Snr C&Q/Validation Engineers(Multiple)- Facility/Utilities/Equipment-Pharma

Process Engineering Specialists; Pennsylvania; On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player is seeking skilled C&Q/Validation Engineers to join their dynamic team. This role involves leading the commissioning, qualification, and validation of pharmaceutical facilities and utilities, ensuring compliance with industry standards. Ideal candidates will possess over five years of experience in validation within the Pharma or Med Device sectors and have a strong understanding of protocol development. With opportunities for growth and the chance to work on impactful projects, this position offers a fulfilling career path in a collaborative environment. If you're ready to make a difference in the life sciences industry, this is the opportunity for you!

Qualifications

• 5+ years of validation experience in Pharma/Med Device.
• Strong background in CQV and project execution.

Responsibilities

• Lead commissioning, qualification, and validation of pharma facilities.
• Manage validation projects with strong client communication.

Skills

Validation/CQV experience

Protocol Development (IQ, OQ, PQ)

Communication skills

Tools

Kneat

Job description

Snr C&Q/Validation Engineers (Multiple) - Facility/Utilities/Equipment - Pharma

PES is an international services company providing Project Management, Construction Management, Commissioning & Qualification and Automation services to our clients in the pharmaceutical, nutritional and related sectors.

With offices across Europe, Asia and US, our core focus is on consistently delivering high-quality outcomes for our multinational clients.

We are currently looking for C&Q / Validation Engineers to join us on a permanent role to help us deliver various projects in the Life Sciences Industry.

We are currently looking for multiple engineers for the following:

• Senior Validation Engineers - Temperature Controlled Equipment (Fridge, Freezers, Autoclaves)
• Senior Validation Engineers - Process Equipment
• Senior Validation Engineers - Facilities & Utilities

Key Attributes/Responsibilities:

• Looking for candidates with 5+ years validation/CQV experience.
• Must come from a CQV background and have executed projects in Pharma/Med Device.
• Leading the commissioning, Qualification and Validation of pharmaceutical Facilities, Utilities and Process equipment.
• Protocol Development (IQ, OQ, PQ).
• Interface with client personnel and with outside vendors when necessary while performing the above.
• Individual will manage all facets of assigned validation projects while maintaining strong communication with client representatives on project status and assistance needed.
• Must have knowledge on working on Kneat.

We are currently looking for candidates who can be on site or travel to site daily.

If you'd like to find out about this opportunity or any other opportunity, please forward your CV to Nelson Anthony ([e-mail]).

PES International operates as an equal opportunity employer. No terminology in this advert is intended to discriminate on the grounds of age, race, religion, sexual orientation or any other factors with no bearing to employment skills and we confirm that we are happy to accept applications from persons of any background for this role.

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Quality Assurance and Engineering
• Industries: Pharmaceutical Manufacturing