Job Description
Key Responsibilities:
Assign tasks and manage schedules for laboratory technicians and analysts.
Oversee daily laboratory operations and workflow that meets operational needs for organization
Monitor equipment maintenance and calibration schedules
Maintaining strong internal relationships to ensure proper liaison with compounding, filling, purchasing, sales and logistics departments
Assist in Interviewing and hiring decisions for QC Laboratory administrate staff
QC lab staff assignment delegation
Providing training to QC lab staff as required on equipment, processes and procedures, with an unwavering focus on ensuring safety and compliance with S.O.P.’s, DEP, EPA, OSHA, FDA, and cGMP’s
Evaluate performance, provide feedback, and address employee concerns.
Qualifications:
Bachelor’s degree in chemistry or related field
Minimum 8-10 years of experience in analytical or Quality Control laboratory, with 5-7 years of Supervisory experience in a cGMP lab environment
Working knowledge of cGMP regulatory requirements for pharmaceutical manufacturing
Previous experience and acumen in testing methods and procedures
Strong interpersonal and communication skills
Analytical, critical thinking, and problem solving skills, and an ability to perform role independently and with strong initiative
Minimum 5-7 years of experience with HPLC, UPLC, and GC testing, including analytical method development and validation
Technically savvy and experienced with Microsoft Office (including proficiency in Microsoft Access), Empower3, Chemstation and Chemstore
Relocation Expense Allowance for non-local applicantsCompany Description
Amris Consulting is a consulting company that assists pharmaceutical manufacturing organizations with placing full time and contract resources. Hiring company name and details will be disclosed during the screening process.
Full-time