Pharm Quality Assurance Associate

Hawkins Inc; Minneapolis (MN); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

LTD/STD

401(k) match

Employee Stock Purchase Program

Paid time off

Paid holidays

Job summary

Hawkins Inc. seeks a Quality Associate (Pharm) to oversee enterprise-wide quality initiatives, ensuring safety, compliance, and customer satisfaction.

You will implement and sustain the Quality Management System while coordinating with internal and external resources for product qualification. Responsibilities include processing regulated docs, conducting line clearance, reviewing batch records, and supporting deviations investigations, with a focus on continuous process improvements across

Qualifications

• Knowledge of cGMP and regulatory requirements.
• Experience documenting batch records and deviations.
• Investigation skills for quality events and impacts.
• Familiarity with SOPs and change controls.

Responsibilities

• Issue, track, and reconcile regulated documentation, including batch records, labels, and logbooks, to production lines.
• Conducts line clearance and post checks in support of manufacturing activities.
• Verify that all manufacturing and testing activities align with approved SOPs.
• Perform reviews of executed batch records, logs and documentation for accuracy and compliance.
• Perform in-process inspections to resolve problems and ensure regulatory compliance.
• Enter test results, generate COAs, and release finished product accordingly.
• Identify, document, and report any quality events or deviations observed during production.

Skills

Safety

Customer Focus

Accountability

Teamwork

Ethics

Communication

Job description

Hawkins Inc. seeks a Quality Associate (Pharm) to oversee enterprise-wide quality initiatives, ensuring safety, compliance, and customer satisfaction.

You will implement and sustain the Quality Management System while coordinating with internal and external resources for product qualification. Responsibilities include processing regulated docs, conducting line clearance, reviewing batch records, and supporting deviations investigations, with a focus on continuous process improvements across