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Remote Director Quality Systems Jobs (NOW HIRING)

... product quality, and strengthen end-to-end service delivery. This role requires deep healthcare ... remote role welcomes candidates anywhere in Canada and the US. Travel is required as needed ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

... product quality, and strengthen end-to-end service delivery. This role requires deep healthcare ... remote role welcomes candidates anywhere in Canada and the US. Travel is required as needed ...

Houston, TX; or Remote #Li-Hybrid #Li-Remote You will mainly be accountable for: * Escalating to ... Familiarity with quality systems concepts and continuous improvement methodologies * Experience ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

... product quality, and strengthen end-to-end service delivery. This role requires deep healthcare ... remote role welcomes candidates anywhere in Canada and the US. Travel is required as needed ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

Hybrid - onsite and remote Overview Join a global medical technology organization undergoing an exciting quality systems integration initiative. This hybrid contract opportunity offers the chance to ...

Showing results 41-60

Remote Director Quality Systems information

See salary details

$31K

$125.6K

$213.5K

How much do remote director quality systems jobs pay per year?

As of Aug 9, 2026, the average yearly pay for remote director quality systems in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

What does a remote director of quality systems do?

A remote director of quality systems oversees an organization’s quality management processes, ensuring compliance with industry standards and regulations. They develop, implement, and monitor quality policies, lead audits, and collaborate with cross-functional teams to improve product or service quality, often using tools like QMS software and requiring certifications such as ISO or Six Sigma. This role involves strategic planning, leadership, and communication skills, typically working remotely with regular virtual meetings.

What is the difference between Remote Director Quality Systems vs Remote Quality Assurance Manager?

AspectRemote Director Quality SystemsRemote Quality Assurance Manager
CredentialsTypically requires advanced degrees (e.g., MBA, PhD) and extensive experience in quality systemsUsually requires a bachelor's or master's degree in quality, engineering, or related field with relevant certifications
Work EnvironmentStrategic leadership role overseeing quality systems across departmentsOperational role focused on implementing and managing quality assurance processes
Employer & Industry UsageCommon in regulated industries like pharmaceuticals, biotech, and medical devicesUsed across manufacturing, healthcare, and biotech sectors

The Remote Director Quality Systems focuses on strategic oversight and development of quality systems, while the Remote Quality Assurance Manager handles day-to-day quality assurance activities. Both roles require strong knowledge of industry standards, but the director position is more senior and strategic.

More about Remote Director Quality Systems jobs
What cities are hiring for Remote Director Quality Systems jobs? Cities with the most Remote Director Quality Systems job openings:
What states have the most Remote Director Quality Systems jobs? States with the most job openings for Remote Director Quality Systems jobs include:
Infographic showing various Remote Director Quality Systems job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 100% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Associate Director, Quality Control (56861)

Praxis Precision Medicines, Inc

Boston, MA • On-site, Remote

$150K - $169K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 9 days ago


Job description

Associate Director, Quality Control
Reports to: Senior Director, Quality Operations, CMC
Location: This position may be performed remotely with travel to the Boston area as needed.
Position Summary
Praxis is seeking a highly experienced, motivated, and innovative quality leader with strong experience in late-stage development and commercialization to join our Quality team as Associate Director, Quality Control to support QC product release and stability activities. Reporting to Senior Director, Quality Operations CMC, this position will be responsible for managing and executing Quality Control activities in support of product testing, release, and stability, and toxicology studies test material inventory support. Ensure GMP activities are conducted in accordance with applicable SOPs, compendia, approved methods, and in accordance with company's and regulatory agencies' policies and procedures.
Primary Responsibilities
  • Quality control oversight of contract lab activities e.g. routine testing, testing results review and approval, generation of Certificate of Analysis, review/approval of technical documents such as method validation and qualification protocols/reports, and regulatory filing documents per project needs as required
  • Manage and lead clinical and commercial quality control compliance for stability, reference standard, and specification programs
  • Support the establishment of QC systems such as product specifications, product expiry, reference standard program, QC documentation including SOP's, material specifications and other quality documents, etc.
  • Support CMC Analytical Development in a QC aspect by review and approval of applicable documents in support of activities such as method development, transfer, characterization, comparability investigations, analytical test method qualification plans/protocols and reports
  • Perform data review of trending for in-process testing, release, and stability and identify data trends, to ensure compliance with regulatory filings and ICH or other global health authority guidance documents, as applicable
  • Support technology transfer and process performance qualification with product characterization/process validation activities
  • QC support in the generation, quality, and compliance review of bioanalytical data from preclinical and clinical projects for proprietary compounds and in some cases support for sample analysis projects
  • Support tox material inventory monitoring process, to ensure no impediments to completing studies
  • Additional responsibilities and ad hoc projects as required

Qualifications and Key Success Factors
  • Bachelors degree strongly preferred, with minimum of 6 years of experience in cGMP Quality Control environment
  • In-depth technical and regulatory understanding of GMP biologics manufacturing and testing including applicable international regulations/standards (GMP and ICH guidelines) in all phases of product development and commercialization
  • Experience managing third party assay laboratories, collaborations, and relevant bioanalytical vendors preferred
  • Extensive knowledge of GMP regulations, ICH guidelines, and stability testing requirements.
  • Proven track record of managing stability programs and COA processes for clinical and commercial products
  • Experience working in QC lab environment with hands-on experience in running, qualifying, and validating analytical methods
  • Ability to work effectively in a fast-paced, dynamic environment
  • Experience managing Contract Test Labs activities
  • Experience with regulatory inspections and interactions with health authorities
  • Excellent communication skills and ability to build key networks and business relationships across all levels of the business

Compensation & Benefits
At Praxis, we're proud to offer an exceptional benefits package that includes:
  • 99% premium cost covered for medical (Blue Cross Blue Shield), dental, and vision plans
  • Bonus program structured to pay on a quarterly basis
  • 401k plan with 100% match up to 6% of employee's contribution (Traditional & Roth)
  • Wellness benefit of $200/month towards incredibly flexible options including travel, fitness equipment & memberships, student loan repayment, sports fees and much more
  • Unlimited PTO, (2) weeklong shutdowns each year, and a generous extended family leave benefit
  • Eligibility for equity awards and Employee Stock Purchase Plan (15% discount)

To round out this world-class total rewards package, we provide base salary compensation in the range of $150,000 to $169,000 annualized. Final salary range may be modified commensurate with job level, education, and experience.
Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE ® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to careers@praxismedicines.com.
Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.