Supervisor, QC Data Review
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Before you apply
LocationMorrisville, NC, US
Work modeon-site
Typefull-time
SeniorityLead
Experience6+ yrs
DepartmentLaboratory Support
Company size1,001–5,000 people
PostedOct 14, 2026 · 3w ago
Verified live2d ago
At a glanceSummarised by Seekless from the posting.
Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Microbiology or equivalent
Minimum 6 years of related pharmaceutical laboratory experience in a cGMP environment
Prior experience in method development/validation and/or transfer/verification, protocols, and troubleshooting
Excellent knowledge of cGMP in a pharmaceutical or regulated environment
Excellent skills in strategic planning, problem solving, root-cause analysis and critical thinking
Excellent verbal communications and presentation skills
Proficiency with Microsoft Office (Word, Excel, PowerPoint)
Proficiency with electronic systems (Empower, MODA, NuGenesis, etc.)
1-2 years of leadership experience
Prior CMO or CDMO experience
Working knowledge of method development/validation and/or transfer/verification and protocols
Working knowledge of pharmaceutical microbiology testing, analytical testing, and quality principles in a cGMP environment
Working knowledge of raw material, in-process and finished product testing, e.g. Microbial Limit Tests, Endotoxin, Sterility, utility testing, ID, appearance, cleaning methods, HPLC, TOC, conductivity and osmolality
Superior documentation skills and thorough understanding of client management
Excellent leadership, communication and presentation skills
Skills
Microsoft Office
Word
Excel
PowerPoint
Empower
MODA
NuGenesis
About the company
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 Supervisor, Data Quality Review is accountable for driving results in a fast-paced environment, continuously challenging performance in regards to quality standards, systems and operating procedures. The Supervisor, Data Quality Review is responsible for scheduling work for the team, developing SOPs or other quality documents as needed, and providing consultation on quality and compliance topics in areas of expertise.
On-Site Expectations
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100% on-site position.
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1st Shift: Monday - Friday, 8:30am - 5:30pm.
Responsibilities
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Interacts with clients and regulatory agencies as needed regarding quality issues, audits, and inspections, and hosts client audits.
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Collaborates with other supervisors in quality, labs, and manufacturing.
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Oversees the distribution of work to ensure efficiency and achievement of department goals.
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Performs data review of lab documentation, protocols, reports, investigations, test procedures, and other documentation on schedule, with accuracy and competency.
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Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
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Attracts, develops, and retains a high performing team to meet the current and evolving needs of the business through effective selection, training and development, coaching, and mentoring and performance management.
Qualifications
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Bachelor’s degree in Pharmaceutical Sciences, Chemistry, Biochemistry, Microbiology or equivalent required.
•
Minimum 6 years of related pharmaceutical laboratory experience in a cGMP environment required.
•
1-2 years of leadership experience preferred.
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Prior CMO or CDMO experience strongly preferred.
•
Prior experience in method development/validation and/or transfer/verification, protocols, and troubleshooting required.
Knowledge, Skills, and Abilities
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Excellent knowledge of cGMP in a pharmaceutical or regulated environment required.
•
Working knowledge of method development/validation and/or transfer/verification and protocols.
•
Working knowledge of pharmaceutical microbiology testing, analytical testing, and quality principles in a cGMP environment.
•
Working knowledge of raw material, in-process and finished product testing, e.g. Microbial Limit Tests, Endotoxin, Sterility, utility testing, ID, appearance, cleaning methods, HPLC, TOC, conductivity and osmolality (or some combination).
•
Superior documentation skills and thorough understanding of client management.
•
Excellent leadership, communication and presentation skills.
•
Excellent skills in strategic planning, problem solving, root-cause analysis and critical thinking required.
•
Excellent verbal communications and presentation skills required.
•
Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
•
Proficiency with electronic systems (Empower, MODA, NuGenesis, etc.)
Travel Expectations
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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 required to frequently talk or hear. The employee is required some of the time to stand, walk, and sit. The employee is required to occasionally use hands to finger, handle, or feel; climb or balance; stoop, kneel, crouch or crawl; reach with hands and arms; taste or smell. The employee must regularly lift and/or move up to 10 pounds, occasionally lift and/or move up to 50 pounds. There is no special vision requirement for this job. The employee may occasionally work in wet or humid conditions, near moving mechanical parts, in high precarious places, near fumes, airborne particles or toxic chemicals.