ACCUCAPS Industries Ltd. is one of the largest full-service contract research & manufacturing organizations (CRMO) in North America. We supply soft gel capsules and encapsulation services for over-the-counter and pharmaceutical (OTC/Rx), health and nutritionals (H&N), and cosmeceutical industries. Guided by highly regarded industry experts, Accucaps has grown into a strong global player serving customers across North and South America, Europe and Asia. Accucaps is seeking driven and knowledgeable individuals who can take products to the next level in the global market. Are you ready to make a difference in the world of Soft Gel Innovation with Accucaps?
 

Reporting to the QA Supervisor the role includes the final product audit for product release, coaching and training operators and supervisors on proper documentation practices and cGMP requirements. Participates in special projects as required in other areas of Quality and Compliance.
 

Primary Responsibilities: 

• Performs in-process document auditing and product quality checks in production and ensures all issues are communicated to production employees, production management and QA management
• Performs Final Release auditing of batch documentation ensure all product has been manufactured in compliance with cGMP''s and SOP''s. This includes performing all duties required to release the final product
• Assists in the investigation of manufacturing issues and manufacturing deviations as reported by the production departments which includes completing quality checks as required
• Performs compliance audits in all production departments and prepares result reports for product and QA management. Follows up on outstanding corrective actions from the audits to ensure timely completion of the action
• Acts as QA representative on shift in decision-making and issue resolution, escalating serious issues to production management and QA management as required
• Participates in special projects as required in other areas of Quality and Compliance
• Coaching and training operators and supervisors on cGMP practices
• Performs sampling for the Environmental Microbial Monitoring program
• Assists in the writing and organization of SOP's
• Responsible for the filing, archiving and review of Quality documents

Success Criteria 

• Bachelor's Degree in Science (Chemistry or Biochemistry preferred) is required
• Minimum 2 years related experience

Additional Skills 

• Advanced computer skills in MS Excel and Word
• Strong analytical skills
• Extremely detailed oriented
• Strong interpersonal skills
• Excellent communication skills - verbal and written
• Able to work independently with minimal supervision
• Demonstrates trustworthiness by being honest, dependable, and reliable

  

This position is for our Strathroy facility which is 20 minute commute from London.

If you are a driven individual who thrives in a challenging and fast paced environment, it’s time you join the Accucaps team. We offer a challenging work environment that fosters innovative thinking and rewards excellence.

Qualified candidates and team players are invited to apply at www.accucaps.com (Corporate>Careers).