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Script Development Jobs in Massachusetts (NOW HIRING)

My3Tech Inc

Salesforce QA Engineer

Everett, MA · On-site

$57.25 - $75.75/hr

Support agile scrum teams in the test script development and execution of system and end-to-end testing for Salesforce based applications. * Automate business processes and data management to improve ...

Stone Search

Endpoint Architect

Foxboro, MA

$257K/yr

US Citizens or GC Holders On-site daily- Foxboro, MA The Endpoint Architect will own endpoint strategic planning & architecture development, systems engineering, script development, application and ...

CERES Group

Data Analyst

Boston, MA · On-site

Experience with visualization tools such as Tableau or Qlikview and writing procedural logic such as script development * Experience with other BI and ETL tools an advantage * Insurance or Financial ...

InterSystems

Senior Quality Development Engineer

Boston, MA · On-site

$96K - $130K/yr

The Senior Quality Development Engineer will work as a technical specialist in an Agile development ... scripts for continuous integration systems. • System management tasks to support testing ...

InterSystems

Senior Quality Development Engineer

Boston, MA · On-site

$96K - $130K/yr

The Senior Quality Development Engineer will work as a technical specialist in a cross-functional ... scripts for continuous integration systems. • System management tasks to support testing ...

General Dynamics Mission Systems, Inc

Test Lead

Dedham, MA · On-site

$146K - $154K/yr

Python script development required * Working knowledge of systems engineering concepts, principles, and theories * Experience developing Systems Design and Requirement Management * Test Procedure ...

InterSystems

Senior Quality Development Engineer

Boston, MA · On-site

$96K - $130K/yr

The Senior Quality Development Engineer will work as a technical specialist within a cross ... scripts for continuous integration systems. • System management tasks to support testing ...

Kelly Honda

Business Development Coordinator

Lynn, MA · On-site

We are looking for a Business Development Coordinator to join our growing Kelly Honda team! The ... Respond quickly to internet, phone and live chat inquiries using email, scripts and templates

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Script Development information

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$108.7K

$125.6K

$140.9K

How much do script development jobs pay per year?

As of Jun 4, 2026, the average yearly pay for script development in Massachusetts is $125,594.00, according to ZipRecruiter salary data. Most workers in this role earn between $117,400.00 and $133,800.00 per year, depending on experience, location, and employer.

What is a Script Development job?

A Script Development job involves working on the creation, refinement, and structuring of scripts for films, television, or other media. Professionals in this role collaborate with writers, producers, and directors to develop compelling narratives, strong character arcs, and engaging dialogue. They provide feedback on drafts, suggest revisions, and ensure the script aligns with the project's vision. This process includes researching, editing, and sometimes overseeing multiple rewrites to make the script production-ready.

What are the key skills and qualifications needed to thrive in the Script Development position, and why are they important?

To thrive in Script Development, you need a strong understanding of storytelling, narrative structure, and industry trends, often supported by a background in screenwriting, film studies, or literature. Familiarity with screenwriting software (such as Final Draft or Celtx) and collaborative project management tools is typically required. Excellent communication, feedback, and creative problem-solving skills help you build productive relationships with writers and production teams. These abilities are crucial for shaping compelling scripts that meet both creative and production objectives in media projects.

What are the typical responsibilities of someone working in Script Development?

Professionals in Script Development are responsible for evaluating, editing, and providing feedback on scripts to ensure they align with the project's vision and production requirements. They often collaborate closely with writers, directors, and producers to refine storylines, characters, and dialogue, as well as to guide revisions throughout the development process. The role may also involve researching market trends, identifying promising scripts or concepts, and helping shape proposals for new projects. Script Development specialists typically balance several projects at once and must adapt to shifting priorities and creative directions. This dynamic role offers great opportunities for creativity, industry networking, and eventual advancement into production or executive positions.
More about Script Development jobs
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Script Development jobs near you
Infographic showing various Script Development job openings in Massachusetts as of May 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $125,594 per year, or $60.4 per hour.
Director / Senior Director, Quality Control Automation & Digitalization

Director / Senior Director, Quality Control Automation & Digitalization

Beam Therapeutics

Cambridge, MA • On-site

Full-time

Posted 24 days ago

Job description

Company Overview:
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam's suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
We are seeking a Director / Senior Director, Quality Control Automation and Digitalization to lead the strategic transformation of Quality Control operations through advanced automation and digital platforms. This role blends strategic leadership with deep hands-on technical expertise in laboratory automation, digital solutions, and GMP operations. The position will serve as the QC Automation Lead, responsible for overseeing and coordinating end-to-end automated analytical workflows across multiple functions, including Analytical Development, Automation, Computational Biology, Quality Control, Quality Assurance, Information Technology, and Validation. This leader will drive cross-functional alignment to ensure streamlined processes and timely delivery of robust, compliant analytical methods and procedures in support of GMP testing. In addition, this role is accountable for implementing comprehensive training programs to strengthen QC capabilities in automated and digital platforms, ensuring scientific rigor, data integrity, and operational excellence. The Senior Director/Director will foster a culture of innovation and continuous improvement, positioning QC to support current and future portfolio and regulatory needs.
Primary Responsibilities:
  • Serve as the QC Automation Lead, providing deep technical expertise and strong compliance acumen to design, deploy, and sustain automation and digital solutions supporting GMP analytical methods and procedures.
  • Partner strategically with cross-functional stakeholders-including Analytical Development, Automation, Computational Biology, Quality Control, Quality Assurance, Information Technology, and Validation-to define and implement integrated, end-to-end automation workflows.
  • Oversee the full lifecycle of automated solutions, including instrumentation and software onboarding, qualification, and validation; robust script development and testing; and technical transfer, qualification, and validation of automated analytical methods. This includes complex modalities such as cell-based functional assays, flow cytometry, ddPCR, ELISA, and NGS.
  • Drive alignment on deliverables and exit criteria across Research, Development, and Commercial phases, including pre-qualification package signoffs, SME training completion, and qualification package approvals.
  • Direct and facilitate investigation and resolution of complex technical challenges related to automated systems, ensuring scientific rigor, data integrity, and compliance with GMP expectations.
  • Design and implement comprehensive training programs to build QC capability and confidence in automated and digital platforms, ensuring strong scientific and technical understanding across the organization.
  • Mentor and develop team members in the design, authoring, execution, and lifecycle management of automated analytical protocols within GMP environments.
  • Establish and maintain technical standards, best practices, and governance for automation scripting, validation documentation, system lifecycle management, and troubleshooting methodologies.
  • Recruit, develop, and retain top talent with expertise in laboratory automation, liquid handling platforms, relevant programming languages, and cell and gene therapy analytical techniques.
  • Foster a highly collaborative environment that effectively bridges scientific expertise, automation engineering, and regulatory compliance, enabling innovation while maintaining inspection readiness.

Qualifications:
  • Advanced degree (PhD preferred) with 15+ years of relevant experience in Quality Control, laboratory automation, and pharmaceutical or biotechnology operations, including 8+ years in progressively responsible leadership roles with demonstrated advancement to Director-level scope.
  • Extensive hands-on automation experience, including 8+ years working with liquid handling platforms (e.g., Hamilton, Tecan), with demonstrated expertise in script development, validation, troubleshooting, and lifecycle management within GMP environments.
  • Proven expertise integrating automated workflows with LIMS and other enterprise digital systems to support compliant data management and end-to-end process automation.
  • Deep technical understanding of molecular biology, cellular, and immunoassay techniques, including transfection/transduction workflows, ddPCR/qPCR, flow cytometry, ELISA, and next-generation sequencing (NGS).
  • Strong track record leading cross-functional automation initiatives in regulated biopharmaceutical settings, including oversight of instrument and software IQ/OQ/PQ, analytical method qualification and validation, and method lifecycle management.
  • Demonstrated success in building, leading, and developing high-performing technical teams, with a proven ability to mentor, coach, and retain top talent.
  • Exceptional communication and influence skills, with the ability to engage senior leadership and align diverse stakeholder groups around complex technical and operational initiatives.
  • Strategic mindset with the ability to translate business and portfolio needs into scalable automation strategies, roadmaps, and executable plans.

The salary range below reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on several factors including, but not limited to, relevant experience, education, scope of job, internal comparisons, and market data.
Beam Pay Range
$210,000-$320,000 USD

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