Toronto On Regulatory affairs associate Jobs – 14 Openings This Week

Regulatory Affairs Associate — Canada
Ryvis Pharma —Mississauga, ON
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quality Assurance and Regulatory Affairs Associate - Entry Level
BTNX Inc. —Markham, ON
- $40,000–$45,000 a year
- Full-time
- Master's degree
- Bachelor's
- Quick service & fast food restaurant
- Disability insurance
- Dental care
Quality Assurance Associate
Apollo Health And Beauty Care —Toronto, ON
- $52,000–$60,000 a year
- Full-time
- Engineering
- Data analysis skills
- Bachelor's
- Dental care
Quick apply
7d
Manufacturing Quality Assurance Associate - AM Shift Contract
DECIEM —Etobicoke, ON
- $45,000–$50,000 a year
- Contract
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Paid time off
- Employee assistance program
Senior Specialist, Quality Assurance
Shoppers Drug Mart / Pharmaprix —Toronto, ON
- $68,000–$93,500 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Manufacturing Quality Assurance Associate - Afternoon
DECIEM —Etobicoke, ON
- $45,000–$50,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Paid time off
- Employee assistance program
Manager, Quality Assurance
Shoppers Drug Mart / Pharmaprix —Toronto, ON
- $80,000–$110,000 a year
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
8d
Quality Assurance Manager
Primo Brands —Mississauga, ON
- $107,417–$128,511 a year
- Full-time
- Bilingual
- English
- Master's degree
- Employee stock purchase plan
- Designated paid holidays
Senior Director, Liquidity Products and Accounts Services
CIBC —Toronto, ON
- Full-time
- Analysis skills
- Presentation skills
- In-person
4d

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Quality Assurance and Regulatory Affairs Associate - Entry Level
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Bachelor’s or master’s degree or equivalent in Regulatory Affairs, Medical Science, Life Science or another relevant field. Recognized Degree in Relevant Field.
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Regulatory Affairs Associate — Canada

Ryvis Pharma
Mississauga, ON

Apply Now

Job details

Full-time

Qualifications

Microsoft Powerpoint
Microsoft Word
Computer operation
Microsoft Excel
Microsoft Access
Sales
Filing
Bachelor's
QA/QC
Pharmacy
Chemistry
Manufacturing
Communication skills
Adobe Acrobat
Marketing

Full job description

The Regulatory Affairs Associate is responsible for planning, coordinating, compiling, submitting, obtaining approval, maintaining drug product registrations for Canada and the U.S. and assisting global drug product registrations.

Type:

12-month Contract with an opportunity to convert to full-time based on performance.

Location:

Mississauga, Ontario, Canada

Key Responsibilities:

Your responsibilities encompass a wide range of tasks, all aimed at ensuring the smooth flow of regulatory processes and the successful approval of drug products. Let’s dive into your key areas of focus:

Plan, coordinate, compile and file drug product submissions for Canada and the U.S. for a variety of dosage forms in eCTD format (e.g. DINs, ANDS, NDS, ANDA, NDAs, S/NDSs, CTAs, NCs, provincial formulary submissions etc.) for the successful registration of drug product for domestic and international markets, with limited supervision.
Review and approve various product labelling components and marketing materials.
Prepare submissions in eCTD format, which involves a complete understanding of the use of Adobe Acrobat to create bookmarks and links.
Prepare written responses to deficiency letters from regulatory agencies in the stated time frame.
Plan, coordinate, compile and file post-approval submissions for FDA (CBE supplement, PAS) and TPD (Notifiable Change, Supplement).
Review Change Controls and determine filing requirements.
Liaise with Health Canada and Provincial Formularies on all aspects of the drug submission, follow up for review status and project updates.
Work on more complex projects which involve identifying and resolving issues on time.
In consultation with the Manager, provide regulatory guidance and expertise to Sales & Marketing, QC/QA, and Operations departments of Ryvis Pharma.
Assist in preparing and compiling FDA and TPD pre-approval and GMP inspections.
Maintain current awareness of regulatory guidelines (Health Canada, FDA, ICH, European Medicines Agency – EMeA, Therapeutic Goods Administration –TGA Australia, etc.).
Other duties as required by the Manager.

Knowledge, Skills and Abilities:

Thorough understanding of regulations and guidance published by Health Canada.
GMP & DEL requirements in Canada.
Understanding of Pharmaceutical development and manufacturing processes; analytical, labelling clinical and non-clinical knowledge.
Regulatory submission formats and filing categories.
Expertise in chemistry and manufacturing, labelling and format requirements for drug product registration for Therapeutic Products Directorate (CTA, ANDS, S/ANDS, NDS, DIN) and US FDA (ANDA, NDA, DMF, IND).
Knowledge of the use of eCTD Software for preparing and filing submissions is preferred.
Knowledge of GMP requirements and QA/QC procedures.
Excellent interpersonal, written and verbal communication skills.
Proven ability to anticipate challenges and negotiate through them to achieve the desired outcome
Ability to plan, coordinate and work effectively in a team-oriented environment.
Superior computer software skills (Microsoft Word, Excel, Access, PowerPoint, Adobe Acrobat, Document Management Systems).
Strong organizational ability, management of multiple priorities, and proven ability to meet strict and established timelines.
Multi-tasking various tasks and adhering to strict timelines.

Background and Experience:

Minimum B. Sc. in a Chemistry, Pharmacy or Life Science discipline combined with at least five (5) to seven (7) years of hands-on Regulatory Affairs experience in filing and managing Canadian and USA submissions, including electronic submissions in eCTD formats.

Problem-Solving:

Good problem-solving abilities are required to prepare written responses to deficiency letters from regulatory agencies and obtain approval of changes to approved drug products.

Working Conditions:

Multidisciplinary office.
Extensive use of computer.
Varied work schedule to meet deadlines, as required.

Schedule:

Regular 5 days per week; 7.5 hours per day

What We Offer:

Competitive wages
Bonus program
Dynamic, close-knit team environment
Company Events
Casual dress
On-site parking

This position is open to applicants legally authorized to work in Canada.

We thank all applicants, but only those selected for an interview will be contacted. No phone calls, please.

Ryvis Pharma is an equal-opportunity employer. We welcome applications from women, aboriginal people, people with disabilities and members of visible minorities. Accommodations in relation to the job selection process are available upon request.

NOTE:

All employment is conditional upon completing and obtaining a satisfactory background check which may include educational, employment, references and criminal records (for which a pardon has not been granted) checks.

AGENCY NOTICE:

Ryvis Pharma does not accept unsolicited resumes from recruiters or employment agencies. Without a signed Services Agreement with an agency/recruiter, Ryvis Pharma will not consider any referrals or agree to payment of referral or recruitment fees. In the event a recruiter or an agency submits a resume or candidate without a previously signed agreement, Ryvis Pharma explicitly reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.

Apply Now

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regulatory affairs associate jobs in toronto on

Regulatory Affairs Associate — Canada

Quality Assurance and Regulatory Affairs Associate - Entry Level

Quality Assurance Associate

Manufacturing Quality Assurance Associate - AM Shift Contract

Senior Specialist, Quality Assurance

Manufacturing Quality Assurance Associate - Afternoon

Manager, Quality Assurance

Quality Assurance Manager

Senior Director, Liquidity Products and Accounts Services