i-Pharm GxP
We are partnering with a well established, global life sciences organisation with a strong long term presence in North Chicago, Illinois. This site is known for its investment in people, technology, and high quality GMP manufacturing, offering contractors stable projects, clear scope, and strong extension potential.
W2 Contract | 12 Months Initial with Extension Based on Performance
Responsibilities
Support commissioning and qualification of automated GMP systems including PLC SCADA DCS and MES.
Execute FAT SAT and on site commissioning activities.
Author review and execute IQ OQ and support PQ documentation.
Ensure compliance with cGMP GAMP 5 and data integrity requirements.
Support deviations change controls and CAPAs related to automation systems.
Collaborate closely with engineering validation quality and operations teams.
Experience Required
Life sciences automation C&Q experience in a GMP manufacturing environment.
Hands on experience with PLC SCADA DCS or MES platforms.
Proven IQ OQ execution experience for automated systems.
Strong understanding of GAMP 5 CSV and regulatory expectations.
Ability to work effectively on site within cross functional project teams.
Seniority Level
Mid‑Senior level
Employment Type
Contract
Job Function
Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at i‑Pharm GxP by 2x
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W2 Contract | 12 Months Initial with Extension Based on Performance
Responsibilities
Support commissioning and qualification of automated GMP systems including PLC SCADA DCS and MES.
Execute FAT SAT and on site commissioning activities.
Author review and execute IQ OQ and support PQ documentation.
Ensure compliance with cGMP GAMP 5 and data integrity requirements.
Support deviations change controls and CAPAs related to automation systems.
Collaborate closely with engineering validation quality and operations teams.
Experience Required
Life sciences automation C&Q experience in a GMP manufacturing environment.
Hands on experience with PLC SCADA DCS or MES platforms.
Proven IQ OQ execution experience for automated systems.
Strong understanding of GAMP 5 CSV and regulatory expectations.
Ability to work effectively on site within cross functional project teams.
Seniority Level
Mid‑Senior level
Employment Type
Contract
Job Function
Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at i‑Pharm GxP by 2x
#J-18808-Ljbffr