Find work in the United States.

A simpler way to find your next job.

Jobs in the United States

25+ jobs

Save this search

Added 1 day ago
Sample Preparation Technician I - $250 Sign on Bonus
Eurofins US Network
Des Moines, IA
Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis and as needed for quality control tests or regulatory purposes; record test data and…
Added 2 days ago
R-290721 Associate Director Clinical Assay Strategy
CSL Behring
Waltham, MA
The incumbent will part of a specialised non-laboratory based team and provide high level expertise and leadership capacity in the area of bioanalytical and biomarker assays to support…
Added 2 days ago
Sample Preparation Technician I - $250 Sign on Bonus
Eurofins
Des Moines, IA
Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis and as needed for quality control tests or regulatory purposes; record test data and…
Added 3 days ago
ST
Associate Director, Biomarker and Nonclinical Operations
Seismic Therapeutic Inc
Watertown, MA
- $170,000 to $230,000 USD / year
…development decisions are managed with rigor, from the CRO laboratory to long-term storage. Reporting to the Senior Director, Biomarker and Translational Sciences, you will own the…
Added 4 days ago
Senior Associate Scientist LNP Analytical Testing - Cambridge MA
Military Spouse Jobs & VetJobs
United States
Perform routine analytical assays including ELISA, HPLC, and other analytical methods in support of research, process development, stability, and quality control activities
Added 5 days ago
Senior Associate Scientist - Bioanalysis
Regeneron Pharmaceuticals, Inc (USA)
United States
Utilizes the ELN to document experimental procedures. Works closely with Quality Control (QC) to address documentation findings and minimize deviations.
Added 10 days ago
P
Bioanalytical Scientist LC-MS/MS
Pharmaron
Germantown, MD
- $85,000 to $93,000 USD / year
The Bioanalytical Scientist LC-MS Bioanalysis, SMB performs laboratory-based activities, including data processing and review, within established timelines and in accordance with Standard…
Added 10 days ago
Supervisor, Bioanalytical Services - Flow Cytometry
ICON Clinical Research
Lenexa, KS
We are currently seeking a Supervisor, Bioanalytical Services - Flow Cytometry to join our diverse and dynamic team. In this role, you will serve as the operational lead for assigned…
Added 12 days ago
Quality Control Analyst II
Immatics US, Inc.
United States
We are seeking a Quality Control Analyst II to support our Global Quality Operations team. The QC Analyst II will be responsible for executing bioanalytical, cell-based, and/or molecular…
Added 15 days ago
Associate Research Scientist - Immunochemistry
ThermoFisher Scientific
Richmond, VA
As an Associate Research Scientist, you will oversee complex laboratory analysis of pharmaceutical products, calculate and analyze data and record data in adherence with PPD SOP's and the…
Added 15 days ago
Research Associate I, Basic Science and Translational Research (Galveston)
UTMB Health
Galveston, TX
One or more years of practical experience in a bioanalytical or micro-/nanoplastic analytical laboratory. Experience with biological sample preparation, extraction, purification, and…
Added 15 days ago
FSP-Associate Research Scientist
ThermoFisher Scientific
Collegeville, PA
…through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve…
Added 15 days ago
Senior Associate Scientist, LNP Analytical Testing
Bristol Myers Squibb
Cambridge, MA
Perform routine analytical assays including ELISA, HPLC, and other analytical methods in support of research, process development, stability, and quality control activities
Added 15 days ago
Associate Director, Quality Control- Analytical Tech Services
Gilead Sciences, Inc.
Frederick, MD
We are seeking a highly motivated individual to join us as an Associate Director, to lead Quality Control Analytical Tech Services group, reporting to the Senior Director, Quality Control…
Added 16 days ago
Sample Preparation Technician I - $250 Sign on Bonus
Eurofins US Network
Des Moines, IA
Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis and as needed for quality control tests or regulatory purposes; record test data and…
Added 16 days ago
Laboratory Technician I - Micro
Eurofins US Network
Des Moines, IA
Maintain a neat and accurate record system; keep accurate records of work performed on a daily basis and as needed for quality control tests or regulatory purposes; record test data and…
Added 16 days ago
Associate Scientist (Quality)
Danisco US Inc.
Wilmington, DE
The Associate Quality Scientist provides technical and operational support to the Global Technical Quality Bioanalytical Team. In this role, you will support the Standards and Controls…
Added 16 days ago
Senior Associate Scientist, LNP Analytical Testing
E.R. Squibb & Sons,L.L.C.
Cambridge, MA
Perform routine analytical assays including ELISA, HPLC, and other analytical methods in support of research, process development, stability, and quality control activities
Added 17 days ago
Associate Director - Immunoassay
Resolian
Malvern, PA
The Associate Director serves as a scientific subject matter expert and client-facing leader, ensuring delivery of high-quality bioanalytical data that complies with applicable regulatory…
Added 17 days ago
C
Laboratory Operations Assistant - Part-Time
Celerion
Lincoln, NE
- $17 USD / hour
- Part-time
We are seeking a detail-oriented and dependable Laboratory Operations Assistant to support daily activities within our bioanalytical department. This role is essential to maintaining the…
Added 18 days ago
MU
Research Associate - DMPK / Bioanalysis
MEDICILON USA CORP
Lexington, MA
- $55,000 to $60,000 USD / year
Medicilon USA Corp is seeking a motivated and detail-oriented Research Associate to join our DMPK and Bioanalysis team in Lexington, MA. This is a hands-on laboratory role supporting…
Added 19 days ago
Executive Director, PDMB Outsourcing
Merck Sharp & Dohme LLC
PA · MA · NJ · CA
Broad experience in bioanalytical development/validation and quality control (QC) with expert knowledge of regulatory agency requirements for operating in a regulated clinical and GLP…
Added 20 days ago
Associate Director, Lab Automation & Digital Enablement
Charles River
NV
Lead laboratory automation and digital solutions strategy and execution within a Good Laboratory Practices (GLP)-compliant environment. Identify and prioritize high-volume, high-impact,…
Added 21 days ago
Associate BioServices Study Lead
TA US Quintiles Laboratories
Ithaca, NY
…providing scientific oversight throughout the lifecycle of bioanalytical projects. Working under Study Lead Management and in partnership with Project Management, ensure exceptional…
Added 21 days ago
Associate BioServices Study Lead - Hybrid
TA US Quintiles Laboratories
Indianapolis, IN
Provide scientific oversight throughout the lifecycle of bioanalytical projects while delivering exceptional service to internal and external customers. Partner with Project Management,…

Gilead Sciences, Inc.

Associate Director, Quality Control- Analytical Tech Services

Frederick, MD, United States

The salary range for this position is: $165,495.00 - $214,170.00.

Apply About employer

Applications open in a new tab.

Job details

Pay: The salary range for this position is: $165,495.00 - $214,170.00.
Posting language: English
Posted: Oct 25, 2025

Original job description

Onsite Required

United States - Maryland - Frederick

Full time

R0048119

We’re here for one reason and one reason only – to cure cancer. Every moment is dedicated to developing treatments and every action moves us one step closer to our goal. We’ve made incredible scientific breakthroughs and our pioneering personalized CAR T-cell therapies have changed the paradigm. But we're not finished yet.

Join Kite, as we make even bigger advances in cancer therapies, and help shape where our business and medical science goes next.

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Kite and help create more tomorrows.

Job Description

Everyone at Kite is grounded by one common goal – curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work. Join us in our mission!

We are seeking a highly motivated individual to join us as an Associate Director, to lead Quality Control Analytical Tech Services group, reporting to the Senior Director, Quality Control in Frederick, MD. In this role, you will lead a group and work closely with the Senior Director and other Associate Directors on supporting commercial operations in CAR-T technology.

You will work on complex projects involving qPCR/ddPCR, Flow cytometry and cell-based bioassays and lead efforts in automation development for analytical assays . You will have cross-functional interaction with personnel from other groups such as Quality Assurance, Analytical Development, Manufacturing, Material Management (MM) and Corporate teams.

Position Responsibilities (include but not limited to):

Provide technical support, process trending and procedural updates
Lead method validation and method transfers support continuous improvement, to support method/product/invalid trending, and to investigate laboratory/assay related findings.
Lead and support method development, validations, and transfers
Support laboratory investigations, deviations, CAPAs, change control as needed
Assist in investigation, identify root cause for critical deviations and determine CAPA for QC as needed
Establish data analytics to serve as metrics for monitoring trends in methods, products, and invalids
Support incoming tech transfers from AD/PD as needed
Author technical reports and protocols in support of cGMP activities
Supervise, train, and mentor junior staff
Create and/or revise procedures, SOPs, and test methods as needed
Support equipment and software lifecyle process
LIMS development and integration
Provide technical expertise for AD/PD, QA, Regulatory, Manufacturing, and Supply Chain as needed
Support and participate inspection readiness plans and participate during compliance audits (internal and external) and regulatory inspections.
Follow technology changes, recommends new technologies, advises on technology purchases and implementation if appropriate.
Additional duties as assigned.

Basic Qualifications:

Advanced scientific degree (i.e. MD, PharmD, PhD) and 2+ years’ experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment OR
Master’s Degree and 8+ years’ experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment OR
Bachelor’s Degree and 10+ years’ experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment OR
High School Degree and 14+ years’ experience in biologics/cell-gene therapy in QC Analytical, Analytical Development environment

Preferred Qualifications:

Experience supervising/managing analytical labs within the biotechnology or pharmaceutical industry
Well versed and experienced in bioanalytical methods working under GMP conditions.
Deep experience in applying GMP in QC lab in conformance to US, EU and ROW standards.
Experience in conducting investigations, writing deviations, implementing CAPA and initiating change controls.
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211), Quality Control, GMPs, GLP
Ability to effectively negotiate and develop collaboration within teams and amongst individuals.
Demonstrated ability to create and maintain highly functioning teams.
Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment
Comfortable in a fast-pace small company environment with minimal direction and able to adjust workload based on changing priorities.

People Leader Accountabilities:

Create Inclusion - knowing the business value of diverse teams, modeling inclusion, and embedding the value of diversity in the way they manage their teams.
Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.
Empower Teams - connect the team to the organization by aligning goals, purpose, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.

The salary range for this position is: $165,495.00 - $214,170.00. Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.

Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com . Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma .

For jobs in the United States:

Kite Pharma is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact ApplicantAccommodations@gilead.com for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' (https://www.eeoc.gov/employers/eeo-law-poster) poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf)

YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Kite Pharma will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the legal duty to furnish information; or (d) otherwise protected by law.

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Kite Pharma provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Change The World With Us

Everyone at Kite is grounded by one common goal – curing cancer. Every day, we aim to establish a direct line between that purpose and our day-to-day work.

We are creating Kite together, with the recognition that the best teams are built by the best people. We maintain an attitude of curiosity, and creativity with each challenge as we develop a new market for cancer therapies. We appreciate and respect one another, and most importantly, we don’t take success for granted.

While we’ve come a long way to make what others viewed as impossible, possible, we know one thing is certain. Today is just the beginning.

Apply About employer

More about this job

Skills

Quality control
Quality assurance
Technical support
Process improvement
Data analysis
LIMS
Provide technical expertise
PD
Supply chain management
Inspection
Regulatory compliance
Biotechnology
Pharmaceutical industry
Good manufacturing practices
Apply GMP
Quality control systems
Good laboratory practices
Collaboration

Report this job