Sr. Quality Assurance Specialist - 3rd Shift

Alcami Corporation; North Charleston (SC); Presencial; USD 90.000 - 120.000; Jornada completa

Descripción de la vacante

Alcami Corporation in Charleston, SC, seeks a Sr. Quality Assurance Specialist for 3rd shift to uphold GMP compliance and support QA activities. This on-site role involves document reviews, audits, and SOP development.

The ideal candidate holds a Bachelor's degree in Chemistry or Biology and 5+ years of GMP experience, with mentoring responsibilities to Operations personnel.

Formación

• Bachelor's degree in Chemistry, Biology, or related field with GMP experience.
• Experience performing audits and inspections in a GMP environment.
• Strong documentation writing and record-keeping skills.

Responsabilidades

• Performs GMP document creation and issuance (batch records, logbooks, forms).
• Performs quality reviews and approvals of documents, data, and reports.
• Conducts internal quality audits and inspections and supports client/regulatory inspections.
• Maintains quality databases and supports quality systems enhancements.
• Mentors Operations staff to achieve GMP compliance and quality culture.

Conocimientos

GMP expertise

Auditing

Documentation control

Educación

Bachelor's degree in Chemistry, Biology, or related field

Herramientas

QMS software

Descripción del empleo

Sr. Quality Assurance Specialist - 3rd Shift

Job Information

• Location: US-SC-Charleston
• ID: 2026-2314
• Category: Quality Assurance
• Position Type: Full-Time
• Working Hours: 3rd Shift: Monday - Friday, 10:30pm - 7:30am

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.
• 3rd Shift: Monday - Friday, 10:30pm - 7:30am.

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 5-7+ years of GMP related experience, or Master's degree in related field.

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.