Formulation Chemist - Mississauga, Canada - Eurofins Canada BioPharma

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Description
Company Description
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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 1000 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.

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_ 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. develops and manufactures new therapeutics to improve the lives and health of patients. Eurofins CDMO Alphora provides contract research & development services to global pharmaceutical and biotech companies, developing their processes and manufacturing their bulk drug substances (Active Pharmaceutical Ingredients "API's") as well as finished dosage products (tablets, capsules, suspensions) for supply to clinical trials and commercial requirements. Eurofins CDMO Alphora provides a rich and technologically challenging environment with a continuing flow of interesting projects. Our employees work in close concert with clients throughout the development process to achieve their program objectives. Eurofins CDMO Alphora Inc. is growing its stateoftheart organization, with continued investments in modern facilities, equipment, and instrumentation while providing a rich environment for employees to develop their technical skills and careers paths._

Job Description:

The Formulation Chemist is responsible for conducting formulation development activities within Drug Product Operations. Responsibilities include formulation and process development, scale up and transfer from bench to the GMP production scale. The Formulation Chemist will be well versed on oral dosage technologies and process equipment. The responsibilities also include the execution of operations within GMP production.


DUTIES AND RESPONSIBILITIES:


  • Draft protocols and production batch records.
  • Design and execute formulation development studies within an R&D environment
  • Conduct process development and scale up to GMP.
  • Execute GMP production and provide support as required
  • Participate in project updates for client's technical calls.
  • Identify and troubleshoot process challenges during GMP batch execution and propose strategies for formulation and process improvements.
  • Write SOPs, approve formulation related activities in SOLABS and supervise/review recipe creation and other assigned activities in ERP to ensure timely support for projects.
  • Ensure that all work is performed in compliance with the applicable SOPs, EHSP's, cGMPs and GLPs.
  • Adhere to the policies and guidelines set out in the Eurofins Alphora Employee Handbook.
  • Work harmoniously with all fellow employees.
  • Perform other related duties as required.

COMMUNICATION AND CONTACTS:


Within the Company

  • Interact with all staff throughout the company as necessary to implement the business objectives.

Outside of the Company

  • Interact with equipment vendors and material suppliers to support the business objectives.

Qualifications:


  • B.Sc. or M.Sc. in Engineering/Chemistry with >5 years' experience or Ph.
D in Chemistry with >2-3 years' experience in the pharmaceutical-related industry

  • Must have a strong knowledge of drug product development, GMP's and handson experience with oral dosage process equipment and related technologies
  • Must be highly motivated and have a proven record of success in multiple projects
  • Must be well organized and able to meet project timeline commitments
  • Must work well in a multidisciplinary team environment and have excellent written and verbal communication skills.
Additional Information

  • The above information on this description has been designed to indicate the gen

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