Laboratory Analyst

Kelly Services

Lodi (CA)

On-site

USD 36,000 - 39,000

Full time

13 days ago

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Job summary

Kelly Science & Clinical is seeking a Laboratory Analyst for a 12-month contract in Lodi, CA. The role supports Bulk Buffer, Reagents, and Bead production labs in a fast-paced GMP/GLP environment, with opportunities for hands-on reporting and process improvement.

Ideal candidates are recent Life Science graduates or those with GMP manufacturing experience, comfortable with 10-hour shifts and flexible schedules. Day and swing shifts available with shift differential.

Qualifications

  • BS in Life Sciences or equivalent with 0–1 years experience; AA with 1–2 years; HS diploma with 2–4 years.
  • Experience in GMP/GLP/ISO environments and cGDP documentation.
  • Ability to perform analytical testing and operate lab equipment.
  • Familiarity with SOPs and quality records.

Responsibilities

  • Support Bulk Buffer, Reagents, and Bead production labs.
  • Execute bulk buffer formulation, aliquoting, and labeling of reagents.
  • Operate beadulators for bead dropping; manage sieving and lyophilizers.
  • Perform QC checks: pH, density, conductivity, UV spectrophotometry.
  • Maintain Right First Time documentation per cGDP and SOPs.
  • Safely handle hazardous chemicals and manage inventory.

Skills

GMP compliance
GLP
ISO standards
SOP proficiency

Education

Bachelor's degree in Life Sciences
AA or Trade Degree
High School Diploma with 2–4 years experience

Tools

Lyophilizers
Beadulators

Job description

Laboratory Analyst | Lodi, CA

Kickstart your scientific career in Molecular Diagnostics!

Kelly Science & Clinical is seeking innovative and highly motivated Laboratory Analysts for a 12-month contract role with a premier Molecular and Diagnostics company in Lodi, CA. This is an exceptional opportunity for recent Life Science graduates or individuals with GMP manufacturing experience to gain hands‑on experience in a high‑paced, state‑of‑the‑art production laboratory.

Pay & Shift Schedules
  • Day Shift:$26.00/hr
  • Swing Shift:$28.08/hr (includes shift differential)
  • Duration:12-Month Contract
Available Schedules (10-hour shifts):
  • Shift 1:Sun–Wed | 5:00 AM – 3:30 PM
  • Shift 2:Wed–Sat | 5:00 AM – 3:30 PM
  • Shift 3:Sun–Wed | 3:00 PM – 1:30 AM
  • Shift 4:Wed–Sat | 3:00 PM – 1:30 AM
The Role: What You’ll Do

As a Laboratory Analyst, you will support the Bulk Buffer, Reagents, and Bead production labs. This is a dynamic, “hands‑on” role that combines technical science with active production.

  • Manufacturing & Formulation: Execute bulk buffer formulation, aliquoting, and labeling of reagents.
  • Specialized Production: Operate “beadulators” for bead dropping, manage sieving processes, and load/unload lyophilizers (freeze‑dryers).
  • Analytical Testing: Perform critical quality checks including pH, density, conductivity, and UV Spectrophotometry.
  • Quality & Compliance: Maintain “Right First Time” (RFT) documentation in accordance with cGDP (Good Documentation Practices) and SOPs.
  • Safety & Maintenance: Work safely with hazardous chemicals, manage inventory, and identify equipment defects or process improvements.
Physical Requirements

This is a very active, physical role within a production environment.

  • Lifting/Moving: Must be able to lift, push, and pull up to 25 lbs consistently throughout a 10-hour shift.
  • Heavy Equipment: Ability to transport materials up to 400 lbs using appropriate machinery or equipment assistance.
  • Stamina: Must be able to stand for several hours and perform repetitive arm/wrist motions.
Qualifications

We are looking for candidates who meet one of the following educational/experience tracks:

  • Recent Graduate: BS in Life Sciences (Biology, Chemistry, Biotech, etc.) with 0–1 years of experience.
  • Technical/Associate Degree: AA or Trade Degree with 1–2 years of related lab/manufacturing experience.
  • Experienced Professional: High School Diploma with 2–4 years of related work experience.
Core Skills:
  • Ability to strictly follow GMP (Good Manufacturing Practices), GLP, and ISO standards.
  • Strong communication skills; able to understand and execute complex Standard Operating Procedures (SOPs).
  • Bonus Points: Previous experience with Lyophilizers, Molecular assays, or analytical scales is a plus!
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