Lead Validation Specialist
$55 - $65/hr
... from the food, biotechnology or pharmaceutical industry that can support commissioning ... Author and manage Commissioning & Validation Master Plans (CVMPs) * Coordinate with OEMs ...
Quick apply
$55 - $65/hr
... from the food, biotechnology or pharmaceutical industry that can support commissioning ... Author and manage Commissioning & Validation Master Plans (CVMPs) * Coordinate with OEMs ...
Quick apply
$55 - $65/hr
... from the food, biotechnology or pharmaceutical industry that can support commissioning ... Author and manage Commissioning & Validation Master Plans (CVMPs) * Coordinate with OEMs ...
... in fields such as Biotechnology, Life Sciences, Biomedical Sciences, Economics, Business, or related fields * Advanced degree (Master's, PharmD, or Ph.D.) in a relevant life sciences field or other ...
... in fields such as Biotechnology, Life Sciences, Biomedical Sciences, Economics, Business, or related fields * Advanced degree (Master's, PharmD, or Ph.D.) in a relevant life sciences field or other ...
Chicago, IL · On-site
$104.50 - $325/hr
Draft, review, and negotiate a high volume of commercial agreements, including Master Services ... Prior in-house experience within a pharmaceutical, biotech, or life sciences company. * Experience ...
Chicago, IL · On-site
$104.50 - $325/hr
Draft, review, and negotiate a high volume of commercial agreements, including Master Services ... Prior in-house experience within a pharmaceutical, biotech, or life sciences company. * Experience ...
Chicago, IL · On-site +1
$309K/yr
Draft, review, and negotiate a high volume of commercial agreements, including Master Services ... Prior in-house experience within a pharmaceutical, biotech, or life sciences company. * Experience ...
Chicago, IL · On-site +1
$309K/yr
Draft, review, and negotiate a high volume of commercial agreements, including Master Services ... Prior in-house experience within a pharmaceutical, biotech, or life sciences company. * Experience ...
Deerfield, IL · On-site
$150 - $190/hr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Master's degree and 5 years of sales analytics, field effectiveness or life sciences management ...
Deerfield, IL · On-site
$150 - $190/hr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Master's degree and 5 years of sales analytics, field effectiveness or life sciences management ...
Chicago, IL · On-site
$160 - $200/hr
Conduct audits, including Internal, Investigator Site and Trial Master File. * Host and support ... Preferred 5+ years of experience in a Leadership role at a CRO, biotech, or pharma company. * 10+ ...
Chicago, IL · On-site
$160 - $200/hr
Conduct audits, including Internal, Investigator Site and Trial Master File. * Host and support ... Preferred 5+ years of experience in a Leadership role at a CRO, biotech, or pharma company. * 10+ ...
$15.25 - $18.25/hr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Master's degreeOR Bachelor's degree and 2 years of consulting/competitive intelligence/biopharma ...
$15.25 - $18.25/hr
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Master's degreeOR Bachelor's degree and 2 years of consulting/competitive intelligence/biopharma ...
... biotech R&D environments, serving as a subject matter expert on life sciences construction strategies. Preconstruction * Assist in the development of the master project schedule and procurement of ...
... biotech R&D environments, serving as a subject matter expert on life sciences construction strategies. Preconstruction * Assist in the development of the master project schedule and procurement of ...
... biotech R&D environments, serving as a subject matter expert on life sciences construction strategies. Preconstruction * Assist in the development of the master project schedule and procurement of ...
Quick apply
... biotech R&D environments, serving as a subject matter expert on life sciences construction strategies. Preconstruction * Assist in the development of the master project schedule and procurement of ...
... biotech R&D environments, serving as a subject matter expert on life sciences construction strategies. Preconstruction * Assist in the development of the master project schedule and procurement of ...
... biotech R&D environments, serving as a subject matter expert on life sciences construction strategies. Preconstruction * Assist in the development of the master project schedule and procurement of ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Doctorate degree and 2 years of related experience OR Master's degree and 4 years of related ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... Doctorate degree and 2 years of related experience OR Master's degree and 4 years of related ...
Chicago, IL · On-site
$133K/yr
... master and directly contribute code to our existing backend test frameworks. • Act as a ... Preferred : • Previous experience in a regulated industry (Healthcare, MedTech, or BioTech). • ...
Chicago, IL · On-site
$133K/yr
... master and directly contribute code to our existing backend test frameworks. • Act as a ... Preferred : • Previous experience in a regulated industry (Healthcare, MedTech, or BioTech). • ...
Chicago, IL · On-site
$135K - $210K/yr
Master Degree in Mechanical Engineering and 6 years mechanical engineering experience. EPC project ... Biotech). * Experience with cGMP manufacturing environments and FDA/USDA, EMA regulations.
Chicago, IL · On-site
$135K - $210K/yr
Master Degree in Mechanical Engineering and 6 years mechanical engineering experience. EPC project ... Biotech). * Experience with cGMP manufacturing environments and FDA/USDA, EMA regulations.
Chicago, IL · On-site
$135K - $210K/yr
Master Degree in Mechanical Engineering and 6 years mechanical engineering experience. EPC project ... Biotech). * Experience with cGMP manufacturing environments and FDA/USDA, EMA regulations.
Chicago, IL · On-site
$135K - $210K/yr
Master Degree in Mechanical Engineering and 6 years mechanical engineering experience. EPC project ... Biotech). * Experience with cGMP manufacturing environments and FDA/USDA, EMA regulations.
... biotechnology? AtBeckman Coulter Diagnostics, one ofDanaher's15+ operating companies, our work ... Master's degree in Engineering,Operations,or Business. * Certifications such as CMRP, CRE, PMP, or ...
... biotechnology? AtBeckman Coulter Diagnostics, one ofDanaher's15+ operating companies, our work ... Master's degree in Engineering,Operations,or Business. * Certifications such as CMRP, CRE, PMP, or ...
Solves difficult and highly complex technical issues in an evolving regulatory climate. Qualifications * PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree ...
Solves difficult and highly complex technical issues in an evolving regulatory climate. Qualifications * PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree ...
Solves difficult and highly complex technical issues in an evolving regulatory climate. Qualifications * PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree ...
Quick apply
Solves difficult and highly complex technical issues in an evolving regulatory climate. Qualifications * PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree ...
North Chicago, IL · On-site
$206K/yr
Solves difficult and highly complex technical issues in an evolving regulatory climate. Qualifications * PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree ...
North Chicago, IL · On-site
$206K/yr
Solves difficult and highly complex technical issues in an evolving regulatory climate. Qualifications * PhD with at least 15 years of relevant pharma/biotech industry experience or master's degree ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... experience OR Master's degree and 4 years of sales analytics, field effectiveness, management ...
Since 1980, we've helped pioneer the world of biotech in our fight against the world's toughest ... experience OR Master's degree and 4 years of sales analytics, field effectiveness, management ...
... biotech industries. Validation Specialists develop and execute C&Q protocols (e.g., IQ/OQ/PQ) for ... Develop project Commissioning and Validation Master Plans (CVMP) that describe C&Q scope, intent ...
... biotech industries. Validation Specialists develop and execute C&Q protocols (e.g., IQ/OQ/PQ) for ... Develop project Commissioning and Validation Master Plans (CVMP) that describe C&Q scope, intent ...
| Criteria | Master In Biotechnology | Biotechnology Research Associate |
|---|---|---|
| Required Credentials | Master's degree in Biotechnology or related field | Bachelor's or Master's degree in Biotechnology or related field |
| Work Environment | Laboratories, research facilities, academic institutions | Laboratories, biotech companies, research organizations |
| Employer & Industry Usage | Academic, research, biotech industry | Biotech companies, research labs, pharmaceutical firms |
| Common Search & Comparison | Yes | Yes |
The Master In Biotechnology typically prepares individuals for advanced roles in research, development, and academia, requiring a master's degree. A Biotechnology Research Associate usually holds a bachelor's or master's degree and works directly in research projects within biotech companies or labs. While both roles involve laboratory work and research, the Master's degree often leads to more senior or specialized positions.
The top searched job categories for Master In Biotechnology jobs in Deerfield, IL are:
Cities near Deerfield, IL with the most Master In Biotechnology job openings:

$55 - $65/hr
Contractor
Posted 12 days ago
Position: Lead Validation Specialist
Type: Contract to hire, no sponsorship available currently, NO third party representation
Duration: 12+ months contract to hire
Location: Mundelein, IL 60060 (regional travel as projects require) onsite daily
Pay rate $55.00 - $65.00 per hour - must be able to accept a permanent position
I am looking for a Lead Validation Specialist coming from the food, biotechnology or pharmaceutical industry that can support commissioning, qualification, and validation (C&Q) initiatives across facilities, utilities, equipment, and automated systems.
This is a hands-on senior validation specialist role with leadership responsibility—ideal for someone who enjoys owning validation strategy, interfacing with clients and auditors, and mentoring junior validation specialists.
OVERVIEW OF RESPONSIBILITIES
• Lead and execute IQ/OQ/PQ activities for facilities, utilities, equipment, control systems, and HVAC
• Conduct cGMP audits, gap assessments, and impact analyses to scope validation work
• Develop system specifications aligned with GAMP and Good Engineering Practices (GEP)
• Author and manage Commissioning & Validation Master Plans (CVMPs)
• Coordinate with OEMs, construction managers, contractors, and end users during commissioning and qualification
• Build and maintain Traceability Matrices (UR/FS/DS → IQ/OQ/PQ)
• Author Summary Reports and defend validation outcomes during audits and inspections
• Lead validation staff and support their professional development
• Manage multiple projects simultaneously, balancing scope, schedule, and quality
QUALIFICATIONS
• Bachelor’s degree in Engineering, Science, or Technical discipline with 5–7 years in an FDA-regulated environment
OR
an Associate degree / military / technician background with 7–10 years regulated industry experience
• Must have working knowledge of FDA regulations, cGMP, and GAMP - Food, Pharma or Biotech industry experience
• Experience reviewing P&IDs, wiring diagrams, HVAC/mechanical drawings, and specifications
must have experience as a Validation Engineer or
• Comfortable using field measurement and verification instrumentation
• Excellent technical writing, communication, and client-facing skills
• Proven ability to manage scope, change control, and problem resolution