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NEW JOB OPENING
LAB TECHNICIAN - 2ND SHIFT
IN Myerstown, PA, USA!
Date Posted: 03/21/2025
Hiring Organization: Rose International
Position Number: 480084
Job Title: Lab Technician - 2nd shift
Job Location: Myerstown, PA, USA, 17067
Work Model: Onsite
Shift: Monday thru Friday 2nd Shift 3pm to 11pm
Employment Type: Temporary
Estimated Duration (In months): 13
Min Hourly Rate($): 24.00
Max Hourly Rate($): 26.00
Must Have Skills/Attributes: Chemistry, Computer Literacy, GMP, Lab Tech, Science
Job Description
EDUCATION / EXPERIENCE REQUIREMENTS
•   High school degree or equivalent. Associate degree in the science is a plus.
•   At least 2 years of relevant post high school education or experience in the sciences.
REQUIRED SKILLS
•   Must be able to fluently read, write, and speak English; ability to understand verbal and written instructions.
•   Must have good organizational skills, high degree of accuracy in testing and completing paperwork, and legible handwriting.
•   Must have excellent interpersonal skills and have the ability to work effectively in a team environment.
•   Previous experience in good manufacturing practices (GMP) and/or government regulated industry preferred.
•   Personal computer (PC) skills needed.
POSITION SUMMARY
Process all incoming raw materials, intermediates, bulk and finished product samples (i.e. purchased materials, production or process technology batches). Perform standard physical and chemical analysis per the approved procedures, ensuring compliance with the written specifications. This position reports to a QC Manager in a cGMP laboratory.
RESPONSIBILITIES
•   Adhere to all aspects of Corporate and Plant safety programs, GMP’s, ISO standards or other regulatory requirements.
•   Process all incoming laboratory samples and record the respective batches into the laboratory sample logbook. Composite and manual log-in individual batches as required. Create composite samples for chemical testing.
•   Perform or support standard qualitative and quantitative analysis on in-process products, raw materials, packaging components, bulk and finished products in accordance with the approved testing procedures, the National Formulary (NF), and the United States Pharmacopoeia (USP). Perform physical testing on incoming stability samples.
•   Assist with non-compliance investigations for in-process work.
•   Prepare laboratory reagent solutions and sample grinds for testing needs.
•   Adhere to all Bayer and Regulatory guidelines for documentation, ensuring accurate, clear, legible and complete records of all information related to the sample login and release, analytical testing and investigations, preventive maintenance and instrument calibration, inventory and training.
•   Document test results into the laboratory notebooks, form sheets and the laboratory information management system (i.e. SAP-QM). Report all non-compliance results to supervisor for further evaluation.
•   Review and evaluate others documentation and test results for regulatory compliance and against specifications.
•   Perform glassware washing to support the laboratory. Distribute and maintain adequate levels of clean glassware as required for testing needs.
•   Monitor the pipette baths and drying desiccators throughout the laboratory.
•   Submit work orders for laboratory maintenance as needed. Review and change refrigerators chart recorders.
•   Handle the product hazardous waste. Monitor the inventory and use of the recycle and waste drums.
•   Participate in laboratory safety audits and solvent dumping schedule.
•   Responsible for filing the laboratory documentation and the review of the laboratory documentation prior to filing.
•   Update the records for testing procedures and monographs when revised or replaced.
•   Assist with the revising of SOPs or testing procedures as needed.
•   May perform other duties as assigned, including housekeeping tasks.
• **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.).
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About Rose
• Founded in 1993
• Office Locations Across the U.S.
• 150+ Clients: Corporations and Government Agencies
• Employee Oriented Company
• Challenging Assignments Across the U.S.
• Continuous Professional Development
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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.
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