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Director Of Quality Control Jobs in Spring Grove, PA

PSC Biotech

Senior Director of Quality

York, PA

The Quality Director will lead internal QA/QC teams and manage external consultants, driving cross ... Perform independent technical review of documentation during and post-execution of cGMP activities ...

PSC Biotech

Senior Director of Quality

York, PA · On-site

The Quality Director will lead internal QA/QC teams and manage external consultants, driving cross ... Perform independent technical review of documentation during and post-execution of cGMP activities ...

PSC Biotech

Senior Director of Quality

York, PA · On-site

The Quality Director will lead internal QA/QC teams and manage external consultants, driving cross ... of documentation during and post-execution of cGMP activities, ensuring specifications and ...

York Materials Group

QC Technician

York, PA

$18.50 - $23.50/hr

Supportive, family-owned company with 85+ years of stability York Building Products is a trusted East Coast leader in asphalt, aggregates, and construction materials. We're hiring a QC Lab Technician ...

York Building Products

QC Technician

York, PA · On-site

$18.50 - $23.50/hr

Supportive, family-owned company with 85+ years of stability York Building Products is a trusted East Coast leader in asphalt, aggregates, and construction materials. We're hiring a QC Lab Technician ...

York Materials Group

QC Technician

York, PA · On-site

$18.50 - $23.50/hr

Supportive, family-owned company with 85+ years of stability York Building Products is a trusted East Coast leader in asphalt, aggregates, and construction materials. We're hiring a QC Lab Technician ...

Solar Gaines

QC Technician - Solar

Cockeysville, MD

$24 - $35/hr

QA/QC Technician Solar Gaines is expanding! We are seeking a dedicated QA/QC Technician to support ... Conduct on-site quality inspections at all stages of the project lifecycle * Verify compliance with ...

Solar Gaines

QC Technician - Solar

Cockeysville, MD · On-site

$24 - $35/hr

QA/QC Technician Solar Gaines is expanding! We are seeking a dedicated QA/QC Technician to support ... Conduct on-site quality inspections at all stages of the project lifecycle * Verify compliance with ...

Solargaines

Quality Control Manager

Hunt Valley, MD · On-site

Quality Control Manager Solar Gaines is seeking a Quality Control Manager who will oversee ... Work with Subcontractors to monitor quality of all installation methods and ensure that ...

NARDA HOLDINGS INC

Quality Control Technician

Sparks, MD · On-site

$29 - $33/hr

iRF Solutions, an Amphenol company, is seeking a Quality Control (QC) Technician to perform inspection, verification, and rework of electronic assemblies, PCB boards, and RF interconnect products.

Trexon

Quality Control Technician

Gettysburg, PA · On-site

$17 - $22/hr

This is a great opportunity to be part of a dedicated team focused on delivering high-quality products to aerospace and industrial customers. Key Responsibilities: * Perform inspections of incoming ...

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All JobsOf Quality Control JobsDirector Of Quality Control JobsDirector Of Quality Control Jobs in Spring Grove, PA

Director Of Quality Control information

See Spring Grove, PA salary details

$30.4K

$123K

$209.1K

How much do director of quality control jobs pay per year?

As of Sep 2, 2026, the average yearly pay for director of quality control in Spring Grove, PA is $123,010.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,100.00 and $147,900.00 per year, depending on experience, location, and employer.

What is a director of quality control?

A Director of Quality Control is responsible for overseeing and managing quality assurance processes within an organization. They develop and implement quality control policies, ensure compliance with industry standards, and lead teams to identify and resolve product or service issues. This role involves analyzing performance data, conducting audits, and driving continuous improvement initiatives. The director collaborates with other departments to maintain high-quality standards and ensure customer satisfaction.

What are some common challenges a director of quality control faces in their day-to-day work?

Directors Of Quality Control often navigate challenges such as maintaining consistent quality standards across multiple teams or locations, adapting to evolving industry regulations, and effectively managing corrective actions when issues arise. They must balance the need for thorough inspections with production deadlines, while also fostering a culture of continuous improvement. Collaboration with departments like production, engineering, and supply chain is essential to resolve quality concerns and implement preventative measures. Tackling these challenges successfully helps ensure the company's products meet all necessary standards and customer expectations.

What are the key skills and qualifications needed to thrive in the director of quality control position, and why are they important?

A Director Of Quality Control should possess a deep knowledge of quality assurance processes, regulatory standards, and industry best practices, backed by a relevant degree and substantial experience in quality management. Familiarity with quality management systems (QMS), statistical process control software, and certifications such as Six Sigma or ISO 9001 is typically expected. Strong leadership, communication, and problem-solving skills set outstanding candidates apart in this position. These competencies ensure the organization consistently meets quality standards, maintains compliance, and fosters continuous improvement.

What cities near Spring Grove, PA are hiring for Director Of Quality Control jobs?

Cities near Spring Grove, PA with the most Director Of Quality Control job openings:

Director Of Quality Control jobs near you

Senior Director of Quality

PSC Biotech

York, PA

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

BioTechnique is a sterile injectable full service CDMO providing cytotoxic and therapeutic sterile injectable fill-finish services.  From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and lyophilization services for a wide variety of liquid injectables. BioTechnique utilizes our team’s expertise to create a process design for our clients’ products that best suits their needs.

The Experience

With operations spanning the globe and featuring a multi-cultural team, BioTechnique is passionate about bringing the best and brightest together in an effort to form something truly special. When you make the decision to join our team, you will be offered the ability to feel inspired in your career, explore your professional passions, and work alongside a group of people who will value and nurture your talents.

We are firm believers in coaching and developing the next generation of industry leaders and influencers. As such, you will not only be offered a compensation and benefits structure that rewards you, but also be provided with the tools that will help you grow and learn.

At BioTechnique, it’s about more than just a job—it’s about your career and your future.

Your Role

The Quality Director will serve as the strategic and operational leader of BioTechnique’s Quality function, overseeing all aspects of Quality Assurance, Quality Control, Compliance, and Validation. This role is responsible for ensuring that BioTechnique maintains the highest standards of regulatory compliance, product quality, and operational excellence across sterile injectable manufacturing, lyophilization, and clinical logistics.

The Quality Director will lead internal QA/QC teams and manage external consultants, driving cross-functional collaboration to resolve quality events, optimize validation processes, and support manufacturing operations in cleanroom environments. This individual will provide on-the-floor quality guidance, mentor junior staff, and ensure alignment with evolving regulatory expectations and sponsor requirements.

In addition to core quality responsibilities, the Quality Director will play a pivotal role in supporting Business Development (BD) initiatives, Manufacturing Science and Technology (MSAT) projects, and internal product approvals. The role includes project management responsibilities for selected customer programs and strategic input into sponsor engagement and innovation adoption.

  • Provide strategic leadership and independent QA oversight across all cGMP-regulated areas, including: 
    • Critical utilities (WFI, Steam, Automation, HVAC, equipment)
    • Warehouse operations
    • Manufacturing processes
    • Inspection, labeling, and packaging
    • Batch record review and disposition
    • New product introduction and product transfer
    • External laboratories and supplier quality
  • Lead and manage BioTechnique’s quality assurance, compliance, and validation activities, ensuring alignment with FDA, EMA, and international regulatory standards
  • Execute tactical QA operations while overseeing and mentoring junior staff in real-time floor assessments, issue identification, documentation, and resolution
  • Perform independent technical review of documentation during and post-execution of cGMP activities, ensuring specifications and requirements are met
  • Provide guidance and training across GMP areas (Manufacturing, QC, Validation) to ensure regulatory compliance and continuous improvement
  • Sign off, qualify, and train junior staff on QA/QC/Validation responsibilities and ensure readiness for regulatory inspections
  • Analyze findings and report to relevant departments; drive corrective actions and preventive measures through CAPA and deviation management systems
  • Serve as Subject Matter Expert (SME) for internal and external audits, regulatory inspections, and client engagements; lead inspection readiness activities
  • Maintain the approved supplier list and oversee external vendor compliance and investigations
  • Lead validation projects and ensure systems, processes, and documentation meet regulatory and internal standards
  • Provide quality oversight for change management systems, including complex Minor and Major Change Controls, ensuring stakeholder alignment and regulatory compliance
  • Suspend operations when necessary and act as final decision-maker on critical compliance determinations
  • Foster collaboration across QA/QC/Validation/Warehouse teams and promote a culture of quality and accountability
  • Mentor, coach, and train personnel at all levels; support development and implementation of training programs
  • Establish and refine QA processes and procedures to ensure robust compliance with cGMP operations
  • Manage PSC consultants supporting BioTechnique, ensuring alignment with project goals and compliance initiatives
  • Support Business Development (BD) and MSAT initiatives with quality strategy, technical input, and sponsor-facing engagement
  • Drive preparation for Pre-Approval Inspections, regulatory audits, and submissions
  • Communicate effectively with clients, vendors, and cross-functional teams to resolve investigations and ensure compliance
  • Stay current with evolving regulatory requirements and advise BioTechnique on necessary adaptations
  • May serve as consultant on external client projects, as needed
  • Perform other duties as required to support BioTechnique’s mission and operational success.

Requirements
  • Bachelor’s degree or higher from an accredited four-year university, preferably in life sciences, engineering, or a related technical field 
  • Advanced degree (MS, MBA, or equivalent)
  • Minimum of 15 years of experience in pharmaceutical quality assurance, with a focus on aseptic and sterile manufacturing
  • At least 5 years of leadership experience managing teams, projects, and priorities within complex matrixed organizations
  • Extensive experience in cleanroom operations, ISO standards, and cGMP environments
  • Proven track record in quality assurance, regulatory compliance, and validation within pharmaceutical or biotech industries
  • Advanced knowledge of FDA, EMA, and international regulatory frameworks
  • Deep understanding of cGMP, ISO, and other applicable quality standards
  • Experience preparing for and hosting regulatory inspections and client audits
  • Strong independent judgment and decision-making capabilities
  • Proven ability to lead cross-functional teams and external consultants
  • Demonstrated success in driving project execution and quality improvement initiatives
  • Ability to execute both strategic and tactical objectives across departments
  • Skilled in mentoring, training, and developing junior staff
Demonstrated Competencies
  • Quality, Compliance, and Validation Oversight – Deep understanding of FDA, EMA, and global regulatory standards, skilled in risk-based validation and regulatory reporting, and ensures manufacturing and documentation meet compliance expectations.
  • Team Leadership & Supervision – Supervises internal staff and external consultants, provides mentorship and training to improve team performance, and aligns team efforts with compliance goals and operational success
  • Regulatory Compliance & Industry Best Practices – Stays current with evolving regulations and industry trends, advises on necessary process changes to maintain compliance, and implements best practices across quality and validation functions.
  • Hybrid Leadership & Strategic Execution – Communicates effectively across PSC Biotech and BioTechnique, builds trust with cross-functional teams and leadership, and coordinates efforts between onsite and remote teams



Benefits
Offering a full suite of benefits, PSC Biotech™ is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance, so you not only enjoy your work, but also have the time and resources to live your life happy and healthy.
  • Medical, Dental, and Vision - PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents
  • Insurance options for Employee Assistance Programs, Basic Life Insurance, Short/Long Term Disability and more
  • 401(k) and 401(k) matching
  • PTO, Sick Time, and Paid Holidays
  • Education Assistance
  • Pet Insurance
  • Fitness Perks and Discounted Rates
  • Financial Perks and Discounts
Equal Opportunity Employment Statement

BioTechnique is committed to a policy of Equal Employment Opportunity with respect to all employees, interns, and applicants for employment. Consistent with this commitment, our policy is to comply with all applicable federal, state and local laws concerning employment discrimination. Accordingly, the Company prohibits discrimination against qualified employees, interns and applicants in all aspects of employment including, but not limited to: recruitment, interviewing, hiring (or failure or refusal to hire), evaluation, compensation, promotion, job assignment, transfer, demotion, training, leaves of absence, layoff, benefits, use of facilities, working conditions, termination and employer-sponsored activities and programs,  including wellness, social and recreational programs. Employment decisions will be made without regard to an applicant’s, employee’s, or intern’s actual or perceived: race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), national origin, age (40 or older), disability, genetic information, or any other status protected by law.

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