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Fda Contractor Jobs in Massachusetts (NOW HIRING)

Merck Group

Senior Counsel -US Rare Tumors

Boston, MA · On-site

$188K - $283K/yr

Ensure all activities comply with FDA, OIG, CMS, and state requirements, as well as company policies and industry codes (e.g., PhRMA Code). * Contracting & Negotiations: Draft, review, and negotiate ...

IPG Photonics

Senior Imaging Software Engineer

Marlborough, MA · On-site

$127K - $167K/yr

Maintain business relationships with 3rd party consultants, contractors, and suppliers. Including ... Knowledge of Design Controls and Risk Management practices, regulations and standards, such as FDA ...

IPG Photonics

Senior Imaging Software Engineer

Marlborough, MA · On-site

$127K - $167K/yr

Maintain business relationships with 3rd party consultants, contractors, and suppliers. Including ... Knowledge of Design Controls and Risk Management practices, regulations and standards, such as FDA ...

Collabera

Manufacturing Engineer

Littleton, MA · On-site

$75K - $97K/yr

In 2015 we placed more than 6,000 contractors across select 100+ clients that we service. End ... Experience in FDA 21 CFR Part 820 Medical Device Manufacturing. Preferred Qualifications: Master ...

Analog Devices

Engineer, Quality Engineering

Wilmington, MA · On-site

$78K - $101K/yr

... 13485, FDA regulations, and EU MDR. The position also includes responsibilities as a Training ... Coordinate and administer initial, ongoing, and re-training activities for employees, contractors ...

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Fda Contractor information

See Massachusetts salary details

$32.8K

$66.4K

$96.7K

How much do fda contractor jobs pay per year?

As of Aug 20, 2026, the average yearly pay for fda contractor in Massachusetts is $66,434.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,000.00 and $76,400.00 per year, depending on experience, location, and employer.

What is an FDA contractor?

An FDA contractor is an individual or company that provides goods or services to the U.S. Food and Drug Administration (FDA) under a formal agreement or contract. These contractors may work in a wide range of areas including research, information technology, regulatory consulting, laboratory services, or facility maintenance. FDA contractors are not direct employees of the FDA but play a crucial role in supporting the agency’s mission to protect public health by ensuring the safety, efficacy, and security of drugs, biological products, and medical devices. Their work is often governed by strict regulations and requires compliance with federal standards. Contractors are selected through a competitive procurement process to ensure quality and value.

What are the key skills and qualifications needed to thrive as an FDA contractor?

To thrive as an FDA Contractor, you need expertise in regulatory compliance, scientific analysis, and project management, often supported by a degree in life sciences or a related field. Familiarity with FDA regulations, electronic submission systems, and specialized software like eCTD or data analysis tools is typically required. Attention to detail, strong communication skills, and adaptability help contractors excel in collaborative and deadline-driven environments. These skills ensure accurate, timely submissions and effective support for FDA regulatory processes.

What are some common challenges faced by FDA contractors when working with cross-functional teams?

FDA Contractors often collaborate with diverse teams, including regulatory, quality assurance, and clinical staff. One common challenge is aligning different priorities and communication styles while ensuring compliance with regulatory standards and tight project deadlines. Success in this role requires strong organizational skills, adaptability, and proactive communication to keep projects moving smoothly and maintain regulatory integrity. Building rapport and understanding the unique needs of each department can help FDA Contractors effectively bridge gaps and facilitate teamwork.

What is the difference between Fda Contractor vs Fda Auditor?

AspectFda ContractorFda Auditor
Required CredentialsTypically requires knowledge of FDA regulations, compliance, and industry standards; certifications like RAC or CQA are commonRequires similar credentials, often with additional auditing certifications such as CQA or ISO auditor training
Work EnvironmentWorks on projects for FDA-regulated companies, often in labs, manufacturing sites, or officesConducts inspections and audits at facilities, often traveling to various sites
Employer & Industry UsageHired by pharmaceutical, biotech, or medical device companies as external consultantsEmployed by regulatory agencies or contracted to perform compliance audits for FDA oversight

In summary, Fda Contractors focus on supporting companies with compliance projects, while Fda Auditors primarily evaluate and verify adherence to FDA regulations through inspections and audits. Both roles require similar certifications and industry knowledge but differ in their primary functions and work settings.

What are popular job titles related to Fda Contractor jobs in Massachusetts?

For Fda Contractor jobs in Massachusetts, the most frequently searched job titles are:

What job categories do people searching Fda Contractor jobs in Massachusetts look for?

The top searched job categories for Fda Contractor jobs in Massachusetts are:

Fda Contractor jobs near you
Infographic showing various Fda Contractor job openings in Massachusetts as of August 2026, with employment types broken down into 77% Full Time, 4% Part Time, 15% Contract, and 4% Nights. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $66,434 per year, or $31.9 per hour.

Statistical Programming Contractor (16-Month Contract)

Crispr Therapeutics

Boston, MA

$70 - $80/hr

Full-time

Posted 2 days ago

New

Job description

Job Description:

Company Overview

ounded over a decade ago,CRISPR Therapeuticsis a leading biopharmaceutical company focused on developing transformative gene-based medicines for serious human diseases. The Company has evolved from a pioneering research-stage organization into an industry leader, marking a historic milestone with the approval of CASGEVY(exagamglogene autotemcel [exa-cel]), the world's first CRISPR-based therapy, approved for eligible patients with sickle cell disease and transfusion-dependent beta thalassemia.CRISPR Therapeuticsis advancing a broad and diversified pipeline across hemoglobinopathies, cardiovascular, autoimmune, oncology, regenerative medicine and rare diseases. The Company continues to expand its leadership in gene editing through the development of SyNTase editing, a novel and proprietary gene-editing platform designed to enable precise, efficient, and scalable gene correction. To accelerate and expand its impact,CRISPR Therapeuticshas established strategic collaborations with leading biopharmaceutical partners, includingVertex Pharmaceuticals.CRISPR Therapeutics AGis headquartered inZug,Switzerland, with its wholly-ownedU.S.subsidiary,CRISPR Therapeutics, Inc., and R&D operations based inBoston, MassachusettsandSan Francisco,California.

Position Summary

The Statistical Programming Contractor will provide technical support for statistical programming activities for assigned clinical studies, FDA submissions, and the development of initiatives.

Responsibilities

  • Design, develop, evaluate, validate and modify computer programs using SAS to analyze and evaluate clinical data.
  • Have thorough knowledge of CDISC theory and implementation guidelines, able to create and validate CDISC standard datasets
  • Program edit checks and produce quality tables, figures and listings in a timely fashion and high quality.
  • Work closely with Clinical Operations, Data Management and Biostatisticians on various clinical projects so that data analysis can be performed in a timely fashion.

Minimum Qualifications

  • Bachelor's Degree in Statistics, Mathematics, and/or Computer Science/IT background. Master's Degree preferred.
  • Minimum 3years of statistical programming in a pharmaceutical/biotech or CRO setting (depending on level)
  • Strong knowledge in CDISC including SDTM, ADaM, metadata, controlled terminologies, and data flows, as well as in industry standards for electronic submission of data to FDA.
  • Strong hands-on SAS programing skills and working experience for clinical trial reporting for SDTM, ADaM, Table, figure, and Listing.
  • Excellent working knowledge of SAS/BASE, SAS/STAT, SAS/GRAPH and SAS Macro language.
  • Advanced knowledge of GCP/ICH standards, 21 CFR Part 11.

Preferred Qualifications

  • Strong ability to work within cross-functional teams.
  • Excellent interpersonal, organizational, and multi-tasking skills.

Competencies

  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.

CRISPR Therapeutics believes in fostering a dynamic workplace that balances remote work flexibility with the benefits of in-person interactions. Our employees work at least three days on-site, creating a collaborative work environment, where we cultivate mentorship opportunities, increase cross-functional communication and offer opportunities for our employees to connect. Certain lab based and manufacturing positions are located fully on-site.

Base pay range of $70.00 - $80.00 per hour.

The hourly rate provided is the reasonable estimate for this contract position. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy

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