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Biopharmaceutical Processing Jobs (NOW HIRING)

CEDENT

Process Scientist

Philadelphia, PA · On-site

A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical processing that utilizes bioreactors. A ...

GSK Internships & Co-ops powered by Atrium

PA · Hybrid

GSK is a global biopharma company with a special purpose - to unite science, technology and talent ... A passing score is required to proceed in the application process. After completing the assessment ...

LuckyJay Consulting

Automation Engineer, Biopharmaceutical The successful candidate will work very closely with the ... Through collaboration across multiple teams, the Automation engineer will improve process ...

ImmunityBio

Validation Engineer II

El Segundo, CA · On-site

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 ...

NKW NantKwest Inc

Validation Engineer I

El Segundo, CA · On-site

$98K/yr

Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment * Good interpersonal skills and the ability to work well ...

ImmunityBio

Validation Engineer I

El Segundo, CA · On-site

$98K/yr

Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment * Good interpersonal skills and the ability to work well ...

ImmunityBio, Inc.

Validation Engineer I

El Segundo, CA · On-site

$98K/yr

Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment * Good interpersonal skills and the ability to work well ...

NKW NantKwest Inc

Validation Engineer II

El Segundo, CA · On-site

$115K/yr

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 ...

ImmunityBio

Validation Engineer I

Mariposa, CA · On-site

$98K/yr

Working knowledge of GMPs, OSHA compliance, 21 CFR Part 11 and cleanrooms, automated biopharmaceutical processing and plant equipment * Good interpersonal skills and the ability to work well ...

Kedrion S.p.A.

Processing Technician

Lincoln, NE · On-site

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 ...

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Biopharmaceutical Processing information

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How much do biopharmaceutical processing jobs pay per hour?

As of Jul 16, 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 is the highest paying job in pharmaceuticals?

In biopharmaceutical processing, senior roles such as Director of Manufacturing or Vice President of Operations tend to be the highest paying, often earning six-figure salaries. These positions require extensive experience, leadership skills, and knowledge of regulatory compliance and process optimization.

What jobs in the US pay 300,000 a year?

In biopharmaceutical processing, senior roles such as Director of Manufacturing, Vice President of Operations, or Chief Scientific Officer can earn $300,000 or more annually, especially with extensive experience, advanced degrees, and leadership responsibilities. These positions often require expertise in process development, regulatory compliance, and team management, and may include bonuses and stock options that contribute to total compensation.

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 involves the manufacturing of biological drugs, such as vaccines and monoclonal antibodies, through complex techniques like cell culture, fermentation, and purification. Professionals in this field operate specialized equipment, follow strict quality standards, and often require knowledge of Good Manufacturing Practices (GMP).

What can I do with a degree in biopharmaceuticals?

A degree in biopharmaceuticals prepares individuals for roles in drug development, manufacturing, quality control, and regulatory compliance within the biopharmaceutical industry. Graduates can work as process technicians, quality assurance specialists, research scientists, or in production environments that require knowledge of bioprocessing techniques and equipment. Certifications in Good Manufacturing Practices (GMP) and familiarity with laboratory tools are often beneficial for career advancement.
More about Biopharmaceutical Processing jobs
What states have the most Biopharmaceutical Processing jobs? States with the most job openings for Biopharmaceutical Processing jobs include:
What job categories do people searching Biopharmaceutical Processing jobs look for? The top searched job categories for Biopharmaceutical Processing jobs are:
Biopharmaceutical Processing jobs near you
Process Scientist

Process Scientist

CEDENT

Philadelphia, PA • On-site

Full-time

Re-posted 29 days ago

Job description

Title: Process Scientist
Report: CTO
Location: Philadelphia, PA  
Position Type: Full Time, Exempt
Travel: Occasional (0-10%)
Position Summary
This position is part of the Technology team responsible for Client technology development, process development, and assisting in transferring developed process to GMP manufacturing. A Scientist is a mid-level individual with understanding of cell/molecular biology and previous experience in either upstream or downstream biopharmaceutical processing that utilizes bioreactors. A Scientist is responsible for hands-on execution of experiments and technology transfer, as well as authoring experimental protocols, SOPs, and batch documents. A Scientist is expected to independently complete objectives given by supervisor, serve as a role model to junior scientists, collaborate cross-functionally, and provide support with any other technology, process development, and manufacturing needs.
Key Responsibilities
  • Independently contribute to technology/process development for specific bioprocessing steps, ensuring delivery in alignment with Client strategy
  • Support Senior/Principal Scientist with experimental design, execution and data analysis, effectively communicating technical results to management
  • Author protocols, SOPs, and batch documents to ensure the successful transfer of technology/process development to GMP manufacturing
  • Perform as a Subject Matter Expert on a cross-functional team to implement novel process.
  • Work closely with suppliers and other partners to drive forward technology development initiatives
  • Serve as a good financial steward to the Technology team at Client and help to implement budgetary adherence and financial governance
  • Coach and train junior scientists/employees on activities and documentation related to technology development, process development.
  • Other related duties as assigned.
Education and Experience
  • Minimum Bachelor’s degree in Biological Engineering, Biotechnology, Biology, Biochemistry, or other related field. Master’s preferred.
  • 2-3 years of industry or academic experience in combination with Bachelor’s or Master’s degree.
Knowledge, Skills and Abilities
  • Experience with methodologies used for upstream or downstream viral vector production in either industry or academia
  • Experience in experimental design, execution, and data analysis
  • Excellent communication, collaboration, and technical writing skills
  • Innovative and creative mindset, with problem solving capabilities
  • Proficient in Microsoft Office products.
Physical Requirements
  • Ability to lift and carry up to 30lbs
  • Ability to sit and stand for extended periods
  • Excellent manual dexterity and ability to perform repetitive movements with fingers/hands
Other Physical Requirements: PPE and gown training will be required as this individual will be required to enter into Laboratory and Cleanroom areas.
Work Environment: Work is performed primarily onsite in Philadelphia. 50% or more of the time, this role is in the laboratory.
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About Cedent

Sourced by ZipRecruiter

CEDENT strives to attract and retain the best people and provide an environment where they can all develop professionally and build a rewarding career. As a result, we create an inclusive environment that is rich in diversity, acknowledges each individual's uniqueness and promotes respect, personal achievement and stewardship. Our clients are global and so is CEDENT. We build and maintain a global workforce that includes people from different backgrounds, with a vast range of skills and experience all united by a common culture and commitment to help our clients achieve high performance. Cultivating a diverse workforce and inclusive work environment makes business sense. Our peoples varied skills are the talent engine that powers CEDENT, enabling it in turn to deliver the innovative solutions that help our clients outperform competitors.

Industry

It services

Company size

11 - 50 Employees

Headquarters location

Plano, TX, US

Year founded

2008

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