1

Edge Pharma Jobs (NOW HIRING)

... edge * Collaborate with product and marketing teams to translate market insights into solution ... pharma access needs * Deeply understand customer challenges across patient support and ...

Territory Sales Manager

South Plainfield, NJ ยท On-site

$95K - $130K/yr

At Azend Pharma , we're not just another healthcare company-we're redefining how care is delivered ... Through the relentless pursuit of operational excellence, the integration of cutting-edge ...

Work on cutting-edge AI applications in pharma manufacturing * Collaborate with a highly technical and mission-driven team * Solve meaningful problems in pharmaceutical and chemical production * Gain ...

Work on cutting-edge AI applications in pharma manufacturing * Collaborate with a highly technical and mission-driven team * Solve meaningful problems in pharmaceutical and chemical production * Gain ...

Work on cutting-edge AI applications in pharma manufacturing * Collaborate with a highly technical and mission-driven team * Solve meaningful problems in pharmaceutical and chemical production * Gain ...

Pharmacy Delivery Driver

Matawan, NJ ยท On-site

$16 - $17/hr

Previous Pharma or Healthcare setting experience, a Plus Salary: $16-17 Hourly Schedule ... Through the relentless pursuit of operational excellence, the integration of cutting-edge ...

next page

Showing results 1-20

Edge Pharma information

See salary details

$22

$49

$74

How much do edge pharma jobs pay per hour?

As of Jun 1, 2026, the average hourly pay for edge pharma in the United States is $49.88, according to ZipRecruiter salary data. Most workers in this role earn between $36.78 and $58.65 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive at Edge Pharma, and why are they important?

To thrive at Edge Pharma, candidates typically need a background in pharmaceutical sciences, compounding pharmacy, or related fields, often supported by relevant degrees or pharmacy technician certifications. Familiarity with USP <797>/<800> standards, sterile compounding equipment, and quality control systems is crucial. Attention to detail, strong teamwork, and effective communication further distinguish high performers in this environment. These competencies are vital to ensure regulatory compliance, patient safety, and efficient operations within a specialized pharmaceutical setting.

What are some common challenges faced by pharmacists working in a compounding pharmacy like Edge Pharma?

Pharmacists in compounding pharmacies such as Edge Pharma often encounter challenges related to maintaining strict quality control and adhering to rigorous regulatory standards, including USP <795>, <797>, and <800> guidelines. They must manage complex formulations tailored to individual patient needs, requiring high attention to detail and strong problem-solving skills. Additionally, collaboration with physicians and healthcare providers is crucial to ensure patient safety and effective treatment, which can be demanding due to the customized nature of compounded medications.

What is Edge Pharma and what do they do?

Edge Pharma is a pharmaceutical compounding company that specializes in producing customized medications for hospitals, clinics, and healthcare providers. They focus on creating sterile and non-sterile compounded drugs, including injectables, oral medications, and topical treatments, tailored to meet specific patient or institutional needs. Edge Pharma operates under strict regulatory standards to ensure the safety and quality of their products. Their services help healthcare facilities address drug shortages, provide alternative dosage forms, and comply with regulatory requirements. By offering tailored pharmaceutical solutions, Edge Pharma supports patient care across various medical settings.

What jobs in the US pay 300,000 a year?

In the healthcare and pharmaceutical sectors, senior roles such as pharmaceutical executives, medical directors, and specialized researchers at companies like Edge Pharma can earn $300,000 or more annually. High-level management positions in biotech and pharmaceutical companies, as well as experienced sales directors and regulatory affairs leaders, often reach or exceed this salary level with relevant experience and advanced degrees. These roles typically require strong industry knowledge, leadership skills, and often a relevant professional certification or advanced degree.

What is the difference between Edge Pharma vs Clinical Research Associate?

AspectEdge PharmaClinical Research Associate
Required CredentialsBachelor's in Life Sciences, relevant certificationsBachelor's in Life Sciences, certifications like CCR or CRA
Work EnvironmentPharmaceutical companies, labs, clinical trial sitesMonitoring clinical trials at sites, coordinating with sponsors
Industry UsagePharmaceutical and biotech industriesClinical trial management and oversight

Edge Pharma professionals often work within pharmaceutical companies focusing on drug development, while Clinical Research Associates primarily monitor and manage clinical trials at various sites. Both roles require similar educational backgrounds and certifications, but their daily responsibilities and work environments differ slightly, with Edge Pharma being more involved in the broader pharmaceutical process and CRA focusing on trial oversight.

More about Edge Pharma jobs
What states have the most Edge Pharma jobs? States with the most job openings for Edge Pharma jobs include:
What job categories do people searching Edge Pharma jobs look for? The top searched job categories for Edge Pharma jobs are:
Infographic showing various Edge Pharma job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 88% Full Time, 2% Part Time, and 9% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $103,758 per year, or $49.9 per hour.
Director, Quality (PAI Readiness Focus)

Director, Quality (PAI Readiness Focus)

Spyglass Pharma

Aliso Viejo, CA โ€ข On-site

$180K - $200K/yr

Full-time

Medical, Dental, Vision, PTO

Posted 12 days ago


Job description

About SpyGlass Pharma:
At SpyGlass Pharma (NASDAQ: SGP), we are focused on improving and preserving the vision of patients suffering from chronic eye conditions, while minimizing the impact on their daily lives. We aim to achieve this by developing cutting-edge long-term drug delivery products to address common causes of blindness and getting these products to the patients that need them.
We have built a highly collaborative team with deep expertise across ophthalmology, drug delivery, pharmaceuticals, and medical devices. Our scientists, engineers, and clinical leaders bring decades of experience developing and commercializing breakthrough technologies, united by a shared commitment to patients and our guiding principle: "We create for patients." That mindset shapes how we build our products, our teams, and our culture.
Backed by strong clinical progress, significant funding, and a growing organization, SpyGlass Pharma is entering an exciting stage of growth as we advance our lead program, the SpyGlass BIM-IOL, through Phase 3 clinical development.
Summary:
The Director of Quality is responsible for supporting SpyGlass Pharma's Pre-Approval Inspection (PAI) Readiness Program. This role works closely with Senior Director of Quality and is key in ensuring that SpyGlass and contract manufacturing organizations are robust and align with regulatory expectations for commercial manufacturing.
Essential Duties & Responsibilities:
  • Maintain expert knowledge of FDA, USP, cGMP, and other quality system standards and regulations, applying these to SpyGlass Pharma's operations.
  • Support PAI readiness activities and ensure the site and CMO's and Contract Labs are ready for PAI inspections
  • Accountable for execution of QMS Gap Assessment Activities.
  • Lead and coordinate successful gap remediation activities at both SpyGlass and contract manufacturers.
  • Point of contact for functional team remediation activities.
  • Lead and coordinate successful gap remediation activities at both SpyGlass and contract manufacturers.
  • Identify risks and resolve QMS issues and appropriately communicate gating items to senior management and stakeholders.
  • Assist in the development and revision of SOPs and controlled documents to support GxP-regulated activities. This includes building a robust QMS supporting PAI and commercial manufacturing.
  • Ensure the QMS documentation effectively supports system functionality and product quality.
  • Coordinate GxP pre-approval inspection preparation activities for SpyGlass filings/products in support of regulatory filings.
  • Influence and train inspection preparation functional teams before and during audits.
  • Facilitate responses to health authority findings to ensure the corrective actions are robust, reviewed by appropriate leadership and submitted on time. This includes tracking all commitments to timely closure.
  • Strategize corrective action plans and provide compliance support during implementation to ensure successful inspections.
  • Provide hands-on support for functional teams with procedural writing, workflow management, and record uploads.
  • Contribute to cross-functional teams focused on continuous improvement of quality system processes.
  • Support post approval activities such as FDA field alerts, product recalls and withdrawals.
  • Complete Annual Product Reviews and ensure product quality and compliance.

Qualifications Required For Position:
  • Bachelor's degree in scientific discipline or equivalent experience.
  • Minimum of 10 years of progressive experience in the biotechnology or pharmaceutical industry.
  • Recent experience with FDA PAI readiness and PAI audits both front and back-room support is a must.
  • Knowledge of pharmaceutical quality and learning management systems.
  • Working knowledge of product development processes and systems. This includes Pharmaceutical, Medical Devices and/or Clinical Operations.
  • High level of professionalism and ability to collaborate effectively in dynamic team environments.
  • Strong judgment and ability to work independently with minimal supervision
  • Ability to manage tasks with competing priorities and deadlines
  • Proficient in implementing written and verbal instructions at all organizational levels
  • Technical expertise in Microsoft Office (Outlook, Word, Excel, PowerPoint)
  • Alignment with SpyGlass Pharma's culture and values
  • Willingness to travel 10-15% (both domestic and international)

Certificates/Licenses Required For Position:
  • Qualified Auditor Certification preferred

Why SpyGlass Pharma?
  • We are offering a range of $180,000 - $200,000, based on experience and qualifications, along with an Annual Bonus opportunity.
  • Share in our success with stock options, giving you a stake in the company's future.
  • Comprehensive health, dental, and vision insurance plans to keep you and your family healthy and happy, with a variety of plan and coverage options.
  • Generous paid time off, including holidays, vacation days, and personal leave.

SpyGlass Pharma is an Equal Opportunity Employer and participates in E-Verify. SpyGlass Pharma takes pride in maintaining a diverse environment and our policies are not to discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity, marital or veteran status, disability, or any other legally protected status.
SpyGlass Pharma is also committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an email to JOBS@SPYGLASSPHARMA.COM and let us know the nature of your request and your contact information.