Pharmaceutical Manufacturing Technician

About the role

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and c.a. 63,000 employees.

This role is a great fit for candidates with strong mechanical aptitude who are looking to translate their hands-on technical skills into a rewarding career in pharmaceutical manufacturing. You'll have opportunities to operate, troubleshoot, and support complex manufacturing equipment while contributing to the production of products that make a meaningful impact on patients' lives.

Candidates currently living within a commutable distance of Groton, CT are encouraged to apply. Candidates must be authorized to work in the United States indefinitely without restriction or sponsorship.

Responsibilities

• Execute documentation associated with manufacturing operations: Paper and Electronic Batch Records, Log Books, Protocols, Change control, QTS, etc.
• Utilize SOPs and Operating Instructions to manufacture drug product in a controlled clean room environment.
• Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate and patient ready products.
• Set up, operation, break down, and cleaning of complex manufacturing equipment, manage and check documentation generated.
• Complete activities associated with cGMP operations in a clean room manufacturing space.
• Generate, manage and report operational performance associated data.
• Identify, own and lead continuous improvement based projects.

Qualifications

• High school diploma, Associate's, or Bachelor degree in the sciences.
• Must hold a valid driver’s license.
• 1-3 years of Pharmaceutical manufacturing experience; may be substituted with experience in a regulated environment such as GMP, ISO, etc.
• Experience with quality systems.
• Experience completing complex manufacturing operational documents.
• Experience utilizing AI to enhance manufacturing operations.