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Remote Senior Net Developer Jobs in Worcester, MA

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Job Title: Sr. Manager, GMP Quality Contract: 7 Months (Temp coverage) Location: Remote Hours: 40 ... Minimum of Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering ...

Senior QuickBase Developer

Woonsocket, RI · Remote

$55.75 - $73.75/hr

Senior QuickBase Developer Location: 100% Remote Duration: 6 months contract to hire Rate: Market Requirements: * 5 -10 years' experience with QuickBase design & development * Experience with ...

As a senior member of our AI engineering team, you'll provide technical leadership, mentor ... REMOTE Basic Requirements * 8+ years experience in software development * AND 2+ years with AI ...

Sr. Tax Manager (REMOTE)

Waltham, MA · On-site +1

$134K - $167K/yr

Job Title Sr. Tax Manager (REMOTE) Location(s) Australia Remote, US Remote - CT, US Remote - DC, US ... Revvity is a developer and provider of end-to-end solutions designed to help scientists ...

... Senior Infrastructure Mainframe Engineer to join our growing organization. This position is based in our Worcester, MA headquarters or may be performed through a remote work arrangement. POSITION ...

... Senior Infrastructure Mainframe Engineer to join our growing organization. This position is based in our Worcester, MA headquarters or may be performed through a remote work arrangement. POSITION ...

Manage developer tooling * Ensure compliance with regulatory, compliance and security frameworks ... Candidate can live anywhere in the United States. #LI-MP2 #LI-REMOTE Basic Requirements * 8+ years ...

Senior Data Protection Engineer (REMOTE)

Worcester, MA · Remote

$114K - $156K/yr

We are seeking a highly skilled Senior Data Protection Engineer to join our IT Security organization in Worcester, MA or in a remote capacity. POSITION SUMMARY: In this role, you will provide subject ...

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Remote Senior Net Developer information

See Worcester, MA salary details

$36

$60

$78

How much do remote senior net developer jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for remote senior net developer in Worcester, MA is $60.07, according to ZipRecruiter salary data. Most workers in this role earn between $52.79 and $67.16 per hour, depending on experience, location, and employer.

What is the difference between Remote Senior Net Developer vs Remote .NET Developer?

AspectRemote Senior Net DeveloperRemote .NET Developer
Required Experience5+ years, leadership skills1-3 years, technical skills
CertificationsMicrosoft Certified: Azure Developer, MCSDMicrosoft Certified: Azure Developer or similar
Work EnvironmentLeading projects, mentoring teamsDeveloping applications, coding
Industry UsageEnterprise, finance, healthcareStartups, small to medium businesses

The main difference between a Remote Senior Net Developer and a Remote .NET Developer lies in experience, leadership responsibilities, and project scope. Senior roles typically involve mentoring, project management, and strategic planning, while .NET Developers focus on coding and technical tasks. Both roles require strong knowledge of .NET frameworks and certifications, but senior positions demand more experience and leadership skills.

What are popular job titles related to Remote Senior Net Developer jobs in Worcester, MA?

For Remote Senior Net Developer jobs in Worcester, MA, the most frequently searched job titles are:

What cities near Worcester, MA are hiring for Remote Senior Net Developer jobs?

Cities near Worcester, MA with the most Remote Senior Net Developer job openings:

Remote Sr. Manager, GMP Quality

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

This job post has expired 2 days ago. Applications are no longer accepted.


Job description

37609761 Remote Sr. Manager, GMP Quality, 6 Months Contract
Sigma Systems is currently looking for a Remote Sr. Manager, GMP Quality

Responsibilities:

  • Be the QA representative on cross-functional project teams. Responsible for communicating with the Quality and Production departments at domestic and international contract manufacturing organizations, and within SMPA's Quality, Supply Chain, CMC, and Commercial Manufacturing departments.
  • Conducts product release activities for clinical and commercial drug substances and drug products; including review and approval of Master Batch Records, Executed Batch Records, release and stability testing documentation, and batch disposition. These activities must be conducted in a timely manner to ensure continued product supply while ensuring Quality and Safety of the product.
  • Partners with CMC and Commercial Manufacturing to conduct technical transfers and validation of new or existing processes and products to domestic and international contract manufacturing organizations.
  • Supports commercial validation activities by reviewing validation protocols and reports.
  • Ensures compliance to existing procedures and supports continuous improvement opportunities by identifying areas where improvements and efficiencies can be gained through SOP and compliance standard revisions. Authors, reviews and approves standard procedures and electronic systems, as needed.
  • Leads, authors, reviews and/or approves CMOs Quality Events, Investigations, CAPA, Change Controls, and Complaints, as well as initiating in SMPA's eQMS, as needed. This may require timely interface with domestic and international suppliers.
  • Serves as Person-in-the-Plant, as needed.
  • Authors relevant sections of Annual Product Reviews by compiling appropriate data and metrics and making appropriate recommendations.
  • Other duties as assigned.

Requirements:

  • Minimum of Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering, pharmacy) or relevant field of study.
  • 8+ years of experience required, with relevant experience in biotech or pharmaceutical industry with most experience in a Quality role.
  • Advanced knowledge of GMP manufacturing and/or market release of pharmaceutical dosage formsand/or combination products.
  • Experience with managing external CMOs, contract laboratories, and third-party logistics suppliers.
  • Must have experience in reviewing and approving master and executed batch records and performing final disposition of drug substances and products.
  • Experience managing quality events (investigations, CAPA and change control), and working knowledge of formal risk management tools and assessments. The individual must demonstrate the ability to evaluate and assess technically complex quality events, as well as the ability to document these events with excellent technical writing skills.
  • Experience in evolving GMP related quality systems, policies, and procedures to ensure compliance with evolving standards as well as improving the efficiency of related workflows.
  • Strong ability to analyze complex issues to develop relevant and realistic plans, programs, and recommendations.
  • Excellent verbal and written communication skills, including ability to interact effectively with senior management, partners, and project core team members.
  • Self-motivated, flexible, and able to prioritize work and handle multiple assignments in a fast-paced environment, while maintaining a high level of quality and compliance.