Responsible for ensuring compliance with relevant Standard Operating Procedures, while gathering, analyzing and applying information from internal and external sources in order to perform a risk assessment of the impact each process deviation and complaint has on the product, process, and patient health and safety.

• Bachelor’s degree with 1-2 years of experience in pharmaceutical manufacturing or cGMP environment.
• Associates degree with 5 years of experience in pharmaceutical manufacturing or cGMP environment.
• Working knowledge of GMP, EU, and GLP, as well as FDA trends and guidelines.
• Excellent verbal and written communication skills required
• Good deductive and inductive critical thinking skills required.
• Candidate must possess strong interpersonal, written, and verbal communication skills. Incumbent must be able to interface positively with Regulatory Agencies, vendors, and company departments. Good knowledge of MS Office programs, including Word and Excel.

Job Type: Full-time

Pay: $59,190.00 - $83,260.00 per year

Benefits:

• 401(k)
• 401(k) 3% Match
• Dental insurance
• Disability insurance
• Employee assistance program
• Employee discount
• Flexible schedule
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance
• Referral program
• Tuition reimbursement
• Vision insurance

Experience level:

• 1 year
• 2 years

Schedule:

• 8 hour shift
• Day shift

Ability to Relocate:

• Grand Island, NY 14072: Relocate before starting work (Required)

Work Location: In person