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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 ...

Verstela

Pasteurizer

Bellevue, WA

$28.92 - $38.56/hr

Track and document fats, total solids, allergens, and critical control point records in compliance ... to permanent): • Medical, Dental, and Vision insurance • Short Term Disability and Life ...

APS

Senior Print Shop Operator

Phoenix, AZ · On-site

$16 - $20.50/hr

... solids; aqueous coating; pack the blanket and/or plate cylinder to register colors between units ... S. Export Control Laws'). Therefore, some positions may require applicants to be a U.S. person ...

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As of Jun 22, 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

Posted 7 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.