Extractables and Leachables Laboratory Manager

Quality Chemical Laboratories; Wilmington (NC); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Subsidized childcare

Job summary

Quality Chemical Laboratories in Wilmington, NC is seeking a qualified candidate to manage the extractables and leachables (E/L) laboratory. The role requires writing and executing protocols and generating final reports, with five years of experience desirable.

The position offers competitive salaries and excellent benefits, including subsidized childcare at a 5-Star facility. QCL serves the biopharmaceutical industry with cGMP testing and manufacturing support, and is expanding with sterile

Qualifications

• Must write and execute laboratory protocols.
• Experience with extractables and leachables (E/L).
• Ability to generate final reports.

Responsibilities

• Manage the E/L laboratory.
• Develop and execute protocols for E/L testing.
• Prepare and review final laboratory reports.

Skills

Protocol writing

E/L expertise

Final report generation

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.