CMC Regulatory Affairs Associate

Akaasa Technologies; Illinois; Hybrid; USD 85,000 - 105,000; Full time

Job summary

Akaasa Technologies in North Chicago, IL is seeking a CMC Regulatory Affairs Associate on a 2-year contract. You will collaborate with technical teams to prepare regulatory filing dossiers and assess regulatory impact of changes.

The role involves document management, GRPT participation, and collaboration with Operations Brand Teams, ensuring alignment with regulatory requirements under management supervision.

Qualifications

• Bachelor's degree in chemistry, biology, pharmacy, engineering or related subject.
• 2-4 years CMC Regulatory experience.

Responsibilities

• Work with technical teams to prepare regulatory filing dossiers.
• Possibly assess changes for regulatory impact.
• Document management system responsibilities.
• Attend GRPT as needed.
• Attend Operations Brand Teams as needed.

Skills

CMC Regulatory experience

Education

Bachelor's degree in chemistry/ biology/ pharmacy/ engineering/ related

Job description

Role: CMC Regulatory Affairs Associate

Location: North Chicago, IL 60064

Duration: 24 Months

Shift: 8 AM to 4 PM

DO NOT SEND RESUME WITHOUT LINKEDIN PROFILE

Location: hybrid

Contract Length: 2 years

What are the top 3-5 skills, experience or education required for this position:

• Bachelors Degree: Chemistry/ Biology/ Pharmacy/ Engineering/ Other Related Subject
• 2-4 years CMC Regulatory experience

Preferred Experience

• US/ EU Post approval variation support
• Change Management Experience
• International Regulatory Strategy for on market products

Job Duties

• Working with technical team to prepare regulatory filing dossiers
• Potentially assessing changes for regulatory impact
• Document management system responsibilities
• Attend GRPT as needed
• Attend Operations Brand Teams as needed

The Senior Associate, RA CMC works with internal and external partners in order to deliver products to patients.

• Prepares CMC regulatory strategies that enable first pass approvals under management supervision. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new market applications and supplements/variations under management supervision. Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations.
• Represents RA CMC on product development and life-cycle management teams.
• Prepares CMC regulatory submissions under management supervision. Prepares regulatory submissions, including new applications and amendments, renewals, annual reports, supplements, and variations under management supervision.
• Analyzes and interprets information, that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions.
• Reviews and revises regulatory submissions to effectively present data and strategy to regulatory agencies under management supervision.
• Responds to global regulatory information requests under management supervision and regularly informs regulatory management of important timely issues.
• Manages products and change control with an understanding of regulations and company policies and procedures under management supervision. Analyzes and approves manufacturing change requests under management supervision.
• May represent CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations brand teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions Stays abreast of regulatory procedures and changes in the regulatory climate. Maintains awareness of legislation and current developments within specific area of business

Required Education:

• Bachelor's degree in pharmacy, biology, chemistry, pharmacology, engineering or related subject

Preferred Education:

• Relevant advanced degree preferred. Certification a plus.

Required Experience:

• 4 years pharmaceutical or industry related experience.
• 1-2 years in quality systems or cross functional project management

Preferred Experience:

• 5 years pharmaceutical experience including 1-2 years in regulatory affairs or 1-2 years in Discovery, R&D, or Manufacturing
• Experience working in a complex and matrix environment
• Strong oral and written communication skills

Experience Level = 3-5 Years