Quality Control Manager

Location: Whitsett

About the Job

Berkshire is the global contamination control leader for cleanroom and controlled environment consumable products. We provide customers with technically advanced materials aimed at application performance. We focus on total solutions that consistently minimize the risk of product and process contamination. With our customer relationships we continuously focus on complete engineered clean solutions. For over 55 years, Berkshire has understood and delivered world class manufacturing, reliable supply chain, the highest standards for quality, and technically advanced products assuring mutual success each step of the way.

The Quality Control Manager is responsible for comprehensive oversight of all QC laboratory operations including receiving, in-process and finished goods testing across nonwoven, knitted, and textile materials, chemical products, and sterile/cleanroom products. Ensures compliance with ISO 9001, ISO 22716, ISO 13485, and FDA 21 CFR Part 820, including GMP, GDP, and data integrity requirements. Leads laboratory personnel, supports manufacturing and product development, and ensures testing meets all internal, customer, and regulatory specifications.

Berkshire Corporation is looking for a proactive, detail-oriented strategist who balances independent initiative with a collaborative spirit. The ideal candidate is a professional of high integrity who tackles complex problems with a positive, solution-focused mindset.

Description of Candidate:

• Demonstrate integrity and professionalism.
• Demonstrate a positive attitude in the face of challenges.
• Maintain a professional demeanor with both internally and externally with vendors and suppliers.
• Maintain a high attention to detail to ensure compliance to standards.
• Ability to work individually as well as positively and proactively in a team.
• Reacts with an appropriate sense of urgency to production and customer needs.
• Ability to read and comprehend written instructions.

Qualifications of Candidate:

• Bachelor's degree in Chemistry, Biology, Microbiology, Engineering or other related disciplines.
• 6+ years QC experience and 4+ years leadership experience. Experience in textiles/nonwovens/knitted, controlled cleanroom and sterile manufacturing environments, and/or regulated industries (including medical device and/or cosmetic GMP-regulated environments) preferred.
• Proficiency in Microsoft Office, ERP, and LIMS systems.
• Attention to detail and commitment to compliance.
• Be able to independently make decisions and lead a department of Lab Technicians.
• Proficiently and knowledgeably multitask and have excellent organizational skills.
• Possess excellent interpersonal and leadership skills to develop and mentor/coach department staff.
• Competently use advanced mathematics together with the use of specifications, charts, tables, and handbook formulas for presentations.
• Ability to solve problems which require several steps of logic and calculation.
• Ability to use judgement in the analysis of facts and circumstances surrounding individual problems and transactions and in the determination of action to be taken within the limits of standard or accepted practice.
• Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Ability to apply complex instructions that include conditionals to situations described in materials.
• Ability to apply technical terms and jargon and relate them to stated situations.
• Ability to use precision measuring instruments including equipment and personal computers to input data involving advanced skills knowledge.

Job Description:

• Supervise, lead, and train laboratory personnel; maintain staffing coverage aligned with production and QC needs.
• Conduct performance evaluations on direct reports and works to develop employees' knowledge, skills and abilities.
• Ensure laboratory compliance with ISO 9001, ISO 22716, ISO 13485, and 21 CFR Part 820 regulations (including equipment calibration and process controls).
• Maintain lab records, ensure data integrity (ALCOA+), and manage migration to LIMS/QMS systems.
• Support audits (internal, external, FDA) and ensure audit readiness at all times.
• Support CAPA, change…