, sick, etc.)<br><br>Educational<br><span style=\"color:#000000;\">Bachelor’s Degree is required; Sciences; Biology, Biotechnology, Microbiology, Industrial Microbiology or Engineering disciplines is highly preferred OR Associate’s degree plus <a>6 </a><a class=\"msocomanchor\" href=\"#_msocom_1\">[TS1]</a> years of directly experience in a quality role within the regulated industry (pharmaceutical, medical device or biotechnology) OR High School degree plus 8 years of directly in a quality role within the regulated industry (pharmaceutical, medical device or biotechnology)</span></span></span><div><div><div class=\"msocomtxt\"> <ol><li><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">At least five (5) years of directly experience in a manufacturing operation or quality role in Parenteral or Pharmaceutical Industry</span></span></span></span></span></span></span></li><li><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">Previous experience with three (3) to five (5) years of in a supervisory / managerial position, with at least three (3) years of experience in Parenteral or Pharmaceutical Industry </span></span></span></span></span></span></span></li><li><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">Two (2) years of experience in GMP Environmental Monitoring or Utilities Sampling activities is preferred. Experience in clean room environmental monitoring and aseptic technique is a preferred.</span></span></span></span></span></span></span></li></ol></div></div></div><br> <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": "Serves as the subject matter expertise to the EM and sampling activities. Under the direction of the Environmental Monitoring and Sampling Manager, supervise the environmental monitoring program and technicians; serves as a facilitator to the team members.\n Participate in the recruitment and selection of staff; provide or coordinate staff training; work with employees to ensure performance is in accordance to expectations; work with manager and human resources department for guidance in managing any performance deviation.\n Plan, prioritize, assign, supervise and review the work of staff involved in the collection. Establish schedules for the collection of all EM sampling; implement policies and procedures. Ensure all necessary testing is carried out and in accordance with internal procedures, protocols, and cGMP's.\n Conduct performance evaluations for the assigned EM and Sampling Technicians.\n Ensure strict adherence to current Good Manufacturing Practices (cGMPs), established cleaning/preparation practices and procedures, and compliance with quality standards and regulations.\n Provide support to Quality Team in internal investigations, deviations or event reports and ensure the closure of such reports for nonconforming results, in a timely manner.\n Participates in the drafting and review of technical documents and procedures to ensure compliance in the event that changes are required.\n Support continuous operations by periodically evaluating workload versus resources to ensure coverage with changing priorities.\n Support the Environmental Monitoring and Sampling Manager in the development of proposals, as well as in the preparation of consumables and overall budget planning.\n Identify and mitigate risks to ensure compliance and escalate any issues with Environmental Monitoring and Sampling Manager.\n Monitor and improve key performance indicators (KPIs) related to lab efficiency, safety, quality, delivery, inventory and productivity.\n Drive continuous improvement initiatives and lead cross-functional projects as a subject matter expert (SME).\n Oversee the Environmental Monitoring and Sampling team and activities when Environmental Monitoring Manager is not available (vacation, sick, etc.)\nEducational\n Bachelor’s Degree is required; Sciences; Biology, Biotechnology, Microbiology, Industrial Microbiology or Engineering disciplines is highly preferred OR Associate’s degree plus 6 [TS1]  years of directly experience in a quality role within the regulated industry (pharmaceutical, medical device or biotechnology) OR High School degree plus 8 years of directly in a quality role within the regulated industry (pharmaceutical, medical device or biotechnology)   At least five (5) years of directly experience in a manufacturing operation or quality role in Parenteral or Pharmaceutical Industry\n Previous experience with three (3) to five (5) years of in a supervisory / managerial position, with at least three (3) years of experience in Parenteral or Pharmaceutical Industry\n Two (2) years of experience in GMP Environmental Monitoring or Utilities Sampling activities is preferred. Experience in clean room environmental monitoring and aseptic technique is a preferred.\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.",
    "jsonld_jobposting": {
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      "title": "Environmental Monitoring and Sampling Services Supervisor - Tercer Turno",
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      "datePosted": "2026-05-18",
      "description": "<ol style=\"margin-bottom:8px;\"><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Serves as the subject matter expertise to the EM and sampling activities. Under the direction of the Environmental Monitoring and Sampling Manager, supervise the environmental monitoring program and technicians; serves as a facilitator to the team members.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Participate in the recruitment and selection of staff; provide or coordinate staff training; work with employees to ensure performance is in accordance to expectations; work with manager and human resources department for guidance in managing any performance deviation.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Plan, prioritize, assign, supervise and review the work of staff involved in the collection. Establish schedules for the collection of all EM sampling; implement policies and procedures. Ensure all necessary testing is carried out and in accordance with internal procedures, protocols, and cGMP's.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Conduct performance evaluations for the assigned EM and Sampling Technicians.</span></span></span></span></span></li></ol><ol style=\"margin-bottom:8px;\"><li style=\"margin-bottom:8px;text-align:justify;\"><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">Ensure strict adherence to current Good Manufacturing Practices (cGMPs), established cleaning/preparation practices and procedures, and compliance with quality standards and regulations.</span></span></span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Provide support to Quality Team in internal investigations, deviations or event reports and ensure the closure of such reports for nonconforming results, in a timely manner.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Participates in the drafting and review of technical documents and procedures to ensure compliance in the event that changes are required. </span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Support continuous operations by periodically evaluating workload versus resources to ensure coverage with changing priorities. </span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Support the Environmental Monitoring and Sampling Manager in the development of proposals, as well as in the preparation of consumables and overall budget planning.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Identify and mitigate risks to ensure compliance and escalate any issues with Environmental Monitoring and Sampling Manager.</span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Monitor and improve key performance indicators (KPIs) related to lab efficiency, safety, quality, delivery, inventory and productivity. </span></span></span></span></span></li><li style=\"margin-bottom:8px;\"><span style=\"font-size:12pt;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Drive continuous improvement initiatives and lead cross-functional projects as a subject matter expert (SME).</span></span></span></span></span></li></ol><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\">Oversee the Environmental Monitoring and Sampling team and activities when Environmental Monitoring Manager is not available (vacation, sick, etc.)<br><br>Educational<br><span style=\"color:#000000;\">Bachelor’s Degree is required; Sciences; Biology, Biotechnology, Microbiology, Industrial Microbiology or Engineering disciplines is highly preferred OR Associate’s degree plus <a>6 </a><a class=\"msocomanchor\" href=\"#_msocom_1\">[TS1]</a> years of directly experience in a quality role within the regulated industry (pharmaceutical, medical device or biotechnology) OR High School degree plus 8 years of directly in a quality role within the regulated industry (pharmaceutical, medical device or biotechnology)</span></span></span><div><div><div class=\"msocomtxt\"> <ol><li><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">At least five (5) years of directly experience in a manufacturing operation or quality role in Parenteral or Pharmaceutical Industry</span></span></span></span></span></span></span></li><li><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">Previous experience with three (3) to five (5) years of in a supervisory / managerial position, with at least three (3) years of experience in Parenteral or Pharmaceutical Industry </span></span></span></span></span></span></span></li><li><span style=\"font-size:12pt;\"><span style=\"background:#FFFFFF;\"><span><span style=\"font-family:'Times New Roman', serif;\"><span style=\"font-size:10pt;\"><span style=\"font-family:Arial, sans-serif;\"><span style=\"color:#000000;\">Two (2) years of experience in GMP Environmental Monitoring or Utilities Sampling activities is preferred. Experience in clean room environmental monitoring and aseptic technique is a preferred.</span></span></span></span></span></span></span></li></ol></div></div></div><br> <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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