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Protocol Intelligence
Data-driven signals on your job's competitivenessStrong employer brand but senior, niche biopharma automation role limits broad applicant competition.
Specialized PLC/DCS skills, pharma validation, and GxP/regulatory knowledge make cross-industry transfer difficult.
Explicit 10+ years plus mandatory PLC/DCS, validation, and regulatory compliance raise filtering strictness.
Job Description
Structured overview of role & requirementsAbout This Role
Lead design, development, validation, commissioning, and lifecycle management of automation, instrumentation, and electrical systems for biopharmaceutical manufacturing equipment.
Serve as SME for PLC/DCS/SCADA platforms (Siemens, Emerson, TIA Portal, WinCC, PCS7, DeltaV) including software design, configuration, testing, and validation ensuring compliance to GAMP 5, 21 CFR Part 11, ISA, IEC, GMP standards.
Manage FAT, SAT, startup, troubleshooting, customer acceptance, and mentoring junior engineers while collaborating globally to deliver scalable solutions.
Minimum Requirements
Bachelor's degree in Instrumentation, Electrical, Electronics & Telecommunication, Computer Science or equivalent.
Minimum 10+ years post-qualification experience in automation or related engineering roles.
Experience in project engineering/management of biopharmaceutical manufacturing equipment, especially filtration, separation, purification systems; biopharmaceutical domain experience preferred.
Willingness to travel up to 40% for project execution, commissioning, and customer support; role based in Pune (onsite).
Ideal Candidate Profile
Proven expertise in developing and validating automation systems compliant with biopharma regulations and standards such as GAMP 5 and 21 CFR Part 11.
Strong operational experience with industry-leading PLC/DCS/SCADA platforms within regulated manufacturing environments.
Ability to lead complex projects end-to-end including risk mitigation, lifecycle management, and mentoring technical teams in a global matrix organization.