Pharmaceutical Manufacturing Technician

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 final 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 manufacture 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 The 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, breathable air, and/or a filtering face piece, is often required. Must be able to wear appropriate PPE (i.e,. daily uniform, safety glasses, respirator,s 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 Strong computer, scientific, and organizational skills Ability to work independently and as part of a team, self-motivation, adaptability, andapositive attitude Authorization to work in the United States indefinitely without restriction or sponsorship Additional Information Position is full-time, working Monday-Friday 8:00 a.m.-5:00p.movertime as needed May be requested to work on weekends, overtime, and holidays based on business needs. 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

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