1 meilleure offre (research analyst (contract), ancaster, on) (à pourvoir)

QC Analyst
AtomVie Global Radiopharma Inc. —Hamilton, ON
- À partir de 60 000 $ par an
- Fins de semaine au besoin
- Microsoft Excel
- Port de charges lourdes
- Anglais
- Assurance Dentaire
- Programme d'Aide aux Employés
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QC Analyst

AtomVie Global Radiopharma Inc.
Hamilton, ON

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Détails du poste

Temps plein

Avantages

Cotisation égale au RÉER
Assurance Dentaire
Programme d'Aide aux Employés

Compétences

Microsoft Excel
Port de charges lourdes
Anglais
Baccalauréat
Chimie
Diplôme d'études collégiales (hors Québec)
Compétences en communication

Description complète du poste

AtomVie Global Radiopharma Inc. is a global leading GMP manufacturer and distributer of clinical and commercial radiopharmaceuticals. We work with our partners to transform patients’ lives by advancing high quality drugs for the treatment and diagnosis of diseases.

We are a community that challenges ourselves professionally, takes pride in what we can accomplish together and values the impact we can make with our partners and patients across the globe. Start your career with AtomVie today and help us achieve our vision: to transform lives by revolutionizing healthcare.

About the Role

As a QC Analyst, you will be responsible for working in accordance with company policies and within GMPs while contributing your technical expertise to support current products and develop future drugs within the AtomVie portfolio.

This posting is for an existing vacancy to support the expansion of the company.

Location: AtomVie Global Radiopharma Inc, Hamilton ON (Onsite)

What You Will Do

Perform quality control (release & retrospective) testing of finished drug products, raw materials and in-processing testing according to standard testing methods (STMs) which may either be compendial or developed/validated in-house; technique areas include analytical chemistry, biology and microbiology.
Conduct all work in accordance with AtomVie Standard Operating Procedures (SOPs) and raise any deviations immediately to the attention of Lab Management and Quality Assurance. Report testing failure and non-conformances (both orally and in written), assist in conducting investigations and implement corrective actions with supervision.
Proper documentation of analytical data and information.
Write technical documents (e.g. generate Certificate of analysis, test reports, data summaries, etc.).
Perform calibration/maintenance of fundamental lab equipment.
Responsible for maintaining inventory of analytical reagents, critical material, reference standard and laboratory consumables.
Responsible for maintenance of documentation to fulfill applicable regulatory requirements relating to nuclear safety (e.g. radioactive material transfer forms).
Responsible for the housekeeping in accordance with AtomVie Standard Operating Procedures (SOPs).
Coordinate quality control (release &retrospective) testing of drug substances with contract laboratories or contract research organizations according to standard testing procedures, USP or EP.
Plan, implement, and successfully complete assigned tasks in a timely fashion ensuring consistent high quality.
Liaises with higher level laboratory personnel to learn the use of all applicable physical & chemical testing equipment and to acquire a fundamental understanding of departmental and regulatory practices.
Assist in training of other colleagues.
Ensure compliance with Health and Safety for all policies, procedures and regulations applicable to their work.
Adhere to Canadian Nuclear Safety Commission.
Adhere to GMP regulations.
Complete all other related duties assigned.

What You Bring to the Role

Basic understanding and ability to follow test methods/SOPs/compendia and Certificates of Analysis.
Ability to make routine decisions around simple task priorities but governed strictly in their work by SOPs. Typically seeks the input of higher-level team members in non-routine matters.
Ability to work in a safe manner collaborating as a team member to achieve all outcomes.

Requirements

College Diploma or B.Sc. in Chemistry, Biotechnology, or a related field.
1 to 3 years of related experience in analytical chemistry techniques such as HPLC, GC and TLC, microbiology tests such as Bacterial Endotoxins, and/or Biology tests such as IRF, ELISA and SDS-PAGE.
Proficiency with equipment data processing software such as Empower (Waters HPLC).
Proficiency with spreadsheets (e.g. Excel), word processing software (e.g. Word) and ability to write technical documents and reports.
Good communication skills (in English) and ability to work both independently and cooperatively in a team environment.
Experience in a pharmaceutical cGMP environment, experience in aseptic operations (use of a BSC - Biological Safety Cabinet) and working under Canadian Nuclear Safety Commission regulations are assets in this role.
This position requires shift work and alternating weekends.
Ability to lift and move heavy weights up to 23 kilograms is required.

Compensation:

Annual salary starts at $60,000. Compensation is based on relevant industry experience, academic credentials, and qualifications.

AtomVie Offers

Group Health & Dental Benefits (from day 1)
RRSP Matching Program
Perkopolis
Employee Assistance and Wellness Programs
Parking Allowance

AtomVie does not use artificial intelligence or automated decision-making tools in any part of the recruitment, screening, or selection process.

We are committed to fostering a workplace that values diversity, equity, and inclusion. We believe that a diverse and inclusive workforce enhances our ability to innovate, collaborate, and better serve our clients and patients. We thank you for considering a career with AtomVie. Only those candidates selected for an interview will be contacted. Accommodations are available upon request for candidates taking part in all aspects of the recruitment and selection process. We are dedicated to ensuring that every qualified applicant has an equal opportunity to thrive within our organization.

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