Chemist I

Job Description

Job Description

Job Title: Chemist I

Job Description

This entry-level Chemist I role focuses on supporting quality control laboratory operations by performing analytical testing, maintaining a safe and compliant lab environment, and ensuring accurate documentation in alignment with cGLP, cGMP, and regulatory requirements. The position offers an excellent opportunity to develop hands-on experience with wet chemistry and instrumental techniques while contributing to a rapidly growing organization and a collaborative laboratory team.

Responsibilities

• Maintain a safe laboratory environment in compliance with OSHA and applicable laboratory safety standards.
• Perform Total Organic Carbon (TOC) and conductivity testing for Water for Injection (WFI).
• Conduct nitrate analysis using wet chemistry methods.
• Perform identification testing using FTIR and other instrumental techniques as required.
• Execute in-process testing using both instrumental and wet chemistry techniques according to established procedures.
• Support the Quality Control Equipment Validation and Calibration Programs under the guidance of technical staff such as QC Engineers or Chemists.
• Coordinate and manage the progression of laboratory test data, standard operating procedures (SOPs), test methods, and reports in accordance with defined processes.
• Perform routine laboratory cleaning and organization to prepare for internal and regulatory inspections and to maintain strong housekeeping practices.
• Execute test methods in accordance with regulatory guidance such as USP and EP, using appropriate analytical protocols as reference.
• Document all laboratory work in compliance with Current Good Documentation Practices (cGDP) and current Good Laboratory Practices (cGLP).
• Recommend and initiate preventive and corrective actions related to product non-conformances and quality system activities within the chemistry laboratory.
• Support and participate in investigations related to cGLP and cGMP analytical processes.
• Collaborate effectively with peers and staff to meet laboratory and quality objectives.
• Assist in troubleshooting basic laboratory instrument issues with minimal guidance.

Essential Skills

• Bachelors degree in Science or a related discipline such as Chemistry or Chemical Engineering.
• 01 year of previous working experience in a similar laboratory or quality control position.
• Experience or familiarity with quality systems in a cGMP environment (preferred).
• Thorough understanding of cGMP requirements for laboratory operations.
• Thorough understanding of FDA expectations for laboratory operations.
• Hands-on experience or training in wet chemistry techniques.
• Experience with analytical chemistry methods and laboratory testing.
• Ability to perform TOC and conductivity testing or willingness to learn these techniques.
• Ability to perform identification testing using FTIR or similar analytical instruments.
• Ability to support equipment validation and calibration activities under supervision.
• Proven ability to work well with peers in a team-oriented environment.
• Proven ability to troubleshoot basic laboratory instrument issues with minimal guidance.
• Strong analytical and problem-solving skills.
• High attention to detail and accuracy in testing and documentation.
• Strong interpersonal skills and the ability to communicate effectively within the laboratory team.

Additional Skills & Qualifications

• Prior experience working in a regulated cGMP environment is preferred.
• Familiarity with USP and EP analytical methods and regulatory guidance.
• Knowledge of Current Good Laboratory Practices (cGLP) and Current Good Documentation Practices (cGDP).
• Experience working within quality systems and supporting investigations related to laboratory processes.
• Demonstrated ability to follow SOPs, test procedures, and analytical protocols consistently.
• Ability to manage multiple laboratory tasks and documentation requirements in an organized manner.
• Motivation to grow within a rapidly expanding organization and contribute to the development of a growing quality control team.

Work Environment

This role is based in a laboratory setting and involves daily hands-on work with analytical instruments, wet chemistry techniques, and quality control testing. The environment follows strict OSHA, cGMP, cGLP, and FDA guidelines, with a strong emphasis on safety, regulatory compliance, and good housekeeping. Team members work closely with technical staff and peers in a collaborative, growth-oriented atmosphere. As the organization is expanding rapidly, the position offers the opportunity to join a growing team early and contribute to building robust laboratory and quality systems.

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

The pay range for this position is $26.00 - $26.00/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.

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)

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

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

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 View email address on ziprecruiter.com 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.