Upstream Bioprocessing Specialist (Night Shift)

public.client.lonza.display.name

Portsmouth (NH)

On-site

USD 65,000 - 90,000

Full time

14 days+

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Benefits offered by this job

Career development

Medical insurance

Dental insurance

Vision insurance

Team culture

Performance recognition

Job summary

Lonza is seeking a Manufacturing Associate III at our Portsmouth, NH site to support upstream bioprocessing of therapeutic proteins. You will operate manufacturing equipment, follow SOPs, and ensure cGMP and GDP compliance in a hands-on, on-site role.

The position features a 12-hour night shift (7:00 PM–7:00 AM) on a rotating schedule, opportunities to contribute to continuous improvement, and a collaborative, safety‑driven team culture with growth potential.

Qualifications

3+ years of upstream bioprocessing experience.
Experience in GMP manufacturing or a regulated biopharmaceutical environment.
Strong understanding of cGMP, documentation practices, and process flow.
Ability to troubleshoot equipment and support investigations.
Strong communication skills, including technical writing.
Attention to detail with strong problem-solving and decision-making skills.
High school diploma or equivalent; Associate’s or Bachelor’s degree in a science-related field preferred.

Responsibilities

Set up, operate, and monitor manufacturing equipment, including CIP and SIP processes.
Execute production processes following SOPs, cGMP, and GDP requirements.
Perform advanced laboratory tasks such as sampling, pH, and conductivity testing.
Troubleshoot routine and non-routine equipment and process issues.
Review batch records, logbooks, and support deviation initiation.
Train and support other associates on manufacturing tasks and process knowledge.
Perform material movements and maintain equipment through cleaning and sanitization.