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Associate Creative Director Acd Jobs in Oregon (NOW HIRING)

About the Role As an Associate Client Services Director, you'll provide strategic leadership for a ... Partner with Scientific Services, Editorial, Digital, Creative, and Operations teams to deliver ...

The ideal candidate combines exceptional analytical skills with creative problem-solving, enabling them to navigate complex challenges, craft innovative solutions, and deliver value to clients at ...

We are looking for an Associate, Talent Services who will provide support to the Director, Talent ... Very motivated, creative, and willing to take risks-entrepreneurial in spirit * Strong listening ...

Guest Experience Associate

Corvallis, OR

$15.25 - $18.75/hr

Patricia Valian Reser Center for the Creative Arts Special Instructions to Applicants: When ... Politely direct and escort guests to their seats and/or venue entrances. * Provide wayfinding of ...

Front Desk Associate

OR · On-site

$17.13/hr

Ensures that guests and appointments are directed to the appropriate fitness consultant in a prompt ... creative. If this feels like you, we can't wait to get your application!

Ensures that guests and appointments are directed to the appropriate fitness consultant in a prompt ... creative. If this feels like you, we can't wait to get your application!

Showing results 41-60

Associate Creative Director Acd information

What is the difference between Associate Creative Director Acd vs Creative Director?

AspectAssociate Creative Director (ACD)Creative Director (CD)
ResponsibilitiesSupports senior creative teams, manages projects, and oversees junior staffLeads overall creative vision, strategy, and client relationships
Experience & CredentialsTypically 5-8 years in creative roles, relevant portfolio, sometimes certificationsMore extensive experience, leadership skills, and industry recognition
Work EnvironmentCollaborates closely with Creative Directors and teamsSets direction and oversees multiple projects and teams

The Associate Creative Director (ACD) plays a vital supporting role in the creative process, focusing on project management and team oversight. In contrast, the Creative Director (CD) holds the primary responsibility for the overall creative vision and strategic direction of campaigns. While both roles require strong creative credentials and industry experience, the CD typically has more seniority and leadership responsibilities. Understanding these differences helps clarify career progression and expectations within creative agencies.

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For Associate Creative Director Acd jobs in Oregon, the most frequently searched job titles are:

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The top searched job categories for Associate Creative Director Acd jobs in Oregon are:

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Cities in Oregon with the most Associate Creative Director Acd job openings:

Infographic showing various Associate Creative Director Acd job openings in Oregon as of August 2026, with employment types broken down into 1% As Needed, 70% Full Time, 25% Part Time, 1% Temporary, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Associate Director of Quality Assurance, Operations

Serán BioScience

Bend, OR • On-site

Full-time

Re-posted 14 days ago


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.