Smithfield

BioScience

SeniorQualityControlManager

$117–175k Cincinnati, Ohio, United States FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Senior candidates.

The Brief

“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.

BioScience
Problems you'll solve

Analytical Thinker; Critical thinking; Problem-solving skills; Navigate complex QC issues

Eligibility Requirements

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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