Stability Coordinator I

Alcami Corporation; Kirkland (NC); On-site; USD 45,000 - 60,000; Full time

Job summary

Alcami Corporation is seeking a Stability Coordinator I to drive stability programs and manage project logs for laboratory testing. You will handle protocol generation, sample receipt, inventory, and transfer/shipment while ensuring accurate electronic records and up-to-date files for client programs.

The role emphasizes cGMP compliance, safety training, and cross-department collaboration, with on-site duties and standard day shift expectations. DEA documentation support may be required.

Qualifications

• Bachelor’s degree in Pharmaceutical Sciences or related field preferred.
• 0–2+ years of related experience or 4+ years with a high school diploma.
• Prior cGMP experience preferred and laboratory/documentation background.

Responsibilities

• Log in and generate projects for laboratory testing and stability campaigns.
• Maintain stability storage protocols and revisions in electronic systems.
• Generate and review stability storage protocols including schedules and testing.
• Receive samples for stability storage and initiate chain-of-custody tracking.
• Prepare samples for internal and external shipments.
• Support client notification for sample destruction and disposition.
• Assist with DEA Form 222 and related documented controls per policies.
• Respond to environmental monitoring for stability chambers.
• Maintain stability inventory and perform routine reviews.
• Ensure documentation is accurate, complete, and compliant with safety and training requirements.

Skills

Attention to detail

Multi-tasking

Microsoft Office

Lab documentation

Communication skills

Education

Bachelor's degree in Pharmaceutical Sciences

High school or GED with related experience

Tools

LIMS software

Electronic record systems

Job 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, 8:30am - 5:30pm.

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 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 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.