At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future?
There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families.
We believe in giving back to help those in need in the communities where we live and work. And are equally committed to creating a healthier environment and planet through our sustainability efforts.
Here is Job Description in French and English:
Résumé du poste :
Rattaché au manager de département dans le cadre de son apprentissage, l’Apprenti Ingénieur Production participe à la gestion du processus de fabrication de produits à usage pharmaceutique aux meilleures conditions de sécurité, qualité, couts et délais.
Assure la conduite des projets qui lui sont confiés, notamment coordonne des projets techniques dans le cadre de l’amélioration continue.
Recherche des moyens d’optimisation du département de rattachement.
Participe au fonctionnement quotidien du département.
Responsibilités / Activités principales (liste d’activités non exhaustive)
Le titulaire a connaissance des Standards Operating Procédures (SOP) de l’usine qui le concernent, comme décrit dans la politique de la société, étant donné qu’elles sont en liaison avec la position couverte par cette description de poste. Celles-ci sont reliées à leurs fonctions, telles que spécifiées dans leur description de poste.
Organisation :
- Recherche des moyens d’amélioration qualité, sécurité, productivité.
- Modifie les gammes de fabrication, forme et qualifie le personnel.
- Assure un reporting à son responsable.
- Participe à la réalisation des objectifs : productivité, qualité, sécurité, volume, délais.
- Développe ses capacités à manager.
Qualité / HSE :
- Garantit l’application de la réglementation (qualité, HSE).
- Audite et faire respecter les standards.
- Adapte et décline les GMP sur son secteur.
- Suit, analyse et propose des actions à tout taux de déchet hors standard.
- Coordonne les investigations suite à réclamation clients, refus interne, ou sécurité.
- Respecte et fait respecter des règles ISO, GMP et de toutes les certifications du site
Amélioration continue :
- Participe et est force de proposition dans le domaine de l’amélioration continue en coopération avec les services supports.
- Participe au développement de nouveaux produits, process, équipements, services clients .
Economique :
-Recherche et met en place les réductions de cout possibles en formulant le retour de saving.
Dans le cadre de la politique GMP, des objectifs et des plans d’actions établis : veille scrupuleusement au respect des règles et à la bonne application des procédures notamment en ce qui concerne l’hygiène personnelle, la propreté, la manipulation des produits, la contamination croisée sur les mélanges d’articles.
Profil :
Actuellement en formation au sein d'une école d'ingénieur, vous recherchez une alternance à partir de septembre 2024.
Qualification :
- Pack MS Office. Maitrise de MS Forms et Power BI serait un plus
- Notions mécaniques, hydrauliques et électriques
- Capacité d’identifier un besoin de remise en question des règles, et les faire respecter
- Esprit d’équipe, d’analyse, de synthèse et d’initiative
- Rigueur, discipline, et attention aux règles sécurité et qualité
- Capacité de formateur et de support de ses collègues de travail
Job summary:
Reporting to the department manager as part of his/her apprenticeship, the Production Engineer Apprentice participates in the management of the manufacturing process of products for pharmaceutical use under the best conditions of safety, quality, costs and deadlines.
Manages projects assigned to him/her, in particular coordinating technical projects within the framework of continuous improvement.
Seeks ways of optimizing the department.
Participates in the day-to-day running of the department.
Main responsibilities / Activities (non-exhaustive list)
The incumbent is familiar with the plant's relevant Standards Operating Procedures (SOPs), as described in company policy, as they relate to the position covered by this job description.
Organization:
- Looks for ways to improve quality, safety and productivity.
- Modifies manufacturing ranges, trains and qualifies personnel.
- Reports to his/her manager.
- Participates in achieving objectives: productivity, quality, safety, volume, deadlines.
- Develops management skills.
Quality / HSE :
- Ensures compliance with regulations (quality, HSE).
- Audits and ensures compliance with standards.
- Adapts and implements GMP in its sector.
- Monitors, analyzes and proposes actions for any non-standard waste rate.
- Coordinates investigations following customer complaints, internal refusals or safety issues.
- Complies with and enforces ISO, GMP rules and all site certifications.
Continuous improvement:
- Participates and makes suggestions in the field of continuous improvement in cooperation with support departments.
- Participates in the development of new products, processes, equipment and customer services.
Economic :
-Seeks out and implements possible cost reductions by formulating saving returns.
Within the framework of GMP policy, objectives and established action plans: scrupulously ensures compliance with rules and the correct application of procedures, particularly with regard to personal hygiene, cleanliness, product handling, and cross-contamination/ intermix.
Profile:
Currently studying at an engineering school, you are looking for a work-study contract starting in September 2024.
Qualifications:
- MS Office package. Mastery of MS Forms and Power BI would be a plus.
- Mechanical, hydraulic and electrical basic knowledge
- Ability to identify the need to question rules, and ensure they are respected
- Team spirit, ability to analyze, synthesize and take initiative
- Rigor, discipline and attention to safety and quality rules
- Ability to train and support colleagues
West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.