Pharmaceutical QC Technical Services Manager

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A great job-and a great future-awaits you at Smithfield Foods. We're an $18 billion U.S. food company with nearly 60,000 employees worldwide. We're looking for motivated people who want to join our team and grow lasting and meaningful careers with us. Join our family today. Apply Now!

Your Opportunity

Our team members receive industry-competitive salaries and are eligible for great benefits packages:

• Competitive Pay

• Annual Bonus Earning Potential

• Comprehensive Health Insurance, Retirement Benefits and More

• Education benefit available to full and part time Smithfield team members on their first day of employment.

• Open to moving? We will help! Ask about our Relocation Assistance packages!

• In addition, we offer opportunities for career growth, professional development, and tuition assistance.

This is a full-time position reporting to the Director of Quality Control. The position is one of leading the technical operations related to quality control of the Company's products pursuant to Standard Operating Procedures (SOPs) and in compliance with current Good Manufacturing Practice (cGMP) as required by the U.S. Food and Drug Administration (FDA).

Responsibilities

• Responsible for qualification of testing equipment and validation/verification of quality control methods to ensure active pharmaceutical ingredient is tested and manufactured in accordance with cGMP, SOPs, and safety requirements.

• Lead and assign technical tasks/duties associated with commissioning and qualification of laboratory equipment; analytical method development, transfer and validation / verification; and product lifecycle improvement projects.

• Provide leadership for cross-functional teams, including training, coaching, and mentoring.

• Champion cGMPs, safety, and workplace activities and help develop and meet QC compliance and safety goals.

• Respond to any observed laboratory or safety issues and take action as appropriate.

• Work closely with Engineering/Maintenance, Quality Assurance, Manufacturing and R&D teams.

• Lead QC out-of-specification (OOS) investigations to determine product impact, root causes and identify corrective and preventive actions (CAPA) to prevent recurrence.

• Provide technical expertise to resolve equipment or testing issues and interact with colleagues to ensure QC testing requirements are met.

• Draft, revise and review technical protocols, reports, standard operating procedures, and worksheets, ensuring compliance to cGMP and Good Documentation Practices (GDP).

• Ensure QC metrics and business systems records are properly developed and maintained.

• Counsel employees to promote their success and manage employee performance issues as needed.

The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties, and skills required of personnel so classified. May perform other duties as assigned.

Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals to perform the essential functions.

• Bachelor's degree from an accredited four-year college or university in a chemistry, microbiology or other technical field and 5+ years of demonstrated experience in FDA cGMP compliance environment in a QC laboratory.

• 2+ years of demonstrated experience in team management/development or project leadership is required

• Demonstrated leadership skills and the ability to uphold regulatory, company, and customer standards.

• Proficient with complex mathematical calculations, technical writing, interpersonal and communication skills (written and verbal).

• Ability to structure work plans and organize employees to achieve results with demonstrated ability to manage multiple priorities in a fast-paced environment.

• Capable of working well with cross-functional teams in a dynamic setting to achieve company goals.

• Works well in high pressure situations.

EEO/AA Information

Smithfield is an equal opportunity employer committed to workplace diversity. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, national origin, age, gender identity, protected veterans status, status as a disabled individual or any other protected group status or non-job characteristic as directed by law.

If you are an individual with a disability and would like to request a reasonable accommodation for any part of the employment selection process, please call us at 757-357-1595.

Salary Range

$117,000.00 - $175,125.00