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Aseptic Process Engineer Jobs in Alabama (NOW HIRING)

Actalent

Quality Manager

Bessemer, AL

$110K - $140K/yr

... Aseptic Process Simulations and training plans. * Manage quality risk, deviation investigations ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Evonik

Development Engineer

Birmingham, AL

... focus on engineering solutions, project planning, resourcing, and execution with respect to ... process development in the pharmaceutical industry is required, experience in aseptic ...

Jubilant Pharma, LLC

Quality Site Lead

Mobile, AL · On-site

$80 - $100/hr

Collaborate with Production and QC teams to ensure aseptic processing standards are met. * Support ... Partner with Corporate Quality, Supply Chain, Radiation Safety, Engineering, and Operations to ...

Airswift

Operator I (Shift C)

Birmingham, AL · On-site

$16 - $19.25/hr

... process operations in a controlled production setting. Key Responsibilities * Demonstrate aseptic technique proficiency with minimal supervision. * Accurately execute development, engineering, GLP or ...

Evonik Industries

Operator

Birmingham, AL · On-site

$16.50 - $21.50/hr

... aseptic technique with minimal supervision. * Accurately execute development/engineering, GLP or ... Assemble and disassemble process equipment on multiple unit operations for an extrusion ...

Evonik

Operator

Birmingham, AL

$16.50 - $21.50/hr

... aseptic technique with minimal supervision. * Accurately execute development/engineering, GLP or ... Assemble and disassemble process equipment on multiple unit operations for an extrusion ...

All JobsAseptic Process Engineer JobsAseptic Process Engineer Jobs in Alabama

Aseptic Process Engineer information

See Alabama salary details

$28K

$72K

$107.7K

How much do aseptic process engineer jobs pay per year?

As of Aug 26, 2026, the average yearly pay for aseptic process engineer in Alabama is $72,049.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,300.00 and $81,300.00 per year, depending on experience, location, and employer.

What is an aseptic process engineer?

Aseptic process engineers are professionals who design, develop, and maintain sterile manufacturing systems, primarily in the pharmaceutical, biotechnology, and food industries. Their main responsibility is to ensure that products are produced in a contamination-free environment, using processes that prevent the introduction of microorganisms. This involves overseeing the design of cleanrooms, validating equipment, developing standard operating procedures, and ensuring regulatory compliance. Aseptic process engineers work closely with quality assurance teams to maintain high standards of product safety and efficacy. Their expertise is crucial for industries where product sterility is critical to consumer safety.

What are the key skills and qualifications needed to thrive as an aseptic process engineer, and why are they important?

Aseptic Process Engineers need a strong background in chemical, mechanical, or biomedical engineering, along with experience in aseptic manufacturing environments and a solid understanding of GMP regulations. Familiarity with process automation systems, sterilization equipment, and industry certifications such as Six Sigma or Lean Manufacturing are often required. Attention to detail, strong problem-solving abilities, and effective communication are vital soft skills for ensuring product quality and process efficiency. These skills are crucial for maintaining sterile conditions, regulatory compliance, and the safe production of pharmaceuticals or biotechnology products.

What are some common challenges faced by aseptic process engineers, and how can they be addressed?

Aseptic Process Engineers often encounter challenges such as maintaining strict sterility standards, troubleshooting equipment issues, and ensuring compliance with changing regulatory requirements. Addressing these challenges requires strong attention to detail, proactive communication with cross-functional teams, and staying current with industry best practices and regulations. Collaborating closely with quality assurance, production, and maintenance teams helps to identify and resolve issues quickly, ensuring that processes remain efficient and compliant.

What is the difference between Aseptic Process Engineer vs Pharmaceutical Manufacturing Technician?

AspectAseptic Process EngineerPharmaceutical Manufacturing Technician
CredentialsBachelor's degree in engineering, life sciences, or related field; GMP trainingHigh school diploma or associate degree; GMP training often required
Work EnvironmentCleanroom, sterile environments, manufacturing facilitiesManufacturing floors, production areas, sometimes cleanrooms
Industry UsageDesign, optimize, and validate aseptic processes in pharmaOperate equipment, assemble products, support manufacturing

The Aseptic Process Engineer focuses on designing and validating sterile manufacturing processes, requiring specialized engineering knowledge. In contrast, the Pharmaceutical Manufacturing Technician handles day-to-day production tasks, often with less formal education but essential for maintaining manufacturing flow. Both roles are vital in pharmaceutical production but differ in responsibilities and qualifications.

What are popular job titles related to Aseptic Process Engineer jobs in Alabama?

For Aseptic Process Engineer jobs in Alabama, the most frequently searched job titles are:

What job categories do people searching Aseptic Process Engineer jobs in Alabama look for?

The top searched job categories for Aseptic Process Engineer jobs in Alabama are:

What cities in Alabama are hiring for Aseptic Process Engineer jobs?

Cities in Alabama with the most Aseptic Process Engineer job openings:

Aseptic Process Engineer jobs near you
Infographic showing various Aseptic Process Engineer job openings in Alabama as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, 5% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $72,049 per year, or $34.6 per hour.

Validation Engineer (Aseptic C&Q )

Centstone

Birmingham, AL • On-site

Contractor

Re-posted 19 days ago

Job description

Job Title: Validation Engineer (Aseptic C&Q )
Openings: 1
Location: Birmingham, AL (Onsite)
Start: January 2026
Duration: Minimum 6 months (extendable)
Employment Type: Contract

Job Summary
We are seeking a Validation Engineer with strong experience in aseptic pharmaceutical validation and equipment qualification. The ideal candidate will have hands-on expertise in C&Q activities, documentation, and compliance aligned with FDA/EU/GMP standards. This role will support new and existing aseptic facilities and critical manufacturing systems.

Key Responsibilities

  • Develop and maintain validation/qualification documentation for aseptic facilities and equipment.

  • Create and execute C&Q deliverables including URS, risk assessments, commissioning plans, IQ/OQ/PQ protocols, and final reports.

  • Perform Commissioning (COM), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) activities.

  • Ensure all validation documentation meets internal quality standards and regulatory expectations (FDA/EU/GMP).

  • Conduct risk assessments and define mitigation strategies for aseptic processes and systems.

  • Collaborate cross-functionally with Engineering, Quality, Manufacturing, and other stakeholders to meet project timelines.

  • Support requalification and lifecycle management activities for validated systems and equipment.

  • Lead or support Computer System Validation (CSV) activities, including system classification, test script creation/execution, and compliance reporting.

  • Verify system functionality and data integrity consistent with regulatory requirements.

Required Qualifications

  • Bachelor’s degree in Engineering or Science (preferred).

  • 3–5 years of experience in validation/qualification of aseptic pharmaceutical processes and/or equipment.

  • Strong knowledge of FDA/EU regulatory frameworks, GMPs, and industry best practices.

  • Demonstrated experience authoring and executing URS, protocols, and validation reports.

  • Strong understanding of pharmaceutical manufacturing equipment and process validation.

  • Proficiency with documentation tools and Microsoft Office (Word, Excel, PowerPoint).

  • Excellent communication, organization, and stakeholder management skills.

  • Ability to work independently and within cross-functional teams.

Preferred/Tools & Equipment Exposure

  • Experience with Kaye Validator AVS and ValProbe systems.

  • Knowledge of qualification for equipment such as:

    • Homogenizers

    • Pump skids

    • SIP/CIP skids

    • Temperature control units (CTUs)

    • Tanks and related utilities

  • Experience supporting aseptic facility start-ups, expansions, or technology transfers.
     

Thanks & Regards,

Adarsh Mallik | IT Recruiter
adarsh.mallik@centstone.com
CENTSTONE SERVICES
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About Centstone

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In the dynamic landscape of today’s business environment, flexibility is key. At Centstone, we understand the unique demands of your industry and offer tailored Contract Hiring solutions to empower your organization with the right talent when you need it most.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Hazlet, NJ, US

Year founded

2022

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