Scientist

Actalent; Florida; Vor Ort; USD 40.000 - 54.000; Vollzeit

Benefits dieser Stelle

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Zusammenfassung

Actalent is seeking a Quality Control Scientist to perform routine analytical testing on pharmaceutical samples, including finished products and stability materials, using HPLC/UV-Vis techniques. The role emphasizes accurate documentation, adherence to SOPs, and strict cGMP compliance in a regulated lab environment.

Qualified candidates have a chemistry degree with substantial pharmaceutical analysis experience and proficiency in HPLC/UPLC.

Qualifikationen

• Bachelor's degree in Chemistry or related field with 12 years of experience in pharmaceutical analysis, or a Master’s with 1 year of related 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 applied to pharmaceutical testing.

Aufgaben

• Perform routine testing of finished products, stability samples, raw materials, in-process and process validation samples in a regulated laboratory.
• Conduct assays, chromatographic purity tests, content uniformity analyses using UV-Vis and HPLC, particle size distribution measurements, and water determinations by Karl Fischer.
• Evaluate test results and decide on sample acceptability based on criteria and analytical outcomes.
• Maintain accurate laboratory notebooks and complete related reports and documentation per SOPs.
• Ensure labs operate with good housekeeping and remain in full cGMP compliance.

Kenntnisse

HPLC

UPLC

UV-Vis

Analytical methods

Ausbildung

Bachelor's degree in Chemistry or related field

Master's degree in Chemistry or related field

Jobbeschreibung

Actalent is Hiring a Team of Quality Control Scientists

Job Description

The Associate Scientist performs routine analytical testing on a wide range of pharmaceutical samplesincluding finished products, stability samples, raw materials, process validation samples, and developmental sampleswithin 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.

Job Type & Location

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

Pay and Benefits

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

Job Type & Location

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

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 16, 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.