Senior Counsel, Compliance, Regulatory & Quality

RXinsider LTD.; Exton (PA); Hybrid; USD 170,000 - 210,000; Full time

Benefits offered by this job

Hybrid on-site 3 days/week

Continuous Learning & Development

Generous PTO

Job summary

West Pharmaceutical Services is seeking a Sr. Counsel, Compliance Regulatory and Quality to partner with executives and lead our global compliance, regulatory affairs and quality governance. You will advise on privacy, CAPA, investigations, and regulatory strategy across multiple geographies.

You will build and guide a high-performing team, monitor regulatory developments, and ensure alignment with global quality frameworks and enforcement trends.

Qualifications

• Experience leading a corporate compliance program in a highly regulated industry.
• Strong understanding of regulations and industry standards (pharma, medical devices).
• Excellent oral and written communication skills.
• Ability to adapt to changing regulatory environments and work with cross-functional teams.

Responsibilities

• Lead global compliance strategy and implementation re enterprise risk management.
• Manage and develop the compliance team (attorney, manager, privacy senior manager).
• Oversee audits, monitoring, and internal controls in line with SOX and regulations.
• Provide guidance on FDA and international regulatory requirements; support inspections.

Skills

Compliance leadership

Regulatory affairs

Quality assurance

Investigation management

People management

Education

JD or equivalent

Job description

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

The Sr. Counsel, Compliance Regulatory and Quality role is a strategic, business-oriented partner to provide integrated legal leadership across the Company’s global Compliance, Regulatory Affairs and Quality Assurance functions. Reporting to and working in close partnership with our General Counsel and Chief Compliance Officer, this role is a key legal advisor to the Company in the area of overall Compliance, including privacy, and helps to oversee and manage West’s global compliance program. As a key legal advisor to our Regulatory Affairs and Quality Assurance functions, this position plays an important role of helping ensure that our quality governance frameworks align with global regulatory requirements and enforcement trends.

Essential Duties And Responsibilities

• Help lead global compliance strategy and implementation aligned with enterprise risk management and business objectives, under the oversight of the General Counsel and Chief Compliance Officer.
• Manage and develop the compliance team, currently including one compliance attorney, one compliance manager and one privacy senior manager.
• Execute appropriate compliance audit and monitoring mechanisms to assess the effectiveness of internal controls addressing regulatory, ethical, operational risks and financial controls in accordance with SOX (in collaboration with our Internal Audit and Finance functions).
• Monitor and interpret developments on relevant laws, regulations, and industry best practices, and ensure the company’s compliance with them.
• Identify potential compliance risks both internally and externally, including those associated with third-party vendors and business partners, and develop mitigation strategies to minimize the organization’s exposure to legal and regulatory issues.
• Create and/or revise compliance policies and procedures to address regulatory requirements and industry standards.
• Design and deliver global compliance training and awareness programs to promote compliance with the organization’s policies.
• Help oversee internal investigations across global operations into potential compliance violations and assist as needed with employment-related investigations in partnership with Human Resources and Legal departments.
• Prepare regular compliance reports for senior management and board members, summarizing compliance risks, investigations, program effectiveness and emerging compliance developments.
• Promote a culture of integrity, accountability and ethical decision-making throughout the organization.
• Serve as a key legal advisor to the Quality Assurance and Regulatory Affairs functions.
• Provide legal guidance and support on Quality Management Systems (QMS), CAPA and investigation processes, audit findings (internal, customer, regulatory), supplier quality issues, product quality events and remediation strategies.
• Advise on global regulatory frameworks applicable to pharmaceutical packaging, containment, and delivery systems.
• Provide legal guidance related to: FDA and international health authority requirements; registration, submission, and regulatory approval matters; regulatory inspections and enforcement actions; and supplier and customer regulatory obligations.
• Manage outside counsel relationships when necessary for compliance and regulatory matters, including scope and budget oversight.

Education

• JD Law Degree or equivalent experience

Work Experience

• 12+ years of legal experience, including compliance, regulatory and investigation experience in the life sciences space

Preferred Knowledge, Skills And Abilities

• Experience administering or leading a corporate compliance program in a highly regulated industry, including people-management experience and skills.
• Preferred experience working in pharmaceutical, medical device, biotech or manufacturing industries.
• Strong understanding of relevant regulations and industry standards applicable to the organization, including frameworks impacting pharmaceutical and medical product supply chains.
• Excellent oral and written communication skills.
• Analytical and problem-solving abilities.
• Familiarity with compliance software and tools.
• Ability to adapt to changing regulatory environments and ensure the organization’s ongoing compliance.
• Strong interpersonal skills to work collaboratively with cross-functional teams and multiple stakeholders across multiple geographies.
• Ability to maintain confidentiality at all times.
• Dependability, attention to detail with strong organizational and time management skills a must.
• Strong leadership skills, with the ability to influence and collaborate with senior leadership and legal counsel.
• Able to comply with the Company’s safety and quality policies at all times.

Travel Requirements

20%: Up to 52 business days per year

Physical Requirements

Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.

Additional Requirements

• Must be able to communicate effectively with written and oral skills, make quick decisions, interpret data, read & write, speak in front of groups, express & exchange ideas, understand direction and adhere to procedures
• Organizational skills will enable planning, prioritization & achievement of goals especially of importance for the successful execution of related activities
• Position operates in a professional office environment. May stand or sit for extended periods of time
• This role is sedentary and routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets and fax machines
• Read and interpret data, information and documents
• Must maintain the ability to work well with others in a variety of situations
• Must be able to multi-task, work under time constraints, problem solve, and prioritize
• Ability to make independent and sound judgmentsObserve and interpret situations, analyze and solve problems

What We Offer

• This is a hybrid position requiring the team member to be onsite a minimum of 3 days per week
• Continuous Learning & Development: Opportunities for professional growth through training programs, tuition assistance, leadership development, and skill-certification initiatives.
• Generous Paid Time Off (PTO): Flexible vacation, personal, and holiday leave ensures employees can maintain a healthy work-life balance and recharge effectively.
• Inclusive & Collaborative Culture: A global workforce that values diversity, equity, and inclusion—where all voices are heard and respected in a supportive environment.
• West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [e-mail] . Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.