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Senior Process Technician
Job in
Andover, Essex County, Massachusetts, 05544, USA
Listed on 2026-07-14
Listing for:
HKA Enterprises
Full Time
position Listed on 2026-07-14
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Validation Engineer
Job Description & How to Apply Below
GMP Manufacturing
· Bioprocessing
· Commercial & Clinical Production
We're looking for a Senior Process Technician to drive the execution of Commercial, Clinical, and/or Development manufacturing operations in accordance with SOPs and production schedules. You'll work on interdisciplinary, self-directed teams — leading process improvements, troubleshooting equipment and automation issues, and ensuring right-first-time execution across a regulated GMP manufacturing environment.
What you'll do- Execute manufacturing operations for buffer/media make-up tanks, glass washers, autoclaves, bioreactors, filtration equipment, inoculum preparation, chromatography skids, and UF/DF skids
- Execute SOPs for unit operations including CIPs, SIPs, sanitization, and related procedures
- Lead troubleshooting, technical support, and resolution of equipment, automation, and process issues on the manufacturing floor
- Support equipment commissioning, qualification, and validation activities
- Drive right-first-time execution, timely documentation review, and real-time monitoring of process and compliance trends
- Collaborate with Subject Matter Experts to support QTS investigations and CAPA implementations
- Support GMP audit walkthroughs and observation improvement initiatives
- Implement Lean Manufacturing, Sustainability, and Operational Excellence initiatives across all manufacturing areas
- Utilize enterprise systems including SAP, LIMS, AMPS, PDOCS, and/or QTS to support manufacturing operations
- Maintain inventory accuracy, reconciliation, and task prioritization to support production sustainability and metric adherence
- Experience executing GMP manufacturing operations in a pharmaceutical, biotech, or related environment
- Hands-on experience with bioprocessing equipment — bioreactors, chromatography skids, filtration, autoclaves, and/or UF/DF skids
- Proficiency in enterprise systems such as SAP, LIMS, AMPS, PDOCS, or QTS
- Strong attention to detail and commitment to documentation accuracy and regulatory compliance
- Ability to work independently on cross-functional teams and manage competing priorities in a fast-paced environment
- Experience with CAPA processes and QTS investigation support
- Familiarity with Lean Manufacturing or Operational Excellence frameworks
- Experience supporting equipment commissioning, qualification, and validation activities
Position Requirements
10+ Years
work experience
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