• Organize and oversee the activities related to the manufacturing of tablets and capsules to include delivery, in-process samples in a defined schedule.
• Review and compile the documents generated during the production of tablets and capsules such as Batch Manufacturing Record (BMR), PQ protocol.
• Ensure and compliance with safety, quality, productivity, and performance expectations and execution of manufacturing operations.
• Review batch record after finishing each step for correctness.
• Make sure correct ness of product log in and yield of product with BMR Correctness online.
• Schedule cleaning validation with request as required for equipment.
• Work with Integrated Product Development (IPD)/R&D on the execution of bio-batches (abbreviated new drug applications - ANDA) and validation batches.
• Coordinate to implementation of current good manufacturing practices (cGMP) and safety practices in the operations and manufacturing of products.

Education Qualifications:

High School Diploma (or equivalent experience)

Experience:

Minimum three years of direct work experience in pharmaceutical manufacturing. Preference will be given to candidates with experience in generic pharmaceutical manufacturing.

Job Type: Full-time

Pay: $20.65 - $25.00 per hour

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Health insurance
• Life insurance
• Paid time off
• Vision insurance

Schedule:

• 8 hour shift

Experience:

• Pharmaceutical: 1 year (Preferred)

Ability to Commute:

• Central Islip, NY 11722 (Required)

Ability to Relocate:

• Central Islip, NY 11722: Relocate before starting work (Required)

Work Location: In person