R&D Chemist I (6 Month Contract)
at Deciem
Toronto, ON, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 07 Oct, 2024 | Not Specified | 07 Jul, 2024 | N/A | Documentation Practices,Regulatory Requirements,Research,Gmp | No | No |
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Description:
WHAT ON EARTH IS DECIEM?
Known as “The Abnormal Beauty Company”, DECIEM is the parent company of The Ordinary, NIOD, and other beauty brands & is an industry disruptor with a science first approach to innovation. DECIEM was Co-Founded in 2013 by the late Brandon Truaxe, a visionary who set out to change the beauty industry through authenticity and transparency. He developed DECIEM to be a happy family (of people and beauty brands), rooted in kindness, creativity, diversity, and respect, alongside Co-Founder and CEO, Nicola Kilner.
We are growing rapidly and we’re looking for someone who shares this vision and wants to grow with us!
WHAT WE’RE LOOKING FOR
We are looking for an R&D Chemist I to join our scientific team on a 6-month contract basis. This position will be based out of our Fraser Office in Liberty Village and requires candidates to work in-office, 5-days a week.
SKILLS AND QUALIFICATIONS NEEDED TO GET THE JOB DONE
- Good knowledge and understanding of GLP and GMP, and regulatory requirements applicable to stability of Cosmetics and OTC products
- Candidates must have hands-on experience working in a Lab Environment and willing to stand for long durations of the day
- Ability to troubleshoot and has excellent problem-solving skills
- Good documentation practices
- Relevant education in Science, Research and Development or another relevant field OR equivalent work experience is an asset
Responsibilities:
- Aid in making physical samples/prototypes from initial to final product development stage
- Document and report development cycle of the products
- Aid in researching assigned topics
- Work closely with Research and Development personnel on expected product behaviour throughout development stage and under stability conditions
- Prepare and communicate stability reports according to standards, and regulatory guidelines
- Perform all the necessary testing on sample prototypes and stability samples, including organoleptic properties and other tests such as pH, viscosity, and other necessary tests
- Perform the necessary calibration of weighing scales, viscometer, and pH meter based on written procedures
- Input new ingredients into ingredient database and continually update existing database
- Compile records for analytical studies, Follow and develop new SOPs, Operate and maintain laboratory equipment, Assist R&D Department with lab administration
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
Proficient
1
Toronto, ON, Canada