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Remote Regulatory Affairs Intern Jobs in Indiana

Regulatory Affairs Engineer Full time Americas - North America - United States - Indianapolis - Remote/Home Indiana Accelerate the possible by joining a winning Amcor team that's transforming the ...

New

The preferred arrangement is for this role is hybrid remote (3 days on location work / 2 days ... Work with cross-functional partners, including but not limited to R&D, Clinical Affairs, Regulatory ...

Political Affairs Internship

Notre Dame, IN · Remote

$14.75 - $19.50/hr

Political Affairs Internship The role focuses on making poverty a focus of U.S., Canadian and U.K ... This is a part‐time 12‐hours per week, 12‐week, unpaid remote internship. If your ...

$13.75 - $18.25/hr

Political Affairs Internship: The role focuses on making poverty a focus of U.S., Canadian and U.K. foreign policy. This is a part-time 12-hours per week, 12 week, unpaid remote internship. If your ...

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Remote Regulatory Affairs Intern information

What are the key skills and qualifications needed to thrive as a Remote Regulatory Affairs Intern, and why are they important?

To thrive as a Remote Regulatory Affairs Intern, you need a strong understanding of regulatory guidelines, attention to detail, and typically a background in life sciences or a related field. Familiarity with regulatory submission systems, document management tools, and sometimes certifications like RAC (Regulatory Affairs Certification) are beneficial. Excellent written communication, organizational skills, and the ability to work independently are standout soft skills in this role. These competencies are crucial for ensuring compliance, timely submissions, and effective remote collaboration within regulatory teams.

What are the typical responsibilities of a Remote Regulatory Affairs Intern, and how do they contribute to the team?

As a Remote Regulatory Affairs Intern, you will support the regulatory team by assisting with the preparation and review of regulatory documents, maintaining compliance records, and conducting research on relevant regulations and guidelines. You may help track submission deadlines, update databases, and coordinate with cross-functional teams, such as quality assurance and product development, to gather necessary information. Your contributions are essential in ensuring that products meet all regulatory requirements, which helps facilitate timely approvals and market access.

What are Remote Regulatory Affairs Interns?

Remote Regulatory Affairs Interns are students or recent graduates who support regulatory affairs teams from a remote location, usually working online. Their main responsibilities include assisting with the preparation and review of regulatory documents, researching relevant laws and regulations, and helping ensure that products comply with government requirements. These interns gain valuable experience in regulatory processes within industries like pharmaceuticals, medical devices, or biotechnology while working flexibly from home or another remote setting.
What are popular job titles related to Remote Regulatory Affairs Intern jobs in Indiana? For Remote Regulatory Affairs Intern jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Remote Regulatory Affairs Intern jobs? Cities in Indiana with the most Remote Regulatory Affairs Intern job openings:
Regulatory Affairs Engineer

Regulatory Affairs Engineer

Amcor

Indianapolis, IN • Remote

Full-time

Medical, Dental, Vision

This job post has expired today. Applications are no longer accepted.


Job description

Regulatory Affairs Engineer

Full time Americas - North America - United States - Indianapolis - Remote/Home Indiana

Accelerate the possible by joining a winning Amcor team that's transforming the packaging industry and improving lives around the world.

At Amcor, we unpack possibility through our innovative and responsible packaging to provide solutions that benefit our customers, our people and our planet. More than 10,000 consumers worldwide encounter our products every second and rely on us for safe access to food, medicine and other goods. We value their trust by making safety our guiding principle. It's our core value and integral to how we do business.

Beyond this core principle, our shared values and behaviors unite us as we work together to elevate customers, shape lives and protect the future. We champion our customers and help them succeed. We play to win – adapting quickly in an everchanging world – and make smart choices to safeguard our business, our communities and the people we serve for generations to come. And we invest in our world-class team, empowering our colleagues to unpack their potential, because we believe when our people grow, so does our business.

Job Description

Insure that Amcor Flexibles Converter & Distribution (AFCD) products are safe for their intended end uses and fulfill relevant regulatory compliance requirements. The scope is inclusive of product safety and regulatory guidance for raw material selection, product end use(s), reclaim and disposal.

Maintain and manage product safety and regulatory information in an efficient and confidential manner. Support the business by addressing product safety and regulatory needs of AFCD's internal and external customers. Gather product safety information from suppliers regarding raw materials used in products to facilitate timely response to customer inquiries. Provide feedback and information to fulfill customer regulatory needs. Act as a primary interface for product safety and regulatory affairs.

  • Technical
    • Actively participate in the development of strategic programs for Product Safety, and Regulatory Affairs
    • Prepare/coordinate Product Safety documentation as needed such as migration studies, biocompatibility testing etc., supporting internal and external requests
    • Provide specialized product safety and regulatory support as needed including US EPA pesticide renewals or modifications
    • Actively participate in gathering knowledge of new regulations affecting AFCD products
  • Administrative
    • Maintain and manage the regulatory and product safety files, including confidential information
    • Develop and maintain regulatory databases as needed
    • Develop expertise and knowledge regarding specialized testing associated with product safety, food contact compliance statements and other regulatory requirements
    • Maintain and support the REACH compliance for AFCD products
    • Use of ERP and other tools that holds product safety information including Bill-of-Materials, SDS, Product Safety testing, new chemical review of raw materials proposed for use
  • Customer Requests
    • Meet the regulatory needs of AFCD's internal and external customers including: obtaining product safety information from suppliers; preparation of product Safety Data Sheet (SDS), Article Information Sheet (AIS) or Article Exemption letters; preparation of product regulatory compliance letters which address customer's needs and response to product regulatory questionnaires
    • Provide accurate and timely information to internal and external customers.
    • Use of the Sphera Solutions Intelligent Authoring tool to create SDS/AIS and regulatory declarations
    • Database administration and maintenance of new or completed regulatory requests
    • Consolidation and organization of vendor certifications
    • Supplier interaction, requests and follow up
    • Refine processes and procedures, for issuance of product regulatory certifications
    • Conduct research as needed for product compliance requirements
    • Prepare and submit documentation for review to Agencies such as Health Canada and FDA as required for products requiring registration
    • Regulatory interpretation and ability to read and interpret legal text
    • Strategic problem solving and provide input for policy development
    • Development of Regulatory Data Sheet (RDS) and/or Product Stewardship Information (PSI) documents
    • Other projects and activities will be assigned as necessary to ensure product compliance to customer requirements

General Required

  • BS degree or product regulatory experience
  • Ability to multi-task in a fast-paced environment
  • Strong accountability for completion of goals and objectives
  • Knowledge of FDA Code of Federal Regulations (CFR) Title 21, Regulation (EU) 10/2011, Health Canada regulations, REACh
  • Expertise in establishing sound audit and testing practices applicable to regulatory compliance
  • Ability to use custom regulatory tools, standard office based productivity tools (i.e. MS Office) and ERP tools

Language Skills:

  • Demonstrated ability to effectively establish proper priorities and to communicate complex information clearly and concisely and apply knowledge of subject matter related to product safety and regulatory compliance
  • Speaks and writes clearly and persuasively. Responds well to questions. Employs active listening skills. Demonstrates group presentation skills; presents information, ideas, conclusions and abstract concepts effectively with customers, vendors and internal project teams and individuals

Initiative:

  • Ability and accountability to work independently and as part of a team
  • Seeks assistance from other functional experts as needed
  • Proactively seeks and seizes opportunities to improve the company's offerings and overall positioning. Develops and refines strategic plans and action plans to achieve declared objectives. Effectively communicates / sells those plans to others, gathers and incorporates further input where appropriate and then implements action steps efficiently and prudently

Reasoning Abilities:

  • Ability to read, analyze, and interpret common scientific and technical journals, and legal documents
  • Gathers and analyzes information skillfully and efficiently. Prioritizes and identifies causal connections, related issues and actionable alternatives. Applies practical criteria to decision alternatives in order to choose course of action. Considers and articulates implications for implementation

Preferred Experience:

  • ISO 9001, GFSI standards and ISO14000 experience preferred.
  • Prior experience in product safety and/or regulatory compliance role
  • BS degree in a technical field such as Biology, Chemistry, Engineering

Our Expectations

We expect our people to be guided by The Amcor Way and demonstrate our Values every day to enable the business to win. We are winning when:

  • Our people are engaged and developing as part of a high-performing Amcor team
  • Our customers grow and prosper from Amcor's quality, service, and innovation
  • Our investors benefit from Amcor's consistent growth and superior returns
  • The environment is better off because of Amcor's leadership and products

Equal Opportunity Employer/Minorities/Females/Disabled/Veterans/Sexual Orientation/Gender Identity

Amcor is an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law.

If you would like more information about your EEO rights as an applicant under the law, please click on the "Know Your Rights: Workplace Discrimination is Illegal" Poster. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the employment process, please call 224-313-7000 and let us know the nature of your request and your contact information.

E-Verify

We verify the identity and employment authorization of individuals hired for employment in the United States.

Benefits

When you join Amcor, you will have access to a comprehensive benefits and compensation package that includes:

  • Medical, dental and vision plans
  • Flexible time off, starting at 80 hours paid time per year for full-time salaried employees
  • Company-paid holidays starting at 8 days per year and may vary by location