Quality Control Chemist (FTC)

Bora Pharmaceuticals•Mississauga, ON

12d•Onsite

About The Position

Bora Bora Pharmaceuticals is a premier international contract development and manufacturing organization (CDMO) specializing in formulation development, clinical and commercial manufacturing, and packaging of complex oral solid dose, liquid, semi-solid, biologics, and sterile injectable pharmaceutical products. From world-class sites in North America and Asia, Bora delivers drug products with unparalleled quality to more than 100 markets around the world. Bora’s teams, technologies, and facilities work seamlessly together to enable clients to deliver much-needed therapeutics to patients worldwide. At Bora Pharmaceuticals, the mission, duty, and responsibility are to make their success and their customer’s success more certain. This is a 12 months fixed term contract (FTC) position, reflecting a current, active, and approved vacancy. The role involves performing chemical analyses on Incoming Goods in accordance with local analytical methods or pharmacopeial monographs.

Requirements

1-2 years of quality Control experience in pharmaceutical laboratory environment or TIPT or equivalent diploma.
Good theoretical and practical knowledge of instrumental techniques.
Demonstrated computer proficiency in LIMs software (e.g., Labware), Empower, MS Word and MS Excel.
Demonstrated proficiency in basic analytical techniques.
Good knowledge of laboratory GMP and the Pharmacopoeias.
Minimum College diploma in Chemistry or a related scientific discipline.
Proficiency in MS Word and MS Excel.
Knowledge or experience in GMP environments.

Nice To Haves

University degree in Chemistry.

Responsibilities

Utilize analytical expertise in chemical and instrumental analysis (e.g. HPLC, GC, UV, IR) and wet chemistry measurement techniques.
Work collaboratively with team members to collectively deliver quality results of the highest accuracy and precision.
Maintain data integrity (ALCOA) and working with integrity.
Be an active agent for continuous improvement in Quality control.
Follow all safety policies, maintain a clean and orderly work area, and report any potentially unsafe conditions within the workplace.
Maintain laboratory systems and participate in projects as required.
Assist in investigations of OOS and OOT results.
May be required to approve packaging component specifications.
May be required to review and release products, raw materials & packaging components.