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Biotechnology Director Jobs in Michigan (NOW HIRING)

Proven track record of 12 or more years of successful account management in the biotech or pharmaceutical industry. Extensive customer relationships with key account RX and Medical Directors.

Managing Director

Ann Arbor, MI · On-site

$190 - $230/hr

The Managing Director is a senior leadership role responsible for FFMI's strategic direction ... industry, biotech and governmental agencies. Operations, Budget, and Performance Management

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Biotechnology Director information

What does a biotechnology director do?

A Biotechnology Director oversees research, development, and operational activities within a biotechnology organization. They manage teams of scientists and professionals, set strategic goals, and ensure projects align with company objectives and regulatory standards. Their responsibilities often include budgeting, resource allocation, ensuring compliance with industry regulations, and fostering innovation. In addition, they collaborate with other departments and external partners to drive product development and bring new biotechnologies to market.

What are the key skills and qualifications needed to thrive as a biotechnology director, and why are they important?

To thrive as a Biotechnology Director, you need advanced expertise in biological sciences, leadership experience, and typically a graduate degree such as a PhD or MBA. Familiarity with laboratory management systems, regulatory compliance tools, and project management software is critical. Strategic vision, strong communication, and the ability to inspire multidisciplinary teams are standout soft skills. These competencies are essential for driving innovation, ensuring regulatory adherence, and achieving organizational goals in a complex and rapidly evolving industry.

What are the main challenges a biotechnology director faces when leading cross-functional teams?

A Biotechnology Director often manages diverse teams comprising scientists, regulatory experts, and business professionals. One common challenge is balancing scientific innovation with regulatory compliance and commercial objectives, which can sometimes have competing priorities. Effective communication and strong leadership are essential to align team goals, facilitate collaboration, and ensure project timelines are met. Directors must also stay updated on technological advances and industry trends to guide strategic decision-making within the organization.

What is the difference between Biotechnology Director vs Biotechnology Manager?

AspectBiotechnology DirectorBiotechnology Manager
Required CredentialsAdvanced degrees (PhD or MS), extensive industry experience, leadership skillsBachelor's or Master's degree, relevant industry experience, technical expertise
Work EnvironmentStrategic planning, overseeing multiple projects, high-level decision makingManaging daily operations, supervising teams, project execution
Employer & Industry UsageBiotech companies, research institutions, pharmaceutical firmsBiotech firms, research labs, pharmaceutical companies
Common Search & Comparison IntentUnderstanding leadership roles, career progression, salary differencesOperational responsibilities, team management, project scope

The Biotechnology Director focuses on strategic leadership, overseeing multiple projects and guiding company direction, often requiring advanced degrees and extensive experience. In contrast, the Biotechnology Manager handles daily operations, manages teams, and ensures project execution. Both roles are vital in biotech companies but differ mainly in scope, responsibilities, and seniority.

What are the most commonly searched types of Biotechnology jobs in Michigan?

The most popular types of Biotechnology jobs in Michigan are:

What are popular job titles related to Biotechnology Director jobs in Michigan?

For Biotechnology Director jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Biotechnology Director jobs in Michigan look for?

The top searched job categories for Biotechnology Director jobs in Michigan are:

What cities in Michigan are hiring for Biotechnology Director jobs?

Cities in Michigan with the most Biotechnology Director job openings:

Senior Medical Director, Medical Affairs, Neurology

Warren, MI


Regeneron Pharmaceuticals
Biotechnology Research and Development • 5 - 10K employees

8.5

Company rating: 8.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

19th of 86 rated pharmaceutical

Good employer

Recommended by parents

Respectful managers


Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 7 days ago


Job description

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Director to join our Neurology/Myasthenia Gravis Medical Affairs Team. The Senior Medical Director is responsible for the co-development of medical strategy and planning & execution of medical affairs activities at Regeneron. This hire will provide medical leadership and serve as a key scientific/medical resource. The Senior Medical Director will report to Head of Medical Affairs, Neurology and work in a cross-functional, matrix organization. He/she will also collaborate with external stakeholders such as healthcare practitioners, key opinion leaders and payers.

When & Where:

Location: Sleepy Hollow, New York; Warren, New Jersey; or Cambridge, Massachusetts

*If hired in Warren, NJ or Cambridge, MA frequent travel to Sleepy Hollow, MA may be required*

Discover your role:

  • You maintain deep scientific and medical knowledge of Neurology / Myasthenia Gravis, treatment landscape and clinical decision making

  • undefined

  • You function as an integral member of the cross-functional Medical Team

  • You are responsible for data generation, data analyses and interpretation as it relates to Phase 4 studies, including interventional and observational research

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  • You are responsible for the medical content of post-marketing study reports, analyses of clinical data, safety monitoring, and activities that ensure patient safety

  • You provide scientific and medical support for development of strategic medical, publications, communications and integrated evidence generation plans

  • You participate in developing and presenting medical content at congresses, symposia and advisory boards

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  • You proactively bring patients' & physicians' voice on cross-functional teams, to enable effective and impactful decision making

  • You provide medical training for internal staff on investigational and/or approved products, disease state and unmet needs

This role requires:

  • MD or equivalent with board eligibility/board certification in Neurology with a minimum of 10 years of relevant experience and 5+ years of Medical Affairs experience in Pharma/Biotech

  • PhD or PharmD with a minimum of 12 years of relevant experience and 8+ years of Medical Affairs experience in Pharma/Biotech

  • Direct experience in Myasthenia Gravis or Neurology Rare Disease, and prior launch experience is strongly preferred

  • Experience and ability in working in a dynamic, matrix environment; excellent collaboration and communication skills

  • undefined

  • Ability to demonstrate deep understanding of all medical affairs accountabilities

  • undefined

  • Thorough understanding of Neurology and Myasthenia Gravis healthcare environment and key stakeholders

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


Salary Range (annually)

$333,300.00 - $450,900.00


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