Extractables and Leachables Laboratory Manager

Quality Chemical Laboratories; Wilmington (NC); On-site; USD 90,000 - 140,000; Full time

Benefits offered by this job

Competitive salary

Benefits package

Subsidized childcare

Job summary

Quality Chemical Laboratories in Wilmington, NC seeks a qualified manager to oversee the Extractables and Leachables (E/L) laboratory, write and execute protocols, and generate final reports.

Five years of experience in this area is desirable; the team offers a competitive salary, a strong benefits package, and opportunities for leadership and career advancement, including subsidized childcare at a 5-Star facility.

Qualifications

• Must have hands-on experience with Extractables and Leachables (E/L) programs.
• Ability to write and execute protocols and generate final reports.
• Five years of experience in this area is desirable.

Responsibilities

• Oversee the E/L laboratory operations.
• Write and execute study protocols; generate final reports.
• Provide leadership and contribute to process improvements.

Skills

E/L expertise

Technical writing

Laboratory leadership

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.

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.