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Critical Process Filtration Jobs (NOW HIRING)

Filtration Group

2nd shift Warehouse Associate

Joliet, IL · On-site

$19.63/hr

... mission critical products with high replacement rates. Over 80 percent of the Company's revenue ... processes. With revenues of $1.4 billion, Filtration Group is consistently recognized as the ...

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How much do critical process filtration jobs pay per hour?

As of Jun 4, 2026, the average hourly pay for critical process filtration in the United States is $25.47, according to ZipRecruiter salary data. Most workers in this role earn between $17.55 and $29.57 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Critical Process Filtration Specialist, and why are they important?

To thrive as a Critical Process Filtration Specialist, you need a solid understanding of filtration principles, chemistry, and process engineering, often supported by a degree in a related science or engineering field. Familiarity with filtration systems, quality control protocols, and regulatory standards (such as GMP) is essential, along with experience using laboratory and industrial filtration equipment. Strong problem-solving, attention to detail, and effective communication skills help you troubleshoot issues and collaborate with cross-functional teams. These abilities ensure the integrity, safety, and efficiency of filtration processes critical to industries like pharmaceuticals, food and beverage, and biotechnology.

What are some of the most common challenges faced by professionals in Critical Process Filtration roles, and how can they be addressed?

Professionals in Critical Process Filtration often encounter challenges such as maintaining strict quality standards, troubleshooting equipment malfunctions, and adapting to evolving regulatory requirements. Working in this role requires strong attention to detail and the ability to quickly identify and resolve process deviations to prevent contamination or product loss. Regular collaboration with quality assurance, maintenance, and production teams is essential to ensure seamless operations. Staying current with industry best practices and participating in ongoing training can help address these challenges and support career advancement.

What is Critical Process Filtration?

Critical Process Filtration refers to the use of specialized filtration systems and techniques designed to remove contaminants and ensure product purity in industries such as pharmaceuticals, biotechnology, food and beverage, and microelectronics. These filtration processes are essential in protecting product quality, meeting regulatory standards, and maintaining safety in environments where even minor contamination can have significant consequences. Professionals in this field are responsible for selecting, operating, and maintaining filtration equipment, as well as validating processes to ensure compliance with industry requirements. Expertise in this area is crucial for maintaining the integrity of sensitive manufacturing and research operations.

What is the difference between Critical Process Filtration vs Process Equipment Operator?

AspectCritical Process FiltrationProcess Equipment Operator
CredentialsTechnical certifications, industry-specific trainingOn-the-job training, basic technical knowledge
Work EnvironmentManufacturing plants, cleanroom settingsFactory floors, production lines
Industry UsagePharmaceutical, food processing, chemical manufacturingVarious manufacturing sectors
Job FocusFiltration system setup, maintenance, quality controlOperating and monitoring equipment

Critical Process Filtration specialists focus on maintaining and optimizing filtration systems crucial for product purity and safety, often requiring specialized certifications. Process Equipment Operators handle the day-to-day operation of manufacturing machinery, including filtration equipment, but with broader operational responsibilities. Both roles are vital in manufacturing industries but differ in technical depth and scope.

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What cities are hiring for Critical Process Filtration jobs? Cities with the most Critical Process Filtration job openings:
What job categories do people searching Critical Process Filtration jobs look for? The top searched job categories for Critical Process Filtration jobs are:
Critical Process Filtration jobs near you
Infographic showing various Critical Process Filtration job openings in the United States as of May 2026, with employment types broken down into 83% Full Time, and 17% Contract. Highlights an 100% In-person job distribution, with an average salary of $52,986 per year, or $25.5 per hour.
Engineer - (JP10122)

Engineer - (JP10122)

3 Key Consulting

Thousand Oaks, CA • On-site

Other

Posted 15 hours ago

Job description

Job Title: Engineer - Hybrid (JP10122)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Commercial Drug Product
Duration: 1+ years (with likely extensions)
Notes: Hybrid: Working on site 25-50% of the time. Highly prefer Masters degree with the 3 years of experience, however, will look at Bachelors
Posting Date: 04/25/2022
3 Key Consulting is hiring an Engineer for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
As a member of the process development team, this role will be focused on identifying and developing aspects of drug product to advance process design for parenteral drug products. The candidate will perform experiments, organize data and analyze results with minimal supervision. The candidate will establish the experimental design, develop and implement protocols, obtain reproducible and reliable results, analyze data and communicate results to cross functional groups. Specific responsibilities include but are not limited to:
  • Design, execute and document primary data packages related to drug product design and process development, and communicate key findings in presentations
  • Develop solutions to technical problems during process characterization and aseptic manufacturing
  • Support one or more clinical and commercial process introductions or process transfers into client manufacturing network
  • Author and review technical protocols, reports, product impact assessments, and regulatory sections in support of IND and marketing application submissions
  • Provide ongoing support to clinical and commercial fill/finish manufacturing operations through troubleshooting, root cause analysis, and product impact assessments for non-conformance investigations and process changes/improvements
  • Participate in cross-functional teams working effectively in a highly matrixed team environment to drive change, efficiency, and strong relationships

Preferred Qualifications:
  • MS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology
  • 3+ years of experience within the pharmaceutical/biotechnology industry
  • Experience in development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters
  • Aseptic fill finish manufacturing or manufacturing technical services experience including the development of control strategies and active process performance monitoring
  • Understanding of process related stresses that impact the quality and stability of biologics
  • Ability to use engineering principles to leverage bench and pilot scale models for process performance characterization
  • Fill/finish process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools (e.g. Fish bone diagrams, FMEA, etc.)
  • Familiarity with Design of Experiments (DOE) and Quality by Design (QbD) principles
  • Familiarity with cGMPs, regulatory filings, and compliance issues for sterile injectable products manufactured by aseptic processing
  • Experience in a matrix team environment and interacting with Analytical Sciences, Process Development, Project Management, Manufacturing, Regulatory, Compliance, and/or Quality
  • Organizational, technical problem solving, communication (written and verbal) skills, and regular interactions
  • Ability to learn and act on dynamic information at a rapid pace
  • Familiar or ability to learn to use electronic record keeping, GMP, laboratory notebooks, statistical analysis and software.
  • Laboratory or pilot plant experience with process equipment
  • BS in Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry or Biotechnology with 3+ years of experience within the pharmaceutical/biotechnology industry

Why is the Position Open?
Supplement additional workload on team.
Top Must-Have Skill Sets:
  • Familiar or ability to learn to use electronic record keeping, GMP, laboratory notebooks, statistical analysis and software.
  • Laboratory or pilot plant experience with process equipment, especially aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.)
  • Ability to learn and act on dynamic information at a rapid pace
  • Degree: BS with 3 years of experience (minimum) -Chemical/Biomedical Engineering, Pharmaceutical Sciences, Chemistry/Biochemistry

Day to Day Responsibilities:
  • Engineer will be involved with development/characterization of aseptic fill/finish unit operations (freeze/thaw, mixing, sterile filtration, filling, stoppering, visual inspection, etc.) to define critical process parameters.
  • Engineer will assist with aseptic fill finish manufacturing or manufacturing technical services activities including the development of control strategies and active process performance monitoring
  • Engineer will perform stability or characterization studies to understand process related stresses that impact the quality and stability of biologics
  • Engineer will apply engineering principles to leverage bench and pilot scale models for process performance characterization
  • Engineer will be involved with Fill/finish process scale-up and technology transfer experience including the use of gap analysis, root cause analysis, and risk assessment tools (e.g. Fish bone diagrams, FMEA, etc.)

Interview process:
Phone screening followed by in-person interview.
We invite qualified candidates to sendyour resume toresumes@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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