Top 9 Quality control associate Jobs in Plymouth Meeting Pa

QC Documentation Associate
KVK Tech —Newtown, PA
- Microsoft Word
- Associate's degree
- Communication skills
- Paid holidays
- Dental insurance
4d
Associate QC Specialist
Frontage Laboratories —Exton, PA
- Full-time
- Microsoft Word
- Mid-level
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
Associate – Inspector
Newmark —Lower Gwynedd, PA
- Full-time
- Mid-level
- Bachelor's degree
- Travel
Automotive Quality Control Associate
CarShop Glen Mills-CS906 —Glen Mills, PA
- $15 - $17 an hour
- Full-time
- Background check
- Dealership
- Driver's License
- Paid training
- Paid holidays
Quick Apply
Associate Director, GxP Quality Auditor
Cabaletta Bio —Philadelphia, PA
- 5 years
- Bachelor's degree
- Budgeting
- Health insurance
- Paid time off
8d
Quality Control Intake Associate
Bucks County Estate Traders Inc —Hatfield, PA
- $18 - $22 an hour
- Full-time
- Customer service
- Writing skills
- English
- Paid parental leave
- Tuition reimbursement
Quick Apply
Operations Associate 3
L3Harris Technologies —Camden, NJ
- $32.73 an hour
- Computer literacy
- Mid-level
- High school diploma or GED
- Paid holidays
- Disability insurance
Inventory & Quality Control Associate I
PHILABUNDANCE —Philadelphia, PA
- $18 an hour
- Extended hours
- Background check
- Clean driving record
- OSHA
Quick Apply

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QC Documentation Associate

KVK Tech -
Newtown, PA

Apply Now

Job Details

4 days ago

Benefits

Paid holidays
Dental insurance
Tuition reimbursement
Paid time off
Vision insurance
401(k) matching

Qualifications

Associate's degree

Full Job Description

KVK Tech is seeking a detail-oriented QC Documentation Associate to join our Quality Control (QC) Chemistry department in Newtown, PA.

The QC Documentation Associate will maintain accurate, complete, and compliant documentation throughout the QC data lifecycle. This role supports the creation, revision, versioning, and maintenance of analytical methods, product specifications, controlled spreadsheets, and Empower calculations. The ideal candidate will demonstrate exceptional attention to detail, an understanding of cGMP documentation requirements, and the ability to maintain inspection-ready records in accordance with ALCOA+ data integrity principles.

This position’s responsibilities will include, but not be limited to the following:

Prepare, revise, and maintain analytical methods, test procedures, product specifications, and related records within controlled documentation systems.
Track compendial updates from USP/NF, EP, and JP and support the timely implementation of required changes to impacted methods, specifications, documents, and systems.
Process documentation change control requests, ensuring appropriate review, accurate routing, complete supporting information, and timely closure.
Validate, maintain, and revalidate controlled Excel spreadsheets and Empower calculations to ensure accuracy, traceability, and compliance with data integrity requirements.
Organize, label, file, archive, and retrieve paper-based and electronic QC documentation in accordance with applicable SOPs and record-retention requirements.
Collaborate with QC analysts, supervisors, and QA reviewers to resolve documentation issues, research technical or regulatory requirements, and maintain consistent documentation practices.

We are looking for applicants with:

Associate’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or another related scientific discipline required; Bachelor’s degree preferred.
0-3 years of experience in a GMP-regulated pharmaceutical environment preferred.
Previous experience with QC documentation, document control, analytical method or specification management, controlled spreadsheets, Empower, or laboratory operations strongly preferred.
Working knowledge of cGMP, GLP, FDA expectations, Good Documentation Practices, and ALCOA+ data integrity principles.
Familiarity with compendial sources such as USP/NF, EP, and JP and an understanding of how compendial changes may affect analytical methods and product specifications.
Strong proficiency in Microsoft Word and Excel; experience with controlled spreadsheets, formula validation, or Empower calculations preferred.
Exceptional attention to detail, organizational ability, and written and verbal communication skills, with the ability to manage multiple priorities and collaborate with laboratory and quality personnel.

What we offer:

401(k) with company match
Health, vision, and dental Insurance
Childcare expense reimbursement
Tuition reimbursement
Annual bonus eligibility
Annual merit increases
Paid Time Off and Flexible Holidays

KVK Tech is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status.

We encourage you to apply if you feel that you are a match! We look forward to hearing from you.

Apply Now

Refine Your Search

quality control associate jobs in plymouth meeting pa

QC Documentation Associate

Associate QC Specialist

Associate – Inspector

Automotive Quality Control Associate

Associate Director, GxP Quality Auditor

Quality Control Intake Associate

Operations Associate 3

Inventory & Quality Control Associate I

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