API Manufacturing Technician

BASIC MINIMUM QUALIFICATIONS

High School Diploma or GED

4+ years of relative experience

Demonstrated experience in a cGMP manufacturing environment.

Operational knowledge of Production Control Systems

Ability to think critically and demonstrate troubleshooting and problem-solving skills

After the initial training period of approximately 3 months which will be Monda- Friday from 8am-5pm team members move to swing shift, which alternates between 1st shift and 2nd shift:

1st Shift is Mon-Fri, 6:00 am to 2 pm

2nd Shift is Mon – Thurs, 2 pm to 10 pm

May be requested to work on weekends, overtime, and holidays based on business needs.

Candidates currently living within a commutable distance of

Groton, CT

You will be part of a multi-disciplinary team responsible for the Current Good Manufacturing Practices (cGMP) production of non-commercial size clinical batches supporting Active Pharmaceutical Ingredient (API) development. This includes but is not limited to: supporting the manufacturing operations team, reviewing Standard Operating Procedures, executing batch records, and supporting commissioning and qualification of process equipment. Standard work will involve chemical synthesis of API, which includes these operational tasks: solid / liquid charges to vessels, atmospheric / vacuum distillations, liquid-liquid extractions, phase cut, crystallization, filtrations and drying.

ROLE RESPONSIBILITIES

Execute Process Operating Instructions in a cGMP {part of GxP} environment.

Responsible for equipment preparation, operational adjustment, process monitoring, sampling, and equipment cleaning of complex pharmaceutical manufacturing equipment as defined in standard operating procedures.

Perform manual handling tasks, including lifting, carrying and moving objects weighing up to and exceeding 50 pounds on a routine basis throughout the work shift, using proper material‑handling techniques and safety practices.

Handle and segregate manufacturing waste in accordance with approved waste management, environmental, and safety requirements.

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.