New!
Manufacturing Technician CYNET SYSTEMS
Antioch, CA1 day ago
- $25–$30 Per Hour
- Temporary
- Contractor
- Part-time
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Skills
- Administrative Skillsunmatched
- Asepsisunmatched
- Biotech and Pharmaceuticalunmatched
- CIP (Clean-in-Place)unmatched
- Cleaning Equipmentunmatched
- Current Good Manufacturing Practice (cGMP)unmatched
- Documentationunmatched
- Documentation Reviewunmatched
- Equipment Maintenance/Repairunmatched
- GMP (Good Manufacturing Practices)unmatched
- High School Diplomaunmatched
- Laboratory Testingunmatched
- Manufacturingunmatched
- Product Testingunmatched
- Production Controlunmatched
- SIP (Session Initiation Protocol)unmatched
- Standard Operating Procedures (SOP)unmatched
Description
Rate details:
Day shift (Shift 1): ***/hr
Night shift (Shift 3): ***/hr
- Please keep these standard pay rates aligned with the rest of the department.
- Only submit candidates that are flexible and open to either day or night shift. The hiring team will do their best to adhere to a preference. However, shift details will be confirmed once offer has been extended.
Shifts and Hours schedule:
Upstream Day Shift: 6am - 7pm
Upstream Night Shift: 6pm - 7am
Downstream Day Shift: 6: 30am - 7: 30pm
Downstream Night Shift: 6: 30pm - 7: 30am
- These roles follow a 3-4-3 shift pattern
Role Purpose:
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
20% Attain qualification for all assigned tasks and maintain individual training plan
10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
10% Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
High School Diploma or Equivalent minimum;AS/BS preferred
Preferred area of study: Science related discipline
0-3 years experience;some prior experience in a manufacturing setting preferred.
Proven logic and decision making abilities, critical thinking skills
Day shift (Shift 1): ***/hr
Night shift (Shift 3): ***/hr
- Please keep these standard pay rates aligned with the rest of the department.
- Only submit candidates that are flexible and open to either day or night shift. The hiring team will do their best to adhere to a preference. However, shift details will be confirmed once offer has been extended.
Shifts and Hours schedule:
Upstream Day Shift: 6am - 7pm
Upstream Night Shift: 6pm - 7am
Downstream Day Shift: 6: 30am - 7: 30pm
Downstream Night Shift: 6: 30pm - 7: 30am
- These roles follow a 3-4-3 shift pattern
Role Purpose:
The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials.
40% Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate
20% Attain qualification for all assigned tasks and maintain individual training plan
10% Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
10% Perform material movements, transfer raw materials, chemicals into, out of, across the production areas.
10% Maintain facility and equipment through routine cleaning and sanitization, support 6S programs
10% Administrative tasks attending shift exchange, meetings, sending/receiving emails, participating in projects, perform other duties as assigned.
High School Diploma or Equivalent minimum;AS/BS preferred
Preferred area of study: Science related discipline
0-3 years experience;some prior experience in a manufacturing setting preferred.
Proven logic and decision making abilities, critical thinking skills
Numbers & Facts
| Location | Vacaville, CA |
| Industry | Staffing/Employment Agencies |
| Salary | $12.56 |
| Company Size | 2,000 to 2,499 employees |
| Year Founded | 2000 |
| Website | http://www.lancesoft.com/ |
About Company
We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc).
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.