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Quality Control Hplc Pharma Jobs (NOW HIRING)

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-40/hour depending upon experience ...

Bachem

Quality Control Project Manager

Vista, CA

$98K - $135K/yr

... biotech/pharma * 3+ years' experience in a biotech/pharma CDMO setting * 4+ years of project ... Chromatography (HPLC), Karl Fischer (KF), etc. * Excellent presentation skills * Ability to ...

System One

QC Chemist

Cranbury, NJ · On-site

$36 - $40/hr

Job Title : QC Chemist (cGMP / HPLC / Solid Dose) Location : Cranbury, NJ (Onsite) Type : Contract-to-Hire Schedule : 40 hrs/week Shift: M-F 8am-5pm Pay : $36-$40 per hour depending upon experience ...

Atp Group

QC Analytics Expert (80-100%)

Indiana, PA · On-site

HPLC, GC, dissolution systems, spectroscopy, stability chambers, balances, sample preparation ... Several years of hands‑on experience in GMP-regulated QC analytical laboratories (pharma or ...

LGM Pharma, LLC

QC CHEMIST II

Irvine, CA · On-site

$32 - $34/hr

... as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus. * Ability to follow standard ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

LGM Pharma, LLC

QC CHEMIST II

Irvine, CA · On-site

... as HPLC, GC, CE, ICP, FTIR, TOC, MS, and dissolution apparatus. * Ability to follow standard ... At LGM Pharma, we always take pride in putting our people first. We are an equal opportunity ...

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Quality Control Hplc Pharma information

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How much do quality control hplc pharma jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for quality control hplc pharma in the United States is $34.52, according to ZipRecruiter salary data. Most workers in this role earn between $24.76 and $39.66 per hour, depending on experience, location, and employer.

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

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

QC Specialist II, Analytical Investigations

Bedford, NH • On-site

PCI Pharma Services
See more jobs at PCI Pharma Servicesexternal

Full-time

Re-posted 24 days ago

PCI Pharma Services rating

6.3

Company rating: 6.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI.


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

What You'll Do

As a QC Specialist, you will:

  • Lead investigations into QC Analytical deviations, OOS/OOT/OOE results, and other quality issues.

  • Serve as a key point of contact during audits and inspections, ensuring timely and compliant responses.

  • Draft and revise change controls, technical reports, cGMP documents, and protocols.

  • Perform QC analytical testing, review data, and identify trends to proactively address risks.

  • Assist in managing analytical equipment to maintain compliance and efficiency.

  • Collaborate cross-functionally to close out quality events and audit findings on time.

  • Help shape and refine QC processes that support continuous improvement.

What You Bring

  • Education/Experience: Bachelor's degree in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or related field; 2-5 years of QC Analytical Chemistry experience (pharma experience preferred).

  • Technical Skills: Hands-on experience with UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer, and Osmometer.

  • Knowledge: Solid understanding of cGMP, ICH, USP, and global compendia guidelines, especially in analytical method validation and stability studies.

  • Strengths: Strong organizational and documentation skills, technical writing ability, and excellent communication skills (written and verbal).

  • Mindset: Ability to thrive in a fast-paced, dynamic environment, juggling multiple priorities while maintaining a sharp eye for detail.

  • Tech: Proficiency in MS Office; experience with lab-based data management systems a plus.

Why Join Us

  • Be part of a collaborative team where your expertise directly impacts patient safety and product quality.

  • Gain exposure to diverse analytical techniques and regulatory processes.

  • Opportunity to work in a GMP environment supporting both clinical and commercial product lifecycles.

  • Professional growth through hands-on problem solving, cross-functional collaboration, and continuous learning.

#LI-LL1

Join us and be part of building the bridge between life changing therapies and patients. Let's talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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