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HomeCompanies2ef40f78 78c9 4e4f 8c8f 7a5add703ae0 19000101 000001Quality Control Manager

Quality Control Manager

2ef40f78 78c9 4e4f 8c8f 7a5add703ae0 19000101 000001 · Woodstock, IL, US, Woodstock, IL · Active · $95,000–$138,000 / year · ADP Workforce Now Recruiting

Job facts

FieldValue
Company2ef40f78 78c9 4e4f 8c8f 7a5add703ae0 19000101 000001
TitleQuality Control Manager
Normalized title-
Department / team-
LocationWoodstock, IL, United States
Work model-
Employment typeFull Time
Salary$95,000–$138,000 / year
Statusactive
ATS providerADP Workforce Now Recruiting
Posted / first seen2026-04-21 / 2026-05-31
Changed / last seen2026-06-19 / 2026-06-19

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PageWhat it containsOpen
Company jobsActive postings from 2ef40f78 78c9 4e4f 8c8f 7a5add703ae0 19000101 000001.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through ADP Workforce Now Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in Woodstock.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

Company2ef40f78 78c9 4e4f 8c8f 7a5add703ae0 19000101 000001
Source783a76fe-5da3-4e0a-ac6a-e56005a04b8e
ATS providerADP Workforce Now Recruiting

Description

Woodstock Sterile Solutions is driven to positively impact global healthcare by providing our partners the best quality solutions to their sterile development and commercial needs. We are a growing organization with a bright future, and we are looking for motivated and experienced team members. We offer a comprehensive benefits and a generous Paid Time Off package. I. Position Overview: We are seeking a dynamic and experienced Quality Control (QC) Manager to lead our Chemistry, Incoming Quality Assurance (IQA) and Stability functions in a fast-paced, cGMP-regulated environment. This is a high-impact leadership role responsible for ensuring compliant, efficient, and timely laboratory operations that directly support manufacturing, product release, stability and overall business performance. The ideal candidate will bring strong leadership experience within a CDMO setting, with a demonstrated ability to manage high-volume testing operations while maintaining strict adherence to regulatory and quality standards. This role requires a hands-on leader who can develop, empower and mentor teams, drive operational excellence, and foster a culture of accountability, safety, and continuous improvement. As a key member of the Quality organization, the QC Manager will play a critical role in ensuring inspection readiness and will serve as a primary representative during customer visits, customer audits and regulatory inspections. Success in this role requires the ability to balance strategic oversight with day-to-day execution, collaborate cross-functionally, and deliver consistent, high-quality on time results in a demanding production environment. The position is responsible for managing all Chemistry, IQA, Stability and method validation /transfer/development departmental activities, including staffing, training and development of staff. Manage departments to ensure products are inspected, sampled, tested and controlled within applicable requirements and quality standards in accordance with business timelines. The laboratory supports manufacturing by testing and releasing raw materials, batch and first acceptable samples, cleaning samples, finished product and stability product. The QC Manager will support New Product Introduction, New Product Development (NPD), Validation and Operations groups with testing or technical expertise. Responsible for providing key leadership, direction, organization, management, monitoring and cGMP compliance of the roles, activities and proceedings of all assigned Chemistry and Incoming Quality Assurance and other selected Quality personnel in order to ensure compliant, cost effective, timely and safe routine testing, stability testing and project support. II. Specific Duties, Activities, and Responsibilities: • Support Manufacturing from a technical perspective. • Drive site improvements from a Chemistry, Stability and IQA perspective. • Serve as resident expert in chemistry testing, method development/validation/transfer, stability and Incoming QA testing requirements. • Direct quality and compliance process improvements and goals in the laboratories and Incoming QA for the site using current regulations and best-demonstrated practices. • Support effective and efficient continuous quality and cost improvement efforts in the laboratories. • Hire, develop and conduct regular performance management activities including goal setting and Performance Reviews to assure highly effective, team-oriented contributors. • Ensure all personnel receive necessary and appropriate training for their job function. • Effectively manage employee relations including hiring, discipline, rewards and recognition, and effective human capital resources allocation. • Participate in customer meetings, customer audits and regulatory inspections and inquiries. • Ensure chemistry testing and NPD project deliverables are executed successfully and on time. • Develop and achieve annual budget for laboratory operations. • Review CMC sections, technical reports, validation reports, method validation reports, specifications, procedures and SOPs. • Collaborate with other groups, activities necessary to ensure project requirements and timelines are met. • Support New Product Introduction activities. • Support and manage method transfer, method validation and method development efforts in line with customer expectations and timelines. • Identify, evaluate, and manage risk to ensure product quality. III. Position Requirements: Education or Equivalent: • BS degree in chemistry, relevant science or equivalent work experience. Experience: • Minimum 10 years of applicable experience in the industry or equivalent combination of education and experience. • Minimum 5 years of formal laboratory management (manager level or higher). Knowledge/Skills Requirements: • Ability to achieve and meet the expected throughput and financial goals of the organization. • Must demonstrate strategic thinking abilities. • Must be able to perform risk assessments in a timely manner and act accordingly. • Possess and demonstrate excellent verbal, written, and interpersonal communications skills. • Strong problem solving and analytical skills. • Strong ability to demonstrate ability to read, understand, interpret and apply technical writing skills and instructions. • Organized and able to multitask. • Detail-oriented. • Proven initiative and self-starter skills. • Must possess and demonstrate knowledge and experience in regulatory standards, cGMPs and relevant Safety Regulations including ISO, ICH, USP, EP and FDA. • Must be able to interact effectively with a variety of individuals within and between departments. • Excellent problem solving and analytical skills. including root cause analysis trouble-shooting experience. • A full complement of business computer literacy skills (e.g., word processing, spreadsheets, database software, LIMs, etc.) is preferred. • Demonstrated ability to read, write, and speak clear English. Physical Requirements: • Frequent sitting, standing, walking, reading written documents and use of computer monitor screen, talking, writing, listening. • Occasional climbing ladders/steps, walking up inclines and uneven terrain, reaching with hands and arms, stooping, kneeling, crouching, crawling, twisting, bending, handling, turning, balancing, carrying, grasping. • Occasional lifting and/or moving up to 30 pounds. Notice to Agency and Search Firm Representatives: Woodstock Sterile Solutions is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Woodstock Sterile Solutions employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Woodstock Sterile Solutions. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Full job record

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Org ID34ec68d1-c3de-4239-9108-272722e146c2
Source ID783a76fe-5da3-4e0a-ac6a-e56005a04b8e
Board ID783a76fe-5da3-4e0a-ac6a-e56005a04b8e
Provideradp_workforcenow
Provider Job Key593065
TitleQuality Control Manager
Normalized Title
Statusactive
Activeyes
Location TextWoodstock, IL, US, Woodstock, IL
Department
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Employment Typefull_time
Workplace Type
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CountryUnited States
RegionIL
CityWoodstock
Salary Raw95000.00 To 138000.00 (USD) Annually
Salary Min95,000
Salary Max138,000
Salary CurrencyUSD
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First Seen At2026-05-31 18:37:48Z
Last Seen At2026-06-19 12:34:37Z
Last Checked At2026-06-19 12:34:37Z
Last Changed At2026-06-19 12:34:37Z
Inactive At
Source Posted At2026-04-21 12:00:00Z
Source Updated At
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    "requisitionDescription": "<div><div><p style=\"line-height: 1;\"><strong>Woodstock Sterile Solutions is driven to positively impact global healthcare by providing our partners the best quality solutions to their sterile development and commercial needs. &nbsp;We are a growing organization with a bright future, and we are looking for motivated and experienced team members. &nbsp;We offer a comprehensive benefits and a generous Paid Time Off package. &nbsp;</strong></p><p data-pasted=\"true\" style=\"line-height: 1;\">I. &nbsp;Position Overview: &nbsp;</p><p style=\"line-height: 1.5;\">We are seeking a dynamic and experienced Quality Control (QC) Manager to lead our Chemistry, Incoming Quality Assurance (IQA) and Stability functions in a fast-paced, cGMP-regulated environment. This is a high-impact leadership role responsible for ensuring compliant, efficient, and timely laboratory operations that directly support manufacturing, product release, stability and overall business performance.</p><p style=\"line-height: 1.5;\">The ideal candidate will bring strong leadership experience within a CDMO setting, with a demonstrated ability to manage high-volume testing operations while maintaining strict adherence to regulatory and quality standards. This role requires a hands-on leader who can develop, empower and mentor teams, drive operational excellence, and foster a culture of accountability, safety, and continuous improvement.</p><p style=\"line-height: 1.5;\">As a key member of the Quality organization, the QC Manager will play a critical role in ensuring inspection readiness and will serve as a primary representative during customer visits, customer audits and regulatory inspections. Success in this role requires the ability to balance strategic oversight with day-to-day execution, collaborate cross-functionally, and deliver consistent, high-quality on time results in a demanding production environment.</p><p style=\"line-height: 1.5;\">The position is responsible for managing all Chemistry, IQA, Stability and method validation /transfer/development departmental activities, including staffing, training and development of staff. &nbsp;Manage departments to ensure products are inspected, sampled, tested and controlled within applicable requirements and quality standards in accordance with business timelines. &nbsp;The laboratory supports manufacturing by testing and releasing raw materials, batch and first acceptable samples, cleaning samples, finished product and stability product.</p><p style=\"line-height: 1.5;\">The QC Manager will support New Product Introduction, New Product Development (NPD), Validation and Operations groups with testing or technical expertise. &nbsp;Responsible for providing key leadership, direction, organization, management, monitoring and cGMP compliance of the roles, activities and proceedings of all assigned Chemistry and Incoming Quality Assurance and other selected Quality personnel in order to ensure compliant, cost effective, timely and safe routine testing, stability testing and project support.</p><p style=\"line-height: 1;\"><br></p><p style=\"line-height: 1;\">II. &nbsp;Specific Duties, Activities, and Responsibilities:</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Support Manufacturing from a technical perspective.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Drive site improvements from a Chemistry, Stability and IQA perspective.&nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Serve as resident expert in chemistry testing, method development/validation/transfer, stability and Incoming QA testing requirements. &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Direct quality and compliance process improvements and goals in the laboratories and Incoming QA for the site using current regulations and best-demonstrated practices.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Support effective and efficient continuous quality and cost improvement efforts in the laboratories.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Hire, develop and conduct regular performance management activities including goal setting and Performance Reviews to assure highly effective, team-oriented contributors.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Ensure all personnel receive necessary and appropriate training for their job function.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Effectively manage employee relations including hiring, discipline, rewards and recognition, and effective human capital resources allocation.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Participate in customer meetings, customer audits and regulatory inspections and inquiries.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Ensure chemistry testing and NPD project deliverables are executed successfully and on time.&nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Develop and achieve annual budget for laboratory operations.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Review CMC sections, technical reports, validation reports, method validation reports, specifications, procedures and SOPs.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Collaborate with other groups, activities necessary to ensure project requirements and timelines are met.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Support New Product Introduction activities.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Support and manage method transfer, method validation and method development efforts in line with customer expectations and timelines.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Identify, evaluate, and manage risk to ensure product quality.&nbsp;</p><p style=\"line-height: 1;\"><br></p><p style=\"line-height: 1;\">III. &nbsp;Position Requirements:</p><p style=\"line-height: 1;\">Education or Equivalent:&nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>BS degree in chemistry, relevant science or equivalent work experience. &nbsp;</p><p style=\"line-height: 1;\">Experience: &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Minimum 10 years of applicable experience in the industry or equivalent combination of education and experience.&nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Minimum 5 years of formal laboratory management (manager level or higher).</p><p style=\"line-height: 1;\">Knowledge/Skills Requirements: &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Ability to achieve and meet the expected throughput and financial goals of the organization.&nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Must demonstrate strategic thinking abilities.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Must be able to perform risk assessments in a timely manner and act accordingly. &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Possess and demonstrate excellent verbal, written, and interpersonal communications skills.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Strong problem solving and analytical skills.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Strong ability to demonstrate ability to read, understand, interpret and apply technical writing skills and instructions.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Organized and able to multitask.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Detail-oriented.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Proven initiative and self-starter skills.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Must possess and demonstrate knowledge and experience in regulatory standards, cGMPs and relevant Safety Regulations including ISO, ICH, USP, EP and FDA. &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Must be able to interact effectively with a variety of individuals within and between departments.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Excellent problem solving and analytical skills. including root cause analysis trouble-shooting experience. &nbsp; &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>A full complement of business computer literacy skills (e.g., word processing, spreadsheets, database software, LIMs, etc.) is preferred.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Demonstrated ability to read, write, and speak clear English.</p><p style=\"line-height: 1;\">Physical Requirements: &nbsp;</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Frequent sitting, standing, walking, reading written documents and use of computer monitor screen, talking, writing, listening.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Occasional climbing ladders/steps, walking up inclines and uneven terrain, reaching with hands and arms, stooping, kneeling, crouching, crawling, twisting, bending, handling, turning, balancing, carrying, grasping.</p><p style=\"line-height: 1;\">&bull;<span style=\"white-space:pre;\">&nbsp; &nbsp;&nbsp;</span>Occasional lifting and/or moving up to 30 pounds.</p><p><br></p><p><em>Notice to Agency and Search Firm Representatives: Woodstock Sterile Solutions is not accepting unsolicited resumes from agencies and/or search firms for this job posting. 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    "requisitionTitle": "Quality Control Manager",
    "clientRequisitionID": "1296",
    "organizationalUnits": [],
    "postingInstructions": [],
    "additionalProperties": {},
    "requisitionLocations": [
      {
        "address": {
          "cityName": "Woodstock",
          "postalCode": "60098",
          "countrySubdivisionLevel1": {
            "codeValue": "IL"
          }
        },
        "nameCode": {
          "shortName": " Woodstock, IL, US"
        },
        "aliasNames": []
      }
    ],
    "screeningRequirements": [],
    "sponsoredVisaTypeCodes": []
  },
  "detail_meta": {
    "url": "https://workforcenow.adp.com/mascsr/default/careercenter/public/events/staffing/v1/job-requisitions/593065?cid=2ef40f78-78c9-4e4f-8c8f-7a5add703ae0&ccId=19000101_000001&lang=en_US&locale=en_US",
    "http_status": 200,
    "content_type": "application/json;charset=UTF-8",
    "response_bytes": 16471
  },
  "detail_errors": []
}
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GET https://api.bluedoor.sh/job-postings/v1/orgs/34ec68d1-c3de-4239-9108-272722e146c2JSON
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