Lab Technician

Contract – Potential to last up to 1 Year, to start
Social Circle, GA
PR: $20-29/hour
 
Shift: M-F, 7:00am-3:30pm
 
Job Summary

• Supports testing a wide range of biological, chemical, or physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods
• Position is applicable to QC Analytical Testing

 
Job 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.

 
Education & Qualifications
Required:

• A Bachelor's Degree and 1-3 years of prior GMP environment experience.
• Prior experience with testing via USP and EP Compendial Methods.
• Skilled in performing assays, as well as analyzing and interpreting their data.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint).

Preferred:

• Proficient in a range of analytical techniques, including both manual and instrumental methods (e.g., GC, HPLC).
• Proficient use of TrackWise, Empower, and MiniTab software a plus.
• 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.
• Ability to consistently follow SOPs to generate reliable results.

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).