QA Operations Supervisor

Posted Yesterday
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New Albany, OH, USA
In-Office
Junior
Pharmaceutical • Manufacturing
The Role
Supervise QA Technicians and lead quality oversight for sterile pharmaceutical manufacturing operations, including materials release, filling, packaging, deviations, investigations, CAPA, and compliance activities. Develop and revise GMP documentation, ensure adherence to company procedures and regulatory standards, and facilitate process improvements. The role requires cleanroom gowning and PPE use, strong organizational and communication skills, and leadership experience in a cGMP environment.
Summary Generated by Built In

Nature and Scope


This position, reporting to the QA Manufacturing Operations Manager, is responsible for leading QA Operations activities at a sterile manufacturing site. 

Essential Duties and Responsibilities

Nothing in this job description restricts management’s right to assign or reassign duties and responsibilities to this job at any time.

·       Supervise QA Technicians to assure timely and quality oversight of daily production activities including materials receipt/release, manufacturing/filling and packaging.

·       Lead on-site QA activities in investigating deviations or compliance issues associated with daily manufacturing operations.

·       Identify and facilitate the resolution of quality issues including deviations, investigations and CAPA in conjunction with senior QA staff.

·       Identify and facilitate quality process improvements to increase efficiencies and performance of systems, operations and personnel. 

·       Write and revise SOP’s and other GMP documentation.

·       Ensure all work is performed and documented in accordance with existing Company policies and procedures, as well as cGMP and health and safety requirements.

·       Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required.

·       Associate’s or Bachelor’s Degree in Life Sciences, Business or related field is required.

·       Minimum of 2 years of work experience in QA, Regulatory, Compliance or Pharmaceutical Operations in a cGMP environment is required.

·        Minimum of 1 year leadership experience required.

·       Experience in sterile pharmaceutical manufacturing preferred.

·       Extensive knowledge of cGMPs and other regulatory standards for Finished Product manufacturing.

·       Demonstrated success in managing multiple activities at the same time and producing outstanding results.

·       Excellent organizational, interpersonal and communication skills (oral and written).

Physical Environment and Requirements

·       Physically able to wear cleanroom/protective gowning and equipment, including but not limited to gowning, goggles, face shields, and protective gloves.  PPE is essential for the health and safety of employees. 

·       Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts) and color vision.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, or protected veteran status.

Applicants have rights under Federal Employment Laws.

  • FMLA poster: https://www.dol.gov/whd/regs/compliance/posters/fmlaen.pdf

  • Know Your Rights: Know Your Rights: Workplace discrimination is illegal (eeoc.gov)

  • Employee Polygraph Protection Act: https://www.dol.gov/whd/regs/compliance/posters/eppac.pdf

Alert: We’re aware of individuals impersonating our staff to target job seekers. Please note:

·         All legitimate communication will come directly from a verified ARI recruiter either by phone or via an americanregent.com email address.

·         Our recruiting process includes multiple in person and/or video interviews and assessments.

·         If you are unsure about the legitimacy of a message, contact John Rossini at [email protected]  before responding.

·         We never request payment, bank information, or personal financial details during our offer process.

Your security is important to us, and we encourage you to stay vigilant when job searching.

American Regent Inc. endeavors to make https://careers.americanregent.com/ accessible to any and all users.  If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please email [email protected].

Skills Required

  • Associate's or Bachelor's degree in Life Sciences, Business, or a related field
  • At least 2 years of experience in QA, Regulatory, Compliance, or Pharmaceutical Operations in a cGMP environment
  • At least 1 year of leadership experience
  • Experience in sterile pharmaceutical manufacturing
  • Extensive knowledge of cGMPs and regulatory standards for finished product manufacturing
  • Ability to manage multiple activities simultaneously and produce strong results
  • Excellent organizational, interpersonal, oral, and written communication skills
  • Ability to wear cleanroom and protective PPE, including gowning, goggles, face shields, and gloves
  • Correctable 20/20 near vision and color vision
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The Company
1,130 Employees

What We Do

American Regent, Inc., a Daiichi Sankyo Group Company, is a leading manufacturer of generic and branded specialty sterile injectable products. Dedicated to improving human and animal health, the company develops, manufactures, and supplies high-quality injectables for healthcare providers, clinics, and hospitals across the United States and Canada. Their expansive portfolio includes a strong focus on IV iron therapy and other critical specialty injectable medications.

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