Analytical QC Analyst II - Remote, GMP Biotech

Revance

Newark (CA)

On-site

USD 90,000 - 105,000

Full time

14 days+
Application generator

Turn this role into an interview — a resume and cover letter built around what this employer wants.

Get past ATS filters

Benefits offered by this job

Telecommuting

Job summary

Revance Therapeutics, Inc. in Newark, CA seeks a Quality Control Analyst II, Analytical to perform routine and non-routine testing for drug substances and products under cGMP. You will conduct ELISA, Western Blot, Karl Fischer, pH and related assays, and author quality records with timely investigations.

Requires a Master’s in Biotechnology or related field, experience in GMP QC labs, and familiarity with US/EU regulations. Salary range $90,000–$105,000 per year; telecommuting is permitted.

Qualifications

  • Master's degree in Biotechnology or a related science.
  • Proficiency with GMP QC lab practices and regulatory requirements.
  • Experience handling biosanitary products and analytical assays.
  • Familiar with US and international guidelines (ICH, GXP).

Responsibilities

  • Perform routine and non-routine release, in-process and stability testing for drug substance, drug product, and other critical reagents and documentation under cGMP.
  • Author quality records such as Deviation, Lab Investigations, CAPA, Change Control including leading thorough and timely investigation and/or implementation activities.
  • Author/ revise SOPs. Review laboratory records, procedures, methods, audit trails and other controlled documents.
  • Support CMC analytical deliverables with Manufacturing, QA and Regulatory.

Skills

ELISA
Western Blot
Karl Fischer
pH

Education

Master's degree in Biotechnology

Tools

LIMS system
Microsoft Office

Job description

Revance Therapeutics, Inc. in Newark, CA seeks a Quality Control Analyst II, Analytical to perform routine and non-routine testing for drug substances and products under cGMP. You will conduct ELISA, Western Blot, Karl Fischer, pH and related assays, and author quality records with timely investigations.

Requires a Master’s in Biotechnology or related field, experience in GMP QC labs, and familiarity with US/EU regulations. Salary range $90,000–$105,000 per year; telecommuting is permitted.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Senior QA Specialist, GxP & Data Integrity Expert
Senior QA Specialist, GxP & Data Integrity Expert

Revance • Newark (CA)

Hybrid
USD 105,000 - 125,000
Quality Control Analyst II — Biotech GMP Lab
Quality Control Analyst II — Biotech GMP Lab

NKGen Biotech, Inc. • Santa Ana (CA), Northern (KY)

Hybrid
USD 45,000 - 48,000
Medical, Dental and Vision Insurance
Business casual work attire
Analyst II
Analyst II

NKGen Biotech, Inc. • Santa Ana (CA), Northern (KY)

Hybrid
USD 45,000 - 48,000
Medical, Dental and Vision Insurance
Business casual work attire
Quality Control Analyst — GMP Biopharma Testing
Quality Control Analyst — GMP Biopharma Testing

avidbio • Costa Mesa (CA)

On-site
USD 34,000 - 44,000
QC Laboratory Analyst - 26-00173
QC Laboratory Analyst - 26-00173

LeadStack Inc. • Durham (NC)

On-site
QC Associate II: GMP Lab Analytics & Compliance
QC Associate II: GMP Lab Analytics & Compliance

Boehringer Ingelheim • Fremont (CA)

On-site
USD 85,000 - 110,000
Biotech QC Analyst II — GMP Microbiology & Testing
Biotech QC Analyst II — GMP Microbiology & Testing

NKGen Biotech • Irvine (CA)

On-site
USD 45,000 - 48,000
Medical, Dental and Vision Insurance
Business casual work attire
Analytical QA Director – Remote
Analytical QA Director – Remote

Travere Therapeutics • Providence (RI)

Hybrid
USD 150,000 - 195,000
Quality Control Analyst I
Quality Control Analyst I

Scorpion Therapeutics • Pittsburgh

On-site
USD 65,000 - 95,000
Analyst II
Analyst II

NKGen Biotech • Irvine (CA)

On-site
USD 45,000 - 48,000
Medical, Dental and Vision Insurance
Business casual work attire