Experienced Engineer Qualification Validation
Ekium
Required skills
About the role
Translated into English from French by Korum. The employer's original wording is on their site.
Welcome to Ekium!
π·πΌββοΈπ¨πΌβπ» 3600 talents π 18 Countries π β¬425M revenue π 36 years
Here, things are buzzing with engineers, experts and enthusiastic technicians who work together to bring industry closer to the challenges of our society.
You have certainly crossed our path or seen our achievements in the industrial landscape. From Industry to Energy, including the Naval sector, Ekium works in many highly specialised areas of expertise!
And because our wealth lies in our employees, we are committed, every day, to protecting their health and safety, because it is together that we build a sustainable future.
π Discover the Ekium universe and the diversity of projects you could work on tomorrow:
Welkium in the EKIUM universe!
Mission
π Location: Jonage (69)
π Sector: Pharmaceutical industry
π
Start date: As soon as possible
β³ Contract type: Technical Assistance
Within a leading pharmaceutical production site based in the RhΓ΄ne, you will join the Qualification team as an experienced expert. Working in an environment subject to Good Manufacturing Practice (GMP), you will actively contribute to ensuring the compliance and performance of production equipment, in interface with many internal functions. You will report directly to the Performance Qualification Manager.
β
Your responsibilities
Lead qualification strategies (IQ/OQ/PQ) for equipment in liaison with Quality Assurance
Write and contribute to qualification deliverables according to defined roles and responsibilities
Plan, coordinate and carry out qualification exercises on site in support of operational teams
Ensure compliance with GMP and regulatory requirements throughout all activities
Profile
π Engineering degree or equivalent, specialising in process engineering, pharmaceuticals or a related field
π Minimum of 7 to 10 years' experience in a pharmaceutical production environment (operating site, investment project or transfer of activity)
π Solid knowledge of GMP requirements and the traceability logic specific to the pharmaceutical industry
π§ Mastery of IQ/OQ/PQ qualification methodologies
π Operational level of English (read, written, spoken)
π€ Excellent communicator, comfortable working across multi-functional interfaces and attentive to internal clients
π― Rigour, organisational skills and ability to manage several topics in parallel
π Collaborative leadership, autonomy and results orientation
The Ekium environment:
β Profit-sharing and incentive scheme, meal vouchers, annual holiday bonus, works council benefits (holiday vouchers, gift cards, ...)
π€ A committed company: EKIUM is a signatory to the engineering charters for climate and diversity
π¬ Close, hands-on management
π’ Remote working possible depending on the assignment
π A friendly environment adapted to people with disabilities
π₯ Colleagues who are passionate like you, with a community of business and software leads!
π§ Collective vigilance that continuously improves the quality and safety of our services
πΌ Opportunities for progression through an internal mobility charter
π Membership of the SNEF Group, which has been on a growth trajectory for more than 115 years
Do you have a CV? So do we!
ππΌCV EKIUM
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