Manager, Quality Control

Job Overview

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Employment Type

Full-time
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Compensation

Salary
Range $11,000.00 - $146,000.00
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Benefits

Generous benefit options eligible first day of employment
Paid training
Paid vacation
Paid holidays
Career advancement opportunities
Education Reimbursement
401k Program with matching contributions
Learning platform

Job Description

Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of expertise in partnering with pharmaceutical and biotech companies to bring life-saving treatments to patients. The company is dedicated to advancing therapies from initial research stages to final cure, aiming to improve patients' lives worldwide. With a strong commitment to quality, innovation, and customer service, Curia offers a collaborative work environment that fosters growth, continuous learning, and career development. The company boasts comprehensive benefit options, including paid training, vacation and holidays starting from the first day of employment, education reimbursement, a 401K program with matching contributions, and access to a learning platform among others. Curia values inclusion and is an Equal Opportunity Employer, promoting a workplace free of discrimination and committed to safety and compliance standards.

The Manager of Quality Control position based in Camarillo, CA, is a pivotal leadership role responsible for overseeing the full spectrum of operations within Curia's Quality Control Laboratory. This role involves managing personnel, including hiring, conducting performance reviews, and scheduling to ensure optimum productivity and a positive work environment. The Manager will prepare and manage budgets, ensure the laboratory maintains audit readiness for all regulatory and customer audits, and develop key departmental metrics to monitor performance and progress. A vital aspect of the position is driving continuous improvement initiatives that enhance the efficiency, effectiveness, and compliance of all laboratory processes.

This role serves as the primary representative of the Quality Control department in both internal and external meetings, fostering strong collaboration with stakeholders and customers to deliver exceptional service. The Manager is tasked with ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), maintaining stringent quality standards critical to the pharmaceutical manufacturing process. Leading a team, this position encourages professional development by mentoring analysts and chemists, promoting analytical problem-solving skills, and guiding the team through complex challenges encountered in laboratory operations.

Additionally, the Manager of Quality Control is responsible for writing, reviewing, and approving essential documentation such as Standard Operating Procedures, project reports, timelines, acceptance methods, and test data summaries. They oversee computer system validation activities, ensuring all analytical equipment and instruments meet compliance standards. By fostering a culture of technical proficiency, ethical standards, and scientific creativity, this role is integral to Curia's mission of producing pharmaceutical products that meet the highest quality benchmarks. This position offers a salary range between $110,000 and $146,000 per year, reflecting the experience, education, and tenure of the successful candidate. Overall, the Manager of Quality Control is a strategic leader essential to the success and compliance of Curia's Quality Control laboratory operations, driving both quality excellence and operational efficiency for the company.

Job Requirements

  • Bachelor's degree in science, chemistry, biology or related field of study
  • Minimum of five years in analytical chemistry, quality assurance or regulatory compliance management
  • Minimum of two years in a leadership role
  • Minimum of five years in an aseptic/sterile product facility, preferred
  • Supervisory responsibilities
  • Must pass a background check
  • Must pass a drug screen
  • May be required to pass Occupational Health Screening
  • May be required to obtain and maintain gowning certification
  • May be required to obtain and maintain media qualification

Job Qualifications

  • Bachelor's degree in science, chemistry, biology or related field of study
  • Minimum of five years in analytical chemistry, quality assurance or regulatory compliance management
  • Minimum of two years in a leadership role
  • Minimum of five years in an aseptic/sterile product facility preferred
  • Supervisory experience
  • Strong analytical and problem-solving skills
  • Excellent oral and written communication skills
  • Ability to multitask and prioritize projects
  • Proven ability to develop continuous improvement plans

Job Duties

  • Complete tasks as required in a timely manner compliant with cGMP, regulatory and corporate requirements and conform to Health, Safety & Environmental responsibilities
  • Mentor chemists and analysts
  • Write, review, revise and approve Standard Operating Procedures, project progress reports, project timelines, acceptance methods, and test data (summary results)
  • Conduct and appropriately document laboratory investigations
  • Write, review and direct the execution of analytical protocols
  • Manage computer system validation (CSV) activities for analytical equipment/instruments
  • Demonstrate success in technical proficiency, scientific creativity, independent thought, and collaboration with others

Job Criteria

Experience

Mid Level (3-7 years)


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