Supplier Quality Specialist I

Résumé du poste

Responsible for the sampling and inspection of raw materials, packaging components, and consumable materials in compliance with cGMP standards. Manages third-party laboratory testing, including purchase order creation and the handling of retention samples.

Détails du poste

Job Type: Current vacancy 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. 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. Job Summary: 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. JOB RESPONSIBILITIES: * 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 ID testing of raw materials using TruScan. * 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. REQUIRED QUALIFICATIONS: Education: * Two-year college diploma preferably in a scientific discipline. Experience: * Minimum of 2 years of pharmaceutical manufacturing experience. Knowledge, Skills, Abilities: * 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 PHYSICAL DEMANDS/WORKING CONDITIONS: * 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.

Ce que vous ferez

Responsible for the sampling and inspection of raw materials, packaging components, and consumable materials in compliance with cGMP standards. Manages third-party laboratory testing, including purchase order creation and the handling of retention samples.

Exigences

Requires a two-year college diploma in a scientific discipline and a minimum of 2 years of pharmaceutical manufacturing experience. Candidates must possess knowledge of cGMP, SAP, and Microsoft Office, along with the physical ability to lift up to 50 lbs.

Avantages

• Deferred profit-sharing plan • Paid time off • Employee assistance program • Work/life balance • Employee recognition program • On-site parking • Discounted gym membership

Compétences indiquées

• SAP · Souhaitée
• Safety Compliance · Souhaitée
• Quality Inspection · Souhaitée
• Communication Skills · Souhaitée
• Gestion des stocks · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• Quality inspection
• Sampling
• Raw materials testing
• Packaging components
• TruScan
• LIMS
• Purchase orders
• cGMP
• SAP
• Microsoft Office Excel
• Communication skills
• Inventory management
• Safety compliance
• Communication
• Innovation
• Microsoft Excel
• Pharmaceuticals
• SAP Applications
• Good Manufacturing Practices
• New Product Development
• Time Off Management
• Employee Assistance Programs
• Written English
• Packaging And Labeling
• Pharmaceutical Manufacturing
• Laboratory Information Management Systems
• Contract Manufacturing

Domaines d’emploi

• Manufacturing
• Science & Research
• Healthcare
• Logistics
• Supplier Quality Specialist
• Unclassified Specialized Occupation