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Cber Jobs (NOW HIRING)

Head of Clinical & Registry Programs

Austin, TX ยท On-site +1

$79K - $108K/yr

Has significant and direct experience interacting with FDA CBER Strongly Preferred * Academic or research-institution registry experience (e.g., investigator-initiated or epidemiologic registries ...

Head of Clinical & Registry Programs

Austin, TX ยท On-site

$79K - $108K/yr

Has significant and direct experience interacting with FDA CBER Strongly Preferred * Academic or research-institution registry experience (e.g., investigator-initiated or epidemiologic registries ...

Quality Engineer 3

San Diego, CA

$76K - $98K/yr

Working knowledge of applicable FDA and ISO regulations and expectations, including CDRH, CBER, 21 CFR Part 820, 21 CFR Part 11, ISO 13485 and ISO 14971. * Cleanroom manufacturing experience ...

Quality Engineer 3

San Diego, CA ยท On-site

$76K - $98K/yr

Working knowledge of applicable FDA and ISO regulations and expectations, including CDRH, CBER, 21 CFR Part 820, 21 CFR Part 11, ISO 13485 and ISO 14971. * Cleanroom manufacturing experience ...

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Cber information

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How much do cber jobs pay per hour?

As of Jul 28, 2026, the average hourly pay for cber in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are CBERs?

CBER stands for Center for Biologics Evaluation and Research, which is a branch of the U.S. Food and Drug Administration (FDA). CBER is responsible for regulating biological products, including vaccines, blood and blood components, gene therapies, and cellular therapies. Its main role is to ensure the safety, purity, potency, and effectiveness of these biologic products through rigorous scientific evaluation and oversight. Professionals working at or with CBER often engage in regulatory review, scientific research, and policy development related to biologics.

What are some common challenges CBER professionals face when ensuring compliance with regulatory standards?

Professionals working within the Center for Biologics Evaluation and Research (CBER) often encounter the challenge of navigating complex and evolving regulatory requirements. Staying current with new guidance, implementing robust documentation practices, and effectively communicating with multidisciplinary teams are key aspects of the role. Additionally, balancing the need for thorough scientific review with tight project timelines can be demanding. Team members regularly collaborate with researchers, regulatory affairs specialists, and external stakeholders to ensure product safety and efficacy while meeting federal standards.

What are the key skills and qualifications needed to thrive as a Cybersecurity Analyst, and why are they important?

To thrive as a Cybersecurity Analyst, you need a strong understanding of network security, risk assessment, and incident response, typically supported by a degree in computer science or related fields. Familiarity with tools like firewalls, SIEM systems, intrusion detection/prevention systems, and certifications such as CISSP, CEH, or CompTIA Security+ is highly valued. Analytical thinking, attention to detail, and effective communication are crucial soft skills for this role. These skills are vital to detect, prevent, and respond to cyber threats, ensuring organizational data and systems remain secure.

What is the difference between Cber vs Coder?

AspectCberCoder
Required CredentialsTypically no formal certification, but some roles may prefer certifications in logistics or supply chainOften requires coding bootcamps, certifications like Microsoft or Cisco, or computer science degrees
Work EnvironmentWarehouse, distribution centers, or logistics companiesOffices, tech companies, or remote work settings
Industry UsageLogistics, transportation, supply chain managementInformation technology, software development, tech industry

While both roles involve operational or technical skills, Cbers focus on logistics and supply chain management, often in physical environments, whereas Coders primarily work on software development in tech settings. The choice depends on your skills and industry interests.

More about Cber jobs
What states have the most Cber jobs? States with the most job openings for Cber jobs include:
Infographic showing various Cber job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 81% Physical, 4% Hybrid, and 15% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
Deputy Center Director

Deputy Center Director

Food and Drug Administration

Silver Spring, MD โ€ข On-site, Remote

$259K - $373K/yr

Full-time

Posted 21 days ago


Job description

Summary
This position is being filled under a stream-lined hiring authority, Title 21 of the United States Code (21 US Code 379d-3a) as amended by the 21st Century Cures Act of 2016, section 3072 and the Consolidated Appropriations Act of 2023, Section 3624. The candidate selected for this position will serve under a career or career-conditional appointment and be paid under the provisions of this authority. This position is being recruited based on the Title 21 Pay Table 4, Band H.
Learn more about this agency
Duties
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  • As the Deputy Center Director, participates fully with the Center Director in planning, managing, organizing, and directing all operations, programs segments, functions, and activities of the Center.
  • Represents the Center Director and serves as the Acting Center Director in his or her absence.
  • Serves to organize and coordinate matters brought to the attention of the Office of the Center Director and acts as an advisor to the Center Director on issues requiring decisions based upon comprehensive reviews of the issues.
  • Acts as a principal policy advisor to the Center Director on issues that require the most careful analysis concerning strategic initiatives and regulatory policy programs for CBER.
  • Establishes and maintains effective Center-wide governance and clearance mechanisms for advancing policymaking within the CBER and in collaboration with other FDA Centers and Offices.
  • Participates with the Office Directors in monitoring policy development and policy implementation activities of interest to the Center Director. Evaluates Center-wide ongoing biological product policies.
  • Develops, prepares, and presents authoritative memoranda, briefings, position papers and other materials concerning substantive questions, issues, findings, conclusions and proposed solutions and suggested courses of action.
  • Collaborates with the Center Director and Agency leaders to develop policy on pre-market product access and approvals, labeling, exclusivity and incentives, and emerging biological technologies and tools, including for cross-Center coordination.
  • Directs special studies and workgroups on major issues, reviewing and evaluating Center programs and consulting with Agency officials to address problems with regional, national, and international impact, and recommending actions to resolve them.
  • Provides authoritative guidance to leadership on short- and long-term activities to maximize CBER's public health impact; reviews and analyzes program reports, proposals, memoranda, and other materials affecting Center operations.
  • Shares responsibility with the Center Director to identify opportunities, develop strategies, and cross-Center projects. Oversees improvements in governance, hiring, and strategic planning while building strong coalitions.
  • Leads the Center's strategic engagement on legislative issues, representing the Center with Congress and stakeholders, guiding positions on legislation, and developing implementation plans following enactment of new laws.

Requirements
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Conditions of employment
  • U.S. Citizenship requirement or proof of being a U.S. National must be met by closing date.
  • The candidate selected for this position will serve under a career or career-conditional appointment within the competitive service.
  • Direct Deposit: You will be required to have all federal salary payments electronically deposited into a bank account with a financial institution of your choice.
  • FDA participates in e-Verify: All new hires must complete the I-9 form; this information will be processed through e-Verify to determine your employment eligibility. If a discrepancy arises, you must take affirmative steps to resolve the matter.
  • Males born after December 31, 1959, must be registered with the Selective Service. Please go to http://www.sss.gov for more information.
  • Background Investigation Requirement: All employees must pass a security investigation. Failing to pass the background check may be grounds for removal or legal action. If hired, you may be subject to additional investigations at a later time.
  • Certification of Accuracy: All information concerning eligibility and qualification is subject to investigation and verification. False representation may be grounds for non-consideration, non-selection, or appropriate legal action.
  • All applicants tentatively selected for this position will be required to submit to urinalysis to screen for illegal drug use prior to appointment and be subject to random, reasonable suspicion, and post-accident drug testing upon hiring.
  • Appointment to the position will be contingent upon a negative applicant drug test result.
  • Probationary periods are required for new employees appointed to competitive service positions for the first time; or reinstated employees who return after a break in service of 30-days or more and who have not completed a probationary period.
  • Ethics Clearance and Financial Disclosure is required.

Qualifications
In order to qualify for the Deputy Center Director position which falls under the 0601 occupational Series, you must meet the following requirements by 11:59 pm EST on 08/05/2026:
The candidate must meet the following qualifications for this Title 21 position:
  1. Scientific, Technical, and/or Professional Fields
  2. Qualified and Outstanding Candidates

a. Qualified applies to all candidates for Cures appointments. The FDA OTS will use the technical qualifications defined below as a baseline for comparing experience levels and other candidate attributes for relevant positions
b, Outstanding candidates can be defined by existing outstanding work experience, outstanding performance rating, or both.
Technical Requirements: (Please do not submit narrative responses these qualifications must be included in your 2-page resume)
  1. Executive Level experience directing a large organization.
  2. Experience establishing organizational policy, including the implementation of new legislative authorities or other significant mandates.
  3. Demonstrated ability to communicate effectively both internally and externally to a large number of staff located in different geographic areas.
  4. Demonstrated ability and experience coordinating complex work and priorities and building coalitions with partners in other organization.
  5. Extensive experience and knowledge of the FDA's regulatory and review process; strong leadership and significant executive management experience.
  6. Demonstrated knowledge and experience in the regulation and development of biological products, including the evaluation of safety, effectiveness, and product quality.

Desired Qualifications:
  1. Knowledge of Federal laws and regulations and DHHS and FDA policies and procedures.
  2. Talent for leading cultural and organizational change management efforts.
  3. Knowledge and awareness of the Director's interests and objectives in all matters involving the application of regulatory and policy judgement.
  4. Experience interacting with the media and with entities that perform oversight activities, such as Congress or the General Accountability Office or a Board of Directors.
  5. An advanced degree in law, science or management from an accredited college or university.

NOTE: Applicants must submit all relevant transcripts that demonstrate you possess the required education to meet the Basic Qualifications.
Supervisory Responsibilities The incumbent is delegated full authority to achieve group goals and objectives through the effective management of available resources. Performance and accomplishments are assessed primarily through work performance indicators, staff discussion, planning sessions, review of individual project outputs, and annual program review.
Leads in a proactive, customer-responsive manner consistent with Agency vision and values, effectively communicating program issues to external audiences. Ensures financial and managerial accountability by acting with prudence when executing fiduciary responsibilities. Demonstrates high integrity and adheres to the highest ethical standards of public service. Uses effective business practices including balanced measures of results, values, and invests in each employee; emphasizes empowerment and two-way communication. Takes a leadership role in advocating for and advancing the priorities of the Agency. Serves as a role model for leadership by encouraging teamwork and a collaborative approach. Timely notifies Agency officials of all significant actions and developments, including but not limited to those related to regulatory matters, legislative matters, budget matters, reports, initiatives, and events and ensures subordinate managers do the same.
Provides reasonable accommodations needed to best utilize qualified people with disabilities.
Organizational Management:
Program Management:
Resource Management:
Personnel Performance Management:
Human Capital Management:
This position is designated as an SES Equivalent position and is covered under the FDA Title 21 Executive Performance Management System and identified as a public filing position for ethics purposes.
Drug Impact Statement for Top Secret Security Clearance: The position requires a Top-Secret/Sensitive Compartmented Information (TS/SCI) security clearance, and the incumbent has access to documents and facilities related to national security.
In accordance with Executive Order 12564 of September 15, 1986, The Department of Health and Human Services (HHS) is A Drug-Free Federal Workplace. The Federal government, as the largest employer in the Nation, can and should show the way towards achieving drug-free workplaces through programs designed to offer drug users a helping hand, and at the same time demonstrating to drug users and potential drug users that drugs will not be tolerated in the Federal workplace.
This is a Testing Designated Position. Incumbent must submit to and successfully pass an urinalysis drug screening prior to appointment. The Incumbent will also be subject to unannounced random drug testing for the duration of their time in this position. The use of illegal drugs, on or off duty, by Federal employees is inconsistent not only with the law-abiding behavior expected of all citizens, but also with the special trust placed in such employees as servants of the public. All applicants tentatively selected for this position will be required to submit to urinalysis to screen for illegal drug use prior to appointment and can be subject to random, reasonable suspicion, and post-accident drug testing upon hiring. Appointment to this non-bargaining unit position will be contingent upon a negative drug test result.
Ethics Preclearance Requirements
This position requires financial disclosure reporting and will be subject to FDA's prohibited financial interest regulation. If you are hired, you may be required to divest of certain financial interests. You are advised to seek additional information on this requirement from the hiring official before accepting any job offers. For more information, please visit the FDA Ethics web page: https://www.fda.gov/about-fda/jobs-and-training-fda/ethics.
All requirements must be met by the closing date of this announcement (08/05/2026); only education and experience gained by this date will be considered. You must continue to meet all requirements throughout the entire hiring process.
Education
Pay careful attention to the Qualifications and Education sections to identify vacancies where a transcript is required. Even if you hold a similar position or are a current employee, you are not exempt from transcript requirements.
Education Requirement: Bachelor's or graduate/higher level degree: major study in an academic field related to the medical field, health sciences or allied sciences appropriate to the work of the position.
TRANSCRIPTS: Positions which are scientific or technical in nature often have very specific educational requirements. You must submit an official transcript, unofficial transcript, including courses, grades earned, completion dates, and quarter and semester hours earned.
Education must be accredited by an accrediting institution recognized by the U.S. Department of Education in order for it to be credited towards qualifications. Therefore, provide only the attendance and/or degrees from schools accredited by accrediting institutions recognized by the U.S. Department of Education.
If you are using education completed in foreign colleges or universities, see the Foreign Education section below for additional requirements.
Electronic Transcript Caution: If you have obtained your transcripts electronically, the file might contain security measures that could prevent our application system from reading the file. Therefore, you should consider asking the institution to provide the file in a non-secured electronic format. Alternatively, you could scan or take a photo of the printed copy of the transcript. If your uploaded transcript cannot be read by our system, you may receive consideration and credit for the information we can access.
Foreign Education: If you are using education completed in foreign colleges or universities to meet the qualification requirements, you must show that the education credentials have been evaluated by a private organization that specializes in interpretation of foreign education programs and such education has been deemed equivalent to that gained in an accredited U.S. education program; or full credit has been given for the courses at a U.S. accredited college or university. For further information, visit the U.S. Department of Education website for Foreign Education Evaluation
To be acceptable, the foreign credential evaluation must include/describe at a minimum, the following information: (1) The type of education received by the applicant; (2