Project Manager

Posted Yesterday
Be an Early Applicant
08540, Princeton, NJ, USA
In-Office
75K-95K Annually
Mid level
Biotech • Pharmaceutical • Chemical • Manufacturing
The Role
Manage project schedules, scope, timelines, budgets, and deliverables for regulated biotech/GMP projects. Coordinate internal and external stakeholders, run meetings, track risks and changes, support POs/invoices/revenue recognition, ensure SOP and regulatory compliance, mentor assistant PMs, and provide status reports. Onsite role with occasional outside-hours work.
Summary Generated by Built In

We are looking for a dedicated and detail-oriented Project Manager to join our team. The successful candidate will be responsible for supporting project management activities, ensuring projects are completed on time, within scope, and on budget, while maintaining high levels of customer satisfaction and collaboration. This position requires the employee to be onsite. The incumbent works cross-functionally with internal departments and external resources on project-management-related issues. The Project Manager supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate. 

JOB RESPONSIBILITIES

•    Develop and manage a detailed project schedule and work plan, tracking project scope, timelines, status, deliverables, shipments, and budget to ensure on-time and on-budget delivery of projects.
•    Adjust project timelines as needed to support changing priorities, client requirements, and business needs.
•    Utilize industry best practices, techniques, and standards throughout the entire project execution process.
•    Communicate with external clients and internal stakeholders; coordinate and conduct meetings; record meeting minutes; organize and store meeting files and documents in designated locations; and track and follow up on action items.
•    Manage client expectations, issue escalations, follow-ups, and project communications.
•    Keep clients and project teams updated with progress reports and current project information.
•    Identify project risks, track issues, escalate blockers, and support mitigation plans.
•    Manage scope changes, document changes, and coordinate impact assessments with internal teams.
•    Support purchase orders, invoices, revenue recognition, cost tracking, project forecasts, and budget reconciliation.
•    Collaborate with Business Development, Finance, Facilities, GMP teams, and R&D teams and contribute to their activities as needed.
•    Partner with management to support safety and quality initiatives within the organization.
•    Develop and maintain strong collaborative working relationships and interact effectively with all levels within the organization and with external clients.
•    Coach and mentor Assistant Project Managers.
•    Perform other tasks and assignments as needed and specified by management.
 

Qualifications

REQUIRED SKILLS AND ABILITIES:

•    Working knowledge of project management principles, including critical paths, timelines, milestones, expectations, and accountability.
•    Strong planning, organization, and time management skills, with the ability to support and prioritize multiple projects.
•    Proficiency with Microsoft Office is required; experience with MS Project is recommended.
•    Proficiency with Smartsheet for project management is required.
•    Excellent verbal and written communication skills, with the ability to communicate effectively with internal and external stakeholders.
•    Strong interpersonal skills and ability to build positive cross-functional working relationships.
•    Ability to work independently and collaboratively with internal and external team members.
•    Analytical thinker with strong problem-solving skills and adaptability to changing priorities and deadlines.
•    Self-motivated and willing to grow and learn new skills.
•    Ability to work outside normal business hours, including occasional nights, weekends, or holidays, as needed to support business needs and accommodate international clients or GMP projects.

EDUCATION AND EXPERIENCE REQUIREMENT:

•    Bachelor’s degree in Chemistry, Biochemistry, Biology, Health Sciences, Project Management, Business, or related discipline required; advanced degree preferred.
•    Minimum 3–5 years of project management experience, preferably in biotech, pharmaceutical, CDMO, GMP, laboratory, manufacturing, or regulated environments.
•    Experience supporting cross-functional, client-facing, or GMP-related project activities preferred.

WORKING ENVIRONMENT:

Office-based position

CERTIFICATIONS & LICENSE REQUIREMENT:

PMP Certification is a Plus

COMPENSATION:

$75,000–$95,000 per year


NJ Bio, Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to their race, color, sex, religion, age, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability or any other characteristic protected by applicable federal, state, or local laws.

Skills Required

  • Working knowledge of project management principles (critical path, timelines, milestones, accountability).
  • Strong planning, organization, and time management skills; ability to prioritize multiple projects.
  • Proficiency with Microsoft Office.
  • Proficiency with Smartsheet for project management.
  • Experience with MS Project.
  • Excellent verbal and written communication skills.
  • Strong interpersonal skills and ability to build cross-functional relationships.
  • Ability to work independently and collaboratively with internal and external teams.
  • Analytical thinker with strong problem-solving skills and adaptability.
  • Self-motivated and willing to learn new skills.
  • Ability to work outside normal business hours, including occasional nights, weekends, or holidays.
  • Bachelor's degree in Chemistry, Biochemistry, Biology, Health Sciences, Project Management, Business, or related discipline.
  • Advanced degree.
  • Minimum 3-5 years of project management experience.
  • Experience in biotech, pharmaceutical, CDMO, GMP, laboratory, manufacturing, or regulated environments.
  • Experience supporting cross-functional, client-facing, or GMP-related project activities.
  • PMP certification.
  • Position requires the employee to be onsite (office-based).
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
146 Employees
Year Founded: 2019

What We Do

NJ Bio, Inc. is a leading Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO) that provides integrated chemistry and biology services to biotechnology and pharmaceutical companies. Specializing in antibody-drug conjugates (ADCs) and bioconjugation, the company supports programs from early-stage discovery through GMP manufacturing, delivering highly tailored and innovative solutions to accelerate the development of complex targeted therapies for patients.

Similar Jobs

Pluralsight Logo Pluralsight

Project Manager

Edtech • Information Technology • Software
Remote or Hybrid
USA
1000 Employees
84K-110K Annually

PwC Logo PwC

Project Manager

Artificial Intelligence • Professional Services • Business Intelligence • Consulting • Cybersecurity • Generative AI
Hybrid
67 Locations
370000 Employees
151K-187K Annually
Hybrid
2 Locations
289097 Employees
Hybrid
Jersey City, NJ, USA
289097 Employees

Similar Companies Hiring

True Anomaly Thumbnail
Aerospace • Artificial Intelligence • Hardware • Machine Learning • Software • Defense • Manufacturing
Centennial, CO
300 Employees
Fortune Brands Innovations Thumbnail
Manufacturing
Deerfield, IL
10000 Employees
Amalgamated Sugar Thumbnail
Food • Greentech • Agriculture • Industrial • Manufacturing
Boise, Idaho
768 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account