Mount Prospect, IL · On-site
$18.75 - $23.75/hr
Knowledge, Skills, Abilities • Ability to function in a dynamic environment and balance multiple priorities simultaneously. • Experience with Quality Systems (Change Control, deviations ...
Mount Prospect, IL · On-site
$18.75 - $23.75/hr
Knowledge, Skills, Abilities • Ability to function in a dynamic environment and balance multiple priorities simultaneously. • Experience with Quality Systems (Change Control, deviations ...
Wood Dale, IL · On-site
$100K - $130K/yr
Lead Change Review Board (CRB) and change control governance * Implement and maintain a risk-based change control framework * Ensure consistent application across teams and functions Supplier Quality
Wood Dale, IL · On-site
$100K - $130K/yr
Lead Change Review Board (CRB) and change control governance * Implement and maintain a risk-based change control framework * Ensure consistent application across teams and functions Supplier Quality
Elwood, IL · On-site
$70K - $100K/yr
Disciplined approach to change control: backups before changes, approvals, testing prior to production use, documentation, and version control; no unauthorized changes and no safety bypasses.
Elwood, IL · On-site
$70K - $100K/yr
Disciplined approach to change control: backups before changes, approvals, testing prior to production use, documentation, and version control; no unauthorized changes and no safety bypasses.
... Change Control • PPAP/FAI Documentation & Validation • Data Accuracy & Validation • Technical Documentation, • Cross-functional Coordination
... Change Control • PPAP/FAI Documentation & Validation • Data Accuracy & Validation • Technical Documentation, • Cross-functional Coordination
Northbrook, IL · On-site
$25 - $30/hr
... change control. Maintain QC laboratory supplies/internal reagents and the integrity and cleanliness of QC work areas. Participate in QC processes to support new product design transfer, process ...
Northbrook, IL · On-site
$25 - $30/hr
... change control. Maintain QC laboratory supplies/internal reagents and the integrity and cleanliness of QC work areas. Participate in QC processes to support new product design transfer, process ...
Northbrook, IL · On-site
$25 - $30/hr
... change control. Maintain QC laboratory supplies/internal reagents and the integrity and cleanliness of QC work areas. Participate in QC processes to support new product design transfer, process ...
Northbrook, IL · On-site
$25 - $30/hr
... change control. Maintain QC laboratory supplies/internal reagents and the integrity and cleanliness of QC work areas. Participate in QC processes to support new product design transfer, process ...
Rockford, IL · On-site
Design Change Control * PPAP/FAI Documentation & Validation * Data Accuracy & Validation * Technical Documentation, * Cross-functional Coordination
Rockford, IL · On-site
Design Change Control * PPAP/FAI Documentation & Validation * Data Accuracy & Validation * Technical Documentation, * Cross-functional Coordination
North Chicago, IL · On-site
This role will focus on packaging design, change control, technical documentation, supplier collaboration, testing activities, and continuous improvement initiatives. Key Responsibilities * Develop ...
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North Chicago, IL · On-site
This role will focus on packaging design, change control, technical documentation, supplier collaboration, testing activities, and continuous improvement initiatives. Key Responsibilities * Develop ...
Chicago, IL · On-site
$25 - $31.25/hr
Experience with SOP Revision, Change Control, CAPAs, Deviations, Investigations, and Batch Record Review. * AS or BS Degree required. Skills * Root Cause Analysis and/or investigation writing ...
Chicago, IL · On-site
$25 - $31.25/hr
Experience with SOP Revision, Change Control, CAPAs, Deviations, Investigations, and Batch Record Review. * AS or BS Degree required. Skills * Root Cause Analysis and/or investigation writing ...
Chicago, IL · On-site +1
$110K - $120K/yr
Establish and manage change control procedures * Ensure quality systems always remain audit-ready Current Good Manufacturing Process (cGMP) Compliance (21 CFR 111): * Ensure Supergut maintains ...
Chicago, IL · On-site +1
$110K - $120K/yr
Establish and manage change control procedures * Ensure quality systems always remain audit-ready Current Good Manufacturing Process (cGMP) Compliance (21 CFR 111): * Ensure Supergut maintains ...
Responsible for compliant change control of documentation and labeling including new and revised procedures, department SOPs, manufacturing specifications and domestic labeling artwork, outside ...
Responsible for compliant change control of documentation and labeling including new and revised procedures, department SOPs, manufacturing specifications and domestic labeling artwork, outside ...
Chicago, IL · On-site
Pillar 2: IT General Controls Adherence The Technology Change Manager supports HUB's change management control environment by ensuring that change activities comply with established IT General ...
Chicago, IL · On-site
Pillar 2: IT General Controls Adherence The Technology Change Manager supports HUB's change management control environment by ensuring that change activities comply with established IT General ...
Pillar 2: IT General Controls Adherence The Technology Change Manager supports HUB's change management control environment by ensuring that change activities comply with established IT General ...
Pillar 2: IT General Controls Adherence The Technology Change Manager supports HUB's change management control environment by ensuring that change activities comply with established IT General ...
Drive lifecycle design change projects in accordance with Design Control and Change Control requirements * Own change management plans, impact assessments, execution strategies, and closure ...
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Drive lifecycle design change projects in accordance with Design Control and Change Control requirements * Own change management plans, impact assessments, execution strategies, and closure ...
The successful candidate will support equipment qualification, protocol execution, documentation, change control, and validation activities associated with solid dose production and packaging ...
The successful candidate will support equipment qualification, protocol execution, documentation, change control, and validation activities associated with solid dose production and packaging ...
$69K - $90K/yr
... complaints, change control, audit processes, standard procedures, test methods, and process controls. * Ensure Business Unit systems are tied into corporate standards via continual reviews and ...
$69K - $90K/yr
... complaints, change control, audit processes, standard procedures, test methods, and process controls. * Ensure Business Unit systems are tied into corporate standards via continual reviews and ...
$69K - $90K/yr
... complaints, change control, audit processes, standard procedures, test methods, and process controls. * Ensure Business Unit systems are tied into corporate standards via continual reviews and ...
$69K - $90K/yr
... complaints, change control, audit processes, standard procedures, test methods, and process controls. * Ensure Business Unit systems are tied into corporate standards via continual reviews and ...
Familiarity with eQMS and RIM capabilities such as document control, training, deviations, CAPA, change control, audits, complaints, supplier quality, and submission/product registration data ...
Familiarity with eQMS and RIM capabilities such as document control, training, deviations, CAPA, change control, audits, complaints, supplier quality, and submission/product registration data ...
Hoffman Estates, IL · On-site
Change Control: Managing changes to project scope, schedule, or resources through formal change control processes to minimize scope creep and maintain project alignment with business goals. Post ...
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Hoffman Estates, IL · On-site
Change Control: Managing changes to project scope, schedule, or resources through formal change control processes to minimize scope creep and maintain project alignment with business goals. Post ...
The position is key to consistent product quality by driving specification governance, change control, and data integrity across internal systems and client portals for both food and OTC drug ...
The position is key to consistent product quality by driving specification governance, change control, and data integrity across internal systems and client portals for both food and OTC drug ...
$41.9K is the 25th percentile. Wages below this are outliers.
$37.8K - $45.3K
46% of jobs
$45.3K - $52.9K
0% of jobs
$52.9K - $60.4K
0% of jobs
$60.4K - $67.9K
0% of jobs
$67.9K - $75.5K
0% of jobs
$75.5K - $83K
0% of jobs
$83K - $90.5K
0% of jobs
The median wage is $92.1K / yr.
$90.5K - $98K
18% of jobs
$98K - $105.6K
5% of jobs
$105.6K - $113.1K
5% of jobs
$113.3K is the 75th percentile. Wages above this are outliers.
$113.1K - $120.6K
26% of jobs
$37.8K
$79.6K
$120.6K
Professionals in Change Control often face challenges like managing competing priorities, coordinating changes across multiple teams, and ensuring proper documentation for audit purposes. They must be prepared to handle urgent change requests while minimizing potential disruptions to business operations. Strong communication skills and a systematic approach are crucial to navigate these challenges effectively. By anticipating potential risks and organizing thorough reviews, Change Control specialists help maintain system stability and compliance while supporting organizational growth.
To thrive in a Change Control role, you need thorough knowledge of change management processes, strong organizational skills, and attention to detail, often supported by a degree in business, IT, or a related field. Familiarity with IT Service Management (ITSM) tools such as ServiceNow or BMC Remedy, and certifications like ITIL, are highly valued. Excellent communication, problem-solving, and teamwork abilities help professionals excel at coordinating changes across departments. These skills ensure that changes are implemented smoothly, minimize risk, and support operational continuity.
A Change Control job involves managing and overseeing changes to processes, systems, or products to ensure they are implemented efficiently with minimal risk. Professionals in this role assess change requests, coordinate approvals, and document modifications to maintain compliance and operational stability. They often work in regulated industries like pharmaceuticals, IT, and manufacturing where controlled changes are crucial. Effective change control helps minimize disruptions, ensures regulatory adherence, and maintains product or service quality.
$18.75 - $23.75/hr
Other
Re-posted 20 days ago
QC Technician - Entry Level
• When you're part of the team at Thermo Fisher Scientific, you'll do important work, like helping customers in finding cures for cancer, protecting the environment, or making sure our food is safe. Your work will have a real-world impact, and you'll be supported in achieving your career goals.
Location/Division Specific Information
• Clinical Trials Division (CTD) partners with pharmaceutical and biotech customers around the world to ensure the right patients get the right therapies in the right doses at the right time - a concept that we internally accept as "There is a Patient Waiting." Our outstanding blend of services includes project management, packaging, distribution, transportation management and specialty logistics, ancillary supply management, clinical supply optimization, bio-repository storage and much more. Our more than 3,000 employees in over 15 countries work hard every day knowing that what they do matters.
What will you do?
• Follows all Thermo Fisher SOPs (standard operating procedure) and performs job responsibilities in a safe and efficient manner.
• Performs process inspections, samplings, and audits
• Participates in continuous improvement initiatives and assists with root cause investigations for nonconforming issues.
• Review production orders to verify all information is accurate per applicable reference documents and align with all customer requirements.
• Review/Approve label part number item specifications to guarantee the information contained within is accurate and stays in sync with requirements.
• Other duties may be assigned to meet business needs.
How will you get here?
• Associates degree and/or equivalent work experience.
Experience
• Good reasoning and problem-solving skills, basic math skills, good interpersonal skills, basic digital literacy.
• 1-2 years experience in Pharmaceutical or of a related field, preferably in a regulated industry.
Knowledge, Skills, Abilities
• Ability to function in a dynamic environment and balance multiple priorities simultaneously.
• Experience with Quality Systems (Change Control, deviations, complaint management, documentation management, among others).
• Ability to work independently or as part of a team, self-motivated, adaptable.
• Proficient in Microsoft Office including Word, Excel, Access, and Outlook. Knowledge or prior experience with Current Good Manufacturing Practices (cGMP) for pharmaceutical products.
Additional Sills: Skills:
Category
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