QC Supervisor - Weekend Shift

Hospira • Rocky Mount, NC

1d • Onsite

About The Position

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. You will play a crucial role in improving patients' lives by ensuring the highest standards of quality and safety in our products. Your leadership will be instrumental in driving innovation and excellence, ultimately making a global impact on patient health. Under the general guidance and functional direction of the CQ Laboratory Manager, the QC Supervisor is responsible for supervision of analysts performing chemical testing in a safe, compliant and efficient manner of raw materials, in process, and finished product samples. This position will evaluate analytical data to determine compliance with established specifications. The QC Supervisor is expected to resolve daily analytical and quality problems, generally without any additional high level technical assistance other than the chemical quality manager/director.

Requirements

• Applicant must have a bachelor's degree with at least 2 years of experience; OR a master's degree with more than 0+ years of experience; OR an associate's degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience.
• Strong written and verbal communication skills
• High level of organizational skills and independence.
• Strong judgment and decision making ability.
• Must be familiar with cGMP and cGLP for a pharmaceutical industry.

Responsibilities

• Consistently adheres to company, site, and laboratory safety rules and immediately raises any safety issues with supervision as soon as they are identified.
• Follows procedures at all times, adopting cGMP, cGDP practices.
• Supervision of QC Chem change control
• Schedule work sequences for documentation personnel and track progress of work sequences and provide feedback and coaching as required
• Participate in daily and weekly planning discussions with team offering suggestions to improve efficiency and schedule adherence.
• Resolve daily problems, generally without any additional high level technical assistance other than the chemical quality manager.
• Review and provide feedback on SOP’s, Investigations, and Reports as needed in the absence of Management.
• Spearhead special projects such as Continuous Improvement initiatives or process flow improvements
• Act as Liaison between lab analyst, data review, change control and investigations were appropriate
• Demonstrated strong technical and leadership skills
• Ability to serve as primary CQ representative on multidisciplinary project teams
• Act as Department representative for Internal and External Business tours and Audits

Benefits

• a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
• paid vacation, holiday and personal days
• paid caregiver/parental and medical leave
• health benefits to include medical, prescription drug, dental and vision coverage

What This Job Offers

• Job Type: Full-time
• Career Level: Manager