Supervisor, Quality Assurance - 2Nd Shift

Under routine supervision, the Quality Assurance Supervisor oversees a staff of QA analysts, inspectors and technicians to ensure that raw materials in process materials, finished products and packaging are in compliance with chemical, biological, microbiological and/or physical quality control programs and external regulations.

• Lead ongoing daily departmental activities for areas of direct responsibility including supervision of assigned personnel, and when required assist other Quality areas in the successful performance of these activities.

• Manage activities of self and direct reports in achieving defined quality goals in an efficient, accurate and timely manner.

• Be directly involved in and where appropriate lead multiple process/product improvement projects which may include, Lean Manufacturing or other focus groups, design of experiments, validation protocols.

• Lead in-plant audit ready status efforts for assigned areas and assist other areas within the facility in understanding FDA, DEA and company quality requirements. Maintain a high level of expertise in current regulatory requirements, and serve as a plant resource for compliance to these requirements.

• Lead in the development of customer awareness and understanding activities for areas of direct responsibility, and where appropriate, assist and support such activities throughout the facility.

• Must be a recognized by all levels of the facility as an expert in their area and be able to demonstrate leadership ability.

• Must have the ability to perform the responsibilities of the Quality Section Manager on an as needed basis.

• Assists and writes validations for equipment, product changes and computer systems.

QUALIFICATIONS

• Minimum: Associates Degree in Science or related field with 10+ years applicable experience.

• Preferred: Bachelor's Degree in Science or related field with 2-3 years' Pharmaceutical Quality experience

EXPERIENCE

• Minimum: 10 years' experience in the pharmaceutical industry, in the fields of Quality Assurance or production

• Preferred: Supervisory Experience

SKILLS

• Understand scientific strategies and be able to invent new methods or new avenues of investigation

• Good interpersonal/communication/influencing/negation skills

• Good project management skills

• Working knowledge of FDA Regulations, Application of Good Laboratory Practices, and Application of Good Manufacturing Practices

• Lead Auditor training, ISO Lead Assessor training, with 2-3 years' experience in auditing techniques, interpreting regulations and quality systems

• Computer knowledge of common office applications required.

What We Offer

• Clean climate-controlled working environment

• Annual performance bonus potential

• 401k employer match up to 6% of your contributions

• 23 vacation/personal days

• 11 paid Company holidays

• Generous healthcare benefits

• Employee discount program

• Wellbeing rewards programs

• Safety and Quality is a top organizational priority

• Career advancement/growth opportunities

• Tuition Reimbursement

• Maternity and Parental Leave

• Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to a specific plan or program terms.

Location:

Cherry Hill, NJ, US, 08003

Nearest Major Market: Philadelphia