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Permanent Solids Control Jobs (NOW HIRING)

Artius Solutions

QC Chemist

Central Islip, NY · On-site

$65K - $90K/wk

Central Islip, NY (Onsite) Job Type: Full-Time | Permanent Shift: 8:30 AM - 5:00 PM (may vary ... Background in testing tablets, capsules, liquids, and solids also acceptable. * Prior exposure to ...

Manpower

Quality Control Tester

Pineville, LA · On-site

$21.50/hr

... analyses of solids, liquids, and gaseous materials. Your work will contribute to product ... and permanent resourcing, providing companies with strategic and operational flexibility and ...

Village of Grafton, WI

Utility Operator

Grafton, WI · On-site

$58K - $82K/yr

Permanent Full-Time Job Number: 202600022 Department: Utility (Water and Wastewater) Division: WWW ... control (fluoride, chlorine, and poly-phosphates) - Perform time-of-sale Clearwater and cross ...

Actalent

Quality Lab Technician

Edgerton, WI

$56K - $66K/yr

... solids, viscosity, color, odor, appearance assessments, titrations, and other wet chemistry ... Prior experience in a quality assurance or quality control laboratory environment is beneficial.

Actalent

Quality Lab Technician

Edgerton, WI

$56K - $66K/yr

... solids, viscosity, color, odor, appearance assessments, titrations, and other wet chemistry ... Prior experience in a quality assurance or quality control laboratory environment is beneficial.

Air National Guard Units

$32.07 - $37.41/hr

Tests various petroleum, cryogenic samples for total solids and microscopic analysis. Extracts ... Monitors vehicle mounted main control panel, gauges, meters and instruments. Operates deadman ...

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As of Aug 2, 2026, the average hourly pay for permanent solids control in the United States is $19.86, according to ZipRecruiter salary data. Most workers in this role earn between $19.23 and $21.15 per hour, depending on experience, location, and employer.
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QC Chemist

Artius Solutions

Central Islip, NY • On-site

$65K - $90K/wk

Full-time

Re-posted 18 days ago

Job description

Job Title: QC Chemist I

Location: Central Islip, NY (Onsite)
Job Type: Full-Time | Permanent
Shift: 8:30 AM – 5:00 PM (may vary)
Industry: Pharmaceutical
Experience Required: 2 to 15 years
Compensation: *,000 – *,000
Visa Sponsorship: Not available
Remote Option: No

Job Overview:

We are looking for a dedicated Quality Control Chemist to join our team and perform analytical testing in a GMP-regulated laboratory environment. The ideal candidate will have experience in pharmaceutical product testing and familiarity with various analytical instruments and techniques.

Responsibilities:

  • Perform standard and advanced laboratory testing on raw materials, in-process samples, and finished products.

  • Operate lab instruments such as HPLC, GC, Karl Fischer, ICP, and particle size analyzers.

  • Ensure compliance with cGMP, data integrity, and good documentation practices.

  • Support deviation investigations, change control activities, and CAPAs.

  • Participate in method validations and support production and quality operations.

  • Maintain accurate and timely documentation in line with regulatory standards.

  • Execute assigned tasks with attention to detail and in alignment with department protocols.

  • Collaborate with team members and other departments to meet project deadlines.

  • Perform other duties as assigned by management.

Required Qualifications:

  • Bachelor’s degree in Chemistry or a related scientific field.

  • 2–15 years of experience in a QC/analytical chemistry role within the pharmaceutical sector.

  • Strong understanding of lab testing and instrumentation.

  • Must be able to read, write, and understand scientific materials in English.

  • Proficiency with MS Office and laboratory software systems.

  • Comfortable working on-site full-time; no remote options.

Preferred Experience:

  • Hands-on experience with Inhalation dosage forms (MDI) is a strong advantage.

  • Background in testing tablets, capsules, liquids, and solids also acceptable.

  • Prior exposure to GMP, FDA regulatory guidelines, and quality systems.

  • Experience conducting investigations or root cause analyses.

Work Environment & Physical Requirements:

  • Work in a controlled laboratory or production area wearing PPE (lab coat, gloves, goggles, etc.).

  • Ability to lift up to 10 kg and stand or walk for extended periods during an 8-hour shift.

  • Comfortable using computers and working at a screen for prolonged periods.

Additional Information:

  • Must be willing to work weekday shifts and occasional weekends depending on business needs.

  • Must be open to working in a pharmaceutical manufacturing environment.

  • No employment sponsorship or visa support available.