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HomeCompaniesCareers Alcami Icims ComStability Coordinator I

Stability Coordinator I

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

Job facts

FieldValue
CompanyCareers Alcami Icims Com
TitleStability Coordinator I
Normalized title-
Department / teamStability
LocationGarner, NC, United States
Work modelOn Site
Employment typeFull Time
Salary-
Statusactive
ATS provideriCIMS
Posted / first seen2026-05-27 / 2026-05-31
Changed / last seen2026-06-01 / 2026-06-06

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City jobsActive postings in Garner.Open
Department jobsActive postings in Stability.Open
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Original postingCanonical source or apply URL captured from the ATS.Open

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 Stability Coordinator I is accountable for driving results in a fast-paced environment by generating protocols and facilitating the log in of samples and projects for lab documentation and reporting of data for client stability programs. This position provides administrative and organizational support related to stability storage activities, including protocol generation, sample receipt, inventory, login for testing, transfer/shipment, and storage. The ideal candidate will maintain electronic documentation and files to assure they are accurate and up-to-date and available to appropriate personnel. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday, 8:00am - 4:30pm. Responsibilities Uses multiple computer software programs to log in / generate projects for laboratory testing. Manage projects, and to maintain stability sample status, pull point, and testing requirements. Manages and maintains testing requirements in electronic systems per the approved stability protocols and revisions. Generates and reviews stability storage protocols, outlining schedule and required testing. Receives incoming samples for stability storage and initiates chain-of-custody tracking in electronic inventory. Completes stability sample pulls and prepares both internal and external shipment of samples for shipment. Supports client notification for sample destruction & prepares dispositioned samples for pickup. This position may be required to complete, organize, and maintain DEA Form 222 and internal company documentation for receipt, transfer, and shipment of controlled substances in accordance with current Alcami and DEA standards. Additional requirements may include support of controlled substances accountability activities, including regular inventory and documentation review. Responds to the environmental monitoring system for stability chambers. Supports stability inventory maintenance and routine review. Performs documentation accurately and completely. Complies with safety policies and procedures. Communicates and collaborates routinely with other departments and clients. Ensures timely completion and compliance with cGMP, EHS, DEA, and all other relevant company training requirements. Other duties as assigned. Qualifications Bachelor’s degree with 0-2+ years of related experience (2 years preferred) or high school diploma/ GED with a minimum of 4+ years of related experience required. Bachelor’s degree in Pharmaceutical Sciences, Chemistry or equivalent preferred. Prior cGMP experience preferred. Laboratory experience and/or experience with compendial testing is preferred, as this experience provides a solid foundation for the technical aspects of project creation and management. Knowledge, Skills, and Abilities Ability to multi-task with high attention to detail skills required. Working knowledge of computer-based networks and document management systems preferred. Strong understanding of pharmaceutical manufacturing and testing preferred. Working knowledge of cGMP in a pharmaceutical or regulated environment preferred. Excellent verbal and written communications and presentation skills required. Proficiency with Microsoft Office (Word, Excel, PowerPoint) required. Self-motivated, reliable, detail-oriented, and a proactive team contributor. Travel Expectations Up to 5% travel required. 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 sit. The employee is occasionally required to stand; walk 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 occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet. While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock 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, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle.

Full job record

Job ID45fd15025ed78d8f6c79df0cfd15debbc6897fc1
Org IDb460a007-52d3-42ae-8629-2d277c0dc6c6
Source ID616edbfb-b00b-461b-b6c9-d3f996abfb46
Board ID616edbfb-b00b-461b-b6c9-d3f996abfb46
Providericims
Provider Job Key1945
TitleStability Coordinator I
Normalized Title
Statusactive
Activeyes
Location TextGarner, NC, US
DepartmentStability
Team
Employment Typefull_time
Workplace Typeon_site
Remote Policy
CountryUnited States
RegionNC
CityGarner
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 Stability Coordinator I is accountable for driving results in a fast-paced environment by generating protocols and facilitating the log in of samples and projects for lab documentation and reporting of data for client stability programs. This position provides administrative and organizational support related to stability storage activities, including protocol generation, sample receipt, inventory, login for testing, transfer/shipment, and storage. The ideal candidate will maintain electronic documentation and files to assure they are accurate and up-to-date and available to appropriate personnel. On-Site Expectations 100% on-site position. 1st Shift: Monday - Friday, 8:00am - 4:30pm. Responsibilities Uses multiple computer software programs to log in / generate projects for laboratory testing. Manage projects, and to maintain stability sample status, pull point, and testing requirements. Manages and maintains testing requirements in electronic systems per the approved stability protocols and revisions. Generates and reviews stability storage protocols, outlining schedule and required testing. Receives incoming samples for stability storage and initiates chain-of-custody tracking in electronic inventory. Completes stability sample pulls and prepares both internal and external shipment of samples for shipment. Supports client notification for sample destruction & prepares dispositioned samples for pickup. This position may be required to complete, organize, and maintain DEA Form 222 and internal company documentation for receipt, transfer, and shipment of controlled substances in accordance with current Alcami and DEA standards. Additional requirements may include support of controlled substances accountability activities, including regular inventory and documentation review. Responds to the environmental monitoring system for stability chambers. Supports stability inventory maintenance and routine review. Performs documentation accurately and completely. Complies with safety policies and procedures. Communicates and collaborates routinely with other departments and clients. Ensures timely completion and compliance with cGMP, EHS, DEA, and all other relevant company training requirements. Other duties as assigned. Qualifications Bachelor’s degree with 0-2+ years of related experience (2 years preferred) or high school diploma/ GED with a minimum of 4+ years of related experience required. Bachelor’s degree in Pharmaceutical Sciences, Chemistry or equivalent preferred. Prior cGMP experience preferred. Laboratory experience and/or experience with compendial testing is preferred, as this experience provides a solid foundation for the technical aspects of project creation and management. Knowledge, Skills, and Abilities Ability to multi-task with high attention to detail skills required. Working knowledge of computer-based networks and document management systems preferred. Strong understanding of pharmaceutical manufacturing and testing preferred. Working knowledge of cGMP in a pharmaceutical or regulated environment preferred. Excellent verbal and written communications and presentation skills required. Proficiency with Microsoft Office (Word, Excel, PowerPoint) required. Self-motivated, reliable, detail-oriented, and a proactive team contributor. Travel Expectations Up to 5% travel required. 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 sit. The employee is occasionally required to stand; walk 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 occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet. While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock 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, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle.
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://careers-alcami.icims.com/jobs/1945/stability-coordinator-i/job
Apply URLhttps://careers-alcami.icims.com/jobs/1945/stability-coordinator-i/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 At2026-05-27 04:00:00Z
Source Updated At2026-03-25 15:39:45Z
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
Event Fields
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Parsed Structured
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Extensions
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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 sit. The employee is occasionally required to stand; walk 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 occasionally exposed to moving mechanical parts and vibration. 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