QC Inspector – Grade I or II or III

VACANCY

QC Inspector Grade I OR II OR III - 3rd Shift (Production)

Hours: 9PM - 7:15AM, Monday - Thursday

The Role: Perform Quality Control functions within the Production areas in order to assure materials and products are sampled, tested, produced, and released in compliance with agreed specifications.

Responsibilities include, but are not limited to:

• Performs regular in-process quality checks on products, processes, room layout, and safety to ensure compliance with GMP and Almac Clinical Services procedures.

• Performs set-up inspections, including setting accept/reject standards, to establish quality criteria for each batch.

• Inspects and approves clinical labels prior to issuance to packaging operations.

• Performs environmental monitoring activities.

• Performs calibration checks on balances and scales used in Almac Clinical Services.

• Performs area and equipment clear / clean inspections.

• Samples clinical materials upon customer request.

• Interacts with Quality, Operations, Project Services, and Logistics personnel to address quality issues.

• Assists in cGMP, SOP, and job skill training of quality control and other Almac Clinical Services personnel.

• Develops and writes departmental and other company SOPs.

• Assists in coordinating the activities of QC Inspectors. Deputizes for the QC Supervisor, as necessary.

Grade I

• Experience in GMP manufacturing, packaging, or quality assurance/control or equivalent preferred.

• Eyesight meets current company Vision Policy requirements for acuity and color blindness.

• GMP training and computer literacy preferred.

• Effective oral and written communication skills.

• Organizational skills.

• Negotiation skills preferred.

• Ability to work overtime on weekdays and weekends, when necessary.

Grade II

• 1-3 years experience in GMP manufacturing, packaging, or quality assurance/control or equivalent preferred.

• Eyesight meets current company Vision Policy requirements for acuity and color blindness.

• GMP training and computer literacy preferred.

• Effective oral and written communication skills.

• Organizational skills.

• Negotiation skills preferred.

• Ability to work overtime on weekdays and weekends, when necessary.

Grade III

• 3 or more years experience in GMP manufacturing, packaging, or quality assurance/control or equivalent (w/o college degree) required.

• Eyesight meets current company Vision Policy requirements for acuity and color blindness.

• Personnel training experience preferred.

• Direct supervision of other personnel preferred.

• GMP training knowledge.

• Computer literacy.

• Knowledge of quality control sampling and inspection techniques preferred.

• Effective oral and written communication skills.

• Technical writing skills preferred.

• Problem analysis and solution skills preferred.

• Ability to form good working relationships with team members and superiors.

• Meticulous, thorough, consistent, decisive, and assertive.

• Ability to work on own initiative.

• Ability to work to consistent high standard under pressure.

• Ability to work overtime on weekdays and weekends, when necessary.

• Willingness to undertake additional responsibilities as required.

Contact Info: To apply, please contact the Recruiting Specialist, Tony Roig, by email or telephone at ext. 7163

Qualifications:

• High School Diploma or Equivalent; Associates or Bachelor's degree with science background preferred 

Posting dealine:  March 5, 2012

Contact Info: To apply, please contact the Recruiting Specialist, Tony Roig, by email or telephone at ext. 7163