Current jobs related to Director of Regulatory Affairs - Chicago - Verano


  • North Chicago, Illinois, United States AbbVie Full time

    Job SummaryAbbVie is seeking a highly skilled Regulatory Affairs Director to join our team. As a key member of our Regulatory Affairs department, you will be responsible for ensuring the successful execution of post-approval change objectives for marketed products.Key ResponsibilitiesProject Management: Independently manage, compile, and author CMC sections...


  • Chicago, Illinois, United States Meitheal Pharmaceuticals Inc Full time

    About the RoleMeitheal Pharmaceuticals Inc is seeking a highly experienced Senior Director of Regulatory Affairs, Specialty Pharmaceuticals to lead our regulatory strategy for specialty pharma products. This is a critical role that will play a key part in the growth and transformation of our regulatory team.Key ResponsibilitiesRegulatory Strategy: Provide...


  • Chicago, United States Meitheal Pharmaceuticals Inc Full time

    DescriptionCompany Overview:Established in 2017 and headquartered in Chicago, Meitheal Pharmaceuticals is a dynamic company dedicated to the development and commercialization of generic injectables. With a recent expansion into fertility, biologics, and biosimilars, Meitheal markets over 50 FDA-approved products across various therapeutic areas. Committed to...


  • Chicago, Illinois, United States Adtalem Global Education Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Expert to join our team at Adtalem Global Education. As a key member of our regulatory affairs team, you will be responsible for ensuring compliance with federal, state, and internal regulations.Key ResponsibilitiesRegulatory Compliance: Interpret and apply statutes, regulations, and...


  • Chicago, Illinois, United States Xeris Pharmaceuticals, Inc. Full time

    Job SummaryXeris Pharmaceuticals, Inc. is seeking a highly experienced Senior Director to lead our Regulatory Affairs and Promotion team. As a key member of our organization, you will be responsible for developing and implementing strategies to ensure compliance with regulatory requirements and promoting our products effectively.Key...


  • Chicago, United States Meitheal Pharmaceuticals Inc Full time

    About Us:Founded in 2017 and headquartered in Chicago, Meitheal Pharmaceuticals is a trailblazing company committed to the development and commercialization of generic injectables. Recently, we've expanded into fertility, biologics and biosimilars, now marketing over 50 FDA-approved products across various therapeutic areas. We embody the Irish principle of...


  • Chicago, Illinois, United States Katalyst HealthCares & Life Sciences Full time

    Position Overview:Katalyst HealthCares & Life Sciences Inc. is seeking entry-level professionals for various roles in contract research focused on clinical trials involving pharmaceuticals, biologics, and medical devices.As an E-Verified organization, we welcome candidates on OPT and CPT, and we offer H1B (both CAP and CAP exempt) and Green Card sponsorship...


  • Chicago, Illinois, United States Katalyst HealthCares & Life Sciences Full time

    Position Overview:Katalyst HealthCares & Life Sciences Inc. is seeking motivated entry-level professionals for various roles in contract research related to clinical trials involving pharmaceuticals, biologics, and medical devices.As an E-Verified organization, we welcome candidates on OPT and CPT, and we offer H1B (both CAP and CAP exempt) and Green Card...


  • Chicago, Illinois, United States Katalyst HealthCares & Life Sciences Full time

    Position Overview:Katalyst HealthCares & Life Sciences Inc. is seeking entry-level professionals for various roles in contract research related to clinical trials involving pharmaceuticals, biologics, and medical devices.As an E-Verified organization, we welcome candidates on OPT and CPT, and we offer H1B (both CAP and CAP exempt) and Green Card sponsorship...


  • North Chicago, Illinois, United States Collabera Full time

    Home Search Jobs Job Description Regulatory Affairs Associate Contract: North Chicago, Illinois, US Salary: $30.00 Per Hour Job Code: End Date: Job Description: Key Responsibilities:Assist in the preparation of regulatory submissions for various product categories including Food, FSMP, Enteral Nutrition, and Pharmaceuticals. Demonstrate proficiency in...


  • Chicago, Illinois, United States Northern Trust Full time

    About Northern TrustNorthern Trust is a leading global financial institution with a rich history dating back to 1889. As a Fortune 500 company, we have established ourselves as a trusted partner for individuals, families, and institutions seeking innovative financial services and guidance.Our commitment to service, expertise, and integrity has enabled us to...


  • North Chicago, Illinois, United States AbbVie Full time

    Job SummaryThe Senior Manager, Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) plays a critical role in ensuring the successful delivery of products to patients. This position requires a strategic thinker who can develop and implement effective CMC regulatory strategies, build strong relationships with internal and external partners, and...


  • North Chicago, Illinois, United States Collabera Full time

    Home Search Jobs Job Description Regulatory Affairs Associate Contract Type: Temporary Location: North Chicago, Illinois, US Compensation: $30.00 Per Hour Job Overview: As a Regulatory Affairs Associate, you will play a crucial role in supporting regulatory submissions for various product categories including Food, FSMP, Enteral Nutrition, and...


  • Chicago, Illinois, United States AbbVie Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Manager to join our team at AbbVie. As a key member of our Global Regulatory Strategy team, you will be responsible for developing and implementing regulatory strategies for assigned products or product lines.Key ResponsibilitiesDevelop and implement regulatory strategies for assigned products or...


  • Chicago, Illinois, United States Meitheal Pharmaceuticals Inc Full time

    Job Summary:The Senior Director/Director of Regulatory Affairs, Biopharma, will provide regulatory guidance for (Bio)Pharma product development and tech transfer, especially biosimilars. This role involves preparing and reviewing submissions and working closely with cross-functional teams within the company and across business partners.Key...


  • Chicago, Illinois, United States PSG Global Solutions Full time

    We are seeking a Regulatory Affairs Associate to join our team at PSG Global Solutions, specializing in the Biotechnology and Medical Devices sectors.Position Overview:In this role, you will be responsible for managing the submission of essential applications and overseeing all interactions with regulatory bodies related to the approval process for products...


  • Chicago, Illinois, United States Medexus Pharma, Inc Full time

    Job DescriptionMedexus Pharma, Inc. is a leading specialty pharmaceutical company with a strong North American commercial platform and a growing portfolio of innovative and rare disease treatment solutions.Position OverviewThe Associate General Counsel and Compliance Officer works closely with the General Counsel and the Chief Operating Officer to enhance...


  • North Chicago, Illinois, United States Collabera Full time

    Home Search Jobs Job Description Regulatory Affairs Associate Contract Type: Contract Location: North Chicago, Illinois, US Compensation: $30.00 Per Hour Job Overview: Responsibilities:Assist in the preparation and submission of regulatory documents for various product categories including Food, FSMP, Enteral Nutrition, and Pharmaceuticals. Demonstrate...

  • Corporate Scientific

    4 months ago


    Chicago, United States Mars Full time

    Job Description:Corporate Scientific & Regulatory Affairs Director, Additives & IngredientsAs an Associate of Mars Inc., the Corporate Scientific & Regulatory Affairs Director, Additives & Ingredients leads cross-segment SRA initiatives related to additives, ingredients, and regulated undesirable substances. The role partners closely with the segments,...


  • North Chicago, United States SPECTRAFORCE Full time

    Job Title: Associate Regulatory Affairs Submission ManagementLocation: Lake County AP50, or Florham Park, NJDuration:12 months 7. What are the top 3-5 skills, experience or education required for this position:1. eCTD submission publishing (advertising and promotional 2253 submissions if possible)2. US regulatory FDA guidelines/CFR3. submission/regulatory...

Director of Regulatory Affairs

4 months ago


Chicago, United States Verano Full time

Verano Holdings Corp. (CSE: VRNO) (OTCQX: VRNOF), one of the U.S. cannabis industrys leading companies based on historical revenue, geographic scope, and brand performance, is a vertically integrated, multi-state operator. Veranos active operations span 13 U.S. states, comprised of 14 production facilities with over 1,000,000 square feet of cultivation capacity and 138 dispensaries. Learn more at www.verano.com.

This role, which reports to the companys Executive Vice President of Regulatory Strategy & Government Affairs, focuses on public and regulatory affairs at the state and local level across our national footprint. This position will work cross-functionally with the compliance, legal, corporate communications, investor relations, finance, operations, and marketing departments to understand the companys global public and regulatory affairs goals. Qualified individuals will demonstrate several years of high-level experience in state and local government relations, with a specific background in advocacy, policy formulation, and public strategy in a highly regulated industry.

A demonstrated track record in publicly advocating for legislation and local zoning, leading policy initiatives through trade associations and lobbying efforts, and overseeing public relations for national organizations in a highly regulated industry is required. The ideal candidate must have strong organizational skills, be able to work collaboratively to oversee multiple projects at once and use analytical skills to solve complex problems under rigorous timelines.

Duties and Responsibilities:

Develop, implement, and manage the companys public affairs and outreach strategy to bolster organizational reputation and brand integrity across our national footprint.

Build and maintain relationships with state and local elected officials, regulatory bodies, municipal boards, business leaders, and other community and industry stakeholders in Veranos current and future markets.

Serve as an organizational spokesperson in local public hearings for both current and future markets.

Coordinate with internal company stakeholders and departments to ensure unified messaging and organizational objectives.

Proactively monitor changes to applicable laws, regulations, and ordinances at the state and municipal levels.

Work closely with the government affairs, licensing, and corporate strategy teams to identify and pursue market expansion and other commercial growth opportunities for the company in current and future markets.

Support the companys social equity, inclusion, and diversity efforts and effectively communicate the same to both state and local regulators and community stakeholders.

Qualifications

Bachelors degree required.

Juris Doctorate or masters degree in public policy or related field preferred.

A minimum 5-7 years progressive public and regulatory affairs experience in highly regulated industry preferred.

Specific experience in the cannabis industry is a plus.

Ability and willingness to regularly travel to venues throughout the U.S. required.