Regulatory affairs Jobs in Indianapolis, IN
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Regulatory affairs • indianapolis in
Last updated: 1 day ago
Job Title : Regulatory Specialist.We are seeking a dedicated Regulatory Specialist to join our Scientific Writing group, which supports crop protection.
This role involves drafting high-quality Produ...Show moreLast updated: 6 days ago
Director, Global Regulatory Labeling Strategy.At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients.By focusing...Show moreLast updated: 30+ days ago
A company is looking for a Senior Associate - Regulatory Affairs.Key Responsibilities Coordinate and execute US regulatory submissions in compliance with corporate standards Manage the preparati...Show moreLast updated: 1 day ago
Global Regulatory Affairs Manager.Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and...Show moreLast updated: 30+ days ago
The company’s broad portfolio — including natural flavors, botanical extracts, functional nutrition, cold brew coffee, tea essences, and food protection solutions — enhances taste...Show moreLast updated: 30+ days ago
Regulatory Compliance Project Manager.The candidate must be a self-starter willing to grow with our company.Applicant must be adaptable, and willing to work in a performance and deadline-driven env...Show moreLast updated: 30+ days ago
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.When considering candidates, we look for scientific and business professionals who ...Show moreLast updated: 30+ days ago
The Regulatory Compliance Specialist ensures that all operations within Langham Logistics environment comply with applicable regulatory requirements, industry standards, and client expectations.Thi...Show moreLast updated: 30+ days ago
RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world's first and only adjustable intraocular lens (IOL) that is custom...Show moreLast updated: 20 days ago
Regulatory Specialist-Scientific Writer.The Scientific Writing Team drafts study reports and study summaries to support regulatory submissions for both biotech and crop protection products.Scientif...Show moreLast updated: 6 days ago
Audit Manager- Regulatory Compliance.US-IN-Evansville | US-MN-St Louis Park | US-IL-Chicago | US-IN-Indianapolis.Old National Bank has been serving clients and communities since 1834.With approxima...Show moreLast updated: 22 days ago
Medical Affairs Biostatistician.The role is responsible for statistical activities in support of Medical Affairs, including post approval value evidence generation, secondary publications, post mar...Show moreLast updated: 9 days ago
Responsibilities : The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials.This role ensures adher...Show moreLast updated: 30+ days ago
RxSight® is an ophthalmic medical technology corporation headquartered in Aliso Viejo, California that has commercialized the world’s first and only adjustable intraocular lens (IOL) that...Show moreLast updated: 21 days ago
Associate Director Of Regulatory Intelligence.The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to inter...Show moreLast updated: 12 days ago
A leading global healthcare company is seeking an Associate Vice President, Assistant General Counsel, to join their Regulatory Legal Team based in Indianapolis.
The successful candidate will provid...Show moreLast updated: 9 days ago
The Regulatory Coordinator is responsible for the coordination, preparation, and maintenance of regulatory documentation and compliance for clinical trials.
This role ensures adherence to local, sta...Show moreLast updated: 30+ days ago
Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success.
We translate unique clinical, medical affairs and commercial insights into ...Show moreLast updated: 30+ days ago
External Affairs Specialist & Driver.Begin a fulfilling career with the State of Indiana by joining one of the largest employers in the state, offering a range of opportunities across 60+ agencies....Show moreLast updated: 3 days ago
- Promoted
Regulatory Specialist
ActalentIndianapolis, IN, USFull-time
- Promoted
Director, Global Regulatory Labeling Strategy
Takeda PharmaceuticalsIndianapolis, IN, USFull-time
- Promoted
Senior Associate Regulatory Affairs
VirtualVocationsIndianapolis, Indiana, United StatesFull-time
- Promoted
Senior Manager, Global Regulatory Affairs
Indianapolis StaffingIndianapolis, IN, USFull-time
- Promoted
Regulatory Specialist
Vibrant IngredientsIndianapolis, IN, USFull-time
- Promoted
Regulatory Compliance Project Manager
Commonwealth Engineers, Inc.Indianapolis, IN, USFull-time
- Promoted
Director, Regulatory Affairs
BeiGeneIndianapolis, IN, USFull-time
- Promoted
Regulatory Compliance Specialist
Langham LogisticsIndianapolis, IN, USFull-time
- Promoted
Clinical Affairs Training Specialist
RxSight, Inc.Indianapolis, IN, United StatesFull-time
Regulatory Specialist
Managed StaffingIndianapolis, IN, USFull-time
Audit Manager- Regulatory Compliance
Old National BankIndianapolis, IN, United StatesFull-time
- Promoted
Principal Biostatistician FSP - Medical Affairs
CytelIndianapolis, IN, United StatesFull-time
- Promoted
Regulatory Affairs Coordinator
Katalyst Healthcares & Life SciencesIndianapolis, IN, USFull-time
- Promoted
Clinical Affairs Training Specialist
RXSIGHT INCIndianapolis, IN, USFull-time
Associate Director, Regulatory Intelligence
Otsuka PharmaceuticalIndianapolis, IN, USFull-time
- Promoted
AVP, Regulatory Counsel Americas
Eli LillyIndianapolis, IN, United StatesFull-time
Regulatory Affairs Coordinator
Katalyst HealthCares & Life SciencesIndianapolis, INFull-time
Sr. Medical Writer (Regulatory)
Syneos Health / inVentiv Health Commercial LLCIndianapolis, IN, United StatesFull-time
- Promoted
External Affairs Specialist & Driver
State of IndianaIndianapolis, IN, USFull-time
The average salary range is between $ 83,350 and $ 132,700 year , with the average salary hovering around $ 104,300 year .
- mail carrier (from $ 44,265 to $ 300,000 year)
- owner operator (from $ 78,770 to $ 250,000 year)
- chief medical officer (from $ 193,102 to $ 250,000 year)
- hospitalist (from $ 30,000 to $ 250,000 year)
- subcontractor (from $ 101,250 to $ 241,250 year)
- pediatrician (from $ 80,000 to $ 235,000 year)
- medical director (from $ 75,633 to $ 230,000 year)
- physician (from $ 50,000 to $ 230,000 year)
- crna (from $ 175,000 to $ 230,000 year)
- dentist (from $ 150,000 to $ 225,000 year)
- Boston, MA (from $ 125,771 to $ 200,600 year)
- Cambridge, MA (from $ 113,100 to $ 200,200 year)
- Atlanta, GA (from $ 87,750 to $ 195,950 year)
- San Francisco, CA (from $ 103,208 to $ 195,773 year)
- San Jose, CA (from $ 104,003 to $ 194,780 year)
- San Diego, CA (from $ 104,546 to $ 193,259 year)
- New York, NY (from $ 90,142 to $ 189,903 year)
- Seattle, WA (from $ 95,000 to $ 185,000 year)
- Pittsburgh, PA (from $ 49,920 to $ 177,310 year)
- Houston, TX (from $ 69,257 to $ 170,000 year)
The average salary range is between $ 74,006 and $ 170,765 year , with the average salary hovering around $ 105,135 year .
Regulatory Specialist
ActalentIndianapolis, IN, US6 days ago
Job type
- Full-time
Job descriptionBachelor's Degree in Life Science or related field. Demonstrated experience in scientific writing, preferably within the regulatory or crop protection industry. Strong understanding of Good Laboratory Practice (GLP) standards and regulatory guidelines. Excellent attention to detail and ability to perform quality control reviews on scientific documents and raw data. Proficiency in using Microsoft Office Suite and document management systems. Effective communication and collaboration skills with cross-functional teams and stakeholders. Ability to manage multiple projects simultaneously and meet tight deadlines. BS in Chemistry / Biochemistry preferred, MS acceptable, PhD considered overqualified. Prior experience with scientific writing and GLP experience is highly preferred. Strong attention to detail and capability in writing technical documents while understanding chemistry discipline. Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off / Leave (PTO, Vacation or Sick Leave)
Job Description
Job Description
Job Title : Regulatory Specialist
Job Description
We are seeking a dedicated Regulatory Specialist to join our Scientific Writing group, which supports crop protection. This role involves drafting high-quality Product Chemistry study reports and summaries for regulatory submissions. The position requires strong scientific writing skills, experience in a chemistry or a related science, and an understanding of Good Laboratory Practice (GLP).
Responsibilities
- Draft high-quality Product Chemistry study reports and summaries to support Crop Protection regulatory submissions.
- Perform quality control reviews on draft reports and raw data.
- Assist in developing new report templates, optimizing processes, and assessing stakeholder feedback for continuous improvement.
- Facilitate the finalization of reports and audit responses.
- Communicate effectively with key stakeholders and customers to understand regulatory reporting requirements.
Essential Skills
Additional Skills & Qualifications
Work Environment
The candidate will work a 1st shift (8am-5pm) Monday-Friday, both independently and as part of a team. The work is conducted in an office setting, and the necessary computer and supplies will be provided.
Job Type & Location
This is a Contract position based out of Indianapolis, IN.
Pay and Benefits
The pay range for this position is $28.00 - $32.00 / hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following :
Workplace Type
This is a hybrid position in Indianapolis,IN.
Application Deadline
This position is anticipated to close on Jan 30, 2026.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.