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Bioprocess Technology Jobs (NOW HIRING)

Merck Group

Account Manager, Life Sciences

Burlington, MA · On-site

$107K - $179K/yr

Generates accurate business forecasts Preferred Qualifications: * 3+ years of experience in bioprocess technology operations or process manufacturing development in life sciences * Ability to work ...

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Bioprocess Technology information

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How much do bioprocess technology jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for bioprocess technology in the United States is $18.71, according to ZipRecruiter salary data. Most workers in this role earn between $15.38 and $25.00 per hour, depending on experience, location, and employer.

What is bioprocess technology?

Bioprocess technology is a branch of biotechnology that uses living cells or their components, such as enzymes, to create products and processes for various industries. It involves designing and optimizing biological processes for the production of pharmaceuticals, biofuels, food, and chemicals. Key steps include fermentation, cell culture, downstream processing, and quality control. This field is crucial for developing sustainable and efficient ways to manufacture products using biological systems.

What can you do with a bioprocessing degree?

A bioprocess technology degree prepares individuals for roles in biopharmaceutical manufacturing, including process development, production, and quality control. Graduates often work with bioreactors, fermentation processes, and regulatory compliance, utilizing skills in laboratory techniques and process optimization.

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

To thrive as a Bioprocess Technologist, you need a solid background in biotechnology, microbiology, or chemical engineering, typically supported by a relevant degree. Familiarity with bioprocess equipment, fermentation technology, and industry-standard laboratory information management systems (LIMS) is essential, along with certifications like GMP (Good Manufacturing Practice). Attention to detail, problem-solving, and strong teamwork skills help you excel in process optimization and troubleshooting. These competencies are crucial to ensure efficient, safe, and compliant production of biopharmaceuticals or other biotech products.

What is bioprocessing technology?

Bioprocessing technology involves using living cells, enzymes, and biological systems to produce products such as pharmaceuticals, vaccines, and biofuels. Bioprocess technologists design, optimize, and monitor these processes often using bioreactors and require knowledge of microbiology, chemistry, and engineering principles.

What are 5 careers in biotechnology?

Bioprocess technology professionals can pursue careers such as bioprocess engineer, quality control analyst, research scientist, manufacturing technician, and regulatory affairs specialist. These roles involve working with bioreactors, lab equipment, and compliance standards to develop and produce biopharmaceuticals and other biotech products. Strong knowledge of biology, chemistry, and process optimization is essential for success in these careers.

What is the difference between Bioprocess Technology vs Bioprocess Engineering?

AspectBioprocess TechnologyBioprocess Engineering
CredentialsTypically requires a degree in biotechnology, biology, or chemical engineeringRequires a degree in chemical, biochemical, or biological engineering
Work EnvironmentLaboratories, production facilities, quality controlDesign, optimization, and scale-up of bioprocesses in industrial settings
Industry UsageResearch, development, manufacturing of biopharmaceuticals, vaccinesProcess design, scale-up, and troubleshooting in bioprocess industries

Bioprocess Technology focuses on the hands-on development and operation of bioprocesses, while Bioprocess Engineering emphasizes designing and optimizing these processes for large-scale production. Both roles require similar educational backgrounds but differ in scope and responsibilities within the biopharmaceutical industry.

What are some common challenges faced by professionals working in bioprocess technology, and how can they be addressed?

Professionals in bioprocess technology often encounter challenges such as maintaining consistent product quality, troubleshooting process deviations, and adapting to rapidly evolving regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams, ongoing training in new technologies, and rigorous documentation practices. Staying updated with industry best practices and actively participating in process optimization initiatives can also help professionals overcome these hurdles and contribute to successful bioproduction outcomes.

What does a bioprocess technician do?

A bioprocess technician is responsible for operating, monitoring, and maintaining equipment used in the production of biopharmaceuticals and other biological products. They follow strict protocols, document processes, and ensure quality control during manufacturing processes, often working in cleanroom environments and using tools like bioreactors and lab instruments.
More about Bioprocess Technology jobs
What cities are hiring for Bioprocess Technology jobs? Cities with the most Bioprocess Technology job openings:
What job categories do people searching Bioprocess Technology jobs look for? The top searched job categories for Bioprocess Technology jobs are:
Bioprocess Technology jobs near you

Principal Scientist - BioProcess Development

Wacker Chemical Corporation

San Diego, CA

Other

Medical, Dental, Vision, Retirement, PTO

Posted 13 days ago

Wacker Chemical Corporation rating

9.1

Company rating: 9.1 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

5th of 90 rated chemical manufacturers

Job description

Do you want to take responsibility and make a difference with your work? With your expertise, we can achieve great goals together. We are WACKER - Reliable. Determined. Ambitious. As one of the world's most research-intensive chemical companies, we've been making countless products that are an integral part of your everyday life possible for over 100 years. From vegan food to resource-efficient buildings to solar cells, we develop sustainable solutions that change the future.
To strengthen our team in San Diego,
we are looking for you as a(n) Principal Scientist - BioProcess Development.

The Principal Scientist, BioProcess Development is a senior technical leadership role responsible for the design, development, optimization, and scale-up of bioprocesses for plasmid DNA, protein biologics, and emerging modalities. This position serves as a scientific authority and technical project lead, bridging hands-on process development with strategic program execution. The Principal Scientist independently leads complex development programs, drives platform and technology innovation, and ensures successful technology transfer to Manufacturing and MSAT.

  • Lead complex upstream/downstream bioprocess development programs. Act as technical escalation point for complex process, scale up, and manufacturability challenges across development programs.
  • Serve as technical project lead and define development strategies aligned with client requirements and timelines, regulatory phase, and manufacturing constraints. Ensure development activities comply with EHS, quality, and data integrity requirements.
  • Design scalable processes using QbD principles. Evaluate and implement new technologies, materials, and unit operations to improve yield, robustness, and cost of goods. Drive process characterization, process definition, and comparability studies in support of process changes or scale transitions.
  • Author and review development protocols, development SOPs, development reports, technical documentation, and tech transfer documentation. Support technical presentations/publications.
  • Coordinate tech transfer with Manufacturing, QC, and MSAT. Review and provide critical input to batch records, development protocols, and technical instructions supporting GMP execution. Partner with MSAT and Manufacturing to support process validation readiness and late stage development activities, as needed. Support root cause investigations and CAPA development for process related deviations impacting development or manufacturing.
  • Support RFPs and customer technical discussions. Support client onboarding and technical due diligence, including assessment of incoming processes and data packages.
  • Provide technical mentorship. Contribute to technical governance forums, development reviews, or internal scientific committees.
  • Provide scientific input to cost modeling, process economics, and capacity planning discussions. Represent Process Development in cross functional decision making related to program strategy, timelines, and risk.
  • Contribute to platform and continuous improvement initiatives. Champion standardization, platform processes, and best practices while maintaining flexibility for clientspecific needs

Position Requirements:

  • Bachelor of Science degree in Biochemistry, Biological Sciences, Bioengineering, Chemistry, or related scientific discipline; Master's Degree or PhD in Biology, Chemistry, Engineering or related scientific field is preferred.
  • Minimum 10 years of relevant experience with 5 years in Contract Development and Manufacturing services of Biopharmaceuticals.
  • Experience in Plasmid and Protein development and/or manufacturing is required. Additional experience in RNA, LNP preferred.
  • Ability to travel up to 10%.
  • Experience in and good technical knowledge of biotherapeutic process development and manufacturing is required. Proven track record of independent decision making on complex technical issues with appropriate risk assessment and escalation. High level of scientific accountability and ownership, with a proactive approach to problem solving.
  • In-depth knowledge in upstream fermentation process development and downstream purification development to support development of pipeline projects, platforms, and innovative technologies.
  • Strong analytical skills with experience in process mapping and process design.
  • Proficiency in data analysis and performance measurement tools.
  • Demonstrated ability to operate effectively in a client facing CDMO environment, balancing scientific rigor, timelines, and customer expectations. Ability to clearly communicate complex technical concepts to diverse audiences, including non technical stakeholders and clients.
  • Extensive experience as a project lead for biologics pipeline programs. Strong capability in managing evolving timelines, program risks and mitigation strategies. Strong understanding of phase appropriate development, including early stage, clinical, and commercial readiness considerations.
  • Experience supporting or leading technical due diligence, feasibility assessments, and program onboarding activities. Comfortable contributing to proposal development, technical justifications, and cost/scope discussions.
  • Innovative mind-set demonstrated by technical accomplishments, external presentations, and publications is a plus. Commitment to maintaining awareness of emerging technologies, regulatory trends, and competitive landscape relevant to bioprocess development.
  • Knowledge in authoring and providing critical input to the regulatory submissions including but not limited to Investigational New Drugs, Investigational Medicinal Product Dossiers, and Clinical Trial Applications is a plus.
  • Ability to work closely with cross-functional stakeholders to ensure team alignment with functional objectives. Ability to manage ambiguity and rapidly evolving priorities across multiple client programs and internal initiatives.
  • Ability to lead technically without direct authority. Demonstrated ability to mentor and elevate technical capability of junior scientists through coaching, review, and example.
  • Strong collaboration skills in matrixed and cross functional organizations, including global or multi-site teams. Willingness to support occasional nonstandard work hours to meet critical project milestones.

The anticipated salary range for candidates who will work in San Diego is $140,000 - $155,000. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc . Wacker is a multi-state employer and this salary range may not reflect positions that work in other states.

What do we offer?
WACKER strives to reward its employees in a fair and equitable manner. Our Total Rewards Package considers employee wellbeing and is comprised of compensation, benefits, work-life balance, performance & recognition, and career development.
  • Compensation and Incentive plans
  • Medical, Dental, and Vision Insurance effective day 1
  • Paid Time Off in addition to personal days and holidays
  • Paid parental leave
  • Wellbeing fund
  • Flexible hybrid work arrangements
  • 401(k) with company match
  • Education Assistance Program
  • Career development and advancement opportunities
  • Support for Community Involvement
We are looking forward to your online application at www.wacker.com.
Reference Code:30937

The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. A minimum requirement for this US-based position is the ability to work legally in the United States on a permanent unrestricted basis. Visa sponsorship is not available for this position, including any type of US permanent residency (e.g., for a green card).

Wacker is an Equal Opportunity Employer. We actively promote the equality of opportunity for all who are qualified and bring the requisite experience, talent, skill and potential, without regard to age, disability, sex, race, religion or belief, marriage/civil partnership, pregnancy/maternity, sexual orientation, or any other protected characteristics. We welcome all applications from a wide range of candidates. Selection for roles will be based on individual merit alone.

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