Lateral Flow QC Supervisor
Neogen Corporation · Lansing, MI · 1 mo ago
Quality AssuranceFull-time
We need to output HTML fragment with headings for sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections if posting has real specific content. No job title heading. No Job ID. Remove boilerplate. Must preserve all substantive info.
Let's parse the posting.
First paragraph: "Come Be Part of a Mission that Matters! The Lateral Flow QC Supervisor will provide leadership and first line management to the Quality Technicians to ensure an effective quality of services for the Quality Control department. To provide specialist advice and knowledge to the laboratory staff to ensure the successful implementation of Quality Management Systems that adhere to the requirements of ISO17025 and similar mandated quality standards. To manage the QMS to ensure we remain ‘audit ready’. To provide leadership and assistance in the laboratory’s day to day functions. Provide effective direct line management including appraisal, development, performance monitoring and competency assessments as well as supporting and motivating staff to problem solve and promote good practice. Engage with Accreditation Body assessment audits, delivering evidence of compliance, recognizing valid improvement actions, and managing their resolution. Be responsible for pro-actively seeking improvement to service delivery, responding to complaints or dissatisfaction, and implementing effective corrective actions. Work with Managers to identify opportunities to develop capabilities, innovation, improve efficiencies, and reducing costs where applicable. Responsible for implementation of quality management systems that meet accredited quality standards for ISO 17025, leading project plans and working closely with Technical Managers and Unit Managers to ensure compliance. Supervise and assist in the day-to-day activities in the laboratory with frequent updates provided to the Laboratory Manager. To carry out any other duties deemed reasonable by management. Support the product line across internal departments (manufacturing, quality control, purchasing, R&D, sales, marketing etc.) Support new product development and manage project team meetings. Tabulates and graphs data and prepares technical reports for senior personnel. Work with R&D and technical services on necessary product validations."
That's responsibilities.
Then "Education and/or Experience: Minimum Bachelor’s Degree in physical science, chemistry, or related fields Minimum 3 years work experience with laboratory setting. Minimum 1 year experience in a technical management role is preferred. Prior experience of successfully implementing and managing a quality management system accredited to ISO17025 or a similarly robust conformity assessment standard is desirable. Experience in presenting scientific results to diverse audiences is preferred. Experience in diagnostic kit validation is preferred."
That's qualifications/requirements.
Then "Why Neogen At Neogen we believe that taking care of our employees allows them to do their best work. When you join our team, you'll enjoy competitive benefits and the opportunity to make a meaningful difference every day. Benefits include: Benefits starting on Day One – Medical, dental, and vision coverage begin on your first day of employment. 401(k) with company match – Invest in your future with retirement savings and company contributions. Paid Time Off (PTO) – Enjoy generous paid time off so you can rest, recharge, and spend time with those who matter most. Career Growth Opportunities – We are committed to promoting from within and providing the tools, training, and support to help you grow your career. Meaningful Work – Be part of a team whose work has a real impact on our customers, communities, and the world around us. Collaborative Culture – Join a team that values innovation, respect, teamwork, and continuous improvement. Come build your future with us while making a difference every day. #Applynow"
That's benefits.
Then "WHO IS NEOGEN: From farm to fork, we offer solutions to enhance the quality, quantity and safety of the global food supply. Our food safety diagnostics are used within farming operations to the production facilities of most of the world’s best-known food companies. Neogen’s solutions are critical to the health and well-being of our customers’ operations – and in turn their consumers. What we do matters! Neogen’s culture combines stability with a deep believe in providing professional and personal growth. Our Pillars of Trust – the principles which guide our everyday decision—making, include Openness, Honesty, Credibility, Respect, and Service. It’s the belief in these characteristics that provide a consistent, happy and healthy work environment for our employees."
That's about the company, maybe "About the role"? Actually "About the role" could be the initial mission statement: "Come Be Part of a Mission that Matters! The Lateral Flow QC Supervisor will provide leadership..." That's more about role. Could treat as "About the role". Then responsibilities separate. But we have overlapping content. The instructions: Use headings for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide which sections have content.
We have:
- About the role: maybe the introductory paragraph describing mission and role purpose.
- Responsibilities: list of duties (the long paragraph with many responsibilities). Could break into bullet list.
- Requirements: maybe education and experience (minimum Bachelor's, 3 years lab, etc.) That's requirements.
- Qualifications: maybe preferred qualifications (technical management experience, ISO17025, presenting results, diagnostic kit validation). Could be separate.
- Skills: maybe not explicitly listed; could infer but we shouldn't invent. So we should not create Skills section if no explicit skill list.
- Benefits: we have benefits list.
- Pay: not mentioned; do not create.
- Schedule: not mentioned; do not create.
Thus we will output sections: About the role, Responsibilities, Requirements, Qualifications, Benefits.
We need to use
for sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections if posting has real specific content. No job title heading. No Job ID. Remove boilerplate. Must preserve all substantive info.
Let's parse the posting.
First paragraph: "Come Be Part of a Mission that Matters! The Lateral Flow QC Supervisor will provide leadership and first line management to the Quality Technicians to ensure an effective quality of services for the Quality Control department. To provide specialist advice and knowledge to the laboratory staff to ensure the successful implementation of Quality Management Systems that adhere to the requirements of ISO17025 and similar mandated quality standards. To manage the QMS to ensure we remain ‘audit ready’. To provide leadership and assistance in the laboratory’s day to day functions. Provide effective direct line management including appraisal, development, performance monitoring and competency assessments as well as supporting and motivating staff to problem solve and promote good practice. Engage with Accreditation Body assessment audits, delivering evidence of compliance, recognizing valid improvement actions, and managing their resolution. Be responsible for pro-actively seeking improvement to service delivery, responding to complaints or dissatisfaction, and implementing effective corrective actions. Work with Managers to identify opportunities to develop capabilities, innovation, improve efficiencies, and reducing costs where applicable. Responsible for implementation of quality management systems that meet accredited quality standards for ISO 17025, leading project plans and working closely with Technical Managers and Unit Managers to ensure compliance. Supervise and assist in the day-to-day activities in the laboratory with frequent updates provided to the Laboratory Manager. To carry out any other duties deemed reasonable by management. Support the product line across internal departments (manufacturing, quality control, purchasing, R&D, sales, marketing etc.) Support new product development and manage project team meetings. Tabulates and graphs data and prepares technical reports for senior personnel. Work with R&D and technical services on necessary product validations."
That's responsibilities.
Then "Education and/or Experience: Minimum Bachelor’s Degree in physical science, chemistry, or related fields Minimum 3 years work experience with laboratory setting. Minimum 1 year experience in a technical management role is preferred. Prior experience of successfully implementing and managing a quality management system accredited to ISO17025 or a similarly robust conformity assessment standard is desirable. Experience in presenting scientific results to diverse audiences is preferred. Experience in diagnostic kit validation is preferred."
That's qualifications/requirements.
Then "Why Neogen At Neogen we believe that taking care of our employees allows them to do their best work. When you join our team, you'll enjoy competitive benefits and the opportunity to make a meaningful difference every day. Benefits include: Benefits starting on Day One – Medical, dental, and vision coverage begin on your first day of employment. 401(k) with company match – Invest in your future with retirement savings and company contributions. Paid Time Off (PTO) – Enjoy generous paid time off so you can rest, recharge, and spend time with those who matter most. Career Growth Opportunities – We are committed to promoting from within and providing the tools, training, and support to help you grow your career. Meaningful Work – Be part of a team whose work has a real impact on our customers, communities, and the world around us. Collaborative Culture – Join a team that values innovation, respect, teamwork, and continuous improvement. Come build your future with us while making a difference every day. #Applynow"
That's benefits.
Then "WHO IS NEOGEN: From farm to fork, we offer solutions to enhance the quality, quantity and safety of the global food supply. Our food safety diagnostics are used within farming operations to the production facilities of most of the world’s best-known food companies. Neogen’s solutions are critical to the health and well-being of our customers’ operations – and in turn their consumers. What we do matters! Neogen’s culture combines stability with a deep believe in providing professional and personal growth. Our Pillars of Trust – the principles which guide our everyday decision—making, include Openness, Honesty, Credibility, Respect, and Service. It’s the belief in these characteristics that provide a consistent, happy and healthy work environment for our employees."
That's about the company, maybe "About the role"? Actually "About the role" could be the initial mission statement: "Come Be Part of a Mission that Matters! The Lateral Flow QC Supervisor will provide leadership..." That's more about role. Could treat as "About the role". Then responsibilities separate. But we have overlapping content. The instructions: Use headings for sections like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. We need to decide which sections have content.
We have:
- About the role: maybe the introductory paragraph describing mission and role purpose.
- Responsibilities: list of duties (the long paragraph with many responsibilities). Could break into bullet list.
- Requirements: maybe education and experience (minimum Bachelor's, 3 years lab, etc.) That's requirements.
- Qualifications: maybe preferred qualifications (technical management experience, ISO17025, presenting results, diagnostic kit validation). Could be separate.
- Skills: maybe not explicitly listed; could infer but we shouldn't invent. So we should not create Skills section if no explicit skill list.
- Benefits: we have benefits list.
- Pay: not mentioned; do not create.
- Schedule: not mentioned; do not create.
Thus we will output sections: About the role, Responsibilities, Requirements, Qualifications, Benefits.
We need to use for each section heading. Then content: use
for prose,
- for lists.
We must preserve all substantive information; not invent or summarize away detail. So we need to keep all details from the posting.
Let's extract each piece.
About the role: The first sentence: "Come Be Part of a Mission that Matters!" plus description: "The Lateral Flow QC Supervisor will provide leadership and first line management to the Quality Technicians to ensure an effective quality of services for the Quality Control department. To provide specialist advice and knowledge to the laboratory staff to ensure the successful implementation of Quality Management Systems that adhere to the requirements of ISO17025 and similar mandated quality standards. To manage the QMS to ensure we remain ‘audit ready’. To provide leadership and assistance in the laboratory’s day to day functions."
We could keep as a paragraph.
Responsibilities: The rest after that up to before Education and/or Experience. Let's list bullet points:
- Provide effective direct line management including appraisal, development, performance monitoring and competency assessments as well as supporting and motivating staff to problem solve and promote good practice.
- Engage with Accreditation Body assessment audits, delivering evidence of compliance, recognizing valid improvement actions, and managing their resolution.
- Be responsible for pro-actively seeking improvement to service delivery, responding to complaints or dissatisfaction, and implementing effective corrective actions.
- Work with Managers to identify opportunities to develop capabilities, innovation, improve efficiencies, and reducing costs where applicable.
- Responsible for implementation of quality management systems that meet accredited quality standards for ISO 17025, leading project plans and working closely with Technical Managers and Unit Managers to ensure compliance.
- Supervise and assist in the day-to-day activities in the laboratory with frequent updates provided to the Laboratory Manager.
- To carry out any other duties deemed reasonable by management.
- Support the product line across internal departments (manufacturing, quality control, purchasing, R&D, sales, marketing etc.)
- Support new product development and manage project team meetings.
- Tabulates and graphs data and prepares technical reports for senior personnel.
- Work with R&D and technical services on necessary product validations.
We need to ensure we didn't miss any: The original also had "Provide effective direct line management including appraisal, development, performance monitoring and competency assessments as well as supporting and motivating staff to problem solve and promote good practice." Already captured.
Also "Engage with Accreditation Body assessment audits, delivering evidence of compliance, recognizing valid improvement actions, and managing their resolution." captured.
Also "Be responsible for pro-actively seeking improvement to service delivery, responding to complaints or dissatisfaction, and implementing effective corrective actions." captured.
Also "Work with Managers to identify opportunities to develop capabilities, innovation, improve efficiencies, and reducing costs where applicable." captured.
Also "Responsible for implementation of quality management systems that meet accredited quality standards for ISO 17025, leading project plans and working closely with Technical Managers and Unit Managers to ensure compliance." captured.
Also "Supervise and assist in the day-to-day activities in the laboratory with frequent updates provided to the Laboratory Manager." captured.
Also "To carry out any other duties deemed reasonable by management." captured.
Also "Support the product line across internal departments (manufacturing, quality control, purchasing, R&D, sales, marketing etc.)" captured.
Also "Support new product development and manage project team meetings." captured.
Also "Tabulates and graphs data and prepares technical reports for senior personnel." captured.
Also "Work with R&D and technical services on necessary product validations." captured.
Also earlier: "Provide leadership and assistance in the laboratory’s day to day functions." That's part of about role maybe but we could include in responsibilities as well. But we already have supervision. Might duplicate. We'll keep it in responsibilities maybe as a bullet: "Provide leadership and assistance in the laboratory’s day to day functions." However we already have supervision bullet. To avoid duplication, we could keep it as part of about role. But we need to preserve all info; duplication is okay but better not to repeat. We'll keep it in about role.
Now Requirements: Education and/or Experience: Minimum Bachelor’s Degree in physical science, chemistry, or related fields Minimum 3 years work experience with laboratory setting. Minimum 1 year experience in a technical management role is preferred. Prior experience of successfully implementing and managing a quality management system accredited to ISO17025 or a similarly robust conformity assessment standard is desirable. Experience in presenting scientific results to diverse audiences is preferred. Experience in diagnostic kit validation is preferred.
We need to separate required vs preferred? The instruction: we can have Requirements and Qualifications sections. Usually Requirements = mandatory, Qualifications = preferred. So we can put mandatory: Bachelor's degree, 3 years lab experience. Preferred: 1 year technical management, ISO17025 QMS experience, presenting results, diagnostic kit validation. We'll put those in Requirements (mandatory) and Qualifications (preferred). Or we could combine but better to follow headings.
Thus:
Requirements (
Requirements
): - Bachelor’s Degree in physical science, chemistry, or related fields - Minimum 3 years work experience with laboratory setting Qualifications (Qualifications
): - Minimum 1 year experience in a technical management role (preferred) - Prior experience of successfully implementing and managing a quality management system accredited to ISO17025 or a similarly robust conformity assessment standard (desirable) - Experience in presenting scientific results to diverse audiences (preferred) - Experience in diagnostic kit validation (preferred) We need to preserve the wording exactly? The instruction: preserve ALL substantive information; do NOT invent or summarize away detail. So we should keep the exact phrases, maybe as list items. We'll use- for each.
Benefits: list as given.
Benefits start: "Benefits starting on Day One – Medical, dental, and vision coverage begin on your first day of employment." etc.
We'll make bullet list.
Now About the role: we need to include the mission statement and role purpose. Let's craft a paragraph: "Come Be Part of a Mission that Matters! The Lateral Flow QC Supervisor will provide leadership and first line management to the Quality Technicians to ensure an effective quality of services for the Quality Control department. To provide specialist advice and knowledge to the laboratory staff to ensure the successful implementation of Quality Management Systems that adhere to the requirements of ISO17025 and similar mandated quality standards. To manage the QMS to ensure we remain ‘audit ready’. To provide leadership and assistance in the laboratory’s day to day functions."
We'll keep as
. Now Responsibilities: we need to include all
- for each.
Benefits: list as given.
Benefits start: "Benefits starting on Day One – Medical, dental, and vision coverage begin on your first day of employment." etc.
We'll make bullet list.
Now About the role: we need to include the mission statement and role purpose. Let's craft a paragraph: "Come Be Part of a Mission that Matters! The Lateral Flow QC Supervisor will provide leadership and first line management to the Quality Technicians to ensure an effective quality of services for the Quality Control department. To provide specialist advice and knowledge to the laboratory staff to ensure the successful implementation of Quality Management Systems that adhere to the requirements of ISO17025 and similar mandated quality standards. To manage the QMS to ensure we remain ‘audit ready’. To provide leadership and assistance in the laboratory’s day to day functions."
We'll keep as