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Jubilant HollisterStier LLC, a well-established member of the business community in Spokane, Washington, provides a complete range of services to support the pharmaceutical and biopharmaceutical industries. The Allergy business is a worldwide leader in the manufacture of allergenic extracts, targeted primarily at treating allergies and asthma. Jubilant HollisterStier is also a nationally recognized contract manufacturer of sterile injectable vials, and lyophilized products. Jubilant HollisterStier is a proud member of the Jubilant Pharma family.

Our Promise:  Caring, Sharing, Growing

We will, with the utmost care for the environment and society, continue to enhance value for our customers and stakeholders by providing innovative products and economically efficient solutions' through growth, cost effectiveness and wise investment of resources.

Job Description:

Quality Assurance (QA) Auditors are responsible for providing QA inspection and auditing of manufacturing operations to ensure that all products produced meet labeling, dating, and packaging requirements as defined by Standard Operating Procedures (SOP's) and current Good Manufacturing Practices (cGMP).  Essential responsibilities include but are not limited to:

1. Process final container samples; perform inspection and sampling according to SOP, Protocol, or client request memo.
2. Review and approve product records and entries for completeness and accuracy.
3. Assure that labeling and packaging lines are clean and free of materials and components from previous lots. Perform visual inspection of product vials and packaging over extended periods of time (8-10 hours/day, with appropriate breaks).
4. Assure through a system of auditing that cGMPs are followed in manufacturing and finished product packaging areas.
5. Recognize potential problems and/or document problems encountered. Follow up with department supervisors to assure corrective actions are taken to resolve any deficiencies in product quality or manufacturing systems and procedures.
6. Conduct annual retention sample inspections.
7. Other tasks as assigned.

Shift: Weekend Days

Basic Qualifications:

• High school diploma or equivalent required.
• Minimum 2 years related experience required with high school diploma. Minimum 1 year related experience required with an Associate's degree. No experience required with a Bachelor's degree.
• Working knowledge of Microsoft Word required, Excel desired.
• Problem solving, basic exchange of information, and interpersonal relation skills required.
• cGMP and pharmaceutical manufacturing knowledge required, specifically an ability to recognize deficiencies in product quality and report to the appropriate supervisor(s).
• Thorough understanding of QA and manufacturing systems as related to the testing and packaging operation and batch records required.
• Ability to tactfully manage conflict and influence outcomes required.
• Ability to influence corrective actions by indicating what is needed for deviations to be in compliance. Must render interpretations relative to compliance with cGMP and other governmental regulations.
• Minimal travel (<10%) required.
• Physical requirements: 14/14 Corrected Near-Point vision, must pass color deficiency test, ability to lift 40 lbs. unassisted, exposure to allergens, prolonged standing, bending and reaching, ability to stoop to access lower shelves for samples/inspection.

Preferred Qualifications:

• Associate's of Science degree or Bachelor's degree desired.
• Ability to fulfill a leadership or controlling role on end results desired.

Compensation:

This position pays $26.15 to $35.37 per hour, depending on