Chemist, R&d (qc)

Mississauga, ON, CA, Canada

Job Description

Overview



Candoo Pharmatech is seeking a dedicated and detail-oriented

Quality Control Chemist

to join our dynamic team. In this role, you will provide analytical support for the development of new drug products across various dosage forms. The ideal candidate will perform analytical testing, maintain accurate documentation, ensure compliance with GMP standards, and contribute to the continued success of our R&D and manufacturing operations.

Key Responsibilities



Perform

release, in-process, and stability testing

using analytical techniques such as FTIR, KF titration, dissolution, and HPLC assay, in accordance with established methods and SOPs. Conduct

purified water monitoring

and

cleaning validation

analyses using a TOC analyzer. Perform

daily verification and calibration

of laboratory instruments and assist with annual calibrations per SOP requirements. Load and pull

stability samples

as assigned, following approved procedures. Coordinate with equipment service vendors for

preventive maintenance and calibration

, maintaining proper documentation for audit purposes. Document all experimental data in compliance with

Good Documentation Practices (GDP)

. Report

unexpected or Out of Specification (OOS)

results immediately to the Manager, assist in laboratory investigations, and complete CAPA as required. Prepare

raw data packages

and

OpenLab reports

for clients as needed. Summarize analytical results and prepare

technical reports

as assigned. Properly

collect and dispose of laboratory waste

according to company policy. Maintain a

clean, organized, and audit-ready

laboratory environment, ensuring compliance with applicable SOPs, regulations, and safety standards. Support

internal, client, and regulatory audits

. Perform other related duties as assigned.

Qualifications



Bachelor's degree in

Analytical Chemistry, Chemistry, Pharmaceutical Science

, or a related discipline. Minimum

1 year of experience

in analytical R&D or quality control within the

pharmaceutical industry

. Hands-on experience with analytical instruments such as

HPLC, GC, Dissolution Apparatus, TOC, FTIR, UV, and KF

is a strong asset. Solid understanding of

cGMP, regulatory compliance

, and

laboratory safety standards

.

Self-motivated

, detail-oriented, and adaptable to a

fast-paced, growth-oriented

environment. Strong

written and verbal communication skills

in English. Excellent

organizational and report-writing

abilities.

About Candoo Pharmatech



Candoo Pharmatech Company Inc. is a rapidly growing

Contract Development and Manufacturing Organization (CDMO)

specializing in advanced drug delivery and formulation development. We focus on high-technical-barrier and difficult-to-formulate

solid, semi-solid, and liquid dosage forms

. Located in the heart of Mississauga's pharmaceutical business park, our state-of-the-art facility supports our mission to develop

high-quality, affordable medicines

through innovative technology and strong industry partnerships.

At Candoo Pharmatech, we are committed to fostering an

inclusive and accessible work environment

where all employees feel valued, respected, and supported.

Job Types: Full-time, Permanent

Pay: $42,000.00-$60,000.00 per year

Benefits:

Dental care Extended health care On-site parking Paid time off RRSP match Vision care
Work Location: In person

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Job Detail

  • Job Id
    JD3068041
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Mississauga, ON, CA, Canada
  • Education
    Not mentioned