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HomeCompaniesCareers Alcami Icims ComSr. Quality Assurance Specialist

Sr. Quality Assurance Specialist

Careers Alcami Icims Com · Morrisville, NC, US · On Site · Active · iCIMS

Job facts

FieldValue
CompanyCareers Alcami Icims Com
TitleSr. Quality Assurance Specialist
Normalized title-
Department / teamQuality Assurance
LocationMorrisville, NC, United States
Work modelOn Site
Employment typeFull Time
Salary-
Statusactive
ATS provideriCIMS
Posted / first seen2026-04-30 / 2026-05-31
Changed / last seen2026-06-01 / 2026-06-06

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Linked records

CompanyCareers Alcami Icims Com
Source616edbfb-b00b-461b-b6c9-d3f996abfb46
ATS provideriCIMS

Description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures. These activities may include reviewing documents and data, conducting audits and inspections, hosting audits and inspections, and maintaining quality databases. The ideal candidate will assist internal teammates and partner with individuals from other departments for the development of SOPs and associated documents, and process improvements. The Sr. Quality Assurance Specialist will provide guidance and mentoring to Operations personnel in achieving a high level of GMP compliance and instilling quality culture. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday, 8:00am - 5:00pm. Responsibilities Performs quality review and approval of documents, data, protocols, and/or reports. Performs GMP document creation and issuance (batch records, logbooks, forms, etc.). Performs visual inspection of parenteral product (requires qualification). Performs internal quality audits and/or inspections. Supports client audits and inspections, and regulatory inspections. Maintains quality databases. Assists with implementation and supports quality systems, including but not limited to, operations support, batch review and approval, training, vendor management, and overall regulatory inspectional readiness. Assists with quality improvement initiatives as needed. Consults with clients on production and documentation. Assists with development of SOPs or other quality documents. Maintains accurate files and records. Serves as an effective member of the Quality Assurance team and may serve as a mentor to others in area of expertise. Complies with company polices and SOPs. Ensures timely completion and compliance with cGMP and all other relevant company training requirements. Other duties as assigned. Qualifications Bachelor’s degree in Chemistry, Biology, or related field with 10+ years of GMP related experience, or Master’s degree in related field. Minimum five years of related work experience. Knowledge, Skills, and Abilities Aseptic parenteral manufacturing. Grade C gowning. GMP and Annex 1 experience. 20/20 corrected vision for Visual Inspector qualification. Travel Expectations Rarely may be requested to travel to support other Alcami sites. Physical Demands and Work Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and the risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.

Full job record

Job IDa3e3606321d205ddee7a0fc79d8a284d4dc3b637
Org IDb460a007-52d3-42ae-8629-2d277c0dc6c6
Source ID616edbfb-b00b-461b-b6c9-d3f996abfb46
Board ID616edbfb-b00b-461b-b6c9-d3f996abfb46
Providericims
Provider Job Key2070
TitleSr. Quality Assurance Specialist
Normalized Title
Statusactive
Activeyes
Location TextMorrisville, NC, US
DepartmentQuality Assurance
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionNC
CityMorrisville
Salary RawAt Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record. Are you interested in joining our team? Job Summary The Senior Quality Assurance Specialist is accountable for driving results in a fast-paced environment by effectively performing activities as directed to ensure quality and compliance with applicable regulatory requirements and internal procedures. These activities may include reviewing documents and data, conducting audits and inspections, hosting audits and inspections, and maintaining quality databases. The ideal candidate will assist internal teammates and partner with individuals from other departments for the development of SOPs and associated documents, and process improvements. The Sr. Quality Assurance Specialist will provide guidance and mentoring to Operations personnel in achieving a high level of GMP compliance and instilling quality culture. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday, 8:00am - 5:00pm. Responsibilities Performs quality review and approval of documents, data, protocols, and/or reports. Performs GMP document creation and issuance (batch records, logbooks, forms, etc.). Performs visual inspection of parenteral product (requires qualification). Performs internal quality audits and/or inspections. Supports client audits and inspections, and regulatory inspections. Maintains quality databases. Assists with implementation and supports quality systems, including but not limited to, operations support, batch review and approval, training, vendor management, and overall regulatory inspectional readiness. Assists with quality improvement initiatives as needed. Consults with clients on production and documentation. Assists with development of SOPs or other quality documents. Maintains accurate files and records. Serves as an effective member of the Quality Assurance team and may serve as a mentor to others in area of expertise. Complies with company polices and SOPs. Ensures timely completion and compliance with cGMP and all other relevant company training requirements. Other duties as assigned. Qualifications Bachelor’s degree in Chemistry, Biology, or related field with 10+ years of GMP related experience, or Master’s degree in related field. Minimum five years of related work experience. Knowledge, Skills, and Abilities Aseptic parenteral manufacturing. Grade C gowning. GMP and Annex 1 experience. 20/20 corrected vision for Visual Inspector qualification. Travel Expectations Rarely may be requested to travel to support other Alcami sites. Physical Demands and Work Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this job, the employee is frequently exposed to moving mechanical parts and the risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc.
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://careers-alcami.icims.com/jobs/2070/sr.-quality-assurance-specialist/job
Apply URLhttps://careers-alcami.icims.com/jobs/2070/sr.-quality-assurance-specialist/job
First Seen At2026-05-31 18:42:15Z
Last Seen At2026-06-06 20:31:42Z
Last Checked At2026-06-06 20:31:42Z
Last Changed At2026-06-01 13:53:34Z
Inactive At
Source Posted At2026-04-30 04:00:00Z
Source Updated At2026-04-30 14:10:58Z
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=icims/board=careers-alcami.icims.com/date=2026-06-06/2026-06-06T20-31-40-867Z-a2db2b794777dfa2fd89f24c61b1d5baa8291c7214447c7ab3299280541feba0.json
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Parsed Structured
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