Quality Control Data Review Specialist - 2nd Shift

Alcami-5; Morrisville (NC); On-site; USD 70,000 - 100,000; Full time

Job summary

Alcami is seeking a Quality Control Data Review Specialist to join the Laboratory Operations team. The role focuses on reviewing data and documents, conducting audits, and ensuring compliance with cGMP and regulatory requirements. The position may include training and mentoring others and supporting continuous improvement initiatives.

On-site, 2nd shift operates Wednesday to Saturday, 2:00pm – 12:30am. The ideal candidate has a chemistry or biology background with GMP experience and strong

Qualifications

• Bachelor's degree in Chemistry, Biology, or related field with 2+ years GMP experience, or Master's with 1+ year related experience.
• Chromatography experience required.
• Method validation experience preferred.

Responsibilities

• Review and approval of data and documents (protocols, reports, test procedures).
• Maintain process KPIs and quality matrices as required.
• Support SOPs, work instructions, and other quality documents.

Skills

Chromatography

Independent work

Communication

Education

Bachelor's in Chemistry/Biology/related

Master's in related field

Tools

Microsoft Office

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 Quality Control Data Review Specialist is an effective member of the Laboratory Operations team. Position is accountable for driving results in a fast-paced environment by effectively performing various activities at range of complexity to ensure quality and compliance with applicable regulatory requirements. These activities may include reviewing documents and data, conducting basic floor audits and process inspections, consulting on quality and compliance issues, maintaining quality databases and performing trend analysis where needed, and performing quality and compliance-oriented training as necessary. The QC Data Review Specialist assists with the development of SOPs or other quality documents as needed. Business needs and deadlines will require the employee to perform work duties outside of standard work hours on occasion.

On-Site Expectations

• 100% on-site position.
• 2nd Shift: Wednesday - Saturday, 2:00pm - 12:30am.

Responsibilities

• Performs detailed review and approval of all types of data and documents (e.g. protocols, reports, and test procedures).
• Assist in maintaining process KPIs and quality matrix as required.
• Drives alignment of the process with quality and compliance procedures.
• Serves as an effective member of the Laboratory Operations team and may serve as a mentor to other employees in the area of expertise.
• Performs floor inspections with focus on audit trail review and testing process/technique scrutiny as required.
• Provides support to release of materials (e.g. media, reagents) as required.
• Assists with continued improvement initiatives as needed.
• Assists with development/writing of SOPs, Work Instructions, and other documents and/or reports as needed.
• 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 2+ years GMP related experience; OR Master's degree in related field with 1+ years related experience; OR equivalent education and work experience.
• Chromatography experience required.
• Method validation experience preferred.

Knowledge, Skills, and Abilities

• Strong knowledge of regulations and SOPs applicable to area of responsibility and keeps abreast of new regulations and regulatory guidance in areas of expertise.
• Excellent written and oral communication skills.
• Good math skills.
• Ability to be trained and to mentor others.
• Ability to act independently.
• Ability to interact well with employees at all levels.
• Ability to host audits.
• Proficiency with Microsoft Office products.

Travel Expectations

• Up to 5% domestic travel.

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 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.