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Ophthalmic technician • windsor on
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Huron Automotive ServicesWindsor, Windsor, Canada- Calgary, AB (from $ 50,751 to $ 87,263 year)
- Saskatoon, SK (from $ 34,613 to $ 80,087 year)
- London, ON (from $ 51,600 to $ 73,986 year)
- East York, ON (from $ 32,175 to $ 73,471 year)
- North York, ON (from $ 33,150 to $ 69,502 year)
- Coquitlam, BC (from $ 35,588 to $ 63,746 year)
- Victoria, BC (from $ 54,127 to $ 61,487 year)
- Toronto, ON (from $ 50,104 to $ 61,230 year)
- Old toronto, ON (from $ 50,880 to $ 61,230 year)
- Vancouver, BC (from $ 46,313 to $ 59,297 year)
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Senior Manager Regulatory Affairs
AdvagenpharmaWindsor, Windsor, Canada- Full-time
1 week ago Be among the first 25 applicants
Direct message the job poster from AdvaGen Pharma
Human Resources & Talent Acquisition at Rubicon Research I AdvaGen Pharma I Validus Pharma
About Our Parent Company Rubicon Research
Rubicon Research is an IP led, specialty pharmaceutical company focused on a mission to provide
innovative yet affordable patient-centered products and solutions to address unmet needs around the world. We leverage our proprietary technologies and specialized formulation development skills to provide solutions to complex delivery challenges, enabling better patient outcomes.
- Our portfolio spans multiple dosage forms, including oral solids, oral liquids, nasal, ophthalmic, injectable, topical, drug device combinations and fixed-dose combinations.
- We hold more than 50 issued patents in drug delivery technologies, and have launched over 200 SKUs, with over 2 billion extended units sold in the US last year alone.
- In the pipeline are 30 approvals and launches (across oral solids, liquids, nasal sprays and ophthalmic formulations).
For more information visit www.rubicon.co.in
Incorporated in 2017 and operationalized in 2020, AdvaGen Pharma is an integrated specialty
pharmaceutical company, focused on providing innovative solutions for patients, customers, and partners
by developing, manufacturing, and marketing high quality prescription branded and generic
pharmaceutical products.
Job Description
Purpose This position will be responsible for regulatory communications for filings in US, managing meetings with USFDA, preparing regulatory strategies for global regulatory filings, regulatory assessments of MLR assets and filings, REMS activities and coordination, regulatory submissions for specialty / 505b2 projects and co-ordination with global regulatory teams.
Position / Job Title : Manager / Sr. Manager
Department : Regulatory Affairs
Reporting To : Director – Regulatory & IP
Location : New Jersey
Years of Experience : 10-15 years
Qualifications & Pre-Requisites
Seniority level
Seniority level
Mid-Senior level
Employment type
Employment type
Full-time
Job function
Job function
Other
Pharmaceutical Manufacturing
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Inferred from the description for this job
Medical insurance
Vision insurance
401(k)
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