Biotech Analytical Scientist II

Alcami-5; Durham (NC); On-site; USD 70,000 - 90,000; Full time

Job summary

Alcami in Durham, NC is seeking a Scientist II to perform analytical testing in support of pharmaceutical development and manufacturing, including method development and validation using HPLC, CE, icIEF, and UV. The role requires routine and non-routine testing, data interpretation, and documentation in GMP environments.

The position is on-site, 1st shift, with potential travel up to 5%. Candidates must maintain safety, lab accuracy, and proficiency with Empower3, ProCal, Master Control, and ELN

Qualifications

• Masters degree in Chemistry, Biochemistry, or related field with 0+ years of related work experience.
• Bachelor’s degree in Chemistry, Biochemistry, or related field with course work in Chemistry with 4+ years related work experience.
• Or Associates degrees in Chemistry or related field with 10+ years related experience.

Responsibilities

• Develops, validates and transfers analytical methodology for analysis via HPLC (SEC, AEX, CEX), UV, CE and icIEF.
• Performs GMP review of solutions and wet chemical analyses and chromatography.
• Performs analysis of large molecule and biologic samples to assess purity, potency, identity, and product quality attributes.
• Evaluates and interprets generated data.
• Writes test procedures, protocols, and reports.
• 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.

Skills

HPLC

CE

icIEF

UV

GMP compliance

Education

Master's degree in Chemistry or Biochemistry or related field

Bachelor’s degree in Chemistry or Biochemistry or related field with 4+ years related experience

Associate degree in Chemistry or related field with 10+ years related experience

Tools

Empower3

ProCal

Master Control

ELN

Job description

Alcami in Durham, NC is seeking a Scientist II to perform analytical testing in support of pharmaceutical development and manufacturing, including method development and validation using HPLC, CE, icIEF, and UV. The role requires routine and non-routine testing, data interpretation, and documentation in GMP environments.

The position is on-site, 1st shift, with potential travel up to 5%. Candidates must maintain safety, lab accuracy, and proficiency with Empower3, ProCal, Master Control, and ELN