ZipRecruiter

Log In

1

Quality Control Hplc Jobs (NOW HIRING)

Astrix Inc

QC Associate Scientist

Concord, OH · On-site

$75K - $80K/yr

... skilled QC Associate Scientist to join their team in Lake County, OH! Location: Lake County, OH ... This role requires strong expertise in HPLC and GC analysis, experience working within cGMP ...

FIRST PRIORITY, INC

Pharmaceutical QC Chemist

Elgin, IL · On-site

$25 - $30/hr

Analyze raw materials, finished products, and stability samples by HPLC and other specialized testing methodologies. Provide support to other QC lab personnel as required. Requirements: PRIMARY ...

Califesciences

QC Analytical Chemist

San Carlos, CA · On-site

$100 - $125/hr

Medterials is seeking a QC Analytical Chemist with chemistry education and experience to work in a ... HPLC experience is required; LCMS experience is a plus. General Skills: Must be organized and ...

Pepsico

Technician - Quality Control (Nights)

Munster, IN · On-site

$18.25 - $23.50/hr

Experience operating testing instruments (e.g., Carbo Qc, HPLC, Densitometers, Water Testing, etc.) * Experience following standards of operations (SOPs) (e.g., following procedures, etc.

Pepsico

Technician - Quality Control

Johnstown, PA · On-site

$28.30/hr

Experience operating testing instruments (e.g., Carbo Qc, HPLC, Densitometers, Water Testing, etc.) * Experience following standards of operations (SOPs) (e.g., following procedures, etc.

Peregrine Team

Quality Control Analyst

Seattle, WA · On-site

$27.25 - $36.75/hr

Peregrine Team is hiring a Quality Control Analyst to support laboratory testing and ensure product ... Key Responsibilities * Perform analytical testing (HPLC, ELISA, etc.) * Document results in ...

Califesciences

$100 - $125/hr

Medterials is seeking a QC Analytical Chemist with chemistry education and experience to work in a ... HPLC experience is required; LCMS experience is a plus. General Skills: Must be organized and ...

Califesciences

Quality Control Scientist

Vista, CA · On-site

$60 - $80/hr

HPLC, UPLC, Water, Mass Spec, UV, GC, melting point, Optical Rotation, TLC and misc. wet chemistry lab work and other related analytical equipment used for control quality of the GMP facility. This ...

Pepsico

Technician - Quality Control

Riverside, CA · On-site

$23.25/hr

Experience operating testing instruments (e.g., Carbo Qc, HPLC, Densitometers, Water Testing, etc.) * Experience following standards of operations (SOPs) (e.g., following procedures, etc.

TriSearch

QC Chemist

Philadelphia, PA

Analytical Chemist (Quality Control) Location: Horsham, PA About the Opportunity Seeking Analytical ... HPLC/UHPLC * Dissolution systems * ICP-MS * UV/Vis Spectrophotometers * Gas Chromatography (GC)

NCSL International

Quality Control Scientist

Vista, CA · On-site

$60 - $80/hr

HPLC, UPLC, Water, Mass Spec, UV, GC, melting point, Optical Rotation, TLC and misc. wet chemistry lab work and other related analytical equipment used for control quality of the GMP facility. This ...

Bayer AG

quality control specialist

Berkeley, CA · On-site

$150 - $200/hr

Quality control gmp HPLC Job Summary: This position plays a vital role in advancing analytical capabilities within a dynamic Quality Control Chemistry environment. The successful candidate will be ...

New

previous page

Showing results 41-60

All JobsScience JobsChemistry JobsChemist JobsQuality Control Hplc Jobs

Quality Control Hplc information

See salary details

$12

$20

$29

How much do quality control hplc jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for quality control hplc in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What are popular job titles related to Quality Control Hplc jobs?

For Quality Control Hplc jobs, the most frequently searched job titles are:

Infographic showing various Quality Control Hplc job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 3% Contract, and 1% Nights. Highlights an 88% Physical, 1% Hybrid, and 11% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.

Quality Control Supervisor

Sellersville, PA • On-site

Piramal Pharma Limited
See more jobs at Piramal Pharma Limitedexternal

Full-time

Re-posted 6 days ago

Job description

Be the First to Apply

Division

Piramal Pharma Solutions

Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia.

This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation.

Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide.

For more details, please visit : www.piramalpharmasolutions.com

Job Title

Quality Control Supervisor

Job Description

Piramal Pharma Solutions is seeking an experienced and motivated QC Supervisor to lead a team of Quality Control analysts in the Sellersville, PA facility. This role is responsible for supervising laboratory operations, ensuring compliance with GMP requirements, supporting laboratory investigations, and driving operational excellence within the Quality Control department. The QC Supervisor oversees a team of approximately 4-5 analysts performing analytical chemistry and microbiological testing on raw materials, finished products, environmental monitoring samples, cleaning validation samples, and stability studies.Key Responsibilities
  • Supervise daily activities of approximately 4-5 QC analysts.
  • Plan, coordinate, and prioritize laboratory testing activities to support manufacturing and supply chain schedules.
  • Review analytical data generated from HPLC, UPLC, GC, and ICP-MS testing.
  • Ensure testing is performed in accordance with approved SOPs, USP, EP and regulatory requirements.
  • Coordinate sampling, testing, and laboratory support activities for production operations.
  • Manage cleaning validation and cleaning verification testing programs.
  • Facilitate communication and testing activities with external laboratories.
  • Perform data review and auditing to support lot disposition decisions.
  • Lead and document OOS, OOT, deviation investigations, CAPAs, and change controls.
  • Support laboratory inspection readiness and regulatory compliance initiatives.
  • Support Empower, LIMS, and TrackWise systems administration activities.
  • Prepare, review, and approve validation and verification protocols and reports.
  • Maintain and periodically review departmental SOPs.
  • Provide training, coaching, performance management, and development for QC analysts.
  • Participate in site quality initiatives and represent QC on cross-functional project teams.
  • Other duties as deemed necessary
Education & Experience
  • Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, or related scientific discipline.
  • Minimum 7 years of technical laboratory experience in a GMP-regulated environment.
  • Minimum 5 years of leadership or supervisory experience.
  • Experience with analytical chemistry and/or microbiological testing.
  • Hands-on experience with HPLC, UPLC, and GC instrumentation.
  • Knowledge of GMP, FDA, ICH, and USP requirements.
  • Experience with Empower, LIMS, and TrackWise preferred.
Knowledge, Skills & Abilities
  • Strong leadership and team development skills.
  • Excellent written, verbal, and interpersonal communication skills.
  • Strong analytical and problem-solving capabilities.
  • Proficiency in Microsoft Office applications.
  • Knowledge of data integrity principles and laboratory compliance requirements.
  • Ability to manage multiple priorities in a fast-paced environment.

Apply