Qc Supervisor

3 weeks ago


Mississauga, Canada Candoo Pharmatech Company Inc Full time

**Position Overview**:
We are seeking a highly skilled and experienced Analytical QC Supervisor to join our team at Candoo Pharmatech Company Inc., a Contract Development and Manufacturing Organization (CDMO). As an Analytical QC Supervisor, you will be responsible for overseeing the analytical quality control activities within our organization. You will lead a team of analysts and ensure the timely and accurate testing of raw materials, intermediates, and finished products, following established procedures and regulatory requirements. Your expertise in analytical techniques and quality control processes will be instrumental in maintaining the highest standards of product quality and compliance.

**Key Responsibilities**:
**1.** **Supervision and Team Management**:

- Lead and manage a team of analytical chemists, providing guidance, training, and performance feedback.
- Plan and prioritize work assignments, ensuring efficient laboratory operations and adherence to timelines.
- Foster a collaborative and positive work environment, promoting continuous learning and professional development within the team.

**2.** **Analytical Testing and Quality Control**:

- Oversee the execution of analytical tests on raw materials, intermediates, and finished products using a variety of techniques such as HPLC, GC, dissolution, spectroscopy, and titration.
- Ensure compliance with established test methods, protocols, and specifications.
- Review and interpret test results, ensuring accuracy, completeness, and timely reporting.
- Investigate and resolve deviations or out-of-specification results, implementing appropriate corrective and preventive actions.

**3.** **Method Development and Validation**:

- Collaborate with the analytical development team to transfer and validate analytical methods for new products or processes.
- Participate in method development activities, optimizing and improving existing analytical methods.
- Ensure that analytical methods are validated according to regulatory requirements, industry guidelines, and internal standards.

**4.** **Compliance and Documentation**:

- Ensure all analytical activities are conducted in compliance with cGMP regulations, SOPs, and applicable guidelines.
- Maintain accurate and up-to-date laboratory documentation, including test records, reports, and laboratory notebooks.
- Participate in internal and external audits, providing support and addressing findings related to analytical quality control.

**5.** **Equipment and Instrumentation**:

- Oversee the maintenance, calibration, and qualification of analytical instruments and equipment.
- Collaborate with the instrument maintenance team to ensure the availability and reliability of analytical instruments.
- Evaluate new technologies and instrumentation, making recommendations for their implementation to enhance laboratory capabilities.

**Qualifications and Requirements**:

- Bachelor’s degree in Chemistry, Pharmaceutical Sciences, or related field; advanced degree preferred.
- Significant experience (5+ years) in a pharmaceutical or biopharmaceutical analytical laboratory, with a focus on quality control.
- Strong knowledge of analytical techniques such as HPLC, GC, dissolution, spectroscopy, and titration.
- Thorough understanding of cGMP regulations, regulatory guidelines (e.g., Health Canada, FDA, EMA), and industry best practices.
- Previous experience in a supervisory or team leadership role is preferred.
- Proven ability to effectively manage a team, prioritize tasks, and meet deadlines.
- Excellent problem-solving and decision-making skills, with the ability to troubleshoot and resolve analytical challenges.
- Proficient in data analysis, interpretation, and trending using statistical tools.
- Familiarity with laboratory information management systems (LIMS) software and electronic document management systems.
- Strong communication and interpersonal skills, with the ability to collaborate effectively across cross-functional teams.

Join our dynamic and innovative team at Candoo Pharmatech Company Inc. as a QC Supervisor (Analytical), and contribute to the successful development and commercialization of life-saving pharmaceutical products in a highly regulated environment.

**Benefits**:

- Company pension
- Dental care
- Extended health care
- On-site parking
- Paid time off
- RRSP match
- Vision care

Schedule:

- 8 hour shift
- Monday to Friday

Supplemental pay types:

- Bonus pay

Ability to commute/relocate:

- Mississauga, ON L5N 5L9: reliably commute or plan to relocate before starting work (required)

**Education**:

- Bachelor's Degree (required)

**Experience**:

- CDMO: 3 years (preferred)

Work Location: In person


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