API C&Q Project Engineer - Pharmaceutical ManufacturingSRG • Lebanon, IN, US

API C&Q Project Engineer - Pharmaceutical Manufacturing

SRG • Lebanon, IN, US

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Overview

SRG, the leader in the Life Sciences human capital industry, is looking for a Commissioning and Qualification (C+Q) API Project Engineer to join our client's pharmaceutical manufacturing team in Lebanon, IN. The right candidate will be a detail-oriented and proactive CQ Project Engineer to support the execution of commissioning and qualification activities for equipment and systems in our API manufacturing facility. This role is ideal for candidates with technical expertise and a working knowledge of facility, utilities and API manufacturing process systems who excel in documentation, data analysis, and cross-functional coordination.

Fully onsite

1+ years contract

Employment details

Location : Lebanon, IN
Work arrangement : Fully onsite
Contract : 1+ years

Responsibilities

Report directly to the C&Q Node Lead, providing updates on the progress, risks, and issues related to C&Q activities.

Maintain and update C&Q trackers, schedules, and status dashboards to support project visibility and decision-making.

Review and interpret engineering drawings, specifications, and technical documents.

Track procurement progress and equipment arrivals, equipment installations, system MCs, etc. with cross-functional teams (eg : Construction teams, Engineering, C&Q Service Providers, Operations, etc.).

Participate in C&Q execution readiness.

Coordinate and assist with HSE related activities such as Permit to Work, Job Hazard Analyses, Safety Walks, etc.

Coordinate with cross-functional teams (eg : QA, Engineering, C&Q Service Providers, Operations, etc.) for C&Q activities.

Actively track field progress and engage in C&Q field activities (eg : perform walkdowns of systems, equipment, and infrastructure. Ensure alignment with design specifications, HSE, and C&Q operational standards, etc.).

Participate in meetings, take minutes, and follow up on action items related to C&Q activities.

Ensure all documentation is maintained in accordance with GMP and internal quality standards.

Any tasks assigned by the C&Q Program.

Qualifications

Engineering degree. ChemE or Mechanical Engineering will be strongly preferred

7 plus years' experience in commissioning and qualification (this is not a validation engineer position)

Required and proven C&Q skillsets : Synthesis and Purification, APIs, Peptides

Other

Note : Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

EEO Statement

Impellam Group and its brands are equal-opportunity employers committed to diversity and inclusion. All qualified applicants will receive consideration without regard to race, color, religion, gender, sexual orientation, pregnancy or maternity, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application, interview process, pre-employment activity, and the performance of crucial job functions.

If you require additional disability considerations, modifications, or adjustments please let us know by contacting HR-InfoImpellamNA@impellam.com or fill out this form to request accommodations.

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Manufacturing Engineer • Lebanon, IN, US