Top 16 pharmaceutical executive Jobs in remote

Executive Director, GMP Quality Assurance
Apogee Therapeutics —Remote
- $275,000 - $305,000 a year
- Remote
- 11+ years
- Travel
- US work authorization
- Health insurance
- Paid time off
Executive Director, Corporate Development
Medison Pharma —Remote
- $250,000 - $330,000 a year
- Full-time
- Remote
- Mentoring
- Senior level
- Business
Quick Apply
Pharmacy Executive - Pharmacy Enterprise
Vizient, Inc. —Remote
- $135,200 - $236,600 a year
- Master's degree
- Clinic
- Travel
Pharmacy Executive IV - Spend Management Delivery
Vizient, Inc. —Remote
- $135,200 - $236,600 a year
- 7 years
- Master's degree
- Travel
Executive Director, Regulatory Affairs, CMC
BeiGene —Remote
- $274,800 - $354,800 a year
- Full-time
- Computer literacy
- Bachelor of Science
- 8 years
- Health savings account
- Employee stock purchase plan
Pharmacy Executive III-Pharmacy Enterprise Servicers
Vizient, Inc. —Remote
- $117,600 - $206,000 a year
- 5 years
- Analysis skills
- Travel
1d
Pharmacy Executive IV - Pharmacy Advisory
Vizient, Inc. —Remote
- $135,200 - $236,600 a year
- 7 years
- Master's degree
- Team management
2d
Executive Director, Regulatory Affairs – Global Regulatory Leader
Summit Therapeutics —Remote
- $231,000 - $285,000 a year
- Remote
- Doctoral degree
- Master's degree
- Bachelor's degree
13h
Executive Director, Clinical Quality Assurance
Jade Biosciences —Boston, MA
- $265,000 - $300,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- Master's degree
Executive Director, Quality Data Analytics and Process Management
Amgen —Thousand Oaks, CA
- $241,843.70 - $327,200.30 a year
- Remote
- 6 years
- Doctoral degree
- Master's degree
- Disability insurance
- Health insurance
9d
Executive Director Marketing Repatha Brand Lead
Amgen —Thousand Oaks, CA
- $262,534.40 - $355,193.60 a year
- Weekends as needed
- Remote
- 6 years
- Doctoral degree
- Master's degree
- Disability insurance
- Health insurance
Exec Director, Drug Substance Development & Manufacturing
ESPERION THERAPEUTICS INC —Ann Arbor, MI
- $320,500 - $365,000 a year
- Full-time
- Remote
- Bachelor of Science
- 8 years
- Bachelor's degree
- Paid holidays
- Health insurance
Quick Apply
Executive Director of Regulatory Affairs - Obesity and Related Conditions
Amgen —Thousand Oaks, CA
- $187,271.15 - $253,366.85 a year
- Remote
- Doctoral degree
- Master's degree
- Analysis skills
- Disability insurance
- Health insurance
Executive Director, Global Medical Expert
Ultragenyx Pharmaceutical —Novato, CA
- $328,400 - $405,700 a year
- Full-time
- Remote
- Medicine
- 7 years
- Up to 50% travel
- Gym membership
Senior/Executive Director, Quality Management System
Jade Biosciences —Seattle, WA
- $250,000 - $300,000 a year
- Remote
- Microsoft Excel
- Microsoft Outlook
- 3 years
Quick Apply
7h

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Executive Director, GMP Quality Assurance

Apogee Therapeutics
Remote

Apply Now

Job Details

$275,000 - $305,000 a year

Benefits

Health insurance
Paid time off
Retirement plan
Paid sick time

Qualifications

Data integrity assurance
Regulatory inspections
Performance improvement leadership
Strategic management
Investigations regulatory compliance
Team leadership
Preventive action implementation
Coaching
11+ years
Corrective and preventive actions (CAPA)
GMP
Metrics Reporting
Internal investigations
Change management
Team development
Data integrity and documentation
Key Performance Indicators
ICH guidelines
Vendor compliance management
Overseeing compliance functions
Quality risk management
Pharmaceutical company experience
Decision making
Regulatory readiness in healthcare
Vendor quality assurance
Collaboration with manufacturing teams
Implementing quality control processes for products
Clinical research inspection readiness
Quality audits
Quality control communication

Full Job Description

About Apogee Therapeutics

Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.

Apogee Therapeutics is a clinical-stage biotechnology company advancing novel biologics with potential for differentiated efficacy and dosing in the largest I&I markets, Apogee's antibody programs are designed to overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. Zumilokibart (APG777), the company's most advanced program, is being initially developed for the treatment of atopic dermatitis (AD), which is the largest and one of the least penetrated I&I markets, as well as asthma. With four validated targets in its portfolio, Apogee is seeking to achieve best-in-class efficacy and dosing through monotherapies and combinations of its novel antibodies. Based on a broad pipeline and depth of leadership and expertise, the company believes it can deliver value and meaningful benefit to patients underserved by today's standard of care.

We are a fast-paced company committed to building an exceptional culture, founded on our C.O.R.E. values: Caring, Original, Resilient and Egoless and a commitment to refusing to stop at "good enough".

If this sounds like you, keep reading!

Role Summary

We are seeking an Executive Director of GMP Quality Assurance (QA) to serve as a senior quality leader responsible for developing, leading, and executing the global GMP QA strategy in support of a transition from clinical development to commercial readiness. This role verifies compliance with cGMP regulations, company policies and procedures, and industry standards, while deliberately designing quality systems that enable speed, clarity, and confident decision-making as the company scales.

The Executive Director partners closely with cross-functional teams and external manufacturing and testing partners ensuring high standards of product quality and data integrity across GMP operations. They build and lead a high‑performing GMP QA team, provide strategic oversight of audits and inspections, and serve as a trusted advisor to senior leadership on GMP QA risk management. This position reports to the Head of QA.

Key Responsibilities

Head of GMP QA and member of the QA Leadership Team
Build, lead, and scale a high‑performing GMP QA team
Develop and execute the GMP QA functional strategy, ensuring alignment with company objectives and evolving clinical‑to‑commercial needs
Establish a clear GMP QA vision that enables inspection readiness, scalability, and sustainable operations
Provide oversight of GMP QA systems, including deviations, investigations, CAPAs, change control, complaints, and product disposition
Ensure compliance with applicable global GMP regulations and standards (e.g., FDA, EMA, ICH)
Lead organizational readiness for GMP internal audits and regulatory inspections
Provide strategic oversight of GMP QA across CMOs, CDMOs, and external testing partners
Ensure effective quality agreements, oversight models, escalation pathways, and performance metrics are in place and actively managed
Exercise sound judgment in resolving quality issues with external partners in a timely and compliant manner
Engage effectively with leadership and key cross‑functional partners, bringing forward clear recommendations and risk‑based perspectives
Lead the development and presentation of Quality Management Review meetings for GMP QA to highlight compliance needs and to foster continuous improvement initiatives to support speed, clarity, and scalability

Ideal Candidate

15+ years of progressive GMP QA experience within pharmaceutical, biotechnology, and/or medical device environments, with deep understanding of global GMP regulations across clinical and commercial operations
Proven track record leading GMP QA organizations through the transition from clinical development to commercial manufacturing, including launch readiness and post approval operations
Demonstrated success building, scaling, and sustaining GMP Quality Systems to support commercial supply, including serving as functional lead for the Veeva Quality Suite (QMS) with accountability for system strategy, governance, and compliance across internal teams and external partners
Extensive experience overseeing external manufacturing and testing partners, and directly leading regulatory inspections and interactions with global health authorities
Significant leadership experience, including managing managers and senior level professionals; effective at coaching and developing leaders through change and uncertainty
Ability to create and clearly articulate a GMP QA vision aligned with company strategy, establish trust and credibility across teams, and set clear direction while adapting leadership style to organizational and individual needs
Sound, unbiased judgment in complex and ambiguous situations; makes pragmatic, well-reasoned decisions, takes full ownership of outcomes, proactively addresses challenges, seeks feedback, and continuously adapts strategies based on evolving risks and business needs
Strong written and verbal communication skills
Ability to operate effectively in a fast‑paced, evolving environment with incomplete information
Demonstrated commitment to Apogee's C.O.R.E. values and ethical decision‑making
Position requires up to 25% travel including mandatory in-person attendance at All Hands meetings typically held twice per year, additional travel may be required to attend visits to vendors, CDMOs, etc., domestic and international travel is required

The anticipated salary range for candidates for this role will be $275,000-$305,000. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography.

What We Offer

A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless
Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly
Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
We provide competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated paid sick leave
Commitment to growing you professionally and providing access to resources to further your development
Apogee offers regular all team, in-person meetings to build relationships and problem solve

E-Verify Participation: As part of the I9 verification of authorization to work in the US, Apogee participates in E-Verify. To learn more about E-Verify please review this poster.

Apogee Therapeutics is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.

To review our privacy policy, click here

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Apply Now

Refine Your Search

pharmaceutical executive jobs in remote

Executive Director, GMP Quality Assurance

Executive Director, Corporate Development

Pharmacy Executive - Pharmacy Enterprise

Pharmacy Executive IV - Spend Management Delivery

Executive Director, Regulatory Affairs, CMC

Pharmacy Executive III-Pharmacy Enterprise Servicers

Pharmacy Executive IV - Pharmacy Advisory

Executive Director, Regulatory Affairs – Global Regulatory Leader

Executive Director, Clinical Quality Assurance

Executive Director, Quality Data Analytics and Process Management

Executive Director Marketing Repatha Brand Lead

Exec Director, Drug Substance Development & Manufacturing

Executive Director of Regulatory Affairs - Obesity and Related Conditions

Executive Director, Global Medical Expert

Senior/Executive Director, Quality Management System

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