Aequor Technologies
Location: Thousand Oaks, CA - 100% onsite
Contract Duration: 3 years
Standard business hours
The ideal candidate will have a strong attention to detail, effective time management, and clear communication skills. They should have at least a high school diploma or GED and two years of relevant work or military experience, though an associate's degree with six months of experience is also acceptable. A bachelor's degree is preferred but not required. Previous experience with GMP is a plus but not mandatory, as training can be provided. The role is fully onsite in Thousand Oaks, CA, and requires the ability to lift 50+ pounds and pass a vision assessment for inspection work. Candidates must be comfortable working with raw materials and components, though no lab work is required.
Job stability is important. Candidates with multiple short-term roles within a brief period may be deprioritized. Candidates of all backgrounds and experience levels, including those who are overqualified, will be considered if they demonstrate the right attitude and interest in the role. The role offers long-term (3-year) engagement with limited overtime.
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's 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
The ideal candidate will have a strong attention to detail, effective time management, and clear communication skills. They should have at least a high school diploma or GED and two years of relevant work or military experience, though an associate's degree with six months of experience is also acceptable. A bachelor's degree is preferred but not required. Previous experience with GMP is a plus but not mandatory, as training can be provided. The role is fully onsite in Thousand Oaks, CA, and requires the ability to lift 50+ pounds and pass a vision assessment for inspection work. Candidates must be comfortable working with raw materials and components, though no lab work is required.
Job stability is important. Candidates with multiple short-term roles within a brief period may be deprioritized. Candidates of all backgrounds and experience levels, including those who are overqualified, will be considered if they demonstrate the right attitude and interest in the role. The role offers long-term (3-year) engagement with limited overtime.
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's 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