Medical Writer jobs
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- Full-time +1
- Dental care
- Company pension
- Minimum 3 - 5 years of hands-on regulatory affairs experience inpharmaceuticals, biologics, or medical devices.
- Other duties as required by the Head.
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Senior Regulatory Affairs Associate
Easily applyUrgently hiringNutrasourceGuelph, ON- $75,000–$100,000 a year
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Easily applyNewConfidentielSaint-leonard, QC- $28 an hour
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Senior Copywriter
Easily applySaje Natural WellnessToronto, ON M5G 2H6- $85,000–$95,000 a year
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- Paid sick leave
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- We look for individuals who have drive and warmth, agility and passion, and keep customer experience at the centre of everything they do.
- View all Saje Natural Wellness jobs - Toronto jobs
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Senior Copywriter
Easily applySaje Natural WellnessToronto, ON M5G 2H6- $85,000–$95,000 a year
- Paid time off
- Vision care
- Dental care
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- Employee assistance program
- Flexible schedule
- We look for individuals who have drive and warmth, agility and passion, and keep customer experience at the centre of everything they do.
- View all Saje Natural Wellness jobs - Toronto jobs
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Job Post Details
Senior Regulatory Affairs Associate - job post
Job details
Pay
- $70,000–$80,000 a year
Job type
- Permanent
- Full-time
Location
Benefits
Pulled from the full job description
- Dental care
- Company pension
Full job description
BLES Biochemicals Inc. is a privately-owned, proudly Canadian pharmaceutical and medical device manufacturer and distributor. Our pharmaceutical product, BLES®, is a life-saving pulmonary surfactant used to treat premature infants who have respiratory distress syndrome. BLES® was discovered at Western University and continues to be manufactured in London, Ontario. In 2015, BLES® was ranked as one of the top five discoveries at an Ontario university, alongside insulin. Our product is the market-leading surfactant in Canada and several other countries, and it treats tens of thousands of patients annually.
The team at BLES Biochemicals works hard to manufacture exceptional products; the welfare and happiness of patients and their families are our top priorities. Our vision is to live in a world where every premature baby has access to life-saving pulmonary surfactant therapy. There is still a long way to go, and we hope that you’ll join us on this journey.
Job Responsibilities:
- Prepare, compile, file and monitor biologic drug product and medical device submissions for international markets with limited supervision.
- Assist in the preparation of submissions for Health Canada in the eCTD format, including Notifiable Changes, annual reports, and renewals.
- Track domestic and international health regulatory sources (Health Canada, ICH and other relevant international sources) for emerging regulatory guidelines for both drug products and medical devices.
- Evaluate the impact of proposed quality and manufacturing changes, as well as the impact of new or revised regulations and guidelines on registered products globally.
- Assist in the review of marketing and promotional materials.
- Maintain all regulatory electronic files at BLES Biochemicals.
- Other duties as required by the Head.
Qualifications:
- University degree in Life Sciences (biology, chemistry, pharmacology or related field)
- Post-graduate Certification in Regulatory Affairs
- Minimum 3 - 5 years of hands-on regulatory affairs experience inpharmaceuticals, biologics, or medical devices
Pay: $70,000.00-$80,000.00 per year
Benefits:
- Company pension
- Dental care
Work Location: Hybrid remote in London, ON N5V 3K4