Job Description
Shift/scheduled: Monday- Friday, 8am - 5pm/7am -4pm/6-3 pm Must be able to pass a visual test - can't be colour blind Under general supervision, this position is responsible for sampling and inspection of raw materials and components and for performing Quality review of documentation for assigned functions (e.g., equipment and maintenance records). Duties will include the operation and maintenance of instruments and equipment associated with sampling, e.g., Toledo balance, drum lift, pallet jack, etc. Maneuvering of large drums required. Employees will also be responsible for the maintenance of training records, recording, and computing data. Ability to maneuver 50+ pounds General understanding of aseptic techniques, cGMPs, gowning, sampling procedures and safety guidelines Work as a team player and/or independently Multi-task and basic problem-solving skills Excellent communication skills Time management Proficient computer skills (i.e., documentation systems, databases, and spreadsheets). Bachelor’s degree OR Associate degree and 4 years of directly related experience OR High school diploma / GED and 6 years of directly related experience Preferred Qualifications: Bachelor’s Degree in Science OR Associate’s Degree in Science and 3 years of experience in biotechnology/Pharma environment. OR 3 years of experience in regulated biotechnology/Pharma environment
TOP 3 MUST HAVE SKILL SETS:
*Understanding of aseptic techniques, cGMPs, gowning, sampling procedures, safety guidelines, perferred
*Self-motivated
*Ability to maneuver 50+ pounds
*High school diploma / GED and 6 years of directly related experience
*Can't be colored blind
DAY TO DAY RESPONSIBILITIES:
• General inspection of received shipments of raw materials, components, and labels
• Sampling of chemical raw materials and preparation of sample shipments
• Quality inspection and dimensional analysis for component and label batches
• Review of GMP shipment paperwork
• GMP controlled document review
• Receiving operations oversight and consultation (Purposeful Presence on the Floor)
• Initiation of deviation records
Additional Information
All your information will be kept confidential according to EEO guidelines.