QC Analyst I (Afternoon Shift) at Bimeda

Cambridge, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

20 Aug, 26

Salary

52000.0

Posted On

22 May, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical Testing, HPLC, GC, UV-Vis Spectroscopy, IR/FTIR, Wet Chemistry, Titration, pH Measurement, Conductivity Testing, Viscosity Testing, TOC Analysis, cGMP Compliance, SOP Adherence, Equipment Calibration, Data Analysis, Sample Preparation

Industry

Veterinary

Description

Job Title: QC Analyst I (Afternoon Shift) Location: Cambridge, ON (In-Office) Position Type: Full-time regular Shift: Afternoon Shift, Monday - Friday (3:00PM - 11:30PM) Vacancy Status: This role is currently vacant AI Disclosure in Hiring: We do not use artificial intelligence to screen, assess, or select applicants Job Summary Reporting to the QC Supervisor, the QC Analyst I is responsible for the analysis of raw materials, in-process, and finished product samples using various instrumental and analytical techniques while assuring compliance to cGMP, SOPs and Bimeda quality standards and requirements. Key Role Specific Requirements Conducts analytical (physical & chemical) testing of raw materials, in-process samples, finished products, gases and water. ie pH, Conductivity, TOC, Viscosity, Potency tests. Samples and performs identity testing on raw materials according to the schedule or as requested, utilizing approved sampling techniques for QC and Microbiology. Ensures that all work is carried out in compliance with company Safety Policies, Good Manufacturing Practices (GMP/GLP) and Standard Operating Procedures (SOPs). Prepares samples for analysis according to company SOPs & GLP methods. Performs specific analytical tests utilizing HPLC, GC, UV, IR, FTIR and other instruments. Analyzes data, keeps the supervisor informed of discrepancies, deviations, out of specifications (OOS) and unusual trends as they occur. Inform QC Supervisor to ensure that all reagents and supplies are replenished in a timely manner. Ensures work areas and glassware are kept clean and tidy. Conduct basic, daily equipment calibration. Troubleshoots minor issues and maintains equipment in good working order. Other duties as assigned. Please note that this job description is not exhaustive, and the role holder may be required to undertake other relevant duties commensurate with the grading of the post. Activities may be subject to amendment over time as the role develops and/or priorities and requirements evolve. What you bring to the role 1-2 years in a Pharmaceutical Analytical testing lab. Bachelor's degree in science, chemistry, biochemistry or other related field required. Analytical Wet Chemistry Lab experience using the following methods/equipment; titration, pH, Potency, Conductivity, Viscosity, TOC, UV, IR, GC, HPLC assays. High integrity, excellent attention to detail, analytical thinker, ability to organize and prioritize, and work in team environment. Excellent communication skills both verbally and written. Competencies Required for the Role INTEGRITY/PERSONAL CREDIBILITY – Demonstrated ability and concern that one be perceived as responsible, reliable and trustworthy. FOSTERING COLLABORATION/TEAMWORK- is the ability to work jointly with others or together especially in an intellectual endeavor; the ability and desire to work cooperatively with others on a team; as a team leader, the ability to demonstrate interest, skill, and success in getting groups to learn to work together. Builds partnerships for global performance. Respects others. INITIATIVE - Identifying what needs to be done and doing it before being asked or before the situation requires it. THOROUGHNESS/DETAIL ORIENTED – Ensuring that one’s own and others’ work ad information are complete and accurate; carefully preparing for meetings and presentations following up with others to ensure that agreements and commitments have been fulfilled. PLANNING – is the process of thinking about and organizing the activities required to achieve a desired goal. Compensation & Benefits: Competitive salary. 13 paid holidays. Competitive vacation policy effective upon hire. 5 paid personal care days. Employee Assistance Program. Expected Salary Range: $48,000K- $52,000K /Year About Bimeda Bimeda is a leading global innovator, manufacturer and marketer of veterinary pharmaceuticals and animal health products and has over half a century’s experience in providing science-driven solutions to optimize the health, wellbeing and productivity of the world’s animals. Bimeda’s global innovation program sees eight state-of-the art R&D centers across four continents collaborate on an enviable product development pipeline which anticipates the ever-evolving needs of the animal health industry. Bimeda’s nine manufacturing facilities across seven countries allow the company to manufacture a broad range of preventative, curative and nutritional products including sterile injectables, vaccinations, nutritional boluses, feed additives, tablets, water-soluble powders, pastes and non-sterile liquids. Globally, the company focuses on the development, manufacture and commercialization of quality Bimeda-branded products while also being the partner of choice for contract manufacturing and R&D services for prominent companies within the animal health industry. More info at www.bimedacareers.com Equal Opportunity & Accessibility At Bimeda we are committed to fostering an inclusive, barrier-free and accessible environment. Part of this commitment includes arranging accommodations to ensure an equitable opportunity to participate in the recruitment and selection process. If you require an accommodation, we will work with you to meet your needs. We are committed to an inclusive and accessible recruitment process. We are an equal-opportunity employer and assess candidates based on skills and experience. Recruitment records are retained in accordance with Ontario law.

Responsibilities

The QC Analyst I performs physical and chemical analysis of raw materials, in-process, and finished product samples. They ensure all testing complies with cGMP, SOPs, and quality standards while maintaining lab equipment and documenting results.