Lab Technician

Actalent; Newark (CA); On-site; USD 60,000 - 80,000; Full time

Job summary

Actalent is seeking a Manufacturing Associate in Newark, CA. The role focuses on producing reagents in strict compliance with ISO standards, preparing materials, and maintaining the safety and cleanliness of the laboratory environment. This is a contractual position with competitive pay and benefits, ideal for candidates with a Bachelor's degree in Life Sciences and relevant experience in manufacturing.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick Leave)

Qualifications

• Experience in manufacturing is essential.
• Proficiency in pipetting and reagent preparation is required.
• Knowledge of SOP and medical device processes is beneficial.

Responsibilities

• Manufacture reagents according to established procedures.
• Perform in-process testing as needed.
• Document manufacturing steps with good practices.

Skills

Manufacturing

Pipetting

Reagent Preparation

ISO Standards

Education

Bachelor's Degree in Life Sciences

Job description

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Job Description

The role of Manufacturing Associate involves producing reagents and products in compliance with ISO 9001/2015 standards and established procedures. This includes preparing routine reagents for inventory and finished goods through both manual and automated processes for protein purification and conjugations. The position also involves making recommendations for process improvements, documenting manufacturing steps with good documentation practices, and performing in-process testing as needed.

Job Title: Manufacturing Associate

Job Description

The role of Manufacturing Associate involves producing reagents and products in compliance with ISO 9001/2015 standards and established procedures. This includes preparing routine reagents for inventory and finished goods through both manual and automated processes for protein purification and conjugations. The position also involves making recommendations for process improvements, documenting manufacturing steps with good documentation practices, and performing in-process testing as needed.

Responsibilities

• Manufacture reagents and products according to ISO 9001/2015 requirements and established procedures.
• Perform routine reagent preparation for inventory and finished goods using both manual and automated processes.
• Support and recommend process improvements.
• Document all manufacturing steps using good documentation practices.
• Perform in-process testing as required.
• Maintain production equipment and facilities in clean, good working condition using established protocols.
• Work with hazardous materials following specified safety precautions.
• Conduct inventory control of raw materials and supplies.
• Maintain a clean, orderly, and safe laboratory environment following health and safety guidelines.
• Collaborate within the team and department to follow best practices and meet department goals.
• Perform other duties as assigned within the operation.
  
  

Essential Skills

• Experience in manufacturing.
• Proficiency in pipetting and reagent preparation.
• Knowledge of SOP and medical device processes.
• Familiarity with ISO standards.
  
  

Additional Skills & Qualifications

• Bachelor's Degree in Life Sciences concentration.
• Ability to lift 25 lbs. unassisted.
• Capability to work with animal plasma/serum-based products.
• Ability to wear latex gloves and safety glasses.
  
  

Pay and Benefits

The pay range for this position is $24.00 - $26.00/hr.

Eligibility requirements apply to some benefits and may depend on your job

classification and length of employment. Benefits are subject to change and may be

subject to specific elections, plan, or program terms. If eligible, the benefits

Available For This Temporary Role May Include The Following

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
  
  

Workplace Type

This is a fully onsite position in Newark,CA.

Application Deadline

This position is anticipated to close on Jun 24, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Not Applicable

Employment type

• Employment type

  Contract

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Business Consulting and Services

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