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Biotech Manufacturing Associate Jobs in Illinois

bioMerieux

QC Technician II - Accellix.

Lombard, IL · On-site

$25.50 - $36.90/hr

High School Diploma or GED and 4+ years of relevant laboratory, GMP manufacturing, or quality control experience; OR * Associate degree or technical certification in Biotechnology, Biology, Chemistry ...

Biomerieux

QC Technician II - Accellix.

Lombard, IL · On-site

$25.50 - $36.90/hr

High School Diploma or GED and 4+ years of relevant laboratory, GMP manufacturing, or quality control experience; OR * Associate degree or technical certification in Biotechnology, Biology, Chemistry ...

bioMérieux

QC Technician II - Accellix.

Lombard, IL · On-site

$25.50 - $36.90/hr

High School Diploma or GED and 4+ years of relevant laboratory, GMP manufacturing, or quality control experience; OR * Associate degree or technical certification in Biotechnology, Biology, Chemistry ...

bioMerieux

QC Technician II - Accellix.

Lombard, IL

$25.50 - $36.90/hr

High School Diploma or GED and 4+ years of relevant laboratory, GMP manufacturing, or quality control experience; OR * Associate degree or technical certification in Biotechnology, Biology, Chemistry ...

Sotera Health

Lab Analyst I

Itasca, IL

... biotechnology, or another science-related field * Associate degree or relevant laboratory coursework * Previous laboratory, manufacturing, quality, healthcare, or other regulated-industry experience

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Showing results 21-40

All JobsBiotech Manufacturing Associate JobsBiotech Manufacturing Associate Jobs in Illinois

Biotech Manufacturing Associate information

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$32

How much do biotech manufacturing associate jobs pay per hour?

As of Aug 16, 2026, the average hourly pay for biotech manufacturing associate in Illinois is $20.19, according to ZipRecruiter salary data. Most workers in this role earn between $15.82 and $22.60 per hour, depending on experience, location, and employer.

What is a biotech manufacturing associate?

Biotech Manufacturing Associates are professionals who work in the production of biotechnology products, such as pharmaceuticals, vaccines, and other biologically derived materials. They are responsible for operating equipment, following strict protocols, and maintaining sterile environments to ensure product quality and safety. Their duties often include preparing materials, monitoring production processes, troubleshooting equipment issues, and documenting all activities according to regulatory standards. This role is essential in ensuring that biotech products are manufactured efficiently and meet both industry and government regulations.

What does a biotech manufacturing associate do?

A biotech manufacturing associate is responsible for producing biological products in a laboratory or manufacturing setting, following strict safety and quality protocols. They operate equipment, prepare materials, monitor processes, and document production activities to ensure compliance with regulatory standards. Strong attention to detail and knowledge of GMP (Good Manufacturing Practice) are essential for this role.

What is the difference between Biotech Manufacturing Associate vs Laboratory Technician?

AspectBiotech Manufacturing AssociateLaboratory Technician
CredentialsHigh school diploma or equivalent; some roles may require associate degreeHigh school diploma or equivalent; some roles may require associate degree or certification
Work EnvironmentManufacturing floor, production lines, cleanroomsLaboratories, research facilities, testing environments
Industry UsageBiotech manufacturing, pharmaceutical productionResearch labs, quality control, testing labs

While both roles support biotech operations, a Biotech Manufacturing Associate primarily works on production and manufacturing processes in a cleanroom environment, focusing on assembling, monitoring, and maintaining manufacturing equipment. In contrast, a Laboratory Technician typically conducts experiments, tests, and quality control procedures in a laboratory setting. Both roles require attention to detail and adherence to safety protocols, but their daily tasks and work environments differ significantly.

What are some common challenges faced by biotech manufacturing associates, and how can they be managed effectively?

Biotech Manufacturing Associates often encounter challenges such as maintaining strict adherence to Good Manufacturing Practices (GMP), troubleshooting equipment malfunctions, and working under tight production deadlines. Effective management of these challenges involves strong attention to detail, proactive communication with cross-functional teams such as quality assurance and engineering, and continuous learning to stay updated on new protocols and technologies. Developing problem-solving skills and embracing a collaborative mindset can also help associates consistently contribute to high-quality production outcomes.

What are the key skills and qualifications needed to thrive as a biotech manufacturing associate?

To thrive as a Biotech Manufacturing Associate, you typically need a background in biology, chemistry, or a related field, along with experience in GMP-regulated environments. Familiarity with bioprocessing equipment, laboratory instrumentation, and documentation systems such as batch records is crucial. Attention to detail, teamwork, and strong problem-solving abilities help you excel in this collaborative and regulated field. These skills ensure the consistent production of safe, high-quality biotech products while maintaining compliance with industry standards.

What are popular job titles related to Biotech Manufacturing Associate jobs in Illinois?

For Biotech Manufacturing Associate jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Biotech Manufacturing Associate jobs in Illinois look for?

The top searched job categories for Biotech Manufacturing Associate jobs in Illinois are:

What cities in Illinois are hiring for Biotech Manufacturing Associate jobs?

Cities in Illinois with the most Biotech Manufacturing Associate job openings:

Biotech Manufacturing Associate jobs near you
Infographic showing various Biotech Manufacturing Associate job openings in Illinois as of June 2026, with employment types broken down into 67% Full Time, 31% Part Time, 1% Contract, and 1% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $41,999 per year, or $20.2 per hour.

Associate Director, Process Chemistry (External Manufacturing)

AbbVie

North Chicago, IL • On-site

$141K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 17 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

16th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
AbbVie is seeking a highly experienced and strategic Associate Director I, Process Development (External Manufacturing) to join our Synthetic Molecule (SM) CMC organization. In this role, you will lead and support the development and external manufacturing strategy for AbbVie's small molecules (SM), t-LNPs, peptides, and ADC clinical assets across a global network of CROs and CDMOs.
This role is ideal for a seasoned process chemistry leader who thrives in a fast-paced, matrixed environment and can successfully manage multiple projects simultaneously. You will serve as a trusted scientific and operational partner, influencing cross-functional teams, guiding external partners, and ensuring reliable, high-quality, and cost-effective supply for preclinical through cPOC programs. You will also play a critical role in CMC planning, budget stewardship, phase-gate governance, and supplier relationship management.
The successful candidate will bring deep expertise in early- and mid-stage process development, strong technical judgment, and the ability to lead with both scientific credibility and operational discipline. This is a high-visibility role representing AbbVie in strategic partnerships and in-licensing activities, with meaningful impact on development timelines, external manufacturing performance, and overall portfolio success.
Key Responsibilities
  • Lead SCPS responsibilities across multiple AbbVie programs and mentor API teams and PPDST members in developing robust external manufacturing strategies for SM, t-LNPs, peptides, and ADC clinical assets.
  • Serve as the process chemistry subject matter expert for external CROs/CDMOs and provide technical guidance on process development, scale-up, and lifecycle planning.
  • Own CMC timelines, drug substance supply/demand planning, and budgetary oversight, including proactive phase-gate management of external spend and alignment with SM CMC leadership on at-risk spend.
  • Develop and maintain cost of goods estimates to support R&D and clinical development decisions.
  • Identify, escalate, and communicate critical supply chain issues at the program level, partnering with appropriate subject matter experts to develop and execute mitigation plans.
  • Influence cross-functional decisions in a matrix organization, balancing asset team priorities, functional requirements, and business objectives.
  • Build, coach, and retain high-performing talent with strong capabilities in outsourcing, external manufacturing, and matrix teamwork.
  • Drive cross-functional improvements in workflows, CRO/CDMO management practices, in-licensing readiness, and CMC development execution.
  • Partner closely with Purchasing, Finance, Regulatory, and Quality to ensure all CRO/CDMO activities meet AbbVie requirements for quality, finance, ethics, and compliance.
  • Support TQA and MSA activities as needed to enable effective external partnerships.
  • Strengthen leadership capability across the organization to address complex outsourcing challenges and improve decision-making.
  • Drive supplier diversification while actively managing strategic CRO/CDMO relationships.
  • Lead due diligence and onboarding CMC activities for in-licensed assets, including gap assessment and DS/DP supply chain mitigation planning.
  • Support development and manufacturing activities across global CROs/CDMOs and participate in meetings across multiple international time zones as needed.

Qualifications
  • PhD in Process Chemistry with 8+ years of relevant pharmaceutical/biotech industry experience, or MS with 10+ years of relevant experience.
  • Extensive experience in small molecule process development, cGMP manufacturing, tech transfer, and lifecycle management.
  • Strong understanding of CMC regulatory expectations, quality systems, and process safety.
  • Demonstrated success managing multiple projects, priorities, and external partners in a fast-moving environment.
  • Excellent program management skills with a strong sense of ownership and accountability.
  • Proven ability to influence without authority and collaborate effectively across scientific, operational, and leadership teams.
  • Recognized technical expert and strategic thinker with the ability to guide complex external manufacturing decisions.
  • Experience with digital transformation, automation, and operational excellence initiatives is highly desirable.
  • Willingness and ability to travel domestically and internationally up to 25%.

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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