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QC Laboratory Technician

Job in Wilmington, New Castle County, Delaware, 19894, USA
Listing for: Creative Solutions Services, LLC
Contract position
Listed on 2026-07-17
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 30 USD Hourly USD 30.00 HOUR
Job Description & How to Apply Below

On-Board Services is hiring a Quality Control Laboratory Technician in Wilmington, DE

Position Details

Title:

Quality Control Laboratory Technician

Position Type: 6 month contract with additional opportunity contingent upon performance and continued business need

Job Location:

Wilmington, DE

Shift: 2nd Shift 1PM-9:30PM

Benefits: 401K, Dental insurance, Life Insurance, Medical Insurance, Vision Insurance, PTO

Compensation: $30/HR

Duties & Responsibilities
  • Conduct raw material, in-process, and finished goods testing according to established work instructions.
  • Prepare laboratory batches for new and existing products as required.
  • Perform scheduled daily, weekly, and monthly calibration verifications.
  • Support complaint investigations.
  • Clearly label all samples, reagents, and equipment and maintain accurate records of procedures and results.
  • Maintain compliance with all health, safety, and environmental procedures and guidelines.
  • Demonstrate strong written and verbal communication skills, including the ability to interpret and report data.
  • Utilize laboratory software systems such as iLIMS or other laboratory information management systems (LIMS).
  • Perform work in a laboratory environment including walking, standing, and climbing stairs or ladders as needed.
  • Follow Standard Operating Procedures (SOPs) and Work Instructions (WIs).
  • Demonstrate strong attention to detail.
  • Lift bags and boxes weighing up to 25 kg during product sampling activities as needed.
  • Operate a forklift in accordance with site safety procedures.
  • Calibrate and maintain laboratory equipment to ensure reliable and accurate results.
  • Complete daily and weekly housekeeping assignments.
  • Collaborate effectively within a team environment.
  • Wear required Personal Protective Equipment (PPE), including gloves, lab coats, safety shoes, and safety glasses.
  • Maintain inventory of laboratory supplies, raw materials for laboratory batches, and laboratory chemicals.
  • Follow good laboratory practices and established protocols for all activities.
  • Support additional Quality Assurance activities including new product setup, training, internal audits, and process improvement initiatives.
  • Dispose of chemical waste in accordance with applicable regulations and procedures.
  • Maintain a clean and organized laboratory environment.
  • Follow emergency procedures and maintain awareness of safety equipment and exit locations.
  • Handle samples appropriately to prevent contamination or loss and follow proper storage procedures.
  • Implement quality control measures to ensure reliability and accuracy of results.
  • Maintain integrity, accuracy, and confidentiality of laboratory data.
  • Conduct risk assessments and implement appropriate safety precautions.
  • Maintain organized and accurate documentation practices.
  • Investigate Out-of-Specification (OOS) results.
  • Report laboratory deviations.
  • Monitor quality metrics.
  • Conduct stability testing.
  • Review product compliance with applicable compendial standards.
  • Qualify new laboratory equipment.
  • Participate in ongoing training and continuous improvement initiatives.
Minimum Qualifications
  • Bachelor’s degree in chemistry, Biology, or equivalent experience.
  • Minimum of two years of laboratory experience in a regulated industry.
  • Ability to work independently and collaboratively within a team environment.
  • Proficiency with Microsoft Office Suite.
  • Experience with SAP and LIMS systems.
  • Knowledge of cGMP and cGLP requirements.
  • Knowledge of laboratory safety practices.
  • Strong written and verbal communication skills.
Position Requirements
  • Two to three years of experience with ISO 9000 Quality Management Systems, pharmaceutical regulatory compliance, and chemical and/or pharmaceutical quality environments.
  • Strong verbal and written communication skills.
  • Effective decision-making skills.
  • Strong computer proficiency.
  • Knowledge of company products and applications is preferred.
EEO Statement

On-Board Companies provides equal employment opportunities to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics.

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