Top 3 Director of quality Jobs in Redmond, Or

Associate Director of Quality Assurance, Operations
Serán BioScience —Bend, OR
- Full-time
- Analysis skills
- Bachelor's degree
- Mentoring
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Associate Director, Quality Assurance
Lonza —Bend, OR
- Full-time
- Bachelor's degree
- Experience equivalent to degree accepted
- Training & development
- Relocation assistance
- Health insurance
Senior Scientist, Laboratory Director Research and Lab Services
OREGONS WILD HARVEST —Redmond, OR
- Full-time
- Microsoft Outlook
- Analysis skills
- Senior level
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Associate Director of Quality Assurance, Operations
Serán BioScience —Bend, OR
The successful candidate will have excellent problem-solving skills and will identify critical quality objectives, develop cross-functional, collaborative, and…
Quick Apply
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Lonza —Bend, OR
Bachelor’s degree or equivalent experience in a relevant field. Manage and develop QA teams supporting GMP production and documentation processes.

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Associate Director of Quality Assurance, Operations

Serán BioScience -
Bend, OR

Quick Apply

Job Details

Full-time

Qualifications

Regulatory inspections
Customer communication
Stakeholder engagement
Manufacturing management
Staff supervision
Investigations regulatory compliance
Team supervision
Pharmaceutical regulatory compliance
Performance management strategy
GMP
Client relationship development
Internal investigations
Project management experience in manufacturing
Change management
Team development
Bachelor's degree
Pharmaceutical company experience
Team training
Quality assurance experience within pharmaceutical industry
Mentoring
Leading team collaboration initiatives
Managing projects
Managing manufacturing teams
Quality control experience within pharmaceutical industry
Managing product quality assurance teams
Cross-functional team management
Stakeholder relationship building
Cross-functional communication
FDA regulations
Pharmaceutical manufacturing facility experience

Full Job Description

Serán is seeking a QA Associate Director,who oversees the day-to-day operations of the Quality Assurance department with oversite of clinical manufacturing and warehouse activities in addition to disposition of raw materials and drug products. Required attributes include a results-driven and broad-minded quality assurance professional with extensive experience in compliance and regulations, quality systems management, investigations, training and mentoring, client relations, performance management, and change management. Extensive experience with direct or quality oversite of manufacturing operations is required.

The successful candidate will have excellent problem-solving skills and will identify critical quality objectives, develop cross-functional, collaborative, and creative teams, and improve, adapt, and execute practical solutions in competitive and fast-paced environments.

Supervisory Responsibilities

Leads and mentors Quality Assurance personnel.
Recruits, interviews, hires and trains new staff.
Oversees daily workflow of the department.

Responsibilities

Leads and implements continuous improvement initiatives to reduce risk and improve efficiency for the company’s quality systems and department operations
Management and scheduling of department operations
Oversees and conducts review and approval of Investigations, CAPAs, Complaints, and Change Management
Review and approval of SOPs, batch records, raw material records, and certificates of conformance/compliance
Responsible for Quality oversight of activities involving raw material, drug product manufacturing, packaging, labeling, and warehouse activities
Assures cGMP compliance systems and processes are in place to support raw material and drug product review, release, storage, and shipping
Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first-time rate
Supports internal audits, client audits and regulatory inspections

Required Skills and Experience

Expert knowledge of GMP guidelines and Quality expectations for preclinical and clinical phase manufacturing operations
In-depth understanding and application of cGMP principles, concepts, practices, and standards
Experience with regulatory inspections by the FDA and EU authorities
Ability to influence diverse stakeholders and drive accountability and decision-making cross functionally
Demonstrated ability to partner with other functional groups to achieve business objectives
Experience organizing and managing group responsibilities while working independently with minimal oversight
Time and project management skills with the ability to multi-task and meet deadlines
Excellent verbal and written communication skills
Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company
Excellent organizational skills and attention to detail
Strong analytical and problem-solving skills
Strong supervisory and leadership skills

Education and Experience

Minimum of a bachelor’s degree, preferably in a scientific discipline. An advanced degree is preferred
10+ years previous GMP and Quality experience in the Pharmaceutical industry with quality oversite of Oral Solid Dose manufacturing
Experience with regulatory inspections by the FDA and EU authorities

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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Associate Director of Quality Assurance, Operations

Associate Director, Quality Assurance

Senior Scientist, Laboratory Director Research and Lab Services

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