Posted 19 days ago
Quality control analyst
@ Groupe Parima Inc.
Saint-Laurent, Quebec
Overview
Groupe PARIMA, a contract development and manufacturing organization for non-sterile liquids, suspensions and semi-solid drug products, is hiring two Quality Control Analysts: one on weekday days (40 hours a week) and one on weekend shifts (Friday to Sunday, 12-hour days). The work is hands-on laboratory testing under GMP, including HPLC, titration, spectrophotometry and physical tests, with LIMS data entry and training of junior analysts.
Responsibilities:
- Perform chemical and physical analyses to GMP and company specifications
- Run HPLC, titration, spectrophotometry and physical tests
- Enter and review analytical results in the LIMS
- Maintain laboratory instruments, reagents and inventories
- Train junior analysts and take part in investigations
Requirements summary:
- Knowledge of USP and EP/BP pharmacopoeias
- Ability to work independently on analytical testing
- Understanding of GMP and laboratory health and safety rules
- Experience with HPLC and titration methods
Tools & skills
Source and dates
Job-board feed · jobillico
- Employer posting date
- 2026-10-19
- First seen by our source
- 2026-10-20
- Source record updated
- 2026-11-07
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Quality assurance |
| Hours per week | 40 |
| Schedule | day, weekends |
| Travel | air: none · ground: none |
| Work setting | Laboratory |
| Position | Sitting and standing |
| Physical demands | physical low · computer moderate |
Summary and details written by AI from the posting; the employer’s posting is the authority.
Groupe Parima Inc.
| Field | Value |
|---|---|
| Open jobs on Jobsy | 1 |
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/fr/
Quality Control Analyst
Two positions to fill:
- Day: Monday to Friday (40 hours per week)
- Weekend: Friday, Saturday and Sunday (12 hours per day)
The Quality Control Analyst...
Responsibilities:
- Independently perform chemical and physical analyses according to the established schedule, following Groupe Parima's specifications, methods, procedures and Good Manufacturing Practices (GMP).
- Participate in laboratory and instrument maintenance, reagent and inventory management, and the training of junior analysts.Work in compliance with health and safety rules and report health and safety risks to supervisors.
- Good knowledge of the USP and EP/BP Pharmacopoeias.
- Independently perform the following physical tests: pH, density, specific gravity, viscosity, deliverable volume, particle size, particle size distribution (PSD) and loss on drying.
- Independently perform assay tests by volumetric and automatic titration
- Independently perform UV-Visible spectrophotometer tests.
- Prepare mobile phases, diluents and dissolution media.
- Independently perform dissolution, assay and related substances tests by HPLC.
- Analyze results critically and with concern for compliance with the standards set by current procedures.
- Enter analytical results in the LIMS using sound judgment by comparing them with trend analyses.
- Ensure data integrity and quality in the QC laboratory.
- Assist and participate in the training of junior analysts.
- Perform maintenance or calibration of laboratory instruments used in physical tests.
- Help maintain inventories of reagents, solvents and consumables required for analyses or for the proper operation of the laboratory.
- Actively participate in laboratory investigations.
- Participate in laboratory problem solving and continuous improvement.
- Follow health and safety rules and report health and safety risks to supervisors.
- Occasionally cover certain senior analyst tasks based on operational needs.
- Any other tasks required for the proper operation of the laboratory.
Journal
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