Quality Control Analyst

1 week ago


PointeClaire, Quebec, Canada Capcium Full time

Benefits:


At Capcium, all our employees benefit at hire date from competitive compensation packages that include a comprehensive group insurance coverage (Life insurance, Accidental Death & Dismemberment (AD&D), Long Term Disability, Drugs, Extended Health Care, Dental, Vision, Travel, Health Spending Account (HSA), Online Doctors, Second Opinion), in addition to many support programs and resources through our Employee & Family Assistance Program (EFAP).

We also offer matching Group Registered Retirement Saving Plan (RRSP), Referral Reward, Tuition reimbursement and the list goes on.

Development:

Retention of talents is essential to the success of our business. We pride ourselves on offering internal advancement opportunities and investing in the continuous learning and growth of our employees. We are committed to support our employees in developing their skills and reaching their full potential.

Culture:

Capcium has an evolving culture driven by diversity, and passionate people.

With our flexible work arrangements, we create a work environment that promotes a healthy balance between work and personal life.


Diversity, Equality, and Inclusion:

Embracing Diversity, Equality, and Inclusion is one of our core values.

Each employee is considered as an important part of our company regardless of their gender, race, physical or mental disability, religion, nationality, sexual orientation, or age.

Supported by our leadership team, we are committed to attracting diverse backgrounds with unique skillsets whereby colleagues work together to better serve our customers and deliver the best science possible.


  • Version française à suivre_

About Capcium


We are an innovative, fully licensed value-add service platform provider for customers in the Pharmaceutical, Over the Counter and Health & Wellness industries.

Capcium has developed a best-in-class team of softgel encapsulation professionals leveraging decades of manufacturing expertise, customer support experience and formulation customization knowledge from leading softgel manufacturers.

We are dedicated to delivering the best customer experience and providing quality products while keeping our core values at the heart of everything we do.


Why work at Capcium
We are a continuously growing company offering a unique opportunity to learn and be apart of a dynamic team.

While ensuring high-quality service throughout every point in the journey, we strive for open and honest communication to create strong relationships between employees and customers.

We foster a collaborative environment to ensure a drive towards shared goals and success.

Our foundation is based on integrity and agility, ensuring trust amongst coworkers and quick responses to rapid changes in the internal and external environments.


Overview


Under the supervision of the QC Manager, the QC Analyst is responsible for performing analytical tests in daily laboratory operations and execution of testing to support manufacturing operations.

Testing typically includes samples from raw materials, in-process intermediates, final drug product manufacturing, stability and various development studies using approved test methods.

This position requires understanding and ability to perform techniques such as HPLC, HPLC-MS, GC-FID, GC-MS, ICP-MS, UV-VIS, FTIR and Wet Chemistry.

All work is executed following cGMP guidelines and Corporate SOP's.

Main Responsibilities

  • Conducts analytical testing of routine samples (raw material, inprocess, and finished product) using instrumentation (8090%) and wet Chemistry (1020%) techniques.
  • Performs all work activities in a safe manner and in compliance with applicable Health and Safety Regulations.
  • Ensures that all work is performed in compliance with GMPs, GLPs, SOPs, and other established regulatory requirements.
  • Independently or under supervision operates analytical instrumentation like HPLC, GC, GC-MS, LC-MS, ICP-MS.
  • Participate in analytical methods verification and validation.
  • Able to follow planning and to complete the workload in a timely manner.
  • Clearly and efficiently documents test results, calculations, and observations as per the established SOPs.
  • Recognizes OOS, out of trend and anomalous results and inform the supervisor or delegate immediately.
  • Performs general maintenance and calibration of laboratory equipment, according to the department's established calibration program, when assigned.
  • Performs additional related duties, as assigned by Management.
  • Backup for this role is the Quality Control Manager, Chemistry.

Qualifications

  • A University degree in analytical chemistry or organic chemistry. Post-Secondary education in a science field with work experience will be considered.
  • 1+ years related QC work experience in a pharmaceutical laboratory using GC and HPLC instrumentation. Experience with GC-MS, LC-MS, ICP-MS is a strong asset.
  • Able to rigorously apply, follow and maintain rules, proced

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