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Biotech Validation Jobs in Malta, IL (NOW HIRING)

TekWissen LLC

Process Development Scientist

Rockford, IL · On-site

$30 - $35/hr

The job opportunity is for one of our clients specializing in biotechnology product development ... Develop, validate, and implement manufacturing processes and analytical methods. * Perform ...

Great Lakes Group

Be Seen First

Mechanical Automation Designer

Elgin, IL · On-site

$43 - $55/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Experience in the medical device , pharmaceutical, biotechnology, laboratory automation, or life-sciences industry is preferred. * Familiarity with regulated manufacturing practices, validation ...

IMA Automation USA Inc

Service Controls Engineer

Elgin, IL · On-site

$83K - $107K/yr

Support software validation requirements and update documentation as needed. * Book service travel ... Technical understanding of pharmaceutical / biotechnology unit operations a plus. * Fundamental ...

Syngenta Seeds

Genotyping Chemistry Scientist

Malta, IL

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We unite precision breeding, advanced biotechnology trait choice, and digital platforms for ... Proven track record in designing and validating high-multiplex PCR assays (e.g., design of panels ...

Syngenta

Genotyping Chemistry Scientist

Malta, IL · On-site

$104K - $157K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We unite precision breeding, advanced biotechnology trait choice, and digital platforms for ... Proven track record in designing and validating high-multiplex PCR assays (e.g., design of panels ...

Syngenta Group

Genotyping Chemistry Scientist

Malta, IL · On-site

$104K - $157K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

We unite precision breeding, advanced biotechnology trait choice, and digital platforms for ... Proven track record in designing and validating high-multiplex PCR assays (e.g., design of panels ...

PCI Pharma Services

Security Specialist

Rockford, IL

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in the pharmaceutical or biotechnology industry is a plus. Essential Duties and ... A valid driver's license is required. * Strong investigative skills with the ability to analyze ...

PCI Pharma Services

Security Specialist

Rockford, IL · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Experience in the pharmaceutical or biotechnology industry is a plus. Essential Duties and ... A valid driver's license is required. * Strong investigative skills with the ability to analyze ...

IQVIA

Portfolio Sales Specialist

Elgin, IL · On-site

Valid driver's license that meets supplier driving standards. Preferred Qualifications * 3+ years of healthcare, medical device, pharmaceutical, biotech, or related sales experience preferred.

PCI Pharma Services

Package Testing Engineer II

Rockford, IL · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

... biotech * High professional proficiency in industry guidelines and standards such as, but not limited to, USP, ASTM, ISTA and ISO. * Good understanding of Formative/Summative Human Factors Validation ...

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All JobsBiotech Validation JobsBiotech Validation Jobs in Malta, IL

Biotech Validation information

See Malta, IL salary details

$21

$48

$73

How much do biotech validation jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for biotech validation in Malta, IL is $48.77, according to ZipRecruiter salary data. Most workers in this role earn between $36.97 and $59.28 per hour, depending on experience, location, and employer.

What cities near Malta, IL are hiring for Biotech Validation jobs?

Cities near Malta, IL with the most Biotech Validation job openings:

Biotech Validation jobs near you
Infographic showing various Biotech Validation job openings in Malta, IL as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $101,439 per year, or $48.8 per hour.

Manager, Facilities & Software Validations

PCI Pharma Services

Rockford, IL • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 4 days ago

PCI Pharma Services rating

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

439th of 540 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.
Summary of Objective:
The Facilities and Software Validations Manager is responsible for coordinating and managing all validation efforts related to Facility/Utility and Computer Equipment at multiple facilities. The Validations Manager is responsible for designing, maintaining and continually improving the validation system. The Validations Manager is responsible for implementation and ongoing improvements of the validation policies, protocols and testing. Provide technical expertise and guidance to customers, the Validations department as well as working with the range of internal departments. Coordinate with other departments to communicate validations and provide resources to implement protocol executions. The Facilities and Software Validations Manager assures customer requirements are accurately incorporated into PCI systems and assures validation protocols adhere to cGMP requirements.
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 include the following but other duties may be assigned.
  • Oversees and manages Validations Supervisor(s), engineers, and, as required, other Validations personnel Manage, identify, hire, and develop staff.
  • Create and maintain employee and organizational development.
  • Oversee proper training, goal setting and effective organizing and assigning of work.
  • Reviews and approves validation and change control documentation, including protocols, summary reports, etc., for validation activities, process parameters, and validation work practices.
  • Manage and develop facility, utility, and computer validations program that is in compliance with regulatory and customer expectations, which includes developing and maintaining Validation Master Plan and policy and work practices. Design, maintain and continually improving the validation system in line with current national and international standards.
  • Assist with validation harmonization among sites across the PCI Pharma Services organization.
  • Provide Validation technical expertise and guidance to the groups within the organization and customers on validation policies and procedures and the implementation of those within the Operations and Quality Assurance (QA) functional areas.
  • Develops and administers budgets, schedules and performance requirements and evaluations.
  • Plan, execute, and oversee validation of facilities, cleanrooms, and utilities (HVAC, compressed air, water systems, gases).
  • Develop and approve validation documentation including URS, risk assessments, IQ, OQ, PQ, and validation summary reports.
  • Ensure facility changes are evaluated through change control and revalidation activities as required.
  • Support environmental monitoring programs and facility qualification strategies.
  • Lead CSV activities in accordance with GAMP 5, FDA, and ISO requirements.
  • Define validation strategies based on system impact, intended use, and risk.
  • Review and approve system lifecycle documentation (URS, FS, DS, risk assessments, test scripts, traceability matrices).
  • Ensure data integrity principles (ALCOA+) are applied across computerized systems.
  • Serve as a 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.
  • Participates, present and provide rationale for the validation 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.the

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, Computer Science, or a related technical discipline.
  • Minimum of 6-8 years of experience in facilities, utilities, and computer system validation in a regulated industry (medical devices, pharmaceutical, or biotechnology).
  • Advanced Computer Skills: Ability to perform the most complex computer tasks and operate various computer programs.
  • Prior experience supervising or leading validation personnel preferred.
  • Strong understanding of validation lifecycle activities (URS, risk assessments, IQ, OQ, PQ, and validation reports).
  • In-depth knowledge of Computer System Validation (CSV) and GAMP 5 methodology.
  • Working knowledge of FDA regulations (21 CFR Parts 820, 210/211, and 11).
  • Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.
  • 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

Preferred:
  • 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 $108,960.00 -$122,580.00 plus eligibility for an annual 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), flexible spending account, and 401(k).
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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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