
Qms Specialist
Remote · USContract$50–80/hrSeen todaySeen in employer's feed today
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Requirements
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Job overview
The QMS Specialist supports Quality Systems and batch/lot disposition for pharmaceutical and In Vitro Diagnostic products. The role provides hands-on QA oversight across the product lifecycle, ensuring products and quality processes meet FDA, ISO, and internal requirements. It is remote, with travel to New Jersey 10% of the time, and is contract-to-hire.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Job Title: QMS SpecialistJob Description
This role supports Quality Systems and batch/lot disposition for pharmaceutical and In Vitro Diagnostic (IVD) products. The specialist will provide hands-on QA oversight across the product lifecycle, ensuring products and quality processes meet FDA, ISO, and internal requirements.
Responsibilities
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Own and improve Quality Management System (QMS) processes.
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Review and approve deviations, nonconformances, investigations, CAPAs, change controls, SOPs, and controlled documents.
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Perform QA review of batch records, QC results, certificates, and support batch and lot disposition decisions while managing quality-related batch holds.
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Assess root cause, product impact, compliance risk, and determine appropriate CAPA.
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Ensure compliance with FDA requirements, 21 CFR Part 820/QMSR, and ISO risk-management principles.
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Support audits, regulatory inspections, supplier quality activities, and remediation efforts.
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Collaborate cross-functionally with Manufacturing, QC, Regulatory Affairs, and Supply Chain.
Essential Skills
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Strong knowledge of FDA and QMS requirements.
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3+ years of hands-on IVD/medical device Quality Systems experience.
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Experience with batch disposition/release.
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Proficiency in performing regulatory gap assessments and driving remediation.
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Experience with electronic QMS, investigations, CAPAs, deviations, and change controls.
Additional Skills & Qualifications
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Bachelor's degree in a scientific, engineering, or technical discipline.
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CQA or CQE certification is a plus.
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Ability to evaluate quality/compliance risks independently and make risk-based quality decisions.
Work Environment
This is a remote position with the flexibility to travel to New Jersey 10% of the time. The role offers opportunities for growth and visibility in a specialized environment focused on orphan drugs and complex rare disease products.
Job Type & Location
This is a Contract to Hire position based out of Bridgewater, NJ.
Pay and Benefits
The pay range for this position is $50.00 - $80.00/hr.
Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)
Job Type & Location
This is a Contract to Hire position based out of Bridgewater, NJ.
Application Deadline
This position is anticipated to close on Nov 13, 2026.
Workplace Type
This is a fully remote position.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.
Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.
How this job compares
Set against the 4,953 open Quality Assurance jobs on Olive Jobs, counted November 7, 2026.
- Pay
- This posting$50–80/hr
- New Jersey median$24–28/hr30 hourly ranges
- US median$26–31/hr840 hourly ranges
This range's midpoint, $65/hr, is 155% above the New Jersey median midpoint ($26/hr) — in the top quarter of Quality Assurance hourly ranges in New Jersey.
- Openings
- Olive Jobs lists 144 open Quality Assurance jobs in New Jersey and 4,953 across the US. 3% of them nationwide are listed as remote or flexible.
- Hiring the most in New Jersey
- Actalent (this employer)5 open
- Bristol Myers Squibb5 open
- CDM Smith5 open
- Experience
- This posting asks for at least 3 years of experience; Quality Assurance postings that state a minimum ask for 5 years at the median (3,787 postings).
- Education
- This posting asks for a bachelor's degree; 1,722 of the 4,953 open Quality Assurance jobs (35%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 7, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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