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Qa director • usa

Last updated: 4 days ago

Compliance QA Director

ExelixisAlameda, CA, United States
$190,000.00 yearly
Full-time

The Compliance QA Director leads the company's GxP inspection readiness ensuring ongoing preparedness for global health authority inspections.This role manages regulatory inspections and responses,... Show more

QA Director/Capital Markets

Syntricate TechnologiesJersey City, NJ, United States
$230,000.00 yearly
Full-time

The client is now looking for a QA director to lead a team of 40 QA engineers on their trading platform team.Candidates must have director level or higher experience and recent experience working o... Show more

Associate Director, QA Computer System Validation

CytokineticsSouth San Francisco, CA, United States
$184,500.00 yearly
Full-time

Associate Director, Computer System Validation.Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle bio... Show more

Sr Director, QA

SoleraRoanoke, TX, United States
Full-time

Solera is a global leader in data and software services that strives to transform every touchpoint of the vehicle lifecycle into a connected digital experience.In addition, we provide products and ... Show more

Program Director, Knowledge & QA

BullhornRemote, United States
Remote
Full-time

Own the end-to-end KCS program: strategy, governance, adoption metrics, and continuous improvement.Establish and oversee the Knowledge Domain Expert (KDE) program across product areas and global re... Show more

Assistant QC/QA Director

BARRETTMiddletown, OH, US, 45005
Full-time

The Assistant QC/QA Director supports the QC Director in the coordination, planning, and supervision of the contract/project quality management system to ensure contracts and projects meet or excee... Show more

Director of Quality Engineering (QA Director)

Ova TechnologiesAlpharetta, GA, United States
Full-time

Director of Quality Engineering (QA Director).Experience: 18+ Years Role Type: Leadership / Strategic Company Type: Product-Based / SaaS Location: India / Hybrid / Remote.We are seeking a Director ... Show more

Director, US Commercial QA Lead (GMP)

PharvarisLexington, MA, United States
$195,000.00 yearly
Full-time

Director, US Commercial QA Lead (GMP).Quality Assurance Hybrid/Remote US (Greater Boston area).Pharvaris is a Nasdaq listed late-stage biotech company developing bradykinin B2 receptor antagonist... Show more

Associate Director, Clinical QA

AlkermesWaltham, MA, United States
Full-time

This position is an integral part of the CQA team and provides oversight for and participates in, auditing services in support of Alkermes Clinical Programs by conducting clinical site, vendor qual... Show more

QA Director

ExperisTempe, AZ, United States
$160,000.00 yearly
Full-time

Experis is seeking a highly experienced QA Director to own the testing strategy across multiple titles for our partner that is a leader in AAA game and devise development.This role will be critical... Show more

Director, CMC QA

Korro BioCambridge, MA, United States
Full-time

Company Summary: Korro is a biopharmaceutical company focused on developing a new class of genetic medicines for both rare and highly prevalent diseases using its proprietary RNA editing platform.K... Show more

Director of Electrical QA/QC

New Day Executive SearchSaint Augustine, FL, United States
Full-time

Director of Electrical QA/QC - Jacksonville.Position Summary: The Electrical QA/QC Director will oversee and enforce quality control standards and procedures throughout all phases of electrical con... Show more

QA Director

Veracity SolutionsBerkeley Heights, NJ, United States
Full-time

Location: Omaha, NE, Berkeley Heights, NJ (100% Onsite - local only no relocation).Manage and coach 4 direct reports and 36 indirect reports.Drive quality practices and standards across the organiz... Show more

QA Director

Tech Resource Group Inc.New York, NY, United States
Full-time

Consulting firm with 10000+ employees & $10+ billion Revenue.Mandatory Technical / Functional Skills.Software Quality Assurance consultant with at least 10 years' experience in playing QA Director.... Show more

Director QA - GCC

SavianceBoston, MA, United States
Full-time

As a director of software quality assurance and release engineering, you will be responsible for managing Software Quality Assurance teams and processes to support manual and automated testing of t... Show more

Associate Director, GCP QA

Mirum PharmaceuticalsSan Mateo, CA, United States
$190,000.00 yearly
Full-time

Mirum Pharmaceuticals is a biopharmaceutical company dedicated to transforming the treatment of rare diseases.We are passionate about advancing scientific discoveries to become important medicines ... Show more

Director, GPV Compliance & Business Management (QA)

Otsuka PharmaceuticalPrinceton, NJ, United States
$186,489.00 yearly
Full-time

Director, Gpv Compliance & Business Management.The Compliance & Business Management (CBM) team supports key Pharmacovigilance (PV) operational, compliance, and business activities across the organi... Show more

QA Program Manager/Director

My3TechAnn Arbor, MI, United States
Full-time +1

Ann Arbor, MI (Onsite Michigan based is preferred or start remote and willing to travel/relocate).Accountable for managing and coordinating all automation QA across different applications and diffe... Show more

Executive Director, Global GCP QA

Structure TherapeuticsSouth San Francisco, CA, United States
Full-time

Structure Therapeutics develops life-changing medicines for patients using advanced structure-based and computational drug discovery technology.The company's platform combines the latest advancemen... Show more

Associate Director-Quality Assurance (QA-CMC)

Clinical DynamixJersey City, NJ, United States
Full-time

Associate Director-Quality Assurance (QA-CMC).Company is seeking a highly experienced, motivated, and innovative quality leader with strong experience in early and late-stage development to join ou... Show more

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Compliance QA Director

Compliance QA Director

ExelixisAlameda, CA, United States
6 days ago
Salary
$190,000.00 yearly
Job type
  • Full-time
Job description

Compliance QA Director

The Compliance QA Director leads the company's GxP inspection readiness ensuring ongoing preparedness for global health authority inspections. This role manages regulatory inspections and responses, directs internal audits and mock inspections, and provides oversight of corrective and preventive actions to drive timely closure and risk reduction. Serving as a compliance subject matter expert, partners cross-functionally to provide guidance on GxP processes and continuously improves inspection readiness practices across the organization.

Essential Duties/Responsibilities:

  • Leads the management of health authority agency inspections and coordination of responses to any health authority agency observations.
  • Responsible for setting the strategic plan for maintaining organizational inspection readiness across the organization and developing an annual inspection readiness plan, ensures activities are completed, and drives continuous improvement initiatives.
  • Leads projects which have strategic impact on the organization and act as a role model for change by demonstrating commitment to the success of the project.
  • Acts as the Subject Matter Expert for current global regulatory compliance expectations and proactively reviews changes in regulatory requirements and industry environment that would necessitate future changes and drives completion of impact assessments.
  • Partners with other groups including Regulatory Affairs, Clinical Operations, Drug Safety, Pharmaceutical Operations and Supply Chain, and Non-clinical Development, regarding compliance assessments and provide compliance guidance related to GxP processes.
  • Leads cross-functional teams in managing inspection readiness activities.
  • Assesses proposed corrective or preventive actions in response to audit or inspection findings, track and report closure of items, and provide management visibility to areas of risk or concern.
  • Manages implementation, maintenance, execution of internal audits and mock inspections.
  • Represents Compliance QA in internal presentations on quality issues, initiatives and projects regarding audit or inspection readiness processes.
  • Identifies new contract auditors, oversees the establishment of agreements and ensures all commitments are met by contract auditors and monitors auditor assignments and budget.
  • Ensures that inspection and audit tools are appropriate and fit for purposes.
  • As necessary, execute external vendor audits as part of the Supplier Quality Management program.
  • Other responsibilities as required.

Supervisory Responsibilities:

  • No supervisory responsibilities.

Education/Experience/Knowledge & Skills:

Education:

  • Bachelor's degree in biology, sciences, or related STEM disciplines and 13 years of relevant experience; or
  • Master's degree in related STEM disciplines and 11 years of relevant experience; or
  • Equivalent combination of education and experience.

Experience:

  • Must have audit and inspection management work experience within pharmaceutical quality compliance or quality assurance.
  • A minimum of 11 years of related experience in GxP quality compliance or quality assurance, with leadership roles in inspection readiness and audits. Recognized as a knowledgeable resource within the department and from other departments on a range of topics and someone whose opinion is sought as a regulatory resource.

Knowledge, Skills and Abilities:

  • Independent contributor with minimal supervision.
  • Excellent written and oral communication skills.
  • Excellent attention to detail and organizational skills.
  • Demonstrated knowledge of regulatory requirements and applied current regulations and quality standards to deliver high quality work.
  • Demonstrated management experience, particularly in audit or inspection management, is required.
  • Working knowledge of supporting inspection preparation and inspection activities for global regulatory filings (US FDA, EMA, MHRA, PMDA, and ANVISA desired).
  • Experience in supporting regulatory health authority inspections, including preparation, documentation review, coordination of activities, and post-inspection actions.
  • Ability to influence others as part of a collaborative team and negotiate effective solutions, strong interpersonal and social skills.
  • Uses broad expertise or unique knowledge and skills to contribute to development of company objectives and principles, and to achieve goals in creative and effective ways
  • Highly skilled in the ability to work with ambiguity and complexity and can continuously modify options and solutions across all levels of the organization.
  • Develops technical solutions to complex problems.
  • Possesses complete understanding and wide application of technical principles, theories, concepts and techniques.
  • Able to multi-task across multiple studies and multiple stage projects.
  • Exercises independent judgment in methods, techniques and evaluation criteria for projects, programs and people and guides the successful completion of those programs and projects.
  • Works in partnership with cross-functional teams.
  • Work with various contractors and team members to ensure Exelixis project/program goals are met.
  • Strong user of Microsoft Office applications.

Work Environment/Physical Demands :

Our office is a modern, open space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.

  • Travel requirements: 20%.

Our compensation reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $190,000 - $269,000 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors. In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

If you have a disability and need an accommodation in relation to the application and/or recruitment process, please email us at recruiting@exelixis.com.

Working Conditions:

Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.

Disclaimer: The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class.