Quality Technician II

Actalent; Raleigh (NC); On-site; USD 10,000 - 60,000; Full time

Job summary

Actalent is seeking a Quality Technician II in Raleigh, NC, to perform in-process and finished goods testing along with troubleshooting laboratory instruments. This role requires an Associate degree and offers competitive pay in an analytical laboratory environment with opportunities for personal protective measures.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account

Employee Assistance Program

Qualifications

• 1 – 3 years laboratory experience in pharmaceutical manufacturing preferred.
• Working knowledge of cGMP is a plus.
• Familiarity with laboratory equipment and computer skills.

Responsibilities

• Perform in-process testing and maintain records of laboratory analysis.
• Conduct troubleshooting on laboratory instruments.
• Prepare standards and reagents for analytical methods.

Skills

Mathematical calculations

Laboratory procedures

Problem-solving skills

Education

Associate or Technical degree in related field

B.S. degree in Physical Science or related field

Job description

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Job Description

We are seeking a dedicated Quality Technician II to perform in-process testing for internal customers and finished goods, returned goods, and stability testing for external customers as needed. The role involves specified analysis on all process control samples, finished goods, and troubleshooting laboratory instrumentation. The technician will maintain precise records of laboratory analysis and ensure the preparation of standards and reagents required for analytical methods.

Job Title: Quality Technician II

Job Description

We are seeking a dedicated Quality Technician II to perform in-process testing for internal customers and finished goods, returned goods, and stability testing for external customers as needed. The role involves specified analysis on all process control samples, finished goods, and troubleshooting laboratory instrumentation. The technician will maintain precise records of laboratory analysis and ensure the preparation of standards and reagents required for analytical methods.

Responsibilities

• Perform in-process testing for internal customers.
• Conduct finished goods, returned goods, and stability testing for external customers as needed.
• Analyze all process control samples and report results promptly via telephone or computer entry.
• Carry out specified analysis on finished goods using approved written procedures and laboratory techniques.
• Maintain accurate records of laboratory analysis using the appropriate recordkeeping system.
• Troubleshoot and conduct routine maintenance on laboratory instruments.
• Prepare standards and reagents for analytical methods and procedures.
• Prioritize and plan workload and team assignments for maximum efficiency and accuracy.
• Assist in non-routine analytical work to solve plant problems.
• Utilize problem-solving skills for failure investigations and testing issues.
• Participate in a certified 5S Workplace System for good housekeeping and organization.
• Aid in training others as needed.
• Perform non-routine quality control tasks such as resampling, raw material testing, and method and equipment validation.
  
  

Essential Skills

• Ability to perform basic mathematical calculations.
• Familiarity with laboratory procedures, equipment, and computer key punching.
• Sound and correct technical judgments during routine analysis.
• High degree of concentration.
  
  

Additional Skills & Qualifications

• Associate or Technical degree in a related field required.
• B.S. degree in Physical Science or related field preferred.
• 1 – 3 years laboratory experience in pharmaceutical manufacturing preferred.
• Working knowledge of cGMP is a plus.
• Functional/Technical Skills, Priority Setting, Written Communication.
• Customer Focus, Organizing.
  
  

Work Environment

The role is primarily based in a well-equipped analytical laboratory featuring fume hoods, benches, glassware, and instruments. Sampling may occur in a warehouse or processing area, requiring lifting and transporting materials. Exposure to chemical emissions typical for chemical operations should be expected. Normal dexterity is required for handling laboratory glassware and instruments, with the ability to visualize colors and distinguish slight differences in liquid volumes. Wearing personal protective equipment such as hard-hats, steel-toe shoes, and safety glasses is mandatory.

Schedule

Must be comfortable working a dupont schedule (12 hour night and day rotation schedule)

Pay and Benefits

The pay range for this position is $18.00 - $22.00/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 Raleigh,NC.

Application Deadline

This position is anticipated to close on Jun 25, 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

  Entry level

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance

• Industries

  Business Consulting and Services

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