Additionalinformation

Additional Information

• Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.m overtime as needed
• May be requested to work on weekends, overtime, and holidays based on business needs.
• Candidates currently living within a commutable distance of Groton, CT are encouraged to apply.
• Excellent full-time benefits, including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• LinkedIn: #LI-EB1
• Authorization to work in the United States indefinitely without restriction or sponsorship

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Companydescription

Company Description

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.

Jobdescription

Job Description

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.

• 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
• Experience with utilizing Operating Instructions to perform manufacturing tasks
• Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required.
• Must be able to wear appropriate PPE (daily uniform, gloves, safety glasses, respirators, and full protective suits)
• Strong computer, scientific, basic math, and organizational skills
• Ability to communicate effectively within a multi-functional manufacturing team