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Mylan Pharmaceuticals Jobs (NOW HIRING)

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Must possess expert knowledge of pharmaceutical drug development requirements for regulatory ...

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Must possess expert knowledge of pharmaceutical drug development requirements for regulatory ...

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Experience in regulated environments, preferably pharmaceutical or healthcare manufacturing.

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Minimum 10 years of pharmaceutical or biotech marketing experience, including global or regional ...

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Minimum 10 years of pharmaceutical or biotech marketing experience, including global or regional ...

Senior Internal Audit Analyst

Canonsburg, PA · Hybrid

$77K - $96K/yr

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Enhance knowledge base through staying current with industry (pharmaceutical) activities and ...

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Minimum 10 years of pharmaceutical or biotech commercial experience, including global or regional ...

Mylan Inc. Viatris is a global healthcare company uniquely positioned to bridge the traditional ... Minimum 10 years of pharmaceutical or biotech commercial experience, including global or regional ...

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Mylan Pharmaceuticals information

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$11K

$124.8K

$206K

How much do mylan pharmaceuticals jobs pay per year?

As of Sep 3, 2026, the average yearly pay for mylan pharmaceuticals in the United States is $124,835.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,000.00 and $158,500.00 per year, depending on experience, location, and employer.

What is a Mylan Pharmaceuticals job?

A Mylan Pharmaceuticals job involves working for a global pharmaceutical company focused on developing, manufacturing, and distributing generic, brand-name, and over-the-counter medicines. Employees may work in various roles such as research and development, manufacturing, quality control, regulatory affairs, sales, and marketing. Mylan, now part of Viatris, offers career opportunities in a dynamic and highly regulated industry committed to providing affordable and accessible medications.

What are the key skills and qualifications needed to thrive in the Mylan Pharmaceuticals position?

To thrive at Mylan Pharmaceuticals, candidates typically need a strong background in pharmaceuticals, life sciences, or related fields, often complemented by a relevant degree and industry certifications. Familiarity with Good Manufacturing Practices (GMP), regulatory compliance, laboratory information management systems (LIMS), and pharmaceutical production technologies is highly valuable. Excellent problem-solving, teamwork, and communication skills are essential for collaborating across departments and complying with strict industry standards. These competencies help ensure product quality, regulatory compliance, and the ability to innovate within a dynamic pharmaceutical environment.

What is the typical work environment like at Mylan Pharmaceuticals, and how do teams collaborate?

At Mylan Pharmaceuticals, employees often work in a collaborative, fast-paced, and highly regulated environment that spans research labs, manufacturing facilities, and corporate offices. Team members regularly partner with colleagues from quality assurance, regulatory affairs, research and development, and production to ensure that products meet high standards. Cross-functional meetings and ongoing training are common, fostering a culture of continuous improvement and shared responsibility. New hires are supported by experienced teams, and collaboration is encouraged at every stage of the drug development and manufacturing process. This team-oriented approach helps maintain a strong commitment to quality and compliance throughout the organization.

More about Mylan Pharmaceuticals jobs

What cities are hiring for Mylan Pharmaceuticals jobs?

Cities with the most Mylan Pharmaceuticals job openings:

What states have the most Mylan Pharmaceuticals jobs?

States with the most job openings for Mylan Pharmaceuticals jobs include:

Infographic showing various Mylan Pharmaceuticals job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 71% Full Time, 23% Part Time, 3% Contract, and 1% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $124,835 per year, or $60 per hour.

Head of US Regulatory Affairs Advertising and Promotion, Global Regulatory Affairs

Viatris

Washington, DC • Hybrid

$151K - $314K/yr

Full-time

Re-posted 13 days ago


Viatris rating

8.3

Company rating: 8.3 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

Mylan Pharmaceuticals Inc.

Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands, combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every stage of life, we provide access at scale, currently supplying high-quality medicines to approximately 1 billion patients around the world annually and touching all of life's moments, from birth to the end of life, acute conditions to chronic diseases.

We have been included on number of award lists that demonstrate the impact we are making.

Every day, we rise to the challenge to make a difference and here's how the role will make an impact:

The Head of US Regulatory Advertising & Promotion(A&P), Global Regulatory Affairs is a senior leadership role, responsible for ensuring that all U.S. advertising, promotion, and related communications for company products comply with federal regulations, company policies, and industry standards while providing strategic regulatory leadership to enable compliant business growth and innovation and acting as the primary subject matter expert on U.S. promotional regulations.

Key responsibilities for this role include:

  • Develop and implement A&P regulatory strategies; establish and maintain local policies, SOPs, and compliance frameworks aligned with global practices ensuring consistent, risk-based decision-making across all promotional activities.

  • Partner withmedical affairs, legal, marketing, and commercial teamsto ensure promotional materials (e.g., physician/patient sales, marketing, educational materials, press releases) are accurate, balanced, substantiated and aligned with overall brand strategy and business objectives.

  • Serve as the primary contact with the FDA's Office of Prescription Drug Promotion (OPDP) within the U.S. Food and Drug Administration; lead submissions, risk mitigation strategies, and regulatory interactions including advisory comments, Form FDA 2253 submissions, and responses to regulatory enforcement actions.

  • Review and approve promotional materials for completeness, accuracy, and consistency with approved labeling; assess clinical evidence supporting claims.

  • Build abest-in-class A&P local functionwith efficient, compliant review and execution processes including optimization of MLR/PRC review workflows and continuous process improvement initiatives.

  • Management of a 4-5-member team including coaching, performance management, and capability development.

  • Monitor FDA, FTC, and SEC enforcement trends and communicate risks to senior leadership, translating external insights into proactive guidance and risk mitigation strategies for the business.

  • Maintain relationship with Global Head of Labeling, Advertising & Promotion to ensure consistency across regions.

The minimum qualifications for this role are:

  • Minimum of a bachelor's degree (or equivalent) and relevant industry experience required. A degree in scientific discipline is strongly preferred. An advanced degree (MS, PharmD, MD) in a scientific discipline is a plus, A minimum of 10 years of experience in Regulatory Affairs with at least 5 years subject matter expertise as strategic leader in Ad Promo. Related experience and/or education may be considered.

  • Must possess expert knowledge of regulatory guidance pertaining to advertising and promotion for pharmaceutical products. Strong knowledge of regulatory environment and FDA.

  • Deep knowledge ofFDA promotional regulations, guidance, and enforcement trends.

  • Strongcross-functional collaborationand stakeholder management skills.

  • Expertise inpromotional review processes(e.g., PSMR - Promotional Submission Management Review).

  • Ability tolead regulatory committeesand influence business strategy.

  • Experience withmedical, scientific, and promotional materialscompliance.

  • Strong communication and presentation skills for internal and external audiences.

  • Must possess excellent analytical, written and verbal communication, interpersonal, and project management skills.

  • Must possess a strong work ethic and have outstanding organization and time management skills. Must have strong computer skills and be proficient within the Microsoft Office Suite.

  • This position follows a hybrid work model, with an expectation of being onsite at the DC office three days per week. Occasional travel may be required based on business needs.

  • Proficiency in speaking, comprehending, reading, and writing English is required.

Exact compensation may vary based on skills, experience, and location. The salary range for this position is $151,000 - $314,000.

At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.

Viatris is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, religion, age, color, sex, sexual orientation, gender identity, gender expression, disability, or protected veteran status, or any other characteristic protected by local, state, or federal laws, rules, or regulations.


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