Weekend Laboratory Technician - 3rd Shift (Part Time)

Job Description

Job Description

Job Title: Weekend Laboratory Technician (QC/SRP)

Department: Quality

Location: Chestertown, MD

Reports To: OC Supervisor

Pay Rate: $17-$19/hr with a $2 shift differential

Schedule & Hours:

3rd shift, Friday & Saturday, 11 pm - 7:15 am

Position Summary: The Quality Control Technician supports the production of high-quality products by performing routine tests, inspections, and basic laboratory tasks. This role follows written procedures to verify that materials and finished goods meet company quality standards. The QC technician records test results, maintains a clean and organized work area, and ensures that laboratory equipment is functioning properly. All training for testing methods, equipment uses, and documentation requirements is provided. This position is essential in helping the company deliver safe, accurate, and reliable products to customers. This role also supports SRP reagent preparation and coverage for the SRP production area as needed.

Qualifications / Requirements:

• Education & Experience
  • High school diploma or equivalent; High school chemistry, general lab coursework, or hands-on lab/production experience required.
  • Associate or bachelor’s degree in a science field (Chemistry, Biology, or related discipline) is a plus.
  • Experience working with basic laboratory tools (balances, pH meters, glassware, meters) or willingness to learn through provided training.
• Knowledge & Skills
  • Ability to follow detailed written instructions and standard operating procedures.
  • General computer skills, including the ability to use email, enter data, and work in Excel spreadsheets.
  • Excellent math skills including basic math and algebra.
  • Good color perception for tests and inspections involving visual color matching.
  • Strong problem solving and attention to detail.
  • Ability to stay focused and work accurately in a fast-paced environment.
  • Clear written and verbal communication skills for interacting with Production, QC, and R&D teams.
• Work Style & Personal Attributes
  • Ability to work both independently and as part of a team.
  • Ability to prioritize tasks and manage workload to meet deadlines.
  • Reliable, organized, and able to maintain accuracy in documentation.
  • Must be able to learn new test methods and adapt to changes in workflow.
• Physical Requirements
  • Ability to lift, move, or transport up to 40 lbs.
  • Ability to stand for extended periods and perform repetitive laboratory tasks.
  • Ability to wear required PPE, including gloves, safety glasses, lab coat and, as needed, a chemical respirator.

Primary Responsibilities:

• Product Testing & Inspection
  • Perform routine quality checks on materials and finished products following written procedures.
  • Conduct tests such as pH measurements, weight checks, titrations, and basic solution testing.
  • Inspect components (tubes, labels, apparatus, overlays, dip cells, strips, etc.) for defects before use.
  • Support testing across various product lines including reagents, powders, spin disks, test strips, tablets, and SRP solutions.
  • Identify and report out‑of‑spec results or unusual findings to QC leadership.
• Sample & Retains Management
  • Collect, label, organize, and store product retains according to company procedures.
  • Perform routine testing or visual checks on retains as required.
  • Dispose of retains, disk waste, tablet waste, and other materials according to safety and environmental guidelines.
• Solution, Standard, and Material Preparation
  • Prepare simple solutions, standards, vats, and premixes used in testing.
  • Follow documented instructions for measuring, mixing, and labeling materials.
  • Maintain proper storage and expiration tracking for standards and solutions.
  • Assist in preparation and management of Proof Sets as required by specific product lines.
• Equipment Use & Daily Maintenance
  • Use laboratory tools such as balances, pH meters, colorimeters, and specialized meters.
  • Perform daily instrument checks to verify accuracy (balance checks, meter verification, etc.).
  • Keep equipment clean and notify the supervisor of any issues or calibration concerns.
• Documentation & Reporting
  • Record all test results clearly and accurately in logs, forms, batch records, and electronic systems.
  • Determine pass/fail disposition based on written specifications and test results.
  • Generate Certificates of Analysis (COAs) using established templates.
  • Review supplier Certificates of Analysis (COAs) for raw materials as part of incoming inspection.
  • Complete daily QC documents such as lot sheets and testing logs.
  • Ensure all work is documented in real time according to SOPs and quality standards.
• Inventory & Lab Readiness
  • Maintain inventory of lab tools, chemicals, and testing supplies; notify team when stock is low.
  • Perform daily housekeeping to maintain a clean, safe, and organized work environment.
  • Support 6S standards and ensure the lab is always audit‑ready.
• SRP Reagent Support (Newark Location)
  • Prepare SRP reagents, solutions, and related materials in accordance with approved procedures and supply Spin production with reagents as needed.
  • Provide coverage for the SRP production area including performing standard testing, documenting results, and communicating any issues to QC and Production leadership.
  • Maintain cleanliness, organization, and safety compliance within the SRP work area.
• Cross-Functional Support
  • Communicate clearly with Production, R&D, Receiving, and other QC team members regarding test results, component issues, or adjustments.
  • Assist in training new QC Technicians once proficient.
  • Attend daily shift huddles to review priorities, communicate expectations, and address team needs.
  • Participate in improvement activities, Kaizens, and problem‑solving efforts as requested.
• Other Duties
  • Perform additional tasks assigned by QC Supervisors or Management to support departmental needs.
  • Perform backup support for certain laboratory or quality tasks when the primary individual is unavailable (after appropriate training).
  • May support multiple value streams or locations as business needs require.

Miscellaneous

• Participates in Lean activities, including but not limited to:
  • Lean training and lean events such as Kaizen or a 5-day event.
  • 6S program in QA/QC or other assigned areas.
  • DMAICs. Continuously look for ways to improve both the department’s and own individual efficiencies and time management, as well as ways to improve any aspect of the Company’s operations and develop and implement DMAICs accordingly.
• Notifies Supervisors/Managers of any production, equipment, safety, personnel problems, etc., and cooperates in resolving such issues as well. For example, requests assistance when systems prevent the efficient performance of duties or when a system fails.
• Provides Supervisors/Managers with feedback to determine where additional training would benefit and obtain additional training as necessary.
• Assist in other department activities as needed.
• Floats to and works in other manufacturing areas as needed.
• Complies with all company policies (i.e. personnel, safety, etc.).

Environmental Factors & Mental / Physical Demands

• Works indoors in a temperature‑controlled laboratory environment with routine exposure to chemicals, powders, and testing solutions (training and PPE provided).
• May occasionally perform tasks inside a fume hood or near ventilation equipment.
• Requires the ability to stand, walk, sit, bend, reach, and lift up to 40 lbs as part of normal laboratory and material‑handling activities.
• Must be able to visually distinguish colors for tests involving color changes or comparison.
• Requires the ability to focus on detailed tasks, follow written procedures, and maintain accuracy during repetitive testing.
• Must be able to wear required personal protective equipment, which may include a chemical respirator depending on the task.

Work-life and Culture:

LaMotte Company, a 100+ year-old global industry leader in developing and manufacturing premier water analysis solutions, operating in Newark, DE, Chestertown, MD and Warwick, UK. Our products are used around the world to accurately, quickly, and conveniently test water in a multitude of applications.

LaMotte relies on the personal success of our employees. We offer competitive pay with performance and level increases based on skills and more.

LaMotte offers a range of different shifts such as mornings, afternoons, evenings, and 12-hour shifts between both facilities to fit employee’s needs. LaMotte offers paid time off including vacation, sick leave, and paid holidays. We have several employee events including holiday events, employee appreciation events, community events, employee engagement, etc.

Full-time employees, who regularly work at least 30 hours per week, are eligible for employer-provided insurance including health, dental, vision, disability, life insurance, and supplemental insurance. Full-time employees are eligible to contribute to our 401(k) plan with an employer match available.

Chestertown, MD Facility Rates:

Salary information provided is based on general guidelines. LaMotte considers all factors (but not limited to) scope and responsibilities of the position, work experience, education, and key skills as well as market and business considerations.

LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws.