QC Analyst II/III (Biotech Manufacturing) Night Shift

Scismic; Portsmouth (NH); On-site; USD 60,000 - 85,000; Full time

Job summary

A leading biotech company is seeking a QC Analyst II/III for the Night Shift to support production and quality testing. The role involves running tests, reviewing assays, and mentoring team members, requiring a degree in a related science and relevant industry experience. This full-time position offers a dynamic work environment and opportunities for professional growth.

Qualifications

• 2-5+ years industry experience, preferably in a cGMP environment.
• Proficiency with Microsoft Office Suite and laboratory systems.
• Ability to make quality decisions independently and mentor others.

Responsibilities

• Running test samples for In-Process, Lot Release, and Stability studies.
• Writing Quality Records (Deviations, CAPA, Change Control) and Test Methods.
• Managing projects such as method transfers and new instruments.

Skills

Data interpretation

Public speaking

Problem-solving

Communication

Education

Bachelor’s or Associate’s Degree in Microbiology, Biochemistry, or related sciences

Tools

Microsoft Office Suite

Laboratory computer systems

GMP Quality Systems (TrackWise, LIMS)

Job description

QC Analyst II/III (Biotech Manufacturing) Night Shift

Join to apply for the QC Analyst II/III (Biotech Manufacturing) Night Shift role at Scismic.

Scismic supports the growth of a global leader in life sciences and one of the largest healthcare manufacturing organizations worldwide.

We are seeking a Quality Control (QC) Analyst II/III (Night Shift) to join our Quality Control department, supporting production of in-process and final drug lots, and participating in quality testing for customer stability studies. Provide timely, high-quality results to meet manufacturing demands.

Role Overview

A QC Analyst III applies skills and company policies to complete tasks, working on semi-routine assignments where deviation recognition is required. Handles moderate scope problems, analyzing situations or data by reviewing identifiable factors.

Work Schedule

10 Hour Night Shifts:

• Sunday - Wednesday: 8:00 pm to 6:30 am
• Wednesday - Saturday: 8:00 pm to 6:30 am

Key Responsibilities

• Running test samples for In-Process, Lot Release, and Stability studies
• Reviewing assays
• Training team members
• Writing Quality Records (Deviations, CAPA, Change Control) and Test Methods
• Managing projects such as method transfers, new instruments, and method qualifications
• Performing other duties as assigned

Minimum Requirements

• Bachelor’s or Associate’s Degree in Microbiology, Biochemistry, or related sciences
• 2-5+ years industry experience, preferably in a cGMP environment
• Proficiency with Microsoft Office Suite
• Experience with Laboratory computer systems and GMP Quality Systems like TrackWise, LIMS
• Strong data interpretation and public speaking skills
• Ability to make quality decisions independently and mentor others
• Effective prioritization, problem-solving, and communication skills
• Professionalism, punctuality, and team collaboration

Additional Details

• Seniority Level: Associate
• Employment Type: Full-time
• Job Function: Research
• Industries: Biotechnology Research and Pharmaceutical Manufacturing