CSL Plasma Posted October 21, 2026

Associate Director, Lab Operations

Knoxville, United States Full time
Quality Associate Director
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CSL Plasma is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

The Opportunity:

Reporting to the Director of Laboratory Operations, as the Associate Director, Laboratory Operations, you will provide leadership for laboratory operations within the Knoxville Laboratory and is responsible for overall operational performance, quality, compliance, staffing, and resource management across laboratory functions and shifts.  You will lead Managers, Senior Managers, and operational support leaders to ensure the laboratory meets safety, quality, service, financial, and operational goals. You will work closely with the Director, Quality, Validation, Human Resources, Facilities, IT, and other business partners to support a safe, compliant, and efficient operation while preparing the laboratory for future growth.

The Role:

Strategic Execution & Performance Management

Translate lab-wide goals into actionable plans for assigned departments; establish KPIs and lead performance reviews to ensure goal achievement.

Monitor and manage Laboratory Operations Key Performance Indicators (KPIs).

Implement course corrections to achieve goals and contribute to monthly operational reports and presentations.

Operational Excellence & Process Optimization

Lead initiatives to improve lab efficiency, throughput, and quality, including infrastructure upgrades and system enhancements.

Analyze operational data to identify trends, diagnose root causes, and implement corrective actions to improve lab performance.

Manage day-to-day capacity and organizational capability to perform high-volume testing required for the release of plasma per customer specifications.

Regulatory Compliance & Quality Oversight

Ensure adherence to FDA, CLIA, cGMP, and internal SOPs; maintain inspection readiness and lead corrective/preventive actions.

Ensure laboratory operations comply with all relevant regulatory agencies (FDA, CLIA, GHA, etc.). Maintain an "inspection-ready" condition at all times, drive corrective/preventive actions (CAPA), and ensure staff are trained in current SOPs.

Leadership & Talent Development

Leads and develops Managers, Senior Managers, and operational leaders.

Oversees staffing plans, succession planning, leadership development, employee relations, and workforce planning to support current and future operational needs.

Financial & Capital Management

Supports development of operating budgets, staffing plans, and resource requirements.

Monitors financial performance and works with laboratory leadership to ensure resources are aligned with operational demands and business priorities.

Cross-Functional Collaboration

Partners with Quality, Validation, Human Resources, Facilities, IT, Engineering, and other business partners to support laboratory operations, implement improvements, and address operational challenges.

Stakeholder Engagement & Industry Relations

Serves as a key representative for laboratory operations.

Builds effective working relationships with internal and external stakeholders and supports business continuity, benchmarking, customer service, and operational planning activities.

Safety & Facility Oversight

Promote a culture of safety and compliance; ensure facility maintenance meets operational and regulatory standards.

Maintain a clean, efficient, and safe work environment.

Ensure strict adherence to Environmental Health and Safety (EHS), OSHA, and Standard Operating Procedures (SOPs).

Change Leadership & Innovation

Leads major operational changes that affect laboratory functions, staffing, workflows, systems, or business processes.

Supports implementation of new technologies, equipment, and operational improvements while ensuring organizational readiness and adoption.

Your Skills & Abilities:

Bachelor’s degree in chemical, biological, or clinical laboratory science, or medical technology from an accredited institution required.

Medical Technologist preferred.

Minimum of 8 years of relevant laboratory experience, including at least 4 years of leadership experience in a laboratory, healthcare, manufacturing, pharmaceutical, biologics, or other regulated environment.

Regulatory Knowledge: Demonstrated working knowledge of FDA regulations, including GMP, GLP, and CLIA standards.

Financial Acumen: Experience monitoring departmental budgets and managing resource allocations.

Leadership & Communication: Proven ability to manage, motivate, and develop supervisory teams. Strong written, verbal, and presentation skills to effectively communicate metrics and drive operational results.

Problem Solving: Excellent critical reasoning and analytical skills to resolve recurring operational defects and manage shifting priorities under tight deadlines.

Key Leadership Competencies

Strategic thinking

Operational leadership

Organizational effectiveness

Change management

Cross-functional collaboration

Continuous improvement mindset

Quality and Regulatory focus

Working Conditions:

Ability to compute, analyze, and interpret operational data and statistical forecasts.

Fast-paced environment with frequent interruptions.

Frequently sitting, with a moderate amount of time walking the laboratory floor and standing.

Must be able to wear personal protective equipment (PPE) and tolerate occasional exposure to extreme temperatures and bloodborne pathogens. Ability to lift/carry up to 40 lbs.

Overnight travel required up to 15–20% of the time.

Schedule Flexibility: Ability to work a flexible schedule, including weekends, evenings, and holidays, to provide operational oversight across all 7 days of operation and multiple shifts.

Operational Availability: Maintains operational accountability for a 7-day (24/6) high-volume testing environment, requiring occasional visibility and presence on alternate shifts to support leadership teams and manage critical escalations.

Note: All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, veteran status, national origin or other legally protected classifications.

About CSL Plasma

CSL Plasma  operates one of the world’s largest and most sophisticated plasma donation networks, with nearly 330 donation centers in the U.S. and Europe. CSL Plasma is a subsidiary of CSL, a global biopharma company. Plasma collected at CSL Plasma facilities is used by CSL for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company,  CSL  (ASX:CSL; USOTC:CSLLY), headquartered in Melbourne, Australia, employs 29,000+ people.

Learn more about CSL Plasma here https://www.cslplasma.com/ and CSL, CSL Behring, CSL Seqirus and CSL Vifor here https://www.csl.com/ .

Learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor here at https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ .

 

Our Benefits

For more information on CSL Plasma benefits visit https://cslbenefits.com/cslp .

You Belong at CSL

At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future.

To learn more visit https://www.csl.com/careers/inclusion-and-belonging

 

Equal Opportunity Employer

CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .

Job details

Seniority
Associate Director
Function
Quality
Therapeutic area
Not listed
Location
Knoxville, United States
Employment type
Full time

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 416 comparable Associate Director Quality roles across 94 biopharma companies.

416Comparable roles tracked
373Currently active
94Companies hiring similar roles
34Countries represented

Salary context

86 of 416 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Chemist, Senior (Data Review) · Merck KGaA $25/hr – $39/hr (≈ $52,000–$81,120/yr)
Peer group range $66,560 – $201,900 (median $159,000)

Where these roles are based

Top locations among the 416 comparable roles

United States190
China29
Ireland27
India19
Germany17
Netherlands13

+ 28 more countries

Seniority mix

416 of 416 peers have a known seniority level

Manager198
Senior179
Associate Director39

Therapeutic area mix

0 of 416 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Biogen Cambridge, United States Associate Director
Same function Same seniority Same country
60%similar
Lilly Pleasant Prairie, Wisconsin, United States of America Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country
60%similar
Otsuka Pharmaceutical Development and Commercialization, Inc. Remote, United States Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country

Notify me about similar jobs

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
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Biogen · Cambridge, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, GMP Operational Quality (Biologics and Devices)
Vertex Pharmaceuticals Inc (US) · Boston, United States · Associate Director
Function Therapeutic area Seniority Country
60%
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Kite Pharma, Inc. · Frederick, United States · Associate Director
Function Therapeutic area Seniority Country
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GMP Operational Quality Packaging & Labeling Validation Associate Director
Vertex Pharmaceuticals Inc (US) · Boston, United States · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.