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<![CDATA[Coordinator, Regulatory Affairs & Compliance Our client is a pharmaceutical company focusing entirely on finding new and effective therapies for central nervous system disorders. They are seeking a Coordinator, Regulatory Affairs & Compliance who will be responsible for providing technical and administrative support to the RA and GMP compliance group. Responsibilities; • Update budget follow-up and assist in the preparation of forecasts; • Maintain miscellaneous binders up to date (regulatory guidelines, Common Drug Review Directorate (CDR) database and statistics, and consultant agreements, quotes, etc.). • Provide administrative support to Managers, Regulatory projects for the preparation and filing of regulatory submissions. • Act as the Super User for Pluto and Jupiter Systems. • Provide administrative support to GMP Compliance Specialists. • Participate to the preparation of GMP SOPs. • Share information received on conference, seminars, etc. • Organize meetings and travel arrangements. • Prepare other financial related documents for the RA and GMP Compliance teams. • Prepare updates for RA and GMP Compliance BrainWeb. • Participate in meetings. Qualifications: - College Education. - Experience in Scientific and Regulatory affairs and GMP Compliance administration. - Experience in Corporate affairs administration. - Excellent knowledge of oral and written French and English - Good computer skills (Microsoft Office) Once you choose to join the exciting team at this renowned company, you will be rewarded with a very competitive salary and full benefits. Apply today to mcouture@fuzehr.com. While we appreciate receiving your resumes, only the chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you. Coordinateur (trice) des Affaires Réglementaires et Conformité Notre client le leader dans l’industrie pharmaceutique en recherche et conception de nouvelles thérapies pour le system nerveux central. Ils recherchent présentement un(e) Coordinateur (trice) des affaires réglementaires et conformité. Responsabilités ; • Met à jour le suivi du budget et assistance à la préparation des prévisions. • Assure la mise à jour de différents cartables (directives réglementaires, base de données et statistiques du programme commun d’évaluation desmédicaments (PCEM), ententes d’experts-conseils, devis, etc.). • Fournit du soutien administratif aux chefs de projets réglementaires pour la préparation et le dépôt de soumissions réglementaires. • Agit à titre d’usager expert pour les systèmes Pluto et Jupiter (eCTDViewer® Web Edition). • Participe à la préparation de procédures sur les AR. • Tient à jour un système de classement et d'archivage pour toute la documentation relative aux BPF (QAQC). • Participe à la préparation de procédures sur les PBF. • Partage l’information reçue lors de conférences, de colloques, etc. • Organise les réunions et prend les dispositions de déplacement. • Prépare d’autres documents de nature financière pour les équipes des AR et de la conformité aux BPF. • Prépare les mises à jour pour les sections des AR et de la conformité aux BPF du site BrainWeb. • Participe à des réunions. Qualifications ; - Éducation collégiale. - Expérience en administration des affaires réglementaires et scientifiques et de conformité aux BPF. - Expérience en administration des affaires corporatives. - Excellente connaissance du français et de l’anglais oral et écrit. - Maîtrise de l’ordinateur (logiciels Office de Microsoft). En choisissant de vous joindre à l’équipe dynamique de cette entreprise renommée, vous profiterez d’un salaire de base concurrentiel, jumelé à une gamme complète d’avantages sociaux. Posez votre candidature dès aujourd’hui à mcouture@fuzehr.com Nous vous remercions d’avance de votre intérêt, mais seuls les candidats sélectionnés pour une entrevue seront contactés. **Si vous n’êtes pas présentement en recherche d’emploi, mais vous connaissez quelqu’un qui pourrait bénéficier de cette opportunité, n’hésitez pas a lui transmette cette information, Merci. ]]>

<![CDATA[Compliance Supervisor-Pharmaceutical Our client is a Montreal-based pharmaceutical company specializing in the manufacturing and distribution of products in Canada and worldwide. They are currently seeking a Compliance Supervisor. This person will be responsible for the supervision of the employees within the department. Manage and perform, according to an established schedule, self-inspections, external audits of suppliers and sub-contractors and audits by regulatory agencies and clients. Perform activities related to compliance. Manage special projects for compliance. The ideal candidate has a Bachelor's degree in Sciences (Chemistry, Biochemistry, Pharmacy, Chemical Engineering along with minimum five (5) years in the pharmaceutical industry where two (2) were in auditing of pharmaceutical firms; having done foreign audits is an asset. ***Knowledge of the Canadian, American and European regulations for the pharmaceutical industry and for medical devices. Fluently bilingual, along with excellent leadership and management skills. Once you choose to join the exciting team at this renowned company, you will be rewarded with a very competitive salary and full benefits. Apply today to mcouture@fuzehr.com. While we appreciate receiving your resumes, only the chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you. ]]>

<![CDATA[About the Company: You will be working for a Quebec company with one owner and multiple business interests The company is a personal holding/operating company that specializes in the healthcare industry and more specifically the prescription pharmaceutical industry The owner takes on additional entrepreneurial activities based on interest and financial review The Position - Assistant/Analyst - Flexible hours 7 prefers part time Primary Functions: The person will report to the owner and combine executive assistant, analyst, and project management functions Executive assistant Book Travel Organize expenses Coordinate correspondence Arrange catering for meetings Mail/Purolator Setting up meetings Some may be personal Analyst Database management Patent screening Product Forecasting & Screening Developing reports Regulatory updates News updates Briefings Pharmaceutical News Competitive Activities Reviewing potential business proposals Project Management Management contacts for product development with owner Following up on business projects The Candidate Seeking part-time work with flexible hours Prefer a person who has worked in pharmaceutical of healthcare industry and looking for work across multiple areas and is not concerned that some tasks are analytical and some clerical Is able to work independently without need of supervision Preferably a University degree with a marketing and finance background Ability to learn on the job Looking for a longer term commitment and not a job to ‘fill a gap’ until another position arises Must have a high and proven level of confidentiality Computer skills Excel Word Powerpoint Access (Nice to have) An understanding of financial concepts IRR NPV Breakeven analysis Please Contact James at jerb_2005@hotmail.com include: Resume expectation in terms of hours compensation ]]>

<![CDATA[Acheteur(e) Senior- Science Santé Notre Client est un leader Montréalais dans le domaine de la santé. Ils recherchent présentement un(e) Acheteur(e) Senior pour le secteur des emballages. Responsabilités; - Identifier les meilleures sources de fournitures; - Négocier les prix avec les fournisseurs et sous-traitants; - Coordonner les transitions de fournisseurs; - Supporter les lancements de nouveaux produits; - Agir en tant que support pour les acheteurs et les planificateurs de produits; - Travailler en participation avec la production; Qualifications; - Excellente maîtrise de l’anglais et du français; - 5 ans d’expérience en achats et négociations. En choisissant de vous joindre à l’équipe dynamique de cette entreprise renommée, vous profiterez d’un salaire de base concurrentiel, jumelé à une gamme complète d’avantages sociaux. Posez votre candidature dès aujourd’hui à mcouture@fuzehr.com Nous vous remercions d’avance de votre intérêt, mais seuls les candidats sélectionnés pour une entrevue seront contactés. **Si vous n’êtes pas présentement en recherche d’emploi, mais vous connaissez quelqu’un qui pourrait bénéficier de cette opportunité, n’hésitez pas a lui transmette cette information, Merci. ]]>

<![CDATA[Position de nuit evening position CONTRACT : 1 year+ Hours: 11:30pm-7:30am  Fabriquer, mélanger et délivrer des préparations radiopharmaceutiques conformément à la réglementation appropriée, en faisant preuve de la plus grande diligence et en se concentrant sur le respect des engagements en temps opportun, tout en promouvant le travail d’équipe.  Accomplir différentes tâches de laboratoire (nettoyage, installation de matériel, calibration d’instruments, élimination des déchets, gestion des stocks, expédition et réception) en s’adaptant à de multiples priorités qui changent sans arrêt. Tenir à jour avec méticulosité les dossiers couvrant tous les aspects des activités, conformément à la réglementation de la Commission canadienne de sécurité nucléaire (CCSN) et du Programme des produits thérapeutiques (DPT) et aux normes régissant le transport de marchandises dangereuses (TMD), pour s’assurer que les produits sont libérés en temps opportun.  Manipuler les substances radioactives ou présentant un risque biologique, conformément à la réglementation en vigueur (SIMDUT, CCSN, TDM, PPT et MOE), de façon à minimiser les risques pour soi-même et pour autrui.  Utiliser des techniques de radioprotection efficaces, conformément aux principes ALARA, pour réduire au minimum la radioexposition pour soi-même et pour autrui.  Analyser les produits radiopharmaceutiques finis en accomplissant, en temps oppportun, les tâches nécessaires au contrôle de leur qualité pour permettre au personnel concerné d’en autoriser la libération.  Capacité démontrée d’agir vite et de se concentrer sur le respect des engagements en temps opportun tout en entretenant avec les clients, tant internes qu’externes, des rapports basés sur une communication efficace.  Connaissance pratique et théorique de l’application des sciences nucléaires en médecine et en radiopharmacie.  Compréhension des Bonnes pratiques de fabrication et de leur rôle dans l’assurance de la conformité des produits finis et des spécifications des méthodes d’analyse.  Bonnes aptitudes pour la tenue de dossiers et habiletés de communication, tant à l’écrit qu’à l’oral.  Connaissance pratique et théorique des sciences pharmaceutiques, en particulier de la préparation de produits pharmaceutiques, du contrôle de leur qualité, de la tenue des dossiers qui s’y rapportent et de leur délivrance.  Connaissance pratique des systèmes de documentation utilisés en laboratoire, sur le papier ou sur un support électronique.  Connaissance de Microsoft Office.  Conscience de l’importance de respecter les exigences des clients pour maintenir de bons rapports avec eux. *************************************************************************** Hours: 11:30pm-7:30am D.E.C. en techniques de médecine nucléaire ou Laboratoires Manufactures, compounds and dispenses preparations of radiopharmaceuticals in compliance with appropriate regulations, demonstrating urgency and a focus on meeting commitments in a timely fashion, while promoting teamwork. Performs a range of lab duties (cleaning, lab set-up, instrument calibration, waste disposal, inventory maintenance, shipping and receiving) while showing the ability to respond to multiple and changing priorities. Maintains meticulous records of all aspects of the business, in compliance with CNSC, TDG and TPP regulations, ensuring release of products in a timely fashion . Handles radioactive and biohazardous materials in compliance with WHMIS, CNSC, TDG, TPP and MOE regulations, minimising risk to self and others. Practices effective radiation safety techniques, in compliance with ALARA principles, to minimise radiation exposure to self and other employees. Performs QC procedures on finished radiopharmaceuticals in a timely manner, ensuring release by appropriate authorised personnel.  Has demonstrated an urgency and focus on meeting commitments in a timely fashion, while using effective and superior communications skills to deal with internal and external customers. Possesses practical and theoretical understanding of radiopharmacy nuclear medicine sciences. Understands concept of GMPs and their role in ensuring compliant finished products and test method specifications Good record keeping skills as well as effective verbal and oral communications. Practical and theoretical understanding of pharmaceutical sciences, in particular, pharmaceutical preparation, quality control, record keeping and dispensing. Working knowledge of laboratory documentation system, both paper-based and electronic Knowledge of Microsoft Office Understands importance of good customer relations by understanding their requirements. College diploma in Nuclear Medicine or medical laboratory College diploma in sciences ]]>

<![CDATA[The Montreal Neurological Institute and McGill’s Department of Psychiatry are looking for non-smoking, healthy men, age 22-35, to participate in a study about the effects of methylphenidate (Ritalin®). The study involves an interview, medical screening and five test sessions (3 PET scans) over the course of one month. Participants will be compensated for their time. Valid Canadian healthcare card required to participate. The principal investigators are Drs A. Dagher, MD and C. Benkelfat, MD. If interested, please contact Alexandra by email: ritalin.study@gmail.com]]>

<![CDATA[Montreal Neurological Institute and McGill’s Department of Psychiatry are looking for non-smoking, healthy men, age 22-35, to participate in a study about the effects of methylphenidate (Ritalin®). The study involves an interview, medical screening and five test sessions (3 PET scans) over the course of one month. Participants will be compensated for their time. Valid Canadian healthcare card required to participate. The principal investigators are Drs A. Dagher, MD and C. Benkelfat, MD. If interested, please contact Alexandra by email: ritalin.study@gmail.com]]>

<![CDATA[We make green software to help protect the environment Knowledge of REACH European norms. Atrion International Inc. is the leading developer of a Materials Compliance Solution for multinational companies as well as for those companies trading on a global basis. Our platform allows corporations to safely and cost-effectively manage and distribute regulated and non-regulated materials in accordance with regional and local legislation. Atrion's dynamic platform includes sophisticated Software Applications, Chemical & Regulatory Content, Compliance Engines, Professional & Regulatory Services and Integration Solutions for ERP platforms, providing end-to-end compliance functionality. Job Description: Primary function will be to cost-effectively prepare regulatory-compliant MSDS for international customers who outsource this function to Atrion · Assist in establishing the details of the (M)SDSs content to be delivered contractually · Assist in establishing the effort (time) required per (M)SDS for each contract · Author (M)SDSs/SDSs for EU countries · Review (M)SDSs prepared by junior authors in the Atrion team · Review their current (M)SDSs and summarize deficiencies · Participate in the development and improvement of the authoring process · Occasionally provide related services like internal and external authoring training - Have no restrictions on valid passport for entering U.S.A. Personality traits: · Self starting / motivated · Multi-tasking, expect competing deadlines for more than one contract to be common Job Qualifications Languages: Fluent working knowledge of English; French, Dutch, German an asset. Computer Proficiency: The job will require routinely using the Atrion Intelligent Authoring system for producing (M)SDSs. Therefore, candidate must be proficient at data entry and navigation with advanced software solutions; training will be provided Required Experience: University degree in Biochemistry, Chemistry, Environmental Sciences or related fields 3 - 5 years of (M)SDS Authoring experience for the EU 3 - 5 years experience in Environmental, Health and Safety (EH&S) (chemical data; health, safety, and environmental regulations; and/or toxicology) ]]>

<![CDATA[Inventory Control Planner Our client is a Canadian wholesale distributor of medical professional and home healthcare products. This renowned and established company is seeking an Inventory Control Planner for their Montreal office. Responsibilities; • Ensure inventory levels are at the desired levels by maintaining planning module for all “B” and “C” vendors; • Constantly updating the planning module with new information that is being provided by the sales or marketing teams on product sales (highs or lows); • Generate vendor purchase orders based on numbers determined in the planning process; • Follow-up and verification of sales confirmations; • Backup to coordinator position within Inventory Control department Qualifications: • Previous experience working with a custom broker, freight forwarder or in the transport industry; • Ability to prioritize and manage several tasks in a high pressure environment; • Ability to set and meet stringent timelines to ensure completion of tasks and projects; • Excellent numeric skills: must be able to analyze inventory levels / stock turns / margins; • Excellent communication skills at all levels of the organization (both written and oral); • Ability to deal with and be sensitive to diverse cultures at the supplier level (Asia); • Ability to work independently as well as part of a team; • Proficiency in all MS Office applications and the internet • Fluent bilingualism; • University degree considered an asset . Once you choose to join the exciting team at this renowned company, you will be rewarded with a very competitive salary and full benefits. Apply today to mcouture@fuzehr.com. While we appreciate receiving your resumes, only the chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you. ]]>

<![CDATA[Corporate Account Executive Our Client is a $17 billion company; they provide the document industry's broadest portfolio of offerings. Our client’s services expertise is unmatched and includes helping businesses develop online document archives, analyzing how employees can most efficiently share documents and knowledge in the office, operating in-house print shops or mailrooms, and building Web-based processes for personalizing direct mail, invoices, brochures and more Responsibilities; • Market the full line of products and services in a defined vertical market of current customers and non-customers; • Developing and implementing a long-term relationship building strategies; • Achieve sales targets for new business sales and renewals; • Provide existing account coverage and development of new accounts; • Provide existing account coverage and development of new accounts; • Meet our client’s Canadian Customer Satisfaction goals by effectively resolving all customer issues; • Establish and build account relationships at executive levels. Qualifications; • Bachelor’s Degree; • Fluently Bilingual; • Demonstrated organization, planning and communications skills • Demonstrated systems literacy skills (working knowledge of common PC and/or Mac applications). Once you choose to join the exciting team at this renowned company, you will be rewarded with a very competitive salary and full benefits. Apply today to mcouture@fuzehr.com. While we appreciate receiving your resumes, only the chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you. Directeur de Compte Corporatifs Notre Client est le leader mondial en gestion du document, offrant la gamme de technologies, de services de conseil et de solutions la plus complète du marché. Ils sont l'une des entreprises les plus innovantes dans le monde, avec des centres de recherche et de technologie aux États-Unis, au Canada et en France. Cette entreprise est présentement a la recherche d’un(e) Directeur (trice) de Comptes pour le territoire de Montréal. Responsabilités; • Le titulaire commercialise la gamme complète de produits et de services auprès des clients actuels et potentiels du client dans un marché vertical désigné; • l’élaboration et la mise en œuvre d’une stratégie à long terme en vue d’assurer la conservation et le développement des affaires; • Atteindre les objectifs de vente en matière de nouvelles affaires et de renouvellement; • Assurer la couverture des comptes actuels et le développement des nouveaux comptes; • Élaborer des stratégies appropriées (à court et à long terme) pour répondre aux exigences et besoins commerciaux des clients actuels et potentiels; • Atteindre les objectifs de satisfaction de la clientèle en solutionnant efficacement tous les problèmes des clients; • Établir et développer les relations avec les clients, au niveau des cadres et des décideurs dans l’ensemble des services; • Communiquer la stratégie et l’orientation aux cadres supérieurs dans chaque compte. Qualifications; • Baccalauréat en Administration ou un domaine connexe; • Parfaitement Bilingue; • Habiletés manifestes en organisation, planification et communications; • Maîtrise manifeste d’outils informatiques (connaissance pratique des applications courantes en environnement PC ou Mac). En choisissant de vous joindre à l’équipe dynamique de cette entreprise renommée, vous profiterez d’un salaire de base concurrentiel, jumelé à une gamme complète d’avantages sociaux. Posez votre candidature dès aujourd’hui à mcouture@fuzehr.com Nous vous remercions d’avance de votre intérêt, mais seuls les candidats sélectionnés pour une entrevue seront contactés. **Si vous n’êtes pas présentement en recherche d’emploi, mais vous connaissez quelqu’un qui pourrait bénéficier de cette opportunité, n’hésitez pas a lui transmette cette information, Merci. ]]>

<![CDATA[Researchers at McGill University (Health Centre and Department of Psychiatry) are inviting female volunteers to participate in a study about mood regulation in relation to the neurotransmitter serotonin. We are particularly interested in women (age 18-60) who meet at least 4 out of the 8 following criteria: (1) mood fluctuations from one extreme to the other in short periods of time; (2) unstable self-esteem and self-identity as well as (3) feelings of emptiness; (4) chronic and intense fear of abandonment; (5) repeatedly and intentionally injuring themselves (eg: cutting their wrists); (6) problems controlling their temper; (7) impulsive behavior (eg: compulsive spending, substance abuse); and (8) marked difficulty engaging in social relationships, which are often turbulent and chaotic. We are inviting women currently treated for disturbed emotional and social behaviors with medications such as fluoxetine (SSRIs), who have seen improvements in their symptoms as a result. Participants will be compensated ($125) for their time. If interested, you can call Alexandra at 514-398-6973/ 514-398-2011 or email at mood_regulation_study@yahoo.ca for more information without any obligation.]]>

<![CDATA[Various Biotech positions available in Dr. Nada's Laboratory. 1-Lab technician 2-Research assistant Levels available: 1-BSc 2-MSc 3-PhD Responsibilities for each positition vary and include ordering of supplies and reagents, maintenance of purchasing records, and general upkeep of laboratory equipment. The applicant will be expected to help research, including mouse handling of and DNA/RNA-PCR, laboratory maintenance such as glassware washing, and accountings. Supervised by Dr. Nada Kabb. Using biochemical and genetic tools the successful candidate will: test for known genetic mutations, identify novel mutations, and develop new diagnostic tests. He/she will also be responsible for filing reports. Qualifications for each position vary. B.Sc or MSc or PhD in biochemistry or related feild. candidates should have basic experience in molecular biology, cell biology, and small animal work or Yeast experience. Should be highly motivated, attentive to detail, able to work independently, organized, and able to manage multiple tasks as needed. statistical data analyses and Advanced computer software knowledge are desirable. Must be willing to work as part of a team. Good organizational and communication skills are essential. Interested candidates are invited to send their CV as there are 3 positions open. Note: IF YOU HAVE ALREADY APPLIED TO DR. NADA'S PREVIOUS POSTINGS DO NOT APPLY AGAIN Dr. Nada Kabb E-mail: nadkabbani@yahoo.com Dr. Nada Kabb Research Institute Biochemistry, McGill Montreal, QC, Canada Keywords: technician OR biology OR biochemistry OR chemistry OR chemist OR HPLC of flow OR cytometry OR FACS OR yeast OR genomics OR proteomics OR technician OR lab OR laboratory OR masters OR scientist OR assistant OR research OR microbiologist OR microbology OR culture OR tissue OR microscopy]]>

<![CDATA[Our client, a large biopharma player in Eastern Canada, is looking for an SAS programmer. Must be bilingual (French/English) with a master's degree in statistics, and able to program in SAS. Some experience in client's industry would be an asset. For more information about this position, please send your resume to/contact TRUDI at: Hess Associates Executive Search www.hessjobs.com hr@hessjobs.com 416.447.3355]]>

<![CDATA[ Researchers at McGill University (Health Centre and Department of Psychiatry) are inviting female volunteers to participate in a study about mood regulation in relation to the neurotransmitter serotonin. We are particularly interested in women (age 18-60) who meet at least 4 out of the 8 following criteria: (1) mood fluctuations from one extreme to the other in short periods of time; (2) unstable self-esteem and self-identity as well as (3) feelings of emptiness; (4) chronic and intense fear of abandonment; (5) repeatedly and intentionally injuring themselves (eg: cutting their wrists); (6) problems controlling their temper; (7) impulsive behavior (eg: compulsive spending, substance abuse); and (8) marked difficulty engaging in social relationships, which are often turbulent and chaotic. We are inviting women currently treated for disturbed emotional and social behaviors with medications such as fluoxetine (SSRIs), who have seen improvements in their symptoms as a result. Participants will be compensated ($125) for their time. If interested, you can call Alexandra at 514-398-6973/ 514-398-2011 or email at mood_regulation_study@yahoo.ca for more information without any obligation.]]>

<![CDATA[DESCRIPTION DE POSTE / JOB DESCRIPTION LAB TECHNICIAN SERVICE Quality Control Analytical Service SOMMAIRE DU POSTE / JOB SUMMARY Under moderate supervision, analyze pharmaceutical samples such as active raw material and finished products according to House or Pharmacopial methods using physico-chemical and chromatographic techniques. RELATIONS D’AFFAIRES / RELATIONSHIPS RELÈVE DE / REPORTS TO :Laboratory Supervisor TRAVAILLE AVEC /WORKS WITH : Group leader and other technicians and analysts RESPONSABILITÉS & TÂCHES / RESPONSABILITIES & DUTIES •Maintain laboratory note books of clear and concise records of all data, results and calculations respecting GLP. •Select appropriate balance for a given application. Able to use standards to verify accuracy of a balance. •Select and use volumetric glassware, employing proper techniques for accurate sample analysis. •Select and use appropriate filtering medium, filtration techniques and proper set-up of pertinent apparatus (vacuum, gravity, etc…). •Select, maintain and safe use of bench top laboratory apparatus such as centrifuge, hot plate, ovens, stirrer, mechanical shakers, circulator bath, thermometers, Bunsen burners, etc… •Use, maintain and calibrate pH meter with pertinent probes and electrodes. •Perform gravimetric, volumetric, titrimetric (acid/base, complex formation, ox-reduction) analysis as per Pharmacopeia or house method. •Analyze samples using IR, UV, Polarimeter and Flame Spectrophotometers, TLC technique according to House or Pharmacopial methods. Also calibrate and maintain these instruments when necessary. •Analyze sample for assay, content uniformity and dissolution using liquid chromatography methods. •Participate in training and development of new laboratory personnel. •Participate in writing and development of SOP’s related to operation and maintenance of laboratory equipment. •Participate in analysis of samples using gas chromatography. •Support transfer of information between different shifts. VERIFY INTEGRITY OF OTHER TECHNICIANS / ANALYSTS RESULTS. CONDITIONS AMBIANTES & ENVIRONNEMENT PHYSIQUE/ WORKING CONDITIONS & PHYSICAL ENVIRONMENT BENCH WORK IN LABORATORY, ABLE TO WORK UNDER PRESSURE TO MEET DEADLINES. CARACTÉRISTIQUES DU POSTE / JOB SPECIFICATIONS NIVEAU DE SCOLAIRTÉ & PERFECTIONNEMENT / EDUCATION & TRAINING DEC IN CHEMICAL TECHNOLOGY, TECHNIQUE CHIMIE OR CHIMIE ANALYTIQUE OR DEC CHIMIE-MICROBIOLOGY OR B.SC. IN CHEMISTRY OR BIOCHEMISTRY. EXPÉRIENCE / EXPERIENCE HABILETÉS, CONNAISSANCES & APTITUDES / SKILLS, KNOWLEDGE & ABILITIES : BILINGUAL, ORGANIZED, PRECISE, FAST AND FLEXIBLE. ABILITY TO WORK UNDER PRESSURE TO MEET DEADLINES; GOOD KNOWLEDGE OF MS OFFICE, GLP AND HPLC TECHNIQUES; ACQUINTANCE WITH HP CHEMSTATION IS AN ASSET. If you are interested ,please call: Groom & Associates Rana Mukhaimer Recruiter 514 288 3222 ext 328 r.mukhaimer@groomassocies.com ]]>

<![CDATA[Compliance Supervisor-Pharmacoeuticals Our client is a Montreal-based pharmaceutical company specializing in the manufacturing and distribution of products in Canada and worldwide. They are currently seeking a Complaince Supervisor. This person will be responsible for the supervision of the employees within the department. Manage and perform, according to an established schedule, self-inspections, external audits of suppliers and sub-contractors and audits by regulatory agencies and clients. Perform activities related to compliance. Manage special projects for compliance. The ideal candidate has a Bachelor's degree in Sciences (Chemistry, Biochemistry, Pharmacy, Chemical Engineering along with minimum five (5) years in the pharmaceutical industry where two (2) were in auditing of pharmaceutical firms; having done foreign audits is an asset. Knowledge of the Canadian, American and European regulations for the pharmaceutical industry and for medical devices. Bilingual, leadership, good managing skills, dynamic. Once you choose to join the exciting team at this renowned company, you will be rewarded with a very competitive salary and full benefits. Apply today to mcouture@fuzehr.com. While we appreciate receiving your resumes, only the chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you. ]]>

<![CDATA[Do you have experience in the Food Industry? Or verifying the quality? Knowledge of basic laboratory techniques? The candidate will be mainly performing taste tests and common laboratory test of raw products (Physical, Chemical & Microbiological Testing). Maintaining HACCP plans and prerequisites, follow-up of dossiers, corrective actions and daily inspections, collecting and filing all necessary reports. A background in similar field and Food Science a definite asset Send your CV to Gerard through email: gerard.galang@randstad.ca or call 514.695.9556]]>

<![CDATA[Compliance Supervisor-Pharmaceutical Our client is a Montreal-based pharmaceutical company specializing in the manufacturing and distribution of products in Canada and worldwide. They are currently seeking a Complaince Supervisor. This person will be responsible for the supervision of the employees within the department. Manage and perform, according to an established schedule, self-inspections, external audits of suppliers and sub-contractors and audits by regulatory agencies and clients. Perform activities related to compliance. Manage special projects for compliance. The ideal candidate has a Bachelor's degree in Sciences (Chemistry, Biochemistry, Pharmacy, Chemical Engineering along with minimum five (5) years in the pharmaceutical industry where two (2) were in auditing of pharmaceutical firms; having done foreign audits is an asset. Knowledge of the Canadian, American and European regulations for the pharmaceutical industry and for medical devices. Bilingual, leadership, good managing skills, dynamic. Once you choose to join the exciting team at this renowned company, you will be rewarded with a very competitive salary and full benefits. Apply today to mcouture@fuzehr.com. While we appreciate receiving your resumes, only the chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you. ]]>