Extractables and Leachables Laboratory Manager

Quality Chemical Laboratories; Wilmington (NC); On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

Subsidized childcare

Job summary

Quality Chemical Laboratories (QCL) in Wilmington, NC seeks an experienced professional to manage the extractables and leachables (E/L) laboratory. The role requires writing and executing protocols and generating final reports, with five years of relevant experience desirable.

You will lead lab operations, ensure cGMP compliance, and contribute to project execution in a growing facility offering career advancement and a competitive benefits package, including subsidized childcare.

Qualifications

• Must have experience in extractables and leachables (E/L).
• Ability to write and execute protocols and generate final reports.
• Five years of experience in E/L is desirable.

Responsibilities

• Manage the E/L laboratory.
• Write and execute protocols for E/L studies.
• Generate final reports for projects.
• Oversee day-to-day lab operations and compliance.

Skills

Protocol writing

Report generation

Laboratory management

EL experience

Job description

QUALITY CHEMICAL LABS

Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking a highly qualified candidate to manage the extractables and leachables (E/L) laboratory. The candidate must be able to write and execute protocols and generate final reports. Five years of experience in this area is desirable.

QCL offers competitive salaries commensurate with experience and an excellent benefits package, as well as great potential for career advancement and leadership in a rapidly growing company. We now also offer subsidized childcare at our 5-Star childcare facility. For more information about our company and our available positions, please visit our website @ www.qualitychemlabs.com

Quality Chemical Laboratories (QCL) serves the biopharmaceutical industry. We provide expert and cGMP compliant scientific testing services in support of both small and large-molecule drug products, drug substances, in-process materials, and raw materials in all phases of Research, Development, and Commercialization. QCL provides formulation development and solid dose GMP manufacturing supporting early-phase clinical trials. QCL is adding sterile fill/finish and lyophilization services launching in 2024.