QC Investigations Lead – Analytical Chemistry

PCI Pharma Services; Bedford (NH); On-site; USD 60,000 - 80,000; Full time

Benefits offered by this job

Professional growth opportunities

Exposure to diverse analytical techniques

Collaboration with a talented team

Job summary

A global pharmaceutical firm in Bedford, New Hampshire is seeking a QC Specialist to lead investigations and manage quality control processes. The ideal candidate should have a Bachelor's degree in Analytical Chemistry and 2–5 years of experience in QC Analytical Chemistry, preferably in pharma. Strong organizational and technical skills are necessary, along with experience in lab technologies and guidelines. This position offers opportunities for professional growth and collaboration in a GMP environment.

Qualifications

• 2–5 years of QC Analytical Chemistry experience in pharmaceuticals preferred.
• Solid understanding of cGMP, ICH, USP guidelines.
• Ability to thrive in a fast-paced environment.

Responsibilities

• Lead investigations into quality control deviations.
• Draft and revise technical reports and cGMP documents.
• Perform analytical testing and identify trends.

Skills

Analytical Chemistry expertise

Organizational skills

Communication skills

Technical writing

Education

Bachelor’s degree in Analytical Chemistry or related field

Tools

UPLC

HPLC

GC

FTIR

UV/VIS

Karl Fisher

Particle Size Analyzer

Densitometer

Osmometer

Job description

A global pharmaceutical firm in Bedford, New Hampshire is seeking a QC Specialist to lead investigations and manage quality control processes. The ideal candidate should have a Bachelor's degree in Analytical Chemistry and 2–5 years of experience in QC Analytical Chemistry, preferably in pharma. Strong organizational and technical skills are necessary, along with experience in lab technologies and guidelines. This position offers opportunities for professional growth and collaboration in a GMP environment.