Top 6 Quality control associate Jobs in West Chester, Pa

QC Associate Scientist
West Pharmaceutical Services —Exton, PA
- Hybrid work
- Background check
- Public speaking
- Mid-level
Associate QC Specialist
Frontage Laboratories —Exton, PA
- Full-time
- Microsoft Word
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
FSP Associate Scientist-QC Review
Thermo Fisher Scientific —King of Prussia, PA
- Full-time
- Bachelor's degree
- Driving
- Travel
7d
Inventory & Quality Control Associate I
PHILABUNDANCE —Philadelphia, PA
- $18 an hour
- Extended hours
- Background check
- Clean driving record
- OSHA
Quick Apply
Associate Director, GxP Quality Auditor
Cabaletta Bio —Philadelphia, PA
- 5 years
- Bachelor's degree
- Budgeting
- Health insurance
- Paid time off
5d

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QC Associate Scientist

West Pharmaceutical Services -
Exton, PA

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Job Details

Qualifications

Biology
Biological safety protocols
Research design
Experimental data reports
Chemical handling safety procedures
Laboratory safety
Tensile testing
Standard Operating Procedures (SOPs) implementation
Technical documentation
Safety regulations
Public speaking
Chromatographs
Mid-level
Technical report writing
Research project design
Bachelor's degree in biology
Laboratory reports
Bachelor's degree
Pharmaceutical company experience
Scientific protocols
Decision making
Laboratory standard operating procedures
Data interpretation
Experimental design
Laboratory specimen handling
Physical analysis
Chemistry
Pipetting
Quality control experience within pharmaceutical industry
Chemical analysis

Full Job Description

Requisition ID: 74985
Date: Aug 12, 2026

Location:
Exton, PA, US, 19341

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Department: Laboratory

Description:
This is an onsite position requiring the team member to be onsite 5 days a week. No relocation is provided for this opportunity.

At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?

There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.

We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.

Job Summary

In this role, you will be responsible for performing testing of products for internal and external customers using a variety of analytical techniques. You may be assisting in developing procedures for instrumentation, test instructions, and test reports. You may coordinate the day-to-day receipt and shipment of samples in the laboratory and support the Laboratory team in administration and quality systems.

Essential Duties and Responsibilities
Perform analysis using various techniques including established and experimental test methods.
Use instrumentation both qualitatively and quantitatively where appropriate.
With guidance assist in completing projects from protocol to final report.
Train analysts as appropriate.
Develop and validate methods with guidance.
Keep current with new analytical technology.
Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude.
Employ QC analytical techniques including but not limited to spectroscopy and chromatography, titrations, or visual and functional testing.
Assist in preparation of work instructions, SOPs, technical reports, and qualification documentation.
Assist in lab study design and preparation in study plans and protocols.
Willingness to learn and apply new analytical techniques.
Perform lab investigations, OOS, and OOT as required.
Meet individual and departmental goals as required.
Apply required cGMP regulations and internal QA procedures
Adhere to established laboratory safety procedures
Handle hazardous and non-hazardous chemicals as well as limited biological compounds
Other duties as assigned #LI-AP1 #LI-HYBRID
Education
Bachelor's Degree in Biology, Chemistry or a relevant scientific field preferred
Work Experience
No minimum experience required
Experience working in a laboratory or cGMP/pharmaceutical environment preferred
Laboratory administrative/Coordinator/Analyst role preferred
Preferred Knowledge, Skills and Abilities
cGMP
Tensile, force, compression or other compendial physical testing experience. Instron and/or Bluehill software knowledge is a plus
Wet chemistry knowledge and techniques such as Pipetting, Titrations, and Extractions
Spectroscopy and/or Chromatographic knowledge
Able to be aware of all relevant SOPs as per Company policy as they are related to the position covered by this Job Description
Travel Requirements
5%: Up to 13 business days per year
Physical Requirements
Light-Exerting up to 20lbs/9kg of force frequently, and/or negligible amount of force frequently constantly to move objects.
Additional Requirements
Job-related activities that require a physical activity such as standing in laboratory environment
Use hands to finger, handle, feel or operate objects, tools or controls and reach with hands and arms.
Employee must have good color vision acuity
Employee may be required to lift heavy objects (up to 25 lbs.) without assistance
Job-related activities that require a mental skill or ability such as communication, quick decision making, interpreting data, reading or writing, public speaking, etc.
Must be able to express or exchange ideas with employees
Must be able to understand direction and adhere to established procedures
Must be able to multi-task, work under time constraints, problem solve, and prioritize
Read and interpret data, information and documents

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to [email protected]. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening.

Nearest Major Market: Philadelphia

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Refine Your Search

quality control associate jobs in west chester, pa

QC Associate Scientist

Associate QC Specialist

FSP Associate Scientist-QC Review

Inventory & Quality Control Associate I

Associate Director, GxP Quality Auditor

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