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Impiricus

Senior Client Services Manager

Remote, US Exemption Status: Full-time, Exempt Who We Are Impiricus is the first and only AI ... and a senior pharmaceutical executive, Impiricus was created to transform how life sciences ...

Impiricus

Senior Client Services Manager

Remote, US Exemption Status: Full-time, Exempt Who We Are Impiricus is the first and only AI ... and a senior pharmaceutical executive, Impiricus was created to transform how life sciences ...

TechData Service Company LLC

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TEMP Remote Sr. Manager, GMP manufacturing- (37609761)

Waltham, MA · Remote

$91 - $111/hr

Advanced knowledge of GMP manufacturing and/or market release of pharmaceutical dosage form and/or ... Minimum of Bachelor's degree in a scientific discipline (e.g., biology, chemistry, engineering ...

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How much do remote senior pharmaceutical scientist jobs pay per year?

As of Sep 4, 2026, the average yearly pay for remote senior pharmaceutical scientist in the United States is $127,031.00, according to ZipRecruiter salary data. Most workers in this role earn between $109,000.00 and $143,500.00 per year, depending on experience, location, and employer.

What does a remote senior pharmaceutical scientist do?

A Remote Senior Pharmaceutical Scientist leads research and development projects related to new drugs and pharmaceutical products, often working from a remote location. They design and oversee experiments, analyze data, and ensure compliance with regulatory standards. In addition, they collaborate with cross-functional teams, prepare detailed reports, and contribute to the development of scientific strategies for their organization. Their expertise helps bring safe and effective medications to market more efficiently.

What are the key skills and qualifications needed to thrive as a remote senior pharmaceutical scientist?

To thrive as a Remote Senior Pharmaceutical Scientist, you need an advanced degree in pharmaceutical sciences or a related field, extensive experience in drug development, and a strong understanding of regulatory requirements. Familiarity with data analysis software, laboratory information management systems (LIMS), and relevant industry certifications are typically required. Exceptional problem-solving, project management, and virtual collaboration skills set standout candidates apart in remote settings. These competencies ensure the effective design, execution, and oversight of pharmaceutical projects while maintaining compliance and team synergy from a distance.

How does remote work impact collaboration and project management for senior pharmaceutical scientists?

As a Remote Senior Pharmaceutical Scientist, you'll collaborate frequently with cross-functional teams, including regulatory, clinical, and analytical groups, primarily through virtual meetings and project management platforms. While remote work provides flexibility, it also requires strong communication skills and proactive organization to ensure projects stay on track. You may face challenges like coordinating across time zones or ensuring clear documentation, but most organizations support remote scientists with robust digital tools and regular check-ins. Building trust and maintaining transparency with colleagues are key to successful remote collaboration in this role.

What is the difference between Remote Senior Pharmaceutical Scientist vs Remote Pharmaceutical Scientist?

AspectRemote Senior Pharmaceutical ScientistRemote Pharmaceutical Scientist
Required CredentialsAdvanced degree (PhD or PharmD), extensive experienceBachelor's or Master's degree, relevant industry experience
Work EnvironmentLeading research projects, mentoring teams, strategic planningConducting experiments, data analysis, supporting research teams
Employer & Industry UsagePharmaceutical companies, biotech firms, research institutionsPharmaceutical companies, contract research organizations, biotech firms

The main difference between a Remote Senior Pharmaceutical Scientist and a Remote Pharmaceutical Scientist lies in experience, responsibilities, and leadership. Senior roles involve strategic oversight and mentoring, while standard roles focus on executing research tasks. Both positions are vital in the pharmaceutical industry and often share similar educational backgrounds and work environments.

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Remote Senior Pharmaceutical Scientist jobs near you
Infographic showing various Remote Senior Pharmaceutical Scientist job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, 1% Temporary, 2% Contract, and 1% Nights. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $127,031 per year, or $61.1 per hour.

Remote Sr. Manager, GMP Quality

Sigma Systems, Inc.

Marlborough, MA • Remote

Contractor

This job post has expired today. 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.