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Masters In Biotechnology Jobs in Philadelphia, PA

OCUGEN OPCO INC

VP of Finance Operations

Malvern, PA · On-site

Bachelor's in Accounting, Finance, or related field, Masters or MBA a plus. * Certified Public ... Relevant experience in biotech is highly desired. * Management experience required. * Excellent ...

Ocugen Inc

VP of Finance Operations

Malvern, PA · On-site

Bachelor's in Accounting, Finance, or related field, Masters or MBA a plus. * Certified Public ... Relevant experience in biotech is highly desired. * Management experience required. * Excellent ...

Cytokinetics, Inc.

Associate Director, FP&A

Radnor, PA · Hybrid

$200K - $234K/yr

Bachelor's degree in finance, Accounting, Economics, or related discipline; MBA a plus. * 10+ years ... Commercial-stage biotechnology or pharmaceutical experience. * Demonstrated experience supporting ...

Cytokinetics

Associate Director, FP&A

Radnor, PA · On-site

$200K - $234K/yr

Bachelor's degree in finance, Accounting, Economics, or related discipline; MBA a plus. * 10+ years ... Commercial-stage biotechnology or pharmaceutical experience. * Demonstrated experience supporting ...

Merck & Co., Inc.

Director, Operations

Wilmington, DE · On-site

Bachelor's degree + 12 years industry experience Or Masters + 10 years Or PhD + 8 years * 6 or more ... Demonstrated experience in a biotech/vaccines/pharma manufacturing site, project, or other relevant ...

New

MSD Malaysia

Director, Operations

Wilmington, DE · On-site

$173 - $273/hr

Bachelor's degree + 12 years industry experience Or Masters + 10 years Or PhD + 8 years * 6 or more ... Demonstrated experience in a biotech/vaccines/pharma manufacturing site, project, or other relevant ...

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All JobsMasters In Biotechnology JobsMasters In Biotechnology Jobs in Philadelphia, PA

Masters In Biotechnology information

See Philadelphia, PA salary details

$27.2K

$78.1K

$118.6K

How much do masters in biotechnology jobs pay per year?

As of Aug 28, 2026, the average yearly pay for masters in biotechnology in Philadelphia, PA is $78,092.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,400.00 and $117,600.00 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.

What cities near Philadelphia, PA are hiring for Masters In Biotechnology jobs?

Cities near Philadelphia, PA with the most Masters In Biotechnology job openings:

Masters In Biotechnology jobs near you
Infographic showing various Masters In Biotechnology job openings in Philadelphia, PA as of August 2026, with employment types broken down into 1% Internship, 2% As Needed, 82% Full Time, 12% Part Time, and 3% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $78,092 per year, or $37.5 per hour.

Vice President, Program Management

Malvern, PA • On-site

Uniquity Bio Inc.
See more jobs at Uniquity Bio Inc.external

Full-time

Re-posted 20 days ago

Job description

Uniquity Bio is a clinical-stage biotechnology company committed to putting science and patients first. We exist to develop transformative new medicines for immune-mediated diseases, and we’re looking for bright-minded professionals driven by a desire to advance science and make a difference for people in need. Our lead asset, solrikitug, is a highly-potent TSLP inhibitor now in Phase 2 clinical trials for asthma, chronic obstructive pulmonary disease (COPD), and eosinophilic esophagitis (EoE) indications. 

Join us in building an organization where people and science thrive together. You’ll have the opportunity to make a meaningful impact while working alongside a talented, agile team in an environment where ideas move quickly, colleagues are trusted, and quality remains a cornerstone.


Position Overview

 

The Vice President of Program Management drives the strategic and operational execution of the company’s late-stage (Phase 2 and Phase 3) development programs. This position will report to the CEO and is a key member of the leadership team. This individual will drive integrated program strategy, execution and decision making partnering closely with cross-functional leaders to ensure clinical and regulatory success, and deliver critical value inflection points in a lean, fast-paced biotech environment.

This role requires a highly experienced, hands-on leader with deep expertise in late-stage clinical development, who can successfully navigate complexity, manage cross functional relationships, and prepare programs for potential registration and commercialization.

 

Key Responsibilities

 

  • Lead the end-to-end program strategy and execution for Phase 2 and Phase 3 programs.
  • Lead team cross functional team meetings to drive decision making and timelines by synthesizing complexity into clear decision options and plans of action.
  • Contribute to development strategies to support regulatory approval, label optimization, and lifecycle planning.
  • Ensure clear alignment of program goals with corporate objectives, investor expectations, and clinical/regulatory milestones.
  • Oversee integrated program plans supporting global Phase 2b/3 clinical trials, including timelines, budgets, and critical path activities.
  • Partner closely with Clinical Development, Clinical Operations, Biostatistics, Regulatory and CMC to ensure trial execution excellence.
  • Anticipate and proactively mitigate risks related to enrollment, endpoints, regulatory expectations, and data integrity.
  • Prepare and deliver communications for Board meetings highlighting key risks, risk mitigation strategies, and progress against timelines and deliverables.
  • Collaborate with Regulatory Affairs to prepare for key interactions (e.g., End-of-Phase 2, pre-BLA/NDA meetings, and global regulatory submissions).
  • Support development of target product profiles and differentiation strategies in competitive immunology markets.
  • Ensure programs are aligned with future commercialization considerations (e.g., payer expectations, labeling, and evidence generation).

Cross-Functional Leadership

  • Act as the central driver of alignment across functions including Clinical, Regulatory, CMC, Commercial, and Quality.
  • Lead program governance meetings and ensure timely, high-quality decision-making.
  • Ensure accountability, performance, and integration of external activities into overall program execution.

Operational Infrastructure & Governance

  • Establish fit-for-purpose program management frameworks tailored to late-stage development in a small biotech setting.
  • Develop clear and concise program reporting for executive leadership, Board of Directors, and investors.
  • Drive scenario planning and contingency strategies to enable rapid decision-making.

Leadership & Team Development

  • Build and lead a small, high-performing Program Management team.
  • Serve as a “player-coach,” remaining deeply engaged in program execution while developing team capabilities.
  • Foster a culture of urgency, accountability, and collaboration.


Qualifications

 

Education & Experience

  • Bachelor’s degree required; Advance degree preferred (PhD, PharmD, MS, MBA)
  • 15+ years in biotech/pharma with substantial experience in late-stage clinical development.
  • Demonstrated leadership of Phase 2 and Phase 3 programs, including global trials.
  • Prior experience in immunology, allergy/inflammation, or respiratory diseases strongly preferred.
  • Experience in small biotech or startup environments highly desirable.
  • Deep understanding of TSLP biology or related epithelial cytokine pathways preferred.
  • Strong knowledge of immunology clinical endpoints, biomarkers, and competitive landscape.
  • Experience with regulatory filings (BLA/NDA/MAA) and health authority interactions.

Leadership & Execution Skills

  • Proven ability to lead complex, cross-functional programs in a matrix environment.
  • Highly hands-on with the ability to operate at both strategic and tactical levels.
  • Strong risk management, problem-solving, and decision-making capabilities.
  • Exceptional communication skills, including Board-level presentations.


Work Environment

At Uniquity Bio, we believe every team member has an impact on the patients we aim to serve. We are a nimble team with a rigorous approach to drug development that requires collaboration and transparency to maximize value, reduce risk, and deliver meaningful, best-in-class products. We are looking for self-starters who enjoy working in a complex, collaborative environment and are motivated to bring critical new medicines to people around the world. We are a small, fast-paced organization with a talented team of in-house employees and external consultants. Candidates must be self-motivated and able to work both independently and collaboratively to achieve success and impact in our dynamic work environment. 

This is a U.S.-based position. Team members who live within commuting distance of our Malvern, PA or San Diego, CA office locations are expected to spend time in the office, and remote employees are expected to travel to an office on a regular basis. Specific details for both local and remote staff will be discussed and agreed upon on a case-by-case basis with the employee’s manager. Business travel may be required depending upon the specific needs of the position. 

The above job description is not intended to be all-inclusive. Requirements of the position may change from time to time based on business needs.


Uniquity Bio is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.


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