Quality Control Chemist - Mississauga, Canada - Bora Pharmaceutical Services

Bora Pharmaceutical Services

Verified Company

Mississauga, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Location:

Mississauga, ON
Date Posted:
6/12/2024
Job Number:
JO Bora Pharmaceuticals is focused on developing and manufacturing branded, generic and over the counter (OTC) healthcare and pharmaceutical products for patients around the globe. At Bora Pharmaceuticals, we see it as our mission and our duty to make our mutual success more certain. As an ambitious, futurefocused company, we know better than most that our own success is shaped by our partners victories. At Bora, we insist on high quality, reliability, and efficiency without any compromises. Dedication to these high standards is how we create a longlasting company culture that is the bedrock for our growth.

We cover the entire pharmaceutical supply chain from research and development to sales and distribution. We focus on manufacturing and selling generic, brand, and over-the-counter (OTC) drugs to clients around the world.

Why join Bora?

Competitive salary
A modern and stateoftheart facility
An onsite cafeteria with dedicated chefs
Onsite gym and basketball court

TITLE:
QC Chemist

DEPARTMENT:
Quality Control

POSITION REPORTING TO:
QC Supervisors in Chemistry (Incoming Goods / Finished Goods)

EMPLOYMENT TYPE:
Permanent Full-Time

General Description:

Perform chemical analyses on Incoming Goods and or Finished Goods in accordance with local analytical methods or pharmacopeial monographs.

Responsibilities:

Utilize analytical expertise in chemical and instrumental analysis (eg 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.

Qualifications:

Experience and Skills

12 years of quality Control experience in pharmaceutical laboratory environment or TIPT or equivalent diploma.
Good theoretical and practical knowledge of instrumental techniques and 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.

Education

Required: