Sr. Scientist I - Analytical Testing , HPLC

Alcami Corporation; Morrisville (NC); On-site; USD 90,000 - 120,000; Full time

Job summary

Alcami Corporation is seeking a Senior Scientist I to perform analytical routine and non-routine testing in support of pharmaceutical product development or manufacturing. Methods include HPLC, dissolution, and GC, with others like titrations, UV, AA, and IR, following USP/EP or client-developed procedures.

This on-site 1st shift role emphasizes cGMP compliance, data evaluation, writing procedures and reports, and safe handling of hazardous materials; knowledge of Empower, ELN, and lab software

Qualifications

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

Responsibilities

• Develops analytical methodology for analysis via HPLC, TOC, UV, and/or particle size.
• Performs GMP review of solutions and wet chemical analyses and chromatography.
• Performs one or more techniques: residual solvents, assays, dissolution, impurities, moisture, identification.
• Evaluates and interprets generated data.
• Writes test procedures, protocols, and reports.
• Maintains knowledge of instrumentation and safety; handles hazardous waste per regulations.

Skills

HPLC

Communication

Detail-oriented

Problem-solving

Safety knowledge

Lab documentation

Method development

Multitask planning

cGMP knowledge

MS Office

Empower/ELN

Education

Bachelor’s degree in Chemistry

Master’s degree

Ph.D.

Tools

Empower3

ProCal

Master Control

ELN

Job description

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, 8:00am - 5:00pm.

Responsibilities

• Develops analytical methodology for analysis via HPLC, TOC, UV, and/or particle size.
• Performs GMP review of solutions and wet chemical analyses and chromatography.
• Performs one or more of the following techniques: residual solvents, assays (potencies, related substances), dissolution, elemental impurities, moisture content, identification, and various other wet chemistry-based measurements.
• Evaluates and interprets generated data.
• Analyzes information for technical correctness and accuracy.
• Understands the theoretical basis of methods/experiments.
• Solves problems of diverse scope in which analysis of data requires evaluation of identifiable factors.
• Writes test procedures, protocols, and reports.
• Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
• Assists in removal of hazardous waste, routine equipment cleaning, and restocking of consumable products and reagents.
• Effectively uses various laboratory software packages (Empower3, ProCal, Master Control, ELN, etc.).
• Maintains a safe, clean, and organized work environment free of safety hazards.
• Safely handles potent compounds.
• This position will be required to supervise, handle, or process hazardous waste under Resource and Conservation guidelines promulgated under 40 CFR 262.177(a)(7), Personnel Training. This includes completion of initial and annual RCRA training and documented as required in Alcami records. This training also includes familiarity with emergency response procedures, emergency equipment, and emergency systems.
• 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

• Hands-on HPLC required.
• 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.
• Empower and ELN experience a plus.

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.