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Q Pharma Jobs (NOW HIRING)

Scorpion Therapeutics

Senior Accountant

Los Angeles, CA · On-site

$100K - $115K/yr

... for Forms 10-Q and 10-K (e.g., rollforwards and disclosure support) * Contribute to segment ... Biotech/pharma/life sciences experience * Big 4 public accounting experience * ERP systems ...

Rocket Pharmaceuticals

NJ · On-site

Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with ... points, Q&A documents, and website content * Assist with quarterly earnings processes, investor ...

Rocket Pharmaceuticals, Inc.

Rocket Pharma is a fully integrated, late-stage biotechnology company advancing gene therapies with ... points, Q&A documents, and website content * Assist with quarterly earnings processes, investor ...

Bruker

Title Research Associate

Boston, MA · On-site

$62K - $100K/yr

... biotech/pharma * Previous experience in working with chromatographic (LC) systems or mass spectrometers using DIA, PRM and MRM methods is an advantage (Q-TOF, triple Quad, Orbitrap) * Previous ...

eTeam

Consumer Care Specialist

... • Pharma/ biotech experience • Experience in consumer healthcare, pharmaceutical, or a ... Q&A inquiries for Gold Bond products • Route medical questions appropriately to the ...

Triveni Bio

Director, Business Development

Watertown, MA · On-site

$220K - $240K/yr

Build and maintain a robust external network across biotech, pharma, academia, and investors ... Lead all external diligence processes (FAQs, Q&As, etc.) * Deal Execution: * Work closely with COO ...

Triveni Bio

Director, Business Development

Watertown, MA · On-site +1

$220K - $240K/yr

Build and maintain a robust external network across biotech, pharma, academia, and investors ... Lead all external diligence processes (FAQs, Q&As, etc.) * Deal Execution: * Work closely with COO ...

Bruker Corporation

Research Associate

Boston, MA · On-site

$62K - $100K/yr

... biotech/pharma * Previous experience in working with chromatographic (LC) systems or mass spectrometers using DIA, PRM and MRM methods is an advantage (Q-TOF, triple Quad, Orbitrap) * Previous ...

Bruker

Research Associate

Boston, MA

$62K - $100K/yr

... biotech/pharma * Previous experience in working with chromatographic (LC) systems or mass spectrometers using DIA, PRM and MRM methods is an advantage (Q-TOF, triple Quad, Orbitrap) * Previous ...

UNAVAILABLE

Research Associate

Boston, MA · On-site

$62K - $100K/yr

... biotech/pharma * Previous experience in working with chromatographic (LC) systems or mass spectrometers using DIA, PRM and MRM methods is an advantage (Q-TOF, triple Quad, Orbitrap) * Previous ...

Fujifilm

Director Data AI & Analytics

Irvine, CA · Hybrid

Lead a crosssite team (CoE + domain squads), partner with QA/CSV, Security, Lab IT, M&Q Systems ... and pharma to tackle the world's biggest health challenges. Imagine being part of a team that ...

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How much do q pharma jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for q pharma in the United States is $54.33, according to ZipRecruiter salary data. Most workers in this role earn between $50.48 and $63.70 per hour, depending on experience, location, and employer.

What is a Q Pharma?

A Q Pharma job typically refers to a position within the pharmaceutical industry that focuses on quality assurance, quality control, or regulatory compliance. Professionals in these roles ensure that pharmaceutical products meet industry standards, regulatory requirements, and safety guidelines. Responsibilities may include reviewing manufacturing processes, conducting audits, and maintaining documentation to comply with FDA and other regulatory bodies. These jobs are critical for maintaining product integrity and patient safety in the pharmaceutical sector.

What are the main responsibilities of someone working in a Q Pharma position?

In a Q Pharma role, your core responsibilities typically include monitoring product quality throughout the manufacturing process, conducting inspections and audits, maintaining meticulous documentation, and ensuring compliance with regulatory guidelines. You might also be involved in investigating quality issues, developing process improvements, and coordinating with production, R&D, and regulatory teams. The position often requires balancing multiple projects while supporting both routine operations and new product introductions. Success relies on close collaboration with cross-functional departments to ensure quality standards are consistently maintained.

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

To thrive in a Q Pharma role, candidates typically need a background in pharmaceutical sciences, quality assurance, or regulatory affairs, often supported by a relevant degree. Familiarity with industry-standard tools and systems such as GMP (Good Manufacturing Practices), LIMS (Laboratory Information Management Systems), and FDA or EMA regulatory standards is crucial. Strong attention to detail, analytical thinking, and excellent communication skills help professionals excel in this position. These competencies ensure pharmaceutical products meet strict quality standards and regulatory compliance, safeguarding consumer safety and organizational reputation.

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Q Pharma jobs near you
Infographic showing various Q Pharma job openings in the United States as of September 2026, with employment types broken down into 79% Full Time, and 21% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $113,000 per year, or $54.3 per hour.

Manager, Accounting (Revenue)

Los Angeles, CA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 15 days ago

Job description

Revenue Accounting Manager for partnership/collaboration accounting and commercial revenue.

Based in Pasadena or San Diego, CA; in office 5 days/week. Reporting to the Senior Accounting Manager, working with the Controller.

Responsibilities
  • Serve as subject-matter expert for revenue accounting under ASC 606 and U.S. GAAP; review complex partnership/customer contracts and determine revenue recognition and disclosure requirements.
  • Establish and maintain revenue accounting policies/procedures; ensure SOX control requirements are met.
  • Partner with FP&A to track actual labor hours, update budgeted resource assumptions, and ensure audit-ready input-method revenue recognition.
  • Lead order-to-cash month-end and quarter-end close: journal entries, balance sheet reconciliations, flux analysis.
  • Support gross-to-net revenue accounting, including review of third-party support.
  • Prepare revenue-related disclosures for Forms 10-Q and 10-K.
  • Prepare and maintain SOX-compliant controls for revenue and accounts receivable cycles.
Requirements
  • Bachelor’s in Accounting, Finance, or related field.
  • 5+ years financial accounting with significant focus on ASC 606 revenue recognition.
  • In-depth U.S. GAAP and SOX knowledge for revenue recognition, receivables, contract assets, and deferred revenue.
  • Ability to manage complex monthly/quarterly close.
  • Communicate complex accounting guidance to non-finance partners.
  • Lead change initiatives and multi-phase projects.
  • Strong organizational skills, accuracy/detail, tight-timeline delivery.
  • Strong oral/written communication; integrity.
  • Adaptable; excellent team player; self-motivated.
  • Occasional travel between locations.
  • Candidates must have current, valid authorization to work in the country where the role is located.
Preferred
  • Technical accounting experience in life sciences/biotech/pharma.
  • Big 4 and/or public company experience.
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