iData Research is a growing international market research firm, based in Vancouver. We specialize in market research for medical and pharmaceutical device markets, and have a 15 year history of serving some of the world’s largest medical device manufacturers.
We are currently looking to add to our expanding team of market research analysts, and seek motivated individuals who are ready to jump into a busy and interesting field.
iData analysts are involved with every aspect of the research and must be capable of conducting their own primary research - this means carrying out professional interviews in person and over the phone. Analysts must also tabulate results, analyze the collected data, and write comprehensive reports.
Our ideal candidates are self starters with superior writing and organizational skills. Our analysts are responsible for directing and managing their projects and have input into what areas of research are explored, so we need critical thinkers with an innovative side.
Minimum Applicant Requirements:
• Bachelor’s degree in commerce, science, or business
• Superior communication skills, both in writing and over the phone
• Background and/or experience in science/medicine is an asset, but not mandatory
• Strong sense of responsibility and adherence to deadlines
• Excellent organizational skills
• Excellent verbal English skills
Job Requirements:
• Primary phone research
• Deadline management
• Ability to multitask
• Ability to quickly learn new skills
• Analytical Capability
• Global perspective
Start Date: As soon as possible.
Salary is competitive and is commensurate with experience. To this is added full extended health including dental, eye-care, prescriptions and paramedics, as well as a substantial profit-sharing program, and a quickly rising career path to senior and management levels.
Apply via email; please list the job title in the subject line please send your resume, cover letter, and transcript. Only qualified candidates need apply.
The primary responsibility of the Regulatory Affairs Officer it to ensure that Flora’s ingredients, labels and marketing materials meet government regulations.
Job Description:
• Prepare regulatory submission documents (Natural Product Number, Drug Identity Number and Cosmetic Notification) in adherence to applicable acts and regulations for submission to Health Canada
• Manage activities associated with generating regulatory submissions, including identifying and sourcing submission content
• Manage and plan submission timelines and projects
• Facilitate regulatory approvals for DIN, NHP through effective communication and negotiation with government agencies
• Evaluate new guideline documents to determine impact on processes
• Manage and ensure maintenance of a positive and productive liaison with internal and external contacts, including regulatory agencies
• Develop and implement process change under the direction of regulatory management
• Identify issues that may delay product or project and recommend appropriate action
• Manage compliance related submissions and activities
• Establish and follow procedures to ensure that products conform to specifications, stability and regulatory requirements
• Maintain a detailed filing system for all applications
• Deal with annual notifications
• Review and approve product labels according to labelling regulations and approved marketing authorization
• Keep up to date on NHP and food regulations in Canada and provide detailed information when needed, including health claims
• Prepare and assist with international applications
• Provide periodic status reports to the QA Manager and other departments
• Conduct continued research to upgrade product claims
Requirements:
• A University Degree or Technical Diploma in related scientific field
• 1-3 years regulatory affairs experience
• Experience with natural health product submissions
• Strong leadership skills
• Excellent verbal and written communication skills
• Strong organizational skills including effective prioritization and follow-up
• Demonstrated ability to work independently as well as part of a team
• Strong proficiency with Excel, Word, Windows, Internet Explorer and Adobe
• Demonstrated ability to multi-task effectively
• Ability to deal with confidential information with a high degree of diplomacy
Production Responsibilities:
• Monitor facility, employees, production, and maintenance process to ensure safety and quality standards are met at all times. Assist Production Supervisor’s in monitoring production and trouble shooting problems that affect quality
• Set up and perform various kinds of tests on materials, parts, and products
• Verify daily implementation and monitoring of net weight and the metal detectors functionality
• Environmental monitoring and test food or raw materials to make sure they are free from contamination
• Accurate recording of all test data, evaluate findings, and write reports
• QC approval and release of finished skids and completion of necessary documentation
• Inspect plastic or mesh totes for cleanliness and/or acceptability prior to next use for blending purposes. Conduct required blend checks
• Conduct required taste tests per blend prior to dispensing while checking for quality and other requirements
GMP Monitoring & Receiving of Raw Materials:
• Responsible for monitoring and verifying the daily implementation of the requirements for GMP, Standard Sanitation Operation and HACCP Programs
• Receive and confirm quantity of shipment; comparing to purchase order, obtain certificate of analysis, specification sheet, allergen statements, and nutritional information for comparison
• Monitor and verify the internal requirements (packaging, labels, etc.)
• Perform daily sanitation check of plant and personnel
• Establish and review product stability test
• Evaluate new raw material based on R & D approved sample, prepare raw material evaluation form for each raw material, and update receiving log
• Prepare necessary documentation for warehouse purposes
Co-Packers
• Receive and confirm finished goods
• Capsules – evaluate samples and prepare for proper storage
• Single Serves – evaluate samples and prepare for proper storage and for distribution to Sales & Marketing
• Bars – evaluate samples and prepare for proper storage
• Reconcile returned packaging to packing slip and purchase order; update receiving log
• Prepare necessary documentation for warehouse
Knowledge, Skills, & Abilities:
• Graduate of a recognized Food Science Program, or minimum 2 year Technical Degree in Food Science
• Prior 2-5 years experience working in a Food Manufacturing environment
• Level 1 or 2 First Aid Certification an asset
• Strongly organized analytical thinker with ability to maintain keen attention to detail
• Ability to operate lab equipment and interpret data
• Ability to prepare reports and make product/method recommendations
• Advanced mathematical and/or scientific skills
• Excellent interpersonal and communication skills (both written and verbal)
• Strong computer skills in Microsoft Office, knowledge of BV an asset
• Adaptable to new technologies and open to updated skills training as required
Plan, design, and implement the evaluation of programs and curricula
- Conduct evaluability assessments, develop frameworks (e.g., develop logic models, conduct stakeholder analyses), identify evaluation questions, plan and apply mixed methods, develop protocols, adapt and/or develop measures, plan and execute analysis procedures, interpret results, disseminate findings and monitor uptake of recommendations.
- Develop, coordinate, and implement work plans for assigned evaluation activities and assigned tasks.
- Review and critique the program evaluation literature to contribute to development and application of new methodologies to evaluation studies.
- Conduct literature reviews to ensure evaluation plans are based on best practices in the field and prepare evaluation reports, contribute to annual reports and other public documents related to evaluation activities.
- Prepare and implement communication plans to guide dissemination of evaluation findings to stakeholders.
- Following existing protocol for qualitative and quantitative data analyses, execute data analyses and preparation of both statistical and qualitative reports from various data sources.
- Utilizing existing frameworks to implement evaluation activities in compliance with ethical requirements.
- Prepare and deliver presentations for scientific, professional, and lay meetings, as well as meetings for decision-makers.
- Write and submit articles for publication
- Assist in preparing grant proposals and applications for external funding.
QUALIFICATIONS:
Education:
Minimum Master's degree required in education, health or social sciences
Experience:
A minimum of six years of relevant experience, including three years of professional experience in program evaluation. Familiarity with medical education and health services an asset. Experience in qualitative and quantitative research/evaluation methods required.. Computer experience and competency with Microsoft Office and statistical packages (e.g., SPSS, SAS, XSight) is required.
Skills:
- Skills in quantitative and qualitative research and evaluation, as well as analysis and interpretation of data.
- Strong communication and organizational skills learned from operating in a team environment.
- Proven ability to work under pressure, meet difficult deadlines, set priorities, and multi-task.
- Ability to review, critique and synthesize evaluation studies literature.
- High level of initiative, self-directedness, and ability to work independently.
- Effective oral and written communication, presentation, and interpersonal skills.
- Ability to work in a confidential environment.
- Meticulous attention to detail.
- Ability to travel as required.
COMPENSATION:
- 59-70K contingent on experience
- Benefits
If you are interested in this position, please apply online using the www.miles.ca application form and quote job reference number 9365.
If you have recently been interviewed by a Miles consultant, please send an email to info@miles.ca with the job number in the subject line.
We thank all applicants for their interest, however, only those selected for an interview will be contacted.
iData Research is a growing international market research firm, based in Vancouver. We specialize in market research for medical and pharmaceutical device markets, and have a 15 year history of serving some of the world’s largest medical device manufacturers.
We are currently looking to add several members to our expanding team of market research analysts, and seek motivated individuals who are ready to jump into a busy and interesting field.
iData analysts are involved with every aspect of the research and must be capable of conducting their own primary research - this means carrying out professional interviews in person and over the phone. Analysts must also tabulate results, analyze the collected data, and write comprehensive reports.
Our ideal candidates are self starters with superior writing and organizational skills. Our analysts are responsible for directing and managing their projects and have input into what areas of research are explored, so we need critical thinkers with an innovative side.
Minimum Applicant Requirements:
• Bachelor’s degree in commerce, science, or business
• Superior communication skills, both in writing and over the phone
• Background and/or experience in science/medicine is an asset, but not mandatory
• Strong sense of responsibility and adherence to deadlines
• Excellent organizational skills
• Excellent verbal English skills
Job Requirements:
• Primary phone research
• Deadline management
• Ability to multitask
• Ability to quickly learn new skills
• Analytical Capability
• Global perspective
Start Date: As soon as possible.
This is an entry-level position with a salary between $40,000 - $50,000 depending on performance on the first project. To this is added full extended health including dental, eye-care, prescriptions and paramedics, as well as a substantial profit-sharing program, and a quickly rising career path to senior and management levels.
Apply via email; please list the job title in the subject line please send your resume, cover letter, and transcript. Only qualified candidates need apply.
Responsibilities:
* Support HACCP coordinator and Production to ensure food safety compliance
* Initiate shelf life studies on new products
* Support production in developing & Implementing SOP
* Review all microbiological results and follow up on corrective action plan
* Interact with all employees on any quality issues, policy changes and general info that might impact their jobs and customers
Requirements:
* Diploma in Technology or BSC in Microbiology or Food Science, or equivalent experience.
* 3+ years experience in a QA Program
* Microbiological Experience, swabbing, pour plate and identification with differential media
* Fluent written and verbal in English, able to speak Mandarin, Punjabi or Tagalog an asset.
* Flexible time and able to work varying shifts including Days, Evenings and weekends.
* Ability to work with people and resolve problems, but to enforce Quality standards.
* Good Problem Solving Skills
* Experience with training people of varying technical levels.
* Adaptable and able to work in a fast paced environment, able to see the entire picture.
* Good time management skills, ability to prioritize
* Able to work in a group setting or alone.
* Detail oriented and able to document effectively.
* Previous HACCP experience and asset.
* Able to audit HACCP program and GMP’s.
* Able to create, maintain and update SOP’s, SOP’s HACCP and GMP programs and documentation.
* Auditing experience an asset.
In its first decade of operations, Viva Pharmaceutical’s facilities have grown to cover a total land area of some 73,000 square feet and total plant area of more than 52,000 square feet. As such, Viva has become the biggest GMP-certified pharmaceutical and natural health food products manufacturer in British Columbia. Through constant improvement of its facilities over the years, Viva now has advanced manufacturing equipment in all stages of production.
Job Title: Quality Control Manager
Starting Date: ASAP
Job Type: Full Time
Salary: To Be Negotiated
Responsibilities:
- Direct and lead the QC team to perform routine chemical and physical testing of pharmaceutical and nutraceutical materials/ingredients, formulation and finished products;
- Ensure all analytical results and documentations are generated of high quality in a timely fashion;
- Participate in Analytical Investigations of OOS (out-of-specification), examine results, change control requests when necessary, generate deviation reports and root cause determination and provide recommendation for corrective actions;
- Ensure compliance with GMP regulations as required by Health Canada and FDA in order to obtain GMP Establishment License renewal, assist in Internal GMP and 3rd party Audit;
- Review and approve certificates of analysis, stability summary reports, calibration reports, analytical monographs, master batch records and packaging records in compliance with GMP regulatory and customer requirements;
- Develop and update policies and SOPs related to GMP regulations;
- Work with manufacturers and suppliers to address regulatory concerns to approved specifications and maintain compliance with regulatory submissions;
- Provide assistance and technical support for equipment or process optimization, validation, calibration, qualification or certification;
- Provide GMP, safety and WHMIS trainings to laboratory staff; and
- Participate in other tasks that may be assigned by the President when required.
Qualifications:
- A B.Sc. degree in an applicable discipline of science (chemistry, biochemistry, biology or related) or specific medical training (pharmacology, pharmacokinetics, nutritional research or related);
- Three or more years of QC experience in the pharmaceutical or nutraceutical related industry;
- Advanced knowledge of GMP and FDA regulations for manufacturing pharmaceutical or nutraceutical products;
- Familiarity with lab equipments (HPLC, GC, AA) and instruments; and
- Proven ability to supervise personnel and excellent verbal/written communication skills.
In its first decade of operations, Viva Pharmaceutical’s facilities have grown to cover a total land area of some 73,000 square feet and total plant area of more than 52,000 square feet. As such, Viva has become the biggest GMP-certified pharmaceutical and natural health food products manufacturer in British Columbia. Through constant improvement of its facilities over the years, Viva now has advanced manufacturing equipment in all stages of production.
Job Title: R&D Lab Assistant
Job Type: Full Time, Permanent
Job Duties:
- Assist research scientists on various projects;
- Perform herb extraction;
- Assist in formulation;
- Perform chemical analysis; and
- Participate in other tasks that may be assigned by the supervisor.
Qualifications:
- Completion of university in an applicable discipline of science (chemistry, biochemistry or related);
- Familiarity with lab equipments and instruments is an asset;
- Detail oriented;
- Ability to work efficiently in fast-paced, multi-tasking environment;
- Knowledge of GMP and/or GLP is definitely an asset;
- New grads are welcomed to apply.
Compensation:
- To be negotiated
- Group benefit available
The Assistant Marketing Manager position is a new position within the company and is being created to take existing product promotion projects and adapt them to ongoing marketing operations, to manage these operations, as well as identify, implement, and monitor effective new revenue generating measures.
The position is a 'hands-on', implementation-oriented position as opposed to being conceptual in nature (e.g., market research, marketing plan development, etc.), and therefore requires a strong background in the biomedical field and an applicable talent in the marketing communications field. If you meet the following criteria, we welcome you to submit your application for consideration:
All applicants are expected to have excellent written and spoken English and proficiency in creative and/or marketing writing. Proficiency in a second language, including Mandarin Chinese, French, or Spanish is an asset.
Applicants must possess one or more of the following skill-sets:
- Working experience with graphic design and publishing (Development and distribution of marketing materials; must be accompanied by strong effective written communications skills)
- Working experience with internet advertising and website programming (Development of a strong internet presence)
- Working experience with public relations and/or direct sales (External visits to potential clients; contract negotiations, establishing classes and workshops, handling of media and other PR matters)
Our company prides itself in innovation, adaptability, and flexibility, and provides dedicated, hard-working, and talented individuals the opportunity to expand their careers to achieve the best of their abilities.
The position is part-time to start, moving to a full-time annual salary basis. The successful applicant will enter a probationary period of up to 3 months before consideration for a full-time position.
Reporting to the Bioinformatics Team Leader or designate, your typical duties will include the following.
* Participation in genomic analyses within a high throughput sequencing facility
* Maintenance, improvement, development and documentation of analysis software and databases
* Analysis and annotation of data from genome and transcriptome sequencing projects
* Reporting research methods and results in meetings and seminars
* Contribution to scientific publications
The ideal candidate should possess a PhD degree and recent proven experience in bioinformatics or computational biology. A strong publication record in the field of bioinformatics is highly desirable.
The Rotary Hearing Clinic at Providence Health Care Research Institute is seeking a Research Coordinator to perform a variety of activities involved in planning, coordinating and conducting research studies in the areas of Otology & Neurotology (ear and hearing disorders), Sinonasal disorders and Head and Neck disorders. Duties include patient recruitment, screening, database management and online Research Ethics Board submissions. The successful applicant will report to Dr’s. Robert Irvine and Brian Westerberg.
Work Performed
* Development of disease-specific quality of life questionnaire for patients (for instance for patients with vestibular schwannomas and for patients with benign thyroid disease).
* Development of prospective computerized database of outcomes of patients with otolaryngology disorders.
* Oversees progress of research projects, including facilitating role of medical students and residents in projects.
* Performs systematic reviews of the literature in preparation for research ethics and grant applications, and helps in writing same applications.
* Schedules research subjects and keeps account of ongoing subject involvement in projects.
* Designs, modifies and performs complex experiments and systems and/or uses technically advanced procedures and conducts complex analysis and interpretation.
* Develops and writes novel protocols and safety procedures.
* Troubleshoots equipment and systems problems.
* Manages and oversees the daily operations and finances of a laboratory or technical operation for a department, including responsibility for budget, large purchase recommendations, inventory, forecasting and maintenance of financial reports, administration of staff.
* Develops operating procedures and makes recommendation on workflow improvements.
* Oversees the progress of projects and participates in complex research activities.
* Provides instruction and training in the use of specialized techniques and equipment.
* Writes reports and assists in writing ethics and grant applications.
* Supervises, schedules and trains staff and may make recommendations with respect to hiring and providing input into staff performance.
* Operates and maintains highly specialized equipment requiring extensive training.
* Carries out any other related duties as required in keeping with the qualifications and requirements of positions in this classification.
Supervision Received
Will work under minimum supervision, receiving specific instructions only on unusual problems or on matters which depart significantly from established policy and procedure; will be responsible for coordinating regular meetings of the research team to ensure suitable progress of research projects.
Supervision Given
Will have supervisory responsibilities for medical students and residents involved in projects, and may have input into staff selection and performance evaluation.
Qualifications
Completion of a university degree in a relevant discipline or technical program and a minimum of four years of related experience or an equivalent combination of education and experience. Must be proficient in patient interview techniques, research subject counseling, database management and online Research Ethics Board submissions. Ability to work both independently and within a team environment.
Please submit your cover letter and resume by 9AM November 12, 2009 to e-mail address above.
Location:
North Vancouver, British Columbia (1 vacancy)
Skill Requirements:
Education:
Completion of high school
Credentials (certificates, licences, memberships, courses, etc.):
Not applicable
Experience:
No experience
Languages:
Speak English, Read English, Write English
Specific Skills:
Supervise, co-ordinate and schedule activities, Identify, investigate, correct and document potential environmental and safety problems, Establish work schedules, Co-ordinate work activities with other units, Recommend measures to improve productivity and product quality, Provide information for maintenance plans to ensure that maintenance and production objectives are met
Additional Skills:
Recommend personnel actions such as hiring and promotions, Train staff in job duties, safety procedures and company policies, Prepare production and other reports
Work Conditions and Physical Capabilities:
Attention to detail
Ability to Supervise:
10 people or less
Essential Skills:
Reading text, Document use, Numeracy, Writing, Oral communication, Working with others, Problem solving, Decision making, Critical thinking, Job task planning and organizing, Significant use of memory, Finding information, Computer use, Continuous learning
*Responsibilities will include, but are not limited to, the following activities:*
• The successful candidate will be independent in project planning and design.
• Select, lead and direct a research team to conduct the research projects
• Develop a safe and effective lentiviral siRNA system for potential medical applications and treatment options.
*To be successful in this role, you will have the following qualifications and experience:*
• Either a M.Sc. or a Ph.D. with a degree in the life sciences
• An additional medical degree will be a significant asset
• Ability to work in a dynamic, fast-paced, team environment
• Proficient technical skills in qPCR and genetic engineering
• Experience in recombinant viral vectors, siRNA expression, and recombinant DNA technology is required
- Experience in diagnostic assays is a plus
Reporting to the General Manager of Centerplate at BC Place Stadium, this individual will be responsible to ensure the strict adherence of food safety sanitation laws, regulations and standards governing the production, processing, storage, transportation and sale of food and related products.
Given the nature of this position, the successful applicant must have a working knowledge of the principles of food production, storage handling and distribution in relationship to local and federal laws and regulations. The applicant must have experience with official inspections, sampling, reporting methods, techniques and practices. The individual will evaluate safety risks, take appropriate steps to ensure that procedures are in place and that all personnel are trained in the necessary systems and workplace requirements. The ability to implement strict workplace standards and critical controls is required. The individual must a strong leader, be administratively strong, have good analytical skills, be detail oriented and have proven experience working within a large operation in a similar capacity. An excellent command of the English language is required and the ability to speak other languages is welcomed.
This is a newly created position and this individual will be instrumental in leading the food safety component of our operation throughout all Olympic related activities.
If you are interested in discussing this position further, please provide a current and detailed resume along with copies of any related certificates to the address noted below. Please reference the position title, posting number and your salary requirements in the subject line of your cover letter. We thank all applicants for their interest in this opportunity but only those who are being considered for this position will be interviewed.
iData Research is a growing international market research firm, based in Vancouver. We specialize in market research for medical and pharmaceutical device markets, and have a 15 year history of serving some of the world’s largest medical device manufacturers.
We are currently looking to add to our expanding team of market research analysts, and seek motivated individuals who are ready to jump into a busy and interesting field.
iData analysts are involved with every aspect of the research and must be capable of conducting their own primary research - this means carrying out professional interviews in person and over the phone. Analysts must also tabulate results, analyze the collected data, and write comprehensive reports.
Our ideal candidates are self starters with superior writing and organizational skills. Our analysts are responsible for directing and managing their projects and have input into what areas of research are explored, so we need critical thinkers with an innovative side.
Minimum Applicant Requirements:
• Bachelor’s degree in commerce, science, or business
• Superior communication skills, both in writing and over the phone
• Background and/or experience in science/medicine is an asset, but not mandatory
• Strong sense of responsibility and adherence to deadlines
• Excellent organizational skills
• Excellent verbal English skills
Job Requirements:
• Primary phone research
• Deadline management
• Ability to multitask
• Ability to quickly learn new skills
• Analytical Capability
• Global perspective
Start Date: As soon as possible.
This is an entry-level position with a salary between $40,000 - $50,000 depending on performance on the first project. To this is added full extended health including dental, eye-care, prescriptions and paramedics, as well as a substantial profit-sharing program, and a quickly rising career path to senior and management levels.
In its first decade of operations, Viva Pharmaceutical’s facilities have grown to cover a total land area of some 73,000 square feet and total plant area of more than 52,000 square feet. As such, Viva has become the biggest GMP-certified pharmaceutical and natural health food products manufacturer in British Columbia. Through constant improvement of its facilities over the years, Viva now has advanced manufacturing equipment in all stages of production.
Job Title: Quality Control Manager
Starting Date: ASAP
Job Type: Full Time
Salary: To Be Negotiated
Responsibilities:
- Direct and lead the QC team to perform routine chemical and physical testing of pharmaceutical and nutraceutical materials/ingredients, formulation and finished products;
- Ensure all analytical results and documentations are generated of high quality in a timely fashion;
- Participate in Analytical Investigations of OOS (out-of-specification), examine results, change control requests when necessary, generate deviation reports and root cause determination and provide recommendation for corrective actions;
- Ensure compliance with GMP regulations as required by Health Canada and FDA in order to obtain GMP Establishment License renewal, assist in Internal GMP and 3rd party Audit;
- Review and approve certificates of analysis, stability summary reports, calibration reports, analytical monographs, master batch records and packaging records in compliance with GMP regulatory and customer requirements;
- Develop and update policies and SOPs related to GMP regulations;
- Work with manufacturers and suppliers to address regulatory concerns to approved specifications and maintain compliance with regulatory submissions;
- Provide assistance and technical support for equipment or process optimization, validation, calibration, qualification or certification;
- Provide GMP, safety and WHMIS trainings to laboratory staff; and
- Participate in other tasks that may be assigned by the President when required.
Qualifications:
- A B.Sc. degree in an applicable discipline of science (chemistry, biochemistry, biology or related) or specific medical training (pharmacology, pharmacokinetics, nutritional research or related);
- Three or more years of QC experience in the pharmaceutical or nutraceutical related industry;
- Advanced knowledge of GMP and FDA regulations for manufacturing pharmaceutical or nutraceutical products;
- Familiarity with lab equipments (HPLC, GC, AA) and instruments; and
- Proven ability to supervise personnel and excellent verbal/written communication skills.