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Associate Director Validation Jobs in Oklahoma (NOW HIRING)

By utilizing our associates' knowledge and experience alongside SSC's extensive training, providing ... Valid driver's license and clean driving record, ensuring safe operation of company vehicles in ...

By utilizing our associates' knowledge and experience alongside SSC's extensive training, providing ... Valid driver's license and clean driving record, ensuring safe operation of company vehicles in ...

By utilizing our associates' knowledge and experience alongside SSC's extensive training, providing ... Valid driver's license and clean driving record, ensuring safe operation of company vehicles in ...

Director of Sales

Tulsa, OK ยท On-site

$90 - $140/hr

Management-level associates are expected to work as much of each workday as is necessary to ... A valid driver's license is required. * Excellent verbal and written communication skills are ...

Management-level associates are expected to work as much of each workday as is necessary to ... A valid driver's license is required. * Excellent verbal and written communication skills are ...

Management-level associates are expected to work as much of each workday as is necessary to ... A valid driver's license is required. * Excellent verbal and written communication skills are ...

Management-level associates are expected to work as much of each workday as is necessary to ... A valid driver's license is required. * Excellent verbal and written communication skills are ...

Program Director - RN

Duncan, OK ยท On-site

$70 - $90/hr

The Program Director, RN, partners both internally and externally to ensure patient wound care is ... An associate's degree in nursing is required; a Bachelor of Science in nursing is preferred * Valid ...

Valid National Provider Identifier (NPI) and DEA registration for controlled substances. * Hospice ... We Offer Benefits for All Associates (Full-Time, Part-Time & Per Diem): * Competitive Pay * 401(k) ...

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Associate Director Validation information

What is an associate director validation?

An Associate Director of Validation is a leadership role in the pharmaceutical, biotechnology, or medical device industries responsible for overseeing validation activities. This includes ensuring that equipment, processes, and systems meet regulatory standards and function as intended. The Associate Director manages validation teams, develops validation strategies, and ensures compliance with industry regulations such as FDA and GMP. They play a key role in quality assurance and help maintain the integrity of products and processes.

How does an associate director validation typically collaborate with cross-functional teams during major projects?

An Associate Director of Validation works closely with departments such as Quality Assurance, Manufacturing, Engineering, and Regulatory Affairs to ensure that validation activities meet both internal standards and regulatory requirements. This often involves leading multi-disciplinary project teams, facilitating communication, and resolving challenges related to process or equipment validation. Regular meetings, joint risk assessments, and coordinated documentation are common, which helps streamline project timelines and maintain compliance. Effective collaboration is essential for successful product launches and ongoing process improvements.

What are the key skills and qualifications needed to thrive as an associate director validation, and why are they important?

To excel as an Associate Director Validation, you need in-depth knowledge of validation principles, regulatory guidelines (such as FDA, EMA), and a background in life sciences or engineering, often supported by advanced degrees. Familiarity with validation software, quality management systems (QMS), and industry-standard protocols like GAMP or ASTM E2500 is crucial. Strong leadership, project management, and cross-functional communication skills help drive teams and ensure compliance. These competencies are essential to maintain product quality, regulatory adherence, and efficient validation processes in a highly regulated environment.

What is the difference between Associate Director Validation vs Validation Manager?

AspectAssociate Director ValidationValidation Manager
CredentialsBachelor's or Master's in Life Sciences, Engineering, or related fields; often requires industry certificationsBachelor's or Master's in similar fields; certifications like ASQ or ISPE are common
Work EnvironmentLeads validation teams, oversees validation strategies, and collaborates with cross-functional departmentsManages validation projects, ensures compliance, and reports to senior management
Employer & Industry UsagePharmaceutical, biotech, and medical device industries; used in large organizationsSimilar industries; common in mid to large-sized companies for validation oversight

The Associate Director Validation typically holds a higher strategic role, overseeing validation teams and strategies, while the Validation Manager focuses on managing validation projects and ensuring compliance. Both roles require similar credentials and are vital in regulated industries, but the Associate Director has broader leadership responsibilities.

What job categories do people searching Associate Director Validation jobs in Oklahoma look for?

The top searched job categories for Associate Director Validation jobs in Oklahoma are:

What cities in Oklahoma are hiring for Associate Director Validation jobs?

Cities in Oklahoma with the most Associate Director Validation job openings:

Associate Director, Oncology Treatment Site Lead - OK-LA Territory (AL, KS, LA, OK)

MSD Malaysia

Oklahoma City, OK โ€ข On-site

$191 - $300/hr

Other

Medical, Dental, Vision, Retirement, PTO

Posted 2 days ago

New


Job description

Job Description Our Company is preparing for the potential U.S. launch of an oncology mRNA-based individualized neoantigen therapy for early stage melanoma which involves operational complexities for treatment sites and requires close coordination with cross-functional partners.

To ensure site readiness and support consistent site execution, we are building a dedicated team of field-based operational roles to help educate treatment sites on the practical, logistical, and operational requirements necessary to onboard the product effectively, inform treatment sites about helpful workflows and tools related to this product, and sustain reliable end-to-end execution through steady-state operations following potential FDA approval.

The Associate Director Oncology Treatment Site Lead (TSL) is the primary field-based point of contact for operational information and support for product treatment sites. This role educates and supports sites so that they can consistently execute the end-to-end product operational journeyโ€”from onboarding and readiness through ordering workflow execution and steady-state operations. TSLs will help support sites by educating them about necessary processes, answering questions about operational issues, and supporting a reliable, seamless experience across the treatment journey. The TSL is focused on operational and process support, and not clinical treatment information. This role requires strong knowledge of treatment-site operations, the ability to navigate complex crossโ€‘functional workflows, and the ability to align internal and external stakeholders to support reliable endโ€‘toโ€‘end site execution as well as timely issue resolution. This is a fieldโ€‘based, customerโ€‘facing, nonโ€“demand generating and nonโ€‘promotional role. The Associate Director Oncology Treatment Site Lead (TSL) role will have responsibility for accounts in the OKโ€‘LA geography, which includes, AL, KS, LA, and OK. The candidate must reside in the designated geographic territory.

Primary Activities & Responsibilities
  • Lead the onboarding and readiness support process for product treatment sites, ensuring treatment sites are educated on the workflow, system setup, and operational requirements
  • Deliver process-focused education for site stakeholders using approved resources to support initial site implementation and ongoing operational support
  • Help ensure treatment sites have the operational capabilities and knowledge required for consistent execution of the product's endโ€‘toโ€‘end treatment journey
  • Serve as the product operational subject matter expert for your assigned treatment sites and provide support regarding the product process, operations, and logistics
  • Act as the primary point of contact for operational issues, triaging and appropriately addressing issues through crossโ€‘functional coordination and defined processes
  • Appropriately collaborate with crossโ€‘functional oncology field teams (as approved) to support coordinated, compliant engagement and a consistent experience for product treatment sites
  • Build trusted business relationships with site operational leaders by delivering consistent, reliable, and responsive operational support
  • Utilize our company generated data and dashboards to assess appropriate site operational metrics (as approved) and identify opportunities for operational improvement
  • Synthesize site feedback and process insights to help HQ team enhance communication, operational workflows, resources and education
Qualifications
  • Bachelor's degree required
  • Minimum of 5 years of relevant experience in healthcare or life sciences, including sales, account management, or provider operations/administration
  • Strong understanding of the healthcare ecosystem
  • Proven track record of working with provider organizations and operational stakeholders to implement workflows for complex therapies
  • Ability to operate effectively in โ€œwhite spaceโ€ environments with evolving processes, unclear paths, and multiple dependencies
  • Strong operational problemโ€‘solving skills, including identifying process friction points, diagnosing root causes, and coordinating next steps with appropriate stakeholders
  • Ability to build and develop meaningful customer relationships with operational stakeholders at treatment sites
  • Excellent interpersonal and communication skills, internally and externally, with ability to interact with individuals from a variety of cultures and disciplines
  • Strong leadership skills and ability to collaborate in crossโ€‘functional, matrix organizations
  • Ability to travel ~50%
  • Valid driverโ€™s license
Required Skills
  • Account Management
  • Business Management
  • Business Relationship Building
  • Cell and Gene Therapy
  • Collaboration
  • Communication
  • Crossโ€‘Functional Collaboration
  • Crossโ€‘Functional Teamwork
  • Cytometry
  • Cytopathology
  • Immunotherapy
  • Logistics Management
  • Messenger RNA
  • Onboarding
  • Oncology
  • Patient Treatment
  • Product Lifecycle
  • Project Implementations
  • Radioimmunoassay (RIA)
  • Radiopharmaceuticals
  • Service Readiness
  • Site Activation
  • Site Operations
  • Stakeholder Engagement

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one anotherโ€™s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is $190,800.00 - $300,300.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employeeโ€™s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and longโ€‘term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

Employee Status: Regular Relocation: No relocation VISA Sponsorship: No Travel Requirements: 50% Flexible Work Arrangements: Remote Shift: 1st - Day Valid Driving License: Yes Hazardous Material(s): NA

Job Posting End Date: 09/17/2026 *A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where we have codified our legacy for over a century. Our success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.

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