Quality Associate

Hawkins Careers•Florida, NY

5d•Onsite

About The Position

The Quality Associate is responsible for providing support to and oversight of operations to verify process control, product quality, product safety, and safe work practices through all stages of manufacturing, packaging, labeling and storage. Completes specific quality-related duties associated with batch manufacturing processes including inspection, monitoring, verification, recordkeeping, and approval. Works with personnel from other departments as needed to identify and resolve quality or production issues. Monitors operations and personnel for compliance with company policy and procedure, GMP, safety and other requirements.

Requirements

BS/BA in a Science background preferred but not required; or related experience and/or training; or equivalent combination of education and experience.
2+ years’ experience in manufacturing, QC lab, or other environment related to food, dietary ingredient, dietary supplement, or pharmaceutical manufacturing.
Able to multi-task in detail-driven environment.
Detail oriented.
Ability to work independently and change focus to meet changing demands.
Able to use independent judgment within company guidelines.
Effective writing and verbal communication skills.
Excellent analytical and problem-solving skills required.
Must meet SQF requirements by following all applicable standards and reporting any food safety problems to Lead Process Technician, Plant Manager, or Quality Supervisor/Manager

Nice To Haves

Knowledge of relevant SOP's, cGMP, OSHA, FDA, and related requirements preferred.
Bilingual Spanish a plus
Knowledge of MS Office Systems preferred.
Knowledge of CRM and ERP Systems such as JDE preferred.

Responsibilities

Recommend, review, approve, conduct, and/or complete documentation for key activities in support of batch manufacturing and to assure compliance with company policy and cGMP including: line clearances; checking-in jobs (verifying material identify/quantity); required approvals and releases; batch record review including master, in-process and completed batch records; process deviations; product rework plans; other assignments as needed.
Inspect and monitor the batch manufacturing process and personnel work practices for compliance with cGMP and company policy.
Assist with development of programs and writing standard operating procedures, work instructions and other procedural documents.
Complete special request documentation including customer questionnaires.
Handle key activities in conjunction with, and as a back-up to, quality specialist including technical documents, sampling/inspecting/testing materials and products, and maintaining database information.
Alert production and quality managers immediately of problems impacting production.