Top 11 Senior analytical chemist Jobs in Durham, Nc

Chemist III/Sr. Chemist Raw Materials
MedPharm —Durham, NC
- Full-time
- 5 years
- Bachelor of Science
- Data analysis skills
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5d
Senior Chemist
Air Clean Systems —Creedmoor, NC
- Full-time
- 5 years
- Bachelor of Science
- Office
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Sr. Manager, CMC Analytical Development
Asahi Kasei —Cary, NC
- $150,000 - $160,000 a year
- Full-time
- Hybrid work
- Microsoft Outlook
- Management
- Bachelor of Science
- Health insurance
Analyst II/Senior Analyst, Quality Control
Kriya Therapeutics —Research Triangle Park, NC
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Paid parental leave
- Paid holidays
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12d
Senior QC Analyst (2nd Shift) – In-Process
KBI Biopharma —Durham, NC
- $63,000 - $86,900 a year
- Full-time
- Mid-level
- Presentation skills
- Military encouraged
Senior Analyst 1, QC Chemistry
FUJIFILM —Holly Springs, NC
- Call employer
- Mid-level
- Ability to sit for extended periods
- 1 year
TALENT PIPELINE - Sr. Scientist I (ARD)
Cambrex Corp. —Durham, NC
- Microsoft Word
- Microsoft Excel
- Computer literacy
- Health insurance
- Life insurance
Senior Specialist 2, Quality Control Instrumentation
FUJIFILM —Holly Springs, NC
- Weekends as needed
- Doctor of Philosophy
- 1 year
- Senior level
Sr. Scientist II - Compendial Testing - 2nd Shift
Alcami Corporation —Morrisville, NC
- Full-time
- Microsoft Excel
- Master's degree
- Ability to lift 50 pounds

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senior analytical chemist jobs near durham, nc

Chemist III/Sr. Chemist Raw Materials

MedPharm -
Durham, NC

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Job Details

Full-time
5 days ago

Qualifications

Bachelor's degree
Materials analysis (analytical chemistry specialty)
Stakeholder relationship building

Full Job Description

Position Summary – The Chemist III/Sr. Chemist Raw Materials ensures that testing, data review, and documentation is compliant with GMP regulations, internal procedures, and applicable compendial requirements. The position will be operating within a GMP environment for a Quality Control CDMO. The ideal candidate will additionally possess superior communication skills, presenting to internal and external clients

Essential Functions

Schedule the QC laboratory Raw Materials workload appropriately to meet manufacturing release testing schedules, stability pull dates and timelines.
Monitor weekly laboratory and data review activities for accuracy and track hours needed for completion of tasks.
Oversight for review of QC and Raw Material data for compliance with specifications and regulatory requirements
Interact with third party laboratories for microbial and analytical testing of raw materials
Generate and/or review shipping paperwork for third part testing and prepare samples for shipment.
Create purchase requisitions for lab supplies and third-party testing
Perform weekly laboratory audit inspections
Perform sampling of raw materials as needed
Review third party laboratory investigations and protocols.
Execute intermediate to advanced chemical and instrumental testing of raw materials using HPLC, GC, FTIR, UV-Vis, Karl Fischer titration, and wet chemistry.
Ensure all testing meets compendial standards (USP/EP/JP) and regulatory expectations. Conduct peer reviews of data, Certificates of Analysis (COAs), and laboratory logbooks.
Author and review GMP documentation including Standard Operating Procedures (SOPs), protocols, deviations, Corrective and Preventive Actions (CAPAs), and change controls.
Provide technical guidance to junior analysts. Lead method verification, validation, and method transfer activities for incoming raw materials.
Oversee the calibration, maintenance, and troubleshooting of laboratory equipment.
Other duties as assigned

Supervisory responsibilities

Direct Reports: No
Indirect Reports: None

Key Relationships

Manufacturing Operations
Quality Assurance
Analytical R&D
Program Management

Travel requirements:

None

Education and Experience

Minimum BA or BS in a scientific discipline required
Minimum 5-8 years of Analytical chemistry experience with a cGMP/GLP environment, preferably at a CDMO or pharmaceutical company.

Knowledge, Skills, and Abilities

Knowledge of cGMPs
Good communication, organization and computer skills are required.
Knowledge of Empower required; LIMS and Microsoft Office programs knowledge is desired.
Ability and willingness to work additional hours as required by business need
At least 5 years’ experience in a CRO environment
Experience with USP, EP and JP monographs.
Experience with laboratory equipment such as HPLC (UV, Ion detectors, RI detectors), GC (Headspace, FID, TCD), FTIR, Auto Titrators, Karl Fischer Titrators (Volumetric and Coulometric), and Particle size.
Excellent interpersonal skills and ability to establish and maintain effective working relationships with both internal and external stakeholders
Excellent verbal and written communication skills
Ability to work with minimal supervision
Experience in Data Review of Analytical data per GDP guidelines.
Proven ability to review and evaluate the compliance and completeness of analytical data.
Able to multi-task productively, applying time management processes and procedures effectively.
Works toward common goals by supporting, encouraging, and sharing information with colleagues.
Strong analytical skills and ability to understand business and financial implications of contracts
Self-directed

Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.

Requires frequent sitting and walking
Requires carrying under 20 LBS, occasionally 20 – 60 LBS
Requires pushing, & pulling under 20 LBS, occasionally 20-60 LBS
Requires occasional bending, twisting, reaching, & gripping
Requires constant seeing & hearing

Other Duties

You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.

Limitations and Disclaimer

The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.

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Refine Your Search

senior analytical chemist jobs in durham, nc

Chemist III/Sr. Chemist Raw Materials

Senior Chemist

Sr. Manager, CMC Analytical Development

Analyst II/Senior Analyst, Quality Control

Senior QC Analyst (2nd Shift) – In-Process

Senior Analyst 1, QC Chemistry

TALENT PIPELINE - Sr. Scientist I (ARD)

Senior Specialist 2, Quality Control Instrumentation

Sr. Scientist II - Compendial Testing - 2nd Shift

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