Lab Technician

Actalent; Sidney (OH); On-site; Full time

Job summary

A leading company is seeking a Lab Technician to ensure quality control in a QC manufacturing lab. Responsibilities include testing raw materials and finished goods, supporting quality assurance systems, and maintaining compliance with FDA regulations. The ideal candidate will have a BS in Chemistry or similar, with experience in analytical chemistry and quality control. This fully onsite role offers competitive pay and benefits, including medical, dental, and retirement plans.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Transportation benefits

Employee Assistance Program

Time Off/Leave

Qualifications

• Experience in a QC lab environment is a plus.
• Good verbal and written communication skills.

Responsibilities

• Provide accurate testing of raw materials and finished goods.
• Support implementation of Quality System for FDA compliance.
• Perform routine verification of instrument calibration.

Skills

Quality assurance

Wet chemistry

Analytical chemistry

Quality control

Education

BS in Chemistry

A.S in lab sciences

Tools

FTIR

HPLC

GC

Job description

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Interested candidates can send updated resumes to [e-mail] or text Marisa at 330-397-1302 to set up a phone interview.

Job Description

The primary purpose of this position is to provide a quality control function, including technical and analytical support for all areas of the facility. Additionally, the personnel in this position will support the continuous development of Quality Assurance systems in manufacturing and packaging areas.

Responsibilities

1. Provide accurate and timely testing of raw materials, bulk formulations, and finished goods in accordance with established procedures and work instructions as well as FDA and GLP standards.
2. Assure inspection and control of incoming raw materials and components, as well as finished goods.
3. Verify line end-of-shift and end-of-run reconciliation.
4. Assemble and verify all batch records.
5. Support implementation of Quality System to ensure compliance with all FDA-related regulations.
6. Coordinate with lines to identify and document nonconformities and report results as required.
7. Perform routine verification of instrument calibration and preventive maintenance on laboratory equipment, supporting the calibration and verification program for testing equipment on lines.
8. Assist with training of line personnel, batching personnel, and office staff as required.
9. Perform routine environmental microbiological testing.
10. Ensure laboratory supplies are current and sufficiently stocked to provide timely service for the plant.
11. Accurately prepare and document the preparation of standards, standard solutions, and other reagents as required.
12. Champion quality both in the lab and the plant.
13. Maintain an effective, efficient laboratory that processes samples accurately and precisely.
14. Promote a team environment where people feel free to seek support and advice on quality matters.
15. Assure compliance with FDA regulations regarding inspection and testing.
16. Interpret and report analytical data.
17. Manage product release/rejection with approval from QC Supervisor/QA Specialist.

Essential Skills

• Quality assurance
• Wet chemistry
• Analytical chemistry
• Quality control
• Experience with FTIR, HPLC, GC
• Understanding of GMP and GLP

Additional Skills & Qualifications

• Must have a BS in Chemistry or similar lab sciences; open to an A.S with a couple of years of lab experience.
• Good computer skills; working knowledge of Microsoft Office (Word, Excel, PowerPoint, and Access) and flowcharting.
• Good verbal and written communication skills; ability to work in a team environment.
• Experience in a QC lab environment is a plus.
• Ideally, experience in a pharmaceutical or cosmetic lab - GMP/GLP environment.
• Skilled in the operation and maintenance of various analytical instruments including GC, HPLC, FTIR.
• Microbiological experience is a plus.

Work Environment

This role is based in a QC manufacturing lab that follows GMP/GLP regulations. The schedule is a first shift, Monday through Thursday from 7 AM to 5 PM, with potential overtime on Fridays and Saturdays. The work is split between two technicians, with the candidate expected to work every other weekend, which may ramp down at the beginning of the year.

Pay and Benefits

The pay range for this position is $21.00/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, plans, or program terms. If eligible, benefits may include:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital coverage
• 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 Sidney, OH.

Application Deadline

This position is anticipated to close on May 30, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help companies advance their engineering and science initiatives through access to specialized experts. With nearly 30,000 consultants and over 4,500 clients worldwide, we serve many Fortune 500 companies.

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

For reasonable accommodations during the application process due to a disability, contact [e-mail].