1

Qc Associate Pharma Jobs (NOW HIRING)

Client is seeking a contract role in Quality Control Raw Materials Associate II based at their Norwood, MA site and surrounding locations. The individual in this role will perform QC Raw Material ...

Posted today

QC Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the quality control plan. This includes working with employees as ...

QC Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the quality control plan. This includes working with employees as ...

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

Quality Control Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the HITT quality control plan. This includes working ...

Quality Control Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the HITT quality control plan. This includes working ...

NC · On-site

Quality Control Associate Location: Research Triangle Park, NC Duration: 12+ months (possibility of extension) ROLES & RESPOSNISBILTIES: * The Quality Control Raw Materials Associate I is responsible ...

NY · On-site

Quality Control Associate Full Time Professional Maitland, Maitland, FL, US At K2 Medical Research , we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing ...

Quality Control Associate

Richmond, VA · On-site

$63K - $90K/yr

Quality Control Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the HITT quality control plan. This includes working ...

Quality Control Associate

Richmond, VA · On-site

$63K - $90K/yr

Quality Control Associate The purpose of Quality Control Associate is to update and coordinate the planning, implementation, and supervision of the HITT quality control plan. This includes working ...

The Quality Control Associate is responsible for inspecting all food products in the warehouse and discerning whether or not they meet our high standards of quality. The Quality Control Associate ...

next page

Showing results 1-20

Qc Associate Pharma information

See salary details

$11

$25

$38

How much do qc associate pharma jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for qc associate pharma in the United States is $25.46, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.01 per hour, depending on experience, location, and employer.

What are popular job titles related to Qc Associate Pharma jobs?

For Qc Associate Pharma jobs, the most frequently searched job titles are:

Infographic showing various Qc Associate Pharma job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $52,962 per year, or $25.5 per hour.

Pharma Quality Control Associate

Norwood, MA

Randstad
Recruiting and Staffing Services • 5 - 10K employees

$36 - $36.11/hr

Full-time

Posted 13 hours ago

Posted today


Job description

Ready to Make an Impact in Biopharm Quality Control?

Client is seeking a contract role in Quality Control Raw Materials Associate II based at their Norwood, MA site and surrounding locations. The individual in this role will perform QC Raw Material activities in support of GMP Manufacturing. Also, this individual may support special projects as assigned. This role is 1st shift, Monday to Friday.Join a high-performing team dedicated to advancing life-saving therapies! We are seeking a detail-oriented Quality Control Associate II to support cGMP QC testing for raw materials, drug substances, and finished products at our state-of-the-art manufacturing facility.

In this hands-on, on-site role, you will execute and troubleshoot core analytical methods, drive method transfers, and ensure absolute compliance with cGMP standards. If you excel in a fast-paced environment and want to apply your testing expertise directly to patient safety, this opportunity is for you!

The Role The Quality Control Associate II will support cGMP QC testing for raw materials, drug substances, and finished products at the company's manufacturing facility and affiliated contract organizations. This role includes executing and troubleshooting analytical methods, supporting method transfers, qualification activities, and ensuring compliance with cGMP standards. This is an on-site position.Here’s What You’ll Need (Basic Qualifications) Education: BA/BS DegreeExperience: STEM degree with 3-5 years’ of experience in a cGMP laboratory setting, with hands-on experience in mammalian cell culture, cell based and potency assays, ELISA, molecular biology, and Protein Analysis.INTERESTED? APPLY NOW! THESE POSITIONS FILL FAST! salary: $36 - $36.11 per hour
shift: First
work hours: 8 AM - 4 PM
education: Bachelors

Responsibilities

Here’s What You’ll Do:

  • Requesting, sampling, releasing and shipping of raw materials
  • Sample coordination including cross functional collaboration with internal and external labs
  • Train and perform testing for methods including Bioanalyzer, osmolality, pH, conductivity, TruScan
  • RM spectroscopy, appearance and dimensional verification
  • Supporting domestic and international sample shipments
  • Inspect product and raw material retain samples
  • LIMS (LabVantage) sample logging and result entry
  • Raw material and consumable component inspection and release
  • Controlled temperature unit management, maintenance and troubleshooting
  • Clean room gowning and aseptic techniques
  • Managing/stocking of QC lab supplies and routine lab cleaning
  • Write/revise SOPs, protocols and reports
  • Complete and maintain cGMP documentation for work performed
  • Participate in authoring quality systems records such as deviations, change controls, CAPAs
  • Support non-conformance investigations
  • Establish and maintain a safe laboratory working environment

Skills
  • Quality Control
  • Quality Assurance
  • cGMP
  • GMP
  • raw materials
  • Drug Substance
  • ELISA (1 year of experience is required)
  • mammalian cell culture
  • molecular biology

  • Qualifications
  • Years of experience: 2 years
  • Experience level: Experienced

  • Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


    Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
    At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
    Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
    This posting is open for thirty (30) days.
    It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.


Randstad USA logo

About Randstad USA

Sourced by ZipRecruiter

Our business is supporting business productivity, from matching the right people with great jobs to custom project solutions and consulting. We use innovative technologies and a passion for people to provide you with the best experience possible. We provide outsourcing, staffing, consulting and workforce solutions within the areas of engineering, accounting and finance, healthcare, human resources, IT, legal, life sciences, manufacturing and logistics, office and administration and sales and marketing. We can’t wait to tell you all about it.

Industry

Recruiting and staffing services

Company size

5,001 - 10,000 Employees

Headquarters location

Minneapolis, MN, US