Top 10 Quality control associate Jobs in Pottstown Pa

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 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
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Quality Control Associate
Buck Mason —Mohnton, PA
- Overtime
- Spanish
- English
- Mid-level
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Associate Director, Quality Control
PPL Healthcare LLC —Sellersville, PA
- Full-time
- 7 years
- Analysis skills
- Mentoring
3d
Quality Packaging Associate II 2nd Shift
Sharp Clinical Services —Macungie, PA
- From $19 an hour
- Overtime
- Background check
- Mid-level
- High school diploma or GED
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Inline Quality Control Associate
Buck Mason —Mohnton, PA
- Overtime
- Spanish
- English
- Ability to lift 50 pounds
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Associate – Inspector
Newmark —Lower Gwynedd, PA
- Full-time
- Mid-level
- Bachelor's degree
- Travel

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quality control associate jobs near pottstown pa

Associate QC Specialist

Frontage Laboratories -
Exton, PA

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Job Details

Full-time

Benefits

Disability insurance
Health insurance
Dental insurance
401(k)
Life insurance

Qualifications

Microsoft Word
Data integrity assurance
Biology
Biotechnology
Immunological assays
Biochemistry
Quality records maintenance
Data validation techniques
Standard Operating Procedures (SOPs) implementation
Immunological laboratory techniques
Spreadsheets
Regulatory compliance
Continuous improvement (laboratory quality control method)
Mid-level
Bachelor's degree in biology
Quality control data reporting
Data integrity and documentation
Laboratory quality control records management
Bachelor's degree
Quality assurance standard operating procedures
Pharmaceutical company experience
Data quality monitoring
Laboratory standard operating procedures
Bachelor's degree in pharmaceutical sciences
Quality inspection
Clinical research inspection readiness
Technical writing quality assurance
Laboratory information systems (LIS)
Quality control communication
Cross-functional collaboration

Full Job Description

Associate QC Specialist

Title: Associate QC Specialist

Department: Large Molecule

Location: Exton, PA

Full-time

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.

Position/Job Summary: The Associate QC Specialist supports quality control activities for Large molecule (PK, PD, ADA, Nab etc.) bioanalytical studies conducted in a GLP-regulated contract research organization (CRO) environment. This role is responsible for the independent quality review of bioanalytical data, laboratory documentation, and study reports to ensure accuracy, completeness, and compliance with Standard Operating Procedures (SOPs), Good Laboratory Practice (GLP), and sponsor requirements.

The position plays a key role in ensuring the integrity of data delivered to clients by reviewing analytical datasets, validating report content, and supporting preparation and quality control of data tables used in clinical and regulatory reports.

Roles & Responsibilities

Bioanalytical Data QC Review

Perform independent quality control review of biomarker bioanalytical data including laboratory notebooks, raw instrument data, electronic files, and Laboratory Information Management System (LIMS) records.
Verify accuracy, traceability, completeness, and consistency of analytical data in accordance with SOPs, GLP regulations, and study protocols.
Identify discrepancies or documentation gaps and work with laboratory scientists and study teams to resolve issues prior to final reporting.

Study Report Review

Review method development, qualification, and validation reports to ensure scientific accuracy and consistency between narrative text, tables, figures, and source data.
Review bioanalytical sample analysis reports for completeness, data integrity, and compliance with internal procedures and client requirements.
Ensure reported results are supported by verified raw data and documentation.

Data Tables and Client Deliverables

Prepare and QC bioanalytical result tables for clinical study reports and biomarker testing reports.
Review and interpret client Data Transfer Specifications (DTS) to ensure correct formatting, variable definitions, and dataset structure.
Generate, QC, and transmit client-ready datasets and data tables according to sponsor specifications and project timelines.

Data Integrity and Compliance

Ensure all QC review activities maintain data integrity and meet regulatory expectations.
Maintain documentation supporting QC review processes for audit and inspection readiness.
Assist in maintaining standardized templates and QC checklists to support efficient report review.

Cross-Functional Collaboration

Collaborate with laboratory scientists, project managers, data management teams, and quality assurance personnel to support timely study reporting and client deliverables.
Communicate QC findings clearly and track issue resolution to ensure high-quality final reports.

Additional Responsibilities

Support continuous improvement initiatives for QC processes and documentation standards.
Assist with preparation for internal audits and regulatory inspections.
Perform other duties as assigned.

Qualifications:

Education

Bachelor’s degree in Biology, Biochemistry, Immunology, Pharmaceutical Sciences, or related life sciences discipline.

Experience

0–3 years of experience in a bioanalytical laboratory, biomarker research, or quality control role in a CRO, pharmaceutical, or biotechnology environment.
Experience with GLP-regulated studies or regulated documentation practices is preferred.

Technical Skills

Familiarity with PK, PD, ADA, Nab etc. bioanalytical workflows (e.g., ligand-binding assays, ELISA, multiplex immunoassays, molecular assays, or emerging biomarker platforms).
Experience reviewing scientific reports, analytical datasets, and laboratory documentation.
Knowledge of LIMS systems and electronic laboratory documentation practices.
Proficiency with Microsoft Excel, Word, and data formatting tools for dataset preparation.

Core Competencies

Strong attention to detail with a focus on data accuracy and data integrity.
Ability to review complex datasets and identify inconsistencies.
Strong written and verbal communication skills.
Ability to manage multiple priorities in a fast-paced CRO environment.
Strong collaboration skills when working with cross-functional teams.

Salary and Benefits

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.

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Refine Your Search

quality control associate jobs in pottstown pa

Associate QC Specialist

Validation Associate

Quality Control Intake Associate

Quality Control Associate

Associate Director, Quality Control

Quality Packaging Associate II 2nd Shift

Inline Quality Control Associate

Associate – Inspector

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