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Quality Engineering Manager Pharmaceutical Jobs

Honeywell

Quality Engineering Manager

Woonsocket, RI · On-site

As a Quality Engineering Manager here at Honeywell, you will help shape our unwavering commitment to quality excellence. You are integral to ensuring the delivery of high-quality products and ...

nLIGHT

Supplier Quality Engineering Manager

Camas, WA · On-site

Position Summary The Supplier Quality Engineering Manager leads a team responsible for ensuring external suppliers meet nLIGHT's standards for quality, capability, and performance. This role provides ...

nLIGHT

Supplier Quality Engineering Manager

Camas, WA · On-site

$90K - $120K/yr

Position Summary The Supplier Quality Engineering Manager leads a team responsible for ensuring external suppliers meet nLIGHT's standards for quality, capability, and performance. This role provides ...

Flex

Supplier Quality Engineering Manager

Austin, TX · On-site

Job Summary To support our extraordinary teams who build great products and contribute to our growth, we're looking to add a Supplier Quality Engineering Manager located in Austin, TX. Reporting to ...

Apple Inc.

$237K - $356K/yr

Engineering Manager, Quality Engineering -- MapKit Cupertino, California, United States Software and Services Embark on a new route in your career! Offering a host of innovative features and rich ...

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Quality Engineering Manager Pharmaceutical information

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$60K

$111.7K

$158.5K

How much do quality engineering manager pharmaceutical jobs pay per year?

As of Sep 13, 2026, the average yearly pay for quality engineering manager pharmaceutical in the United States is $111,650.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,000.00 and $131,000.00 per year, depending on experience, location, and employer.

What does a quality engineering manager do in the pharmaceutical industry?

A Quality Engineering Manager in the pharmaceutical industry is responsible for overseeing quality assurance and control processes to ensure that products meet regulatory and company standards. They lead teams to develop, implement, and monitor quality systems, conduct risk assessments, and resolve quality-related issues. Their role includes collaborating with other departments, managing audits, and ensuring compliance with Good Manufacturing Practices (GMP). Ultimately, they help guarantee the safety, efficacy, and consistency of pharmaceutical products.

What are the key skills and qualifications needed to thrive as a quality engineering manager in the pharmaceutical industry?

To thrive as a Quality Engineering Manager in the pharmaceutical industry, you need a solid background in quality assurance, regulatory compliance (such as GMP, FDA, or ISO standards), and a relevant engineering or science degree. Familiarity with quality management systems (QMS), risk assessment tools, and process validation techniques is crucial, and certifications like Six Sigma or ASQ are highly valued. Strong leadership, problem-solving abilities, and effective communication are essential soft skills for managing teams and driving continuous improvement. These skills ensure product safety, regulatory compliance, and operational excellence, which are critical for success in the highly regulated pharmaceutical sector.

How does a quality engineering manager in the pharmaceutical industry typically collaborate with cross-functional teams to ensure compliance and product quality?

A Quality Engineering Manager in the pharmaceutical sector works closely with departments such as manufacturing, regulatory affairs, R&D, and supply chain to ensure that all products meet stringent quality and compliance standards. They facilitate regular meetings, coordinate audits, and provide training on quality systems and best practices. By fostering open communication and aligning team objectives, they help identify potential risks early and implement corrective actions efficiently. This collaborative approach is crucial for maintaining regulatory compliance and ensuring the consistent delivery of safe and effective pharmaceutical products.

What are popular job titles related to Quality Engineering Manager Pharmaceutical jobs?

For Quality Engineering Manager Pharmaceutical jobs, the most frequently searched job titles are:

Manufacturing Quality Engineering Manager

San Diego, CA • On-site

ASML
Manufacturing • 10K+ employees
Learn more about ASMLexternal

$118K - $178K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Key responsibilities

  • Manage and report on team performance of quality engineers and inspectors.

  • Drive the execution of quality initiatives, analyze KPI progress, and suggest improvements.

  • Collaborate with cross-functional teams to address quality-related issues and participate in audits.

ASML rating

9.1

Company rating: 9.1 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

Job description

Introduction to the Job:
Join ASML in San Diego as a Manufacturing Quality Engineering Manager and help shape the future of semiconductor manufacturing. Your work will ensure our deep ultraviolet (DUV) systems meet the highest standards of quality and reliability. You will improve parts and processes, strengthen performance, and support customer success across factory.
As a Manufacturing Quality Engineering Manager, you will lead a team of quality professionals and drive cross-functional improvement initiatives. You will use data, structured methods, and clear communication to drive and lead quality initiatives. This role requires key management/leadership skills summarized above, as well as working in a cleanroom environment, wearing protective gear for the entire shift. You will be onsite 100% during working hours. You will be responsible for managing activities of the assigned team, in line with the department & sector strategy, business plans and relevant policies; for people development & performance.
Roles and Responsibilities:
  • Contributes to the Q&E strategy and business plan for the department and translates into annual operational plan for own group.
  • Drives execution of quality roadmap, integrates quality deliverables within scope.
  • Contributes to the definition of department Quality KPIs in line with sector priorities and strategic roadmaps.
  • Analyzes KPI progress and suggests improvements to mitigate risks.
  • Responsible for directly managing quality engineers and quality inspectors.
  • Ensures highly qualified workforce and drives people performance & development.
  • Manage and report on team performance.
  • Creates relevant network of stakeholders of internal and external counterparts.
  • Organizes adequate feedback loop on achieved results and secures feedback.
  • Live the Living Quality & Excellence culture & enable employees to own quality.
  • Manages internal/external customer interactions, collaborating with cross-functional teams to address intricate quality-related issues.
  • Participates in audits, addressing customer concerns, and ensuring adherence to established quality protocols.
  • Works closely with other departments to address customer needs, and plays a role in improving overall customer satisfaction.
  • Lead Quality Review Board, facilitate Quality meetings and deploy Quality Programs.

Education and Experience:
  • Master's degree in a technical field such as electrical engineering, manufacturing, industrial engineering, mechatronics, or mechanical engineering, or other relevant area with thorough experience or Bachelor degree with deep/extensive experience.
  • Proven performance in one or more of the related areas (Supplier/Manufacturing Quality, Lean, Six Sigma Problem Solving, ISO Auditor, SPC, etc.)
  • Preferably has experience in working in a global technology environment within manufacturing and/or quality engineering.
  • Strong professional with 'hands on' mentality to lead, drive and sustain changes.
  • Proven track record in creating sense of urgency, leading and managing escalations to systematically drive the development and implementation of solutions.
  • Able to functionally influence, inspire and engage SMEs (Subject Matter Experts).
  • Develop and share Quality data, reports, other Quality initiatives presentations.
  • Required minimum of ten years' experience in related areas of expertise.
  • Experience with leading direct or indirect reports.
  • Experience with leading and facilitating quality meetings. (cross-functional/sectoral)

Skills:
Working at the cutting edge of tech, you'll always have new challenges and new problems to solve - and working together is the only way to do that. You won't work in a silo. Instead, you'll be part of a creative, dynamic work environment where you'll collaborate with supportive colleagues. To thrive in this job, you'll need the following skills:
  • Communicate clearly with stakeholders and present data-driven insights.
  • Collaborate across functions and build trusted relationships.
  • Plan and lead projects with structure and accountability.
  • Lead Problem Solving with curiosity and a continuous improvement mindset.
  • Work proactively, manage priorities, and deliver under deadlines.
  • Drive process development and documentation. Document decisions with clarity and consistency.
  • Uphold safety, quality, and customer focus in all activities.
  • Lead and develop team.

The current base annual salary range for this role is currently:
$118,875-178,313
Pay scales are determined by role, level, location and alignment with market data. Individual pay is determined through interviews and an assessment of several factors that that are unique to each candidate, including but not limited to job-related skills, relevant education and experience, certifications, abilities of the candidate and pay relative to other team members.
The Company offers employees and their families, medical, dental, vision, and basic life insurance. Employees are able to participate in the Company's 401k plan. Employees will also receive eight (8) hours of vacation leave every month and (13) paid holidays throughout the calendar year. For more information, please contact the Recruiter or click on this link Compensation & Benefits in the US.
All new ASML jobs have a minimum application deadline of 10 days.
This position requires access to controlled technology, as defined in the United States Export Administration Regulations (15 C.F.R. § 730, et seq.). Qualified candidates must be legally authorized to access such controlled technology prior to beginning work. Business demands may require ASML to proceed with candidates who are immediately eligible to access controlled technology.
Inclusion and diversity
ASML is an Equal Opportunity Employer that values and respects the importance of a diverse and inclusive workforce. It is the policy of the company to recruit, hire, train and promote persons in all job titles without regard to race, color, religion, sex, age, national origin, veteran status, disability, sexual orientation, or gender identity. We recognize that inclusion and diversity is a driving force in the success of our company.
Need to know more about applying for a job at ASML? Read our frequently asked questions.
Request an Accommodation
ASML provides reasonable accommodations to applicants for ASML employment and ASML employees with disabilities. An accommodation is a change in work rules, facilities, or conditions which enable an individual with a disability to apply for a job, perform the essential functions of a job, and/or enjoy equal access to the benefits and privileges of employment. If you are in need of an accommodation to complete an application, participate in an interview, or otherwise participate in the employee pre-selection process, please send an email to USHR_Accommodation@asml.com to initiate the company's reasonable accommodation process.
Please note: This email address is solely intended to provide a method for applicants to initiate ASML's process to request accommodation(s). Any recruitment questions should be directed to the designated Talent Acquisition member for the position.

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