In-Process QC Analyst - Biopharma Testing & Compliance

avidbio

Tustin (CA)

On-site

USD 35,817 - 44,083

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Benefits offered by this job

Health insurance
401(k) matching
Paid time off

Job summary

Avid Bioservices is seeking a Quality Control In-Process Analyst to perform testing and sampling in a GMP environment, supporting manufacturing, validation, and development studies. The role requires attention to accuracy and adherence to protocols, with responsibilities spanning routine QC testing, writing procedures, and cross‑department collaboration.

The position is full-time on a 4x10 schedule (Sunday to Wednesday) with potential overtime.

Qualifications

  • Bachelor’s degree or 2-4+ years in biotech QC/analytical lab.
  • Experience with analytical testing, GMPs, and regulatory audits.
  • Experience with most methodologies listed (e.g., LAL, pH, conductivity).
  • Basic maintenance and troubleshooting of analytical instrumentation desirable.

Responsibilities

  • Perform basic compendial test methods without supervision following protocols.
  • Formulate buffers and reagents for test methods.
  • Write and revise test methods and procedures.
  • Perform aseptic sampling and various QC tests (endotoxin, pH, conductivity, osmolality).
  • Work with other departments to develop and implement QC procedures.
  • Prepare study protocols and reports.
  • Adhere to cGMPs and regulatory requirements.
  • Overtime and weekend shifts may be needed.

Skills

Analytical testing
GMP compliance
Regulatory audits
Test method writing

Education

Bachelor’s degree in biotech or life sciences

Tools

LAL endotoxin testing

Job description

Avid Bioservices is seeking a Quality Control In-Process Analyst to perform testing and sampling in a GMP environment, supporting manufacturing, validation, and development studies. The role requires attention to accuracy and adherence to protocols, with responsibilities spanning routine QC testing, writing procedures, and cross‑department collaboration.

The position is full-time on a 4x10 schedule (Sunday to Wednesday) with potential overtime.

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

Similar jobs worth comparing

In-Process QC Analyst — Biotech GMP Impact
In-Process QC Analyst — Biotech GMP Impact

Avid Bioservices • Tustin (CA)

On-site
USD 35,500 - 44,372
Biopharma In-Process QC Analyst – GMP Testing & Compliance
Biopharma In-Process QC Analyst – GMP Testing & Compliance

BioTalent • Tustin (CA)

On-site
USD 65,000 - 90,000
Analyst (In-Process), Quality Control (Flex)
Analyst (In-Process), Quality Control (Flex)

avidbio • Tustin (CA)

On-site
USD 35,817 - 44,083
Health insurance
401(k) matching
Paid time off
Analyst (In-Process), Quality Control (Flex)
Analyst (In-Process), Quality Control (Flex)

Avid Bioservices • Tustin (CA)

On-site
USD 35,500 - 44,372
Quality Control In-Process Analyst
Quality Control In-Process Analyst

BioTalent • Tustin (CA)

On-site
USD 65,000 - 90,000
Quality Control In-Process Analyst
Quality Control In-Process Analyst

BioTalent • California (MO)

On-site
Health insurance
Dental insurance
Vision insurance
+2
Supervisor, Quality Control In-Process (Flex)
Supervisor, Quality Control In-Process (Flex)

avidbio • Tustin (CA)

On-site
USD 67,000 - 91,000
Health insurance
Dental insurance
Vision insurance
+2
Supervisor, Quality Control In-Process (Flex)
Supervisor, Quality Control In-Process (Flex)

Avid Bioservices • Tustin (CA)

On-site
USD 67,000 - 91,000
Health insurance
Dental insurance
Vision insurance
+2
Quality Control Analyst I
Quality Control Analyst I

Vyriad Inc. • Holiday (FL)

On-site
USD 50,000 - 70,000
Group Healthcare Plan
Company paid dental and vision
Short- and long-term disability insurance
+1
Quality Control Analytical In-Process (QCA-IP) Analyst
Quality Control Analytical In-Process (QCA-IP) Analyst

Planet Pharma • Novato (CA)

On-site
USD 52,000 - 62,000