Quality Chemical Laboratories

QUALITY CHEMICAL LABS – X-ray Laboratory Manager Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking an experienced X-ray Lab Manager to join our team. This person will be responsible for managing and supervising all activities within the X-ray laboratory, including scheduling, equipment maintenance, personnel oversight, and compliance with all safety regulations. Must be able to operate and maintain X-ray equipment and associated software and write testing protocols and reports for clients. Bachelor’s degree in Chemistry, Physics, or Materials Science required with at least 3 years of experience in X-ray diffraction and/or solid-state techniques. Advanced degree preferred. 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...

QUALITY CHEMICAL LABS – X-ray Laboratory Manager Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking an experienced X-ray Lab Manager to join our team. This person will be responsible for managing and supervising all activities within the X-ray laboratory, including scheduling, equipment maintenance, personnel oversight, and compliance with all safety regulations. Must be able to operate and maintain X-ray equipment and associated software and write testing protocols and reports for clients. Bachelor’s degree in Chemistry, Physics, or Materials Science required with at least 3 years of experience in X-ray diffraction and/or solid-state techniques. Advanced degree preferred. 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...

Quality Chemical Laboratories (QCL), a pharmaceutical testing and development lab in Wilmington, is seeking highly motivated candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/validation, Document Control Associates, Computer System Validation and Data Integrity Specialists, Scientists (all levels) with experience in Mass Spec, LC, GC, QC compendial testing, Wet Chemistry, Microbiology, Sterility, Synthetic Chemistry, Pharmaceutical Formulation (with knowledge of manufacturing equipment), Metrology, and Sample Log-In Associates. Special attention given to candidates with advanced degree in Chemistry or related science and experience in method development/validation. Special consideration also given to experienced GMP data reviewers. 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.  Quality Chemical...

Quality Chemical Laboratories (QCL),  a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Manufacturing Quality Assurance Associate. This position, in the Manufacturing Quality Assurance department, requires a Bachelor’s degree or higher in a scientific or engineering discipline with either 3 years of experience or an equivalent combination of education and experience in a GMP laboratory or GMP manufacturing environment. Responsibilities include performing GMP review of manufacturing records and data, review and release manufacturing product batches, review and approve deviations, SOPs, calibration records, and protocols, perform AQLs as required, and assist with client audits. 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. Quality Chemical Laboratories (QCL)...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of QA Associate – Report Generation. The candidate will be responsible for review and approval of reports generated from laboratory data, such as certificate of analysis and stability study tables and will be expected to review reports for completeness and accuracy to ensure compliance with GMPs and SOPs. This position requires outstanding attention to detail, documentation, communication, problem-solving and organization skills. With experience, the candidate may be required to review technical reports such as method verifications, validations, transfer activities and other protocol driven work. Candidate must be proficient in Word and formatting documents. Additional quality assurance responsibilities may be required. QCL offers competitive salaries commensurate with experience and an excellent benefits package as well...

Quality Chemical Laboratories (QCL), a leading Pharmaceutical testing and manufacturing laboratory in Wilmington, is seeking a qualified candidate for the position of Validation Engineer. This position, in the Manufacturing and Formulations Services department, requires a Bachelor’s degree or higher in a scientific or engineering discipline with either 3 years of experience or an equivalent combination of education and experience in a GMP laboratory or manufacturing environment.  Special consideration given to candidates with experience with automated filling equipment especially in a sterile manufacturing environment.  Responsibilities include:  Create and execute equipment installation and operational qualification/requalification, calibration, and preventative maintenance for manufacturing instruments and equipment, as well as facilities and utilities qualifications /development. Standard Operating Procedures and training materials for manufacturing equipment / perform....

Quality Chemical Laboratories (QCL), a pharmaceutical testing, manufacturing, and development lab in Wilmington, is seeking a highly motivated scientist for our formulation development laboratory. The focus of this position is solid oral dosage forms but other dosage form experience, especially parenteral, will be considered as this is an area of growth for the company. Must be capable of working independently from concept and product prototype through transfer to cGMP Manufacturing.  The ideal candidate will possess strong problem solving abilities, excellent customer service mindset, and a positive can do attitude. A college degree is required with at least 3 years’ experience in formulation development. Experience in process development and technology transfer into cGMP manufacturing, familiarity with analytical techniques, regulatory requirements, and early phase cGMP manufacturing is preferred. QCL offers competitive salaries commensurate with experience and an excellent...

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 Qualified candidates may also apply via our website, or email resumes by clicking APPLY Equal Opportunity Employer: We don’t just accept difference - we celebrate it, we support it, and we thrive on it for the...

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 Qualified candidates may also apply via our website, or email resumes to  hrassistant@qualitychemlabs.com     Quality Chemical Laboratories (QCL) serves the biopharmaceutical industry.  We provide expert and...

QUALITY CHEMICAL LABS   Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking an experienced and dedicated Utilities Engineer to join our team. This person will be responsible and accountable for overseeing the qualification, validation, maintenance and repair of our utilities and HVAC systems, ensuring that all are compliant with applicable regulations for GMP pharmaceutical operations and meet safety standards. The Utilities engineer role is to ensure that the organization’s clean utilities that support GMP manufacturing operations in both sterile and non-sterile sites remain in a validated state of control with minimum downtown and operate efficiently and safely. The ideal candidate is a strategic planner with an excellent project management mindset, experienced with GMP documentation, comfortable in a fast-paced environment managing a multitude of contractors, and preferably specialized in...

Quality Chemical Laboratories (QCL) is a rapidly growing pharmaceutical testing and manufacturing lab in Wilmington, NC. We are seeking an experienced and dedicated Utilities Engineer to join our team. This person will be responsible and accountable for overseeing the qualification, validation, maintenance and repair of our utilities and HVAC systems, ensuring that all are compliant with applicable regulations for GMP pharmaceutical operations and meet safety standards. The Utilities engineer role is to ensure that the organization’s clean utilities that support GMP manufacturing operations in both sterile and non-sterile sites remain in a validated state of control with minimum downtown and operate efficiently and safely. The ideal candidate is a strategic planner with an excellent project management mindset, experienced with GMP documentation, comfortable in a fast-paced environment managing a multitude of contractors, and preferably specialized in working in sterile fill/finish...