Supervisor, PDS Sterile Manufacturing

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7i6rri

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

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7i6rri