Theranostics Quality Assurance Specialist jobs in United States
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PharmaLogic · 2 hours ago

Theranostics Quality Assurance Specialist

PharmaLogic is at the forefront of precision medicine and is seeking a Theranostics Quality Assurance Specialist. This role is responsible for Quality Assurance support for manufacturing operations, ensuring compliance with current Good Manufacturing Practices (cGMP) and driving continuous product quality improvement.

Pharmaceuticals

Responsibilities

Provide quality oversight for all sterile manufacturing operations, including aseptic processing, terminally sterilized processes, and related support areas
Manage the QA program to provide coverage and decision-making support across a variable radiopharmaceutical manufacturing schedule, including off-shift and potential weekend operations as needed
Ensure the integrity of sterile product manufacturing through robust sterility assurance practices
Manage QA review and approval of cGMP documentation, including procedures, protocols, deviations, out of specifications, CAPAs and change controls
Collaborate with cross-functional departments (Manufacturing, QC, Engineering, Safety, Regulatory, etc.) to resolve quality-related issues and support new products and product lifecycle management
Promote a proactive quality culture focused on patient safety, product quality, and regulatory compliance
Perform other job-related duties as assigned

Qualification

GMP manufacturing knowledgeFDA regulations experienceQuality systems managementRadiopharmacy manufacturingAnalytical methods expertiseCommunicationProject management skillsCritical thinkingProblem-solving skillsContinuous learning

Required

3-5 years of radiopharmacy manufacturing or equivalent experience
Excellent communication and collaboration skills with all stakeholders, including Quality, PET Manufacturing, and Pharmacy
Ability to work varying shifts both independently and as part of a team and be reachable at all hours
Strong knowledge of a GMP manufacturing environment and working with FDA and FDA cGMP regulations
Experience with quality systems, deviation/investigation management, change control, and CAPA
Ability to analyze complex problems, identify root causes, and drive corrective actions
Excellent project management, critical thinking, and problem-solving skills required to manage competing projects, timelines, and deliverables
A passion for continuous learning and curiosity to find innovative ways to improve our ways of working
Required are a mechanical aptitude, manual dexterity for manipulating small items; ability to lift between 16 and 50 lbs., and to handle frequent crawling, stooping, crouching, and kneeling

Preferred

Bachelor's degree in a scientific discipline
Knowledge of molecular imaging techniques and pharmaceutical study design and execution
Experience with laboratory procedures, radiochemistry techniques, analytical methods, equipment (HPLC, GC, TLC, and radiometric measures), radiochemistry synthesis, US FDA cGMP, Radiation Safety Principles, Isotopes production, and analytical equipment troubleshooting

Benefits

401(k) retirement benefit program
Medical
Dental care
Disability insurance
Employee assistance program
Life insurance
On-site parking
Paid time off
Vision care

Company

PharmaLogic

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PharmaLogic is a leading global contract development and manufacturing organization (CDMO) specialized in diagnostic and therapeutic radiopharmaceuticals.

Funding

Current Stage
Late Stage

Leadership Team

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Keith Kennedy
Chief Financial Officer
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Deborah Vanerka
Chief Revenue Officer (CRO)
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Company data provided by crunchbase