Chemist

Actalent; Boca Raton (FL); On-site; USD 56,000 - 76,000; Full time

Benefits offered by this job

Medical

Dental & Vision

Critical Illness

Accident, and Hospital

401(k) Retirement Plan

Pre‑tax and Roth post‑tax contribution

Life Insurance

Short and long‑term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent is seeking a Quality Control Chemist for a pharmaceutical manufacturing environment in Boca Raton, FL. You will perform analytical testing of materials and finished products, develop specifications and SOPs, and support method validation and investigations.

The role requires a bachelor's in a scientific field, 5+ years of QC experience, and knowledge of cGMP, GLP, and FDA regulations. This contract‑to‑hire position offers competitive pay and benefits.

Qualifications

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, Microbiology, or a related scientific field.
• 5+ years of Quality Control experience in the pharmaceutical industry.
• Hands-on experience with GC, FTIR, TOC, UV-Vis, and other analytical instrumentation.
• Experience supporting sterile injectable manufacturing environments.
• Strong knowledge of cGMP, GLP, FDA regulations, USP, ICH guidelines, and data integrity requirements.

Responsibilities

• Perform analytical testing of raw materials, packaging materials, in-process samples, finished products, and utility systems.
• Develop and maintain specifications, test methods, SOPs, and laboratory documentation.
• Conduct method validations, transfers, and suitability studies.
• Investigate OOS/OOT results and support deviations, CAPAs, change controls, and quality risk assessments.
• Review analytical data and approve Certificates of Analysis (COAs).
• Manage laboratory equipment qualification, calibration, maintenance, and documentation.
• Support internal, customer, and regulatory audits while maintaining inspection readiness.
• Ensure compliance with data integrity, GMP, GLP, and laboratory best practices.

Skills

GC, FTIR, TOC, UV-Vis

Quality Control in pharma

Sterile injectable manufacturing

cGMP, GLP, FDA regulations

Analytical data review & COA approval

Education

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Microbiology, or related field

Tools

LIMS

Job description

Actalent is Hiring a Chemist for a Pharmaceutical Manufacturing Company!!

Job Description

We are seeking an experienced Quality Control Chemist to support analytical testing, method validation, laboratory investigations, and regulatory compliance within a pharmaceutical manufacturing environment. This role ensures the quality and release of raw materials, in-process materials, packaging components, and finished products while maintaining compliance with cGMP, GLP, and FDA requirements.

Responsibilities

• Perform analytical testing of raw materials, packaging materials, in-process samples, finished products, and utility systems.
• Develop and maintain specifications, test methods, SOPs, and laboratory documentation.
• Conduct method validations, transfers, and suitability studies.
• Investigate OOS/OOT results and support deviations, CAPAs, change controls, and quality risk assessments.
• Review analytical data and approve Certificates of Analysis (COAs).
• Manage laboratory equipment qualification, calibration, maintenance, and documentation.
• Support internal, customer, and regulatory audits while maintaining inspection readiness.
• Ensure compliance with data integrity, GMP, GLP, and laboratory best practices.

Essential Skills

• Bachelor's degree in Chemistry, Pharmaceutical Sciences, Microbiology, or a related scientific field.
• 5+ years of Quality Control experience in the pharmaceutical industry.
• Hands-on experience with GC, FTIR, TOC, UV-Vis, and other analytical instrumentation.
• Experience supporting sterile injectable manufacturing environments.
• Strong knowledge of cGMP, GLP, FDA regulations, USP, ICH guidelines, and data integrity requirements.

Additional Skills & Qualifications

• Experience with method validation, equipment qualification (IQ/OQ/PQ), and laboratory investigations.
• Familiarity with LIMS and electronic laboratory systems.
• Excellent technical writing, problem-solving, and communication skills.

Work Environment

The position operates within a GMP Clean Room environment with a standard shift from 8:30 am to 5 pm. Flexibility may be required if demands change.

Job Type & Location

This is a Contract to Hire position based out of Boca Raton, FL.

Pay and Benefits

The pay range for this position is $40.87 - $55.29/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)

• 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 to Hire position based out of Boca Raton, FL.

Application Deadline

This position is anticipated to close on Nov 13, 2026.

Workplace Type

This is a fully onsite position in Boca Raton,FL.

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.