Job Description

Groupe PARIMA

is a Contract Development and Manufacturing Organization (CDMO), established in 1994. For over 30 years, we have developed an expertise in the development and manufacturing of non-sterile liquids, suspensions and semi-solid drug products.

https://www.groupeparima.com

Quality Control Supervisor

The Quality Control supervisor is responsible for the quality management of the QC Chemistry laboratory to ensure high standards and superior services while remaining compliant with regulations and safety programs. He/she ensures testing and release services (materials and products) are provided in support of established schedules.

Responsibilities:

Oversee and manage daily activities of the Quality Control team in an efficient manner Oversee and coordinate raw material testing and release internally and externally Oversee and support of internal and outsourced cGMP release and stability programs Participate actively of thorough completeness of Deviations, Out of Trend (OOT) or Out of Specification (OOS) investigations. Provide technical expertise and troubleshooting support, and ensure testing are completed in a timely manner Responsible of all results released by the Quality control team and approve the certificate of Analysis Lead and coach a team of QC Analysts Built a development and objective plans for each analyst and perform a follow-up on a monthly basis Assure the technical and safety trainings are kept updated Develop an action plan for the process improvement and increase the performance for the QC Laboratory Support internal, client and regulatory agency audits as needed and develop action plans for continuous improvement Serve as point person of all internal and external Quality Control data for commercial product Ensure that instruments and equipment are kept in a qualified and calibrated state Review periodical SOP revisions Support the achievement of Groupe Parima global objectives

Skills and experience required

B.Sc. in Science (Chemistry, Biochemistry, pharmaceutical field) or related field from a Canadian University, or an equivalent scientific diploma recognized by a Canadian University or an accredited Canadian organism Minimum of Ten (10) years of experience in Quality Control in the pharmaceutical industry, with a minimum of Five (5) years in a supervisory position Thorough knowledge and understanding of Canadian, US and European regulations. Experience with cGMP and ICH regulations and guidelines Supervisory experience Excellent interpersonal, organizational and communication skills Knowledge in computer software (Microsoft Office, Outlook) Bilingual (French and English)

What we offer:

Flexible work schedule Medical - dental & travel benefits Group retirement plan Recognition program & social activities Personal days Employee assistance program & online medical service Hot Beverages (Hot chocolate, Coffee, Mokaccino) Accessible by public transit or free parking Referral program Subsidized meal service
Type d'emploi : Temps plein, Permanent

Avantages:

Assurance Dentaire Assurance Invalidite Assurance Maladie Complementaire Assurance Vie Conges payes Cotisation egale au REER Evenements d'Entreprise Heures d'arrivee et de depart flexibles Nourriture a Prix Reduit ou Gratuite Programme d'Aide aux Employes Stationnement sur place
Horaire:

Du Lundi au Vendredi
Lieu du poste : En presentiel