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Biotechnology Manager Jobs in Minnesota (NOW HIRING)

Lab Systems Manager

Minneapolis, MN · On-site

$90K - $125K/yr

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of ... our hiring manager(s), executive team members, or employees directly. We require that all ...

Celcuity is a clinical-stage, publicly traded biotechnology company seeking to extend the lives of ... our hiring manager(s), executive team members, or employees directly. We require that all ...

Regional Manager

Minneapolis, MN · On-site

$106K - $198K/yr

Inizio Engage has a long-standing partnership with a leading biotechnology organization across Commercial, Patient Solutions and Medical Affairs businesses. We are seeking a Regional Manager to lead ...

University Degree (BS or MS) in Life Sciences, Biotech , or a related field. Emphasis in molecular ... Relationship Management: Outstanding interpersonal and networking skills, with the ability to ...

University Degree (BS or MS) in Life Sciences, Biotech , or a related field. Emphasis in molecular ... Relationship Management: Outstanding interpersonal and networking skills, with the ability to ...

University Degree (BS or MS) in Life Sciences, Biotech , or a related field. Emphasis in molecular ... Relationship Management: Outstanding interpersonal and networking skills, with the ability to ...

University Degree (BS or MS) in Life Sciences, Biotech , or a related field. Emphasis in molecular ... Relationship Management: Outstanding interpersonal and networking skills, with the ability to ...

... biotech clients. PURPOSE The National Accounts Director is responsible for the management of all aspects of payer account management and manages targeted market access accounts. May lead a team or ...

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Biotechnology Manager information

What is the difference between Biotechnology Manager vs Research Scientist?

AspectBiotechnology ManagerResearch Scientist
Required CredentialsBachelor's or Master's in Biotechnology, Biology, or related field; often some management experienceTypically a Master's or Ph.D. in Biotechnology, Biology, or related field
Work EnvironmentLeads teams, manages projects, oversees operations in biotech companies or labsConducts experiments, develops new techniques, and analyzes data primarily in research settings
Employer & Industry UsageUsed in biotech firms, pharmaceutical companies, and research institutions for leadership rolesCommon in academic, government, and industry research labs focused on scientific discovery

The Biotechnology Manager focuses on overseeing projects, managing teams, and ensuring operational success, often requiring leadership skills and management experience. In contrast, the Research Scientist primarily conducts experiments and develops new scientific knowledge. Both roles require strong scientific credentials, but their daily responsibilities and career focus differ significantly.

What does a Biotechnology Manager do?

A Biotechnology Manager oversees the research, development, and production processes within biotechnology organizations. They are responsible for managing teams of scientists and technicians, ensuring projects meet regulatory and safety standards, and coordinating with other departments to achieve company goals. Their role often involves budgeting, project management, and staying updated on the latest technological advancements in the field. Effective communication and leadership skills are essential for this position.

How does a Biotechnology Manager typically collaborate with cross-functional teams to drive project success?

As a Biotechnology Manager, you will frequently work with multidisciplinary teams, including scientists, engineers, regulatory specialists, and business development professionals. Your role involves coordinating efforts, setting project timelines, and ensuring clear communication across departments to meet research and development goals. Effective collaboration is essential for troubleshooting technical challenges, aligning project objectives, and delivering innovative solutions within budget and regulatory guidelines. Building strong relationships and facilitating regular team meetings are key practices for success in this role.

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

To thrive as a Biotechnology Manager, you need a solid background in biological sciences, project management experience, and usually an advanced degree such as a Master's or Ph.D. in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), regulatory compliance tools, and certifications like PMP or Six Sigma are often required. Strong leadership, problem-solving abilities, and effective communication distinguish top performers in this role. These competencies are crucial to successfully lead teams, ensure regulatory adherence, and drive innovation in a highly technical and regulated industry.
What are the most commonly searched types of Biotechnology jobs in Minnesota? The most popular types of Biotechnology jobs in Minnesota are:
What cities in Minnesota are hiring for Biotechnology Manager jobs? Cities in Minnesota with the most Biotechnology Manager job openings:
Infographic showing various Biotechnology Manager job openings in Minnesota as of July 2026, with employment types broken down into 81% Full Time, 14% Part Time, 1% Temporary, 3% Contract, and 1% Summer. Highlights an 75% Physical, 3% Hybrid, and 22% Remote job distribution.

Global Product Registration Manager

Pivot Bio

Minnetonka, MN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 days ago


Job description

About Pivot Bio:
Fueled by an innovative drive and a deep understanding of microbiology, genomics, crop nutrition and agriculture, Pivot Bio is pioneering game-changing advances in fertilizer technology. Our first commercial product harnesses the power of naturally-occurring microbes, modern gene editing and application technologies to provide nitrogen to crops. We are dedicated to providing new solutions for farmers to improve yield as they work to help feed the world's growing population. Read/Hear more about Pivot Bio on Forbes or PBS News Hour.
The Global Product Registration Manager will lead regulatory strategy and execution for the registration and commercialization of Pivot Bio products, with a strong emphasis on United States federal and state regulatory requirements. This role is responsible for ensuring timely product approvals, maintaining compliance across jurisdictions, and enabling market access through proactive engagement with regulatory authorities.
Essential Functions
  • Develop and execute global regulatory strategies for Pivot Bio products, with primary focus on U.S. regulatory frameworks, including federal and state-level registrations (e.g., soil amendment, biostimulant, and biofertilizer requirements).
  • Lead the preparation, submission, and management of regulatory dossiers to U.S. agencies and individual state departments of agriculture, ensuring alignment with varying state data requirements, labeling standards, and review timelines.
  • Coordinate and manage state registration processes across all states required for product commercial launch, including renewals, amendments, and tonnage reporting
  • Serve as the primary regulatory contact for U.S. state agencies, building relationships and effectively responding to inquiries and data requests.
  • Interpret evolving regulatory guidance related to gene-edited organisms, microbial products, and biotechnology, translating requirements into actionable plans.
  • Partner cross-functionally with regulatory science, product development, manufacturing, quality, and commercial teams to create product labels and compile data packages supporting product safety, efficacy, and environmental impact.
  • Partner with growth team to inform new partnership strategy with regards to potential regulatory pathways, requirements, resources, and timelines.
  • Forecast product registration resource needs based on commercial plans and build resources internally and/or externally to meet commercial timelines
  • Monitor regulatory developments at both federal and state levels, identifying risks and opportunities, and advising internal stakeholders on strategic implications.
  • Ensure compliance with post-registration obligations, including adverse event reporting, tonnage reporting, and label updates.
  • Support global registrations outside the U.S. as needed, ensuring consistency in regulatory strategy and documentation.
  • Contribute to regulatory policy and advocacy efforts through engagement with industry groups and stakeholders.

Competencies
Knowledge & Application
  • Demonstrated experience with U.S. federal and state registration processes, particularly for microbial products such as biopesticides, biofertilizers, or biostimulants.
  • Strong working knowledge of U.S. regulatory agencies and frameworks, including familiarity with state-specific requirements and registration systems.
  • Experience preparing and submitting regulatory dossiers, including data related to product characterization, toxicology, environmental fate, and efficacy.
  • Understanding of gene editing technologies (e.g., CRISPR) and their regulatory implications preferred.
  • AI proficiency, including the ability to responsibly leverage AI-enabled tools to improve regulatory research, dossier development, data synthesis, workflow efficiency, and cross-functional decision support.

Complexity & Problem Solving
  • Proven ability to manage multiple complex projects and regulatory submissions simultaneously.
  • High attention to detail, strong organizational skills, and a proactive, solutions-oriented mindset.

Collaboration & Interaction
  • Excellent communication, technical writing, and stakeholder engagement skills.
  • Ability to work effectively in a cross-functional, global environment and influence without direct authority.
  • Collaborate cross-functionally with regulatory science, product development, manufacturing, quality, and commercial teams

Required Education & Experience
  • Bachelors degree in Microbiology, Molecular Biology, Biotechnology, Plant Sciences, or a related scientific discipline.
  • Minimum of 8 years of regulatory affairs experience in agricultural biologicals, biotechnology, or related industry.

Must be authorized to work in the United States
What We Offer:
  • Incentive Bonus Plan
  • Competitive package in a disruptive startup
  • Stock options
  • Health/Dental/Vision insurance with employer-paid premiums
  • Life, Short-Term and Long-Term Disability policies
  • Employee Assistance Program with free referrals and discounts
  • 401(k) plan, 3% Match
  • Commuter benefits
  • Annual Training & Development support
  • Flexible vacation policy with a generous holiday schedule
  • Exciting opportunity to work with a talented and fun team

#LI-Onsite
Hiring Compensation Range
$105,984-$132,480 USD