Supervisor, PDS Sterile Manufacturing

Location: Ferentino

This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Work Schedule
Standard (Mon-Fri)  Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

At  Thermo Fisher Scientific , you’ll do meaningful work that makes a positive impact on a global scale. Join our team and help bring our Mission to life every day—enabling our customers to make the world healthier, cleaner, and safer. We empower our employees with the resources and opportunities to achieve their career goals while developing innovative solutions to some of the world’s toughest challenges, from protecting the environment to ensuring food safety and supporting the search for cancer treatments.

Position Summary  We are seeking a  PDS Sterile Manufacturing Supervisor  to join our manufacturing operations team. In this role, you will lead and support production teams involved in sterile pharmaceutical manufacturing, ensuring operational excellence, product quality, and full compliance with cGMP standards and FDA regulations.

This position combines strong technical expertise with people leadership. You will coordinate production activities, oversee manufacturing processes, and drive continuous improvement initiatives while fostering a culture of safety, quality, and accountability.

Key Responsibilities    Supervise and coordinate daily sterile manufacturing operations

Ensure compliance with cGMP, FDA, and company quality standards

Monitor production performance and maintain adherence to schedules

Review batch records and ensure accurate documentation

Lead, coach, and develop manufacturing team members

Support investigations, deviations, and corrective actions

Promote a strong culture of safety, quality, and continuous improvement

Collaborate cross-functionally with Quality, Engineering, and other departments

Identify and implement process and operational improvements

Education     Bachelor’s degree in Science, Engineering, Chemistry, Economics, Business or a related STEM field (preferred)

Experience      3+ years  of experience in pharmaceutical or biotechnology manufacturing,

2+ years  of supervisory or leadership experience in a GMP-regulated environment

Preferred Qualifications     Strong knowledge of  cGMP regulations  and  FDA requirements

Experience with  aseptic processing  and  cleanroom operations

Familiarity with  environmental monitoring  and aseptic techniques

Experience with  batch record review  and manufacturing documentation

Knowledge of  Lean, Six Sigma , or other continuous improvement methodologies

Strong project management and organizational skills

Ability to manage multiple priorities in a fast-paced environment

Experience driving operational excellence and quality improvements

Proficiency with Microsoft Office and manufacturing systems

Excellent written and verbal communication skills

Strong interpersonal skills and ability to work cross-functionally

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