Chemist II

Actalent; Bedford (OH); On-site; USD 33,000 - 47,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

Actalent is seeking a Chemist II to maintain a safe laboratory environment and perform analyses using TOC, conductivity, nitrates, FTIR, chromatography, and in-process testing. The role supports QC equipment validation and calibration with minimal supervision, ensuring CGMP and FDA compliance.

The position is contract-based and based in Bedford, OH, onsite, with a pay rate of $28.85/hr. Requires a Bachelor's in science and 2+ years in a similar role, strong teamwork, and instrument

Qualifications

• Bachelor's degree in science or related field.
• Minimum 2 years in a similar role, preferably cGMP.
• Strong understanding of CGMP and FDA lab requirements.
• Ability to work effectively in a team.
• Troubleshoot basic lab instruments with minimal guidance.
• Proficient with existing lab systems.

Responsibilities

• Qualify laboratory equipment by authoring and executing IQ/OQ/PQ protocols and reports.
• Conduct testing to support method validation/verification, method transfer, routine and non-routine testing.
• Coordinate and manage progression of lab test data, SOPs, test procedures, and reports.
• Review and approve lab test data, SOPs, test procedures, validation protocols, and reports.
• Perform routine lab cleaning in preparation for inspections and ensure good housekeeping.
• Execute test methods per regulatory guidance (USP/EP) using appropriate protocols.
• Identify bottlenecks and propose continuous improvement ideas for QC Laboratory.
• Document all work per current Good Documentation Practices and cGLPs.
• Recommend preventive and corrective actions for non-conformances and quality system activities.

Skills

Teamwork

Troubleshooting

Laboratory systems

CGMP knowledge

Analytical mindset

Education

Bachelor's Degree in Science

Job description

Job Title: Chemist IIJob Description

The Chemist II will ensure the laboratory is maintained in a safe working environment and adheres to OSHA and other laboratory safety standards. The role includes performing various analyses using techniques such as TOC, Conductivity for WFI, Nitrates via wet methods, FTIR identification, chromatography analysis, and in-process testing by instrumental and wet chemistry techniques. The position supports the QC Equipment Validation and Calibration Programs and requires minimal supervision in qualifying laboratory equipment.

Responsibilities

• Qualify laboratory equipment including authoring and executing IQ/OQ/PQ protocols and reports.

• Conduct testing to support method validation/verification, method and tech transfer, routine and non-routine testing.

• Coordinate and manage the progression of laboratory test data, SOPs, test procedures, and reports.

• Review and approve laboratory test data, SOPs, test procedures, method/equipment validation protocols, and reports.

• Perform routine laboratory cleaning in preparation for inspections and ensure good housekeeping.

• Execute test methods according to regulatory guidance such as USP/EP using appropriate analysis protocols.

• Identify process bottlenecks and provide ideas for continuous improvement for the QC Laboratory.

• Document all work performed according to applicable Current Good Documentation Practices and cGLPs.

• Recommend and initiate preventive and corrective actions regarding product non-conformances and quality system activities.

Essential Skills

• Bachelor's Degree in Science or a related discipline (Chemistry or Chemical Engineering).

• Minimum of 2 years of experience in a similar position, preferably in a cGMP environment.

• Thorough understanding of CGMPs and FDA requirements for laboratory operations.

• Ability to work effectively in a team environment.

• Capability to troubleshoot basic laboratory instrument issues with minimal guidance.

• Proficiency in utilizing existing laboratory systems.

Additional Skills & Qualifications

• Experience with continuous improvement initiatives is preferred.

• Strong analytical, attention to detail, and interpersonal skills.

Work Environment

The position is based in a laboratory setting where the candidate will engage in hands‑on work with various scientific instruments. The environment is structured to ensure adherence to safety standards and regulatory compliance, providing a collaborative atmosphere for scientific exploration and innovation.

Job Type & Location

This is a Contract position based out of Bedford, OH.

Pay and Benefits

The pay range for this position is $28.85 - $28.85/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job‑related factors.

• 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)

Job Type & Location

This is a Contract position based out of Bedford, OH.

Application Deadline

This position is anticipated to close on Nov 6, 2026.

Workplace Type

This is a fully onsite position in Bedford,OH.

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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

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 process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.