Associate Scientist

Alcami Corporation; Wilmington (NC, DE); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated Associate Scientist to join its dynamic team. This role focuses on analytical testing to support pharmaceutical product development and manufacturing. The ideal candidate will thrive in a fast-paced environment, utilizing techniques such as HPLC and UV-Vis spectroscopy. With a commitment to quality and safety, you'll ensure compliance with GMP standards while contributing to innovative projects that unlock the potential of transformative medicines. If you're passionate about science and eager to make a difference, this opportunity is perfect for you.

Qualifications

• Bachelor's degree in Chemistry or related field is required.
• 0 - 4+ years of related work experience preferred.

Responsibilities

• Performs various analytical techniques including assays and elemental impurities.
• Maintains knowledge of instrumentation and scientific methodologies.

Skills

Verbal Communication

Written Communication

Detail Orientation

Problem Solving

Organizational Skills

Education

Bachelor's degree in Chemistry

Related Field Degree

Tools

HPLC

GC

UV-Vis Spectroscopy

FTIR

Titration

Job description

Associate Scientist

Location

US-NC-Wilmington

ID

2025-1323

Category

Development Services

Position Type

Full-Time

Working Hours

1st Shift: Monday - Friday, 8:30am - 5:30pm

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

The Associate Scientist is accountable for driving results in a fast-paced environment by performing analytical routine and non-routine testing in support of pharmaceutical product development or pharmaceutical manufacturing. The Associate Scientist may also assist with method development/method validation projects. For this position, UV-Vis, FTIR, HPLC, GC, Titration, and/or AA based methodologies are commonly employed in the described testing.

On-Site Expectations

100% on-site position.

• 1st Shift: Monday - Friday, 8:30am - 5:30pm.

Responsibilities

• Performs one or more of the following techniques: residual solvents, assays (potencies, related substances), dissolution, elemental impurities, moisture content, identification, and other various analytical techniques.
• Maintains working knowledge of routine instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
• Performs assigned tasks carefully and on schedule according to standard operating procedure and supervisor instructions.
• Analyzes information for technical correctness and accuracy.
• Complies with applicable GMPs, peer checks information and signs for GMP review. Brings aberrant information to the attention of supervisor.
• Maintains a safe, clean, and organized work environment free of safety hazards.
• Suggests improvements for safety, work quality, and productivity.
• Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
• Seeks to cultivate mentorship, build leadership skills, and foster a culture of 'team first'.
• Other duties as assigned.

Qualifications

• Bachelor's degree in chemistry or a related field.
• 0 - 4+ years of related work experience.
• Prior laboratory experience or work experience in Pharmaceutical, CDMO, or cGMP 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.
• Basic knowledge of Laboratory equipment and safety required.
• Basic knowledge of Laboratory Documentation is required.
• Working knowledge of cGMP in a pharmaceutical or regulated environment preferred.
• Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
• Applies job skills, company policies and SOPs to complete a variety of tasks.
• Receives general instructions on routine work, detailed instructions on new projects or assignments.

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 use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to stand. The employee is occasionally required to walk; sit 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 frequently exposed to moving mechanical parts and the risk of electrical shock, burn hazards and microbial contamination. The employee is occasionally exposed to fumes or airborne particles, toxic or caustic chemicals 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, lab coats, full protective body coverings, various types of gloves, etc.