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Tanvex Biopharma Jobs (NOW HIRING)

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Tanvex Biopharma information

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$35K

$73.7K

$115K

How much do tanvex biopharma jobs pay per year?

As of Aug 9, 2026, the average yearly pay for tanvex biopharma in the United States is $73,667.00, according to ZipRecruiter salary data. Most workers in this role earn between $59,000.00 and $85,000.00 per year, depending on experience, location, and employer.

What is the difference between Tanvex Biopharma vs Biotech Research Associate?

AspectTanvex BiopharmaBiotech Research Associate
Required CredentialsBachelor's or Master's in Life Sciences, relevant biotech experienceBachelor's or Master's in related fields, laboratory experience often preferred
Work EnvironmentBiopharmaceutical manufacturing, R&D labs, quality controlLaboratory research, experimental testing, data analysis
Employer & Industry UsageBiopharmaceutical companies, biotech firmsResearch institutions, biotech and pharma companies

Tanvex Biopharma focuses on biopharmaceutical manufacturing and R&D, requiring specific biotech credentials. Biotech Research Associates typically work in laboratory research and testing. While both roles involve biotech expertise, Tanvex emphasizes manufacturing and quality, whereas Research Associates focus on experimental research and data analysis.

More about Tanvex Biopharma jobs
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Tanvex Biopharma jobs near you
Infographic showing various Tanvex Biopharma job openings in the United States as of July 2026, with employment types broken down into 97% Full Time, 1% Part Time, 1% Contract, and 1% Nights. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $73,667 per year, or $35.4 per hour.

QC Associate I, Microbiology

TANVEX BIOPHARMA USA INC

San Diego, CA • On-site

Full-time

Posted yesterday

New

Job description

Description:

Summary

The Quality Control Associate I, Microbiology is responsible for performing routine environmental and utilities monitoring of the cGMP manufacturing facilities. Conducts microbiological and chemical testing including endotoxin, bioburden, total organic carbon (TOC), and conductivity to support product release and facility compliance. Additional responsibilities include assisting with data trending, supporting method validation activities, and contributing to the drafting of protocols, reports, and SOPs related to microbiological operations. The role also involves timely and compliant reporting of test results and participation in investigations as needed.


Job Responsibilities

Essential Functions

  • Conduct Bioburden and endotoxin testing of in-process and products samples.
  • Perform environmental monitoring (EM) of classified cleanrooms and controlled areas.
  • Collect and test water samples from purified water and WFI systems.
  • Maintain accurate and compliant documentation in accordance with cGMP, GDP, and internal SOPs.
  • Assist in investigations of microbiological deviations and support CAPA implementation.
  • Collaborate cross-functionally with Manufacturing, QA, and Validation teams.
  • Perform sample management functions, such as receiving, logging, tracking, storing, and disposal of samples in accordance with SOPs and regulatory requirements.

Supplemental Functions

  • Other duties as assigned.
Requirements:

Education and Experience

  • BS or advanced degree in a related scientific discipline, or equivalent combination of education and experience.
  • BS with 0-2 years of progressively responsible experience in pharmaceutical or biologics production environments, or equivalent combination of education and experience.

Knowledge, Skills, and Abilities

  • Working knowledge of GLP and cGMP regulations 21 CFR Part 11, 210, 211, 600 & EU guidelines and good documentation practices.
  • Knowledge of standard laboratory equipment.
  • Basic understanding of microbiological techniques, aseptic practices, and laboratory safety.
  • Good organizational and problem-solving skills.
  • Ability to follow written procedures and work in a regulated environment.
  • Must always adhere to good documentation practices.
  • Detail oriented with strong written and verbal communication skills.
  • Ability to work independently, within prescribed guidelines, or as a team member.
  • Willingness to work in cleanroom settings and handle biohazardous materials under proper PPE and gowning protocols.
  • Experience with Microsoft suite (e.g. PowerPoint, Word, and Excel).