ZipRecruiter

Log In

Partners Internal Quality Control

60 Partners Internal Quality Control Jobs Hiring Near You

Trexon

Quality Control Technician

Chandler, AZ · On-site

$22 - $27/hr

Quality Control Technician C.E. Precision Assemblies (CEPA) | Chandler, AZ Compensation: $22.00 ... Support internal and external audits, including customer audits Cross-Functional Support * Partner ...

Trexon

Quality Control Technician

Chandler, AZ · On-site

$22 - $27/hr

Quality Control Technician C.E. Precision Assemblies (CEPA) | Chandler, AZ Compensation: $22.00 ... Support internal and external audits, including customer audits Cross-Functional Support * Partner ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

System One

Quality Control Specialist

Miami, FL · On-site

$48K/yr

... internal quality standards. Responsibilities * Implement and monitor quality control standards and ... System One not only serves as a valued partner for our clients, but we offer eligible employees ...

Sebela Pharma

Director, Quality Control

Holbrook, MA · On-site

$150K - $190K/yr

Ensure all testing is performed in accordance with internal procedures and cGMP requirements ... Partner with Quality Assurance, Manufacturing, and external stakeholders to investigate product ...

previous page

Showing results 41-60

All JobsPartners Internal Quality Control Jobs

Partners Internal Quality Control Jobs Information

Infographic showing various job openings at Partners Internal Quality Control in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 91% Physical, and 9% Hybrid job distribution.

QC Analyst, Quality Control Laboratory

Coherus Oncology

Camarillo, CA • On-site

$90K - $110K/yr

Full-time

Re-posted 23 days ago

Job description

Title:                          QC Analyst, Quality Control Laboratory
Reports to:            Director, Quality Laboratory
Location:                Camarillo, CA
Classification:    Exempt
 

Overview:

This laboratory position will be in the Quality Control Department and support activities associated with routine in-process testing, Certificate of Analysis (COA) release testing, and stability program support for biologics. This position will demonstrate strong technical proficiency with analytical methods, operate as a technical leader within the QC team, supporting complex testing, driving investigation quality, and ensuring compliant execution of analytical programs.

In addition, this position will support laboratory investigations, identify and help implement CAPAs, and participate in analytical method lifecycle activities including protocol drafting and execution of method validation, verification, and transfer in accordance with regulatory expectations.


Responsibilities:

  • Perform and review routine in-process, release, and stability testing for biologic drug substances and drug products while adhering to GMP/GDP QC requirements
  • Experience performing plate-based ELISA, ligand binding assays required
  • Execute and troubleshoot a range of analytical methods including HPLC/UPLC (SEC, RP, CEX, Peptide Mapping), capillary electrophoresis testing (cIEF, CE-SDS)
  • Perform compendial methods relevant to large molecule therapeutics (USP/EP/JP)
  • Support laboratory investigations, including OOS, OOT, and atypical result investigations
  • Conduct root cause analysis and identify, implement, and verify effectiveness of CAPAs
  • Draft and oversee protocols for method validation, verification, and transfer
  • Interpret results, perform statistical analyses, and prepare validation reports aligned to ICH Q2 and US FDA expectations
  • Author and review SOPs, test methods, protocols, and technical reports
  • Ensure all work is performed in compliance with cGMP, data integrity principles, and internal QA/QC policies
  • Support regulatory inspections and audits as a subject matter expert
  • Maintain departmental instruments and ensure timely execution of QC quality system records
  • Mentor team members and oversee analytical workflows to meet project goals

Qualifications:

  • Bachelor's or Master's in Biology, Chemistry, Biochemistry, or a related scientific field.
  • Minimum of 3 years of direct, hands-on QC experience in a GMP Quality Control laboratory supporting biologics.
  • Technical proficiency with HPLC, ELISA, capillary electrophoresis, and compendial testing.
  • Background in laboratory investigations, OOS management, and CAPA implementation.
  • Hands-on QC experience with method validation aligned to ICH Q2 and US FDA regulations.
  • Excellent technical writing, documentation, and analytical troubleshooting skills.
  • Ability to work independently while collaborating effectively across QC, QA, and Regulatory.
  • Experience in a commercial-stage or late-phase biologics environment is preferred.
  • Familiarity with LIMS and chromatography data systems (e.g., Chromeleon) is highly desirable.
  • Strong familiarity with GxP requirements.
  • Excellent communication, interpersonal and organizational skills are required.

The Base Salary Range for this position is $90,000 to $110,000. Coherus considers various factors, including professional background and work experience, when determining base pay. These considerations mean actual compensation will vary.

Coherus provides equal employment opportunities to all employees and applicants for employment and prohibits unlawful discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. We also prohibit discrimination based on the perception that anyone has any of these characteristics or is associated with a person who has or is perceived as having any of these characteristics.

Apply