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Remote Quality Control Biotech Jobs in Worcester, MA

Synex Talent

Oncology Data Specialist

Northborough, MA · Remote

$150K - $200K/yr

This full-time, remote position allows you to leverage your expertise in the health and fitness ... Provide support in data entry, validation, and quality control processes * Utilize statistical ...

Clinton Savings Bank

Loan Operations Manager

Clinton, MA · On-site +1

$66K - $90K/yr

Loan Operations Manager Pay Range $66,971 - $90,413 annually Hybrid with 2 days remote. Standard ... quality control Ensure accurate maintenance of loan terms, rates, collateral, insurance, taxes ...

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

As of Aug 7, 2026, the average hourly pay for remote quality control biotech in Worcester, MA is $21.43, according to ZipRecruiter salary data. Most workers in this role earn between $17.26 and $23.99 per hour, depending on experience, location, and employer.

What skills and qualifications are needed for a remote quality control biotech?

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?

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 Worcester, MA? For Remote Quality Control Biotech jobs in Worcester, MA, the most frequently searched job titles are:
What job categories do people searching Remote Quality Control Biotech jobs in Worcester, MA look for? The top searched job categories for Remote Quality Control Biotech jobs in Worcester, MA are:
What cities near Worcester, MA are hiring for Remote Quality Control Biotech jobs? Cities near Worcester, MA with the most Remote Quality Control Biotech job openings:
Remote Quality Control Biotech jobs near you

Manager, Quality Operations

Viridian Therapeutics, Inc.

Waltham, MA • On-site, Remote

$118K - $145K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago

Job description

Description
At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets.
Reporting to the Director, Quality Operations, the Manager, Quality Operations, will take the lead in overseeing and optimizing GMP systems and processes to ensure alignment with corporate goals and strict adherence to regulatory standards. This role requires a strategic thinker and a hands-on leader, responsible for ensuring compliance with all relevant policies and procedures while working closely with internal teams to drive quality excellence. In addition, the Manager, Quality Operations will serve as the key liaison with external partners, including CMOs, and vendors, fostering strong relationships to ensure seamless quality operations across the board.
This role may be based in our Waltham, MA headquarters or remote. Office-based employees are required to work in the office three (3) days a week. For remote role, travel to headquarters may be required at the discretion of management.
Responsibilities (including, but not limited to):
  • Oversee CMO activities to ensure products are manufactured in accordance with regulatory requirements, product registrations, and quality agreements
  • Perform batch record reviews and lot dispositions per established procedures
  • Conduct and review product and/or lot-related deviations, complaints, CAPAs, change controls, and annual product quality reviews (APQRs)
  • Support new product introductions (NPI) and ensure GMP readiness for manufacturing and supply chain operations
  • Review and approve controlled documents supporting product manufacture and testing, including master batch records, product specifications, analytical methods, protocols, and reports.
  • Lead continuous improvement initiatives to enhance quality assurance processes
  • Collaborate cross-functionally with departments such as CMC, Regulatory Affairs, and Supply Chain to ensure quality standards are met
  • Ensure compliance with internal quality systems, including document control, training, and audit readiness
  • Assist with regulatory inspections and internal audits, ensuring resolution of observations and implementation of corrective actions
  • Quality review of regulatory filings
  • Establish and track Key Performance Indicators (KPIs) for CDMO quality performance
  • Participate in Quality Management Reviews

Requirements
  • Minimum of 5+ years of Quality Assurance experience in Biotechnology and/or pharmaceutical industry
  • Bachelor's degree in Life Science or Engineering is required
  • Strong experience working with CDMOs
  • Experience in combination products ideal, although not required
  • Demonstrated strong written and verbal communication skills
  • Proven mindset of proactive continuous improvement
  • Efficient independent worker with ability to focus and drive for results
  • Strong knowledge of US and global GMP regulations, ICH guidelines, and industry best practices
  • Experience supporting clinical phases through commercialization and lifecycle management
  • Proficiency in electronic Quality Management Systems (e.g., Veeva, TrackWise)
  • Demonstrated ability to manage batch disposition, deviation investigations, and change control processes
  • Strong analytical and problem-solving skills with a proactive continuous improvement mindset
  • Excellent attention to detail, organizational, and time management skills
  • Strong written and verbal communication skills
  • Ability to work independently and collaboratively in a fast-paced, team-oriented environment
  • Strong commitment to ethical standards
  • Proficient with Microsoft Office suite (i.e., Word, PowerPoint, Excel, Outlook, SharePoint, etc.)
  • Ability to travel up to 20% domestically and internationally, including visits to CMOs and Viridian's offices
  • The salary range for this position is commensurate with experience

Viridian offers a comprehensive benefits package including:
• Competitive pay and stock options for all employees
• Medical, dental, and vision insurance
• 100% Paid Parental leave
• Short- and long-term disability coverage
• Life, Travel and AD&D
• 401(k) Company Match with immediate company vest
• Employee Stock Purchase plan
• Generous vacation plan and paid company holiday shutdowns
• Various fertility, mental, financial, and proactive physical health programs
Viridian Therapeutics, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination, harassment, or retaliation of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by Federal, State, and Local laws. Viridian will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
Viridian Therapeutics, Inc. participates in E-Verify, the federal program for electronic verification of employment eligibility.

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