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Program Biotech Jobs in Piscataway, NJ (NOW HIRING)

Legend Biotech US

Manager, Regulatory CMC

Somerset, NJ · Hybrid

Legend Biotech is seeking a Manager, Regulatory CMC as part of the Regulatory Affairs team based in ... Partner closely with Regulatory CMC Program Leads and cross-functional subject matter experts to ...

Legend Biotech US

Director, Regulatory Affairs

Somerset, NJ · On-site

$158K - $209K/yr

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... programs. * Lead the team efforts required for the submission of INDs, CTAs, and BLAs as well as ...

Legend Biotech US

Operations Manager

Raritan, NJ · On-site

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... projects/programs forward in a matrixed environment. * Ability to work independently and ...

Legend Biotech US

Metrology Tech I

Raritan, NJ · On-site

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... Provides technical expertise in support of an effective calibration program that supports daily ...

Legend Biotech US

Operations Supervisor

Raritan, NJ · On-site

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life ... projects/programs forward in a matrixed environment. * Clear and succinct verbal and written ...

Legend Biotech US

Investigations Supervisor

Raritan, NJ · On-site

Ability to utilize various standard programs for data entry and word processing. * Language(s): English #Li-BZ1 #Li-Onsite The base pay range below is what Legend Biotech USA Inc. reasonably expects ...

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Showing results 41-60

All JobsProgram Biotech JobsProgram Biotech Jobs in Piscataway, NJ

Program Biotech information

See Piscataway, NJ salary details

$25.5K

$53.3K

$92.2K

How much do program biotech jobs pay per year?

As of Sep 2, 2026, the average yearly pay for program biotech in Piscataway, NJ is $53,349.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,800.00 and $60,600.00 per year, depending on experience, location, and employer.

What is a program biotech?

A Program Biotech is a professional who manages and coordinates biotechnology projects or programs within an organization. They oversee research and development activities, ensure compliance with regulations, manage budgets, and facilitate collaboration between scientists, engineers, and other stakeholders. Their role is crucial in bringing biotech innovations from concept to market by ensuring projects stay on schedule and meet organizational goals.

What are the key skills and qualifications needed to thrive as a program biotech professional?

To excel as a Program Biotech professional, you need a solid background in life sciences, project management, and regulatory knowledge, often supported by an advanced degree in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), project management software, and compliance frameworks like GLP or GMP is common. Strong leadership, problem-solving abilities, and effective communication are crucial soft skills for coordinating multidisciplinary teams. These skills and qualifications are essential to drive innovation, ensure regulatory compliance, and achieve successful outcomes in complex biotech projects.

What are some common challenges faced by program biotech professionals when managing cross-functional teams?

Program Biotech professionals often coordinate projects that involve diverse teams, including research scientists, regulatory specialists, and business development staff. One key challenge is ensuring clear communication and alignment among team members with varying backgrounds and priorities. Additionally, balancing project timelines with regulatory requirements and scientific uncertainties can require strong problem-solving skills. Being proactive in facilitating collaboration and adapting to shifting project goals are essential for success in this role.

What is the difference between Program Biotech vs Laboratory Technician?

AspectProgram BiotechLaboratory Technician
Required CredentialsBiotech degree or certification, specialized trainingAssociate degree or certification in laboratory sciences
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or industrial labs
Employer & Industry UsageBiotech firms, research institutions, pharma companiesHospitals, research labs, manufacturing plants
Common Search & ComparisonYesNo

Program Biotech professionals focus on research, development, and overseeing biotech projects, often requiring advanced degrees and specialized training. Laboratory Technicians perform routine lab tests and support research or manufacturing processes, typically with an associate degree. While both roles work in lab environments within the biotech and healthcare industries, Program Biotech roles are more research-oriented, whereas Laboratory Technicians handle day-to-day testing and sample analysis.

What job categories do people searching Program Biotech jobs in Piscataway, NJ look for?

The top searched job categories for Program Biotech jobs in Piscataway, NJ are:

What cities near Piscataway, NJ are hiring for Program Biotech jobs?

Cities near Piscataway, NJ with the most Program Biotech job openings:

Program Biotech jobs near you

Manager, Project Management, Regulatory

Legend Biotech US

Somerset, NJ • Hybrid

Full-time

Posted 29 days ago

Job description

Legend Biotech is seeking a Manager, Regulatory Project Management as part of the Regulatory team based in Somerset, NJ. 

Role Overview

This role will be reporting to the Director of Project Management Regulatory. We are seeking a motivated, detail-oriented Project Manager to support the planning and execution of Cell & Gene Therapy development programs. Working closely with cross-functional teams, this individual will coordinate project activities, monitor timelines, facilitate effective communication, and provide administrative support to ensure projects are executed efficiently and meet key development milestones. This opportunity is well suited to an individual with early-career project management experience in the biotechnology or pharmaceutical industry who is eager to grow in a fast-paced, collaborative environment. The successful candidate will play a key role in project coordination, documentation, meeting management, and operational support throughout the product development lifecycle.

Key Responsibilities

  • Coordinate day-to-day project activities across cross-functional teams, including Research, CMC, Quality, Regulatory Affairs, Clinical Operations, and external partners.
  • Develop and maintain project timelines, action-item trackers, meeting agendas, and other key project documentation.
  • Schedule and facilitate project team meetings, prepare meeting minutes, and follow up on action items to support timely completion.
  • Monitor project progress and promptly escalate potential risks, delays, and resource constraints to project leadership.
  • Support the preparation and coordination of activities related to Investigational New Drug (IND) submissions and other regulatory filings.
  • Track project budgets, purchase orders, invoices, and resource utilization in collaboration with Finance and functional leads.
  • Assist with preparation of project dashboards, presentations, reports, and materials for leadership reviews, governance meetings, and investor or partner updates.
  • Assist with onboarding new project team members by coordinating access to systems, project documentation, and team resources.
  • Provide general administrative support to the cross function as needed.
  • Support vendor onboarding, contract routing, purchase requisitions, and invoice processing in partnership with Procurement and Finance.
  • Facilitate clear, effective communication among internal stakeholders and external collaborators, including contract research organizations (CROs) and contract development and manufacturing organizations (CDMOs).
  • Ensure project documentation is accurate, well organized, and maintained in accordance with company procedures.
  • Contribute to the continuous improvement of project management processes, templates, and best practices.

Requirements

  • Bachelor's degree in Life Sciences, Biotechnology, Biomedical Engineering, Pharmacy, or a related scientific field. Master's degree preferred.
  • 1-3 years of experience in project coordination, project management, program support, or administrative project support within the biotechnology, pharmaceutical, or life sciences industry.
  • Familiarity with Cell & Gene Therapy, biologics, or related therapeutic development is preferred.
  • Basic understanding of the drug development process, including preclinical development, CMC activities, and IND submissions.
  • Experience working in cross-functional teams within a regulated environment is preferred.
  • Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
  • Excellent written, verbal, and interpersonal communication skills.
  • Proficiency with Microsoft Office (Excel, PowerPoint, Word) and project management tools such as Microsoft Project, Smartsheet, or similar platforms.
  • PMP or CAPM certification is a plus but not required.

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