Bilingual (Spanish) Quality Control Coordinator 2nd shift
Position Description:
The QC Coordinator is tasked with developing, training and growing Quality Control Inspectors. The Leader's responsibility includes conducting inspections, identifying production, process or product issues and presenting solutions.
Responsibilities:
- Ability to perform all job duties of the Quality Control Inspector.
- Act as a liaison between Quality Control Inspectors and QC Management.
- Assist all manufacturing managers in various quality related matters.
- Ensure the Quality Control Inspectors understand line and/or room clearance.
- Train new Quality Inspectors to understand the batch record and the batch record reconciliation in all phases of the manufacturing process.
- Ensure that the line clearances are performed per product in all manufacturing areas.
- Ensure that packers and operators in all areas understand all quality aspects of their position.
- Coordinate with Quality to ensure that all documents are properly reviewed and approved.
- Ensure the inspection and sample retention of all processes are being taken, at the actual manufacturing process, and documented on the correct forms and retained correctly.
- Assist fellow employees with their tasks per manager's instruction.
- Adhere to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices.
- Conduct thorough inspections of staged raw materials in pharmacy, in-process components in manufacturing and packaging, and finished products to ensure they meet quality standards.
- Perform routine in-process checks using established methods in manufacturing and packaging to verify product quality, integrity, and safety.
- Inspect the lines and/or room clearance for pharmacy, blending, manufacturing, and packaging.
- Inspect all processes of the departments as assigned.
- Inspect the information white board at each phase of the process to confirm the work-in-process products match records on hand.
- Review the batch record and the batch record reconciliation in all phases of the manufacturing process.
- Accurately document in-process checks, inspection results, and deviations from approved standards like batch records.
- Maintain comprehensive and up-to-date records of quality control activities like sample logs, retains, temperature logs, cleaning logs for rooms/lines etc.
- Collaborate with cross-functional teams as needed.
- Responsible for communicating quality defects with supervisors.
- Assist as needed in providing information or retain samples required to complete investigations for customer complaints, deviations and/or CAPA.
- Work at different stations as production requires.
- Maintain a clean and safe work environment.
- Show a desire and willingness to learn and succeed.
- Complete all required training activities.
- Demonstrate a commitment to the organization by maintaining regular, on-site attendance, acting in a reliable manner and following through on responsibilities.
- Other duties as assigned.
Qualifications:
- Experience in Quality and/or Manufacturing in a cGMP environment.
- Knowledge of quality systems, cGMP, and Good Documentation Practice (GDP).
- Able to work in a timely manner in a fast-paced environment.
- Strong organizational skills, multitasking, and attention to detail.
- Strong experience of Microsoft Excel.
- Excellent communication skills and ability to work in a team.
- Strong willingness to learn and grow.
- Basic math skills, keen observation ability.
- Bilingual, must be able to read and write English.
Schedule:
40 hour week, Mon-Thurs, 2nd shift, 3:30 p.m. - 2:00 a.m.
Benefits:
- Health insurance
- Sick days
- Paid holidays
- Vision insurance
- Life insurance
- 401(k) matching
Seniority level: Entry level
Employment type: Full-time
Job function: Quality Assurance
Industries: Wellness and Fitness Services