Sr. Scientist I - Analytical Testing , HPLC

Davita Inc.; Morrisville (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

A leading company in pharmaceutical services seeks a Senior Scientist I to conduct analytical testing and method development within a collaborative team. The successful candidate will utilize HPLC and other methodologies to support drug product development, ensuring compliance with regulatory standards and internal protocols.

Qualifications

• 8+ years of experience if Bachelor's; 4+ years if Master's; 2+ years if PhD.
• Experience in pharmaceuticals drug product development under cGMP required.
• CDMO experience preferred.

Responsibilities

• Performs analytical routine and non-routine testing with HPLC and related methods.
• Develops and validates methods, test procedures, protocols, and reports.
• Analyzes information for technical correctness and accuracy.

Skills

Communication

Detail orientation

Problem-solving

HPLC experience

Laboratory documentation

Education

Bachelor's degree in Chemistry

Master's degree with 4+ years experience

PhD with 2+ years experience

Job description

Sr. Scientist I - Analytical Testing , HPLC

Location

US-NC-Morrisville

ID

2025-1491

Category

Analytical

Position Type

Full-Time

Working Hours

1st Shift: Monday - Friday, 9:00am - 5:00pm

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.

Are you interested in joining our team?

Job Summary

A Senior Scientist I performs analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. HPLC, dissolution and/or GC based methodologies are commonly employed in the described testing. Other key methodologies applied include titrations, UV, AA, IR. Test methods employed may be compendial (i.e. USP, EP) or proprietary (client supplied or developed by The Company).

On-Site Expectations

100% on-site position.

• 1st Shift: Monday - Friday, 9:00am - 5:00pm.

Responsibilities

• Uses advanced skills in multiple techniques, to include assays (potencies, related substances), dissolution/drug release, residual solvents, elemental impurities, moisture content, identification, and various other wet chemistry-based measurements.
• Develops and validates methods, test procedures, protocols, and reports.
• Understands the theoretical basis of methods/experiments.
• Maintains strong knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
• Analyzes information for technical correctness and accuracy.
• Evaluates and interprets data.
• Achieves results by solving problems of a diverse scope.
• Interacts with clients and participates in regulatory agency and/or client audits.
• Leads investigations and root cause analysis.
• Drives initiatives outside of standard work function.
• Maintains a safe, clean, and organized work environment free of safety hazards.
• Safely handles potent compounds.
• Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
• Other duties as assigned.

Qualifications

• Bachelor's degree in Chemistry with 8+ years of experience, or Master's degree with 4+ years of experience, or Ph.D. with 2+ years of experience required.
• 2+ years of experience in Pharmaceuticals drug product development under cGMP is required.
• CDMO experience is preferred.

Knowledge, Skills, and Abilities

• Excellent verbal and written communication and documentation skills required.
• Excellent detail orientation and organizational skills required.
• Excellent problem-solving and basic trouble-shooting ability required.
• Excellent knowledge of laboratory equipment and safety required.
• Expert knowledge of Laboratory Documentation is required.
• Ability to develop and implement new methods/processes required.
• Ability to plan and manage multiple tasks for timely achievement of results.
• Working knowledge of cGMP in a pharmaceutical or regulated environment required.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
• Hands-on HPLC experience required.

Travel Expectations

• Up to 5% domestic travel.

Physical Demands and Work Environment

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is occasionally required to walk; sit; climb or balance and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.

While performing the duties of this job, the employee is occasionally exposed to wet and/or humid conditions; moving mechanical parts; fumes or airborne particles; toxic or caustic chemicals; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, various types of respirators/breathing apparatus, half face and full-face respirator, lab coats, full protective body coverings, various types of gloves, etc.