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Masters In Biotechnology Jobs (NOW HIRING)

Jobtailor

NY · On-site

$150 - $230/hr

... * MBA or equivalent business training/experience (preferred); MD or MD/PhD also considered * 7-10 years in biotech/pharma/medtech, with 3-5 years in translational R&D (neuro-oncology, CNS delivery ...

DGN Technologies

Senior QC Technician

Oceanside, CA · On-site

Domain knowledge in biotechnology, chemistry, biochemistry, microbiology, analytical chemistry, or ... Masters degree and 6-9 years experience in Computer Science (Software Development) or Life Science ...

Revolution Medicines

Senior Manager, Commercialization FP&A

$111K - $152K/yr

... in biotechnology industry. * Highly proficient in Excel, PowerPoint and AI automation (Codex ... Preferred Skills: * CPA or MBA preferred. * Demonstrated experience utilizing financial systems and ...

AbbVie

Data Scientist

Worcester, MA · On-site

Masters in Data Engineering, Data Science or related * Prior experience in biotech or pharmaceuticals preferred * Strong experience in programming, including Python, SQL, etc. * Experience with ...

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How much do masters in biotechnology jobs pay per year?

As of Aug 28, 2026, the average yearly pay for masters in biotechnology in the United States is $77,389.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $116,500.00 per year, depending on experience, location, and employer.

What can you do with a master's in biotechnology?

A Master's in Biotechnology opens up a wide range of career opportunities in industries such as pharmaceuticals, healthcare, agriculture, environmental science, and research and development. Graduates can work as research scientists, bioprocess engineers, clinical research associates, regulatory affairs specialists, or quality control analysts. This degree also provides a strong foundation for those who wish to pursue a Ph.D. or move into management or business roles related to biotech innovation.

What types of career paths are available to professionals with a master's in biotechnology, and how can graduates position themselves for advancement?

With a Masters in Biotechnology, graduates can pursue diverse career paths in research and development, quality assurance, regulatory affairs, clinical trials, and product management within pharmaceutical, agricultural, and medical device industries. To position themselves for advancement, professionals should gain hands-on laboratory experience, stay updated on emerging biotech trends, and develop strong project management and communication skills. Networking through industry conferences and professional associations also opens doors to leadership or specialized roles. Many organizations value candidates who can bridge scientific expertise with business acumen, so additional certifications or training in management can further enhance career progression.

What are the key skills and qualifications needed to thrive in a role with a master's in biotechnology, and why are they important?

A Master's in Biotechnology requires a solid background in molecular biology, genetics, and laboratory techniques, supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory equipment, data analysis software, and compliance certifications such as GLP or GMP is commonly expected. Strong analytical thinking, problem-solving skills, and effective communication are crucial soft skills for collaborating in multidisciplinary environments. These competencies ensure successful research, innovation, and adherence to industry standards in the rapidly evolving biotechnology sector.

What is the difference between Masters In Biotechnology vs Biotechnology Research Associate?

AspectMasters In BiotechnologyBiotechnology Research Associate
Required CredentialsMaster's degree in Biotechnology or related fieldBachelor's degree often required; master's preferred
Work EnvironmentLaboratories, research facilities, academia, biotech companiesLaboratories, research institutions, biotech firms
Employer & Industry UsageAcademic institutions, biotech companies, research labsBiotech companies, research organizations, pharmaceutical firms
Common Search & ComparisonYesYes

Masters In Biotechnology provides advanced theoretical knowledge and research skills, often leading to roles in research, development, or academia. A Biotechnology Research Associate typically holds a bachelor's or master's degree and focuses on executing research projects under supervision. While both roles work in similar environments, a master's degree can open doors to more senior or specialized positions within the biotech industry.

Is a Masters in Biotechnology a good career?

A Masters in Biotechnology prepares individuals for careers in research, development, and quality control within biotech, pharmaceutical, and healthcare industries. It can lead to roles such as biotechnologist, research scientist, or lab manager, often requiring strong laboratory skills and knowledge of molecular biology and bioinformatics. Job prospects are generally favorable due to ongoing advancements in medical and agricultural fields.

Is a Masters in Biotechnology worth it?

A Masters in Biotechnology can enhance job prospects in research, development, and quality control roles within biotech and pharmaceutical industries. It provides specialized knowledge, laboratory skills, and often requires hands-on experience or internships, which can improve employability and earning potential.
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Infographic showing various Masters In Biotechnology job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 2% As Needed, 83% Full Time, 11% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $77,389 per year, or $37.2 per hour.

Director, Program Management I & I Full Life Cycle

Boston, MA • On-site

Monte Rosa Therapeutics, Inc
Biotechnology Research and Development • 11 - 50 employees
Learn more about Monte Rosa Therapeutics, Incexternal

$150K - $225K/yr

Full-time

Re-posted 29 days ago

Job description

Overview
The Associate Director of Program Management will serve as a strategic and operational leader for priority immunology and inflammation programs, driving assets from mid- to late-stage development through regulatory submission. This role is designed for a hands-on, agile leader who thrives in a fast-paced biotechnology environment and can rapidly translate evolving science into executable development strategy.
As a core member of the Program Team, the Director will partner closely with Clinical, Regulatory, CMC, Nonclinical, Biomarkers, Translational Sciences, and Commercial leaders to integrate strategy and execution across the full development lifecycle. This individual will ensure alignment to the Target Product Profile (TPP) and Integrated Development Plan (IDP), while enabling flexibility as data emerge and scientific understanding evolves.
Success in this role requires deep familiarity with immunology and inflammation drug development, comfort operating amid uncertainty, and the ability to balance scientific rigor with speed, capital efficiency, and enterprise priorities.
Responsibilities
  • Serve as a strategic and operational lead for one or more immunology/inflammation programs, ensuring alignment between clinical strategy, translational insights, and regulatory pathways.
  • Develop and maintain integrated, cross-functional development plans across clinical, regulatory, CMC, manufacturing, and translational functions.
  • Lead scenario planning exercises to evaluate alternative development pathways, indication sequencing, acceleration opportunities, and capital-efficient trade-offs.
  • Continuously pressure-test timelines and critical paths, proactively identifying opportunities to streamline execution without compromising quality.
  • Establish proactive risk identification and mitigation frameworks tailored to immunology/inflammation programs, including biomarker risk, patient heterogeneity, regulatory complexity, and competitive landscape shifts.
  • Lead high-quality risk discussions at the Global Program Team level with timely escalation of high-impact issues.
  • Develop contingency strategies for clinical, manufacturing, or regulatory inflection points.
  • Monitor program-level budget and resource health in alignment with corporate priorities.
  • Ensure clarity of functional accountabilities and decision rights in a lean, matrixed biotech structure.
  • Partner with functional leaders during long-range planning and portfolio prioritization exercises.
  • Build and maintain practical, real-time tracking tools (e.g., Smartsheet dashboards, integrated timelines, risk logs) that enable rapid visibility and decision-making.
  • Prepare concise, executive-ready materials that distill complex scientific and operational issues into clear recommendations.
  • Lead continuous improvement initiatives within Program Management to enhance agility, transparency, and execution discipline.

Qualifications
• 12+ years of experience in biotechnology or pharmaceutical drug development.
• Minimum 8 years of program/project management experience leading cross-functional development teams.
• Demonstrated experience advancing immunology and/or inflammation assets through Phase 2 and Phase 3 development.
• Experience preparing for and supporting major regulatory interactions (e.g., End-of-Phase 2 meetings, NDA/BLA submissions).
• Experience operating in small-to-mid-sized biotech environments where agility and hands-on leadership are required.
Education
• BS required; advanced degree (MS, PhD, or MBA) strongly preferred.
• PMP certification desirable but not required.
Technical & Leadership Capabilities
• Strong understanding of immunology and inflammation biology, clinical endpoints, biomarker strategy, and regulatory considerations.
• Deep knowledge of end-to-end drug development within a resource-conscious biotech setting.
• Demonstrated ability to lead through ambiguity and adapt strategy as data emerge.
• Proven success influencing senior stakeholders in a highly matrixed environment.
• Expertise in integrated planning, risk management, and scenario modeling.
• Strong executive presence with the ability to communicate complex scientific and operational topics clearly and concisely.
• Proficiency with modern project management and collaboration tools (e.g., Smartsheet, MS Project, Teams).
• Exceptional organizational skills with the ability to manage multiple interdependent workstreams simultaneously.
• High emotional intelligence, strong conflict resolution skills, and the ability to build trust across scientific and operational teams.
• Comfort operating with urgency, limited infrastructure, and evolving priorities typical of innovative biotech companies.

Apply