Pharmaceutical Manufacturing Technician

Eurofins USA; Groton (CT); On-site; USD 40,000 - 70,000; Full time

Job summary

Join a dynamic and innovative life sciences company that prioritizes safety and sustainability. This role involves executing and managing documentation for complex manufacturing processes, operating equipment, and ensuring compliance with safety protocols. You will be part of a dedicated team, contributing to the production of essential products that impact health and safety globally. With a commitment to employee well-being, the company offers excellent benefits, including comprehensive medical coverage and a supportive work environment. If you are motivated, adaptable, and ready to make a difference, this opportunity is perfect for you.

Benefits

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Qualifications

• High school diploma required; pharmaceutical manufacturing experience is a plus.
• Strong communication, organizational skills, and attention to detail are essential.

Responsibilities

• Complete complex bulk product manufacturing activities and manage documentation.
• Set up and operate manufacturing equipment in a classified space.

Skills

Pharmaceutical manufacturing experience

Strong computer skills

Excellent communication skills

Attention to detail

Ability to perform heavy lifting

Self-motivation

Adaptability

Teamwork

Education

High school diploma

Job description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.

Job Description

• Generate, assist and execute documentation associated with manufacture, Batch Documents, Log Books, Labels, check sheets, protocols, Change control, QTS etc.
• Complete complex bulk product manufacturing activities to convert incoming raw materials into intermediate product.
• Complete complex processing of intermediate bulk to convert this to a final patient ready presentation.
• Set up complex manufacturing equipment, manage and check documentation generated.
• Complete activities associated with the operation and maintenance of a classified manufacturing space.
• Complete activities identified as operator care tasks associated with the maintenance and operation of complex manufacturing equipment.
• Generate, manage and report operational performance associated data.
• Identify, own and lead continuous improvement based projects.

Qualifications

• High school diploma.
• Must hold a valid driver’s license.
• Pharmaceutical manufacturing experience is a plus.
• Role requires a Groton site presence. The job requires the operation of manufacturing equipment in the Groton manufacturing area. Standing, bending, climbing, reaching, and lifting upward of 55 pounds may be required. Personal Protective Equipment such as gloves, a full Tyvek suit and breathable air and/or filtering face piece is often required.
• Must be able to wear appropriate PPE (i.e. daily uniform, safety glasses, respirators and full protective suits) when necessary.
• Strong computer, scientific, and organizational skills.
• Excellent communication (oral and written) and attention to detail.
• Ability to perform heavy lifting (up to 55lbs).
• Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies.
• Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude.
• Authorization to work in the United States indefinitely without restriction or sponsorship.

Additional Information

Position is Monday-Friday 8:00 am- 5:00 pm. Overtime as needed. 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.
• #LI-EB1

Eurofins USA PSS Insourcing Solutions is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.