Chemist I

Chemist I is an entrylevel position and is accountable to the Department Supervisor. The Chemist I is responsible for performing various analytical activities associated with incoming materials bulk finished products stability and complaints.

There are various functional areas within the chemistry laboratory to which a Chemist I will be assigned. In addition to the general responsibilities the Chemist I will be assigned a focus area as outlined below. Note that while a person may be predominantly involved in one specific area crosstraining may be performed as needed to support other areas.

GENERAL RESPONSIBILITIES:

• Completes testing in accordance with internal policies procedures and specifications.
• Reviews testing performed by other analysts as needed.
• Maintains and calibrates laboratory equipment.
• Provides support during internal and external audits as required.
• Follows GMP and regulatory requirements and ensures quality standards are met.
• Notifies management of deviations out of trend suspect or out of specification results in a timely manner and participates in investigations as necessary.
• Observes and supports all safety guidelines and regulations.
• Demonstrates the Company Mission Vision and Values Statements policies and current standard business practices.
• Performs other related duties as assigned.

FOCUS AREA BULK/FINISHED PRODUCT/COMPLAINTS

• Performs chemical and functionality testing for commercial drug product samples including bulk in process finished product and complaints.
• Completes testing of nonroutine samples related to special studies investigations validation etc.

FOCUS AREA RAW MATERIALS

• Performs chemical testing of commercial raw materials including excipients and APIs as well as some operating supplies (e.g. disinfectants).
• Testing is performed using internal methods or various compendia (USP EP FCC)

FOCUS AREA COMPONENTS/OPERATING SUPPLIES/IMPORTED FINISHED PRODUCTS

• Performs testing of incoming materials used by Production for commercial products:
  • Primary Components e.g. product contact items such as cartridges plungers caps plastic bottles
  • Printed Materials e.g. printed cartons inserts box end labels cartridge labels
  • Operating Supplies e.g. filters tubing sterile materials
  • Secondary Components e.g. backing paper PVC film
  • Devices e.g. auto injectors
• Completes verification testing of Imported Finished Products prior to shipping.

FOCUS AREA STABILITY AND ANALYTICAL SERVICES

• Performs testing of stability samples for both commercial and noncommercial products using equipment such as HPLC UPLC ICPOES GC Ion chromatograph Optical comparator and other wet chemistry techniques.
• Performs testing of raw materials components and other incoming items needed for development or other noncommercial purposes.
• Completes testing of nonroutine samples related to special studies e.g. bulk hold studies cleaning validation and process validation samples.
• Performs Technology Transfer for analytical methods from CDMO and R&D labs to Stability and Analytical Services department.

Education

• Degree or diploma in Chemistry or related discipline.

Experience

• One to two years of experience in pharmaceutical or related industry is an asset.
• Strong attention to detail.
• Proven analytical skills with the ability to solve problems.
• Proficient time management skills with the ability to manage multiple priorities.
• Ability to work in a selfdirected team environment.
• Proficiency with Microsoft Office application especially Excel.
• Experience with Empower and LIMS is an asset.

What we offer:

• Excellent compensation/benefits package.
• Bonus and reward programs
• Discounted gym memberships
• Programs supporting work life balance
• Employee recognition program
• Professional and personal development programs
• Social events and spirit days

We are committed to diversity and inclusion and thank all applicants in advance; however we will be corresponding only with those selected for an interview.

In accordance with the Ontario Human Rights Code and the Accessibility for Ontarians with Disabilities Act we are committed to providing an inclusive and barrier free recruitment and selection process.

Recruitment Fraud please be aware of recruitment fraud. Novocol Pharmaceutical of Canada Inc. will never ask for banking information money or any personal information up front. We will only respond to official applications submitted through our careers site. In addition we will only use official corporate email addresses or to communicate with applicants. Should you be contacted without submitting an application please delete the message and advise your email provider.

Internal Job Posting Grade 7. The due date for internal applicants to apply for this role is May 5. 2025.