Analytical method validation jobs

Manager, Microbiology (CVRM)

Roche · Posted Nov 6, 2026

Open

Holly Springs, North Carolina, United States
Manager
$100K–$185K per year
5+ years

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Manager, Microbiology (CVRM)

Roche · Posted Nov 6, 2026

Open

Holly Springs, North Carolina, United States
Manager
$100K–$185K per year
5+ years

Apply with Referso

Manager, Microbiology (CVRM)

Genentech · Posted Nov 6, 2026

Open

Holly Springs, North Carolina, United States
On-site
Full-time · Manager
$100K–$185K per year
5+ years

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Lead and build the QC Microbiology team at Genentech’s Holly Springs facility, overseeing laboratory start‑up, compliance, and operational excellence.

Compensation

The expected salary range for this position based on the primary location for this position of Holly Springs, North Carolina is $99,500 - $184,700. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

Responsibilities

Establish and lead QC Microbiology team
Build and maintain QC capabilities for CVRM products
Develop and implement QC processes and SOPs
Ensure compliance with cGMP, ICH, FDA, EMA
Drive continuous improvement and Lean initiatives

Requirements

Bachelor's or Master's in a science related discipline
Nice to have: Greenfield project experience
Nice to have: Lean Six Sigma Green/Black Belt
Nice to have: 5S
Nice to have: Kaizen

Skills

Microbiology methods Laboratory instrumentation Analytical method validation Contamination control

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Pfizer · Posted Nov 6, 2026

Open

Toluca, Mexico
On-site
Contract
4+ years

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Support the planning and execution of analytical method validation activities for chemical and physicochemical methods in a GMP-regulated laboratory.

Responsibilities

Support planning and execution of analytical method validation activities
Prepare and organize samples, standards, reagents, solutions, reference materials and documentation
Execute validation tests such as specificity, accuracy, precision, linearity, range, robustness, system suitability, detection limit, quantitation limit and method equivalency
Ensure training records reflect current qualification
Verify instrument readiness, calibration status and system suitability

Requirements

Bachelor's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, Biology, Biochemistry or related scientific discipline
Nice to have: HPLC
Nice to have: GC
Nice to have: UV-Vis
Nice to have: dissolution

Skills

analytical method validation verification transfer lifecycle activities GMP

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Pfizer · Posted Nov 6, 2026

Open

Toluca, Estado de México, Mexico
On-site
Temporary · Associate
4+ years

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Support the planning and execution of analytical method validation activities for chemical and physicochemical methods in accordance with approved protocols.

Responsibilities

Support the planning and execution of analytical method validation activities for chemical and physicochemical methods in accordance with approved protocols.
Prepare and organize samples, standards, reagents, solutions, reference materials, and documentation required for validation studies.
Execute validation tests such as specificity, accuracy, precision, linearity, range, robustness, system suitability, detection limit, quantitation limit, and method equivalency, as applicable.
Ensure training records reflect current qualification to perform validation, verification, and routine analytical method activities.
Verify instrument readiness, calibration status, analytical conditions, and system suitability requirements before executing validation or verification testing.

Requirements

Bachelor's degree in Chemistry
Pharmaceutical Sciences
Chemical Engineering
Biology
Biochemistry

Skills

Analytical method validation Good Manufacturing Practices (GMP)

Scientist

Aditi Consulting · Posted Nov 5, 2026

Open

Thousand Oaks, California, United States
Full-time
$35–$38 per hour
2+ years

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Scientist in Commercial Process Development responsible for method transfer, validation, and statistical analysis for quality control.

Compensation

Payrate: $35.00 - $38.00/hr.

Responsibilities

Provide technical support for critical large projects
Support clinical and commercial programs and locations
Perform method transfer and validation
Conduct statistical analysis and documentation
Author protocols and reports according to regulatory guidelines

Requirements

Bachelor's degree in Biochemistry, Analytical Chemistry, Physical or Life Sciences
Master’s degree and 2 years of Operations or Scientific experience OR Bachelor’s degree and 4 years of Operations or Scientific experience
Nice to have: Direct experience with method transfer and validation processes from a Pharmaceutical or Biotechnology Company
Nice to have: Knowledge of analytical methods used in biologic and synthetic development and manufacturing
Nice to have: Excellent written and oral communication

Skills

Analytical method validation Method transfer Chromatography

Senior Scientist II – Analytical Chemistry

Pharmaron · Posted Nov 4, 2026

Open

Coventry, Rhode Island, United States
Senior
$90K–$130K per year
1–10 years

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Senior Scientist II – Analytical Chemistry

Compensation

Salary Range: $90k - $130k

Responsibilities

Support analytical method validation, verification, and transfer activities within the QC laboratory.
Troubleshoot complex analytical challenges related to API characterization and GMP testing.
Review analytical data, laboratory notebooks, and instrument qualification documentation to ensure scientific accuracy and regulatory compliance.
Lead or support laboratory investigations, deviations, and root cause analyses.
Maintain laboratory equipment and serve as system owner for analytical instrumentation, including qualification and maintenance activities.

Requirements

Ph.D. in Chemistry
MS in Chemistry
BS in Chemistry
Nice to have: mentoring
Nice to have: supervising laboratory personnel

Skills

HPLC UPLC GC FTIR UV

Sr. Specialist - Quality Control

Julphar · Posted Nov 4, 2026

Open

Ras Al Khaima, United Arab Emirates
Full-time · Senior
5+ years

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Oversee and coordinate Quality Control laboratory operations, ensuring accurate, timely, and compliant testing of finished products and stability samples in accordance with approved specifications, analytical methods, GMP, GLP, pharmacopoeial standards, and regulatory requirements.

Responsibilities

Supervise and coordinate chemical and physical analysis of finished products and stability samples
Allocate testing activities to analysts and monitor workload
Ensure finished products comply with approved specifications and regulatory requirements
Oversee operation, maintenance, calibration, and performance monitoring of QC laboratory instruments
Develop and implement analytical methods

Requirements

Bachelor’s or Master’s degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a relevant scientific discipline

Skills

GMP GLP GDP pharmacopoeial standards HPLC GC chromatographic techniques

Global QC Product Lead

AbbVie · Posted Nov 4, 2026

Open

North Chicago, Illinois, United States
Full-time · Senior
8+ years

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The Global QC Product Lead provides strategic Quality leadership and governance for the implementation and lifecycle management of commercial analytical methods across AbbVie’s global QC network, integrating scientific, Quality, operational, and product considerations.

Responsibilities

Lead the global QC analytical implementation and lifecycle strategy for assigned late-stage and commercial products.
Represent Global QC as a key Quality and scientific decision-maker in cross-functional product, CMC, analytical, validation, and transfer discussions.
Translate development analytical strategies into robust, compliant, and sustainable approaches for routine QC execution.
Provide strategic QC input from late-stage development through validation, co-validation, transfer, commercialization, troubleshooting, and ongoing lifecycle management.
Independently review, challenge, and approve proposed validation, co-validation, and analytical method transfer strategies from a QC implementation perspective.

Requirements

Bachelor’s degree
Master’s degree
PhD
Nice to have: analytical development
Nice to have: commercial QC environments

Skills

analytical chemistry biochemistry biological sciences

Manager, Microbiology (CVRM)

Manager, Microbiology (CVRM)

Compensation

Responsibilities

Requirements

Skills

Manager, Microbiology (CVRM)

Compensation

Responsibilities

Requirements

Skills

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Responsibilities

Requirements

Skills

Químico Analista de Soporte Analítico (Posicion Temporal - 12 meses)

Responsibilities

Requirements

Skills

Scientist

Compensation

Responsibilities

Requirements

Skills

Senior Scientist II – Analytical Chemistry

Compensation

Responsibilities

Requirements

Skills

Sr. Specialist - Quality Control

Responsibilities

Requirements

Skills

Global QC Product Lead

Responsibilities

Requirements

Skills

Benefits

Benefits

Benefits