Senior Counsel, Regulatory Compliance
for each section. Use - for lists. Use
for prose.
We need to decide which sections to include:
- About the role: prose summarizing role purpose, context, reporting line, etc.
- Responsibilities: list from Key Responsibilities.
- Requirements: maybe combine Minimum Requirements and Authorization? Could also include "Must be authorized to work in the United States; sponsorship is not available." Also maybe include "Hybrid work model" not a requirement but schedule.
- Qualifications: maybe the Critical Skills & Experience list (the bullet list). Or we could treat that as Skills. The instruction: Use sections for Requirements, Qualifications, Skills. We need to decide what goes where. The posting has "Minimum Requirements" and "Critical Skills & Experience" and "Preferred Qualifications". We could map:
Requirements: Minimum Requirements (JD, bar, 7-10 years experience, experience advising on healthcare regulatory etc.) plus Authorization.
Qualifications: Critical Skills & Experience (the list of skills/experience).
Skills: maybe Preferred Qualifications? Or we could treat Preferred Qualifications as Skills. But better to follow typical: Requirements = mandatory; Qualifications = preferred? But we have both. Let's assign:
- Requirements: Minimum Requirements + Authorization.
- Qualifications: Critical Skills & Experience (the list).
- Skills: Preferred Qualifications (the list). Or we could combine Preferred Qualifications into Qualifications and leave Skills empty? But we should not create empty sections. So we need to decide if we have content for Skills. Preferred Qualifications is a list of experiences; could be considered skills. We'll put them under Skills.
Thus we have sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Pay, Schedule.
Check if we have content for each:
About the role: we have description of role: "The MMS Legal Department is seeking Senior Counsel, Regulatory Compliance to join its Technology, Risk & People (TRP) pillar. This role is critical to MMS’s transition to a standalone company. The TRP team provides practical, business-oriented legal support across operations, technology, data, compliance, and risk-related matters, helping the business achieve its objectives while appropriately managing legal and regulatory risk. The role reports to the Managing Principal Counsel, Technology, Risk & People. This role will provide day-to-day legal support on healthcare regulatory and compliance matters, including support for regulatory risk assessments, policy development, investigations, compliance monitoring, training, and enterprise risk management initiatives. The successful candidate will partner closely with Compliance, Enterprise Risk Management, and business stakeholders to identify legal and regulatory risks, develop practical solutions, and support informed business decision-making. The ideal candidate exercises sound judgment, communicates effectively with both legal and business audiences, and thrives in a dynamic environment with evolving priorities. This position offers the opportunity to help build scalable compliance processes and contribute to the growth of a newly independent healthcare organization." That's substantive.
Responsibilities: list from Key Responsibilities.
Requirements: Minimum Requirements: JD from accredited law school and active U.S. bar membership. 7-10 years of relevant legal experience in a law firm, government agency, and/or in-house legal department. Experience advising on healthcare regulatory, compliance, risk management, or related legal matters. Plus Authorization: Must be authorized to work in the United States; sponsorship is not available.
Qualifications: Critical Skills & Experience list: Experience with: Healthcare regulatory compliance counseling; Compliance program development and support; Regulatory risk assessment and mitigation; Policy and procedure development; Internal investigations, audits, monitoring, or corrective action initiatives; Cross-functional counseling in a highly regulated industry; Working knowledge of healthcare regulatory frameworks and compliance requirements; Foundational knowledge of regulations applicable to medical devices, controlled substances, and related healthcare products and services; Familiarity with enterprise risk management principles and processes; Strong drafting, issue-spotting, and legal analysis skills; Strong research and problem-solving skills; Ability to provide clear, practical legal guidance; Proven ability to adapt to evolving business needs and operate effectively in ambiguous situations; Strong collaboration and communication skills.
Skills: Preferred Qualifications list: Experience in the healthcare, life sciences, pharmaceutical, medical device, healthcare technology, or healthcare distribution industries. Experience supporting compliance programs involving FDA-regulated products, controlled substance compliance, quality systems, or related healthcare regulatory frameworks.
Pay: Base Pay Range $132,000 - $220,000. Also mention additional compensation: annual bonus or long-term incentive opportunities may be offered. That's substantive.
Schedule: Hybrid work model (Richmond, VA (Preferred); Jacksonville, FL; Alpharetta, GA). Up to 25% travel.
We should not include the "About McKesson Medical-Surgical" description. Could we incorporate into About the role? It's about the company, not the role. But maybe we can include a brief sentence about MMS being a subsidiary etc. However the instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." If we omit that description, we are losing substantive info about the company. But is that considered required? The sections allowed do not include a company description heading. However we could fold it into About the role as context. That would preserve the info, albeit under About the role heading. That seems acceptable.
Thus we can add a sentence: "McKesson Medical-Surgical (MMS), which is expected to become Wellverse in early 2027, is a subsidiary and publicly reported segment of the McKesson Corporation. MMS distributes medical-surgical supplies, pharmaceuticals, diagnostic equipment and supplies, along with other solutions and services to virtually every type of healthcare setting and provider outside of the traditional hospital..." etc. That is substantive.
We need to ensure we don't repeat the job title. The job title is Senior Counsel, Regulatory Compliance. We must not repeat it as a heading. We can mention it in prose.
Now produce HTML.
We must not include any markdown code fences. Just raw HTML.
Let's craft:
About the role
...
Responsibilities
- ...
...
Requirements
- JD from an accredited law school and active U.S. bar membership.
- 7-10 years of relevant legal experience in a law firm, government agency, and/or in-house legal department.
- Experience advising on healthcare regulatory, compliance, risk management, or related legal matters.
- Must be authorized to work in the United States; sponsorship is not available.
Qualifications
- Experience with healthcare regulatory compliance counseling
- Compliance program development and support
- Regulatory risk assessment and mitigation
- Policy and procedure development
- Internal investigations, audits, monitoring, or corrective action initiatives
- Cross-functional counseling in a highly regulated industry
- Working knowledge of healthcare regulatory frameworks and compliance requirements
- Foundational knowledge of regulations applicable to medical devices, controlled substances, and related healthcare products and services
- Familiarity with enterprise risk management principles and processes
- Strong drafting, issue-spotting, and legal analysis skills
- Strong research and problem-solving skills
- Ability to provide clear, practical legal guidance
- Proven ability to adapt to evolving business needs and operate effectively in ambiguous situations
- Strong collaboration and communication skills
Skills
- Experience in the healthcare, life sciences, pharmaceutical, medical device, healthcare technology, or healthcare distribution industries
- Experience supporting compliance programs involving FDA-regulated
for prose. We need to decide which sections to include: - About the role: prose summarizing role purpose, context, reporting line, etc. - Responsibilities: list from Key Responsibilities. - Requirements: maybe combine Minimum Requirements and Authorization? Could also include "Must be authorized to work in the United States; sponsorship is not available." Also maybe include "Hybrid work model" not a requirement but schedule. - Qualifications: maybe the Critical Skills & Experience list (the bullet list). Or we could treat that as Skills. The instruction: Use sections for Requirements, Qualifications, Skills. We need to decide what goes where. The posting has "Minimum Requirements" and "Critical Skills & Experience" and "Preferred Qualifications". We could map: Requirements: Minimum Requirements (JD, bar, 7-10 years experience, experience advising on healthcare regulatory etc.) plus Authorization. Qualifications: Critical Skills & Experience (the list of skills/experience). Skills: maybe Preferred Qualifications? Or we could treat Preferred Qualifications as Skills. But better to follow typical: Requirements = mandatory; Qualifications = preferred? But we have both. Let's assign: - Requirements: Minimum Requirements + Authorization. - Qualifications: Critical Skills & Experience (the list). - Skills: Preferred Qualifications (the list). Or we could combine Preferred Qualifications into Qualifications and leave Skills empty? But we should not create empty sections. So we need to decide if we have content for Skills. Preferred Qualifications is a list of experiences; could be considered skills. We'll put them under Skills. Thus we have sections: About the role, Responsibilities, Requirements, Qualifications, Skills, Pay, Schedule. Check if we have content for each: About the role: we have description of role: "The MMS Legal Department is seeking Senior Counsel, Regulatory Compliance to join its Technology, Risk & People (TRP) pillar. This role is critical to MMS’s transition to a standalone company. The TRP team provides practical, business-oriented legal support across operations, technology, data, compliance, and risk-related matters, helping the business achieve its objectives while appropriately managing legal and regulatory risk. The role reports to the Managing Principal Counsel, Technology, Risk & People. This role will provide day-to-day legal support on healthcare regulatory and compliance matters, including support for regulatory risk assessments, policy development, investigations, compliance monitoring, training, and enterprise risk management initiatives. The successful candidate will partner closely with Compliance, Enterprise Risk Management, and business stakeholders to identify legal and regulatory risks, develop practical solutions, and support informed business decision-making. The ideal candidate exercises sound judgment, communicates effectively with both legal and business audiences, and thrives in a dynamic environment with evolving priorities. This position offers the opportunity to help build scalable compliance processes and contribute to the growth of a newly independent healthcare organization." That's substantive. Responsibilities: list from Key Responsibilities. Requirements: Minimum Requirements: JD from accredited law school and active U.S. bar membership. 7-10 years of relevant legal experience in a law firm, government agency, and/or in-house legal department. Experience advising on healthcare regulatory, compliance, risk management, or related legal matters. Plus Authorization: Must be authorized to work in the United States; sponsorship is not available. Qualifications: Critical Skills & Experience list: Experience with: Healthcare regulatory compliance counseling; Compliance program development and support; Regulatory risk assessment and mitigation; Policy and procedure development; Internal investigations, audits, monitoring, or corrective action initiatives; Cross-functional counseling in a highly regulated industry; Working knowledge of healthcare regulatory frameworks and compliance requirements; Foundational knowledge of regulations applicable to medical devices, controlled substances, and related healthcare products and services; Familiarity with enterprise risk management principles and processes; Strong drafting, issue-spotting, and legal analysis skills; Strong research and problem-solving skills; Ability to provide clear, practical legal guidance; Proven ability to adapt to evolving business needs and operate effectively in ambiguous situations; Strong collaboration and communication skills. Skills: Preferred Qualifications list: Experience in the healthcare, life sciences, pharmaceutical, medical device, healthcare technology, or healthcare distribution industries. Experience supporting compliance programs involving FDA-regulated products, controlled substance compliance, quality systems, or related healthcare regulatory frameworks. Pay: Base Pay Range $132,000 - $220,000. Also mention additional compensation: annual bonus or long-term incentive opportunities may be offered. That's substantive. Schedule: Hybrid work model (Richmond, VA (Preferred); Jacksonville, FL; Alpharetta, GA). Up to 25% travel. We should not include the "About McKesson Medical-Surgical" description. Could we incorporate into About the role? It's about the company, not the role. But maybe we can include a brief sentence about MMS being a subsidiary etc. However the instruction: "Preserve ALL substantive information; do NOT invent or summarize away detail." If we omit that description, we are losing substantive info about the company. But is that considered required? The sections allowed do not include a company description heading. However we could fold it into About the role as context. That would preserve the info, albeit under About the role heading. That seems acceptable. Thus we can add a sentence: "McKesson Medical-Surgical (MMS), which is expected to become Wellverse in early 2027, is a subsidiary and publicly reported segment of the McKesson Corporation. MMS distributes medical-surgical supplies, pharmaceuticals, diagnostic equipment and supplies, along with other solutions and services to virtually every type of healthcare setting and provider outside of the traditional hospital..." etc. That is substantive. We need to ensure we don't repeat the job title. The job title is Senior Counsel, Regulatory Compliance. We must not repeat it as a heading. We can mention it in prose. Now produce HTML. We must not include any markdown code fences. Just raw HTML. Let's craft:
About the role
...
Responsibilities
- ... ...
Requirements
- JD from an accredited law school and active U.S. bar membership.
- 7-10 years of relevant legal experience in a law firm, government agency, and/or in-house legal department.
- Experience advising on healthcare regulatory, compliance, risk management, or related legal matters.
- Must be authorized to work in the United States; sponsorship is not available.
Qualifications
- Experience with healthcare regulatory compliance counseling
- Compliance program development and support
- Regulatory risk assessment and mitigation
- Policy and procedure development
- Internal investigations, audits, monitoring, or corrective action initiatives
- Cross-functional counseling in a highly regulated industry
- Working knowledge of healthcare regulatory frameworks and compliance requirements
- Foundational knowledge of regulations applicable to medical devices, controlled substances, and related healthcare products and services
- Familiarity with enterprise risk management principles and processes
- Strong drafting, issue-spotting, and legal analysis skills
- Strong research and problem-solving skills
- Ability to provide clear, practical legal guidance
- Proven ability to adapt to evolving business needs and operate effectively in ambiguous situations
- Strong collaboration and communication skills
Skills
- Experience in the healthcare, life sciences, pharmaceutical, medical device, healthcare technology, or healthcare distribution industries
- Experience supporting compliance programs involving FDA-regulated