This Laboratory Operations role in Temecula, CA, is ideal for a life science professional with a bachelor's degree or 3-5 years of relevant experience. You'll be crucial in manufacturing products, performing diverse lab operations, and ensuring compliance with cGMP and regulatory standards. The position requires strong aseptic technique, experience with lab equipment, and proficiency in data entry and reporting. You will contribute to process improvements, new product development, and assist in troubleshooting manufacturing issues, all while working in a dynamic team environment.
location: Temecula, California
job type: Contract
salary: $20 - 25 per hour
work hours: 9 to 5
education: Bachelors
responsibilities:
- Perform bulk laboratory operations such as fractionation of antiserum, dialysis, filtration, labeling and bottling, using available resources to coordinate daily manufacturing requirements.
- Perform various testing methods such as Heidelberger titers, total protein, OD280, IEP and SDS-Page
- On time Manufacture of products as needed per Planning department
- Perform standard and new operating procedures
- Execute complex laboratory methods per established procedures; support activities to resolve process and testing issues under guidance of senior staff
- Perform procedures involving calculations and material measurements. Collect and evaluate data per defined specifications
- Safely and correctly operate standard laboratory equipment
- Prepare routine solutions and reagents
- Utilize software for data entry and recordkeeping in conformance with company and regulatory policies and standards
- Ensure compliance with all quality and regulatory specifications
- Execute the manufacturing performance metrics (productivity, customer satisfaction and quality improvements)
- Execute on objectives and planned schedules as outlined by supervisor
- Train other lab personnel in established procedures
- Filling, labeling, and packaging of products
- Contribute to completion of specific programs and projects
- Comply with applicable established cGMP, FDA, OSHA, EPA, and Quality System regulations
- Develop, write and update documents pertaining to lab procedures and product manufacturing to maintain cGMP and/or ISO compliance
- Problem-solve Manufacturing-related issues:
- Actively participate in troubleshooting and the identification of manufacturing and production issues
- May assist with the research of new methods or steps in a process at direction of team management, including revising SOPs
- Improve manufacturing processes:
- Identify inefficiencies and opportunities for process improvements
- Assist in the implementation of manufacturing procedures intended to optimize existing processes, such as yield, time and cost, and ensure achievement of regulatory and customer requirements
- Support new product development:
- Support R&D and Tech Transfer functions in bringing new products to manufacturing
- Train on new SOPs, technologies etc. to support the manufacture of new products
qualifications:
Required:
- Bachelor's in Life Science (preferred) OR 5+ years relevant experience.
- Basic lab techniques: sterile/aseptic, buffer prep, protein purification (large/small scale).
- Basic scientific equipment knowledge (pipettes, scales, pH meters, etc.).
- Proficient in sterile/aseptic technique.
- Cell culture techniques; basic antibody/protein production knowledge.
- Follows SOPs, completes Batch Records accurately.
- Basic knowledge of cell-based/immuno/molecular techniques.
- Safe handling of biohazards.
- Computer skills (Office 365, Excel).
- Basic math skills.
- Multi-tasking, meets production schedules.
- Good organization and detail-oriented.
- Good written/verbal communication; clear reports, accurate records.
- Follows, writes, edits SOPs.
- Adheres to Quality/Regulatory requirements.
- Adaptable to change.
- Knowledge of lab safety procedures.
- Self-directed, motivated; works independently and in a team.
- Working knowledge of manufacturing ERP systems (Oracle/SAP).
skills: SOP, GLP (Good Laboratory Practice), GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers.
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.
