Lynx, Phase II Manufacturing Supervisor

Lonza•Portsmouth, NH

4d•Onsite

About The Position

We are seeking a dynamic and collaborative leader to join our production team in Portsmouth, NH, as a Manufacturing Supervisor for our expanding 2K asset. This newly created position offers an exciting opportunity to build, onboard, and lead a brand-new manufacturing team from the ground up. Initially overseeing 4 direct reports during the preparatory phase, you will guide your team through the expansion, ultimately scaling to lead a team of 8–10 associates once operational water runs and routine cGMP campaigns begin.

Requirements

3–5+ years of experience in cGMP biological manufacturing (large-scale mammalian or microbial assets preferred), with previous experience in a step-up, lead, or supervisory capacity.
Proven track record of mentoring junior staff, driving accountability, and managing team dynamics, with a strong passion for developing people.
Deep familiarity with core biomanufacturing equipment, automated control systems (such as DeltaV), electronic batch records, and standard cleanroom flows.
Flexibility to manage a phased schedule transition (from Monday–Friday to rotating shift work) and navigate the shifting priorities of an active asset expansion.
High School Diploma or equivalent is required.
Strong operational alignment with EHS objectives, strict adherence to SOPs, and an uncompromising commitment to Good Documentation Practices (GDP).

Nice To Haves

An Associate’s or Bachelor’s Degree in a science or engineering discipline is preferred.

Responsibilities

Directly supervise, coach, and develop an initial team of 4 direct reports, successfully scaling the squad to 8–10 associates as the 2K asset expansion becomes fully operational.
Own the onboarding, cGMP training, and qualifications for your new team, fostering a positive, safe, and highly collaborative floor culture.
Lead the preparatory activities for the asset expansion, ensuring equipment, suite readiness, and standard operating procedures (SOPs) are aligned ahead of water runs.
Oversee the safe and compliant execution of cGMP manufacturing runs, ensuring total adherence to batch records, validation protocols, and data integrity standards.
Manage shift transitions, resource allocation, and daily manufacturing schedules to maintain seamless project continuity and asset efficiency.
Recognize, investigate, and escalate process deviations, participating in root cause analysis (RCA) and implementing corrective and preventive actions (CAPAs).
Act as the primary point of contact for your shift, collaborating closely with Quality Assurance, Engineering, Maintenance, and MSAT to achieve site production goals.