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Project Control Analyst Jobs in New York (NOW HIRING)

Legend Biotech US

Sr. QC Analyst

Raritan, NJ · On-site

$24.50 - $33/hr

Shift: 3rd shift Wed-Sat Role Overview The Sr. QC Analyst is an exempt level position with ... Employs good project management principles to appropriately align time, resources, and budgets.

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Project Control Analyst information

See New York salary details

$50.3K

$106.1K

$147.7K

How much do project control analyst jobs pay per year?

As of Jul 3, 2026, the average yearly pay for project control analyst in New York is $106,083.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,900.00 and $114,900.00 per year, depending on experience, location, and employer.

What Does a Project Control Analyst Do?

A project control analyst oversees a project to ensure it stays within budget and is completed on time. As a project control analyst, you keep accurate records of expenditures and timelines, track regulatory compliance of each phase, and monitors any market changes that may affect the project. You compile this data and process reports for management to determine whether or not changes should be made to the project.

What is a Project Control Analyst?

A Project Control Analyst is a professional responsible for monitoring, analyzing, and reporting on the progress and performance of projects. They support project managers by tracking budgets, timelines, risks, and resource allocation to ensure projects stay on track and within scope. Their role often involves creating and updating project schedules, preparing financial reports, and identifying any potential issues that could impact project outcomes. Project Control Analysts play a critical role in ensuring successful project delivery by providing valuable insights and recommendations.

What is the difference between Project Control Analyst vs Cost Analyst?

AspectProject Control AnalystCost Analyst
Required CredentialsBachelor's in project management, finance, or related field; certifications like PMP or CCPBachelor's in finance, accounting, or related; certifications like CPA or CMA
Work EnvironmentConstruction, engineering, IT, or manufacturing projectsFinance departments, consulting firms, or corporate accounting
Employer & Industry UsageProject-based industries requiring schedule and resource managementOrganizations focusing on budgeting, cost control, and financial analysis

The Project Control Analyst primarily manages project schedules, resources, and overall project performance, while the Cost Analyst focuses on budgeting, cost tracking, and financial analysis. Both roles require strong analytical skills and relevant certifications, but they serve different aspects of project and financial management within organizations.

What are the key skills and qualifications needed to thrive as a Project Control Analyst, and why are they important?

To thrive as a Project Control Analyst, you need strong analytical skills, attention to detail, and a background in project management or finance, often supported by a relevant degree or certification. Familiarity with project management software (such as MS Project or Primavera), ERP systems, and advanced Excel skills is typically required. Excellent communication, problem-solving, and organizational abilities help you collaborate with project teams and stakeholders. These competencies are crucial for monitoring project performance, ensuring budget adherence, and supporting successful project delivery.

How does a Project Control Analyst typically collaborate with project managers and other stakeholders?

Project Control Analysts work closely with project managers, finance teams, and engineers to monitor project progress, track budgets, and ensure timelines are met. They often participate in regular project meetings, provide data-driven updates, and flag any potential risks or deviations from the project plan. Effective communication and collaboration are essential, as they must coordinate between multiple departments to gather accurate information and help keep projects on track. This role is highly cross-functional, making strong interpersonal skills and attention to detail important for success.
More about Project Control Analyst jobs
What are the most commonly searched types of Project Control Analyst jobs in New York? The most popular types of Project Control Analyst jobs in New York are:
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What are popular job titles related to Project Control Analyst jobs in NY? For Project Control Analyst jobs in NY, the most frequently searched job titles are:
Project Control Analyst jobs near you
Infographic showing various Project Control Analyst job openings in New York as of June 2026, with employment types broken down into 33% Full Time, 54% Part Time, 11% Contract, and 2% Nights. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $106,083 per year, or $51 per hour.

Sr. QC Analyst

Legend Biotech US

Raritan, NJ • On-site

$24.50 - $33/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 21 days ago

Job description

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.
Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.
Legend Biotech is seeking a Sr. QC Analyst as part of the Quality team based in Raritan, NJ.
Shift: 3rd shift Wed-Sat
Role Overview
The Sr. QC Analyst is an exempt level position with responsibilities for performing QC testing related to the manufacturing of cell therapy products for clinical trials and commercial operations in a controlled GMP environment.
Key Responsibilities
  • Be responsible for the completion of QC testing related to the manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment.
  • Ensure testing is completed in compliance with all applicable procedures, standards and GMP regulations.
  • Conduct analytical testing of raw material/utility, in-process, or final product samples submitted to the QC laboratories.
  • Perform peer review/approval of laboratory data.
  • Utilize electronic systems (LIMS) for execution and documentation of testing.
  • Create, review and approve relevant QC documents, SOP's and WI's.
  • Perform tasks in a manner consistent with the safety policies, quality systems and cGMP requirements.
  • Work in a collaborative team setting with quality counterparts that include Quality Assurance, Manufacturing Operations, and Analytical/Process Development.
  • Job duties performed require routine exposure to and handling of biological materials and hazardous chemicals.

Requirements
  • Bachelor's Degree in Science, Engineering or equivalent technical discipline is required.
  • Minimum of 1 year relevant work experience, preferably within a biological and/or pharmaceutical industry is required.
  • Experience in a Quality Control setting is preferred.
  • Experience with processing samples in biosafety cabinets utilizing aseptic technique is strongly preferred.
  • Knowledge of cGMP regulations and FDA/EU guidance related to manufacturing of cell-based products is strongly preferred.
  • Knowledge of Good Tissue Practices is required.
  • Knowledge of CAR-T QC test methods and related equipment is preferred.
  • Excellent written and oral communication skill are required.
  • Candidates must be able to accommodate shift schedule. Shifts include routine weekend and evening work as required by the manufacturing process.
  • Candidates must be able to accommodate unplanned overtime (including nights and weekends) on little to no prior notice.
  • The candidate must be highly organized and capable of working in a team environment with a positive attitude under some supervision.
  • Comfortable with speaking and interacting with regulatory inspectors.
  • This position may require occasional travel to partner sites in NJ or PA as business demands.
  • This position may require up to 5% domestic or international travel as business demands.
  • Takes responsibility for one's results and deliverables; sets and achieves goals to support organizational priorities.
  • Takes initiative; willing to take unpopular positions/actions when necessary; courageous and assertive.
  • Works effectively in the face of ambiguity, shifting priorities, and rapid change; maintains a positive outlook in difficult situations; a change agent.
  • Identifies and focuses on activities of highest value and impact; makes informed decisions quickly.
  • Results oriented; defines goals, metrics and actionable plans and manages work to deliver desired outcomes; has a sense of urgency.
  • Considers resources, alternatives, constraints and desired outcomes to make effective decisions.
  • Employs good project management principles to appropriately align time, resources, and budgets.
  • Appreciates diverse perspectives and is actively inclusive of others' input and ideas; treats others with respect.
  • Articulates ideas clearly and succinctly in a variety of settings and styles; can get messages across that have the desired effect.
  • Leverages personal credibility and interpersonal skills to help others make better decisions and positively impact outcomes; able to develop/maintain effective working relationships internally and externally.
  • Employs a global mindset in decision-making and errs on the side of over-communicating to create organizational transparency, trust and alignment.
  • Takes initiative, actively shares knowledge, builds skills, promotes new ideas and embraces change.
  • Generates new solutions to problems by challenging the status quo and conventional thinking.

#Li-RP1
#Li-Onsite
The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.
Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.
Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.
Pay Range (Base Pay):
$83,711-$109,870 USD
Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.
EEO Statement
It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.
Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.
For information related to our privacy notice, please review: Legend Biotech Privacy Notice.

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