Onsite Manufacturing Process Support Associate

Initial Therapeutics, Inc.; West Lebanon (NH); On-site; USD 65,000 - 88,000; Full time

Benefits offered by this job

Competitive pay

Performance bonus

Paid time off

401K with match

Parental leave

Product access

Job summary

Novo Nordisk is seeking an on-site Process Support role in West Lebanon, NH to back manufacturing operations across training, documentation, deviations, change control and projects. You will coordinate improvements, review quality records, and train technicians to run processes per cGMP at our bioproduction site.

The position is Monday–Friday onsite in West Lebanon, NH, with cross-functional collaboration and a strong focus on quality systems and regulatory compliance.

Qualifications

• High School diploma or equivalent with six (6) years relevant manufacturing experience.
• Bachelor's degree or equivalent with two (2) years of experience preferred.
• Pharmaceutical or biotechnology experience strongly preferred.
• Knowledge and understanding of cGMPs and quality regulations.

Responsibilities

• Liaison between Production Support and Manufacturing for process/equipment improvements and data trending/analysis.
• Review and approval of completed process documentation.
• Ability to train others on the manufacturing process and QMS systems.
• Revise and create documentation (SOP, batch records, FT's) for manufacturing.
• Investigate Deviation events using Root Cause Analysis.
• Support on-floor manufacturing and training to run according to cGMP.

Skills

Excellent communication skills

Analytical abilities

Problem-solving

Attention to detail

Lean manufacturing principles

Education

High School diploma or equivalent

Bachelor's degree in science or engineering

Job description

Novo Nordisk is seeking an on-site Process Support role in West Lebanon, NH to back manufacturing operations across training, documentation, deviations, change control and projects. You will coordinate improvements, review quality records, and train technicians to run processes per cGMP at our bioproduction site.

The position is Monday–Friday onsite in West Lebanon, NH, with cross-functional collaboration and a strong focus on quality systems and regulatory compliance.