Laboratory Supervisor

Overview

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.

Selution, in partnership with Cordis, specializes in the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery disease. Our mission is to revolutionize healthcare by creating next-generation solutions that address unmet and critical medical needs.

The Laboratory Supervisor is responsible for overseeing daily laboratory operations related to formulation, characterization, and testing. This role ensures safe, compliant, and efficient execution of laboratory activities while supervising technical staff, maintaining data integrity, and supporting process development and scale-up efforts.

• Team Management:
  Supervise, train, and mentor laboratory technicians and scientists.
• Team Management:
  Assign work, set priorities, and monitor performance against timelines and quality expectations.
• Team Management:
  Conduct performance reviews and support development plans.
• Team Management:
  Promote a culture of safety, accountability, and continuous improvement.
• Laboratory Operations:
  Supervise day-to-day laboratory activities, including formulation preparation, and control.
• Laboratory Operations:
  Ensure adherence to approved procedures, protocols, and work instructions.
• Laboratory Operations:
  Oversee use and maintenance of laboratory equipment (e.g., mixers, reactors, particle sizers, microscopes, refrigerators, etc.).
• Laboratory Operations:
  Support method development, optimization, and transfer to manufacturing or pilot scale.
• Laboratory Operations:
  Review laboratory data for accuracy, completeness, and compliance.
• Quality, Compliance & Data Integrity:
  Ensure compliance with GMP, ISO 13485, and internal quality system requirements.
• Quality, Compliance & Data Integrity:
  Enforce proper documentation practices, including batch records, lab notebooks, and electronic data systems.
• Quality, Compliance & Data Integrity:
  Participate in investigations, deviations, CAPAs, and change controls related to lab processes.
• Quality, Compliance & Data Integrity:
  Support internal and external audits and regulatory inspections.
• Safety & EHS:
  Ensure compliance with laboratory safety, chemical handling, and waste disposal requirements.
• Safety & EHS:
  Conduct or support safety training and risk assessments.
• Safety & EHS:
  Investigate and report safety incidents or near misses.
• Cross-Functional Collaboration:
  
  Collaborate with R&D, Manufacturing, Quality, Engineering, and Regulatory teams.
• Cross-Functional Collaboration:
  
  Support scale-up activities and technology transfers.
• Cross-Functional Collaboration:
  
  Provide technical input to project teams and leadership.

Required Qualifications:

• Bachelor’s degree in Chemistry, Chemical Engineering, Materials Science, Biomedical Engineering, or related field or the equivalent combination of education and experience.
• 4+ years of laboratory experience.
• Experience working under GMP/GLP or ISO-regulated systems.

Preferred Qualifications:

• 2+ years of supervisory or team-lead experience in a regulated laboratory environment.
• Experience in medical device or pharmaceutical manufacturing.
• ASQ or related analytical chemistry certification.

• Familiarity with analytical tools (e.g., particle size analysis, microscopy, and efficiency testing).
• Understanding process development and scale-up principles.
• Proficient in documentation and electronic data systems.
• Strong people-management and coaching skills.
• Excellent communication and organizational abilities.
• Detail-oriented with strong problem-solving skills.
• Ability to manage multiple priorities in a fast-paced environment.

• On-time completion of laboratory activities and projects
• Right-first-time documentation and data integrity compliance
• Red…