JP

JAMP Pharma Group

Verified Job Source

A healthier future for all

Boucherville, Québec

Pharmaceutical Manufacturing
501–1,000 people

About

JAMP Pharma Group is a Canadian organization headquartered in Boucherville, in the Greater Montreal area. Having experienced exceptional growth over the past 10 years, JAMP Pharma Group operates across all segments of the pharmaceutical market and now offers the widest range of generic drugs in Canada, with nearly 350 molecules. In addition to its generic division, JAMP Pharma Group operates several divisions, including Orimed, BioJAMP®, and JAMP Acute Care and Injectables, offering prescription, branded, and biosimilar products. The Group is also a leader in the over-the-counter market through its subsidiary, Groupe Wampole S.E.C., which encompasses 12 brands of natural health and cosmetic products. Since 2024, the JAMP Pharma Group has also operated its own manufacturing facility, located in Lévis. As part of JAMP Pharma, you will be able to: • Achieve your professional goals while having a significant impact on the success of the company. • Perform in a fast, agile, entrepreneurial and friendly environment. • Work with talented and multicultural professionals in order to achieve common goals. • Be part of a stable, successful and ambitious company at the forefront of innovation • Take advantage of our new, bright and welcoming offices. • Get involved socially with employees as well as the community. WANT TO MAKE HISTORY WITH US?

Open positions

Préparateur(trice) de commandes à l'unité (UPA1) (Soir)

On-site · Boucherville

The individual will be responsible for daily order picking, packing, and shipping tasks within a computerized environment. They will also handle product labeling, display assembly, and cycle counts while maintaining a clean and safe workspace.

Tehcnicien (ne) en environnement

Hybrid · Lévis

The technician will perform environmental sampling and analysis to ensure compliance with environmental monitoring programs for facilities and utilities. They are also responsible for compiling data, interpreting results, and drafting periodic reports.

Sales Manager

On-site

The Sales Manager is responsible for leading and developing a high-performing sales team to achieve growth objectives and strengthen market position in the generic pharmaceutical sector. They will manage regional action plans, conduct performance evaluations, and build strong relationships with key corporate customers.

Territory Manager - GP (London)

On-site

The Territory Manager is responsible for promoting and strategically positioning the product portfolio to healthcare professionals to achieve annual sales objectives. They will build long-term, value-based relationships and execute a robust territory business plan in compliance with industry regulations.

Territory Manager - Specialty (Ontario)

On-site · Toronto

The Territory Manager is responsible for promoting the product portfolio to specialists in ophthalmology and psychiatry to achieve annual sales objectives. They will develop and execute territory business plans while maintaining a strategic network of healthcare professionals.

Territory Manager - British Columbia

On-site

The Territory Manager is responsible for prospecting new customers and managing business relationships to drive growth within the British Columbia region. They will promote products and services while ensuring high-quality service standards and achieving established sales targets.

Gestionnaire de comptes stratégiques - Oncologie (Montréal)

On-site · Boucherville

The Strategic Account Manager will act as the primary point of contact for oncology centers across Canada to drive sales performance and execute strategic account plans. They will build relationships with healthcare professionals, communicate clinical information, and collaborate with internal teams to ensure market access and product growth.

Chargé(e) de projets ingénierie et maintenance

On-site · Lévis

The role involves managing engineering projects for production equipment and buildings, including planning and optimization. Key tasks include drafting specifications, coordinating with international suppliers, and overseeing budget and change controls.

Analyste, laboratoire chimie - Contrôle de la qualité (quart de jour)

On-site · Boucherville

Perform a variety of physico-chemical and qualitative/quantitative analyses to ensure pharmaceutical products comply with current standards and regulations. Responsible for monitoring laboratory equipment, documenting quality control activities, and participating in continuous improvement processes.

Analyste de données maîtres

Hybrid · Boucherville

The Master Data Analyst is responsible for ensuring the integrity of the product database within SAP and supporting data platforms. This includes maintaining product data governance, validating technical specifications, and advising supply chain teams on product configuration.

Conseiller(ère), Ressources humaines

Hybrid · Boucherville

Manage the full recruitment process and provide daily HR support to assigned client groups. Lead organizational transformation initiatives and oversee the onboarding and integration of new employees.

Technicien(ne) en projets d'ingénierie et maintenance

On-site · Lévis

The technician will manage engineering projects for production equipment and facilities while supporting the maintenance and engineering team. Responsibilities include project planning, vendor coordination, factory layout design, and managing budget tracking and regulatory documentation.

Technicien(ne) en projets d'ingénierie et maintenance

On-site · Lévis

The Project Manager in Maintenance will manage engineering projects related to production equipment and facilities. This role involves supporting maintenance and engineering team members on a daily basis.

Acheteur(euse)

On-site · Lévis

The strategic buyer is responsible for defining and implementing procurement strategies for essential materials and services in pharmaceutical manufacturing. This role contributes to competitiveness, regulatory compliance, and securing supplies.

Spécialiste assurance qualité Senior (Produits)

On-site · Lévis

The Senior Quality Assurance Specialist is primarily responsible for developing specifications for raw materials, packaging materials, and finished products during technology transfers and product introductions at the site. Daily tasks include drafting specifications, writing risk analyses (in English), reviewing change controls related to specification modifications, and revising laboratory quality control analytical methods.

Spécialiste investigation contrôle qualité

Hybrid · Lévis

The specialist conducts investigations into out-of-specification (OOS) and out-of-trend (OOT) results and quality events. They are responsible for performing root cause analysis and implementing corrective and preventive actions (CAPA) to ensure regulatory compliance.