Date Posted: 10/29/2024
Hiring Organization: Rose International
Position Number: 473572
Job Title: Quality Lab Associate
Job Location: Marion, NC, USA, 28752
Work Model: Onsite
Shift:
12 hour rotating shift
Hours will be 7am-7pm
Candidates will be required to enter clean rooms and will need to be fully gowned for that piece of the process.
Employment Type: Temporary
Estimated Duration (In months): 10
Min Hourly Rate($): 27.00
Max Hourly Rate($): 28.00
Must Have Skills/Attributes: GMP, Investigations, Medical device, Quality Assurance
Job Description
The client is seeking a Laboratory Technician with a microbiology or related sciences background. The ideal candidate will operate and maintain laboratory equipment, perform microbiological testing, and ensure compliance with safety and documentation standards. They should be detail-oriented, capable of multitasking, and possess effective communication skills. Experience in the Pharmaceutical or Medical Device industry is preferred, along with a solid understanding of regulatory standards.
Job Responsibilities
• Operate lab equipment such as laminar flow hoods, autoclaves, incubators, and other equipment
• Read plates and enter test results and other data into LIMS
• Initiate paperwork for microbial out-of-limit investigations and provide needed information to Investigators
• Perform monthly safety audits
• Sustain a clean and safe work environment utilizing 6S principles
• Perform growth promotion testing and media sterility verification; release media in BLAS and LIMS
• Approve paperwork including Microbial Identification forms, media production, growth tests, and incubator logs
• Assist in assimilating the monthly Microbial Identification report
• Prepare media used for microbiological testing such as TSA and TSB
• Perform Thermal Death Time testing
• Responsible for general housekeeping of the Laboratory
Knowledge, Skills, and Abilities
• Computer literate/knowledge of Microsoft Office applications (Word, Excel)
• Familiarity with quality-based computer systems such as LIMS
• Attention to detail and ability to prioritize multiple tasks promptly
• Must have a basic understanding of laboratory instrumentation and equipment such as laminar flow hoods, autoclaves, incubators
• Good documentation skills and knowledge of GDPs (Good Documentation Practices)
• Knowledge of aseptic sampling and testing techniques and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
• Must be able to communicate effectively with supervisors and peers
• Knowledge of aseptic technique and microbiological testing according to FDA, cGMP, GLPs and USP testing methodology
• Must be experienced in executing general microbiology procedures
• Must be able to lift 50 lbs
Required Education and Experience
• B.S. degree in Microbiology, Biology, or related science
• 0-2 years of experience; minimum 1 year experience in the Pharmaceutical/Medical Device industry
preferred
- **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
Working for Rose International was the most pleasant assignment I have ever had. They were always on top of situations when necessary, and very helpful. I was very proud to be an employee of Rose International, and would recommend anyone to try to work with them.
Melvon, Consultant
Thanks for the opportunity. If in the future I ever need a job, I would like to work for Rose International.
David, Consultant
Any time I did have a question and called, the phone was always answered, and my question/concern was immediately resolved.
Sally, Consultant
My on-boarding with Rose was outstanding. The packets of information, the process, and great attention to detail each person gave me allowed me to get started quickly.I appreciated each person's friendly and helpful attitude.
Diana, Consultant
It is a great pleasure being a part of the Rose International Team.
Toni, Consultant
EMPLOYEE COMMENTS