Lead Engineer - Automation Systems, Cell Therapy Devens
Bristol Myers Squibb
2 months ago
On-site
Devens, MA
Operations
Responsibilities:
- Technical lead and subject matter expert for process automation systems and equipment (DeltaV, PI, BAS, and integrated process equipment).
- Lead substantial technical efforts (e.g., major system upgrades, new process introductions).
- Integrate with cross-functional site teams to perform qualification and validation.
- Troubleshoot automation systems supporting Manufacturing; participate in a 24/7 on-call rotation.
- Support audits as a front room representative.
Required Qualifications/Skills:
- 5+ years experience with DeltaV, PI, BAS, and OT Infrastructure.
- Expert understanding of S88, S95, and batch processing operations.
- Expert knowledge of engineering documentation (P&IDs, network diagrams, process flow diagrams, SOPs).
- Expert knowledge of Validation Lifecycle Management (planning, IQ/OQ/PQ execution).
- Experience with QMS systems (Veeva or similar) and GMP Quality Processes (Deviation Management, Change Controls, etc.).
- Ability to troubleshoot network/control systems from field elements through operator interfaces and databases.
- Experience with IT ticketing systems (ServiceNow or similar).
- Excellent oral/written communication and presentation skills.
Preferred:
- Control system networking/PC networking; SQL/Server/Oracle/relational databases.
- Validation Lifecycle Management systems (Valgenesis or similar).
- Building automation systems; .Net scripting.
Education:
- Bachelor’s degree in engineering or equivalent.
- 5–7 years experience with control systems (DeltaV, PI, BAS, PLCs) in pharmaceutical/biotech.
Compensation (Devens, MA, US): $131,370–$159,187. Additional incentive may be available (eligibility-based).
- Technical lead and subject matter expert for process automation systems and equipment (DeltaV, PI, BAS, and integrated process equipment).
- Lead substantial technical efforts (e.g., major system upgrades, new process introductions).
- Integrate with cross-functional site teams to perform qualification and validation.
- Troubleshoot automation systems supporting Manufacturing; participate in a 24/7 on-call rotation.
- Support audits as a front room representative.
Required Qualifications/Skills:
- 5+ years experience with DeltaV, PI, BAS, and OT Infrastructure.
- Expert understanding of S88, S95, and batch processing operations.
- Expert knowledge of engineering documentation (P&IDs, network diagrams, process flow diagrams, SOPs).
- Expert knowledge of Validation Lifecycle Management (planning, IQ/OQ/PQ execution).
- Experience with QMS systems (Veeva or similar) and GMP Quality Processes (Deviation Management, Change Controls, etc.).
- Ability to troubleshoot network/control systems from field elements through operator interfaces and databases.
- Experience with IT ticketing systems (ServiceNow or similar).
- Excellent oral/written communication and presentation skills.
Preferred:
- Control system networking/PC networking; SQL/Server/Oracle/relational databases.
- Validation Lifecycle Management systems (Valgenesis or similar).
- Building automation systems; .Net scripting.
Education:
- Bachelor’s degree in engineering or equivalent.
- 5–7 years experience with control systems (DeltaV, PI, BAS, PLCs) in pharmaceutical/biotech.
Compensation (Devens, MA, US): $131,370–$159,187. Additional incentive may be available (eligibility-based).