Top 1388 Qc associate i Jobs

QC Associate I/II - Contract
Abzena Inc. —San Diego, CA
- $40 - $60 an hour
- Temporary
- Mid-level
- 3 years
- Bachelor's degree
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QC Associate I/II - Contract
Abzena —San Diego, CA
- $40 - $60 an hour
- Temporary
- Mid-level
- 3 years
- Bachelor's degree
QC Technician I
Sensient Technologies Corporation —Turlock, CA
- $24.80 an hour
- High school diploma or GED
- US work authorization
- Entry level
Specialist I, QC Logistics (Contract)
ElevateBio —Waltham, MA
- $43 - $57 an hour
- Contract
- Mid-level
- 3 years
- Organizational skills
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11d
Quality Control Associate Bioanalytical Laboratory
Meso Scale Diagnostics, LLC. —Gaithersburg, MD
- $45,500 - $66,000 a year
- Writing skills
- Mid-level
- Office
- Paid parental leave
- AD&D insurance
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Quality Control Analyst I
LGC Group —Milford, MA
- $26 - $39 an hour
- Full-time
- Microsoft Excel
- Basic math
- Data analysis skills
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QC/Production Associate I
SOFIE —Kansas City, MO
- $22 - $24 an hour
- Weekends as needed
- Engineering
- High school diploma or GED
- Ability to lift 50 pounds
9d
Associate QC Specialist
Frontage Laboratories —Exton, PA
- Full-time
- Microsoft Word
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
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Validation Associate
Accupac —Mainland, PA
- $44,000 - $60,000 a year
- Online Application
- Microsoft Excel
- English
- Mid-level
- Health savings account
- Paid holidays
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Quality Control Associate - 3rd Shift
Intellyk —Boston, MA
- $35.41 - $48.00 an hour
- Contract
- Word processing
- Mid-level
- Bachelor's degree
Quick Apply
10d
Analytical QA Associate I - DPI
Cipla —Hauppauge, NY
- $76,000 - $85,000 a year
- Weekends as needed
- English
- Master's degree
- Analysis skills
Quality Control Analyst I
Meso Scale Diagnostics, LLC. —Rockville, MD
- $52,400 - $76,000 a year
- Weekends as needed
- Databases
- High school diploma or GED
- Bachelor's degree
- Paid parental leave
- AD&D insurance
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QC Associate I
Software Technology Inc —San Diego, CA
- 8 hour shift
- Microsoft Word
- Computer literacy
- Bachelor of Science
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Quality Technician I -2nd Shift
JOHN B SANFILIPPO & SON, INC —Bainbridge, GA
- $18.70 - $25.75 an hour
- Overtime
- Basic math
- Ability to climb stairs
- High school diploma or GED
- Health insurance
- Paid time off
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QA Associate
ANI Pharmaceuticals —East Windsor, NJ
- $52,000 - $70,000 a year
- Full-time
- 5 years
- Computer literacy
- Mid-level
- Paid holidays
- Disability insurance
Contract Quality Administrator / Quality Engineer I - Vera Beach, FL
STRATOSPHERE QUALITY —Vero Beach, FL
- $45 - $55 an hour
- Contract
- Ability to walk for extended periods
- Mid-level
- Office
Quick Apply
Quality Technician I
Mayville Engineering Co Inc —Neillsville, WI
- 8 hour shift
- Ability to walk for extended periods
- High school diploma or GED
- 1 year
Quick Apply
Quality Control Associate
SMSbiotech, Inc —San Diego, CA
- $60,000 - $68,000 a year
- Full-time
- Data analysis skills
- Mid-level
- Driver's License
- Mileage reimbursement
- Health insurance
Quick Apply
Quality Inspector I
Prototek Digital Manufacturing —Blue Mounds, WI
- $21 - $25 an hour
- Email
- US work authorization
- 1 year
- Hand tools
- Paid holidays
- Disability insurance
Quick Apply
Manufacturing Quality Technician I
PGT Industries —Fort Myers, FL
- From $20.50 an hour
- Full-time
- Word processing
- Mid-level
- Office
- Store discount
- Paid holidays
Quick Apply
12d

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QC Associate I/II - Contract

Abzena Inc. -
San Diego, CA

Quick Apply

Job Details

Temporary | Contract
$40 - $60 an hour

Qualifications

Data integrity assurance
High-performance liquid chromatographs
GMP
Bachelor's degree

Full Job Description

With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing.

Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely.

We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services.

We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient.

The Quality Control (QC) Associate I / II is responsible for performing analytical testing and laboratory activities that support stability, qualification/validation, and supporting release testing of biologics in a cGMP-regulated environment. This role supports routine QC operations through the execution of analytical methods, data review, laboratory investigations, method transfer activities, equipment maintenance, and continuous improvement initiatives while ensuring compliance with current Good Manufacturing Practices (cGMP), Good Documentation Practices (GDP), and applicable regulatory requirements.

The successful candidate will demonstrate strong technical expertise, attention to detail, data integrity awareness, and a commitment to maintaining inspection readiness while supporting internal and client-driven programs.

Responsibilities

Analytical Testing and Laboratory Operations

Perform routine and non-routine analytical testing of in-process, release, stability, characterization, reference standard, raw material, and investigational samples using approved methods and procedures.
Execute a variety of analytical techniques commonly used for biologics and large-molecule products, including but not limited to:
- HPLC/UHPLC
- CE-SDS
- cIEF/icIEF
- ELISA
- UV-Vis Spectroscopy
- Compendial testing
- Other biochemical and physicochemical methods as applicable.
Ensure all testing activities are completed accurately, efficiently, and within established timelines.
Maintain laboratory notebooks, worksheets, logbooks, and electronic records in accordance with GDP and ALCOA+ data integrity principles.
Ensure all activities comply with GMP, ALCOA+ principles, and data integrity regulations (FDA, EMA, ICH guidelines).
Review and support validation documentation, test scripts, and execution records. LIMS knowledge is a plus.
Identify and escalate compliance risks during system transition.
Support analytical method transfer, qualification, verification, and validation activities from Analytical Development or external clients into GMP QC laboratories.

Other Lab Responsibilities/Skills

Participate in comparability, bridging, and lifecycle management activities for analytical methods and reference standards.
Perform first-person review of analytical data to ensure completeness, accuracy, and compliance with applicable procedures and regulatory requirements.
Assist in the preparation and review of: Certificates of Analysis (CoA), Stability Summary Sheets (SSS), Analytical reports, Method qualification and validation reports, technical memoranda and laboratory documentation. Ensure documentation is complete, contemporaneous, attributable, and inspection ready.
Participate in laboratory investigations involving: OOS, OOT, invalids, and other lab investigations as needed.
Maintain laboratory equipment records and ensure equipment remains in a qualified state.
Support laboratory readiness for internal audits, client audits, regulatory inspections, and quality assessments.
Participate in process improvement initiatives to enhance laboratory efficiency, compliance, and data integrity.
Collaborate effectively with cross-functional teams including QA, AMD, Manufacturing, MSAT, and Materials Management.
Support implementation of new technologies, systems, and laboratory processes.

Qualifications

Required Qualifications and Skills:

Bachelor’s degree in chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific field.

3–7+ years of experience in GMP Quality Control laboratory environment.

Hands-on experience with HPLC/UPLC systems and chromatography data systems.

Direct experience with either Empower CDS or LIMS implementation preferred.

Strong understanding of GMP regulations and data integrity expectations.

Preferred Skills & Experience:

Prior experience transitioning from OpenLab, ChemStation, or similar CDS to Empower.

Exposure to LIMS configuration or implementation projects.

Experience supporting CSV (Computer System Validation) activities.

Strong problem-solving and troubleshooting skills in analytical environments.

Ability to work independently in a fast-paced project environment.

Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local Jaws.

This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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qc associate i jobs

QC Associate I/II - Contract

QC Associate I/II - Contract

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Quality Control Associate Bioanalytical Laboratory

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