Lab Technician Position Available In Walton, Georgia
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Job Description
job summary: This 1-year contract Lab Technician role in Social Circle, GA, offers an excellent opportunity for a detail-oriented professional with a Bachelor’s Degree and 1-3 years of GMP experience. You’ll be instrumental in performing critical biological, chemical, and physical analyses of raw materials, in-process, and final products, ensuring adherence to USP and EP Compendial Methods, FDA, GLP, QSR, and cGMP regulations. The role requires precise analytical skills, strong documentation practices, and proficiency in Microsoft Office, with a consistent Monday through Friday, 8 AM – 5 PM shift. If you’re skilled in conducting assays, interpreting data, and maintaining the highest standards of data integrity in a regulated lab environment, this position is a great fit for you.
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 RequirementsConduct 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 andunderstanding 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 requirerespiratory 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:
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. #LI-KH1 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 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: 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 detailssummary$20 – $29 per hourcontracthigh schoolcategorylife, physical, and social science occupationsreference51095job details job summary: This 1-year contract Lab Technician role in Social Circle, GA, offers an excellent opportunity for a detail-oriented professional with a Bachelor’s Degree and 1-3 years of GMP experience. You’ll be instrumental in performing critical biological, chemical, and physical analyses of raw materials, in-process, and final products, ensuring adherence to USP and EP Compendial Methods, FDA, GLP, QSR, and cGMP regulations. The role requires precise analytical skills, strong documentation practices, and proficiency in Microsoft Office, with a consistent Monday through Friday, 8 AM – 5 PM shift. If you’re skilled in conducting assays, interpreting data, and maintaining the highest standards of data integrity in a regulated lab environment, this position is a great fit for you.
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 RequirementsConduct 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 andunderstanding 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 requirerespiratory 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:
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. #LI-KH1 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 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: 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.
