Hiring QC/scientist ASAP

ACTalent; Florida; On-site; USD 40,000 - 54,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Time Off/Leave (PTO)

Transportation benefits

Employee Assistance Program

Job summary

ACTalent is seeking an Associate Scientist to perform routine analytical testing in a GMP-regulated lab in Coral Springs, FL. The role focuses on UV-Vis, HPLC, and related QC procedures for finished products, stability, and raw materials.

Training occurs on first shift, with second shift support. The position requires a chemistry degree with substantial pharma analysis experience and strong chromatographic skills.

Qualifications

• Bachelor's degree in chemistry or related field with 12 years of pharma analysis experience, or Master's with 1 year of pharma analysis experience.
• Proficiency in HPLC techniques for pharmaceutical analysis.
• Proficiency in UPLC methods and related chromatographic techniques.
• Strong working knowledge of UV-Vis spectroscopy for routine testing.
• Solid analytical experience in chemistry and pharmaceutical testing.

Responsibilities

• Perform routine testing of finished products, stability samples, raw materials, in-process and process validation samples in a regulated lab.
• Conduct assays, chromatographic purity tests, content uniformity analyses using UV-Vis and HPLC; measure particle size distribution and water by Karl Fischer.
• Evaluate test results and decide sample acceptability based on established criteria.
• Maintain laboratory notebooks and complete analytical reports and documentation per SOPs and cGMP.
• Ensure laboratories maintain good housekeeping and comply with cGMP requirements.

Skills

HPLC

UPLC

UV-Vis spectroscopy

Analytical chemistry

Education

Bachelor's degree in Chemistry or related field + 12 years pharma analysis experience

Master's degree in Chemistry or related field + 1 year pharma analysis experience

Job description

Job Description

The Associate Scientist performs routine analytical testing on a wide range of pharmaceutical samples including finished products, stability samples, raw materials, process validation samples, and developmental samples within an FDA- and GMP-regulated laboratory. Using techniques such as UV-Vis and HPLC, this role evaluates test results, determines sample acceptability, and maintains complete and accurate documentation in compliance with SOPs and cGMP standards. The position supports both first and second shift operations, with all training conducted on first shift.

Hiring For Scientist/ Quality Chemist

The Associate Scientist performs routine analytical testing on a wide range of pharmaceutical samples including finished products, stability samples, raw materials, process validation samples, and developmental samples within an FDA- and GMP-regulated laboratory. Using techniques such as UV-Vis and HPLC, this role evaluates test results, determines sample acceptability, and maintains complete and accurate documentation in compliance with SOPs and cGMP standards. The position supports both first and second shift operations, with all training conducted on first shift.

Responsibilities

• Perform routine testing of finished products, stability samples, raw materials, in-process and process validation samples, CV samples, and developmental samples in a regulated laboratory environment.
• Conduct assays, chromatographic purity tests, content uniformity analyses using UV-Vis and HPLC, particle size distribution measurements using various techniques, and water determination by Karl Fischer, following in-house monographs and USP methods.
• Evaluate test results and decide on the acceptability of samples based on established criteria and analytical outcomes.
• Maintain accurate laboratory notebooks and complete all related analytical reports, summaries, and documentation in strict compliance with SOPs.
• Ensure laboratories are maintained with good housekeeping practices and remain in full compliance with cGMP requirements.

Additional Skills & Qualifications

• Bachelors degree in Chemistry or a related scientific field with 12 years of related experience in pharmaceutical analysis, or a Masters degree in Chemistry or a related scientific field with 1 year of related experience in pharmaceutical analysis.
• Proficiency in HPLC techniques for pharmaceutical analysis.
• Proficiency in UPLC methods and related chromatographic techniques.
• Strong working knowledge of UV-Vis spectroscopy for routine testing.
• Solid analytical experience in chemistry, with the ability to apply principles to pharmaceutical testing.

Work Environment

• The position operates on either first shift (typically 8:00 a.m. to 5:00 p.m.) or second shift (typically 2:00 p.m. to 11:00 p.m.), with all training conducted during first shift hours.

Pay And Benefits

The pay range for this position is $29.00 - $39.00/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)

Job Type & Location

This is a Contract to Hire position based out of Coral Springs, FL.

Application Deadline

This position is anticipated to close on Nov 19, 2026.

Workplace Type

This is a fully onsite position in Coral Springs,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.