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Cerapedics

Peptide-enhanced bone grafts for orthopedics

Operations Engineer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeWestminster, CO, USAIn-person

About the Job

Requirements

  • Communicate succinctly, clearly, and accurately in verbal and written communications, and create engineering reports detailing change qualifications.
  • Develop technical expertise in new therapeutic areas.
  • Demonstrate strong analytical and problem-solving skills.
  • Work effectively in a cross-functional environment.
  • Be self-motivated and assertive, and approach work with a positive attitude.
  • Cultivate and maintain relationships with thought leaders, establishing trust through scientific expertise and follow-through on requests.
  • Have knowledge of FDA and ISO guidelines for medical devices or pharmaceuticals.
  • Hold a bachelor's degree in an engineering or scientific discipline, or have an equivalent combination of education and work experience.
  • Have 3–5 years of experience with progressively increasing responsibility or complexity.
  • Have at least 2 years of experience in the medical device, biomedical, or pharmaceutical industries.

Responsibilities

  • Ensure changes to raw materials, regulations, equipment, and processes meet applicable FDA, BSI, quality-system, and internal-procedure requirements.
  • Monitor external changes to standards and regulations and ensure products remain compliant.
  • Support the Engineering Change Control Process and assess changes with key stakeholders; improve processes to ensure continuity of supply.
  • Participate in managing engineering change controls and reviews, and assess the impact of proposed solutions on operational processes and procedures.
  • Communicate project status, risk analyses, and mitigation plans, answer detailed questions, and prepare concise project summaries for leadership and management.
  • Evaluate changes and execute appropriate qualification activities, ensuring required documentation is completed in accordance with the quality system.

Desired Qualifications

  • Experience with orthopedics or spinal medical devices is highly desirable.
  • An advanced degree or MBA is preferred.

About the Company

Cerapedics

Peptide-enhanced bone grafts for orthopedics

Cerapedics develops and commercializes peptide-enhanced bone grafts for orthopedic and spine procedures. Its flagship product, i-FACTOR Peptide Enhanced Bone Graft, combines a small P-15 peptide attached to anorganic bone mineral (ABM) to mimic the way autograft bone heals, promoting safe and predictable bone formation. The company differentiates itself by offering a biologically guided graft that relies on clinical data to support safety and efficacy, reducing the need for autograft harvest. Cerapedics aims to improve patient outcomes by providing clinicians with evidence-based graft solutions that enhance bone healing and fusion in bone grafting procedures.

Company size
51-200
Company stage
Late Stage VC
Total funding
$150.9M
Headquarters
Westminster, CO
Founded
2000

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