Longueuil, Qc Chargé de travaux Jobs – 1 Openings This Week

QC Reviewer, LBA
Altasciences —Laval, QC
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Designated paid holidays
- Dental care
13d

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QC Reviewer, LBA

Altasciences
Laval, QC

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Job details

Full-time
13 days ago

Benefits

RRSP match
Designated paid holidays
Dental care
Paid vacation
Vision care

Skills

Microsoft Powerpoint
Microsoft Word
French
Biochemistry
Microsoft Excel
GLP
Microsoft Outlook
Equipment calibration
Document preparation
Personal protective equipment (PPE) use
Workplace safety policies
English
Quality Control
Written report writing
Chemistry
Standard operating procedures (SOPs)
Communication skills

Full job description

About The Role

Le/la Réviseur(se) contrôle qualité, LBA est chargé(e) d'effectuer les contrôles de qualité des données générées et des travaux réalisés au sein du laboratoire afin de garantir leur exactitude, leur conformité et le respect des normes applicables.

What You’ll Do Here

Ensure that all batch-related documentation is completed accurately and on time by the analysts, and that all procedures are followed in accordance with the company’s standard operating procedures (SOPs)
Conduct daily in-process quality control for batches currently being processed in the laboratory
Provide support in responding to quality assurance reports
Monitor quality within the laboratory in accordance with Good Laboratory Practice (GLP), regulatory requirements, and internal Standard Operating Procedures (SOPs)
Guide and supervise analysts in the laboratory’s daily documentation procedures and processes
Ensure that laboratory instrument calibration is performed in accordance with internal procedures.
Ensure consistency in techniques, processes, and documentation among laboratory analysts.
Report quality issues or trends to the line manager and participate in resolving them.
May be required to participate in laboratory inspections: identify and report nonconformities as well as any health and safety issues.
Based on their training, be able to draft study documents for review by the bioanalytical manager (BPI), such as notes for inclusion in the file, reports on deviations from standard operating procedures (SOPs), the protocol, or the study plan; perform quality control on batches by conducting trend analyses across multiple batches; and compile study documentation
Depending on their training, be able to provide reports and/or final results within the study’s specified deadlines, ensure that any deviations, exceptions, or events are properly documented, and ensure that all analyses performed are recorded and accurate for review by the principal investigator in bioanalysis
Contribute to the planning of sample analysis by meeting deadlines and honoring scheduling commitments.
Stay informed about standard operating procedures (SOPs), procedures, and techniques through training sessions, team meetings, and internal communication channels, and comply with all company guidelines and policies
Comply with health and safety standards regarding personal protective equipment, laboratory maintenance, and work procedures

What You’ll Need to Succeed

College degree in Chemistry, Biochemistry or Immunology or equivalent field.
Minimum of 2 years of experience in the medical and/or pharmaceutical fields
MS Word, Excel, Outlook and Power Point
Ability to read and interpret technical documents and industry specific manuals.
Ability to write advanced reports and correspondence.
Ability to speak effectively before groups of employees of the organization.
Bilingual proficiency in French may be required, depending on location.
Excellent verbal and written communication skills.
Well developed interpersonal skills are required.
Personal/professional integrity and proven discretion in handling confidential information.
Ability to develop strong trusting relationships in order to gain support and achieve results.
Capable of managing multiple conflicting priorities.
Must be self-directed, motivated, and have a willingness to take the initiative to identify and anticipate client needs and make recommendations for implementation.

Altasciences strives to provide a French work environment for its employees in Quebec. Altasciences has taken all reasonable measures to avoid imposing the above language requirement. This requirement is essential for the position of QC Reviewer, LBA in particular, but without limitation, for the following reason(s):

The requirement to have study protocols read and documented in English as required by industry regulatory agencies

What We Offer:

Altasciences offers a wide variety of benefits to help our employees live healthy and fulfilling lives both at and outside of work.

Altasciences' Benefits Package Includes:

Health/Dental/Vision Insurance Plans
401(k)/RRSP with Employer Match
Paid Vacation and Holidays
Paid Sick and Bereavement Leave

Altasciences' Incentive Programs Include:

Training & Development Programs
Employee Referral Bonus Program

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