Develop and implement quality control testing and product inspection at various production stages.
Create reports documenting production or incoming raw material issues.
Oversee the QC Department, including the distribution of projects, priorities, workloads, and deadlines within the QC Department.
Responsible for management, discipline, and evaluation of QC staff.
Train staff and determine work quality expectations. Provide advice and assistance on work techniques, best practices, and subject matter expertise to team members.
Oversee general QC approval (Work in Progress Raw Material). Responsible for inspecting final product specifications and approving or rejecting finished products.
Manage QC retains, testing schedule, data and reports, and related Standard Operating Procedures (SOPs) documents. Review and make decisions regarding retaining testing and final QC long-term results.
Oversee raw material qualification, re-qualification, and disposal.
Coordinate and oversee instrument and equipment validation and equipment maintenance.
Requirements and Qualifications:
M.S. in Biology or a related field with 5+ years of QC experience
1-3 years of supervisory experience
Knowledge and experience with Quality Control Management is preferred.
Excellent writing and communication skills.
Detail-oriented and excellent at record keeping.
Able to think critically and analyze and troubleshoot data.
Able to lift and move up to 40 pounds.
Familiarity with a laboratory setting and handling of lab-related materials.
Strong computer literacy and experience with Microsoft Word, Excel, and PowerPoint
Able to work in the cold room periodically, kept at 2 - 8°C (35.6 - 46.4°F).
Able to provide a vaccination record and confirm current Hepatitis B status after hiring.
Desired Skills and Experience
QC, Quality Control Management, biotech, SOPs, laboratory, Word, Excel, PowerPoint
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