QC Analyst II - Full Time (10 Hours Shift)

Bimeda, Inc.; Cambridge; On-site; CAD 50,000 - 80,000; Full time

Job summary

An established industry player in veterinary pharmaceuticals is seeking a QC Analyst II to join their dynamic team. In this pivotal role, you will analyze raw materials and finished products using advanced analytical techniques, ensuring compliance with stringent quality standards. Your expertise in HPLC, GC, and other instrumentation will be essential in maintaining the integrity of the Stability Program. This is a fantastic opportunity to contribute to a company that values quality and innovation, while working collaboratively with a talented team. If you have a passion for analytical chemistry and a commitment to excellence, this position is perfect for you.

Qualifications

• 3-5 years of experience in a pharmaceutical analytical testing lab.
• Experience with wet chemistry methods and equipment.

Responsibilities

• Conducting physical and chemical testing of raw materials and stability samples.
• Reviewing data and ensuring compliance with safety policies and SOPs.
• Training and guiding junior analysts.

Skills

Analytical thinking

Problem-solving skills

Attention to detail

Collaboration

Adaptability

Education

B.Sc. in Chemistry

B.Sc. in Biochemistry

Tools

HPLC

GC

UV

IR

FTIR

KF

Job description

QC Analyst II - Full Time (10 Hours Shift)

Reporting to the Quality Control Project Lead, the QC Analyst II is responsible for analyzing raw materials, in-process, finished products, and stability samples using various wet chemistry and instrumentation techniques to ensure compliance with cGMP, SOPs, and Bimeda quality standards. This position also supports the Stability Program and is experienced with laboratory equipment, troubleshooting instrumentation issues, and guiding junior QC Analysts.

Shift Availability: Friday - Saturday - Sunday - Monday: 10 Hours

Responsibilities include but are not limited to:

1. Conducting physical and chemical testing of raw materials, in-process samples, finished products, gases, water, and stability samples (e.g., pH, conductivity, TOC, viscosity, potency, impurities).
2. Reviewing data, results, and documentation for QC analytical testing.
3. Ensuring all work complies with safety policies, GMP/GLP, and SOPs.
4. Preparing samples for analysis according to methods, SOPs, and compendia (USP/EP).
5. Performing analytical tests using HPLC, GC, UV, IR, FTIR, KF, and other instruments.
6. Documenting test results in logbooks and production dockets.
7. Analyzing data and informing supervisors of discrepancies, deviations, OOS data, and trends.
8. Assisting with quality investigations.
9. Replenishing reagents and supplies, informing supervisors or preparing PO requisitions.
10. Calibrating equipment, troubleshooting issues, and arranging repairs.
11. Training and guiding junior analysts.
12. Maintaining clean work areas and cleaning glassware.
13. Performing other duties as assigned.

Requirements:

• 3-5 years of experience in a pharmaceutical analytical testing lab supporting stability programs.
• B.Sc. in Chemistry, Biochemistry, or related discipline.
• Experience with wet chemistry methods and equipment such as titration, pH, potency, conductivity, viscosity, TOC, UV, IR, GC, HPLC.

Core Behaviors, Skills & Abilities:

• Thoroughness and attention to detail.
• Integrity and personal credibility.
• Analytical thinking and problem-solving skills.
• Change agility and adaptability.
• Collaboration and teamwork skills.

About Bimeda:

Bimeda is a global leader in veterinary pharmaceuticals and animal health products, with over 50 years of experience. The company operates R&D centers worldwide and has manufacturing facilities across multiple continents, producing a broad range of animal health products. Bimeda focuses on quality, innovation, and global presence, serving markets in over eighty countries.

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