Pharmaceutical Process Operator
1 week ago
Company 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 works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies._**
**_ In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 58,000 staff across a network of more than 1,000 independent companies in over 54 countries and operating more than 900 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing._**
**_ In 2021, Eurofins generated total revenues of EUR € 6.7 billion, and has been among the best performing stocks in Europe over the past 20 years._**
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- Eurofins CDMO Alphora Inc. provides a fully integrated suite of services to support drug substance and drug product development from the IND enabling development stage, through to phase II & III supply, and commercial validation and manufacturing for niche APIs. In addition to a continuing flow of interesting and challenging projects for global pharmaceutical and biotech companies, Eurofins CDMO Alphora Inc. is committed to growing its state-of-the-art organization, with continued investments in its people, modern facilities, equipment, and instrumentation._
**Job Description**:
**Description of Department**:
The Kilo Laboratory/Pilot Plant is responsible for the manufacture of Active Pharmaceutical Ingredients (API) and intermediates up to multi-kilogram quantities in accordance with current Good Manufacturing Practices (cGMP). These products are critical supplies to client programs and clinical efforts for the development of life saving and improvement therapies for various unmet needs.
**Major Responsibilities**:
- Carry out pharmaceutical processing operations using state-of-the-art reactors and supporting process equipment
- Perform cleaning of processing equipment’s and facilities.
- Receive, sample, label and ship chemicals and products.
- Work in accordance with Environmental, Health and Safety Procedures, Standard Operating Procedures, Production Batch Records and Good Manufacturing Practices.
**Qualifications**:
- Minimum of College Diploma or Degree
- 7-10 years of experience in a chemical manufacturing facility preferably in a cGMP environment
- Experience handling chemicals
- Experience working with API or formulation pharmaceutical processing equipment, or related experience in food, cosmetics or specialty chemicals
- Flexibility to adapt to and perform continental shift work
- Knowledge and ability to operate computerized equipment
- Good verbal and written English communication skills
Additional Information
**_ We thank all applicants within commuting distance of Oakville, Ontario for showing an interest in this position. Only those selected for an interview will be contacted._**
**_ NO AGENCIES, CALLS OR EMAILS PLEASE._
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