Supplier Quality Specialist

Who We Are

At CPL, we are passionate about pharmaceutical product development and contract manufacturing. Our aim is to be the top choice CDMO in the non-sterile liquid and semi-solid pharmaceutical products domain, and ultimately bring benefits to the customers using our manufactured products.

Current vacancy

At CPL, we are passionate about pharmaceutical product development and contract manufacturing. Our aim is to be the top choice CDMO in the non-sterile liquid and semi-solid pharmaceutical products domain, and ultimately bring benefits to the customers using our manufactured products.

For more than 30 years CPL has partnered with the world’s leading pharmaceutical companies to provide full-service product development and manufacturing, singularly focused on innovation and efficiency.

We recognize our employees are our number one asset and support their career growth. We also offer a benefits program, deferred profit-sharing plan, paid time off, employee’s assistance program, work/life balance, employee recognition program, on-site parking, discounted gym membership.

Responsible for all activities related to sampling and inspection of packaging components and raw materials, as well as sampling and release of consumable materials. Creates and closes purchase orders for third party laboratories. Manages retention samples.

• Responsible for working in compliance with established safe work practices and procedures; properly uses personal protection and safety equipment as required by CPL; reports any injury of illness immediately and notifies CPL of any hazards, unsafe acts or conditions in the workplace.
• Performs incoming inspection and sampling of packaging components and raw materials, including customer-supplied materials.
• Performs  of raw materials using Tru Scan.
• Sends samples of raw materials, packaging components, bulk and finished product to testing laboratory for analysis against approved specification. Enters samples in LIMs.
• Creates purchase orders for testing done at third party laboratories. Closes purchase order once testing results are received. Follows up and verifies costs of testing with testing laboratories where required.
• Responsible for proper storage and destruction of packaging component, raw material, bulk product and finished product retain samples.
• Performs sampling and release of consumable materials.
• Performs responsibilities in an efficient and timely manner. Identifies areas where efficiencies can be improved.
• Other duties as required.

• Two-year college diploma preferably in a scientific discipline.

• Minimum of 2 years of pharmaceutical manufacturing experience.

• Knowledge of cGMP requirements for pharmaceutical manufacturing.
• Knowledge of computer systems such as SAP and Microsoft Office Excel.
• Good verbal and written English communication skills.
• Flexible with the ability to adapt, respond quickly and manage change in a fast- paced environment.
• Demonstrated competencies in CPL's core values

• Some flexibility in work schedule to ensure assigned activities are completed as scheduled.
• Physically demanding job which requires daily movement of skids and lifting of bags and boxes up to 50 lbs.

CPL is an equal opportunity employer committed to diversity and inclusion. We welcome applications from all qualified individuals. CPL is committed to accommodating persons with disabilities. If you need accommodation at any stage of the application process or want more information on our accommodation policies, please contact us.

We thank all applicants for their expression of interest; however only those selected for an interview will be contacted. No phone calls or agencies please.