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Remote Quality Control Biotech Jobs in Boston, MA

Vor Bio

Quality Systems Manager

Boston, MA · Remote

$170K - $180K/yr

... the biotech industry. Key Responsibilities * Documentation Management: Perform document control ... Ability to work effectively with communication and office tools in a remote, fast-paced, and ...

Cytel

Senior Statistical Programmer FSP

Cambridge, MA · On-site +1

Production and QC / validation programming * Generating complex ad-hoc reports utilizing raw data ... Biotech industry with a bachelor's degree or equivalent. At least 6 years of related experience ...

Vrtx

Principal Statistical Programmer

Boston, MA · Remote

$149K - $223K/yr

Performs quality control checks of SAS code and output produced by other Statistical Programmers to ... Remote Company Information Vertex is a global biotechnology company that invests in scientific ...

UL Solutions

Remote Inspector - Jewelry

Canton, MA · Remote

$33 - $37.50/hr

High school diploma or equivalent plus a minimum of 2 years demonstrated proficiency in quality ... We also provide sick time off (72 hours). #LI-MB1 #LI-Remote * Evaluate raw materials, associated ...

Danaher

Inside Sales Representative (REMOTE)

Boston, MA · On-site +1

$33.65 - $43.27/hr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... We bring together deep scientific expertise, an unwavering commitment to quality, and a ...

UL Solutions

Remote Inspector - Jewelry

Canton, MA · On-site +1

$33 - $37.50/hr

High school diploma or equivalent plus a minimum of 2 years demonstrated proficiency in quality ... We also provide sick time off (72 hours). #LI-MB1 #LI-Remote About Us A global leader in applied ...

Danaher

Inside Sales Representative (REMOTE)

Boston, MA · On-site +1

$33.65 - $43.27/hr

... biotechnology? At Aldevron, one of Danaher's 15+ operating companies, our work saves lives-and we ... We bring together deep scientific expertise, an unwavering commitment to quality, and a ...

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Remote Quality Control Biotech information

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$12

$23

$36

How much do remote quality control biotech jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for remote quality control biotech in Boston, MA is $23.33, according to ZipRecruiter salary data. Most workers in this role earn between $18.80 and $26.11 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Remote Quality Control Biotech position, and why are they important?

To thrive as a Remote Quality Control Biotech, you generally need a solid background in biology or biotechnology, laboratory techniques, and quality assurance processes, often supported by a relevant degree in life sciences or biotechnology. Familiarity with regulatory standards such as GMP or ISO, data analysis software, and laboratory information management systems (LIMS) is typically required. Strong attention to detail, effective communication, and the ability to work independently are important soft skills in remote settings. These competencies ensure accurate quality assessments, regulatory compliance, and effective collaboration with distributed teams.

What are the most common challenges faced by remote quality control professionals in the biotech industry?

One of the main challenges faced by remote quality control biotech professionals is maintaining effective communication and collaboration with on-site laboratory teams and cross-functional departments. Since much of the data review, reporting, and troubleshooting are performed remotely, it can also be challenging to stay updated with real-time lab processes and quickly resolve discrepancies. To address these issues, many companies use digital collaboration tools, regular virtual meetings, and thorough documentation practices. Adapting to these remote workflows ensures that quality standards are consistently met even from a distance.

What is a Remote Quality Control Biotech job?

A Remote Quality Control Biotech job involves ensuring the quality, safety, and compliance of biotechnological products and processes while working remotely. Responsibilities may include reviewing data, conducting virtual audits, ensuring regulatory compliance, and collaborating with teams to maintain product integrity. Professionals in this role use digital tools to analyze laboratory results, monitor production processes, and document findings. Strong attention to detail, knowledge of industry regulations, and proficiency in data analysis are essential. This position is critical in maintaining high-quality biotech products while allowing flexibility through remote work.

What are popular job titles related to Remote Quality Control Biotech jobs in Boston, MA? For Remote Quality Control Biotech jobs in Boston, MA, the most frequently searched job titles are:
What job categories do people searching Remote Quality Control Biotech jobs in Boston, MA look for? The top searched job categories for Remote Quality Control Biotech jobs in Boston, MA are:
What cities near Boston, MA are hiring for Remote Quality Control Biotech jobs? Cities near Boston, MA with the most Remote Quality Control Biotech job openings:
Remote Quality Control Biotech jobs near you
Infographic showing various Remote Quality Control Biotech job openings in Boston, MA as of July 2026, with employment types broken down into 77% Full Time, 9% Part Time, and 14% Contract. Highlights an 100% Remote job distribution, with an average salary of $48,528 per year, or $23.3 per hour.
Associate Director, Quality Operations

Associate Director, Quality Operations

Amylyx Pharmaceuticals

Cambridge, MA • On-site, Remote

Other

Posted 8 days ago

Job description

The Opportunity

This position is responsible for providing CMC quality oversight of drug substance, drug product, and finished drug product manufacturing, testing, packaging, labeling and distribution for non-commercial products that are in various development stages.

As the GMP quality expert, this role is accountable for ensuring all company, regional, and global GMP and GDP standards and regulations are met, and that the GMP Quality department performs to a standard that ensures the quality of products and materials produced by Amylyx contracted partners. 

We anticipate hiring the Associate Director, Quality Operations in September 2026.

Responsibilities

  • Provide quality oversight of production, labeling and testing activities, including warehousing and distribution of clinical trial materials.
    • Provide QA review and approval on quality technical agreements, master production records, product specifications (in-process, release, and stability), analytical method qualification/validation documents, method transfer documents, and stability plans.
    • Review executed Batch Production and QC Control Records to ensure all approved procedures were followed and all specifications are met.
    • Prepare and /or approve batch disposition packages.
    • Provide QA review and approval on quality system records, including but not limited to deviations, OOS, change controls, CAPAs, and product quality complaints.
    • Lead or participate in regular meetings internally and externally as CMC Quality SME to ensure Amylyx's quality expectations are met in the areas of Good Manufacturing Practice, Good Distribution Practice, and Good Documentation Practice.
  • Provide QA review on INDs. Assure that source data and information used in regulatory submissions and validation activities is maintained and traceable.
  • Write, review and/or approve SOPs as QA SME for manufacturing, testing, labeling, packaging, and transportation of early-stage products.
  • Support FDA, EMA or other regulatory agency inspections.

Required Qualifications

  • Bachelors degree
  • 8+ years of experience within the Pharmaceutical or Biotechnology industry in a quality role.
  • Experience with authoring and reviewing IND CMC sections and addressing Regulatory Filing requirements in FDA cGMP regulations, Eudralex and ICH Guidance, as well as other Biopharma industry guidance and regulations.
  • Ability to work with all levels of the organization and external contract service providers to ensure compliance with current regulations.
  • Travel may be required up to 10%, which may include on-site review of third-party operations.

Preferred Requirements

  • QC/AD experience 
  • Small molecule and peptides experience

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested.
  • You must have access to work in setting which enables meeting all requirements of the role (including privacy, reliable internet access, phone, ability to video conference, etc.) at your remote location.

Apply