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L3Harris Technologies

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Manager, Quality Engineering
Seen active today Posted Jun 18
Camden, NJ, United States Mid Full Time $128.5k-185k/yr

Role highlights

  • Oversee quality team is involved in Engineering design reviews, review engineering drawings for conformance to quality requirements and sig…
  • Verify test requirements and assist Engineering in the development of test procedures and the design of test equipment.

L3HHCM20

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Manager, Quality Engineering
Seen active today Posted Jun 17
Camden, NJ, United States Mid $128.5k-185k/yr

Role highlights

  • Oversee quality team is involved in Engineering design reviews, review engineering drawings for conformance to quality requirements and sig…
  • Verify test requirements and assist Engineering in the development of test procedures and the design of test equipment.

L3Harris Technologies

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Specialist, Quality Engineering (Suppliers)
Seen active today Posted Aug 13
Camden, NJ, United States Mid Full Time $84k-156k/yr

Role highlights

  • The SQE will be an active and significant contributor in the evaluation, development and monitoring of key Suppliers and Subcontractors,…
  • Visit suppliers to review product & process issues and perform investigation, root cause analysis, and corrective actions to drive improvem…

L3HHCM20

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Specialist, Quality Engineering (Suppliers)
Seen active today Posted Aug 12
Camden, NJ, United States Mid $84k-156k/yr

Role highlights

  • The SQE will be an active and significant contributor in the evaluation, development and monitoring of key Suppliers and Subcontractors,…
  • Visit suppliers to review product & process issues and perform investigation, root cause analysis, and corrective actions to drive improvem…

Oatly AB

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SQA Manager (Direct Material & Release), North America
Seen active today Posted Aug 18
Philadelphia, PA, United States Mid Full Time $115k/yr

Role highlights

  • This role manages supplier quality and food safety for direct materials and serves as release authority, ensuring products produced at…

Children’s Hospital of Philadelphia

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GMP Manufacturing Associate
Seen active today Posted Aug 18
Philadelphia, PA, United States Entry Full Time $58.3k-72.9k/yr

Role highlights

  • What you will do Performs tasks per manufacturing records commensurate with training and experience General advanced lab duties Reviews SOP…
  • The position requires good documentation practices, aseptic processing, team work, and an ability to consistently perform delicate tasks ac…

Catalent

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Regional Supervisor, GO, US
Seen active today Posted Aug 18
Philadelphia, PA, United States Mid Full Time

Role highlights

  • This role involves working in a dynamic environment with a focus on operational excellence and compliance.
  • Community engagement and green initiatives.

Hikma Pharmaceuticals PLC

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Specialist, Lab Support
Seen active today Posted Aug 13
Cherry Hill, NJ, United States Entry $48.2k-80.4k/yr

Role highlights

  • Experience: 0-2 years of experience in a QC laboratory, preferably in a GMP-regulated environment (pharma, biotech, or chemicals).
  • Experience with LIMS, ERP, or inventory management systems.

Catalent

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Clinical Production Specialist
Seen active today Posted Aug 13
Philadelphia, PA, United States Entry Full Time

Role highlights

  • In this role, you will oversee the execution, training, and supervision of clinical production staff within a specific clinical packaging…

Charles River Laboratories, Inc.

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Technician I Methods Qualification and Validation
Seen active today Posted Aug 11
Wayne, PA, United States Senior $24.70/hr

Role highlights

  • Perform tasks using aseptic techniques including work within a biological safety cabinet.
  • Job Overview Under direct supervision, responsible for performing daily laboratory activities necessary for analytical and/or bioanalytical…

Catalent

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Clinical Production Specialist
Seen active today Posted Aug 13
Philadelphia, PA, United States Entry Full Time

Role highlights

  • In this role, you will oversee the execution, training, and supervision of clinical production staff within a specific clinical packaging…

Alnylam Pharmaceuticals

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Associate Director, Study Management
Seen active today Posted Aug 7
Philadelphia, PA, United States Senior Full Time $172.6k-233.4k/yr

Role highlights

  • Lead and ensure inspection readiness for the trial/s * Build knowledgeable and skilled team with competencies and capabilities to successfu…
  • Lead or participate in process improvement activities at a trial and department level as needed * Participate in preparation for,…

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CAI

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Validation Engineer
Seen active today Posted Aug 7
Philadelphia, PA, United States Senior Full Time

Role highlights

  • Technical Responsibilities - Develop documentation for CQV activities - Write and execute protocols (field verification) - Develop summary…
  • For mission-critical and regulated industries needing to deliver essential solutions in high-stakes environments, we provide accelerated op…

The Campbell's Company

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Scientist I
Seen active today Posted Aug 6
Camden, NJ, United States Mid Full Time $75.8k-104.2k/yr

Role highlights

  • Who you will work with… This role partners closely with Product Development, Quality, Regulatory, Procurement, Supply Chain, and external s…
  • Experience supporting pilot plant studies and manufacturing commercialization.

Iovance Biotherapeutics

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Analytical Sciences and Technology Specialist I
Seen active yesterday Posted Jul 31
Philadelphia, PA, United States Mid

Role highlights

  • Overview The ASaT Specialist is accountable for the technical development of quality control methods and processes, method and instrument v…
  • Proficient in performing technical writing (e.g., test methods, SOPs, protocols, etc.).

Health Network Laboratories LLC

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Technical Coordinator - Supporting Jefferson Hospital Laboratories
Seen active today Posted Jul 31
Abington, PA, United States Mid Full Time

Role highlights

  • Prepares and revises laboratory procedure manuals and provides technical in-service and orientation of new staff and develops training/comp…
  • Provides technical expertise, continuing education and training to all staff within a designated clinical operations area.

Hikma Pharmaceuticals PLC

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Director, Operations
Seen active today Posted Jul 29
Cherry Hill, NJ, United States Senior

Role highlights

  • Drive process optimization, waste reduction, and continuous improvement initiatives (Lean, Six Sigma).
  • Key Accountabilities: Lead all site operations (manufacturing and maintenance), including compounding, equipment prep, filling, inspection,…

Children’s Hospital of Philadelphia

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Cellular Therapy & Transplant Quality Specialist
Seen active today Posted Jul 24
Philadelphia, PA, United States Mid Full Time $76.1k-97k/yr

Role highlights

  • The Departmental Quality Specialist works to improve quality assurance, workflows, and processes within the Department of Pathology and Lab…
  • Along with quality manager and Education and Development manager, acts as an administrator of the departmental electronic document control…

More roles at Children’s Hospital of Philadelphia

Charles River Laboratories, Inc.

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Technician I Process Evaluation
Seen active 3 days ago Posted Jul 22
Wayne, PA, United States Senior $24.70/hr

Role highlights

  • Job Overview Under direct supervision, responsible for performing daily laboratory tasks as they relate to Process Evaluation Testing Servi…
  • Offering a variety of services such as contamination and impurity testing, protein characterization, bioassays, viral clearance studies and…

More roles at Charles River Laboratories, Inc.

BAYADA Home Health Care

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Associate Director, Quality Assurance-Hospice
Seen active today Posted Jul 17
Pennsauken, NJ, United States Senior Full Time $110k-114k/yr

Role highlights

  • Develop, create and execute an annual QA plan by specialty practice including identification and testing of key requirements based on…
  • Ensure objectivity & appropriate competence/skill of QA staff.

More roles at BAYADA Home Health Care

IPS-Integrated Project Services

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CQV Engineer, General Application
Seen active today Posted Jul 7
Cherry Hill, NJ, United States Mid Full Time

Role highlights

  • Primary responsibilities include C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medi…

Clarkston Consulting

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Quality Systems (Veeva) Senior Consultant
Seen active today Posted Jul 3
Philadelphia, PA, United States Senior Full Time

Role highlights

  • Come join us as a Quality Systems (Veeva) Senior Consultant, and in this role, you will deliver creative business solutions…
  • What You’ll Do As a Quality Systems (Veeva) Senior Consultant at Clarkston, you will: Participate in projects at life sciences…

LAPORTE L.C.C.

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Process & Validation Project Manager
Seen active yesterday Posted Jul 1
Philadelphia, PA, United States Mid

Role highlights

  • The Process & Validation Project Manager is responsible for leading the coordination of projects of various systems across the pharmaceutic…
  • Process & Validation Project Manager (a minimum of 5 years of experience required) Location: Philadelphia, PA Employment Type: Full-time, m…

Cytokinetics, Inc.

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Director, REMS Strategy & Operations
Seen active today Posted Jun 17
Radnor, PA, United States Senior Full Time $220.5k-257.2k/yr

Role highlights

  • This role provides strategic leadership across REMS and REMS-adjacent patient services, ensuring alignment of regulatory requirements with…
  • Align patient services initiatives with REMS requirements, organizational goals, compliance standards, and market access strategies.

West Pharmaceutical Services

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Medical Affairs Specialist
Seen active 3 days ago Posted Apr 9
Radnor, PA, United States Mid

Role highlights

  • Essential Duties and Responsibilities Act as the primary liaison between clinical experts and cross functional teams (quality, operations,…
  • Must have excellent project management skills and excellent written and verbal communication skills Prior supervisory experience preferred…
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