Top 41 Pharmaceutical qms Jobs in Remote

Sr. Manager, Quality Systems - Audits & CAPAs (2026-8012)
CareTria —Remote
- $90,000 - $110,000 a year
- Full-time
- Writing skills
- Bachelor's degree
- Mentoring
- Paid parental leave
- Health insurance
Document Control & Quality Systems Administrator
Noctrix Health —Remote
- $120,000 - $140,000 a year
- Full-time
- Remote
- 3 years
- Continuous improvement
- Neurology
Quick Apply
3d
Senior Manager, GCP Quality Assurance
Spyre Therapeutics —Remote
- $149,000 - $175,000 a year
- Remote
- 6 years
- Bachelor of Science
- Bachelor's degree
- Health insurance
- Retirement plan
Associate Director - Corporate Quality Compliance (QMS)
Zimmer Biomet —Remote
- $130,000 - $165,000 a year
- Full-time
- 7 years
- Computer literacy
- Writing skills
- Wellness program
Quality Systems Implementation Specialist
RQM+ —Remote
- Ability to walk for extended periods
- Engineering
- Mid-level
Quick Apply
Contract Opportunity - Medical Device Auditors
SGS —Remote
- Contract
- Spanish
- Computer literacy
- English
Quick Apply
4d
Senior Manager, Clinical Quality Assurance
Gan & Lee Pharmaceuticals —Remote
- Full-time
- Writing skills
- English
- Analysis skills
Quick Apply
Senior Clinical Quality Assurance Associate
WEP Clinical —Remote
- Full-time
- Remote
- 3 years
- Analysis skills
- Bachelor's degree
- Paid parental leave
- Health savings account
Quality Assurance Specialist
Hims & Hers —New Albany, OH
- Full-time
- Remote
- Mid-level
- 3 years
- Analysis skills
- Employee stock purchase plan
- Health insurance
3d
Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management
BeiGene —Remote
- $172,000 - $232,000 a year
- Full-time
- 6 years
- Microsoft Outlook
- Computer literacy
- Health savings account
- Employee stock purchase plan
Sr. Manager, Quality Systems
TG Therapeutics —Remote
- Email
- Remote
- 5 years
- Mentoring
- US work authorization
Director, Central Quality Audit, Pharmacovigilance
GE HEALTHCARE —Remote
- $142,400 - $213,600 a year
- 5 years
- Pass drug screening
- English
- Health insurance
- Dental insurance
11d
Manager, Statistical Programming
Penumbra —Remote
- $158,000 - $227,000 a year
- 6 years
- Computer Science
- Office
- Paid parental leave
- AD&D insurance
Data Engineer Lead- PMS & QA
CooperSurgical —Trumbull, CT
- $120,000 - $160,000 a year
- Full-time
- Remote
- Databases
- In-person
- Senior level
- Health insurance
- Paid time off
Field Technical Specialist - Southeast US
Impulse Dynamics —Remote
- $90,000 - $120,000 a year
- Weekends as needed
- Remote
- Surgery
- Ability to walk for extended periods
- English
- Paid holidays
- Health insurance
Quick Apply
IT Senior Analyst - QARA
Zimmer Biomet —Remote
- $100,000 - $125,000 a year
- Full-time
- Computer Science
- 5 years
- Master's degree
- Wellness program
Director, Clinical Quality Assurance
Jazz Pharmaceuticals —Philadelphia, PA
- $184,000 - $276,000 a year
- Remote
- Writing skills
- 11+ years
- Master's degree
- Health insurance
- Dental insurance
10d
Quality Audit Specialist
LabConnect, LLC —Johnson City, TN
- Online Application
- Remote
- Mid-level
- Bachelor's degree
- Continuous improvement
- AD&D insurance
- Paid holidays
Quick Apply
Clinical Quality Assurance Manager
WEP Clinical —Remote
- Full-time
- Remote
- 5 years
- Supervising experience
- Bachelor's degree
- Paid parental leave
- Health savings account
10d
Field Technical Specialist - Northeast US
Impulse Dynamics —Remote
- $80,000 - $90,000 a year
- Weekends as needed
- Remote
- Surgery
- Ability to walk for extended periods
- English
- Paid holidays
- Health insurance
Quick Apply

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Sr. Manager, Quality Systems - Audits & CAPAs (2026-8012)

CareTria
Remote

Apply Now

Job Details

Full-time
$90,000 - $110,000 a year

Benefits

Paid parental leave
Health insurance
Dental insurance
Paid time off
Parental leave
Employee assistance program
Vision insurance
Retirement plan

Qualifications

Data analysis reporting
Audit report preparation
Writing skills
Drug regulation
Good documentation practices (GDP)
Corrective and preventive actions (CAPA)
GMP
Trend analysis
Bachelor's degree
Quality assurance experience within pharmaceutical industry
Investigative reports
FDA regulations

Full Job Description

The Sr. Manager, Quality Systems -Audits & CAPAs is responsible for the day-to-day management and hands-on execution of CareTria’s internal audit, supplier audit, and Corrective and Preventive Action (CAPA) programs. This role manages the operational delivery of the full audit lifecycle including planning, scheduling, execution, reporting, and findings closure for internal, supplier, and third-party audits in alignment with cGMP, GDP, PDMA, and DSCSA requirements. The Sr. Manager leads the qualification, ongoing monitoring, and periodic reevaluation of service providers to ensure continued compliance with cGMP, GDP, QMS expectations, and client requirements.

Responsible to drive continuous improvement across the Quality Management System by ensuring audit outcomes and CAPA activities strengthen operational controls, mitigate risk, and support a constant state of inspection readiness for clients and regulatory authorities. This role ensures that all quality events including deviations, distribution errors, temperature excursions, and other nonconformances—are thoroughly investigated using sound root-cause methodologies and that effective, sustainable corrective and preventive actions are implemented and closed on time.

**Must reside within a commutable distance from our Lakewood, NJ location.

KEY RESPONSIBILITIES:

Oversee the day-to-day operational administrator of the eQMS, managing user access, workflow routing, training assignments, and system accuracy.
Execute and manage the annual Internal Audit Plan and Supplier/Third-Party Audit Plan under the direction of the department senior management, including scheduling, conducting audits, drafting comprehensive audit reports, and driving timely closure of all audit findings.
Develop and maintain audit questionnaires and checklists to standardize compliance assessments across all supplier and client interactions; recommend updates to the department senior management as regulations or program needs evolve.
Manage the Investigations and CAPA process in accordance with cGMP, GDP, PDMA, and DSCSA requirements, ensuring root cause analyses are thorough and that corrective/preventive actions are assigned, tracked, and closed within approved timelines.
Coordinate client-specific audit CAPAs and questionnaires, ensuring responses are professional, accurate, and submitted within contractual timelines; escalate complex or high-risk client quality matters to the Associate Director. Partner with the Quality Control organization on shared quality events and investigations.
Manage the lifecycle of QMS events, including deviations, change controls, and non-conformances, ensuring they are documented, investigated, and mitigated per approved SOPs and within required timeframes.

PEOPLE MANAGEMENT & TEAM LEADERSHIP:

Directly manage, mentor, and develop QA staff within the Audits & CAPAs team, establishing clear performance goals and supporting professional development in audit and investigation competencies.
Manage daily activities and workloads of QA staff to ensure all audit schedules, investigation timelines, corrective action plans, and compliance deadlines are met; escalate resource conflicts or program risks to the Associate Director.
Conduct regular performance check-ins and formal evaluations; provide ongoing coaching and technical guidance to ensure staff proficiency in audit execution, root cause analysis, and CAPA writing.
Track, trend, and compile Quality KPIs (e.g., CAPA cycle time, audit findings closure rate, overdue investigations) and prepare reporting packages for presentation to Senior Leadership at Management Review Meetings.
Monitor team workflows daily to ensure no investigation or CAPA reaches “Overdue” status without a pre-approved extension and documented impact assessment; escalate imminent overdue items to department senior management in advance.

The above duties are meant to be representative of the position and not all-inclusive.

MINIMUM JOB REQUIREMENTS:

Education: Bachelor’s degree in Life Sciences, Supply Chain Management, or a related technical field.
Experience: Minimum of 4–6 years in Quality Assurance within the pharmaceutical or 3PL industry, with at least 2 years specifically focused on Audits, CAPA, and Investigations.
Professional Certification: ASQ Certified Quality Auditor (CQA), RAPS RAC, or equivalent quality/compliance certification is desirable.

KNOWLEDGE, SKILLS & ABILITIES:

Demonstrated ability to author clear, concise, and defensible investigation reports and CAPA responses suitable for regulatory and client review.
Experience using enterprise eQMS platforms (e.g., MasterControl, TrackWise, Veeva).
Ability to evaluate analytical and technical quality data to identify, track, and resolve unfavorable quality trends; strong working knowledge of cGMP, GDP, PDMA, DSCSA, and applicable FDA regulations governing pharmaceutical distribution.

PHYSICAL DEMANDS:

Ability to sit, stand, and work at a computer for extended periods.
Location of job activities 100% inside
Extensive manual dexterity (keyboarding, mouse, phone)
Expected to support Audits remotely or physically present at facility as needed.

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

The expected base pay range for this position is $90,000-$110,000 per year. The actual compensation for the position may vary based on market differences and on factors such as skills, experience, qualifications and can vary based on location and/or work schedule. In addition to base pay, CareTria offers a comprehensive benefits package. Full-Time benefits include access to health, dental, and vision insurance; retirement plan options; paid time off; paid parental leave; employee assistance programs; and other perks. Eligible employees may also have access to performance bonuses.

CareTria is an Equal Opportunity Employer

Apply Now

Refine Your Search

pharmaceutical qms jobs in remote

Sr. Manager, Quality Systems - Audits & CAPAs (2026-8012)

Document Control & Quality Systems Administrator

Senior Manager, GCP Quality Assurance

Associate Director - Corporate Quality Compliance (QMS)

Quality Systems Implementation Specialist

Contract Opportunity - Medical Device Auditors

Senior Manager, Clinical Quality Assurance

Senior Clinical Quality Assurance Associate

Quality Assurance Specialist

Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management

Sr. Manager, Quality Systems

Director, Central Quality Audit, Pharmacovigilance

Manager, Statistical Programming

Data Engineer Lead- PMS & QA

Field Technical Specialist - Southeast US

IT Senior Analyst - QARA

Director, Clinical Quality Assurance

Quality Audit Specialist

Clinical Quality Assurance Manager

Field Technical Specialist - Northeast US

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