1

Biopharmaceutical Processing Jobs (NOW HIRING)

Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation ... Want to be part of the process that turns plasma donations into life-saving therapies? As a ...

... biopharmaceutical company. As a member of the process development team, the candidate will be focused on supporting senior staff to develop and characterize drug product technologies and ...

Processing Lead

Houston, TX · On-site

$98K - $128K/yr

Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation ... Want to be part of the process that turns plasma donations into life-saving therapies? As a ...

Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation ... As a Processing Lead , you'll manage the behind-the-scenes operations that ensure plasma is ...

Strategic Product Manager

Burlington, MA · On-site

$128K - $192K/yr

You demonstrate an innovative, proactive mindset and strong business acumen, with familiarity in BioProcessing applications relevant to biopharmaceutical processing. Pay Range for this position: $128 ...

Senior Process Engineer

Burlington, MA · On-site

$113K - $146K/yr

... processing, etc. * Experience making decisions and resolving process design problems typical to biopharmaceutical projects: selecting optimum Water for Injection generation & distribution ...

Senior Process Engineer

Burlington, MA · On-site

$113K - $146K/yr

... processing, etc. * Experience making decisions and resolving process design problems typical to biopharmaceutical projects: selecting optimum Water for Injection generation & distribution ...

next page

Showing results 1-20

Biopharmaceutical Processing information

See salary details

$13

$21

$33

How much do biopharmaceutical processing jobs pay per hour?

As of Jun 26, 2026, the average hourly pay for biopharmaceutical processing in the United States is $21.13, according to ZipRecruiter salary data. Most workers in this role earn between $16.35 and $24.76 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in Biopharmaceutical Processing, and why are they important?

To thrive in Biopharmaceutical Processing, you need a solid background in biology, chemistry, or engineering, often with a relevant degree and experience in GMP-regulated environments. Familiarity with bioprocessing equipment, automation systems like SCADA, and knowledge of regulatory standards such as FDA and EMA guidelines are commonly required. Strong problem-solving skills, attention to detail, and effective teamwork are crucial soft skills for success in this role. These competencies are vital to ensure the safe, efficient, and compliant production of high-quality biopharmaceutical products.

What are some common challenges faced in biopharmaceutical processing, and how can new hires best prepare to address them?

Professionals in biopharmaceutical processing frequently encounter challenges such as maintaining strict regulatory compliance, ensuring product quality, and adapting to rapidly evolving technologies. New hires can best prepare by familiarizing themselves with Good Manufacturing Practices (GMP), learning about cleanroom protocols, and staying updated on the latest process automation trends. Collaborating closely with cross-functional teams—including quality assurance, engineering, and research—also helps in troubleshooting and optimizing production workflows. Proactive communication and a commitment to continuous learning are key for success in this dynamic environment.

What is biopharmaceutical processing?

Biopharmaceutical processing refers to the methods and technologies used to produce biopharmaceutical drugs, such as vaccines, antibodies, and therapeutic proteins, from living cells. This process involves multiple steps, including cell culture, fermentation, purification, and quality control to ensure the final product is safe and effective. Biopharmaceutical processing is a vital part of the biotechnology and pharmaceutical industries, and requires strict regulatory compliance to maintain product consistency and safety. Professionals in this field work to optimize processes to improve yield, efficiency, and product quality.
More about Biopharmaceutical Processing jobs
What states have the most Biopharmaceutical Processing jobs? States with the most job openings for Biopharmaceutical Processing jobs include:
Infographic showing various Biopharmaceutical Processing job openings in the United States as of June 2026, with employment types broken down into 94% Full Time, 1% Temporary, 4% Contract, and 1% Nights. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $43,948 per year, or $21.1 per hour.

$115K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago


Job description

Company Overview
ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can conquer it, thanks to the biological wonder that is the human immune system. Our scientists are working to develop novel therapies that harness that inherent power by amplifying both branches of the immune system, attacking cancerous or infected cells today while building immunological memory for tomorrow. The goal: to reprogram the patient's immune system and treat the host rather than just the disease.
Why ImmunityBio?
ImmunityBio is developing cutting-edge technology with the goal to transform the lives of patients with cancer and develop next-generation therapies and vaccines that complement, harness and amplify the immune system to defeat cancers and infectious diseases.
Opportunity to join a publicly traded biopharmaceutical company with headquarters in Southern California.
Work with a collaborative team with the ability to work across different areas of the company.
Ability to join a growing company with professional development opportunities.

Position Summary

The Validation Engineer II is responsible for generating and executing protocols, creating summary reports and executing validation activities in FDA regulated biopharmaceutical environments. Coordinates all validation activities by constant communication with affected departments and personnel. Will report to a manager or head of the department. The Validation Engineer II works on many phases/sub-tasks of projects of moderate complexity and working under general supervision or mostly independently with minimal supervision.

Essential Functions

  • Collaborate with cross-functional departments to meet company expectations,
  • Perform validation activities for equipment, utility systems, facilities, processes, and automation systems in compliance with approved SOPs, cGMPs, and applicable regulatory requirements.
  • Generate, support and execute validation protocols (IQ/OQ/PQ/CV/PV) of all site equipment including laboratory equipment, production equipment, utilities (as applicable) and other related systems in an FDA regulated environment,
  • Author and review SOPs, protocols, reports, and validation master plans for GMP equipment, instruments, and computerized systems,
  • Generate and keep current inventory of GMP systems and requalification/periodic review schedules,
  • Perform and lead risk assessments for GMP systems as required,
  • Plan validation efforts according to risk,
  • Collaborate with clients, CMOs, and vendors to meet project and company objectives,
  • Assist with vendor communications,
  • Troubleshoots and resolve discrepancy reported during validation/qualification.
  • Performs ad-hoc and cross-functional duties and/or projects assigned to support business needs and provide developmental opportunities.

Basic Qualifications

  • Bachelor's degree in science or related discipline is required.
  • 3+ years of relevant validation or GMPregulated industry experience is required.
  • Experience with facility commissioning and validation of equipment and facilities is required.

Preferred Qualifications

  • Strong technical document writing and reviewing with teams
  • Strong understanding and application of validation principles, concepts, practices, and industry standards.
  • Working knowledge of validation principles including commissioning, IQ/OQ/PQs related to equipment and facilities
  • Working knowledge of related quality systems such as change control; CAPA (including deviations/OOSs); training and document control is required.
  • Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment
  • Strong interpersonal skills and the ability to work well independently and in a team environment
  • Strong communication and organizational skills

Working Environment / Physical Environment

  • This position works on-site.
  • Exposure to onsite in-lab environment
  • Must be able to don and wear Personal Protective Equipment (PPE) as required
  • Lifting, standing, climbing, bending, grasping, sitting, pulling, pushing, stooping, stretching, and carrying are generally required to perform the functions of this position
  • Must possess mobility to work in a standard office setting and to use standard office equipment, including a computer.
  • Must be able to lift frequently lift up to 35 pounds and occasionally lift/move 50 pounds

This position is eligible for a discretionary bonus and equity award. The annual base pay range for this position is below. The specific rate will depend on the successful candidate's qualifications, prior experience as well as geographic location.

$103,500 (entry-level qualifications) to $115,000 (highly experienced) annually

The application window is anticipated to close on 60 days from when it is posted or sooner if the position is filled or closed.

ImmunityBio employees are as valuable as the people we serve. We have built a resource of robust benefit offerings to best support the total wellbeing of our team members and their families. Our competitive total rewards benefits package, for eligible employees, include: Medical, Dental and Vision Plan Options Health and Financial Wellness Programs Employer Assistance Program (EAP) Company Paid and Voluntary Life/AD&D, Short-Term and Long-Term Disability Healthcare and Dependent Care Flexible Spending Accounts 401(k) Retirement Plan with Company Match 529 Education Savings Program Voluntary Legal Services, Identity Theft Protection, Pet Insurance and Employee Discounts, Rewards and Perks Paid Time Off (PTO) includes: 11 Holidays Exempt Employees are eligible for Unlimited PTO Non-Exempt Employees are eligible for 10 Vacation Days, 56 Hours of Health Pay, 2 Personal Days and 1 Cultural Day We are committed to providing you with the tools and resources you need to optimize your Health and Wellness.

At ImmunityBio, we are an equal opportunity employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law.