Quality Control

Adecco US, Inc.; Fremont (CA); Presencial; USD 41.000 - 45.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Medical, Dental, Vision

401K plan

Paid leave

Descripción de la vacante

Adecco US, Inc. has a contract opportunity for a Quality Control Engineer/Scientist I in Fremont, CA. The role focuses on QC testing of raw materials and intermediates in a regulated laboratory, with a background in chemistry or related life sciences.

The position offers an hourly pay range and a standard M-F day shift. The candidate should have GMP/cGMP familiarity, strong lab skills, and proficiency in Excel/Word to document results and maintain compliance.

Formación

• Bachelor's degree in Chemistry, Biochemistry, Biology, Bioscience, or a related scientific discipline.
• 0–2 years of QC or QA experience preferred.
• Experience in medical diagnostics, biotechnology, pharmaceutical, or life sciences environments preferred.
• Strong laboratory skills including pipetting, sample handling, and laboratory safety.
• Familiarity with GMP/cGMP regulations and laboratory procedures preferred.

Responsabilidades

• Perform analytical and functional testing of raw materials and intermediate products per SOPs.
• Conduct laboratory testing using chemistry and clinical analyzers.
• Document laboratory results accurately using Excel and quality records.
• Complete batch records and ensure cGMP compliance in documentation.

Conocimientos

Pipetting

Data analysis

Documentation

Excel

Attention to detail

Communication

Educación

Bachelor's degree in Chemistry/Biochemistry/Biology

Herramientas

Microsoft Excel

Clinical analyzers

Descripción del empleo

Quality Control Engineer / Scientist I

Location: Fremont, CA

Pay Rate: $30–$33 per hour

Schedule: Monday–Friday, 9:00 AM–5:00 PM

Shift: Day Shift

Employment Type: Contract Opportunity

Position Overview

We are seeking a detail-oriented Quality Control Engineer/Scientist I to join a laboratory team in Fremont, California. This position will perform quality control testing of raw materials and intermediate products in a regulated laboratory environment.

The ideal candidate will have a background in Chemistry, Biochemistry, Biology, or a related life science field, along with strong laboratory skills and an understanding of Good Manufacturing Practices (GMP).

This role is an excellent opportunity for an early-career scientist looking to gain hands‑on experience in quality control, laboratory testing, and regulated manufacturing operations.

Key Responsibilities

• Perform analytical and functional testing of raw materials and intermediate products in accordance with approved Standard Operating Procedures (SOPs).
• Conduct laboratory testing using chemistry and clinical analyzers.
• Perform sample receipt, preparation, testing, data collection, and analysis.
• Accurately document laboratory results using Excel spreadsheets, workbooks, and applicable quality records.
• Complete batch records and maintain accurate documentation in compliance with current Good Manufacturing Practices (cGMP).
• Operate laboratory instruments and equipment while following established safety procedures.
• Review and summarize test data, maintain lot histories, and identify trends or discrepancies.
• Assist with revisions and updates to quality control SOPs, worksheets, and procedures.
• Initiate procedure change requests when necessary.
• Support additional laboratory and quality control activities as assigned.

Required Qualifications

• Bachelor's degree in Chemistry, Biochemistry, Biology, Bioscience, or a related scientific discipline.
• 0–2 years of Quality Control (QC) or Quality Assurance (QA) experience preferred.
• Previous laboratory experience, preferably within medical diagnostics, biotechnology, pharmaceutical, or life sciences environments.
• Strong laboratory skills, including pipetting, sample handling, and laboratory safety.
• Familiarity with GMP/cGMP regulations and laboratory procedures preferred.
• Ability to accurately follow written and verbal instructions.
• Strong attention to detail and documentation skills.
• Proficiency in Microsoft Excel and Word.
• Ability to perform basic mathematical calculations, including concentrations, dilutions, and algebraic calculations.
• Ability to analyze data, summarize findings, and identify discrepancies.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities and work independently in a laboratory environment.

Compensation & Schedule

• Pay: $30–$33 per hour
• Monday–Friday
• 9:00 AM–5:00 PM
• Day shift
• Location: Fremont, California

Why Consider This Opportunity?

• Gain hands‑on experience in a regulated laboratory environment.
• Work with analytical testing and clinical chemistry equipment.
• Develop experience in quality control, GMP compliance, and laboratory documentation.
• Opportunity to build a career in biotechnology, pharmaceutical, and medical diagnostics industries.

Pay Details

$30.00 to $33.00 per hour

Adecco is an Equal Opportunity Employer.

Benefit offerings available for our associates include medical, dental, vision, life insurance, short‑term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

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