Training Specialist

Are you interested in an exciting and rewarding career within a growing company? Are you motivated to collaborate with a team to achieve goals? Do you have passion for improving the lives of others?

Bryllan is looking for respectful, empathetic, courageous individuals who are eager to utilize their skills in a rewarding career. Bring the knowledge and experience you've gained from your education and career, along with passion to proactively develop and maintain the Quality training program within the pharmaceutical manufacturing industry. Bryllan LLC in Brighton, Michigan, is a contract manufacturing organization (CMO) with a focus in sterile injectable pharmaceuticals. Bryllan embraces a management philosophy built around the principles of Quality, Integrity, and Service. If you feel invigorated by the thought of contributing to the creation of life enhancing or lifesaving products, this opportunity could be for you!

Training Specialist Responsibilities:

• Support management in the development of training curriculums for all departments at Bryllan
• Create training material, coach Subject Matter Experts to design and develop training materials to improve knowledge and skills in their function and site performance.
• Participate in the investigation of deviations associated with learning gap errors and recommend appropriate learning solutions to aid in reducing human errors to improve business process and site performance.
• Evaluate the effectiveness of employee training methods against key business objectives and propose solutions to improve training delivery.
• Provide continuous improvement recommendations for training throughout the site.
• Ensure that the training items that require periodic retraining/requalification are managed effectively.
• Contribute to completion of project milestones and organize own work to meet project tasks deadlines.
• Perform necessary assessment of site operations and update necessary documents.
• Support management to accurately determine their team training status prior to assigning GMP tasks.
• Maintain all training documentation and records.
• May require work beyond the hours typically defined as a regular workday to support off shift operations.
• Must have the ability to simultaneously multitask across multiple capabilities and functions and handle multiple competing priorities and requirements.

Behavioral Expectations:

• Demonstrates leadership both by words and leading by example to foster Bryllan One Team culture.
• Personal Competencies: self-awareness, integrity, judgement, vision, adaptability, decision making, coaching, highly motivated.
• Strong work ethic and ability to accomplish tasks without supervision.
• Adhere to and follow all Company Policy and Procedures.
• Excellent interpersonal skills including team building, consensus building, conflict resolution, with the ability to cooperate with others in a high-performance setting.
• Excellent English communication skills: verbal, written, and listening.
• Experience with US, EU, and Canadian pharmaceutical and medical device regulations and ISO standards.
• Expert knowledge and application of cGMP and regulatory principles.
• Demonstrate ownership and accountability to production schedule without compromising product quality.
• Basic computer skills (proficient in Microsoft Office applications).
• Strong mathematical and organizational skills.
• Must possess honesty and integrity, commitment to the highest legal and ethical standards.
• Ability to treat every person with courtesy and respect.

Work Experience and Education Requirements:

• Minimum of 3 years' experience in pharmaceutical manufacturing.
• 2 or more years of experience in quality and/or quality systems.
• Experience in continuous improvement methodologies, i.e. lean, six sigma, statistical process control preferred.
• Minimum qualification of a four-year Degree in engineering, quality or related field.

Employment at Bryllan (Biovire) is contingent upon a successful background check.