Unleash Your Analytical Prowess!
Are you a highly meticulous and driven individual with a solid foundation in laboratory techniques? Do you excel at performing precise analyses and ensuring data integrity in a fast-paced environment? If you possess strong analytical skills, are proficient in both manual and instrumental methods (including techniques like GC and HPLC), and are committed to upholding the highest standards of quality and compliance, then we want to hear from you!
We're seeking a dedicated Lab Technician to join our client's team in Social Circle, GA, for a 1-year contract. In this pivotal role, you'll be at the forefront of critical biological, chemical, and physical analyses of raw materials, in-process, and final products, directly contributing to our manufacturing facility's production schedules.
You'll be instrumental in performing advanced assays, meticulously documenting and reviewing test data, and entering final results into LIMS and other computerized systems. Beyond the bench, you'll play a key part in maintaining data integrity, investigating deviations, and ensuring strict adherence to company SOPs, FDA, GLP, QSR, and cGMP regulations. Your ability to consistently follow protocols and identify procedural deviations will be crucial. While not required, prior experience with USP and EP Compendial Methods testing would be a significant advantage!
This is an exceptional opportunity to apply your technical problem-solving skills, expand your expertise in a regulated environment, and directly impact product quality. If you're ready to contribute your analytical talents and thrive in a collaborative laboratory setting, apply today!
location: Social Circle, Georgia
job type: Contract
salary: $20 - 29 per hour
work hours: 9 to 5
education: High School
responsibilities:
- Testing via USP and EP Compendial Methods and Requirements
- Conduct critical biological, chemical and physical analyses of Raw Materials, in-process and final products to support manufacturing facility production schedules.
- Perform documentation and review of test data following good documentation practices.
- Enter final data in LIMS and other computerized systems.
- Perform advanced biological and chemical assays requiring precise analytical skills and
- understanding of biology and chemistry principles.
- Complete all testing, including special project / protocol testing in a timely and appropriate manner.
- Maintain data integrity and ensure compliance with company SOPs, product specifications, FDA, GLP, QSR and cGMP regulations.
- Investigate deviations and write exception documents.
- Participate in team functions to address production, increase efficiency, solve problems, generate cost savings and improve quality.
- Conduct other duties as assigned.
- General laboratory housekeeping.
- Cleaning of laboratory glassware and equipment.
- Operation of equipment preparation and cleaning systems in QC (QC glasswashers).
- Maintenance and stocking of departmental consumable inventory.
- Routine verification of operating parameters of temperature controlled units.
- Routine cleaning and maintenance of temperature controlled units.
- Perform non-batch release testing (e.g. raw materials, cleaning).
- Assist in filling and archiving of departmental data, binders, reports, investigations, etc.
- Maintenance and disposal of waste generated throughout the laboratory.
- Retrieves and receives all samples into the QC Laboratories.
- Logs samples into logbooks.
- Receives samples into LIMS, EBM, and/or JDE.
- Enter data into LIMS.
- Initiate and pull Stability Studies / Samples.
- May lift, push, pull and carry up to approximately 25 lbs.
- Will work around chemicals such as alcohol, acids, and buffers that may require
- respiratory protection.
- May be required to work or be assigned to a different shift to meet business needs. Must be willing to work off shifts hours.
- Must be able to work supplemental hours as necessary to complete work commitments.
- May be required to work in a confined area.
- Primarily inside working conditions.
- Some clean room and cool/hot storage conditions.
qualifications:
Required:
- Proficient in a range of analytical techniques, including both manual and instrumental methods (e.g., GC, HPLC).
- Skilled in performing, analyzing, and interpreting analytical assays.
- Strong technical problem-solving abilities, supported by basic statistical knowledge.
- Adept at identifying and addressing deviations from standard procedures.
- Familiar with basic chemical and biological safety procedures.
- Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to consistently follow SOPs to generate reliable results.
- Prior experience with testing via USP and EP Compendial Methods.
- Proficient use of TrackWise, Empower, and MiniTab software a plus.
skills: Quality control, HPLC, SOP, MS-EXCEL, MS-Powerpoint, GMP (Good Manufacturing Practice), Sanitation, LIMS (Laboratory Information Management System
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 ....
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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Job ID: 482420462
Originally Posted on: 6/23/2025