Thermo Fisher
Thermo Fisher

Supervisor, Visual Inspection PFS (CAPO REPARTO)

職種オペレーション
経験リード級
勤務地Ferentino, Italy
勤務オンサイト
雇用正社員
掲載2週間前
応募する

ポジションについて

Visual Inspection PFS Supervisor

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office Job

About the Role

Join our manufacturing team as a Visual Inspection PFS Supervisor, where you'll manage teams in producing pharmaceutical products. You'll maintain operational excellence while ensuring compliance with cGMP standards and FDA regulations. This role combines technical expertise with people leadership to deliver high-quality products that improve healthcare outcomes. You'll coordinate production schedules, oversee manufacturing processes, and support continuous improvement initiatives. Your leadership will be essential in maintaining quality standards, developing team members, and fostering a culture of safety and innovation.

About Thermo Fisher Scientific

As the world leader in serving science, with annual revenue of more than $40 billion, our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Requirements

  • Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in pharmaceutical or biotechnology manufacturing
  • Preferred Fields of Study: Science, Engineering, Chemistry, or related STEM field
  • 2+ years of supervisory/leadership experience in a GMP environment
  • Strong knowledge of cGMP regulations and FDA requirements
  • Expertise in visual inspection process
  • Demonstrated ability to lead and develop teams
  • Experience with batch record review and documentation
  • Strong problem-solving and decision-making capabilities
  • Excellence in written and verbal communication skills
  • Proficiency with Microsoft Office applications and manufacturing systems
  • Ability to work rotating shifts, including nights/weekends as needed
  • Physical ability to stand for extended periods and lift up to 50 pounds
  • Strong project management and organizational skills
  • Experience with continuous improvement methodologies (Lean, Six Sigma)
  • Ability to effectively manage multiple priorities
  • Demonstrated experience in operational excellence and quality improvements
  • Knowledge of aseptic techniques and environmental monitoring
  • Excellent interpersonal skills and ability to work cross-functionally

Equal Opportunity Statement

Thermo Fisher Scientific will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.

必須スキル

Team Leadership

cGMP regulations

FDA requirements

Visual inspection

Batch record review

Problem-Solving

Communication

Project Management

Aseptic techniques

Environmental monitoring

Thermo Fisherについて

Ferentino

本社所在地