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Biotech Operations Jobs in Worcester, MA (NOW HIRING)

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Biotech Operations information

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How much do biotech operations jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for biotech operations in Worcester, MA is $26.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $30.24 per hour, depending on experience, location, and employer.

What is biotech operations?

Biotech operations refer to the management and coordination of processes involved in developing, manufacturing, and distributing biotechnology products. This includes overseeing laboratory research, quality control, regulatory compliance, production scaling, and supply chain logistics. Professionals in biotech operations ensure that products such as pharmaceuticals, vaccines, or genetically engineered organisms are produced safely, efficiently, and in compliance with industry standards. Their work is critical in bringing scientific discoveries from the lab to market and ultimately to patients or consumers.

What are the key skills and qualifications needed to thrive in biotech operations, and why are they important?

Thriving in Biotech Operations requires a solid background in life sciences or engineering, experience with regulatory compliance, and a relevant degree such as a B.S. or M.S. in biotechnology or a related field. Familiarity with laboratory information management systems (LIMS), quality management systems (QMS), and certifications like Six Sigma or GMP training are highly valuable. Excellent problem-solving abilities, attention to detail, and strong collaboration skills help individuals excel and adapt in dynamic environments. These competencies are essential for ensuring operational efficiency, regulatory adherence, and successful product development in the biotech industry.

What are some common challenges faced in biotech operations, and how can new team members effectively navigate them?

Biotech Operations professionals often encounter challenges such as stringent regulatory compliance, maintaining production timelines, and managing cross-functional communication between research, quality, and manufacturing teams. New team members can navigate these challenges by proactively seeking mentorship, staying organized with project management tools, and maintaining open communication channels with colleagues in related departments. Embracing a mindset of continuous learning and adaptability is also crucial, as processes and technologies in biotech are constantly evolving.

What is the difference between Biotech Operations vs Laboratory Technician?

AspectBiotech OperationsLaboratory Technician
Required CredentialsBachelor's degree in biotech, biology, or related field; sometimes certifications in GMP or quality assuranceAssociate's or bachelor's degree in biology, chemistry, or related field; lab safety certifications often preferred
Work EnvironmentManufacturing facilities, quality control labs, production linesResearch labs, clinical labs, testing facilities
Employer & Industry UsageBiotech companies, pharmaceutical manufacturers, biotech startupsResearch institutions, hospitals, biotech and pharma labs

Biotech Operations roles focus on managing production processes, quality assurance, and ensuring compliance in manufacturing settings. Laboratory Technicians primarily perform experiments, testing, and data collection in research or clinical labs. While both roles require scientific knowledge, Biotech Operations emphasizes process management and compliance, whereas Laboratory Technicians focus on hands-on lab work and data analysis.

What job categories do people searching Biotech Operations jobs in Worcester, MA look for?

The top searched job categories for Biotech Operations jobs in Worcester, MA are:

What cities near Worcester, MA are hiring for Biotech Operations jobs?

Cities near Worcester, MA with the most Biotech Operations job openings:

Infographic showing various Biotech Operations job openings in Worcester, MA as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $54,470 per year, or $26.2 per hour.

Director, Patient Advocacy and Operations

Initial Therapeutics, Inc.

Waltham, MA โ€ข On-site

$196 - $240/hr

Other

Posted 15 days ago


Job description

Company Overview

Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease. At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at https://www.dyne-tx.com/, and follow us on X, LinkedIn and Facebook.

Role Summary

The Director, Patient Advocacy & Operations works as part of the Corporate & Patient Affairs (C&PA) team with two key areas of focus: 1) Cultivating and supporting strategic partnerships with patient advocacy organizations and 2) day-to-day management of key Patient Advocacy and Corporate Affairs operations.

Reporting to the VP, Patient Advocacy, this role is highly integrated with internal crossโ€‘functional teams and partners with external organizations.

This role is based in Waltham, MA and does not offer a remote option.

Primary Responsibilities
  • In collaboration with the VP of Patient Advocacy, partner closely with advocacy leaders and the broader patient community to advance key initiatives, including but not limited to:
    • Executing the patient advocacy strategy in alignment with corporate objectives
    • Fostering strong, strategic relationships with patient leaders, caregivers, and advocacy organizations to inform company programs and priorities.
    • Leading the planning and management of Patient Community Advisory Panels/Boards.
    • Conducting oneโ€‘onโ€‘one engagements with patient advocacy leaders to identifyโ€‘ needs, insights, and opportunities for collaboration.
    • Supporting clinical trial awareness and recruitment efforts through patient engagement and community focusedโ€‘ initiatives.
    • Collaborating with Medical Affairs, Marketing, Market Access/Patient Services, and Corporate Affairs to integrate the patient voice into R&D, clinical trial design, and commercialization efforts.
    • Representing Dyne at patient advocacy events, conferences, and advisory boards.
    • Collecting, synthesizing, and sharing patient community insights across functional teams.
    • Identifying and coordinating community participants for Dyneโ€‘led events (internal and external).
  • Partner with the VP of Patient Advocacy to plan and execute conference and patient advocacy organization (PAO) engagement activities:
    • Supporting Dyneโ€™s presence at patient advocacy and select scientific/medical conferences including event planning, session development, patientโ€‘facing materials, symposia, presentations, and onโ€‘site event execution.
    • Staffing events; willingness to travel approximately 20%.
  • Serve as the operational lead for the Patient Advocacy Grants, Sponsorships & Donations committee, including budget oversight and endโ€‘toโ€‘end management of the submission process, such as coordinating with requestors, ensuring proper documentation, and overseeing contracting and payment workflows.
  • Support the planning and execution of enterpriseโ€‘wide events (e.g., advocacy walks) that bring patient community voices into the organization, serving as a Patient Advocacy representative on cross functional teams and supporting coordination tasks when needed to support the delivery of highโ€‘quality experiences.
  • Manage and own patient engagementโ€‘related contracting, ensuring compliance and timely execution.
  • Lead operational processes for advancing patient advocacy materials through Medical Legal Review (MLR), ensuring accuracy, alignment, and compliance.
Education and Skills Requirements
  • Bachelorโ€™s degree in a relevant field and a minimum of 10+ years of related experience (social work, genetic counseling, nursing, public health preferred).
  • 8+ years of experience in patient advocacy in the biotech/pharmaceutical industry, preferably within a clinical stage biotechnology company.
  • Proven experience developing and sustaining partnerships with patient advocacy organizations and community leaders.
  • Deep understanding of rare diseases and the unique needs of rare disease communities.
  • Strong understanding of the Patientโ€‘Focused Drug Development (PFDD).
  • Exceptional communication, diplomacy, and crossโ€‘functional collaboration skills.
  • Experience managing budgets, teams, and compliance sensitive partnerships within a regulated environment.
  • Proven experience partnering with clinical teams on trial awareness and recruitment efforts.
  • Broad knowledge of the biopharma landscape and a solid working understanding of the drug development process.
  • Strong interpersonal skills with the ability to influence without authority and work effectively across diverse functions and personalities.
  • Compassionate, patient centered mindset, and a high degree of personal integrity.
  • Ability to manage multiple simultaneous projects, navigate ambiguity, and thrive in a fast paced, dynamic environment.
  • Experience with Patient Advocacy sponsorship contracting processes.
  • Proven operations experience and excellent project, vendor, and budget management capabilities with a demonstrated ability to deliver results.
  • Strong organizational skills and attention to detail.
  • Bilingual fluency in Spanish is a plus.
  • Overnight travel will be required; up to 20%.

MA Pay Range

$196,000 - $240,000 USD

The statements contained herein reflect general details as necessary to describe the principles functions for this job, the level of knowledge and skill typically required, and the scope of responsibility, but should not be considered an allโ€‘inclusive listing of work requirements. Individuals may perform other duties as assigned, including work in other functional areas to cover absences or relief, to equalize peak work periods or otherwise balance workload.

Dyne Therapeutics is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

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