ZipRecruiter

Log In

2

Entry Level Biotech Product Manager Jobs in Delaware

AllSTEM Connections

Lab Tech - I (Associate)

Millsboro, DE · On-site

$41K - $46K/yr

... biotechnology products in a regulated manufacturing environment. Team members work with a Safety ... Handle, label, and manage hazardous waste when appropriately trained. * Support non-aseptic ...

Prism Biotech

Sales Rep - BioPharma

Dover, DE · On-site

$85K - $116K/yr

Pharmaceutical Sales Representative (Specialty to entry level both available) Pharmaceutical Sales ... Reporting to a District Sales Manager, the Pharmaceutical Sales Rep role will be responsible for ...

Prism Biotech, Inc

Sales Rep - BioPharma

Dover, DE · On-site

$85K - $116K/yr

Pharmaceutical Sales Representative (Specialty to entry level both available) Pharmaceutical Sales ... Reporting to a District Sales Manager, the Pharmaceutical Sales Rep role will be responsible for ...

CROSSMARK1

PRODUCT / EVENT DEMONSTRATOR

Dover, DE · On-site

... directed by management. Qualifications Friendly, respectful, willing and able to take direction ... Company-provided training (Ideal for entry-level or those looking to obtain new skills.

CROSSMARK1

Product/Event Demonstrator

Dover, DE · On-site

... directed by management. Qualifications Friendly, respectful, willing and able to take direction ... Company-provided training (Ideal for entry-level or those looking to obtain new skills.

CROSSMARK1

Product Event Demonstrator

Selbyville, DE · On-site

... management. CROSSMARK is looking for associates to complete in-store food and product ... Company-provided training (Ideal for entry-level or those looking to obtain new skills.) *Crossmark ...

next page

Showing results 1-20

All JobsBiotech Product JobsEntry Level Biotech Product Manager JobsEntry Level Biotech Product Manager Jobs in Delaware

Entry Level Biotech Product Manager information

What are some typical challenges faced by entry level biotech product managers in their first year?

Entry level biotech product managers often face the challenge of quickly mastering complex scientific concepts while also learning the nuances of product development cycles. Navigating cross-functional collaboration between research, regulatory, and marketing teams can be demanding, especially when balancing technical accuracy with business objectives. Additionally, adapting to fast-paced changes in priorities and ensuring effective communication between departments are key hurdles. Overcoming these challenges usually leads to valuable experience and career growth within the company.

What is the difference between Entry Level Biotech Product Manager vs Associate Biotech Product Manager?

AspectEntry Level Biotech Product ManagerAssociate Biotech Product Manager
Required CredentialsBachelor's degree in life sciences, business, or related field; some roles may prefer internships or related experienceBachelor's degree, often with some industry experience or internship background
Work EnvironmentCross-functional teams, product development, marketing, and R&D departments within biotech companiesSimilar environment, supporting product lifecycle activities under supervision
Employer & Industry UsageBiotech firms, pharmaceutical companies, healthcare startupsBiotech and pharmaceutical sectors, often as entry-level support roles

The main difference is that Entry Level Biotech Product Managers typically have less industry experience and may focus more on learning product processes, while Associate Biotech Product Managers support product teams with more defined responsibilities. Both roles serve as entry points into biotech product management, with the associate role often acting as a stepping stone to a full product manager position.

What does an entry level biotech product manager do?

An Entry Level Biotech Product Manager helps coordinate the development, launch, and marketing of biotechnology products. They work closely with cross-functional teams such as research and development, marketing, and sales to ensure products meet customer needs and regulatory requirements. Their responsibilities typically include market research, project management, gathering user feedback, and supporting senior product managers in strategic planning. This role is crucial for bringing innovative biotech solutions to market efficiently and effectively.

What are the key skills and qualifications needed to thrive as an entry level biotech product manager?

To thrive as an Entry Level Biotech Product Manager, you need a background in life sciences or biotechnology, strong analytical abilities, and a foundational understanding of product lifecycle management. Familiarity with tools like CRM systems, project management software, and data analysis platforms, as well as certifications such as PMP or relevant biotech training, is highly valuable. Excellent communication, teamwork, and problem-solving skills help you collaborate across scientific, marketing, and sales teams. These competencies are essential to successfully bridge technical concepts and market needs, ensuring product success in a dynamic biotech environment.
What are the most commonly searched types of Biotech Product Manager jobs in Delaware? The most popular types of Biotech Product Manager jobs in Delaware are:
What are popular job titles related to Entry Level Biotech Product Manager jobs in Delaware? For Entry Level Biotech Product Manager jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Entry Level Biotech Product Manager jobs in Delaware look for? The top searched job categories for Entry Level Biotech Product Manager jobs in Delaware are:
Entry Level Biotech Product Manager jobs near you
Infographic showing various Entry Level Biotech Product Manager job openings in Delaware as of August 2026, with employment types broken down into 77% Full Time, 15% Part Time, and 8% Temporary. Highlights an 100% In-person job distribution.

Senior Manager, Regulatory Affairs CMC

Incyte Corporation

Wilmington, DE • On-site

Full-time

Posted 19 days ago

Job description

Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
Job Summary (Primary function)
This role will primarily be responsible for managing regulatory CMC submissions and strategy for Incyte development and marketed products, including both small molecules and biologics, from early development through late-stage (phase 3, registration and post-approval).
Essential Functions of the Job (Key responsibilities)
  • Participates in outside professional development meetings and conferences to ensure the latest thinking is applied to CMC strategies.
  • Maintains current knowledge of relevant US and international guidance's, laws and regulations, and proposed and final rules which affect CMC pharmaceutical drug development.
  • Liaises with FDA and other global health authorities as needed (e.g. telephone contacts, submissions). Leads or participates in regulatory CMC related health authority meetings for assigned projects. Prepare summaries of meetings and contacts for inclusion in the regulatory archives.
  • Ensures regulatory CMC submissions comply with current regulatory standards, are of high quality, consistent, and complete. Provides thorough review of the CMC data packages from team representatives to support clinical trial and marketing applications. Collaborates with CMC experts to provide timely responses to CMC regulatory questions from global health authorities. Oversees post-approval global product activities such as change control, product feedback, marketing application supplements, and variations.
  • Leads or participates in meetings with internal and external stakeholders/business partners or teams for clinical development programs, in order to communicate regulatory CMC guidance and strategies.
  • Leads or manages regulatory CMC strategy and submission aspects for both small and large molecule development programs.
  • Ensures compliance to global regulatory guidance documents, regulations and laws, as well as internal policies and procedures.

Qualifications (Minimal acceptable level of education, work experience, and competency)
  • In-depth knowledge of pharmaceutical drug development, and CMC regulations/ guidelines governing development of pharmaceuticals and/or biotechnology products.
  • Minimum of relevant experience in regulatory affairs CMC or a related pharmaceutical development field. Experience with regulatory CMC aspects of both large and small molecule drugs desirable.
  • Experience with global clinical trial and marketing applications, eCTD submissions and electronic document management systems.
  • A degree in a relevant field is required. Advanced degrees in scientific, Regulatory Affairs, or related pharmaceutical fields are desirable, but equivalent experience will also be considered.
  • Willingness to travel domestically up to 10% with reasonable accommodations provided for individuals with disabilities.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.

Apply