Smithfield
BioScience
SeniorQualityControlManager
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“Senior Quality Control Manager at Smithfield. Skills: Quality Control, cGMP compliance, Leadership, Regulatory compliance. Take charge of QC operations. Ensure testing is accurate”
What You'll Achieve.
Uphold and elevate quality across all laboratory operations; Ensure every procedure aligns with global regulatory standards; Safeguard operations; Achieve results
Industry & Context.
Analytical Thinker; Critical thinking; Problem-solving skills; Navigate complex QC issues
Relocation Package Available
What They're Looking For.
Must Have
Bachelor's degree from an accredited four-year college or university in a chemistry, microbiology or other relevant technical field, 8+ 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, Demonstrated leadership skills, Ability to uphold regulatory, company, and customer standards, Proficient with complex mathematical calculations, Technical writing skills, Interpersonal skills, Communication skills (written and verbal), Ability to structure work plans, Ability to organize employees to achieve results, Demonstrated ability to manage multiple priorities in a fast-paced environment, Capable of working well with cross-functional teams in a dynamic setting, Works well in high pressure situations, Exceptional written and verbal communication skills, Capable of articulating complex technical issues clearly and concisely across all levels of the organization
Nice to Have
Master’s Degree chemistry, microbiology or other relevant technical field from an accredited four-year college or university and 6+ years relevant experience, Bilingual communication in Mandarin and English
What You'll Do.
Take charge of QC operations
Ensure testing is accurate
Report testing promptly
Meet regulatory standards
Provide hands-on leadership
Lead investigations for OOS
Lead investigations for CAPA
Lead investigations for Complaints
Lead investigations for Deviations
Ensure thorough resolution
Ensure timely resolution
Maintain inspection readiness
Support regulatory inspections
Report laboratory deviations
Ensure appropriate follow-up
Assist in testing raw materials
Assist in testing in-process samples
Assist in testing finished goods
Monitor quality metrics
Report quality metrics
Support continuous improvement
Review laboratory SOPs
Collaborate on SOP updates
Develop new laboratory methods
Validate new laboratory methods
Support computer system validations
Manage lab equipment usage
Manage lab equipment maintenance
Ensure peak equipment performance
Ensure cGMP compliance for equipment
Support training of QC analysts
Support onboarding of QC analysts
Support training of QC management
Support onboarding of QC management
How You'll Work.
Team & Collaboration
Serve as QC voice in cross-functional discussions; Work closely with Quality Assurance; Work closely with Production teams; Keep manufacturing workflows efficient; Keep product release timelines on point; Collaborate effectively in a fast-paced, cross-functional team environment; Work well with cross-functional teams; Achieve company goals
Communication Scope
Exceptional written and verbal communication skills; Articulate technical issues across all levels; Technical writing skills; Interpersonal and communication skills (written and verbal); Articulate complex technical issues clearly and concisely
Process & Methodology
Ability to structure work plans, Ability to organize employees to achieve results, Demonstrated ability to manage multiple priorities
Full Job Description
**If you are currently employed at Smithfield, please log into Workday and submit your application through the Jobs Hub.** Have a seat at our table. When you join Smithfield, you become part of something special – a company that's sustainably feeding people around the world, producing good food the right way with respect for our people, animals, communities and planet. With opportunities across locations and functions, a culture grounded in our Core Four values - gratitude, communication, respect and accountability - and a strong commitment to learning, collaboration, and innovation, Smithfield offers challenging and rewarding careers where you can grow, contribute and make a real impact. **Apply Now!** **THE VALUE YOU’LL BRING:** _The position summary states the general nature and purpose of the job. Overall accountabilities are defined in this section._ Are you ready to play a pivotal role in ensuring the highest standards in pharmaceutical and medical device manufacturing? We're looking for a passionate and driven professional to take on a **full-time position** reporting to the **Head of Quality**. In this key leadership role, you’ll be at the forefront of **Quality Control operations** , championing **compliance with current Good Manufacturing Practices (cGMP)** and driving the integrity and excellence of our products and quality systems. Your mission: to uphold and elevate quality across all laboratory operations, from testing **Active Pharmaceutical Ingredients (APIs)** to critical **medical device components**. You’ll ensure every procedure aligns with global regulatory standards, including **21 CFR Parts 210/211** , **ICH Q7** , **ISO 22442** , and **EU guidelines** —safeguarding not just our operations, but ultimately the patients who rely on our products. If you thrive in a fast-paced, quality-first environment where precision and leadership matter, this is the opportunity to make a real impact. **WHAT YOU’LL DO:** _The below statements are intended to de
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