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Remote Quality Control Biotech Jobs in Illinois (NOW HIRING)

This is a FULLY REMOTE opportunity: Essential Duties and Responsibilities: To perform this job ... Lead a team of Quality Professionals responsible for managing Design Control activities for NPI ...

VDC QA/QC Manager, Electrical

Chicago, IL · On-site +1

$100K - $130K/yr

This is a remote role within the United States. US work authorization is required. About VIATechnik ... Exceptional attention to detail, with a track record of building and enforcing QA/QC frameworks ...

... Control, in accordance with FDA QSR (Quality System Regulation), ISO 13485, CAP/CLIA/NYS ... requirements and other applicable global regulations. This individual also supports the Quality ...

Remote Job Type: Contractor Pay: $60-$65/hour Job Overview We are looking for an experienced ... TFL production & QC * Regulatory submissions & CSR review * Strong documentation, communication ...

... biotech) * 3+ years experience in Computer System Validation (CSV). * Experience with industry ... Additionally, for remote roles open to individuals in unincorporated Los Angeles - including remote ...

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Remote Quality Control Biotech information

What is a remote quality control biotech?

A Remote Quality Control Biotech job involves ensuring the quality, safety, and compliance of biotechnological products and processes while working remotely. Responsibilities may include reviewing data, conducting virtual audits, ensuring regulatory compliance, and collaborating with teams to maintain product integrity. Professionals in this role use digital tools to analyze laboratory results, monitor production processes, and document findings. Strong attention to detail, knowledge of industry regulations, and proficiency in data analysis are essential. This position is critical in maintaining high-quality biotech products while allowing flexibility through remote work.

What skills and qualifications are needed for a remote quality control biotech?

To thrive as a Remote Quality Control Biotech, you generally need a solid background in biology or biotechnology, laboratory techniques, and quality assurance processes, often supported by a relevant degree in life sciences or biotechnology. Familiarity with regulatory standards such as GMP or ISO, data analysis software, and laboratory information management systems (LIMS) is typically required. Strong attention to detail, effective communication, and the ability to work independently are important soft skills in remote settings. These competencies ensure accurate quality assessments, regulatory compliance, and effective collaboration with distributed teams.

What are the most common challenges faced by remote quality control professionals in the biotech industry?

One of the main challenges faced by remote quality control biotech professionals is maintaining effective communication and collaboration with on-site laboratory teams and cross-functional departments. Since much of the data review, reporting, and troubleshooting are performed remotely, it can also be challenging to stay updated with real-time lab processes and quickly resolve discrepancies. To address these issues, many companies use digital collaboration tools, regular virtual meetings, and thorough documentation practices. Adapting to these remote workflows ensures that quality standards are consistently met even from a distance.

What job categories do people searching Remote Quality Control Biotech jobs in Illinois look for?

The top searched job categories for Remote Quality Control Biotech jobs in Illinois are:

What cities in Illinois are hiring for Remote Quality Control Biotech jobs?

Cities in Illinois with the most Remote Quality Control Biotech job openings:

Infographic showing various Remote Quality Control Biotech job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 65% Full Time, 31% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Quality Manager, NPI

PCI Pharma Services

Rockford, IL • Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 7 days ago


PCI Pharma Services rating

6.3

Company rating: 6.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

492nd of 545 rated manufacturers


Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI.


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

This is a FULLY REMOTE opportunity:

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities are the following but other duties may be assigned.

  • Lead a team of Quality Professionals responsible for managing Design Control activities for NPI projects and direct cross-functional team members to achieve on-time quality deliverables, pristine customer service, value-add results.
  • Ensures delivery of all quality elements needed to facilitate new product introductions of combination products.
  • Develop Advanced Drug Delivery Product Quality Assurance strategies and implements agreed strategy to support the development of NPI projects.
  • Makes key decisions on product quality, compliance, and regulatory conformance issues for combination products and ensures risk-based escalations to leadership.
  • Working with the programmer and project managers manage project timelines to ensure Quality elements of projects are delivered on time and critical paths are identified and monitored throughout their lifecycle.
  • Promote engagement at all levels and stages of the program. Encourage individuals to contribute to the success of each project and illustrate benefits brought about.
  • Manage risks within the program - ensuring risks are identified, evaluated, and controlled through the program lifecycle.
  • Follow and comply with the NPI process as per company procedures and policies.
  • Display strong leadership to the various project teams from concept to handover. Lead by example in day-to-day project and team management.
  • Manage change at varying levels ensuring site procedures are followed and change controls are raised at the appropriate time with the relevant approvers engaged from the outset.
  • Create and sustain a working environment that promotes the PCI Values and Behaviors.
  • Collaborate with Customer to define KPI's and lead reporting of KPI's to Site and Customer Teams
  • Manage and ensure the quality element of all new products/devices and their associated project phases. It is a requirement of this role that on occasion the individual will be required to travel on company business. This may be vendor/supplier or customer based.
  • Maintain, continually improve, and ensure a compliant NPI Change Requests that promotes sound technical review of product development changes, design reviews, impact assessments, relevant documentation, and compliant closure.
  • Serve as a an NPI risk management representative on cross-functional and multi-site teams to support integrating risk management into various product quality systems such as Change Control and CAPA.
  • Collaborate with internal stakeholders and clients in providing feedback on issue management, escalation, evaluation, and resolution for quality, operational, and regulatory concerns.
  • Participate in, present on, and/or provide rationale for the NPI program during periodic audits and regulatory inspection and customer visits/conference calls as required.
  • This position may require overtime and/or weekend work.
  • Performs other duties as assigned by Director.

Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

Required:

  • Bachelor's degree in engineering, Life Sciences, or related technical discipline.
  • Minimum of 10+ years of progressive experience within pharmaceutical, biotech, or medical device industries.Expert knowledge of GAMP 5, 21 CFR Parts 820, 210/211, and 11, and data integrity regulations.
  • Strong understanding of Product Life Cycle Management, Design Assurance, and Project Management.
  • Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.
  • Strong quality assurance/control, manufacturing, laboratory, technical support, regulatory, and/or validation background is required
  • Highest Reasoning Ability: Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems and deal with nonverbal symbolism in its most difficult phases while dealing with concrete/abstract variables.
  • High Standard of Report Writing
  • Ability to effectively present information to various people as the job requires.
  • Ability to identify and resolve problems in a timely manner.
  • Ability to display original thinking and creativity.
  • Ability to show success in managing employees.
  • Ability to demonstrate attention to detail.
  • Ability to set and achieve challenging goals.

The hiring rate for this position is $86,880-$97,740 plus eligibility for an annual 10% performance bonus. Final offer amounts are determined by multiple factors, including but not limited to specific and relevant experience, education, credentials, geography, and subject matter expertise. PCI offers full-time employees a competitive benefits package that includes paid time off, health insurance coverage (including dental and vision), a flexible spending account, and a 401(k) plan.

#LI-SW1

Join us and be part of building the bridge between life changing therapies and patients. Let's talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.


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