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Project Manager Quality Control Jobs in New Jersey

QuVa Pharma

Manager, Quality Control Lab

Bloomsbury, NJ · On-site

$98K - $135K/yr

Our Manager Quality Control- Lab plays a vital role within our organization. Once you complete our ... Understands how various issues affect each other and the outcome of projects; Improves upon ...

PIM BRANDS LLC

Assistant Manager, Quality Control

NJ · On-site

$66K - $72K/yr

Manages the Quality Control function, monitors and audits quality of the product. Functions as the key decision maker on issues related to acceptability of ingredients, materials in process and ...

Valiant

Quality Control Manager

Lakehurst, NJ · On-site

Perform quality control management on multiple federal DB and DBB construction projects. The QCM will review, process, and track submittals. The QCM will utilize the USACE-established three phases of ...

Teya Development LLC

Quality Control Manager

Lakehurst, NJ · On-site

$107K - $130K/yr

Perform quality control management on multiple federal DB and DBB construction projects. The QCM will review, process, and track submittals. The QCM will utilize the USACE-established three phases of ...

Epicur

Quality Control Manager

Mount Laurel Township, NJ · On-site

$75K/yr

Project Management * Results Driven * Technical Capacity * Innovation Supervisory Responsibility This position has supervisory responsibilities for the Quality Control Department Work Environment ...

INA Solution Inc

Quality control Manager

Fort Dix, NJ · On-site

Candidates must have NAVFAC, USACE, or other Federal/Government construction project experience and be available to start immediately. Responsibilities: * Manage the Contractor Quality Control (CQC ...

Ardena

Scientist - Quality Control (QC)

Somerset, NJ · On-site

Quality Control Location: Somerset, New Jersey FLSA Status: Exempt Employment Type: Full-Time ... Ability to effectively manage multiple priorities while meeting project deadlines. * Fluent in ...

Valiant

Quality Control Manager/SSHO

Lakehurst, NJ · On-site

Perform quality control management on multiple federal DB and DBB construction projects. The QCM will review, process, and track submittals. The QCM will utilize the USACE-established three phases of ...

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Project Manager Quality Control information

What is a project manager quality control?

Project Manager Quality Control professionals are responsible for overseeing the quality assurance and quality control aspects of a project. They ensure that all project deliverables meet established standards and regulatory requirements by developing quality management plans, conducting inspections, and coordinating with various teams. Their role is crucial in identifying defects, implementing corrective actions, and maintaining documentation throughout the project lifecycle. By focusing on quality, they help minimize risks, reduce costs, and ensure customer satisfaction.

What are the key skills and qualifications needed to thrive as a project manager quality control?

To thrive as a Project Manager Quality Control, you need expertise in quality assurance methodologies, project management principles, and a relevant degree such as engineering or quality management. Familiarity with tools like Six Sigma, ISO standards, project management software (e.g., MS Project), and quality control systems is typically required, along with certifications like PMP or CQE. Strong leadership, problem-solving, and communication skills help ensure effective team coordination and issue resolution. These competencies are crucial for maintaining project quality, meeting regulatory requirements, and delivering successful outcomes on time and within budget.

How does a project manager quality control typically collaborate with cross-functional teams to ensure project deliverables meet quality standards?

A Project Manager in Quality Control works closely with departments such as engineering, production, and compliance to establish quality requirements for each project phase. They facilitate regular meetings to review progress and address quality concerns, coordinate testing and inspection activities, and ensure all stakeholders are aligned on quality objectives. This collaboration helps identify potential issues early and ensures corrective actions are taken promptly, ultimately maintaining the integrity of the project’s deliverables. Building strong communication channels and fostering a culture of accountability are key aspects of this role.

What is the difference between Project Manager Quality Control vs Construction Supervisor?

AspectProject Manager Quality ControlConstruction Supervisor
CertificationsPMI-PMP, Quality certificationsOSHA, OSHA-related certifications
Work EnvironmentOffice, site inspections, quality auditsConstruction sites, overseeing daily operations
Employer & IndustryConstruction firms, project management companiesConstruction companies, general contractors
Primary FocusEnsuring quality standards and complianceManaging daily construction activities and safety

The main difference is that Project Manager Quality Control focuses on maintaining quality standards and compliance throughout a project, often working closely with inspectors and clients. Construction Supervisors oversee daily construction activities, safety, and workforce management on-site. Both roles are essential in construction projects but serve distinct functions.

What cities in New Jersey are hiring for Project Manager Quality Control jobs?

Cities in New Jersey with the most Project Manager Quality Control job openings:

Project Manager Quality Control jobs near you

Manager, Quality Control Chemistry

Pennington, NJ • On-site

BeiGene, Inc.
Health Care and Social Assistance • 5 - 10K employees
Learn more about BeiGene, Inc.external

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
Manages all Quality Control (QC) Chemistry Laboratory - Capillary Electrophoresis (CE) activities to support GMP manufacturing, testing and release of materials, intermediates, and finished products under FDA/EU regulations, applicable International Regulations, BeOne processes and procedures. Establishes and implements QC Chemistry procedures including but not limited to capillary electrophoresis and supports regulatory compliance inspections. Ensures efficient and effective day-to-day operations of the CE laboratory. This position reports to the Senior Manager QC and is located full-time at the Hopewell, NJ site.
Essential Functions of the Job:
  • Lead the QC Chemistry (CE) laboratory daily workflow.
  • Establish and maintain QC Chemistry (CE) laboratory related quality systems to ensure conformance with regulations and BeOne Global quality standards.
  • Manage QC Chemistry (CE) laboratory routine operations, including but not limited to validation, SOPs, specifications, testing records, personnel training and assessment, scheduling, etc.
  • Ensure QC Chemistry (CE) laboratory compliance with Environmental Health and Safety (EHS) standards.
  • Ensure timely completion of testing (e.g., In-process control, DS release, DP release, and stability testing) to ensure timely generation and reporting of test results in support of manufacturing operations.
  • Review of laboratory test results, ensuring adherence to Good Documentation Practices.
  • Ensure appropriate investigation of OOS events, discrepancies, lab errors, and equipment failures.
  • Implementation of effective corrective actions and preventive actions (CAPAs).
  • Participate in internal and external GMP audits where possible.
  • Ensure that the QC Chemistry (CE) laboratory meets or improves on budget, cost, volume, and efficiency targets (KPIs) in line with business objectives.
  • Expertise in Quality Control (QC) within a Good Manufacturing Practice (GMP) environment, ensuring compliance with industry standards and regulations through hands-on laboratory experience.
  • Working knowledge and experience with capillary electrophoretic analytical methods such as reduced and non-reduced CGE, CZE, and cIEF/icIEF, etc.
  • Knowledgeable with USP/EP and cGMP/EU GMP regulations.
  • Familiar with instrument and equipment validation.
  • Expert knowledge of quality control principles, practices and standards for the biopharmaceutical industry.
  • Impressive, demonstrable track record and skills/experience gained within a similar position(s), at a similar level.
  • Strong leadership/team management skills and experience.
  • Manage, motivate, coach and mentor direct reports.
  • Credible and confident communicator (written and verbal) at all levels.
  • Strong analytical, problem-solving ability, with excellent attention to detail, with the ability to work accurately in a busy and demanding environment.
  • Excellent project management skills.
  • Hands-on approach, with a 'can do' attitude.
  • Ability to prioritize, demonstrating good time management skills.
  • Self-motivated, with the ability to work proactively using own initiative.
  • Committed to learning and development.
  • Interacts with all levels of BeOne employees
  • Undertake any other duties as required

Supervisory Responsibilities:
  • Manage direct reports from QC Chemistry (CE) laboratory
  • 2+ years of managerial experience directly managing people required
  • Leadership experience leading teams, projects, programs or directing the allocation of resources.

Computer Skills:
  • Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).
  • Ability to work on a computer for extended periods of time

Travel:
  • Must be willing to travel approximately 10%

Education Required:
  • Bachelor's Degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline with 5+ years of GMP testing using capillary electrophoresis techniques in an FDA-regulated biotechnology, pharmaceutical company is required.
  • Bachelor's degree in Chemistry, Biology, Molecular Biology, Biotechnology, Biochemistry, or related scientific discipline preferred.
  • Master's degree and 4+ years of relative experience preferred.

Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $110,800.00 - $150,800.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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