Mid Level Analytical Technician Jobs
Mid level analytical technician jobs go to professionals ready to own test protocols end to end, interpret results with minimal oversight, and guide junior technicians through complex procedures. Openings run across Biotechnology & Pharmaceuticals, Chemicals & Materials, and Medical Devices, with employers like Amneal Pharmaceuticals, Eurofins, and dsm-firmenich hiring at this level now.
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Open roles23
Top stateNew Jersey
Top employerAmneal Pharmaceuticals
Top cityBranchburg, NJ
Work type83% On-site
Top industryBiotechnology
Showing 5 of 23+ Mid Level Analytical Technician jobs
Scientist III, Analytical Development (Contract to Hire 6-9 Months)
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Added 2d ago
MannKind Corporation
Scientist III, Analytical Development (Contract to Hire 6-9 Months)
Danbury, Connecticut
Added 2d ago
mRNA Analytical Development Senior Scientist
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Added 1w ago
Sanofi
mRNA Analytical Development Senior Scientist
Waltham, Massachusetts
Added 1w ago
Senior Scientist I, Analytical Sciences
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Added 1mo ago
Sail Biomedicines
Senior Scientist I, Analytical Sciences
Cambridge, Massachusetts
Added 1mo ago
QC Analytical Chemist - 6am-6pm
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Added 1mo ago
Eurofins
QC Analytical Chemist - 6am-6pm
Albany, New York
Added 1mo ago
QC Analytical Chemist - 6pm-6am
We won't show you this job again
Added 1mo ago
Eurofins
QC Analytical Chemist - 6pm-6am
Albany, New York
Added 1mo ago
Added 2d ago
Scientist III, Analytical Development (Contract to Hire 6-9 Months)
MannKind Corporation·Danbury, Connecticut
Job functions:
$40 - $60/hr
3+ yrs exp.
Bachelor of Science
Contract
201-500 employees
Job Description
MannKind
MannKind Corporation (Nasdaq: MNKD) is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient-centric solutions. Focused on cardiometabolic and orphan lung diseases, we develop and commercialize treatments that address serious unmet medical needs, including diabetes, pulmonary hypertension, and fluid overload in heart failure and chronic kidney disease. With deep expertise in drug-device combinations, MannKind aims to deliver therapies designed to fit seamlessly into daily life.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Summary
The Scientist III Validation is responsible for execution of analytical method validation, verification, and lifecycle activities to support clinical and early commercial programs. This role focuses on hands-on validation work, protocol execution, data analysis, and documentation, ensuring methods are fit-for-purpose and compliant with global regulatory expectations (ICH Q2(R2), ICH Q14, USP <1220>, FDA/EMA guidance).
Scientist III works under minimum supervision, contributes to cross-functional projects, and supports regulatory submissions.
Key Responsibilities
- Analytical Method Development: Independently develop and optimize analytical methods for assigned drug substances and products using techniques such as HPLC, LC-MS, GC, UV, and dissolution. Make sound technical decisions on method design and execution within the scope of the assigned work.
- Method Validation & Transfer: Execute phase-appropriate validation and method transfer activities, including protocol execution, data generation, and report contribution, under the guidance of senior staff who define the overall validation strategy.
- Data Generation & Interpretation: Execute experiments, analyze data, and draw conclusions to support formulation development, stability studies, and clinical release testing.
- Documentation: Draft analytical protocols, method development reports, and contribute to regulatory documentation (e.g., IND sections).
- Cross-Functional Support: Collaborate with Formulation, Process Development, and Quality teams to ensure alignment of analytical activities with program needs.
- Compliance & Data Integrity: Ensure all work is conducted in accordance with GLP/GMP standards and internal quality systems. Maintain accurate and complete laboratory records.
- Problem Solving: Troubleshoot analytical methods and instrumentation issues with increasing independence.
- Mentorship & Training: Provide informal mentorship to junior scientists and analysts. Assist in onboarding and training activities.
- Continuous Improvement: Identify opportunities to improve workflows, documentation practices, or analytical robustness. Drive implementation of improvements within the scope of assigned work, with senior support on broader changes.
- Scientific Communication: Present experimental results and recommendations in team meetings and contribute to technical discussions.
Required Qualifications
- Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field with 1–3 years of experience, or M.S. with 3–5 years, or B.S. with 4–6 years of relevant experience.
- Hands-on experience with analytical instrumentation and method development.
- Familiarity with ICH guidelines, GMP/GLP, and regulatory expectations.
- Strong organizational, documentation, and communication skills.
Preferred Qualifications
- Experience supporting clinical-stage pharmaceutical development.
- Exposure to regulatory submissions and method validation.
- Experience working with CROs or CDMOs.
- Familiarity with LIMS or electronic lab notebooks.
Core Competencies (Aligned to Company Values)
- Do Right: Follows SOPs and quality standards; ensures data integrity and compliance.
- Win Together: Collaborates effectively with team members and cross-functional partners.
- Own It: Takes ownership of assigned analytical work end to end, including planning, execution, documentation, and follow-through.
- Be Tenacious: Independently resolves routine technical challenges and pursues continuous improvement in assigned areas.
- Push Boundaries: Suggests improvements to methods, workflows, or technologies.
MannKind Corporation
Scientist III, Analytical Development (Contract to Hire 6-9 Months)
Danbury, Connecticut
Added 2d ago201-500 employees
Job functions:
$40 - $60/hr
3+ yrs exp.
Bachelor of Science
Contract
Job Description
MannKind
MannKind Corporation (Nasdaq: MNKD) is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient-centric solutions. Focused on cardiometabolic and orphan lung diseases, we develop and commercialize treatments that address serious unmet medical needs, including diabetes, pulmonary hypertension, and fluid overload in heart failure and chronic kidney disease. With deep expertise in drug-device combinations, MannKind aims to deliver therapies designed to fit seamlessly into daily life.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Summary
The Scientist III Validation is responsible for execution of analytical method validation, verification, and lifecycle activities to support clinical and early commercial programs. This role focuses on hands-on validation work, protocol execution, data analysis, and documentation, ensuring methods are fit-for-purpose and compliant with global regulatory expectations (ICH Q2(R2), ICH Q14, USP <1220>, FDA/EMA guidance).
Scientist III works under minimum supervision, contributes to cross-functional projects, and supports regulatory submissions.
Key Responsibilities
- Analytical Method Development: Independently develop and optimize analytical methods for assigned drug substances and products using techniques such as HPLC, LC-MS, GC, UV, and dissolution. Make sound technical decisions on method design and execution within the scope of the assigned work.
- Method Validation & Transfer: Execute phase-appropriate validation and method transfer activities, including protocol execution, data generation, and report contribution, under the guidance of senior staff who define the overall validation strategy.
- Data Generation & Interpretation: Execute experiments, analyze data, and draw conclusions to support formulation development, stability studies, and clinical release testing.
- Documentation: Draft analytical protocols, method development reports, and contribute to regulatory documentation (e.g., IND sections).
- Cross-Functional Support: Collaborate with Formulation, Process Development, and Quality teams to ensure alignment of analytical activities with program needs.
- Compliance & Data Integrity: Ensure all work is conducted in accordance with GLP/GMP standards and internal quality systems. Maintain accurate and complete laboratory records.
- Problem Solving: Troubleshoot analytical methods and instrumentation issues with increasing independence.
- Mentorship & Training: Provide informal mentorship to junior scientists and analysts. Assist in onboarding and training activities.
- Continuous Improvement: Identify opportunities to improve workflows, documentation practices, or analytical robustness. Drive implementation of improvements within the scope of assigned work, with senior support on broader changes.
- Scientific Communication: Present experimental results and recommendations in team meetings and contribute to technical discussions.
Required Qualifications
- Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field with 1–3 years of experience, or M.S. with 3–5 years, or B.S. with 4–6 years of relevant experience.
- Hands-on experience with analytical instrumentation and method development.
- Familiarity with ICH guidelines, GMP/GLP, and regulatory expectations.
- Strong organizational, documentation, and communication skills.
Preferred Qualifications
- Experience supporting clinical-stage pharmaceutical development.
- Exposure to regulatory submissions and method validation.
- Experience working with CROs or CDMOs.
- Familiarity with LIMS or electronic lab notebooks.
Core Competencies (Aligned to Company Values)
- Do Right: Follows SOPs and quality standards; ensures data integrity and compliance.
- Win Together: Collaborates effectively with team members and cross-functional partners.
- Own It: Takes ownership of assigned analytical work end to end, including planning, execution, documentation, and follow-through.
- Be Tenacious: Independently resolves routine technical challenges and pursues continuous improvement in assigned areas.
- Push Boundaries: Suggests improvements to methods, workflows, or technologies.
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Find JobsMid Level Analytical Technician Job Market
Who's Hiring
Top Industries Hiring
- Biotechnology & Pharmaceuticals12
- Chemicals & Materials3
- Medical Devices2
- Science & Research2
- Education1
Mid Level Analytical Technician Jobs: Frequently Asked Questions
How do I get a mid level analytical technician job?
Position yourself by leading with specific techniques you have mastered, instruments you have operated independently, and projects where your data drove a decision. Tailor your resume to show ownership, not just task completion. Highlight cross-functional collaboration, any method development or validation work, and moments where you caught an issue before it became a problem. Applications that show depth in a core discipline consistently outperform generic ones.
Which companies hire mid level analytical technicians?
Companies hiring mid level analytical technicians right now include Amneal Pharmaceuticals, Eurofins, and dsm-firmenich, based on current listings on Migrate Mate as of November 2026. Hiring at this level tends to come from pharmaceutical manufacturers, contract testing labs, chemical producers, and food and beverage companies that need technicians who can run with minimal supervision.
Are there remote mid level analytical technician jobs?
Yes, though the role is largely lab-based, so fully remote positions are rare. About 17% of mid level analytical technician openings are remote or hybrid as of November 2026, and those tend to involve data review, reporting, or quality systems work rather than hands-on instrument operation. Most openings require at least some on-site presence tied to equipment and samples.
How do I move up to a mid level analytical technician role?
Moving from entry level to mid level takes deliberate depth-building over your first few years. Focus on mastering two or three core techniques rather than spreading across many, take on project ownership whenever offered, and document your contributions with measurable outcomes. Demonstrating that you can troubleshoot independently, write or revise SOPs, and mentor newer colleagues signals readiness for mid level responsibility to most hiring managers.
Which industries hire the most mid level analytical technicians?
Mid Level analytical technician roles concentrate in Biotechnology & Pharmaceuticals, Chemicals & Materials, and Medical Devices, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because they require consistent, validated testing at scale and depend on experienced technicians to maintain data integrity and regulatory compliance across ongoing production or research workflows.