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Test Method Validation (TMV) jobs

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Test Method Validation (TMV)

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Skill:Test Method Validation (TMV)

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1–4 jobs· newest first

Quality Assurance Specialist with focus on Production supportNew
Getinge · Solna, Sweden
On-site
R&D Engineer
LanceSoft Inc · Plymouth, US
Senior
R&D Engineer
LanceSoft Inc · Minnetonka, US
Contract · Entry
Supervisor, QC (Chemistry) Method Transfer
Cardinal Health · Indianapolis, US
$82K–$117K

+10K new in the last hour

Quality Assurance Specialist with focus on Production support

Getinge · Posted Nov 12, 2026

Solna, Stockholm County, Sweden
On-site
3–5 years

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Support manufacturing quality processes, perform audits, manage CAPA, and validate software applications used in manufacturing and quality management.

Compensation

We offer a competitive compensation and benefits package, including wellness allowances, generous family benefits and joint company activities.

Responsibilities

Act as independent reviewer of production process changes, including process validation and production process risk assessments
Support non-conformance handling in manufacturing and coordinate product holds for high-risk non-conforming products
Support the organization on quality issues and improve procedures in the management system, specifically for manufacturing controls
Support implementation, validation and management of software applications used in manufacturing and within the quality management system
Perform internal audits and track non-conformances to closure, and support preparation of external audits and the CAPA process

Requirements

M.Sc. or B.Sc. in science or engineering

Skills

quality and compliance manufacturing of medical devices ISO 13485 MDSAP QMSR ISO 14001 Swedish English cross-functional communication test method validation computerized system validation software applications used in manufacturing and quality management system

Benefits

wellness allowances
generous family benefits
joint company activities

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L

R&D Engineer

LanceSoft Inc · Posted Nov 10, 2026

Plymouth, Minnesota, United States
Senior
4–10 years

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Senior R&D Engineer to lead integration of acquisition into PLM and quality systems for medical device products.

Responsibilities

Review and transfer specifications into PLM system
Update design inputs and outputs
Transfer and validate test methods
Support verification and validation protocols
Collaborate with Quality, Manufacturing, and Regulatory teams

Requirements

Bachelor’s degree in Mechanical, Biomedical, Electrical, or related field
Master’s degree in Mechanical, Biomedical, Electrical, or related field

Skills

test method validation equipment qualification medical device design controls PDP processes regulatory requirements verification and validation testing statistical methods and tools

L

R&D Engineer

LanceSoft Inc · Posted Nov 9, 2026

Minnetonka, Minnesota, United States
Contract · Entry
1–3 years

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Responsibilities

Author and execute Process Validations including Test Method Validation (TMV), Inspection Method Validation (IMV), Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), Product Performance Qualification (PPQ)
Responsible for process development, equipment specification, acquisition and implementation
Analyzes and solves problems from basic engineering principles
Completes design of experiments, validation, completion of testing and analysis of data for continuous improvement activities
Suggests and supports new methods or materials for continual improvement of quality and efficiency

Requirements

Bachelor's degree

Skills

Process Validation Test Method Validation (TMV)Inspection Method Validation (IMV)Installation Qualification (IQ)Operational Qualification (OQ)

Supervisor, QC (Chemistry) Method Transfer

Cardinal Health · Posted Nov 9, 2026

Indianapolis, Indiana, United States
$82K–$117K per year
5+ years

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Supervisor, Quality Control (Chemistry) overseeing method transfer and quality processes at Cardinal Health.

Compensation

Anticipated salary range: $82,100.00-$117,200.00

Responsibilities

Coordinates and supervises the daily activities of Chemists or business support staff in the performance of technology transfer, method validation/verification and method optimization
Serves as the liaison between Cardinal Health Quality Control and Client Quality Control in the performance of technology transfer, method validation/verification/development/optimization
Is a quality lead for the QC Chemistry team
Identifies quality events and works with QA/QC management to ensure each event is handled in accordance with site procedures and regulatory requirements
Oversees chemists and contractors who operate analytical equipment, perform analytical tests, interpret results and documents findings in accordance with SOPs and regulatory requirements

Requirements

Bachelor’s degree in chemistry or related science field
Nice to have: experience in radiochemistry
Nice to have: nuclear pharmacy
Nice to have: health physics

Skills

experience with equipment qualification

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Performance Qualification (PQ)

Product Performance Qualification (PPQ)

Design of Experiments

Standard Operating Procedures (SOPs)

Risk Assessment

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software validation

test method validation

process validation

Change Controls

Deviations (Nonconformance)

Laboratory Investigations

Microsoft Excel

technical writing

Benefits

Medical coverage
Dental coverage
Vision coverage
Paid time off plan
Health savings account (HSA)

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